The Natural Repertory of Prof. William Nelson

Edited by Professor Emeritus Desire’ Dubounet, IMUNE ISBN 978-615-5169-68-7

The Natural Repertory

Prof. William Nelson

An In-Depth Understanding of Nelsonian Homeopathy

Including a Catalogue of all two-hundred Nelsonian Homeopathic Remedies

The Natural Repertory of Prof. William Nelson

Revised edition, 2008, William J. Cunningham White Dove Healing Arts, Ltd.

All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means electronic or mechanical, including photocopying, recording, or any other information retrieval system, without permission in writing from:

White Dove Healing Arts, Ltd. 10959 Lynne Avenue, Lafayette, Colorado 80026

Telephone (303) 828-4439

TABLE OF CONTENTS Introduction ______1 Quantum Quality Control ~ QQCTM______4 Combination Homeopathy______8 Regarding the Remedies______10 Homeopathy______15 Possible Mechanisms of Homeopathic Information Transfer______22 The Hormetic Philosophy______29 Nosodes______34 Isodes ______46 The Liquitrophic Philosophy______55 The Anodyne Philosophy______77 The Combination Philosophy______83 The Restorative Philosophy______94 Sarcodes ______96 Oriental Herbal Philosophy______106 Chinese Herbology and Homeopathy______115 The Miasm Philosophy______123 The Psychological Philosophy______127 Imponderable Homeopathy______131 Allersodes______138 The Dehabituate Philosophy______157 Vitamins and Powdered Products______159 Screening Groups Used in the Academy of Applied Quantum Biotechnology Computer Program______164 List of Homeopathic Remedies with Similar Herbal Action______188 An Advanced Treatise in Quantum Biology______198 Alphabetical List of Health Disorders and Chromosome Locations______214 Lectins______231 Venoms______239 Gemmotherapy______259 Classical Hahnemanian Singulars______262 A New Perspective on Research______264 Metabolic Pathways ______301

TABLES AND CHARTS

Periodic Table – Crystal Structure______12

Duplication Study______25

Comparison Chart: New Homeopathy – Allopathy______26

Inflammation: Part of the Defense Phase of Life______27

Chromosome Homeopathic______230

Snake Venoms Containing NGF______245

Distribution of Hemorrhagic, Lethal and Proteolytic Activities in Snake Venoms______247

Effect of Venoms from Different Species of Snakes on the Histamine (H) and Serotonin (S) Content of Isolated Rabbit Platelets______248

Summary of Immunopathology, Histopathology, and Electro-microscopic findings of the Kidney in Snakebite______254

Renal Failure with Known Lesions in Various Snakebites______255

DR. RECOMMENDS’ PLEDGE

First, do no harm

¾ We pledge to provide safe products and to educate practitioners in understanding their efficacy and using them safely.

Help ease misery and suffering

¾ We pledge to test and develop the highest quality products, and to educate practitioners in relieving causes of disease and to stimulate recovery.

Respect the natural process of God’s living world

¾ We pledge to remember that we do not know and that nature does know, thus, we shall use as natural a healing process as possible.

Provide research, consulting and education in natural, homeopathic and nutritional healing

¾ We pledge to broaden confidence through the realization that natural healing methods are superior to synthetic ones in the long run and often in the short term.

***

INTRODUCTION

A repertory is a compilation of the homeopathics used by a practitioner, and many have been written by homeopaths throughout the ages. This particular one is the Natural Repertory of Dr. William Nelson. With this book, homeopathy enters into the modern age in regard to toxicity, hormones, amino acids, minerals, vitamins, sarcodes, nosodes, allersodes, isodes, and classical homeopathy. This is by far, to date, the most extensive repertory ever compiled by any homeopath. Within these pages, there are many remedies that are used for the entire human condition. For every known disease, we have developed nosodes, sarcodes, isodes, allersodes, and classical treatments. Within this document, we propose a new vision of statistical analysis that will modernize homeopathy and bring it into the new age of modern medicine. We also offer a new definition of homeopathy here, one that is broader; from reversal (which is not apropos to all of homeopathy) to herbology, naturopathy, and all forms of natural medicine. Our new definition will show how homeopathy is the science of using the body to respond, rather than using external means, which is the philosophy of allopathy. Allopathy tries to artificially reduce symptoms, which can sometimes make the patient dependent on an external agent. In homeopathy, it is about working with a natural entity to try to balance the patient’s metabolism. At times, allopathy is used but only in its most gentle form in trying to stimulate the body to achieve balance by itself. We can fight symptoms allopathically while trying to produce harmony and natural health in the patient. Homeopathy is equivalent to system balance, and allopathy implies an external treatment of the symptoms. Within these pages, we present a new era of homeopathy, a new era of understanding and expansion of homeopathy from its limited confines to a broader based, total m edical system. 1

Many classic homeopaths may not completely understand everything within this treatise. They may struggle and try to rationalize against using the remedies. We only can hope that they will embrace the vision and understand how homeopathy can be used in dramatic, new ways. We feel history is being expanded within these pages, allowing the homeopath to broaden their base of understanding to encompass the total concept of biology and medicine. We welcome the open-minded reader to this exciting, new concept of homeopathic thinking.

Protocol for Wellness

¾ Relieve or diminish the causes of disease as much as possible, and improve on one’s lifestyle.

¾ Treat the organs of involvement by rebuilding, draining, de-toxing, and reconstructing. Use sarcodes (glandulars) and the correct structure and flow.

¾ Re-establish the balance of flow through adjustment, yoga, acupuncture, acupressure, electric field work, polarity techniques, etc.

¾ Relieve symptoms by balancing homeostasis through homeopathy. The use of combination homeopathics makes it safe and easy.

¾ Use nutrition, exercise, affirmation, massage, and stress reduction programs.

Our next challenge concerns the politics of free choice. We need to develop a safe system in which we can train and watch over these different wellness consultants, and to encourage the people of the United States to freely choose wellness intervention over crisis intervention.

Quantum Quality Control ~ QQCTM

Quantum Quality Control or Double QC (QQCTM) is a trademark of Dr. Nelson’s, developed by him to determine the finest quality control that can be utilized in the development of homeopathics. Walter Shewhart came up with the idea of superb quality control as the hallmark of a good business that would last through financial difficulties. He offered this technology to the Americans in the 1950s and early 60s, and American industry scoffed at him. W. Edward Deming collaborated with Shewhart and when the boom markets were not interested in incentives for quality, he eventually left America and found a welcome home in the Japanese market where quality control became the pinnacle of Japanese businesses. This helped the small nation which was recovering after the devastation of the World War to become a new economic power dominating the car market and electronics industries as well as many others through the utilization of quality control. Many surmise that purchases from the Orient are junk but these are rarely from Japan; more often they are from Taiwan or Hong Kong. The Japanese try to excel in quality control and make it a hallmark of their industry. Quality is the best way to build a business and quality control is the best tool. Using this model, we try to develop a quality control technique for homeopathy that would allow us to produce the finest homeopathic products. A complete description of this double QC process is included in the Quantum Vibrational Medicine of Dr. Nelson, in which the analysis of the different techniques and how they came about are explained. We go into the magnetic, static and conductance patterns and the trivector fields produced by bio-quantum homeopathics, and we explain the logical capacities of these homeopathics. Looking at the polymorphic state or liquid crystal effect is also well discussed in the book.

We wish to briefly discuss quality control to help doctors understand how Dr. Recommends can develop the finest homeopathics in the world. Many techniques are used, including superb intake or initial acceptance criteria to allow only the finest quality herb, hormone, enzyme, sarcode, nosode, isode or allersode. This way there is control each step of the process through the shape, structure, electrodynamics, Kirlian photography, and other dramatic means. Below are some profiles used to develop this QQCTM process. The QQCTM process includes developing the best statistical information on the product in a clinical setting, to make sure that the products not only fit our QQCTM process but also work in patient populations, guaranteeing safety and efficacy. Dr. Recommends has developed the finest in homeopathy, as well as the most extensive remedy list in the industry today. With these different compounds we have the finest medical pharmaceutical house in the world for the widest variety of ailments. We insist on:

¾ Statistical evaluation of clinical results to confirm safety and efficacy ¾ Raw material intake must begin with the best ¾ Kirlian photography to confirm bio-energy field stability ¾ Trivector analysis to confirm polymorphic liquid crystal state ¾ Cryogenic photography to confirm polymorphic liquid crystal state ¾ Spectro-photometry and atomic absorption to confirm bio-photon absorption and release ¾ Culture to confirm safety ¾ Chromatography to confirm safety ¾ Pro bono programs to give back by helping the poor ¾ Education for the doctor and the public

On the first page is the Dr. Recommends’ pledge which includes safety first, then efficacy. We revere nature in all that we do even though we realize that sometimes we must use synthetic pharmaceuticals to break up the damage done before. We revere the natural process in every way possible. We also provide education. A repertory can only outline products, and not really spell out their use. To obtain more information the reader is pointed to a list of books by Dr. Nelson that can be found at http://www.whitedovehealing.com/training/books.htm. (White Dove Healing Arts, Ltd.) Many of these books are on video and audio tape, which will help the practitioner with the wide range of health issues and encourage the use of some of these simple homeopathic techniques thus increasing cure rate, and helping patients in many new ways. It is hoped that these books offer data needed to continue broadening the ability to cure, so that diseases on earth can be a thing of the past by helping to provide simple, natural, safe, medical solutions. These techniques are utilized only by Dr. Recommends for quality control management to develop the finest homeopathics. Only by using the finest quality products can homeopaths truly succeed. The people of the world want natural medicines and a medical philosophy that works with the body, not against it. Homeopaths now need to maximize their results and can do so if the industry will focus on quality. The Dr. Recommends’ Quantum Quality Control consists of spectrophotometry and atomic absorption, electrolyte potential, Kirlian field analysis, bacteria and fungal cultures, rickettsia and viral detection, trivector analysis, cryogenic photography, and pilot and clinical testing. This thorough policy of product control provides the quality of product that everyone deserves. Double QC is the process of quality control which will assure the finest energetic remedies. The Nelsonian manufacturing process gives a more active homeopathic. Sea life, brain hormones, and enzymes are mixed 6 into each batch and an electrical potential current is run through the base alcohol and water to produce the finest homeopathics in the world.

The eight steps in Quantum Quality Control ~ QQCTM

¾ Raw materials intake (make sure you begin with the best) ¾ Kirlian photography (confirm bio-energy field stability) ¾ Trivector analysis (confirm electronic, magnetic, capacitance state) ¾ Cryogenic photography (confirm polymorphic liquid crystal state) ¾ Spectrophotometry and atomic absorption (confirm bio-photon absorption and release)

¾ Culture (confirm safety – no micro-organism growth) ¾ Chromatography (confirm safety – proper protein, hormone and enzyme existence)

¾ Statistical evaluation of clinical results (confirm safety and efficacy)

Combination Homeopathy

Classic homeopathy uses singular compounds in their basic form which were devised by Samuel Hahnemann. Hahnemann never realized the important fact that all the compounds he was using were combinations of many other compounds and elements. Apis mellifica is a very complex combination that nature has developed into a single energy pattern. There are over 50,000 known compounds in this singular remedy. The very principle of nature is combination in which many elements are blended into life. If we were to blend Apis mellifica with Lachesis, two biological compounds, we would get a new entity unlike each of them separately. Their effects might be amplified, cancelled or synergistically changed. The skill is to treat the combination as a new entity that needs scientific validation. Combination homeopathy involves one to blend or prepare different remedies for broader based action which most classic homeopathic combinations are used for. For just one patient we might take a specific group of allergens, isodes, nosodes, or sarcodes and combine them in a way that produces a combination specifically for the patient. The scientific art in combination homeopathy is covered in Quantum Vibrational Medicine. Much of combination homeopathy was developed to make the principles of homeopathy easy for practitioners to use. With combination homeopathy, doctors no longer have to remember the profile of each individual entity. They can remember simple terms such as “pain, heat improves” or “pain, cold improves.” The practitioner only has to know two different concepts in the face of pain; heat and cold. Combination homeopathy offers safety as well as an increased band of efficacy over most singular homeopathics. The argument for combination homeopathy includes several justifiable concepts that most singular 8

homeopaths may not truly know about. Most singular homeopaths argue circularly, and may never have tried combinations because they have superstitious or vague beliefs that only Hahnemann truly understood homeopathy, not even considering the fact that the world has changed dramatically since his time. This belief is often fostered by minds that resist new thinking and scientific improvements. This way of thinking and lack of science has held homeopathy back long enough. Dr. Nelson has devised many combination homeopathics that are easy to use by practitioners. These homeopathics are tested in statistical ways. If we look into the chapter called “A New Perspective on Research,” in Bio-Quantum Matrix, we can read some new statistical information that will prove the safety and efficacy of such formulas. In The Experimental Data on Homeopathy clinical tests validate results that prove homeopathy’s effectiveness. These many combinations teach homeopaths to use homeopathy in broader ways. Combination homeopathy offers the best techniques to entice allopathic medical doctors into the homeopathic camp as it can be taught very quickly and easily. A list of the many different combination remedies used by Dr. Recommends is included here. It goes way beyond homeopathic lines that existed before. We welcome the reader and practitioner to a new world of homeopathy and a deep understanding of how to utilize the combinations more significantly. After presenting this list, different types of remedies used for circulation, nerve disorders, digestion problems, immunology, and other types of sicknesses will be covered. This will allow the practitioner some viable shortcuts in using homeopathy.

Regarding the Remedies

The Dr. Recommends’ combination remedies are developed with several advantageous points in mind. They are as follows:

¾ Ease of use: Designed for the busy doctor to learn about and use. ¾ Guaranteed safety: Engineered to be safe – first don’t hurt. ¾ Effectiveness: Passed crucial quantum quality control procedures that surpass other homeopathics in the world. ¾ Affordable: Easily affordable. ¾ High quality service: Delivery on special order items beats most regular deliver. ¾ FDA registered: Registered with the FDA (National Drug Code/ NDC numbers) and are also registered in Canada (Drug Identification Number/DIN), Australia, and the Common Market. ¾ World wide distribution.

This catalog contains the most dramatic homeopathic remedies ever engineered. The Dr. Recommends’ remedies are scientifically formulated and contain many trace elements from the Polymorphic Periodic Table developed by Dr. James Isaacs. Trace elements have profound biological effects by producing stimulating and stabilizing effects on the body. Trace element therapies are used in conjunction with scientifically developed sarcodes, nosodes and isodes. The shape and atomic structure of these elements are used in making the Dr. Recommends’ remedies the most effective homeopathics in the world. Dr. Recommends’ remedies use very high potencies, along with lower potencies, in a homochord blend. This unique, scientific combining of the homochords guarantee their safety and effectiveness. To ensure the quality of the product, Dr. Recommends’ remedies are quantum quality

controlled using the QQCTM techniques. This produces the finest and most profound healing combinations. Dr. Recommends’ remedies are made with the Nelsonian manufacturing process which activates electrical, synergistic, polymorphic and energetic potentials. Unfortunately, the Nelsonian process increases the energy so well that electronic duplicators and imprinters cannot duplicate these formulas. The Dr. Recommends’ remedies are designed to blend with each other and work together for health. Any contraindication to the mixing of these remedies will be noted. These remedies are safe and easy to use.

Periodic Table – Crystal Structure

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 H He 1 Hex Hex Li Be B C N O F Ne 2 Cub Hex Rhom Hex Hex Cub Cub Cub

Na Mg Al Si P S Cl Ar 3 Cub Hex Cub Cub Mono Ortho Ortho Cub K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 4 Cub Cub Hex Hex Cub Cub Cub Cub Hex Cub Cub Hex Ortho Cub Rhom Hex Ortho Cub Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe 5 Cub Cub Hex Hex Cub Cub Hex Hex Cub Cub Cub Hex Tet Tet Rhom Hex Ortho Cub Cs Ba * Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn 6 Cub Cub Hex Cub Cub Hex Hex Cub Cub Cub Rhom Hex Cub Rhom Mono ? Cub Fr Ra ** Rf Db Sg Bh Hs Mt Uun Uuu Uub 7 Cub Cub ? ? ? ? ? ? ? ? ?

* La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hex Cub Hex Hex Hex Rhom Cub Hex Hex Hex Hex Hex Hex Cub Hex ** Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr Cub Cub Ortho Ortho Ortho Mono Hex ? ? ? ? ? ? ? ? Crystal Structure Abbreviations Hex Hexagonal Rhom Rhombohedral Cub Cubic Mono Monoclinic Ortho Orthorhombic Tet Tetragonal ? Unknown http://www.chemicalelements.com/show/crystalstructure.html

HOW THE COMBINATION REMEDIES ARE USED

¾ Homeopathy can be used as nutritional supplementation. If we use a homeopathic compound such as Vitamin B to supplement the body’s deficiency syndrome, then homeopathy is used in a nutritional sense. A concentrated source of B-12 which is diluted, one part to ten, six times, arrives at a 6x. This is approximately equal to the RDA of B12, 5 micrograms. Homeopathic remedies made for nutritional supplementation can be found in the Liquitrophics and Vitamin sections. Vitamins in the minimal dose can also be used to regulate metabolism of the vitamins. The theories of Dr. Royal Lee, the Father of Natural Vitamins, proved that low doses of natural, high quality vitamins can do the job better than mega dose, synthetic vitamins. ¾ Homeopathy can be used to help stimulate the body. If a low dose homeopathic of Belladonna is used, it is possible to achieve the low-dose pharmacological action. This will trigger the body to stimulate its own healing. The vast difference between homeopathy and allopathy is that homeopathy does not incur dependence, but rather uses the minimal dose philosophy and gently shifts the patient towards restoring health. Homeopathy stimulates the body where allopathy works against the symptoms. ¾ Homeopathy can be used in classic ways to help reverse symptoms. Homeopathy can help reverse symptoms and stimulate the body to return to the balance of its cybernetic systems. Homeopathy encourages homeostasis and cure without side effects. In homeopathy, the symptoms are messengers of underlying imbalances; whereas allopathy works in synthetic ways to only control symptoms. ¾ Homeopathy works to encourage energetic stabilization. Homeopathy encourages energetic stabilization by encouraging 13

correct tissue development with sarcodes, reducing allergic reactivity with allersodes, increasing hormetic detox with nosodes, stabilizing synthetic reactions with isodes and producing healing effects with imponderables and classic remedies.

Classification of the Remedies

Dr. Recommends’ remedies are classified in the following manner: ¾ Over the counter (OTC). This category does not require a prescription from a medical doctor. It is sold to the public and it is safe to use. It does not require professional training to be obtained. ¾ Professional Use. This category includes such practitioners as licensed naturopaths, massage therapists, or other professionals who do not have a license to dispense pharmaceuticals. ¾ Rx. The remedies in this category can only be prescribed by a licensed medical professional within the states.

Homeopathy

The theory and practice of homeopathy is strange to those of us who are accustomed to conventional Western medicine. But we all sense the rightness of a healing system which conceives of all symptoms as parts of a larger whole, which appears to stimulate the body’s natural healing force rather than attack its parts. Homeopathy seems to work with us, not on us. It assists our innate biological intelligence to be healthy. When we break a bone, it is our innate intelligence that repairs it. In fact, our bodies can heal themselves of dramatic diseases. Homeopathy encourages and maximizes our innate intelligence to cure ourselves. At one time, homeopathy was the number one form of medicine in the United States. Allopathy rose to precedence when the culture turned towards the economically driven development of synthetic chemicals and turned its back on natural healing techniques. Now homeopathy is experiencing regeneration in the United States. The rise in iatrogenic diseases and synthetic chemical problems has reintroduced the importance of choosing natural healing techniques. Homeopathy is the science of healing from within, or prompting the organism to heal itself. Homeopathics are used to stimulate the organism toward its own state of homeostasis (balance). Homeopathy is a concept of minimal dose which Samuel Hahnemann, the Father of Homeopathy, discovered while trying to determine the smallest amount of a pharmacological agent that could gently nudge the patient back into the biological cybernetics of health. Using a “feather” to stimulate such a balance is the principle of homeopathy. Throughout history, disease has been viewed from two fundamentally different perspectives: One, as a malfunction of specific components of the body, where symptoms are seen as the disease itself, and two, where symptoms are a result of a deeper disturbance or imbalance of the person as a whole, and where symptoms are simply the outward 15 manifestation. Disease is the blockage of the flow of life, and symptoms are the body’s way of dealing with the blockage. Symptoms just point the way towards natural homeostasis and homeopathic cure. Perspective number one is the basis underlying modern orthodox medicine. Whatever symptoms arise, they are counteracted by drugs, e.g., an antihistamine for a histamine reaction, an analgesic for pain, steroids for inflammation, an MAO inhibitor for depression, an antipyretic for fever, etc. In allopathy, 95 percent of all pharmacology works against symptoms and against the body. However, perspective number two is an ancient concept which underlies the entire holistic health movement, including homeopathy. Nature is revered and utilized to balance the system. The innate intelligence is worked with, not against. With homeopathy, side effects are relatively unknown. Symptoms are not the disease, they merely accompany the disease. Symptoms are evidence of disease. But treating symptoms is like killing the messenger for bringing bad news. In fact, by treating symptoms you are suppressing the body’s natural responses and inhibiting the healing process, interfering with life. As far back as 190 years ago, long before the term “holistic health” was coined, homeopaths recognized the inseparability of body and mind. Homeopaths have always stressed the importance of assessing the totality of the person. Homeopathic medicines thus have physiological activity. Violinist Yehudi Menuhin once said, “Homeopathy is one of the rare medical approaches which carries no penalties – only benefits.” In theory, there is no reason why orthodox medicine should not embrace homeopathy as an ally.

Significance of Homeopathy

There is a growing consensus in the world that the massive expenditures on medical research have failed to demonstrate any significant improvement in society’s level of health. The incidence of major chronic diseases like cancer, diabetes and heart disease has continued to climb, and medical costs have soared beyond the means of the average person. More and more, doctors and lay people alike are searching for alternatives. Homeopathy offers a time tested method which satisfies the need for a more economical and non-toxic therapy. It encompasses all areas of medical care – prevention, emergency and acute care, and chronic disease treatment. Homeopathy offers the individual and society improved health, productivity, and enjoyment of life.

Advantages of Combination Homeopathic Therapy

¾ Combination homeopathic remedies are safe, effective and compatible with all types of medical, surgical, psychological, physical and nutritional therapies.

¾ Homeopathy is the safest method for treating infants, children, elderly patients and individuals who have an allergic history of drug reaction.

¾ Combination homeopathic remedies provide a wider range of utility.

¾ Combination homeopathics offer increased safety due to fewer side effects.

¾ Iatrogenic or toxic reactions are rare.

¾ Fatal poisoning is unheard of.

¾ Recovery is usually progressive.

¾ Disorders for which no specific medication is available may respond to homeopathics.

¾ Homeopathy can rescue the medical establishment from its drug addiction.

¾ The expense is minimal.

¾ Homeopathy stimulates the body into a healing process – it goes beyond just treating the symptoms.

¾ Combination homeopathy is easy to learn and to use.

AMERICA IS PREPARED MEDICALLY FOR EVERYTHING

We have: The most hospitals The most drug stores The most pharmacists The most nursing homes The most medical doctors The most medical schools The most surgical operations The most clinical laboratories The most nurses and nurses’ aides The most education about disease The most publicity about diseases The most “sick” insurance policies The most medical scientific research The most pharmaceutical companies The most “sick” insurance companies The most physician office laboratories The most medical research in the world The most health societies and associations The most radio and television “sick” talk about disease The most federal government medical agencies A USDA, FDA, HCFA, CDC AND SURGEON GENERAL The most State and local health agencies

WITH

THE WORLDS’S HIGHEST MEDICAL COSTS EVERYTHING BUT GOOD HEALTH

“Any serious proposal that is genuinely designed to prevent disease will be sure to meet with stubborn opposition from those who have a vested interest in disease. Prevention, if genuine, would put the disease treaters out of business. Without the sick man the entire medical industry would collapse, consequently, it becomes necessary that there shall always be a sick man.” - Herbert Sheldon

BUT IT DOESN’T’ HAVE TO BE.

PREVENTION OF DISEASE

Every person can prevent disease. Every person can attract disease. The list of diseases below can create more suffering and affect more lives and more people than earthquakes, floods or other natural disasters in the United States. Yet man devotes more time and money to control natural disasters than to prevent disease. The cause for most of the non-infectious diseases listed below can be food related.

One does not have to be ¾ One of the 1 million who will be diagnosed with cancer this year ¾ One of the 1 million who die of cancer each year. ¾ One of the 1 million who die of heart disease ¾ One of the 400,000 new cases of skin cancer each year. ¾ One of the 126,000 new cases of colon cancer each year. ¾ One of the 99,000 new cases of uterine cancer each year. ¾ One of the 38,000 new cases of bladder cancer each year. ¾ One of the 45 million who suffer headaches. ¾ One of the 35 million who suffer from allergy. ¾ One of the 7 million who have coronary artery disease. ¾ One of the 37 million who suffer from hypertension. ¾ One of the 9 million who suffer from asthma. ¾ One of the 1.6 million suffering from gout. ¾ One of the 100 million who suffer from chronic back pain. ¾ One of the 36 million who suffer from hearing loss. ¾ One of the 24.5 million who have cataracts. ¾ One of the 26 million who suffer from gallstones. ¾ One of the 6.5 million who suffer from osteoporosis. ¾ One of the 225,000 to undergo angioplasty. ¾ One of the 35 million to suffer from candidiasis. ¾ One of the 35 million to undergo surgery each year. ¾ One of 36 million who can’t afford ‘sick’ insurance. ¾ One of the 6.9 million currently confined to a nursing home for long term nursing care. The projection for the year 2040 is 18 million.

Dangers of Homeopathic Utilization

¾ Masking a major disorder: This may provoke a patient to not seek proper medical care. If symptoms persist, seek medical attention; always work with a doctor’s supervision for maximum safety. Try to choose a physician who is reverent of nature and reluctant to use synthetics.

¾ Alcohol sensitivities: If alcohol sensitive, the homeopathic drops may be put into a 3 oz. glass of warm water. Allow 1 minute for alcohol to evaporate. If the problem persists, alcohol sensitive persons may get remedies in pills without alcohol.

¾ Provings: This is a symptom caused by a homeopathic, and it is usually mild in appearance. If the homeopathic is terminated and symptoms abate in 24 hours, it could be a proving; if symptoms continue after 24 hours, then it is unlikely they were caused by the homeopathic. It is natural for modest symptoms to be exhibited during the healing and cleansing of the body. When symptoms grow in intensity or for a prolonged length of time seek professional help.

The Food and Drug Administration (FDA) recognizes the Homeopathic Pharmacopoeia of the United States (HPUS) regulations, which indicate how remedies should be made, dispensed and utilized by homeopathic practitioners. The remedies in this catalog are registered with the FDA, following HPUS guidelines.

POSSIBLE MECHANISMS OF HOMEOPATHIC INFORMATION TRANSFER

Homeopathy is a medical art used for centuries to treat illness. But what are the ways in which a homeopathic can work? Please see the list below:

¾ Pharmacology: Low potency products which in dilute form follow two laws: Arundt-Schultz Law – A very small dose of a poison has reverse effects of the larger mega dose, i.e., homeopathic belladonna relieves the redness and dryness that raw belladonna produces. Law of Initial Values – As the quantity of substance is proportionately reduced the potent effectiveness can elevate, paradoxically reverse, or reduce depending on the substance itself. ¾ Imprinting of a message into the polymorphic structure of the carrier water and alcohol mixture. Here the clath-rate structure of water is changed to receive a message and transfer this message to a patient. The receptors for this message would be on the cell membrane and be similar to olfactory receptors of the nose. This might explain the ability of strong odors to block homeopathy. ¾ Quantic storage of information in the quantic states of the electrons, atoms, and molecules of the carrier fluid. This transfer would be disrupted by sunlight, x-ray, or other photon or particle release. Homeopathics are sensitive to the same. Energy is needed for this shift and possibly could be supplied by succussion. (There seems to be a minimum of times a product needs to be succussed: 10 to 15 times).

¾ Energetic and electrical pattern of the homeopathic. By analyzing the spectral reactions of the homeopathic to conductance, electrons, inductance (magnetic relativity), and capacitance (static reactance). This gives a trivector analysis of the electrical signature of the homeopathic. ¾ Storage might take place in dimensions beyond the 1st, 2nd, 3rd, and 4th. Some shift of matter in dimensions 4, 5, and 6 might be a possible place for memory storage of a homeopathic. This might explain the imponderables of homeopathy or the power of energy healing. This is measured by correlating the virtual biophotons of a homeopathic.

In the second mode, the memory ability of water and alcohol is mentioned. This phenomena can be studied through photon scattering tests, nuclear magnetic resonance and simplest of all, freezing. If the water holds a plastic amorphous memory in liquid form as it enters solid form, this shape should have some effect on the ice patterns. A freezer that maintains -5c within 1 degree was used to crystallize the substances. The homeopathics used were less than 5% alcohol to allow proper freezing. They were put into 1 in. circular 1/8 in. deep trays, and then allowed to cool in the refrigerator for 2 hours at +5c before insertion into the freezer at -5c. After 12 hours, the disks were frozen and allowed investigation. Patterns would form on the homeopathics. There was indeed some shape transfer even beyond 25x where probabilities of product existing are minuscule. Another easy way to measure energetic homeopathics is through Kirlian photography. This involves simply placing the product in a highly charged electrical field through a container or rare electron gasses. The electric charge fluoresces the gas, but the homeopathic acts as a prism to direct the charge and each homeopathic produces its own fingerprint or pattern of colors to identify it. These charged particles will be enhanced 23 by the polymorphic shape of the water, the quantic states of the sub- molecular bodies and perhaps by the quasi-dimensional memory. It is also interesting to note that so called duplicated remedies show no fingerprint under freezing or Kirlian photography.

Duplicated Remedies and Homoepathic Information Transfer

As has been discussed, there are several possible modes of information transfer. Duplicators work on a supposed magnetic transfer. In the first mode, which involves chemical action, magnetics would not work for information transfer. In the second and third modes, the mechanical force of succussion could change electron or molecular quantic states. Magnetics cannot effect this change. If magnetics could indeed do so, then homeopathy would be useless. The magnetic interference from a T.V. set or a telephone unit would change the information. Transport of a homeopathic through the magnetic lines of the earth would change the information and nullify homeopathic effectiveness. As mentioned, duplicated remedies show no change in freezing patterns or in Kirlian photography. Duplicated remedies are probably advanced placebo at best. To test this supposition, an experiment was performed with double blind capacity. Procedure: 35 patients were chosen from a naturopathic Doctor’s practice. All patients were using certain homeopathics on a regular basis and knew what results to expect. Some patients used a Candida nosode to control bloating or other bodily symptoms; others used Belladonna or Lachesis. All were familiar with their remedy’s effect. Each patient was given either a regular homeopathic or a duplicated remedy. Each patient was also given either a placebo sugar pill, or a pill with 5mg. Narcan (Naloxone). Naloxone is used to block endorphin response and has been found to block the placebo effect in placebo responsive patients. Patient profiles were chosen to exclude those with 24

symptoms of pain as Naloxone can increase pain perception. The test was double blind with neither patient nor practitioner knowing which formula was given. Patients were given questionnaires to evaluate the efficacy of the remedy. Results of the effectiveness are shown in the accompanying diagram. Results: The tests show that the duplicated remedy performed significantly lower than the real remedy. The placebo blocking Narcan pill significantly lowered efficacy (63% is approximately the predicted placebo effect). Perhaps the information transfer of mode number 4 (multi-dimensional transfer) could account for the transfer of duplicators; Narcan with its endorphin blocking action might also block other dimensional information transfer. Even so, the study shows a markedly decreased efficacy with the duplicated remedy. Radionic remedies have no pharmacology, quantic state or polymorphic state, thus, they are not homeopathics and homeopathy is continually blamed for radionic remedies that fail. Here again, quality is often not paramount to homeopaths. Some prefer the greater monetary reward duplicators or imprinters provide. This lack of focus on quality and maximization of effectiveness could erode our industry. Only through quality and dedication to developing and delivering the finest homeopathics can we truly succeed. If you want the best, at affordable prices, Dr. Recommend’s remedies are for you.

DUPLICATION STUDY Placebo Duplicated Real (Imprinted) Homeopathic Placebo 55% 63% 97% Narcan 10% 11% 96%

COMPARISON CHART

NEW HOMEOPATHY ALLOPATHY Very small chance of side effects Very great chance of side effects Minimal cost Usually high costs Safe for children and elderly Warning of risks if not used correctly Non-addictive Creates dependency Works by letting patient reestablish Works by externally blocking, homeostasis stimulating, or interfering with the body Little if any malpractice, due to Major malpractice suits. Iatrogenic safety disease is on the increase Philosophy: body’s reactions are an Philosophy: Body is stupid and intelligent attempt to deal with malfunctions often; it then needs to toxicity and other disease-causing be stimulated, blocked, or fooled by conditions the doctor and his synthetic medication Easy to use Takes years of experience Safe for environment, natural Manufacturing hurts environment Tries to cure Tries to sedate reactions

Tries to treat whole body Tries to reduce patients to mere metabolically symptoms The patient is an individual The patient is a set of symptoms

Symptoms are only a part of a Symptoms are bearers of bad news, complex set of problems and we should kill the messenger Pain is God’s gift, and life’s way of Pain is the enemy and must be telling us about underlying covered up. Improperly reduces problems inflammation Stimulates immune system Weakens immune system. Sensitive to energetic problems of Ignores energetic nature of the the body body

INFLAMMATION Part of the Defense Phase of Life Sympathetic, Acidosis, Hyaluronidase, Hydrolysis, Tissue Bouillon, Hypertony, Histamine

Homeopathy/Naturopathy Allopathy Holistically Driven Symptom Driven

Defense Management Suppression Restoration of Homeostasis Chemotherapeutics Release of Etiology Antibiotics, Antipyretics Minimal Dose Steroids, Anti-Inflammatories NSAID

Precipitate Develops as System Balance Restored Biology/Reacts to Synthetic Compounds/Mega-Doses of Drugs/Builds Dependency

System Release of Auto Produces Wild (Illegal/Improper) Toxins Peptides (Overdose of Drugs) Reduced Cascades Induces Anti-Body Cascade

Proper Anti-Body Release Produces Improper Auto Anti-Bodies

Cure Produces Auto Aggression Diseases: Lupus, Arthritis, Asthma, etc.

HOMEOPATHIC INSTRUCTION

¾ Take nothing by mouth 10 – 15 minutes prior to and following dosage. This includes food, drink, cigarettes, chewing gum, toothpaste, etc.

¾ Limit caffeine or nicotine in any form, such as soda pop, coffee, chocolate, cigarettes. If necessary use one hour after taking a homeopathic

¾ Limit mint in any form, such as candy mints, mint toothpaste, mint mouthwash.

¾ No camphor, as in muscle and joint rubs. Avoid moth ball fumes.

¾ If dental drilling or trauma to mouth occurs, use topically for 48 hours.

¾ Limit breathing of strong smells, such as paint thinner, eucalyptus, cigarette smoke (especially menthol).

¾ Limit raw garlic, onions and strong spices to one hour after taking a homeopathic. Cooked garlic is ok.

¾ Place drops under the tongue and hold for 10 seconds to allow for absorption.

¾ Keep homeopathics out of direct sunlight and x-ray.

¾ Homeopathics may generally be taken at the same time with other suggested homeopathics.

¾ Homeopathics should not be mixed with Liquitrophics and should be taken 20 minutes apart.

CAUTION: Alcohol sensitivities – If a person is sensitive to alcohol, put the drops into a 3 oz. glass of warm water. Allow one minute for alcohol to evaporate. Pills are also available without alcohol. By following these guidelines, you will give the remedies the greatest opportunity to succeed.

THE HORMETIC PHILOSOPHY

Over the last hundred years, man has drastically increased his toxic exposure through the development of synthetics. Present day scientists have found in a new study of hormesis that tickle doses, small trace doses of a toxin, can have stimulatory effects on the body. Hormesis stimulates a cell’s defense system. In hormesis the homeostatic balance is tipped, forcing the body to take measures to protect itself or the effect where a toxic substance acts like a stimulant in small doses but acts as an inhibitor in large doses. The Dr. Recommends’ hormetic remedies cover a wide variety of toxic conditions including asbestos poisoning, beauty shop toxins, environmental toxins, industrial toxins, mercury amalgams and more. The Dr. Recommends’ formulas are safe yet powerful in their ability to stimulate the individual to detoxify without inducing a healing crisis. The high-end potencies used in the Dr. Recommends’ remedies are counterbalanced by the lower dose remedies mixed in the homochords. These highly engineered hormetic remedies can be used for increased safety and effectiveness, producing a more stable and safer remedy for doctors to use with their patients.

HORMETIC REMEDIES

AMEBA-FUGE (1 fl. oz.) Catalog No. 0005 Indication: Ameba infections Ingredients: Diloxanide Furoate Metronidazole 3x. Artemisia absinthium, Bismuthum Metallicum, Allium sativum, Ipecacuanha 6x. Ammonium Phosphoricum 6x, 12x. Ferrum phosphoricum 6x, 12x, 30x. Ameba, Entamoeba histolytica, Naegleria fowleri 24x, 40x, 75x, 120x, 300x, 500x.

ASBESTOS (1 fl. oz.) Catalog No. 0006 Indication: Asbestos sensitivity, Assists in detox Ingredients: Zincum Valerianicum 5x. Lung sarcode 6x, 12x, 30x, 60x, 100x. Iodium 12x. Silicea 12x, 30x, 60x. Asbestos 25x, 60x, 100x, 350x, 500x.

BACTERIA-FUGE (1 fl. oz.) Catalog No. 0007 Indication: Bacterial infections Ingredients: Hydrastis canadensis 3x, 6x, 12x, 30x, 100x. Zincum Metallicum 4x, 12x. Aloe socotrina 6x. Allium sativum, Arum maculatum 12x. Mercurius Vivus 16x. Broad-based Bacillinum, Pyrogenium, Anthracinum, Staphysagria 16x-30x, 100x. Diphtherinum, Streptococcinum, Staphylococcinum, Pneumococcinum, Syphilinum, Botulinum, Tuberculinum 16x-30x, 100x, 500-1000x. Eucalyptol 20x. Lac caninum, Lac vaccinum 30x.

COSMETIC MATERIALS (1 fl. oz.) Catalog No. 0008 Indication: Cosmetic material sensitivity, Assists in detox Ingredients: Natrum Carbonicum 4x. Manganum Metallicum 6x. Formalinum 10x, 30x, 100x, 500x. Nitricum Acidum, Phosphoricum Acidum, Hypophysis, Sulphur 12x. Miscellaneous Beauty Shop Toxins 30x, 60x, 100x, 750x, 1100x. Kali Cyanatum 20x, 30x, 60x, 100x.

DENTAL MATERIALS (1 fl. oz.) Catalog No. 0004 Indication: Dental material sensitivity, Assists in detox Ingredients: Caries, Gingivitis, Periodontitis 16x, 20x, 30x. Root Ostitis 20x, 30x. Argentum Metallicum, Mercurius Solubilis, Aurum Metallicum, Platinum Metallicum, Dental Materials (Amalgams, Composites, Bonding Resins, Dentin Bonders, Cavity Liners, Metals, Ceramics, Cements, Temporary Restoratives, Root Canal Materials, Anesthetics, Denture Materials, Flourides) 30x, 60x, 100x, 500x, 1000x.

ENVIRONMENTAL POLLUTANTS (1 fl. oz.) Catalog No. 0011 Indication: Water and air pollution sensitivity, Assists in detox Ingredients: Zincum Metallicum 3x. Chlorophyllum 5x. Manganum Metallicum 5x, 12x. Taraxacum officinale 6x, 12x, 30x. Formalinum 8x, 12x, 30x, 100x, 500x. Petroleum 16x, 20x, 30x, 60x, 100x, 500x, 1000x. Air Pollution 50x, 155x, 700x. Water Pollution 50x, 500x. Hydrocarbonum 60x.

FOOD ADDITIVES (1 fl. oz.) Catalog No. 0001 Indication: Food additive sensitivity, Assists in detox Ingredients: Berberis vulgaris, Plantago major 3x, 6x, 12x, 30x. Zincum Metallicum, Lycopodium clavatum, Selenium Metallicum 6x, 30x. Graphites, Taraxacum officinale, Arctium 8x, 12x. Petroleum 13x, 24x, 100x, 500x. Miscellaneous Food Additives 30x, 60x, 100x, 500x, 1000x.

FUNGI-FUGE (1 fl. oz.) Catalog No. 0012 Indication: Fungal infections Ingredients: Tabebuia impetiginosa, Equisetum arvense 3x. Natrum Muriaticum 4x. Colostrum 6x, 12x. Bovine Glandulars: Thymus, Liver, Lymph, Spleen 5x, 12x, 30x, 60x, 100x. Manganum Metallicum, Selenium Metallicum, Zincum Metallicum, Allium sativum 6x. Bovista 6x, 12x. Usnea barbata, Amanita muscaria, Saccharomyces, Ustilago maidis, Borax 6x, 12x, 30x. Apis mellifica 12x. Graphites 16x, 30x. Chlorinum, Iodium 20x, 30x, 100x. Candida albicans, Candida parapsilosis, Blastomyces, Molds, Epidermophyton, Chlamydia, Geotrichum 30x, 60x, 100x, 500x, 1000x, 50m. Mercurius Solubilis, Salarinum, Antibiotics 50x, 100x.

HALOGENS (1 fl. oz.) Catalog No. 0010 Indication: Chlorine or fluorine sensitivity, Assists in detox Ingredients: Zincum Metallicum, Selenium Metallicum 6x. Chlorinum, Bromium, Fluorine 6x, 12x, 30x, 40x, 100x, 500x, 1000x. Diatomum 12x, 30x, 60x. Mercury 100x.

INDUSTRIAL POLLUTANTS (1 fl. oz.) Catalog No. 0013 Indication: Industrial pollution sensitivity, Assists in detox Ingredients: Taraxacum officinale, Chlorophyllum, Plantago major 4x, 12x, 30x. Selenium Metallicum 6x. Silicea 7x. Plumbum Metallicum 12x. Zincum Metallicum, Iodium 30x, 60x, 100x. Industrial Toxins 40x, 40c, 40m.

INSECTICIDES (1 fl oz.) Catalog No. 0002 Indication: Insecticide sensitivity, Assists in detoxification. Ingredients: Taraxacum officinale, Plantago major 3x. Carduus marianus 4x. Natrum Muriaticum 6x. Cholecystokinin, Acetylcholinesterase, Acetylcholine 20x, 30x, 60x, 100x. Organo Phosphates, Miscellaneous Synthetic Insecticides and Herbicides 30x, 60x, 100x, 500x, 1000x.

METALS (1 fl. oz.) Catalog No. 0014 Indication: Metal sensitivity, Assists in detox Ingredients: Plantago major 4x, 6x-12x. Silicea 6x, 12x, 30x. Kali Muriaticum, Kali Phosphoricum, Liver Sarcode, Kidney Sarcode: 6x, 12x, 30x, 60x, 100x. Aluminum Metallicum, Aurum Metallicum, Cadmium Metallicum, Beryllium Metallicum, Niccolum Metallicum, Mercurius Vivus, Amalgam, Argentum Metallicum, Plumbum Metallicum, Stannum Metallicum, Selenium Metallicum, Rubidium, Radon, Radium, Cobaltum Metallicum, Molybdenum, Antimony, Uranium, Bismuthum Metallicum, Platinum Metallicum 30x-30c, 30m.

RADIATION (1 fl. oz.) Catalog No. 0003 Indication: Radiation sensitivity, Assists in detox Ingredients: Sodium Alginate 2x. Citrus limonum 3x. Hydrangea arborescens 4x. Iodium, Sarcodes: Adrenalinum, Brain, Thyroidinum 6x, 12x, 30x, 60x, 100x. Imponderables: X-ray, Color TV, Microwave, Gamma Radiations 6x, 12x, 30x. Phosphorus 12x. Radium Bromatum 22x, 60x, 100x, 500x, 1000x. EMR Spectrum 100x.

SYNTHETIC CHEMICALS (1 fl. oz.) Catalog No. 0009 Indication: Synthetic pharmaceutical sensitivity, Assists in detox Ingredients: Natrum Muriaticum 3x. Kali Nitricum 6x. Platinum Metallicum 8x. Plumbum Metallicum, Graphites, Lac defloratum 8x, 12x, 30x, 100x. Vaccinotoxinum 16x, 30x, 60x. Pharmaceutical Toxins 60x, 100x, 500x, 1000x.

VERMI-FUGE (1 fl. oz.) Catalog No. 0015 Indication: Intestinal parasite infections Ingredients: Absinthium 3x, 6x. Sulphur 4x. Rhamnus purshiana, Cinchona officinalis, Juglans nigra, Ferrum Phosphoricum 6x. Magnesium Metallicum 7x. Cymbopogon citratus 8x. Mercurius Solubilis 12x. Nosodes of Various Helminths, Nematodes and Intestinal Parasites 12x-30x, 60x, 100x, 500x, 1000x.

VIRAL-FUGE (1 fl. oz.) Catalog No. 0016 Indication: Viral infections Ingredients: Trifolium pratense, Echinacea purpurea, Natrum Muriaticum, Asclepias tuberosa, Ferrum Iodatum, Zincum Metallicum 3x. Ferrum Phosphoricum 4x. Lac Vaccinum, Euphrasia officinalis 6x. Thuja occidentalis 6x, 12x, 30x, 60x, 100x. Camphora, Calcarea Arsenicica, Arium Virus, Ichthyolum, Selenium Metallicum 12x. Vaccinotoxinum, Morinum, Variolinum, Miscellaneous Influenzinum, Psorinum, Vincetoxicum 12x, 30x, 60x, 100x, 500x, 1000x, 50m. Aurum Metallicum, Platinum Metallicum, Uranium 60x-100x.

NOSODES

Nosodal therapy involves using disease-causing or disease-containing tissues and diluting them to cause reversal effects. This is the basic principle of vaccination and homeopathy. Diseased tissue can be used to alleviate disease conditions. This is the science of nosodal homeopathy. A nosode is a homeopathic or diluted and energized form of the diseased entity. Within this treatise, a list of the following are included: bacteria, worms, viruses, fungi, protozoa, rickettsia, and many other tissues; as well as medical nosodes of various diseases and diseased tissues. Also included are: dental toxins that allow the dentist to use different disease- causing dental material from the nosodal tray. There is a wide range of nosodal factors used by modern homeopaths. Those known to Dr. Nelson are contained in this document. To reference some experimental data behind nosodal homeopathy we point the reader to The Experimental Data on Homeopathy, by Dr. William Nelson. Within the pages of that document one can read about how nosodal homeopathy is used to reverse disease conditions. Homeopathy offers a safe alternative to vaccination which has very similar modes of operation. Even new ideas of DNA and RNA theory can be ascertained with this new homeopathy.

VIRUSES

CONJUNTIVITIS, VIRAL MALARIA COMMON WARTS AND MONILA ALBACANS VIRAL CONDOMYLOMA COMPONENT COXSACKIE NOSLAMINT DIPTHERIA PLANTERS WARTS EPSTEIN BARR POLIO MYELITIS ESCHERICOLI VIRAL Q FEVER COMPONENT RETRO-VIR FAEKALALK RHINOPNEUMONIA HEPATITIS A ROCKY MOUNTAIN SPOTTED HEPATITIS B FEVER HERPES PROGENTALIS SWINE INFLUENZA HERPES SIMPLEX TRICHINOSIS HERPES ZOSTER V GRIPPE HUMAN PAPPILOMA VIRUS VAPCH GRIPPE INFECTIOUS MONONUCLEOSIS VA2 GRIPPE INFLUENCINIUM VA2 LGRIPPE INFLUENZA V2 GRIPPE INFLUENZA (BERIN 55) V3 GRIPPE INFLUENZA 83 V4 GRIPPE INFLUENZA 84 V5 GRIPPE INFLUENZA 85 V20 GRIPPE–V50 GRIPPE INFLUENZA 86 V60 GRIPPE–V76 GRIPPE INFLUENZA 87 RETROVIRUS1–RETROVIRUS10 INFLUENZA 88 VIRUS

FUNGUS

ADNEXITIS CRYPTOTOCCUS 4 ASPERGILLUS, FLAVUS, CRYPTOTOCCUS 5 FUMIGATUS, GLAUCUS, CYRTOCOCUS NEOFORMS NIGER, TERRUS EPIDERMOPHYTON 1 BLASTOMYCOCES 1 EPIDERMOPHYTON 2 BLASTOMYCOCES 2 EPIDERMOPHYTON 3 BLASTOMYCOCES 3 EPIDERMOPHYTON 4 BLASTOMYCOCES 4 FUNGUS FLORA CANDIDA ALBICANS HISTOPLASMOSIS 1 CANDIDA GLABRATA HISTOPLASMOSIS 2 CANDIDA GUILLIER HISTOPLASMOSIS 3 CANDIDA KRUSEI HISTOPLAMSOSIS 4 CANDIDA LAUERENTI HISTOPLASMOSIS 5 CANDIDA LIPOLYTI NEOFORMS 1 CANDIDA LUSITANI NEOFORMS 2 CANDIDA ORIENTALIS NEOFORMS 3 CANDIDA PARAPSILOSA PNEUMOCYSTOSIS CANDIDA PSEUDOTROPICALIS SACROMYCOSES 1 – CANDIDA RUGOSA SACROMYCOSES 7 CANDIDA STELLATO SCEREVISI CANDIDA TAMATA TINEA CURTIS CANDIDA TROPICALIS TINEA CURVIS CRYPTOTOCCUS 1 TINEA PEDIS CRYPTOTOCCUS 2 TYCO SPORON CRYPTOTOCCUS 3

BACTERIA

ACTINOMYSOSIS ADNEXITIS AEROBACTER AMOEBA AMOEBA HEPAR ABSCESSUS ANTHRAX ASCARIDINUM BAC. GARTNER BAC. MORGAN BACILLUS ANTHRACIS – ANTHRAX, MALIGNANT PUSTULE BACTEROIDES BARTONELLOSIS BIFIDUS BOTULINUM BRUCELLOSIS CARIES CAUCAUOUS CHLAMYDIA TRACHOMATIS CHOLERA DYSENTERY ECOLI ENCEPHALITIS ENTEROCOCCINUM FRANCISELLA TULARENIS – TULAREMIA GASTROENTEROCOLI HAEMOPHILUS INFLUENZA KAWASAKI KLEBSIELLA PNEUMONIAE LEGIONELLA LISTERIA MONOCYTOGENES LYMES MELIOIDOSIS MENINGOCOCCINUM MORBILLINUM MYCOPLASMA PNEUMONIAE MYOBACTERIUM LEPRAE – LEPROMATOUS LEPROSY NEISSERIA GONORRHOEAE NOCARDIA NOS. ELEPHANTIASIS NOS. FISHPYROGENIUM (FRESHWATER) NOS. RHINOPNEUMONITIS OXYUREN PEPTOSTREPTOCOCCUS ANAER. PLASMODIUM SPP. – MALARIA 37

BACTERIA, cont.

PNEUMOCCIN PNEUMOCOCCUS PROGENIUM PROPIONIBACTERIUM ACNES – ACNE PROTEUS PSEUDOMONAS PYOCYANEUS R. MOOSERI R. QUINTANA – TRENCH FEVER R. RICKETTESII RICKETTSIA PROWAZEKII RUBEOLA SAB ACIDOPHILUS/BIFIDUS SALMONELLA TP SCARLATINUM SHIGA KRUSE SHIGELLA PARADYSENTERIAE SPRILLUL MINUS – RAT-BITE FEVER STAPHYL AUREUS STAPHYL PYOGENES – IMPETIGO STAPHYLOCOCCIN STAPHYLOCOCCUS EPIDERMIDIS – ACNE STREPTOBACILLUS MONILIFORMIS – RAT-BITE FEVER STREPTOCOCCIN STREPTOCOCCUS HAEMOLYTICUS SYPHILIS TERSENIA PESTIS – PLAGUE TETANUS THERMAL BACTERIA TOXOPLASMOSIS TREPONEMA CARATEUM – PINTA TREPONEMA PALLIDUM – SYPHILIS (SECONDARY) TREPONEMA PERTENUE – YAWS TRICHINELLA SPIRALIS, MAN TUBERCULINUM TULEREMIA TYPHOIDINUM TYPHUS VACCININUM

NOSODES, DENTAL

ASTRO 1180 KETAC-CEM AUTOPOLYMERISAT LIFE (AUTOACRYLAT) LUCITONE 199 BARRIER MARCAINE BIO C MOLYBDENUM BIO H NOBILIUM C & B METABOND NOS. ACUTE BACTERIAL CARBOCAINE 2% OSTITIS OF THE JAW CARBOCAINE 3% NOS. ACUTE PULPITIS CARBOXYLAT-CEMENT NOS. APICAL GRANULOMA CAVIT-G NOS. CARIES CERAMCO II NOS. CHRON. BACT. OSTITIS COMPOS FULL MATERIAL OF JAW COMPSPAN OPAQUE NOS. CHRON. PULPITIS COMPSPAN RESIN NOS. CORYNEBACTERIUM CONCEPT NOS. CYST EPITHELIAL CONQUEST DF NOS. DENTAL SACK COPALITE NOS. EAR SCLEROSIS COPPERAMALGAM NOS. EPULIS DEGUNDENT G NOS. EXUDATIVE OSTITIS DENTAL GOLD NOS. FATTY OSTITIS OF JAW DG-63 NOS. FISTULA DENTALIS DICOR NOS. FOLLICLUARE CYST DISPERSAL NOS. FUNDUS ABSCESS CURELON NOS. GANGRANOSE PULPA DYCAL NOS. GINGIVITIS E-2713 NOS. GRANULMOA PURULENT EBA NOS. JAW OSTITIS FIRMILAY NOS. NECROTIC GINGIVITIS FLECK’S NOS. OSTEOSCLEROSIS GC DENTIN CEMENT OF THE JAW GEL KAM NOS. PARODONTOSE GINGIVITIS NOS. PAROTIS DENTAL GLUMA PART 3 CALCULI GUTTA PERCHA NOS. PARULIS (STAPH. AUX.) HELIOBOND NOS. PARULIS (STREPTOC. HELIOMOLAR MUC.) HERCULITE XR NOS. PERIODONTAL FIBROM HYDROXYAPATITE NOS. PERIODONTAL POCKET HYDROXYLINE NOS. PERIODONTITIS HP-3 NOS. PULPAL STONE IN-CERAM NOS. RADICULAR CYST JELENKO O NOS. ROOT CANAL TX JET ACRYLIC NOS. ROOT GRANULOMIUM 39

NOSODES, DENTAL, cont.

NOS. ULCERATIVE GINGIVITIS PURE ALLOY NUPRO NEUTRAL REXILLIUM V OCCLUSIN ROOT GRANULOMIUM OLYMPIA RX-IV OPTEC DENTIN SCOTCHBOND II OPTEC HSP SCOTCHPREP OPTEC U-BOND SEALAPEX ORAL MUCOCUTANEUS SILUX PLUS PAPILOMA SODIUM FLUORIDE P-10 SPC PERIODONTO COMPLEX P-50 STAINLESS STEEL PALLADIUM SILVER TERM PERTAC TICONIUM PHOSPHATE-CEMENT TITANIUM POLYMERISAT (ACRYLAT) TITANIUM ALLOY PORSELITE DUAL TRIADVLC POST-COM II VINYLPOLYMERISAT PRISMA APH VITA VMK 68 PRISMA DENTIN VITADUR N PRISMA U-BOND 3 VITRA BOND PROFILE 2-1 PROTEMP XR BAND PULP CANAL SEALER XR DENTIN PULPDENT XYLOCAINE 2% ZOE 2200 ZONE

NOSODES, MEDICAL

ACID PHOSPHATES CONTARACTA SENILIS ALBUMIN, COWMILK CO2 CONTENT ALKALINE PHOSPHATASE COPPER SERUM ALPHA GLOBULIN CPK ALPHA1 GLOBULIN CR. WHOLE BLOOD ALPHA2 GLOBULIN CU. WHOLE BLOOD ALUMINUM SERUM CREATINE ALUMINUM WHOLE BLOOD CREATINI AMPYCILLIN DIFFERENTIAL TESTS ARTERIAL OXYGEN AFTER ENCEPHALOMELOMALACIA PURE OXYGEN ENDOMETRITIS ARTERIAL OXYGEN TUBERCULOSSA SATURATION EOSINOPHIL ASTHMA BRONCHITIS FASTING BLOOD SUGAR BASOS GALACTOSE IN BLOOD BETA GLOBULIN GAMMA GLOBULIN BICARBONATE SERUM GLOBULIN BLEEDING TIME GLUCOSE BLOOD AMMONIA HEMOGLOBIN BLOOD LACTATE LEVEL HEPATITIS BLOOD PYRUVATE LEVEL IRON SERUM BLOOD UREA NITRATE IRON WHOLE BLOOD LEVEL LACTIC DEHYDROGENASE BLOOD VOLUME LDH BUN LEAD SERUM CADMIUM SERUM LEAD WHOLE BLOOD CADMIUM WHOLE BLOOD LIPID TRIGLYCER CALCIUM SERUM LIPOPROTEIN SERUM CALCIUM WHOLE BLOOD LUPUS CALCULI PROSTATAE LUPUS ERYTHEMATOSIS CALCULI RENALES LYMPHS CALCULI RENALES MANGANESE OXALIC ACID MERCURY SERUM CALCULI VESICALES MERCURY WHOLE BLOOD CAPILLARY FRAGILITY MN. WHOLE BLOOD CATARACTA BRUNESCENS MONOS CATARACTA COMPLICAT MULTIPLE SCLEROSIS CELL MORPHOLOGY NERUALGIE CHOLESTEROL NEUROFIBROM CHOLESTEROL ESTER NICKEL SERUM SERUM NICKEL WHOLE BLOOD CHROMIUM SERUM NODULAR PROSTATIC CHRONIC CYSTITIS AND HYPERPLASIA ENDOMETRIOSIS NOS. BLADDER BIHARZIOSIS 41

NOSODES, MEDICAL, cont. SODIUM SERUM SODIUM WHOLE BLOOD NOS. BLADDER POLYP SPIROMETRIC STUDIES NOS. BLADDER Tbc THROMBIN TIME NOS. CYSTOPYELITIS TIMED VITAL CAPACITY NOS. FIBROADENOM TONSILLA MAMMA TONSILLA PHARYNGEA NOS. KIDNEY PAPILOMA TOTAL BILIRUBIN NOS. MAMMA FIBROMATOSIS TOTAL LIPIDS NOS. MASTITIS TOTAL LUNG CAPACITY NOS. MASTOPATHIA CYSTICA TOTAL PROTEIN NOS. OXALIC ACID URICA TRANSAMINASES NOS. PERIORCHITIS TRICHOMONAS VAGINITIS NOS. PROSTATA-ADENOM T3 VERTEBRAE NOS. SOLITARY CYST (KIDNEY) T4 VERTEBRAE NOS. TESTICULAR FISTULA Tbc T7 VERTEBRAE NOS URETHRITIS POST MASC URIC ACID PARTIAL THROMBOPLASTIN VAGINITIS TIME VITAL CAPACITY PHOSPHATE SERUM WBC PHOSPHATE WHOLE BLOOD WILSON PHOSPHOLIPIDS ZINC SERUM PLASMA KETONES ZINC WHOLE BLOOD PLATELET COUNT 2 HOUR POSTPRANDIAL PLEURITIS BLOOD SERUM POTASSIUM SERUM POTASSIUM WHOLE BLOOD PROGRESSIVE MUSCULAR DYSTROPHIE PROTHROMBIN CONSUMPTION PROTHROMBIN TIME PSA PSORIASIS RED BLOOD COUNT RESIDUAL VOLUME

RETICULOCYTE SE. WHOLE BLOOD SEGS PMN SELENIUM SERUM SGOT SGPT SINUSITIS FLONTALIS SINUSITIS MAXILLARIS 42

PARASITES

AMIDOSTOMUM ANSERIS, BIRD ANCYLOSTOMA CANIUM, DOG, CAT ANCYLOSTOMA DUODENALE, MAN ANCYLOSTOMA TUBAEFORME, CAT ANGIOSTRONGYLUS CANTONENSIS, MAN ANGIOSTRONGYLUS VASORUM, DOG ANOPLOCEPHALA MAGNA, HORSE APOPHALLUS DONICUS, DOG, CAT ASCARIDIA GALLI, BIRD ASCARIS LUMBRICOIDES, MAN ASCAROPS STRONGYLINA, PIG ASPICULIRIS TETRAPTERA, MOUSE, RAT CAPILLARIA AEROPHILA, CAT, DOG CAPILLARIA BREVIPES, BIRD CAPILLARIA FELIS-CATI, CAT CAPILLARIA OBSIGNATA, BIRD CAPILLARIA PLICA, DOG CAPILLARIA PUTORII, DOG, CAT CATATROPIS VERRUCOSA, BIRD CHILOMASTIX MESNILI, MAN CYATHOSTOMA SPP., HORSE CYSTICAULUS OCREATUS, SHEEP DAVAINEA PROGLOTTINA, BIRD DELAFONDIA VULGARIS, HORSE DICROCOELIUM LANCEATUM, MAN DICTYOCAULUS FILARIA, SHEEP DIENTAMOEBA FRAGILIS, MAN DIOCTOPHYMA RENALE, DOG DIPHYLLOBOTHRIUM LATUM, MAN, DOG, CAT DIPYLIDIUM CANINUM, MAN, DOG, CAT DIROFILARIA IMMITIS, DOG ECHINOCOCCUS GRANULOSUS, DOG ECHINOCOCCUS MULTILOCULARIS, DOG ECHINOSTOMA RECURVATUM, BIRD ECHINOSTOMA REVOLUTUM, BIRD ENDOLIMAX NANA, MAN ENTAMOEBA COLI, MAN ENTAMOEBA GINGIVALIS, MAN ENTAMOEBA HISTOLYTICA, MAN ENTEROBIUS VERMICULARIS, MAN FASCIOLA HEPATICA, MAN GIARDIA LAMBLIA GRAPHIDIUM STRIGOSUM, HARE

PARASITES, cont.

HABRONEMA MUSCAE, HORSE HAEMONCUS CONTORTUS, SHEEP HAEMONCUS PLACEI, CATTLE HETERAKIS GALLINARUM, BIRD HYDATIGERA TAENIAEFORMIS, DOG, CAT HYMENOLEPIS DIMINUTA, MAN HYMENOLEPIS NANA, MAN IODAMOEBA WILLIAMS, MAN MARSHALLAGIA MARSHALLI, MAN MESOCESTOIDES LINEATUS, DOG, CAT MESOSTEPHANUS SP., CAT METASTRONGYLINAE, PIG MEULTBRAU MUELLERIUS CAPILLARIS, SHEEP MULTICEPS GAIGERI, DOG MULTICEPS MULTICEPS, DOG MULTICEPS SERIALIS, DOG MULTICEPS SMYTHI, DOG NECATOR AMERICANUS, MAN NEMATODIRUS FILICOLLIS, CATTLE NEMATODIRUS SPATHIGER, CATTLE NEMATOSPIROIDES DUBIA, RAT, MOUSE NIPPOSTRONGYLUS BRASILIENSIS, RAT, MOUSE OESOPHAGOSTOMUM DENTATUM, PIC OLLULANUS TRICUSPIS, DOG, CAT ONCHOCERCA, MAN OPISTORCHIS FELINEUS, MAN PARAMPHIS CERVI, CATTLE PROBSTMAYRIA VIVIPARA, HORSE PROSTHOGONUMUS OVATUS, BIRD PROTOSTRONGYLUS RUFESCENS, SHEEP RAILLIETINA ECHINOBOTHRIDA, BIRD SCHISTOSOMA BOVIS, CATTLE SCHISTOSOMA HAEMATOBIUM, MAN SCHISTOSOMA MANSONI, MAN SPIROCERCA LUPI, DOG STEPHANURUS DENTATUS, PIG STRONGYLOIDES STERCORALIS, MAN, DOG, CAT STRONGYLUS EQUINUS, HORSE SYNGAMUS TRACHEA, BIRDS SYPHACIA MURIS, RAT, MOUSE SYPHACIA OBVELATA, MOUSE, RAT TAENIA CERVI, DOG TAENIA CRASSICEPS, DOG 44

PARASITES, cont.

TAENIA HYDATIGENA, DOG, CAT TAENIA KRABBEI, DOG TAENIA OVIS, DOG TAENIA PISIFORMIS, DOG, CAT TAENIA SAGINATUM, MAN TAENIA SOLIUM, MAN THELAZIA RHODESII, CATTLE TOXASCARIS LEONINA, DOG TOXOCARA CANIS, DOG TOXOCARA CATI, CAT TRICHINELLA SPIRALIS, MAN TRICHOMONAS HOMINIS, MAN TRICHOSTRONGYLUS AXEI, CATTLE TRICHOSTRONGYLUS TENUIS, BIRDS TRICHURIS SERRATA, CAT TRICHURIS TRICHIURA, MAN TRICHURIS VULPIS, DOG TROPISURUS FISSIINUS, BIRD UNCINARIA STENOCEPHALA, DOG, CAT

ISODES

It is stated in The Experimental Data on Homeopathy by Dr. William Nelson, that isodal homeopathy includes using different synthetic compounds that can cause disease, even including body secretions. The form of isodal therapy that we will concentrate on is that of different synthetic compounds and pollutants that can cause disease. Dr. Nelson has devised many combinations known as xenobiotics that deal with broad-based detoxification. There is also a large list of pollutants that can be developed in homeopathic form and various combinations for trained homeopaths to use. In this chapter there is a long list of pollutants and disease-causing factors caused from heavy metals, insecticides, food additives, etc., included. This challenging form of homeopathy offers exciting new ways to deal with an increasingly polluted world. Many of these compounds have the potential to be extremely dangerous and must have strict controls which are exercised by Dr. Recommends. It is necessary to make sure that the items rendered by licensed doctors are safe to use. The pledge of Dr. Recommends is to make safety very important. Welcome reader to an exciting new world of expanded homeopathy, a world that was unknown to Hahnemann as many of these chemicals did not exist during his time, but they are a big part of the structure of disease today. Our patients must be cleansed and detoxified of these noxious chemicals. In The Experimental Data on Homeopathy, evidence is offered for homeopathy’s effectiveness in this area. The new field of hormesis research also offers additional evidence for isodal homeopathy’s ability to help the patient.

POLLUTANTS I

ABIETIC ACID ALUMINUM FLUORIDE ABRIN ALUMINUM FORMATE ACENAPHTHENE ALUMINUM METHYL ACERDOL ALUMINUM PICRATE ACETAL ALVARTHR ACETAMIDE ALYPIN ACETAMIDINE AMATOL HYDROCHLORIDE AMINOMETHANE ACETATE RAYON AMINOPTERIN ACETOACET-o-CHLORANILIDE AMINOPYRINE ACETOACETIC ACID AMMONIA-d3 ACETOGUANAMINE AMMONIA GAS ACETONE PEROXIDE AMMONIUM ARSENATE ACETONE SEMICARBAZONE AMMONIUM AZIDE ACETULAN AMMONIUM BICHROMATE ACETYL IODIDE AMMONIUM BIFLUORIDE ACETYL TRIETHYL CITRATE AMMONIUM BINOXALATE ACETYBUTYROLACTONE AMMONIUM BROMATE ACETYLENE AMMONIUM CHLORATE ACETYLENE TETRACHLORIDE AMMONIUM CHLOROOSMATE ACETYLSALICYLIC ACID AMMONIUM ACRIDINE CHLOROPALLADITE ACROLEIN AMMONIUM CYANIDE ACTINIUM AMMONIUM EMBELATE ADIPIC ACID AMMONIUM FLUOGALLATE ADIPONITRILE AMMONIUM PICRATE ALDRIN AMMONIUM SELENITE ALIZARIN AMMONIUM THIOCYANATE ALKALOID SALTS AMYL ALCOHOL ALLOXANTIN AMYL NITRITE ALLYL AMINE AMYL SILICATE ALLYL CHLORIDE AMYLOFORM ALLYL CHLOROPHENYL ANABASINE CARBONATE ANILINE ALLYL FLUORIDE ANILINE BRILLIANT GREEN ALLYL FORMATE ANILINE FLUORIDE ALLYL IODIDE ANILINE GREEN ALLYL THIOUREA ANILINE HYDROCHLORIDE ALLYLENE ANILITE ALUMINUM BROMIDE ANISOLE ALUMINUM BROMATE ANTHRAROBIN ALUMINUM CARBIDE ANTIMONY TRIETHYL ALUMINUM CHLORATE ANTIPYRINE ALUMINUM CHLORIDE APHRODINE, YOHIMBINE 47

POLLUTANTS I, cont.

APOMORPHINE BEETHLE ARSANILIC ACID BENZALDEHYDE ARSENIC BENZEDRINE ARSENIC TRISELENIDE BENZENE ARSENIC TRISULFIDE BENZENE HEXACHLORIDE ARSENOBENZENE BENZHYDROL ARSINE BENZIDINE ASCARIDOLE BENZIL ASPIRIN BENZOIC ACID ATROPINE BENZOIN AUROUS CYANIDE BENZYL MRCAPTAN AUTUNITE BENZYLAMINE AZOBENZENE BERYL AZOCHLORAMIDE BERBERINE n-AMYLENE BETA RAYS o-AMINOETHYLBENZENE BETEL p-AMINOBENZOIC ACID BIMETHYL sec-AMYL ACETATE BISMUTH sec-n-AMYL ALCOHOL BISULFITES 2-ACETAMIDOFLUORENE BITHIONOL 2-AMINOETHANOL BORAX BARBITUATES BORAZOLE BARIUM ARSENIDE BORIC ACID BARIUM CARBIDE BOROCAINE BARIUM CHLORIDE BROMATES BARIUM CHROMATE BROMIDES BARIUM CYANIDE BUTYLATED HYDROXYANISOLE BARIUM MYRISTATE n-BUTYL GLYCIDYL ETHER BARIUM NITRATE DI-TERT-BUTYL –p-CRESOL HIGH EXPLOSIVES

POLLUTANTS II

BROMINE CHLORAL HYDRATE BROMOPHORM CHLORATES BROMOPICRIN CHLORAZINE BRUCINE CHLORDANE BUTANE CHLOREX BUTANOL ALCOHOL CHLORIC ACID BUTYL ALCOHOL CHLORINATED NAPHTHALENES BUTESIN CHLORINE DIOXIDE BUTOXYL CHLORINE HYDRATE BUTYLAMINE CHLORINE TRIFLUORIDE BUTYN CHLOROACETONE BUTYRIC ACID CHLOROALDEHYDE BUTYRONE CHLORHYDO 2-BUTYNE CHLORIDES CACODYL CHLORINE CADMIUM SERUM CHLOROBENZENE CAFFEINE CHLOROBENZOL CALCIMINE CHLOROBUTANOL CALCITE CHLOROETHENE CALCIUM CYANAMIDE CHLOROETHYNE CALCIUM HYDROXIDE CHLOROFORMIUM CAMPHENE CHLOROPICRIN CAMPHOR CHLOROPRENE CANNABIS CYCLOHEXANE CANTHARIDES m-CHLOROANILINE CAPROIC ACID m-CHLORONITROBENZENE CAPRYLIC ACID m-CHLOROPHENOL CARBAMIDE o-CHLOROPHENOL CARBITOL m-CHLOROPHENYL CARBOLIC ACID ISOCYANATE CARBOLINEUM o-CHLOROPHENYL ISOCYANATE CARBON TETRACHLORIDE p-CHLORO-o-NITROANILINE CARBONYLS 2-CHLORO-6-NITROTOLUENE CARBORUNDUM DECALIN CARBOWAX DEMETON CARNAUBA WAX DIBORANE CELLOIDIN DICOBALT OCTACARBONYL CELLULOID DIETHYL CARBONATE CERIUM DIETHYL SULFATE CESIUM DIETHYLAMINE CETAB DIETHYLENE GLYCOL CEVADINE DIETHYLPHOSPHINE CHELIDONINE DIHYDROPYRAN CHLORAL DIIODOACETYLENE 49

POLLUTANTS II, cont.

DIIODOFORMOXIME ETHYL OXALATE DIKETENE ETHYL SILICATE DIMETHYL BERYLLIUM ETHYL TRICHLOROSILANE DIMETHYL ETHER ETHYLAMINE DIMETHYL SULFATE ETHYLBENZENE DIMETHYLDIOXANE ETHYLDICHLOROARSINE DINITRO-o-sec-BUTYL PHENOL ETHYLENE CHLOROBROMIDE DINITROCHLOROHYDRIN ETHYLENE GLYCOL DINITRODICHLOROBENZENE ETHYLENEDIAMINE DINITROGEN TRIOXIDE ETHYLIDENE CHLORIDE DIONIN FERBAM DIPHENYL FERRIC NITRATE DIPHENYLCYANOARSINE FERRIC OXALATE DIPHOSGENE FERRIC SULFIDE DITAINE FIBERGLASS o-DIMETHYL PHTHALATE FLUOACETATES ECGONINE FLUOBERYLLATES EMERY FLUORIDES EPHEDRINE HCL FLUOROACETIC ACIDE ETHYL ACETATE FLUOSILICATES ETHYL ACRYLATE FLUOSULFONIC ACID ETHYL ALCOHOL FORMALDEHYDE ETHYL BROMIDE DEHYDROGENASE ETHYL BUTYL KETONE FORMIC ACID ETHYL ETHER FORMYL FLUORIDE ETHYL FLUOROSULFONATE FURAN ETHYL IODIDE FURFURAL ETHYL ISOTHIOCYANATE GAMBOGE ETHYL MERCAPTAN GASOLINE ETHYL NITRATE

POLLUTANTS III

GILSONITE LACQUERS SLYCERYL DIACETATE LACTIC ACID GLYOXAL LANTHANUM SULFATE GRANITE DUST LAUDANINE HANANE LEAD AZIDE HENNA LITHIUM ORATATE (PILL) HEPTAFLUOROUTYRIC ACID LUMINAL HEPTANE LUPERCO HEPTYL ACETATE LUPERSOL HEXACHLOROACETONE LUPININE HEXACHLOROMETHYL ETHER LYCONINE HEXACHLORONAPHTHALENE NICKEL ARSENIDE HEXACHLOROPROPENE NICKEL CARBIDE HEXAETHYL TETRAPHOSPHATE NICKEL CARBONYL HEXENE-1 NICKEL CHLORATE HYDRAZINE NICKEL CHLORIDE HYDRAZOIC ACID NICKEL IODIDE HYDROCHLORIC ACID NICKEL NITRATE HYDROFLUORIC ACID NICKEL PEROXIDE HYDROFLUOSILICIC ACID NICKEL SULFATE HYDROGEN PEROXIDE NICOTINE HYDROGEN SELENIDE NICOTINE SULFATE HYDROXYLAMINE NIRVANOL HYPOIODOUS ACID NITRIC ACID p-HYDROQUINONE NITRIC OXIDE INDIUM NITRITES IODIC ACID NITROBENZENE IODOFORM NITROETHANE IPECAC NITROGEN CHLORIDE IROKO NITROGLYCERIN IRON PENTACARBONYL NITRONAPHTHALENE ISOAMYL ACETATE NITROPRUSSIDES ISOAMYL FORMATE NITROSYL BROMIDE ISOBUTYL ALCOHOL NITROSYL SULFURIC ACID ISOOCTANE NITRYL CHLORIDE ISOPRENE NORNICOTINE ISOPROPYL ALCOHOL p-NITROPHENOL ISOPROPYL ETHER OCTACHLORO-CAMPHENE ISOPROPYLAMINE OCTADECYL JUNIPER BERRIES TRICHLOROSILANE KAPOK OCTAMETHYL KEROSENE PYROPHOSPHORAMIDE KETENE OCTANE KRYOFIN OCTYL ALDEHYDE 51

POLLUTANTS III, cont.

OLEFINS OLEUM OPIUM ORRIS ORTOL OXALATES OXALIC ACID OXALYL CHLORIDE

POLLUTANTS IV

OZONE PYRROLIDINE PARAFORMALDEHYDE QUARTZ PARALDEHYDE QUINOLINE PARATHION QUINONE PELARGONIC MORPHOLIDE RADON PENTACHLOROMETHYL ETHER RESOURCINOL PENTACHLORONAPHTHALENE RICIN PENTACHLOROPHENOL RICININE PENTASOL ROSIN PERBENZOIOC ACID ROTENONE PERCHLORATES RUBIDIUM PERCHLORIC ACID RUTHENIUM PERCHLOROETHYLENE SAFROLE PERIODIC ACID SALICYLICANILIDE PERONINE SAPONINS PEROXY SULFURIC ACID SARIN PERTHANE SILANES PHENACAINE HYDROCHLORIDE SILICA PHENOTHIAZINE SILICON CHLORIDE PHENOTHIOXIN SISAL PHENYL CARBYLAMINE SODIUM CHLORATE CHLORIDE SODIUM ETHYL XANTHATE PHENYL MUSTARD OIL SODIUM HYDROXIDE PHENYLHYDRAZINE SODIUM NITROPRUSSIDE PHENYLTRICHLOROSILANE SODIUM PEROXIDE PHOSGENE SOMAN PHOSPHINE SORBIC ACID PHYSOSTIGMA SPARTEINE PICRIC ACID STANNANE POTASSIUM IODIDE STRONTIUM POTASSIUM NITRITE STROPHANTHIN POTASSIUM PERSULFATE STRYCHNINE PROCAINE HYDROCHLORIDE STYRENE OXIDE PROPIOLACTONE SULFUR DIOXIDE PROPIONYL CHLORIDE SULFUR TRIOXIDE (ALPHA) PROPYL ALDEHYDE SULFURIC ACID PROPYLENE SULFUROUS ACID PROPYLENE ETHER TABUN PROPYLENE OXIDE TAR, DEHYDRATED PROTACTINIUM TAR, LIQUID PTOMAINES TARTARIC ACID PYRETHRUM FLOWERS TELLURIUM PYRIDINE TETRACHLORONAPHTHALENE PYROGALLOL TETRACHLOROSILANE 53

POLLUTANTS IV, cont.

TETRAETHYL PYROPHOSPHATE VINYL ETHER TETRAETHYLTHIURAM SULFIDE VINYLTRICHLOROSILANE TETRAHYDROFURAN WARFARIN TETRAHYDRONAPHTHALENE WELDING FUMES TETRANITROMETHANE WHISKY TETRYL XENON THALLIUM XYLIDINE THEBAINE m-XYLYL BROMIDE THEOPHORIN m-XYLYL CHORIDE THIOCETIC ACID m-XYLYNE THIOGLYCOLIC ACID YOHIMBINE THIOGLYCOLLATES ZIRCONIUM THIONYL CHLORIDE FLUORIDE THIONYL FLUORIDE THIOPHOSPHORYL FLUORIDE THIOSEMICARBAZONE THORIUM TIGLIC ACID TITANIUM TETRACHLORIDE TOLUENE TOXAPHENE TREMETOL TRI-o-CRESYL PHOSPHATE TRICHLOROACETYL CHLORIDE TRICHLOROSILANE TRIFLUORONITROSOMETHANE TRIISOBUTYLALUMINUM TRIMETHYLAMINE TRINITROANISOLE TRINITROTULUENE TRISODIUM PHSOPHATE TRITIUM TUMERIC TURPENTINE o-TOLUIDINE p-THOIXENE ULTRAVIOLET RADIATION UNDECANAL URANIUM URIC ACID URUSHIOL VANADIUM VARNISH VINYL CHLORIDE 54

THE LIQUITROPHIC PHILOSOPHY

In the development of a nutritional science we find that the body does indeed need vitamins, enzymes, coenzymes and a multitude of other factors to survive, including protein, carbohydrates, fats, water, air, and exercise. In the field of homeopathy we often deal with just subtle energies, but homeopathy need not always be so dilute. Many homeopathics can be utilized in low concentrations at mother tinctures of 1x, 2x, 3x, or 4x to supply chemical properties to the system for chemical effects. The Dr. Recommends’ Liquitrophics remedies supply the vitamins, minerals, enzymes, alkaloids and hormones needed by the body to regulate biological activities. The Liquitrophics remedies are not in pill form, but in liquid form to maximize the surface area and to trigger the digestive system for absorption at the point in which it works best; the mouth. Inside the nasal pharynx area are many nerve structures running to the brain that help trigger the digestive system for maximum absorption and utilization of the remedy. The liquid formulation of these remedies maximizes their effectiveness. This means less can be used in much safer dosages. The Dr. Recommends’ Liquitrophics remedies are developed to be safe for children within their specific context and are quality controlled within the QQCTM standards.

LIQUITROPHIC REMEDIES

ADRENO LIQUITROPHIC (4 fl. oz.) Catalog No. 0096 Indication: Weak adrenal glands, hypoadrenia Ingredients: Panax Quinquefolium 2x. Sarcodes: Adrenal, Spleen, Pantothenic Acid, Lobelia cardinalis, Rosa canina 3x. Coffea cruda, Paullinia sorbilis 3x, 6x. Ephedra vulgaris 3x, 6x, 12x. Ascorbic acid, Magnesia Phosphorica, Adrenalinum 4x. Arachidonic Acid 5x, 12x, 30x, 60x, 1000x. Sarcodes: Pituitary, Hypothalamus 6x. Adrenocorticotrophin 6x, 12x, 30x.

AMINO LIQUITROPHIC (4 fl. oz.) Catalog No. 0097 Indication: Supplies amino acids and minerals Ingredients: Panax quinquefolium, Hydrocotyle asiatica, Polygonum punctatum, Fucus disticus, Undaria pinnatifida, Gigartina papillata, Porphyra, Arame, Rhodymenia, Alaria esculenta 2x.

ARTHRO LIQUITROPHIC (4 fl. oz.) Catalog No. 0102 Indication: Connective tissue repair, joint strain or sprains Ingredients: Calendula officinalis, Echinacea purpurea, Symphytum officinale, Rhododendron chrysanthum 3x. Shark and Bovine Muscle, Ligament, Cartilage 3x, 6x. Ruta graveolens 4x. Collagen, Elastin 4x, 12x, 60x, 100x, 500x. Silicea 5x, 6x, 12x. Hypericum perforatum, Euphrasia officinalis, Aceticum Acidum, Arnica montana 6x. Glycine, Alanine, Serine, Proline 6x, 12x, 30x, 60x. Formica rufa 20x.

B LIQUITROPHIC (4 fl. oz.) Catalog No. 0098 Indication: Mental depression, pellagra, vaso constriction Ingredients: Hordeum vulgare, Saccharomyces cerevisiae, Angelica archangelica 3x. Sarcodes: Liver, Heart 3x. Vitamins: B1 - B20, 3x, 4x, 12x, 30x, 60x, 100x. Beta vulgaris, Raphanus sativus 4x, 5x, 6x, 16x. Natrum Pyruvate 6x, 12x, 30x.

C LIQUITROPHIC (4 fl. oz.) Catalog No. 0123 Indication: Supplies Vitamin C, infection resistance Ingredients: Citrus limonum, Malpighia punicifolia, Rosa canina, Solanum tuberosum 1x. Calcium Ascorbate, Citrus aurantium, Bone Marrow 2x. Agaricus bisporus, Petroselinum sativum, Capsicum Annuum 3x. Ascorbatase 6x.

CARDIO LIQUITROPHIC (4 fl. oz.) Catalog No. 0107 Indication: Heart repair, infarction risk Ingredients: Crataegus Oxyacantha, Plantago major, Kali Muriaticum, Kali Phosphoricum 3x. Cytisus scoparius 4x, 6x, 12x, 30x. Sarcodes: Thyroidinum, Heart, Vagus Nerve, Cardiac Plexus 4x, 6x, 30x, 100x. Cactus grandiflorus 5x. Digitalis purpurea, Natrum Muriaticum, Carnitine, Valeriana officinalis, Lecithin 6x. Alanine, Methionine, Proline, Leucine 6x, 12x, 30x, 60x.

DERMA LIQUITROPHIC (4 fl. oz.) Catalog No. 0119 Indication: Skin repair, psoriasis Ingredients: Equisetum arvense, Iris germanica, Berberis vulgaris, Mahonia aquifolium 3x. Thuja occidentalis, Nux vomica 6x. Sassafras officinale, Chondrus crispus, Mentha piperita 6x, 12x, 30x, 60x, 100x. Hypericum perforatum 10x. Mercurius Solubilis, Petroleum 12x. Graphites 16x.

FEM LIQUITROPHIC (4 fl. oz.) Catalog No. 0106 Indication: Balance the female system Ingredients: Rubus idaeus, Dioscorea villosa, Glycyrrhiza glabra, Trillium erectum, Liatris spicata 2x. Caulophyllum thalictroides, Ignatia amara 6x. Sarcodes: Ovary, Uterus, Mammary, Pituitary, Hypothalamus 6x, 12x, 30x.

G LIQUITROPHIC (4 fl. oz.) Catalog No. 0101 Indication: Brain repair, dementia, poor memory Ingredients: Ginkgo biloba 2x. Glycerinum, Taurine 3x. Brain Sarcodes 3x, 6x, 12x, 30x, 60x, 100x. Vitamin B2, B6, B15, Niacinamide, Choline, PABA, Inositol, Biotin, Folic Acid, Scutellaria lateriflora, Convallaria majalis, Tyrosine, Glutamine, Glutamic Acid, Phosphatydl Choline 4x. Datura stramonium 8x, 12x. Oxytocin 12x, 30x, 60x, 100x, 500x.

GLUCO LIQUITROPHIC (4 fl. oz.) Catalog No. 0125 Indication: Diabetes, hyperglycemia Ingredients: Aletris farinosa, Ignatia amara, Rhamnus purshiana, Diabatina 2x. Geranium maculatum, Convallaria majalis 3x.

HEMO LIQUITROPHIC (4 fl. oz.) Catalog No. 0099 Indication: Blood cell repair, anemia Ingredients: Ferrum Gluconate, Ferrum Phosphoricum, Ferrum Sulphuricum, Ferrum Muriaticum, Trifolium pratense, Panicum miliaceum, Fagopyrum esculentum, Beta vulgaris, Panax quinquefolium, Hydrocotyle asiatica, Polygonum punctatum, Pyridoxine, Cyanocobalamin, Thiamine, Riboflavin, Folicum Acidum 3x, 12, 60, 500x. Hemoglobin 4x. Sarcodes: Spleen, Bone Marrow, Pituitary, Liver 6x. Intrinsic Factor 6x, 12x, 30x, 60x. Erythropoietin 6x, 12x, 30x, 60x, 100x. Tyrosine, Histidine 30x, 60x, 1000x.

HEMO-A LIQUITROPHIC (4 fl. oz.) Catalog No. 0126 Indication: Auto-immune disorders Ingredients: Cucumis sativus 1x. Phytolacca decandra 2x. Sarcode: Thymus 3x. Trifolium pratense, Sarcodes: Adenoids, Tonsils, Appendix 4x. Vaccinotoxinum 30x, 100x.

HEPATO LIQUITROPHIC (4 fl. oz.) Catalog No. 0112 Indication: Liver repair, liver toxicity Ingredients: Cucurbita, Beta vulgaris, Raphanus sativus, Arctium, Plantago major 2x. Bupleurum, Verbena hastata 2x, 6x. Ascorbicum Acidum 3x. Sarcodes: Liver, Gallbladder 3x, 6x, 12x, 30x, 60x, 100x. Podophyllum peltatum 4x. Glycine, Methionine, Proline, Cytochrome, Flavoprotein, NAD, NADP, Inositol, Choline 5x, 10x, 30x, 100x. Natrum Sulphuricum 6x. Natrum Muriaticum 14x. Creatine Phosphokinase, Glutamic-oxaloacetic transaminase, Lactic Dehydrogenase 16x, 30x, 60x, 100x.

LIENO LIQUITROPHIC (4 fl. oz.) Catalog No. 0120 Indication: Spleen repair Ingredients: Sarcode: Spleen 3x. Quercus robur 4x. Ceanothus americanus 6x. Helianthus annuus 6x, 12x. Natrum Muriaticum 6x, 12x, 30x. Germanium, Arctium lappa, Myeloperoxidase 6x, 12x, 30x, 60x, 100x.

LIPID LIQUITROPHIC (4 fl. oz.) Catalog No. 0105 Indication: Fatty acid deficiencies Ingredients: Oil from: Canola, Olive, Sesame Seed, Safflower, Sunflower, Wheat Germ, Garlic, Carrot, Lemon, Orange, Borage, Linseed (Flax Seed), Cod Liver, Lecithin (from Soybean), Lettuce, Evening Primrose, Rose Hips, Pumpkin Seed, Cinnamon, Apple Seed, Senna, Myrrh, Barley, Apricot Kernel, Currants, Australian Tea Tree, Grape Seed, Hazel Nut.

LYMPHO LIQUITROPHIC (4 fl. oz.) Catalog No. 0114 Indication: Lymphatic repair, cleansing Ingredients: Echinacea purpurea, Trifolium pratense 2x. Arctium, Capsicum annuum, Citrus limonum 3x. Sarcodes: Lymph, Spleen, Mammary, Thymus 3x, 6x, 12x, 30x, 60x, 100x. Hydrastis canadensis 5x. Sarcodes: Adenoids, Tonsils, Appendix 5x, 12x, 30x, 60x, 100x.

NEO LIQUITROPHIC (4 fl. oz.) Catalog No. 0103 Indication: Degenerative tissue Ingredients: Vinca minor, Carduus marianus, Phytolacca decandra, Plantago major 2x. Sanguinaria canadensis, Viscum album, Amygdala amara 3x. Carduus benedictus, Taxus baccata 3x, 6x, 12x, 30x, 60x, 100x. Rhamnus cathartica, Glycyrrhiza glabra 6x.

NEPHRO LIQUITROPHIC (4 fl. oz.) Catalog No. 0110 Indication: Kidney repair, detoxification of protein waste Ingredients: Hydrangea arborescens 2x. Eupatorium purpureum, Pareira brava, Pisum sativum, Taraxacum officinale 3x. Natrum Phosphoricum 3x, 6x, 12x, 30x, 60x, 100x. Kali Carbonicum, Natrum Nitricum 4x, 6x, 12x, 30x, 60x, 100x. Berberis vulgaris, Uva ursi, Sarcodes: Kidney, Bladder 6x, 12x, 30x, 60x, 100x, 500x. Urea, Ammonium, Rennin, Aldosterone 24x, 40x, 60x, 100x.

OSTEO LIQUITROPHIC (4 fl. oz.) Catalog No. 0100 Indication: Bone repair, cold & flu Ingredients: Bone Meal, Liquid Calcium, Lactuca sativa 3x, 6x, 12x, 60x, 100x, 1500x. Calcarea Fluorica, Calcarea Sulphurica, Calcarea Phosphorica, Calcarea Muriatica, Calcarea Carbonica, Manganum Metallicum, Magnesium Metallicum, Equisetum arvense, Juglans nigra, Vitamin D, D2, D3, A, F 4x, 8x, 12x, 60x, 100x. Niccolum Metallicum 5x, 12x, 30x, 60x, 100x. Osteoclasts, Osteoblasts 6x, 12x, 30x, 60x, 100x. Thyrocalcitonin 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Sarcodes: Bone, Thyroidinum, Parathyroid, Liver, Kidney, Skin 6x, 30x, 60x, 100x, 1000x. Fluorine, Molybdenum 12x, 30x, 100x.

OXY LIQUITROPHIC (4 fl. oz.) Catalog No. 0109 Indication: Oxygenator and energizing aid Contraindication: Flower, yeast, bee pollen allergies Ingredients: Bee Pollen, Flower Pollen, RNA-DNA from Yeast 2x. Amygdala amara, Laminaria, Medicago sativa, Symphytum officinale 3x. Vitamins B12-B18, Chelated Zinc 6x. Oxytocin, Carbonic Anhydrase, Hemoglobin, Taurine 6x, 12x, 60x, 100x.

PITUI LIQUITROPHIC (4 fl. oz.) Catalog No. 0116 Indication: Pituitary repair, Assists in detox Ingredients: Amygdala amara 3x. Cimicifuga racemosa, Sarcode: Hypothalamus 3x, 6x, 12x, 30x. Sarcodes: Pituitary Anterior, Pituitary Posterior 4x. Caulophyllum thalictroides 6x. Arginine, Lysine, Ornithine 6x, 12x, 30x. Adrenocorticotrophin 6x, 12x, 30x, 60x, 100x.

PROPEPSIA LIQUITROPHIC (4 fl. oz.) Catalog No. 0104 Indication: Stimulates and balances digestive enzyme release Ingredients: Pancreatinum 2x. Bromelain, Papain, Coriandrum sativum, Cinnamomum, Eugenia caryophyllata, Berberis vulgaris, Herbal Bitters, Mentha piperita, Ananas comosus 3x. Sarcodes: Parotid, Stomach, Pancreas, Liver, Small and Large Intestine, Vagus Nerve 6x. Pancreozymin-cholecystokinin, Lysozyme, Pepsinogen, Trypsinogen, Chymotrypsin, Lipase, Amylase, Cellulase, Protease, 6x, 12x, 30x, 60x, 100x, 500x.

PULMO LIQUITROPHIC (4 fl. oz.) Catalog No. 0113 Indication: Lung repair Ingredients: Eucalyptus globulus 2x. Sarcode: Lung 3x. Adrenalinum 4x. Sanguinaria canadensis 6x. Carbon Dioxide, Ferrum Metallicum, Zincum Metallicum, Oxygen, Carbonic Anhydrase, Verbascum thapsus, Curare 6x, 12x, 30x, 60x, 100x. Belladonna 12x.

SEROTO LIQUITROPHIC (4 fl. oz.) Catalog No. 0117 Indication: Parkinsonian symptoms, depression Contraindication: High blood pressure Ingredients: Musa paradisiaca, Medicago sativa, Scutellaria lateriflora, Valeriana officinalis, Nerium odorum, Magnesia Phosphorica, GABA, Choline Chloride, Inositol, Niacinum, Pyridoxine 3x, 6x, 12x, 30x, 60x, 100x. Serotonin, Dopamine 4x, 12x, 60x, 100x. 5-Hydroxy-L- Tryptophan, Niacinamide 6x, 12x, 30x, 60x, 100x. Amygdala amara 30x, 100x.

THYMO LIQUITROPHIC (4 fl. oz.) Catalog No. 0121 Indication: Thymus repair Contraindication: Disease involving excess white blood cell count Ingredients: Sarcode: Thymus 3x. Thymol, Natrum Muriaticum 6x. Phytolacca decandra, Arctium lappa 6x, 12x, 30x.

THYRO LIQUITROPHIC (1 fl. oz.) Catalog No. 0122 Indication: Thyroid repair Contraindication: Hyperthyroid conditions Ingredients: Olive Oil, Canola Oil, Sesame Oil. Thyroidinum 3x, 5x, 6x, 12x, 30x, 100x. Lac defloratum 4x, 6x, 8x. Fucus vesiculosus 6x, 12x, 30x. Molybdenum 8x. Plumbum Metallicum, Mercurius Vivus, Argentum Metallicum, Platinum Metallicum, Alumina, Bismuthum Metallicum, Carboneum, Selenium Metallicum, Stannum Metallicum, Silicea, Sulphur 30x, 60x, 100x.

LIQUITROPHIC INSTRUCTION

¾ Liquitrophics may be taken with meals, although they should not be mixed with piping hot foods over 106 degrees F.

¾ Refrigerate after opening.

¾ Liquitrophics and homeopathics should be taken 20 minutes apart.

¾ Do not store Liquitrophics in sunlight.

¾ Liquitrophics may be taken at the same time with other Liquitrophics. The exception to this would be that Lipid Liquitrophic and Thyro Liquitrophic should not be mixed with other homeopathics or Liquitrophics.

CAUTION: Alcohol sensitivities: If a person is sensitive to alcohol, put the dosage into a 3 oz. glass of warm water. Allow one minute for the alcohol to evaporate.

By following these guidelines, you will give the remedies the greatest opportunity to succeed.

AMINO ACIDS ALANINE (L-ALANINAMIDE) ARGININE (L-ARGININAMIDE) ASPARAGINE (NA-T-BOC-N-Y-XANTHYL-L-ASPARAGINE) ASPARTIC ACID (L-ASPARTIC ACID AMIDE) ASPARTIC ACID (P-NITROPHENYL ESTER) CYSTEINE GLUTAMIC ACID GLUTAMINE GLYCINAMIDE GLYCINE HISTIDINE ISOGLUTAMINE ISOLEUCINE L-LYSINE L-METHIONINE L-TAURINE LEUCINE METHIONINE N-CBZ-EZ-AMINO-N-CAPROIC ACID N-CBZ-D-3-(2-NAPHTHYL) ALANINE N-CBZ-L-HOMOSERINE N-CBZ-Y-AMIN0-N-BUTYRIC ACID N-T-BOC-L-HOMOSERINE N-T-BOC-Y-AMINOBUTYRIC ACID NORLEUCINE NORVALINE ORNITHINE PHENYLALANINE PROLINE PYROGLUTAMIC ACID SARCOSINE SERINE STATINE THREONINE TRYPTOPHAN TYROSINE VALINE

LIPIDS

Fatty Acid Anhydrides C 2:0 Acetic C 4:0 Butyric C 6:0 Caproic C 8:0 Caprylic C 10:0 Capric C 12:0 Lauric C 14:0 Myristic C 16:0 Palmitic C 17:0 Heptadecanoic C 18:0 Stearic C 18:1, cis-9 Oleic C 18:1, trans-9 Elaidic C 18:2, cis-9, 12 Linoleic C 20:0 Arachidonic C 22:1, cis-11 11-Eicosenoic C 22:0 Behenic

Diglycerides

C 6:0 Dicaproin, 1,3 isomer C 8:0 Dicaprylin, 1,2-, 1,3-and mixed isomers C 10:0 Dicaprin, 1, 2-, 1, 3- and mixed isomers C 12:0 Dilaurin, 1, 2-, 1, 3- and mixed isomers C 14:0 Dimyristin, 1, 2-, 1, 3- and mixed isomers C 15:0 Dipentadecanoin, 1, 3-isomer C 16:0 Dipalmitin, 1,2-, 1,3- and mixed isomers C 18:0 Disteaarin, 1, 2-, 1, 3- and mixed isomers C 18:1, cis-9 Diolein, 1,2- 1,3- and mixed isomers C 18:1, cis-9, C2:0 1-Oleoyl-2-Acetyl C 18:1, trans-9 Dielaidin, 1,3-isomer C 18:2, cis-9, 12 Dilinolein, 1,3-isomer C 20:0 Diarachidin, 1,3-and mixed isomers C 20:1, cis-11 Di-11-Eicosenoin, mixed isomers C22:1, cis-13 Dierucin, mixed isomers

LIPIDS, cont. Monoglycerides

C 8:0 1-Monocapryloyl-rac-glycerol C 10:0 1-Monodecanoyl-rac-glycerol C 12:0 1-Monolauroyl-rac-glycerol C 14:0 1-Monomyristoyl-rac-glycerol C 16:0 1-Monopalmitoyl-rac-glycerol C 16:1, cis-9 1-Monopalmitoleoyl-rac-glycerol C 18:0 1-Monostearoyl-rac-glycerol C 18:1, cis 9 1-Monooleoyl-rac-glycerol C 18:1, trans-9 Monoelaidin C 18:2, cis-9, 12 1-Monolinoleoyl-rac-glycerol C 18:3, cis-9,12,15 1-Monolinoleoyl-rac-glycerol C 20:1, cis-11 Mono-11-eicosenooin, 1-isomer C 22:1, cis-13 Monoerucin, 1-isomer

Lipids, cont.

Triglycerides

C 2:0 Triacetin C 4:0 Tributyrin C 6:0 Tricaproin C 8:0 Tricaprylin C 9:0 Trinonanoin C 10:0 Tricaprin C 12:0 Trilaurin C 13:0 Tritridecanoin C 14:0 Trimyristin C 14:1, cis-9 Trimyristolein C 15:0 Tripentadecanoin C 16:0 Tripalmitin C 16:1, cis-9 Trielaidin C 17:0 Triheptadecanoin C 18:0 Tristearin C 18:1, trans-9 Trielaidin C 18:1, cis-9 Triolein C 18:1, cis-6 Tripetroselinin C 18:2, cis-9, 12 Trilinolelaidin C 18:3, cis-9, 12, 15 Trilinolenin C 19:0 Trinonadecanoin C 20: Triarachidin C 20:1, cis-5, 8, 11, 14 Triarachidonin C 22:0 Tribehenin C 22:1, cis-13 Trierucin C 24:1, cis-15 Trinervonin

HORMONES

ACETYL CHOLINASE ACETYL CHOLINE ADRENAL PEPTIDE E ADRENALIN ADRENOCORTICOTROPIC HORMONE (ACTH: CORTICOTROPIN A) ALDOSTERONE AMASTATIN ANGIOTENSIN (CONVERTING ENZYME INHIBITOR) ANGIOTENSIN I ANGIOTENSIN II (HYPERTENSIN II) ANGIOTENSIN III INHIBITOR ANGIOTENSINOGEN (FRAGMENT) ANTI-PAIN ANTI-REPRODUCTIVE TRIPEPTIDE ATRIOPEPTIN I ATRIOPEPTIN II ATRIOPEPTIN III BEAUVERICIN BRADYKININ BRADYKININ POTENTIATOR C B-CASOMORPHIN B-LIPOTROPIN FRAGMENTS BRADYKININ POTENTIATOR B CAERULEIN CALCITONIN (THYRO) CHOLECYSTOKININ CHYMOSTATIN CORTICOTROPIN RELEASING FACTOR DERMORPHIN DYNORPHIN A (PORCINE) CYNORPHIN B (PORCINE) ELASTIN CHEMOTACTIC FRAGMENT ELEDOISIN ENKEPHALINAMIDE EPINEPHRINE ERYTHROPOIETIN ESTROGEN a-ENDORPHIN GALANIN GASTRIC INHIBITORY POLYPEPTIDE GASTRIN GASTRIN RELEASING PEPTIDE GASTRIN I FRAGMENTS GASTRIN II

HORMONES, cont.

GLUCAGON GLUTATHIONE GROWTH HORMONE GROWTH HORMON RELEASING FACTOR INSULIN KALLIDIN KATACALCIN KEMPTIDE KENTSIN KETOSTEROIDS (ALL) KYOTORPHIN L-ALANYLGLYCYL-L-SERYL-L-GLUTAMIC ACID L-METHIONYL-L-LEUCYL-L-PHENYLALANINE L-TYROSYLGLYCYLCLYCINE L-VALYLGLYCYL-L-SERYL-L-GLUTAMIC ACID LEUCINE ENKEPHALIN-LYS LEUPEPTIN LEUTINIZING HORMONE LEUTINIZING RELEASING HORMONE METHIONINE ENKEPHALINE MINERAL CORTICOID MORPHICEPTIN MOTILIN a-MELANOCYTE STIMULATING HORMONE a1-MATING FACTOR (D-TRP2)-METHIONINE ENKEPHALIN N-ACETYL-L-METHIONYL-L-LEUCYL-L-PHENYLALANYL-L-METHIONINE N-FORMYL-L-METHIONYL-L-LEUCYL-L-PHENYLALANINE METHYL N-FORMYL-L-METHIONYL-L-LEUCYL-L-TYROSINE N-FORMYL-L-METHIONYL-L-PHENYLALANYL-L-LYSINE N-FORMYL N-FORMYL-L-NORLEUCYL-L-LEUCYL-L-PHENYLALANINE N-T-BOC-L-LEUCYL-L-PHENYLALANINE N-T-BOC-L-METHIONYL-L-LEUCYL-L-PHENYLALANINE N-T-BOC-L-METHIONYL-L-LEUCYL-L-TYROSINE NEOENDORPHIN NERVE GROWTH FACTOR NEUROMEDIN C NEUROTENSIN NOREPINEPHRINE a-NEOENDORPHIN OXYTOCIN PANCREATIC POLYPEPTIDE PANCREOZYMIN PARATHYROID HORMONE 68

PEPTIDE YY PITUITARY DIURETIC HORMONE (POSTERIOR) PITUITARY RELEASE (ANTERIOR) PRESSINOIC ACID PROCTOLIN PROENKEPHALIN PROGESTERONE PROLACTIN RENIN RENIN INHIBITOR SCHIZOPHRENIA RELATED PEPTIDE SECRETIN SOMATOSTATIN SOMATOSTATIN 25 SOMATOSTATIN 28 SYNDYPHALIN-20 TESTOSTERONE THYMOPOIETIN 32-36 THYMOSIN THYROCALCITONIN THYROID STIMULATING HORMONE VAL-GLY-VAL-ALA-PRO-GLY VASOPRESSIN VASOTOCIN XENOPSIN YEAST a-FACTOR

HOMRONES/BIOACTIVE PEPTIDES

Adrenocorticotropic Hormone (ACTH: Corticotropin A) Angiotensin I Angiotensin II (Hypertensin II) Angiotensin III Angiotensin III Inhibitor Angiotensin-Converting Enzyme Inhibitor (pGlu-Trp-Pro-Arg-Pr9o-Gin- lie-Pro-Pro) Angiotensinogen (Fragment 1-14) Renin Bradykinin (Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg) Bradykinin Potentiator B (pGlu-Gly-Leu-Pro-Pro-Arg-Pro-Lys-11e-Pro- Pro) Bradykinin Poetntiator C (pGlu-Gly-Leu-Pro-Pro-Gly-Pro-Pro-11e-Pro- Pro)

CHEMOTACTIC PEPTIDES

N-Acetyl-L-Methionyl-L-Lefucyl-L-Phenylalanine L-Alanylglycyl-L-Seryl-L-Glutamic Acid (Eosinophil chemotactic factor of anaphylaxis) N-t-BOC-L-Methionyl-L-Leucyl-L-Phenylalanine (Chemotactic peptide antagonist) N-t-BOC-L-Phenylalanyl-D-Leucyl-L-Phenylalanyl-D-Leucyl-L- Phenylalanin (Chemotactic peptide inhibitor) N-Formyl-L-Methionyl-L-Leucyl-L-Phenylalanine Methyl Ester (A potent chemotactic peptide for human blood monocytes) N-Formyl-L-Methionyl-L-Leucyl-L-Phenylalanyl-L-Lysine (Acetate salt) N-Formyl-L-Methionyl-L-Leucyl-L-Tyrosine (Dicyclohexylammonium salt) N-Formyl-L-Norleucyl-L-Leucryl-L-Phenylalanine (Chemotactic peptide) N-Formyl-L-Norleucyl-L-Leucyl-L-Phenylalanyl-L-Tyrosine L-Methionyl-L-Leucyl-L-Phenylalanine (Acetate Salt – Exhibits very weak chemotactic properties) Val-Gly-Val-Ala-Pro-Gly (Elastin chemotactic fragment) L-Valylglycyl-L-Seryl-L-Glutamic Acid (Esinophil chemotactic factor of anaphylaxis) Dynorphin A (Porcine) Dynorphin B (Porcine) a-Endorphin Leucine Enkephalin Leucine Enkephalin-Lys Enkephalinamide Methionine Enkephaline (Tyr-Gly-Gly-Phe-Leu-Lys) [D-Trp 2]-Methionine Enkephalin 70

Proenkephalin Syndyphalin Syndyphalin-20 L-Tyrosylglycylglycine

ENZYME INHIBITORS

Amastatin Angiotensin-Converting Enzyme Inhibitor Antipain Chymostatin Leupeptin

GASTROINTESTINAL PEPTIDES

Caerulein Cholecystokinin Galanin Gastric Inhibitory Polypeptide Gastrin Gastrin I Fragments Gastrin II (Sulfated) Gastrin Releasing Peptide (Porcine) Glucagon (Crystalline) Pancreatic Polypeptide Pancreozymin Peptide YY Secretin Growth Hormone Releasing Factor (1-44) a-Melanocyte Stimulating Hormone Neurotensin

OPIOID PEPTIDES

Adrenal Peptide E B-Casomorphin Dermorphin Kyotorphin Morphiceptin Oxytocin Pressinoic Acid Vasopressin Vasotocin Somatostatin Somatotstatin 25 71

Somatostatin 28 (Fragment 1-14)

MISCELLANEOUS

Amastatin Antipain Beauvericin Calcitonin Cholecystokinin Corticotropin Releasing Factor Elastin Chemotactic Fragment Eledoisin Erythropoietin Glucagon Glutathione Insulin Katacalcin Kentsin Neuromedin C Pancreozymin Proctolin Proenkephalin Thymosin a Thyrocalcitonin Xenopsin

ENZYMES ACETYL CHOLINE ESTER ACETYLESTERASE ACID MALTASE – POMPE’S DISEASE ACID PHOSPHATASE ADENOSINE 5’-DIPHOSPHATE ALKALINE PHOSPHATASE ALAKALINEPROTEASE ALDOASE ALPHA 1, 4 GLUCOSIDASE – POMPE’S DISEASE AMINO ACID DECARBOXYLASES AMINO ACID OXIDASE AMINOBUTYRIC ACID TRANSAMINASE AMYLO-1, 6 GLUCOSIDASE – CORI’S DISEASE ANGIOTENSIN-CONVERTING ENZYME INHIBITOR ARGINASE ARGININE DECARBOXYLASE ASCORBATE OXIDASE ASPARAGINASE ASPARTIC ACID DECARBOXYLASE ATPase a-AMYLAST b-AMYLASE BILE ACID DEHYRDROGENASE BUTYL CHOLINESTERASE CALCULASE CANDIDA PSEUDOTROPICALIS CANDIDA UTILIS CARBONIC ANHYDRASE CARBOXYPEPTIDASE A CARNITINE PALMITOYLTRANSFERASE –MYOPATHY CAROBXYPEPTIDASE B CATALASE CELLULASE CHOLESTEROL OXIDASE CHOLINE KINASE CHOLINESTERASE, ACETYL CHLOROPEROXIDASE CHOLESTEROL ESTERASE CHOLINE ACETYLTRANSFERASE CHOLINE OXIDASE CHOLINESTERASE, BUTYRYL CHYRO TRYPSIN COENZYME A DEHYDROGENASE

ENZYMES, cont. COLLAGENASE CORTISONE REDUCTASE CREATINASE CREATININASE CREATININE PHOSPHOKINASE CYTOCHROME b2 CYTOCHROME C REDUCTASE a-CHYMOTRYPSIN DEOXYRIBONUCLEASE (ATP DEPENDENT) DEOXYRIBONUCLEASE 1 DEOXYRIBONUCLEASE 2 DEOXYRIBONUCLEIC ACID LIGASE DEOXYRIBONUCLEIC ACID POLYMERASE DEXTRANASE DNA LIGASE DNA POLYMERASE DOPAMINE B-MYDROXYLAST ELASTASE ENTEROKINASE FORMALDEHYDE DEHYDROGENASE FUCOSE DEHYDROGENASE GABASE GLUTAMINASE GLUTATHIONE PEROXIDASE BLUATHIONE REDUCTASE GLUCOSE DEHYDROGENASE GLUTAMIC DECARBOXYLASE GLUTAMIC DEHYDROGENASE GLYCEROL DEHYDROGENASE GLYCOGEN PHOSPHORYLASE GLYCOGEN SYNTHETASE HISTAMINE HISTIDASE HYALURONIDASE HYDROXYPYRUVATE REDUCTASE HYDROXYSTEROID DEHYDROGENASE INVERTASE ISOAMYLASE ISOCITRATE LYASE ISOMALTASE LACTASE LACTATE DEHYDROGENASE LACTATE 2-MONOOXYGENASE

ENZYMES, cont. LACTIC DEHYDROGENASE LACTOPEROXIDASE LDH LECITHINASE A LECITHINASE B LECITHINASE C LECITHINASE D LEUCINE DEHYDROGENASE LIPASE LIPOXIDASE LYSIN LYSINE DECARBOXYLASE LYSOZYME LYTIC ENZYMES MALATHION HYDROLASE MALTASE MERCURIPAPAIN MONOAMINE OXIDASE MYLEO PEROXIDASE MYOPHOSPHORYLASE – McARDLE’S DISEASE MYOSIN NADASE NEURAMINIDASE NUCLEASE OTNIHINE DECARBOXYLASE OXALATE OXIDASE PANCREATIN PANCREOZYMIN PAPAIN PARATHION HYDROLASE PECTINASE PECTOLYASE PENICILLINASE PEP CARBOXYLASSE PEPSIN PEPSINOGEN PEPTIDASE PEROXIDASE PHOSPHATASE, ACID PHOSPHODIESTERASE PHOSPHOFRUCTOKINASE – MYOPATHY PHOSPHOLIPASE A2 PHOSPHORYLASE

ENZYMES, cont. PHYTASE PROSTAGLANDID DEHYDROGENASE PROTEASE PYRUVATE DEHYDROGENASE PYRUVATE KINASE PYRUVATE OXIDASE PYTALIN TRYPSIN RENIN RENNIN RIBONUCLEASE SACCHARASE SBP BROMELAIN PAPIN STEROID DEHYDROGENASE SUCRASE TRYPSIN TRYPSINOGEN TRYPTOPHAN TYROSINASE URICASE VANILMANDELIC ACID DEHYDROGENASE VITAMIN C ASE XANTHINE OXIDASE

THE ANODYNE PHILOSOPHY

Anodyne is the medical word for a remedy used to treat pain conditions. The neurology of pain involves many sensory neurons and their ability to project neurological signals through the nervous system to the brain, which then perceives these signals as pain. The physiology of pain is akin to the physiology of neurology and perception. Pain results when there is an over or under balance in the neurons of any area resulting in an energetic overload. The Dr. Recommends’ anodyne remedies are formulated to help in a wide variety of pain conditions. They are not designed to cover up the pain, nor are they designed as pain killers. They are designed to help in healing the factors behind the pain and to stimulate the organism into a healing process, thereby reducing the amount of pain through natural means. Anodyne formulas give us a broad-based collection of easy-to-use remedies to help many types of pain conditions in the body and are quality controlled within the QQCTM guidelines. Pain is not the enemy; pain is indeed the messenger of a problem and must not be fought against. It is the purpose of homoeopathy to work with the pain. If pain persists, it is a further indication that there is a serious underlying condition and the patient should be referred to a professional who can treat the patient effectively.

ANODYNE REMEDIES

ABDOMINAL ANODYNE (1 fl. oz.) Catalog No. 0017 Indication: Cramping, Pre-appendicitis Ingredients: Ferrum Metallicum, Chamomilla 3x. Bismuthum Metallicum, Borax 4x. Lycopodium clavatum 5x. Carbo Vegetabilis, Solar Plexus, Vagus Nerve, Bovine Stomach Tissue, Natrum Sulphuricum 6x, 12x, 30x, 60x, 100x. Bromium 7x. Sulphur 8x, 30x, 60x. Muriaticum Acidum, Platinum Metallicum, Alumen 12x, 30x, 60x, 100x. Plumbum Metallicum, Mercurius Vivus, Nux vomica 30x, 60x, 100x.

ANODYNE-ACD (1 fl. oz.) Catalog No. 0286 Indication: Pain from acid conditions Ingredients: Natrum Bicarbonate 3x. Full spectrum Fatty Acids, Coca, Ferrum Metallicum 5x. Antimonium Tartaricum 6x. Chemoreceptors 6x, 12x, 30x. Sepia, Muriaticum Acidum 8x, 16x, 30x. Oxalicum Acidum, Uricum Acidum 16x, 30x. Endorphins 20x, 60x, 100x.

ANODYNE-ALK (1 fl. oz.) Catalog No. 0287 Indication: Pain from alkaline conditions Ingredients: Ascorbicum Acidum, Smilax 3x. Coca 5x. Zincum Metallicum, RNA-DNA, Magnesium Thiosulfate, Propionaldehyde 6x. Chemoreceptors 6x, 12x, 30x. Natrum Bicarbonate 8x, 16x, 30x. Causticum, Calcarea Sulphurica, Calcarea Phosphorica, Calcarea Magnesia 12x. Endorphins 20x, 60x, 100x.

ANODYNE-AUTOX (1 fl. oz.) Catalog No. 0288 Indication: Pain from self-made toxins, injury Ingredients: Smilax 3x. Symphytum officinale 4x. Arnica montana 4x, 10x, 30x. Calendula officinalis 5x, 15x, 30x. Isotonic Plasma 6x, 20x. Mechanoreceptors 6x, 12x, 30x. Aurum Metallicum, Carbo Animalis 12x. Endorphins, Gate Receptors (Spine & Brain) 20x, 60x, 100x. Vaccinotoxinum 60x, 100x, 500x, 1000x.

ANODYNE-C (1 fl. oz.) Catalog No. 0058 Indication: Pain where cold improves Ingredients: Pulsatilla 4x. Natrum Sulphuricum 6x. Dulcamara 6x, 12x, 30x. Ferrum Metallicum 6x, 12x, 30x, 100x. Sarcodes: Temperature Sensor Nerve Cells 6x, 12x, 30x, 60x, 100x. Arsenicum Metallicum 8x. Rhododendron chrysanthum 12x. Echinacea purpurea, Lachesis mutus 12x, 30x, 100x. Aluminium Metallicum, Aurum Metallicum, Bismuthum Metallicum, Borax, Plumbum Metallicum, Silicea 16x, 20x, 50x, 100x.

ANODYNE-ELC (1 fl. oz.) Catalog No. 0289 Indication: Pain provoked by exposure to electric or energetic fields, television, microwaves, etc. Ingredients: Euphrasia officinalis, Pilocarpus 3x. Agate 4x, 5x, 6x. Cuprum Metallicum 6x, 12x. Electromagnetic Nerve Receptors 6x, 12x, 30x, 60x, 100x. Full spectrum EMR, Full spectrum magnetic oscillations 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Glonoine 12x, 30x. Corallium Nigra 30x.

ANODYNE-NT (1 fl. oz.) Catalog No. 0050 Indication: Pain where no touch improves Ingredients: Zincum Metallicum 3x. Selenium Metallicum 4x, 6x, 30x, 100x. Bryonia 5x. Nux vomica 6x. Zincum Metallicum 6x, 12x, 30x, 60x. Sarcodes: Kruski Cells (Pressure Sensors) 6x, 12x, 30x, 60x, 100x. Silicea 6x, 12x, 30x, 100x. Arsenicum Album, Gelsemium sempervirens, Plumbum Metallicum, Lachesis mutus 8x, 12x, 30x.

ANODYNE-T (1 fl. oz.) Catalog No. 0049 Indication: Pain where touch improves Ingredients: Coffea cruda 3x. Belladonna 4x. Bryonia, Aconitum napellus 5x. Spigelia marilandica 6x. Sarcodes: Kruski Cells (Pressure Sensors) 6x, 12x, 30x, 60x, 100x. Bismuthum Metallicum, Magnesia Phosphorica 12x. Iodium 16x-24x. Borax 16x-30x.

CEPHALO ANODYNE (1 fl. oz.) Catalog No. 0036 Indication: Sub-orbital, migraine, temporal headache Ingredients: Iris versicolor, Chrysanthemum parthenium, Salix nigra 2x. Sanguinaria canadensis 3x. Endorphins 6x, 12x, 30x. Ammonium Carbonicum 5x. Silicea, Manganum Metallicum, Cimicifuga racemosa 6x. Bovine Pituitary Glandular, Antimonium, Arsenicum Metallicum 12x. Cuprum Metallicum, Graphites, Iodium 16x.

ANODYNE-G (1 fl. oz.) Catalog No. 0048 Indication: General pain Ingredients: Salix alba 3x, 6x. Selenium Metallicum, Zincum Metallicum, Vitamins A, C, E 6x. Acetaminophen, Ibuprofen, Acetylsalicylic Acid 6x-30x. Arsenicum Metallicum, Arum maculatum 6x, 12x, 30x. Sarcodes: Major Nerves 6x, 12x, 30x, 60x, 100x. Barium, Mercurius Vivus 30x.

ANODYNE-H (1 fl. oz.) Catalog No. 0057 Indication: Pain where heat improves Ingredients: Kali Carbonicum, Bryonia, Manganum Metallicum 6x. Sarcodes: Temperature Sensor Nerve Cells 6x, 12x, 30x, 60x, 100x. Sulphur, Zincum Metallicum 6x, 100x. Borax 8x, 12x. Belladonna, Apis mellifica, Ruta graveolens, Rhus toxicodendron 12x, 30x. Fluorine, Arnica montana 12x, 30x, 100x. Arsenicum Metallicum 12x, 30x, 100x, 500x. Mercurius Vivus 30x.

ANODYNE-M (1 fl. oz.) Catalog No. 0051 Indication: Pain where motion improves Ingredients: Valeriana officinalis 1x. Pulsatilla 2x. Dioscorea villosa 3x. Kali Iodatum 4x, 6x, 12x, 70x. Ignatia amara, Oxalicum Acidum 5x. Rhus toxicodendron 6x. Phosphorus 8x, 12x, 25x. Cuprum Metallicum 12x, 30x. Sarcodes: Nerve Sensors of Proprioceptors 12x, 30x, 60x, 100x. Silicea 100x, 500x.

ANODYNE-NM (1 fl. oz.) Catalog No. 0052 Indication: Pain where no motion improves Ingredients: Magnesia Phosphorica 3x, 6x. Bryonia 8x. Manganum Metallicum 8x, 12x, 30x. Kreosotum, Nux vomica 9x. Sarcodes: Nerve Sensors of Proprioceptors 12x, 30x, 60x, 100x. Platinum Metallicum 20x, 50x, 100x. Mercurius Vivus 30x, 60x, 100x.

FACIAL ANODYNE (1 fl. oz.) Catalog No. 0031 Indication: Facial pain, Symptoms relating to Bell's Palsy Ingredients: Salix nigra 3x. Aconitum napellus 4x. Zincum Metallicum, Manganum Metallicum, Silicea, Belladonna 6x. Argentum Metallicum 8x. Phosphorus, Chromium 12x. Trigeminal Nerve 16x, 30x, 60x, 100x, 500x.

INTERCOSTO ANODYNE (1 fl. oz.) Catalog No. 0059 Indication: Intercostal neuralgia Ingredients: Ruta graveolens 6x, 12x. Arsenicum Album 12x. Intercostal Cartilage, Rib Glandular 12x, 30x. Antimonium, Plumbum Metallicum, Rhus toxicodendron 30x.

LARGE JOINT ANODYNE (1 fl. oz.) Catalog No. 0044 Indication: Large joint discomfort, knees, elbows, shoulders Ingredients: Bryonia 4x. Magnesium Metallicum, Manganum Metallicum, Calcarea, Arnica montana, Sulphuricum Acidum 6x. Zincum Metallicum 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Niccolum Metallicum 8x. Ledum palustre 10x. Sulphur 12x. Ligament, Cartilage 12x, 30x. Strontium 20x.

LUMBO ANODYNE(1 fl. oz.) Catalog No. 0070 Indication: Low back pain Ingredients: Niacinamide 3x. Nux vomica, Atropinum 4x. Rhus toxicodendron 5x. Nicotinum 6x. Sarcodes: Kidney, Liver, Lumbar and Sacral Vertebrae, Sciatic and Femoral Nerve 6x, 12x, 30x, 60x, 100x. Arnica montana 30x, 100x.

SCIATIC ANODYNE (1 fl. oz.) Catalog No. 0060 Indication: Sciatic, Low back pain Ingredients: Manganum Metallicum 4x, 12x, 30x, 60x, 100x, 1000x. Sarcode: Sciatic Nerve 6x, 12x. Magnesia Phosphorica 8x. Atropinum 12x. Aconitum napellus 12x. Arsenicum Album 30x.

SMALL JOINT ANODYNE (1 fl. oz.) Catalog No. 0045 Indication: Small joint pain in fingers, toes Ingredients: Lithium Carbonicum 2X, 12x. Atropinum 4x. Calendula officinalis, Nitricum Acidum, Magnesium Metallicum, Manganum Metallicum, Calcarea 6x. Rhododendron chrysanthum 6x, 12x, 30x, 60x, 1000x. Zincum Metallicum 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Niccolum Metallicum 8x. Platinum Metallicum, Sulphur 12x. Ligament, Cartilage 12x, 30x. Ammonium Phosphoricum 12x, 30x, 100x. Strontium, Plumbum Metallicum 20x. Natrum Sulphuricum, Nux vomica 30x.

THORACIC ANODYNE (1 fl. oz.) Catalog No. 0067 Indication: Acute chest pains Ingredients: Crataegus oxyacantha, Cactus grandiflorus, Scilla maritima 2x. Kali Carbonicum, Kalmia latifolia, Spigelia marilandica 3x. Digitalis purpurea 4x. Arsenicum Album, Phosphorus 5x. Manganum Metallicum 6x, 12x, 30x, 60x, 100x. Selenium Metallicum 8x. Creatine Phosphokinase, Rennin, Histaminum 12x, 20x, 60x, 100x. Zincum Metallicum, Platinum Metallicum 12x, 30x, 60x.

THE COMBINATION PHILOSOPHY

Combination homeopathy is the most popular type of homeopathy used in the world today. Combination ingredients are chosen based on a symptomatic picture. Therefore, combinations can be engineered for broader based ranges of effectiveness, whereas, singular homeopathics usually have profoundly small realms of utilization. Combination homeopathy is easy to learn, as a minimal amount of training is needed for the doctor to perceive the symptomatic picture that is presented. In nature, everything exists in a combination form. Thus, Apis mellifica, or honey bee, is a very complex combination that nature has brought together to yield one energetic substance. This is the law of “synergy” – the sum of the whole is greater than that of the parts. “Combining” is the secret of life. This type of synergy is culminated in the Dr. Recommends’ combination remedies. The combination remedies have been developed with QQCTM techniques, to ensure that the blending of the ingredients have a synergistic effect and become a new singular formula. The Dr. Recommends’ combination remedies are safe and effective formulas that will minimize healing crises and help to reduce risk to the patient. The combination remedies also utilize the best of trace element work in achieving their glandular activity.

COMBINATION REMEDIES

ARRHYTH-1 (1 fl. oz.) Catalog No. 0043 Indication: Irregularities of the pulse Ingredients: Crataegus oxyacantha, Valeriana officinalis, Kali Phosphoricum, Amni visnaga, Leonurus Cardiac, Cytisus scoparius, Sumbul 2x. Heart, Nerium oleander 3x. Zincum Metallicum 5x. Iberis amara 6x. Sulphur, Platinum Metallicum 12x.

ARTHRO 1 (1 fl. oz.) Catalog No. 0032 Indication: Joint stiffness and pain Ingredients: Angelica archangelica, Du Huo 2x. Magnesia Phosphorica 2x, 3x, 6x. Dong Quai, Cnidium, Achyranthes, Gambir, Kali Muriaticum, Manganum Metallicum, Yucca filamentosa 3x. Cartilage 3x, 6x, 12x. Rhus toxicodendron 5x. Arsenicum Metallicum 6x. Hordeum vulgare 8x. Oxalicum Acidum 8x, 12x. Arnica montana 8x, 100x, 1000x. Antimonium, Borax, Baryta, Arsenicum Metallicum, Platinum Metallicum, Sulphur, Elastin, Elastase, Collagen, Collagenase 12x.

CEPHALO-LD (1 fl. oz.) Catalog No. 0064 Indication: Learning disabilities, Mental clarity Ingredients: Convallaria majalis 2x, 6x. Cistus canadensis, Impatiens, Clematis erecta 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Bovine Brain Tissue 6x, 12x. Sepia 8x. Phosphorus 10x. Zincum Metallicum, Belladonna 12x. Plumbum Metallicum, Platinum Metallicum 25x, 75x, 100x. Mercurius Vivus 25x, 75x, 100x, 500x. Bovine Kidney Glandular, Lycopodium clavatum 30x.

CEPHALO-M (1 fl. oz.) Catalog No. 0065 Indication: Stimulates blood flow to brain, Memory Ingredients: Euphrasia officinalis, Rosmarinus officinalis 2x. Salvia officinalis 2x, 6x. Artemisia vulgaris, Asparagus officinalis 3x. Ilex paraguariensis 5x. Convallaria majalis, Allium sativum, Calcarea Phosphorica 6x. Brain 6x, 12x, 30x, 60x, 100x. Baryta Carbonica 8x. Sulphur, Silicea, Selenium Metallicum, Zincum Metallicum 12x, 100x, 1000x. Plumbum Metallicum 30x.

CEPHALO-SD (1 fl. oz.) Catalog No. 0172 Indication: Memory, Brain power Ingredients: Gingko biloba, Choline, Phosphatydl Choline 2x. Taurine, Tyrosine 3x. Niacin, Niacinamide, Biotin 4x. Phenylalanine 5x. Nerve Growth Factor 6x. Brain Sarcode 6x, 12x, 30x, 60x, 100x. Vitamins: B1-B20 8x. Paullinia cupana 3x.

COUGH SYRUP (4 fl. oz.) Catalog No. 0027 Indication: Cough Ingredients: Laurocerasus, Spongia tosta, Rumex crispus, Belladonna, Ipecacuanha, Drosera rotundifolia 3x. Mentha, Adrenalinum, Ligusticum porteri 4x. Convallaria majalis, Alumen, Bromium, Ferrum Phosphoricum, Zincum Metallicum, Manganum Metallicum, Magnesia Phosphorica, Baryta, Bismuthum Metallicum, Dextromethorphan 6x. Sarcodes: Cough Center, Lung 6x, 12x, 30x, 60x, 100x. Arsenicum Metallicum 8x. Stannum Metallicum 9x. Platinum Metallicum, Sulphur 12x, 24x, 30x, 60x.

CoQ (1 fl. oz.) Catalog No. 0300 Indication: Deficiencies of CoQ Ingredients: Sesame Seed oil, Avocado oil, Biotin, Folic acid, CoQ10 3x. CoA, CoQ6, CoQ7, CoQ9, Ascorbic palmitate 6x, 12x, 24x, 30x.

DERMA-A (1 fl. oz.) Catalog No. 0018 Indication: Comedones, Pustules, Blackheads, Whiteheads Ingredients: Selenium Metallicum, Zincum Metallicum 4x. Cimicifuga racemosa 6x, 12x, 24x. Lymph 6x, 12x, 30x. Natrum Muriaticum 6x, 200x. Argentum Metallicum, Aurum Metallicum, Gelsemium sempervirens, Iodium, Manganum Metallicum 8x. Placenta 9x. Kali Bromatum, Alumen, 12x, 24x, 60x. Juglans nigra 12x, 30x. Ledum palustre, Hepar Sulphuris Calcareum, Mercurius Vivus 30x, 60x, 100x.

DERMA-I (1 fl. oz.) Catalog No. 0020 Indication: Itching Ingredients: Sarcodes: Liver, Lymph 3x, 6x, 12x, 30x, 60x, 100x. Selenium Metallicum, Zincum Metallicum, Borax, Magnesium Metallicum, Manganum Metallicum, Pangamicum Acidum 4x. Silicea, Graphites, Calcarea Carbonica 6x. Alumen, Arsenicum Metallicum, Baryta, Bismuthum Metallicum, Cuprum Metallicum, Stannum Metallicum, Nitricum Acidum 8x. Muriaticum Acidum, Sulphuricum Acidum 8x, 12x, 30x, 60x. Iodium, Phenylalanine, Tyrosine, Phenylpyruvic Acid 12x, 30x, 60x. Phenylalanine Hydroxylase, Glutamic-oxaloacetic Transaminase, Creatine Phosphokinase, Lactate Dehydrogenase 60x, 100x, 500x.

EAR DROPS (1 fl. oz.) Catalog No. 0173 Indication: Ear ache and excess ear wax (external use) Ingredients: Olive Oil, Sesame Seed Oil. Verbascum thapsus 1x. Anthemis nobilis 2x. Plantago major 3x. Vanilla, Ferrum Phosphoricum 4x, 6x.

ENTERO-B (1 fl. oz.) Catalog No. 0047 Indication: Bowel flora disorders Ingredients: Large Intestine Sarcode, Colostrum 4x. Manganum Metallicum 6x. Natrum Muriaticum 6x, 100x, 1000x. Argentum Metallicum, Arsenicum Metallicum, Arum maculatum, Lactobacillus 12x. Bacteroidum 30x.

ENTERO-C (1 fl. oz.) Catalog No. 0035 Indication: Constipation Ingredients: Senna, Cascara sagrada, Zincum Metallicum 3x. Borax, Ferrum Metallicum 6x. Alumina, Phosphorus 8x. Sulphur, Barium, Aurum Metallicum, Antimonium, Arsenicum Metallicum 12x. Iodium 16x. Lycopodium clavatum 30x.

EU-STRESS (1 fl. oz.) Catalog No. 0023 Indication: Stress Ingredients: Apis mellifica 2x, 6x. Royal Jelly 3x. Adrenalinum 3x, 6x, 12x, 30x, 60x, 100x. Citrullus, Cistus canadensis, Impatiens, Clematis erecta, Zincum Metallicum, Ferrum Metallicum, Silicea 6x. Hypothalamus, Amygdala amara 6x, 12x, 30x, 60x, 100x. Vanadium Metallicum 8x, 12x, 30x. Lithium Carbonicum 12x, 30x, 60x. Neurotensin 16x, 30x, 60x, 100x. 86

FEM-B (1 fl. oz.) Catalog No. 0068 Indication: Balance female organ systems Ingredients: Caulophyllum thalictroides 2x, 6x. Rubus idaeus, Cimicifuga racemosa 6x. Sarcodes: Ovary, Corpus Luteum, Uterus, Mammary, Hypothalamus, Pituitary, Adrenal, Estrogen, Progesterone 6x, 12x, 30x, 100x, 500x, 1000x. Mercurius Vivus, Petroleum, Baryta, Sulphur 20x.

FEM-M (1 fl. oz.) Catalog No. 0046 Indication: Menopausal conditions Ingredients: Chamomilla 3x, 30x, 100x, 500x, 1000x. Cimicifuga racemosa, Sanguinaria canadensis, Ovarian Sarcode 6x. Silicea 8x. Borax, Graphites, Iodium, Phosphorus, Estrogen 12x. Lachesis mutus 16x.

FEM-PMS (1 fl. oz.) Catalog No. 0066 Indication: Premenstrual cramping, Irritability and depression Ingredients: Chamomilla, Vitamin B6 3x. Caulophyllum thalictroides 3x, 6x. Cimicifuga racemosa 4x. Magnesia Phosphorica, Magnesia Carbonica, Natrum Muriaticum 6x. Manganum Metallicum 6x, 12x, 30x. Estrogen, Progesterone 6x, 12x. Natrum Carbonicum 12x. Phosphorus 30x. Platinum Metallicum 30x, 100x.

GASTRO-I (1 fl. oz.) Catalog No. 0062 Indication: Stomach lining ulcerations Ingredients: Oryza sativa, Panicum miliaceum, Triticum repens, Poria, Raphanus sativus, Brassica, Zingiber officinale, Glycyrrhiza glabra, Disodium Phosphate 2x. Borax 6x. Sarcodes: Stomach, Small Intestine 6x, 12x, 30x, 60x, 100x. Calcarea Carbonica 8x. Carbo Vegetabilis 8x, 12x, 30x. Mercurius Vivus, Arsenicum Metallicum 30x. Plumbum Metallicum 100x. Sulphur, Cuprum Metallicum, Selenium Metallicum 200x.

GLUCO-H (1 fl. oz.) Catalog No. 0038 Indications: Hypoglycemia Ingredients: Oenothera biennis 3x. Chromium Metallicum 6x. ATP, Insulin, Pancreas 6x, 12x, 30x. Plumbum Metallicum, Antimonium Metallicum, Arsenicum Metallicum 20x. Nux vomica 30x. Saccharum Officinale 30x, 200x, 1000x.

GLUCO-I (1 fl. oz.) Catalog No. 0029 Indication: Hereditary tendency toward diabetes Ingredients: Lycopodium clavatum, Selenium Metallicum, Zincum Metallicum, Sulphur, Chromium, Alumen 6x. Sarcodes: Hypothalamus, Posterior Pituitary, Kidney, Pancreas 6x, 12x, 30x, 60x, 100x. Argentum Metallicum, Bismuthum Metallicum, Barium 12x. DNA, Insulin 12x, 60x, 100x, 1000x. Gelsemium sempervirens, Iodium, Plumbum Metallicum 20x. Uranium, Phosphoricum Acidum 30x. Radium Bromatum, ATPase, Antidiuretic Hormone 60x. Glucose, Glycogen 1000x.

HEMO-L (1 fl. oz.) Catalog No. 0299 Indication: White blood cell disorders Ingredients: Ceanothus americanus 2x. Nux vomica, Thuja occidentalis 3x. Ipecacuanha 4x, 6x, 12x. Leukemia Nosode 6x, 8x, 12x, 30x, 60x, 100x, 1000x. Hapalochlaena maculata, Sarcodes: Lymph, Spleen 6x, 12x, 30x, 60x, 100x. Leukocytes 12x, 30x, 60x, 100x. Phosphorus, Natrum Muriaticum 30x, 60x, 100x.

HYPERTHYRO 1 (1 fl. oz.) Catalog No. 0039 Indication: Iodine sensitivity, Over-active thyroid Ingredients: Selenium Metallicum, Vitamin A 2x. Bovine Pituitary Glandular 6x. Thyroidinum 12x, 24x, 30x. Sulphur, Arsenicum Metallicum 16x. Mercurius Vivus, Molybdenum 20x. Iodium, Natrum Muriaticum 30x. TSH 30x.

HYPERTONIA 2 (4 fl. oz.) Catalog No. 0108 Indication: High blood pressure Ingredients: Valeriana officinalis 2x. Citricum Acidum, Kali Bitartrate 3x. Rauwolfia serpentina, Fucus vesiculosus 4x. Kali Muriaticum, Kali Phosphoricum 4x, 5x, 6x, 12x. Rhamnus purshiana, Allium sativum, Rennin, Sarcodes: Mid Brain, Kidney, Liver, Collective Arterial 6x. Vasopressin, Angiotensin I, II, Neurotensin 8x, 12x, 30x, 60x, 100x, 500x.

HYPOTONIA 1 (1 fl. oz.) Catalog No. 0040 Indication: Low blood pressure Ingredients: Crataegus oxyacantha 2x. Nerium oleander, Laurocerasus, Cytisus scoparius 3x. Zincum Metallicum, Natrum Sulphuricum 6x. Chromium 8x. Angiotensin 12x.

IMMUNOPOIE (1 fl. oz.) Catalog No. 0041 Indication: Stimulates immune system Ingredients: Petroselinum sativum, Natrum Muriaticum 3x. Bovine Glandulars: Thymus, Bone Marrow, Liver, Spleen, Adenoids, Tonsils 5x, 6x, 12x, 30x, 100x. Aurum Metallicum, Argentum Metallicum, Sulphur 12x. Appendix 15x, 30x, 100x. Mercury Amalgam 100x, 500x, 1000x. Saccharinum 100x

INFLU-F (1 fl. oz.) Catalog No. 0033 Indication: Flu and fever like symptoms Ingredients: Euphrasia officinalis, Ulmus fulva 2x. Pulsatilla 2x, 6x, 12x. Dulcamara 3x. Ferrum Phosphoricum, Ruta Graveolens 4x. Zincum Metallicum, Bismuthum Metallicum, Adrenalinum, Thuja occidentalis, Hyssopus officinalis 6x. Aconitum napellus 6x, 8x, 12x. Belladonna 8x. Rhus toxicodendron, Camphora, Manganum Metallicum, Phosphorus, Iodium 12x.

INFLU-I (1 fl. oz.) Catalog No. 0034 Indication: Intestinal flu symptoms Ingredients: Chamomilla, Marrubium vulgare 1x. Mentha piperita, Lavandula officinalis, Ocimum basilicum, Citrus limonum, Populus candicans 2x. Pogostemon patchouli 3x. Zincum Metallicum, Symphytum officinale 6x. Sulphur, Argentum Metallicum, Iodium, Manganum Metallicum, Alumen, Phosphorus 12x.

ME 1 (1 fl. oz.) Catalog No. 0030 Indication: Epstein Barr related conditions Ingredients: Zincum Metallicum, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Natrum Carbonicum 6x. Antimonium, Lithium 12x. Epstein Barr Virus, Mononucleosis, Hemolytic Influenza, Hemolytic Streptococcus, CMV 16x, 24x, 30x, 100x.

METABOLIC 1 (1 fl. oz.) Catalog No. 0157 Indication: Metabolic disorders Ingredients: All Glandulars 5x-30x, 60x-100x, 500x, 1000x. All Cell Salts 6x-12x, 30x-500x, 1000x. All Amino Acids 10x-30x, 50m. All Parts of Krebs Cycle 12x-30x, 50m. RNA/DNA 30x-100x, 50m. Chromosomes 12x, 30x, 60x, 100x, 500x, 1000x. Collective Miasms: Psorinum, Sycosis, Syphilinum 500x, 1000x, 2000x, 50m.

MUCOUSLYSIS (4 fl. oz.) Catalog No. 0115 Indication: Mucous conditions Ingredients: Plantago major, Urtica dioica, Equisetum arvense 1x. Eucalyptus globulus 2x. Lobelia cardinalis, Vinca minor, Ephedra vulgaris 3x. Calcarea Iodata 5x. Sarcodes: Lymph, Pancreas 6x, 12x, 30x, 60x, 100x. Arsenicum Iodatum 8x. Mucin 30x, 60x, 100x. mRNA (4 fl. oz.) Catalog No. 0290 Indication: Resets mesenger RNA for intercellular regulation Ingredients: Mercaptoethanol 12x, 30x, 60x, 100x, 500x, 1000x. mRNA 100x, 500x, 1000x.

NASO-I (1 fl. oz.) Catalog No. 0061 Indication: Rhinitis, Sinusitis Ingredients: Natrum Muriaticum, Manganum Metallicum, Zincum Metallicum 4x, 6x, 12x. Allium cepa, Allium sativum 6x. All Sinuses 6x, 12x, 30x, 60x, 100x. Pulsatilla 12x. Sulphur, Aluminium Metallicum, Mercurius Vivus, Stannum Metallicum, Bromium, Borax 30x, 100x.

NEO-P (1 fl. oz.) Catalog No. 0028 Indication: Degenerative tissue Ingredients: Naja tripudians 5x, 12x, 30x. Zincum Metallicum, Calcarea Phosphorica, Sulphur, Antimonium 6x, 12x, 30x, 60x, 100x. Bovine Glandulars 6x, 16x. Viscum album 6x, 12x, 100x. Cuprum Metallicum, Arsenicum Metallicum 8x, 12x, 30x. Interferon: Alpha, Beta, Gamma, Interleuken: I, II, III 12x, 24x, 30x. Taxus baccata 12x-30x. Carcinum 12x, 30x, 100x, 500x, 1000x.

NEURO-R (4 fl. oz.) Catalog No. 0056 Indication: Stress and nerval over-stimulation Ingredients: Panax quinquefolium, Zincum Valerianicum, Lecithin 3x, 12x, 30x. Serotonin 5x. Cistus canadensis, Impatiens, Clematis erecta 6x. Pulsatilla, Magnesia Phosphorica, Passiflora incarnata, Valeriana officinalis, Coffea cruda, Lithium Carbonicum, GABA 6x, 12x. Acetylcholine 6x, 12x, 30x, 60x, 100x. Aconitum napellus, Selenium Metallicum 8x. Arsenicum Iodatum, Endorphins, Neurotensin 12x, 30x, 60x. Gelsemium sempervirens 18x, 24x, 30x. Cuprum Metallicum, Aluminium Metallicum 30x, 100x.

PROSTA-I (1 fl. oz.) Catalog No. 0054 Indication: Inflamed prostate Ingredients: Bee Pollen, Zincum Metallicum 3x. Prostate 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Capsicum annuum 6x, 12x. Natrum Sulphuricum 6x, 12x, 30x. Baryta Carbonica, Pulsatilla 12x. Plumbum Metallicum, Platinum Metallicum, Cadmium Metallicum 12x, 30x, 60x, 100x, 500x. Tuberculinum, Thuja occidentalis 16x, 30x, 100x, 1000x.

PULMO-A (1 fl. oz.) Catalog No. 0024 Indication: Asthmatic-like conditions Ingredients: Arsenicum Album 4x, 6x, 8x. Bryonia 2x, 6x, 12x. Adrenalinum 3x, 6x. Zincum Metallicum, Silicea, Carbo Vegetabilis 6x. Lung Sarcode 6x, 12x, 30x, 60x, 100x. Lithium Carbonicum 8x. Camphora 12x, 30x. Histamine 16x, 24x, 30x. Belladonna, Natrum Muriaticum 30x. NADP, NAD, NADH 60x, 100x, 500x. Natrum Sulphuricum 200x.

PULMO-P (1 fl. oz.) Catalog No. 0053 Indication: Pulmonary infections and accompanying pain Ingredients: Asclepias tuberosa 3x. Bovine Lung Tissue, Sepia, Cinchona officinalis 6x. Silicea 6x, 12x, 30x. Picricum Acidum 8x. Arsenicum Iodatum, Bryonia 12x. Sulphur 12x, 30x. Selenium Metallicum 12x, 30x, 100x. Cuprum Metallicum, Stannum Metallicum, Aurum Metallicum, Platinum Metallicum 18x, 30x. Calcarea Carbonica, Lycopodium clavatum, Phosphorus 30x. Mercurius Vivus 100x, 500x.

PURATIVE (1 fl. oz.) Catalog No. 0124 Indication: Cleans microorganism infestations from the body Ingredients: Hydrastis canadensis 1x. Citrus paradisi semen 2x. Aloe socotrina, Benzoin 3x. Chrysanthemum coccineum, Vitamins: A, C, E 4x.

REN-P (1 fl. oz.) Catalog No. 0055 Indication: Excess urinary protein, Enzymatic disturbance Ingredients: Kidney 6x, 12x. Vita Mar 8x. Phosphorus, Ledum palustre 12x. Albumin, Petroleum 12x, 30x. Mercurius Vivus 20x, 30x, 100x. Silicea, Sulphur, Zincum Metallicum 30x.

RENLAPIS (1 fl. oz.) Catalog No. 0063 Indication: Kidney pain, Gravel urine Ingredients: Crataegus oxyacantha 2x, 6x. Sarsaparilla 3x. Digitalis purpurea 3x, 6x. Nitricum Acidum, Berberis vulgaris, Lycopodium clavatum 6x. Kidney Sarcode 6x, 12x, 30x, 60x, 100x. Bismuthum Metallicum, Borax 8x. Stannum Metallicum 10x. Lithium, Selenium Metallicum 12x. Oxalicum Acidum, Uricum Acidum 30x.

SARCOESIS (1 fl. oz.) Catalog No. 0019 Indication: Inflammatory and swelling conditions Ingredients: Chrysanthemum parthenium 2x. Zincum Metallicum, Verbascum thapsus 3x. Urtica dioica 4x. Apis mellifica 4x, 6x, 12x, 30x. Adrenalinum 4x, 6x, 12x, 30x, 60x, 100x. Belladonna 5x, 6x, 12x, 30x. Crotalus horridus 6x. Silicea, Triosteum perfoliatum 6x, 12x. Natrum Muriaticum, Magnesia Phosphorica, Kali Sulphuricum, Lymph 6x, 12x, 30x, 60x, 100x. Hepar Sulphuris Calcareum 8x, 16x, 30x. Lachesis mutus 12x, 30x. Chymotrypsin, Histidine, Histamine, ATPase Lysozyme, 12x, 30x, 60x, 100x. Glucose-6-Phosphatase, Coenzyme A Dehydrogenase 30x, 60x, 100x. Biopterin, Hepar Suis 100x, 500x, 1000x

SHARK CARTILAGE (1 fl. oz.) Catalog No. 0118 Contains the nutritional factors of shark cartilage Ingredients: Shark Cartilage 3x, 6x, 12x, 30x. Thymol, Sarcode: Thymus 4x, 6x, 12x. Sarcode: Lymph 5x, 15x, 30x. Natrum Muriaticum, Mentha piperita 6x. Silicea 12x, 30x, 60x.

THERACEPHALIC (1 fl. oz.) Catalog No. 0026 Indication: Brain circulation after stroke or injury Ingredients: Scutellaria lateriflora 3x. Convallaria majalis 3x, 6x, 12x. Taurine, Tyrosine 3x, 12x, 60x. Thyroidinum 5x. Magnesia Phosphorica, Manganum Metallicum 6x, 12x, 30x, 60x, 100x. Variolinum 12x, 30x, 60x, 100x. Stannum Metallicum 8x. Sarcodes: Brain, Arterial Wall 12x, 30x, 60x, 100x.

THERACIRCULO (1 fl. oz.) Catalog No. 0025 Indication: Circulatory disorders Ingredients: Niacinum, Niacinamidum 2x. Adrenalinum, Camphora 4x. Aorta Valve, Ferrum Metallicum 6x, 12x, 30x. Thrombin, Proteolytic Enzymes 8x, 24x, 30x, 100x. Stannum Metallicum 8x, 24x, 50x. Sulphur, Heloderma, Aesculus hippocastanum, Crotalus horridus 12x. Tabacum 12x, 24x. Arterial Tissue 12x, 30x. Baryta 20x. Arnica montana 100x.

TRAUMATIC 1 (1 fl. oz.) Catalog No. 0042 Indication: Injuries, Rebuilds cellular tissue Ingredients: Echinacea purpurea 3x. Arnica montana 3x, 6x, 12x, 100x, 1000x, 50lm. Sulphur 3x, 12x. Calendula officinalis 3x, 12x, 30x, 100x, 1000x, 50lm. Symphytum officinale 5x, 12x, 30x, 60x, 100x. Bone Marrow 6x, 12x, 30x, 60x, 100x, 500x. Niccolum Metallicum 10x, 30x, 100x. Rhus toxicodendron, Barium, Bromium, Bismuthum Metallicum 12x, 30x, 60x, 100x. Arsenicum Metallicum 100x.

VENA-H (1 fl. oz.) Catalog No. 0037 Indication: Hemorrhoidal conditions Ingredients: Aesculus hippocastanum 2x. Collinsonia canadensis 3x. Nux vomica 4x. Lycopodium clavatum, Sulphur 5x. Cuprum Metallicum, Nitricum Acidum, Graphites, Veins 6x. Liver Aliesterase, Proteolytic Enzyme, Chymotrypsin, Vanadium Metallicum 8x.

VIR-H (1 fl. oz.) Catalog No. 0069 Indication: Herpes, Cold sores Ingredients: Silicea 5x. Selenium Metallicum, Euphrasia officinalis, Trifolium pratense 6x. Sulphur, Antimonium Crudum, Arsenicum Metallicum, Iodium 12x. Plumbum Metallicum 16x. Herpes simplex I, II, III, Herpes zoster, Herpes progenitalis 16x, 24x, 30x, 100x. Thuja occidentalis 30x.

THE RESTORATIVE PHILOSOPHY

Sarcode remedies have been used for many years in homeopathy to help rebuild and correct tissues when organ structures are in disease states. Damage caused by disease states in organs can result in malfunctioning on an organic level. The Dr. Recommends’ restorative remedies help the tissues to rebuild. Energetic students have shown that a potent glandular can rectify an energetic imbalance where there is no organic disturbance. This is covered in The Experimental Data on Homeopathy by Dr. William Nelson, and shows the uses and proposed mechanisms of sarcodal homeopathy. Sarcodal homeopathy offers the safest and most gentle form of homeopathy. Results are often the slowest to be seen due to the correct rebuilding of the degenerative cells in the organs. The restorative remedies will work more quickly and successfully in younger patients than in older ones. In the older patient, these remedies can at times be utilized to stimulate cleansing and to stabilize and reduce the risk of a healing crisis. The Dr. Recommends’ restorative homeopathics are engineered in homochords of differing potencies. Maximum efficiency is achieved with a combination of 4x, 6x, 12x, 30x, 60x, 100x, 500x, and 1000x. This allows the body to respond to the frequency of dilution which works best to rebuild tissues. The restorative remedies are safe and effective and quality controlled by the QQCTM techniques to ensure efficacy.

RESTORATIVE REMEDIES

Ingredients: New Zealand or American Ursa and Bovine Glandulars 4x, 6x, 12x, 30x, 60x, 100x, 500x, and 1000x.

Bone and Bone Marrow Brain Cervical Cranial, Sacral Ear Eye Gallbladder Heart, Lung Kidney, Ovarian, Adrenal Kidney, Prostate, Adrenal Liver, Gallbladder Lymph, Spleen, Mammary Major Nerves Muscle, Ligament, Cartilage Orchic Pancreas, Stomach Pineal, Pituitary, Hypothalamus Sinuses Skin and Mucous Membrane Small and Large Intestine Thoracic Thyroid, Thymus, Parathyroid

SARCODES

Sarcodal homeopathy involves using healthy glandular tissue from a healthy organism to treat sick conditions within the body. For an expanded view of sarcodes and the experimental context behind them read The Experimental Data on Homeopathy, by Dr. William Nelson. In the text it outlines exactly how sarcodal homeopathy works. Sarcodal homeopathy promotes growth and development of healthy glandular tissue. Within this treatise, many different sarcodes will be classified that can be used by a knowledgeable homeopath. The list of sarcodal tissues used here is very large and may be beyond the grasp of some homeopaths. We have a variety of tissues being used by homeopaths in many ways. Since these sarcodal tissues help to rebuild tissue, help tissue to organize properly, and increase the probability of the presence of healthy tissue over old tissue, it is possible to see how homeopathy can be used. Sarcodal tissue can go beyond mere tissue to secretions; which include hormones, enzymes, coenzymes, RNA, DNA, and others. Thus, we can see from the long list a wide range of sarcodal tissues that can be brought beyond just tissue to include secretions of the body. This vast array of secretions is broadened to include as many different hormones and enzymes known by Dr. Nelson at this time.

SARCODES I

ADENOIDS ADRENAL ADRENAL GLANDULAR APPENDIX AUDITORY NERVE BONE MARROW BOWEL FLORA BRAIN CEREBRUM CORPUS CALLOSUM CORPUS LEUTEUM CYSTERNA CHYLI EMOTIONS ESONOPHIL FRONTAL LOBE GALLBLADDER HEART HYPOTHALAMUS ILEO CECAL VALVE INTRINSIC FACTOR ISLE OF LANGERHANS KIDNEY LARGE INTESTINE LIMBIC SYSTEM LIVER LEUCOCYTE LUNG LYMPHOCYTE MAMMARY GLANDS MEDULA MICHELLE BALANCE MID BRAIN MONOCYTE MOUTH NERVES OF ABDOMEN (PERIPHERAL SPINAL NERVES) OCCIPITAL OCULOMOTOR 3 (CRANIAL NERVES) OLFACTORY HAIRS (CILIA) (SMELL) OLFACTORY MUCOSA (SMELL) OLFACTORY NEURONS (SMELL) OLFACTORY PLATE (SMELL) OLFACTORY TRACT (SMELL) OLFACTORY 1 (CRANIAL NERVES)

SARCODES I, cont.

OPTIC CHIASMA (RELATED STRUCTURES-BRAIN STEM) OPTIC DISC (LAYERS OF THE EYE: RETINA-EYE) OPTIC NERVE (EYE) OPTIC 2 (CRANIAL NERVES) ORGAN OF CORTI (INTERNAL EAR-EAR) OTIC (GANGLIA-PARASYMP) OTOLOTHS (EQUILIBRIUM: MACULA-EAR) OVAL WINDOW (INTERNAL EAR-EAR) OVARIES PAIN (SENSORY) PANCREAS PARATHYROID PARIETAL LOBE PELVIC/PERINEAL VISCERA (POSTGANGLIONIC NEURONS-AUTOSYMP) PERINEURIUM (MOTOR NERVES) PERSONALITY (BRAIN) PINEAL PITUIPOSTERIOR PITUITANTERIOR PITUITARY POLYMORPH PONS (HINDBRAIN-BRAIN STEM) PONS (MOTOR NERVES) PONTINE CISTERN (SUBARACHNOID SPACES-CERE FLUID) PORE CANAL (TASTE BUDS-TASTE) POST GANGLIONIC AXONS (AUTOSYMP) POST GANGLIONIC CELL BODIES (AUTOSYMP) POSTERIOR FUNICULUS (SPINAL CORD-WHITE MATTER) POSTERIOR HORNS (SPINAL CORD-GRAY MATTER) POSTERIOR MEDIAN SULCUS (SPINAL CORD) POSTERIOR RAMUS (MOTOR NERVES) PRECENTRAL GYRUS (MOTOR NERVES) PREGANGLIONIC AXONS (AUTOSYMP) PREGANGLIONIC CELL BODIES (AUTOSYMP) PREVERTEBRAL GANGLIA (AUTOSYMP) PREVERTEBRAL GANGLIA (POSTGANGLIONIC NEURONS-AUTOSYMP) PRINCIPAL SPEECH AREA (FRONTAL LOBE-CEREBRUM) PROSTAGLANDIN PTERYGOPALATINE (GANGLIA–PARASYMP) PUPIL (EYE) PYRAMIDS (MYELENCEPHALON-BRAIN STEM) RECEPTOR CELLS (TASTE BUDS-TASTE) RECKLESS (EMOTION) RETICULAR FORMATION 98

SARCODES I, cont.

RETINAL ARTERIES (LAYERS OF THE EYE: RETINA-EYE) RHINENCEPHALIN SACCULE/UTRICLE (INTERNAL EAR-EAR) SEMICIRCULAR CANALS (INTERNAL EAR-EAR) SEMICIRCULAR DUCTS (INTERNAL EAR-EAR) SENSORY AREA (PARIETAL LOBE-CEREBRUM) SKELETAL MUSCLES (MOTOR NERVES) SKIN (MOTOR NERVES) SMALL INTESTINE SPINAL CORD (RELATED STRUCTURES-BRAIN STEM) SPINAL NERVES (MOTOR NERVES) SPINAL NERVES (POSTGANGLIONIC NEURONS-AUTOSYMP) SPLANCHNIC NERVE (AUTOSYMP) SPLANCHNIC NERVE (PREGANGLIONIC NEURONS-AUTOSYMP) SPLEEN STALK OF HYPOPHYSIS (RELATED STRUCTURES-BRAIN STEM) STAPES (MIDDLE EAR-EAR) STOMACH STOMACH ACID SUBARACHNOID SPACE (ARACHNOID-MENINGES) SUBMANDIBULAR (GANGLIA-PARASYMP) SUPERFICIAL FASCIA (MOTOR NERVES) SUPERIOR CEREBELLAR PEDUNCLE (MIDBRAIN-BRAIN STEM) SUPERIOR CISTERN (SUBARACHNOID SPACES-CERE FLUID) SUPERIOR COLLICULI (MIDBRAIN-BRAIN STEM) SUPPORTING CELLS (EQUILIBRIUM: CRISTA-EAR) SUPPORTING CELLS (INTERNAL EAR-EAR) SUPPORTING CELLS (SMELL) SUPPORTING CELLS (TASTE BUDS-TASTE) SUSPENSORY LIGAMENT (EYE) SWEAT GLANDS (TO SKIN – AUTOSYMP) SYMPATHETIC CHAIN (POSTGANGLIONIC NEURONS-AUTOSYMP) SYMPATHETIC CHAIN OF GANGLIA (AUTOSYMP) TECTORIAL MEMBRANE (INTERNAL EAR-EAR) TEMPORAL LOBE TEMPORAL MANDIBULAR JOINT TENTORIUM CEREBELLI (DURA MATTER-MENINGES) TESTIS THALAMUS (DIENCEPHALON) THIRD VENTRICULE (DIENCEPHALON) THORACIC DUCT THORACIC VISCERA (POSTGANGLIONIC NERUONS-AUTOSYMP) THYMUS THYROID 99

SARCODES I, cont.

TMJ TONSILS TOUCH-PRESSURE (SENSORY) TRIGEMINAL (PERIPHERAL SPINAL NERVES) UTERUS VAGUS NERVE VALVE OF HOUSTON WBC

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SARCODES II

1ST – 12TH CRANIAL NERVES FRONTAL BONE INFA CONCHA VERTEBRAE INTESTINE, SMALL/LARGE LYMPH, SPLEEN, MAMMARY MAXILLAE M1 3RD – 6TH NERVE OCCIPITAL OCCIPITAL CONDYLES OCCIPUT OLFACTORY NERVE OPTICAL NERVE PALATINE BONE PARIETAL BONE SACROILIAC SACRUM SPHENOID SQUAMA STOMACH, PANCREAS TEAR DUCTS TEMPORAL BONE TRIGEMINAL 5 (CRANIAL NERVES) TROUCHLEAT 4 (CRANIAL NERVES) TYMPANIC MEMBRANE (EXTERNAL EAR-EAR) VAGUS NERVE VENTRAL ROOT (MOTOR NERVES) VENTRAL (ANTERIOR) ROOT (SPINAL CORD-SPINAL NERVES) C1-C7 VERTEBRAE L1-L5 VERTEBRAE T1-T12 VERTEBRAE VESTIBULAR PATHWAY (PERIPHERAL SPINAL NERVES) VESTIBULE (INTERNAL EAR-EAR) VESTIBULOCOCHLEAR 8 (CRANIAL NERVES) VISCERAL AFFERENT PATHWAY (PERIPHERAL SPINAL NERVES) VISUAL AREA (OCCIPITAL LOBE-CEREBRUM) VITREOUS BODY (LAYERS OF THE EYE: SPACES/FLUID-EYE) VOMER BONE WHITE COMMISSURES (SPINAL CORD-WHITE MATTER) WHITE RAMUS COMMUNICANS (AUTOSYMP) ZYGOMA BONE

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SARCODES III

ABDOMINAL VISCERA (POSTGANGLIONIC NEURONS-AUTOSYMP) ABDUCENS 6 (CRANIAL NERVES) ACCESSORY 11 (CRANIAL NERVES) AGGRESSION AMYGDALA (DIENCEPHALON) ANGER (EMOTION) ANTERIOR CORTICOSPINAL TRACT (MOTOR NERVES) ANTERIOR CUTANEOUS DIVISION (MOTOR NERVES) ANTERIOR FUNICULUS (SPINAL CORD-WHITE MATTER) ANTERIOR HORNS (SPINAL CORD-GRAY MATTER) ANTERIOR MEDIAN FISSURE (SPINAL CORD) ANTERIOR RAMUS (MOTOR NERVES) ANXIETY (EMOTION) ARRECTOR PILI (TO SKIN-AUTOSYMP) ASSOCIATION NEURON (MOTOR NERVES) ASSOCIATION TRACTS (SUBDIVISIONS OF WHITE MATTER-CEREBRUM) AUDITORY AREA (TEMPORAL LOBE-CEREBRUM) AUDITORY (EUSTACHIAN) VERSTIBULE (MIDDLE EAR-EAR) AURICLE (EXTERNAL EAR-EAR) AUTISTIC (EMOTION) AXONS (MOTOR NERVES) AXONS (PREGANGLIONIC NEURONS-AUTOSYMP) AXONS – EYE, NASAL, ORAL, ETC. (POSTGANGLIONIC AXONS-PARASYMP) AXONS – HEAD & NECK (POSTGANGLIONIC NEURONS-AUTOSYMP) AXONS – S2, S3, & S4 (PREGANGLIONIC NEURONS-PARASYMP) AXONS – 3, 7, 9, 10 CRANIAL NERVES (PREGANG. NEURONS- PARASYMP) BASILAR MEMBRANE (INTERNAL EAR-EAR) BLOOD VESSELS (TO SKIN-AUTOSYMP) BONY LABYRINTH (INTERNAL EAR-EAR) CARELESS (EMOTION) CAUDATE NUCLEUS (BASAL NUCLEI-CEREBRUM) CAUDATE NUCLEUS (DIENCEPHALON) CELL BODIES (POSTGANGLIONIC AXONS – PARASYMP) CELL BODIES (POSTGANGLIONIC NEURONS- AUTOSYMP) CELL BODIES (PREGANGLIONIC NEURONS – AUTOSYMP) CELL BODIES (PREGANGLIONIC NEURONS – PARASYMP) CENTRAL CANAL CENTRAL CANAL (VENTRICLES-CERE FLUID) CENTRAL SULCUS (MAJOR FISSURES-CEREBRUM) CEREBELLUM (HINDBRAIN-BRAIN STEM) CEREBRAL AQUEDUCT (MIDBRAIN-BRAIN STEM) CEREBRAL AQUEDUCT (VENTRICLES-CERE FLUID) CEREBRAL PEDUNCLE (MIDBRAIN-BRAIN STEM) 102

SARCODES III, cont.

CEREBRAL PEDUNCLE (MOTOR NERVES) CHOROID PLEXUS (CERE FLUID) CILIARY (GANGLIA-PARASYMP) CILIARY BODY CILIARY PROCESSES (LAYERS OF THE EYE: CHOROID-EYE) CIRCUMVALLATE (PAPILLAE-TASTE) COCHLEA (INTERNAL EAR-EAR) COCHLEAR (PERIPHERAL SPINAL NERVES) COCHLEAR DUCT (INTERNAL EAR-EAR) COGNITION (BRAIN) COMMISSURE (SUBDIVISIONS OF WHITE MATTER-CEREBRUM) CONFUSION (EMOTION) CONJUNCTIVA (EYE) CORNEA (LAYERS OF THE EYE: SCLERA-EYE) CORONA RADIATA (MOTOR NERVES) CORONA RADIATA (PROJECTION TRACTS-CEREBRUM) CORPUS CALLOSUM (DIENCEPHALON) CUPOLA (EQUILIBRIUM: CRISTA-EAR) CUTANEOUS DIVISION (MOTOR NERVES) CRIBRIFORM PLATE (SMELL) DELUSION (EMOTION) DEPRESSION (EMOTION) DORSAL ROOT (MOTOR NERVES) DORSAL (POSTERIOR) ROOT (SPINAL CORD-SPINAL NERVES) DORSAL ROOT GANGLION (SPINAL CORD-SPINAL NERVES) EFFECTOR (MOTOR NERVES) EMR (SENSORY) ENDOLYMPHATIC DUCT (INTERNAL EAR-EAR) ENDONEURIUM (MOTOR NERVES) EPINEURIUM (MOTOR NERVES) EPITHALAMUS (DIENCEPHALON) EXTERNAL AUDITORY MEATUS (EXTERNAL EAR-EAR) FACIAL 7 (CRANIAL NERVES) FACILATATING EFFECT (MOTOR NERVES) FALX CEREBRI (DURA MATER-MENINGES) FEAR (EMOTION) FILIFORM (PAPILLAE-TASTE) FILUM TERMINALE (PIA MATTER-MENINGES) FOURTH VENTRICLE (HINDBRAIN-BRAIN STEM) FOURTH VENTRICLE (MYELENCEPHALON-BRAIN STEM) FOVEA CENTRALIS (LAYERS OF THE EYE: RETINA-EYE) FUNGIFORM (PAPILLAE-TASTE) GLOSSOPHARYNGEAL 9 (CRANIAL NERVES) GRAY COMMISSURES (SPINAL CORD-GRAY MATTER) 103

SARCODES III, cont.

GRAY RAMUS COMMUNICANS (AUTOSYMP) GREAT CISTERN (SUBARACHNOID SPACES-CERE FLUID) HAIR CELLS (EQUILIBRIUM: CRISTA-EAR) HAIR CELLS (EQUILIBRIUM: MACULA-EAR) HAIR CELLS (INTERNAL EAR-EAR) HAPTIC (SENSORY) HEAT-COLD (SENSORY) HYPOGLOSSAL 12 (CRANIAL NERVES) HYPOPHYSIS (DIENCEPHALON) HYPOTHALAMUS (DIENCEPHALON) INCUS INFERIOR COLLICULI (MIDBRAIN-BRAIN STEM) INHIBITING EFFECT (MOTOR NERVES) INTERMEDIATE ZONE (SPINAL CORD-GRAY MATTER) INTERNAL CAPSULE (DIENCEPHALON) INTERNAL CAPSULE (MOTOR NERVES) INTERNAL CAPSULE (PROJECTION TRACTS-CEREBRUM) INTERPENDUNCULAR CISTERN (SUBARACHNOID SPACES-CERE FLUID) INTERVENTRICULAR FORAMEN (VENTRICLES-CERE FLUID) INTRAMURAL (GANGLIA-PARASYMP) JOY (EMOTION) LATERAL CORTICOSPINAL TRACT (MOTOR NERVES) LATERAL CUTANEOUS DIVISION (MOTOR NERVES) LATERAL FISSURE (MAJOR FISSURES-CEREBRUM) LATERAL FUNICULUS (SPINAL CORD-WHITE MATTER) LATERAL HORNS (SPINAL CORD-GRAY MATTER) LATERAL RETICULOSPINAL (MOTOR NERVES) LATERAL VENTRICLE (DIENCEPHALON) LATERAL VENTRICLES (SUB CORTICAL AREAS-CEREBRUM) LATERAL 3RD (VENTRICLES-CERE FLUID) LATERAL 4TH (VENTRICLES-CERE FLUID) LENS (EYE) LENTICULA NUCLEUS (BASAL NUCLEI-CEREBRUM) LENTICULA NUCLEUS (DIENCEPHALON) LONGITUDINAL FISSURE (MAJOR FISSURES-CEREBRUM) LUMBAR CISTERN (SUBARACHNOID SPACES-CERE FLUID) LUST (EMOTION) MALLEUS (MIDDLES EAR-EAR) MAMMILLARY BODIES (RELATED STRUCTURES-BRAIN STEM) MEDICAL RETICULOSPINAL (MOTOR NERVES) MEDICAN/LATERAL APERTURES (CERE FLUID) MEDULLARY PYRAMIDS (MOTOR NERVES) MIDDLE CEREBELLAR PEDUNCLES (HINDBRAIN-BRAIN STEM) 104

SARCODES III, cont.

MIDDLE CEREBELLAR PEDUNCLES (MYELENCEPHALON-BRAIN STEM) MOTOR AREA (FRONTAL LOBE-CEREBRUM) MOTOR CELL BODIES (SPINAL CORD-SPINAL NERVES) MOVEMENT (SENSORY) MUSCLES OF THE EYEBALL (EYE) MUSCULAR BRANCH (MOTOR NERVES) MUSCULAR BRANCHES (MOTOR NERVES) NERVE FIBERS (EQUILIBRIUM: CRISTA-EAR) NERVE FIBERS (EQUILIBRIUM: MACULA-EAR) NERVE FIBERS (TASTE BUDS-TASTE) NERVES OF HEAD & FACE (PERIPHERAL SPINAL NERVES) NERVES OF LOWER LIMBS (PERIPHERAL SPINAL NERVES) NERVES OF THORAX (PERIPHERAL SPINAL NERVES) NERVES OF UPPER LIMBS (PERIPHERAL SPINAL NERVES)

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ORIENTAL HERBAL PHILOSOPHY

The Chinese did not have a system of succussion, nor did they have a system of homeopathic dilution, but their pharmacology was much akin to homeopathic processes. Many herbs were diluted to find safer levels of activity. This titration allowed for strong herbs to be used more safely. The Chinese have studied the medicinal effects of herbs for thousands of years. Specific directions were developed on how to pick the herbs, preserve the herbs, and how to prepare the herbal remedy. Often, these remedies were made in dilute quantities, sometimes as low as one part per trillion, which is equivalent to a 9x. They understood how certain herbs could be made more dilute and still achieve pharmacological effectiveness. Nature provides many energetic factors beyond mere chemistry. Subtle energetic effects, mineral balance, electrical regulation abilities, and more are stable in dilution. Dilution also offers safety in compliance with the minimal dose concept of medicine. Many Chinese herbs have excellent effects in low-potency homeopathic form. The Dr. Recommends’ oriental herb remedies combine the compatibility of herbology and homeopathy. This is to insure safety first, while guaranteeing effectiveness. Many compounds can be increased in energetic potency as we make them more and more dilute, while preserving their activity. The oriental herb formulas are quality controlled through QQCTM techniques.

Source: http://www.myhealthandharmony.com/category_s/33.htm

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Quality of Herbs

America has often come under fire because of an inability to supply good quality herbs. This is largely due to the fact that American herbs can be picked at any time, in any place. In following the Chinese protocol, herbs are picked at precise times and in precise ways so that the pharmacological activity of the herb is preserved. Dr. Recommends buys many of its herbs from the Chinese, Japanese and Korean markets. Still, that is not enough; each of these herbs must undergo quality control methods to make sure that the pharmacological activity of the herb is above the satisfactory level and at the highest level of potency in developing the natural pharmaceuticals. Next in developing quality control techniques beyond the chemistry and beyond the range of 12x, Dr. Recommends developed Kirlian photography methods of analysis, freezing studies of the crystalline structure of the liquid crystal effect of water, trivector analysis to analyze the magnetic, dielectric static and conductance fields of the different homeopathics to understand the energetic nature of these compounds; and patient reactivity modes, challenging them on skin resistance, voltage, and other directed activity. As well, Dr. Recommends has researched a photo-multiplier, and has measured the photons coming off of these fields; and how these different compounds affect living tissue with their electromagnetic radiation through the mitogenic process. The development of a quality control process was paramount in developing a way to create the most precise, safe and effective remedies for doctors to use with their patients. Dr. Recommends realized that this needed to have a global expression, and has developed manufacturing in Ireland and Canada. Dr. Recommends has developed a global strategy to supply doctors and practitioners throughout the USA, Europe, and Canada with product,

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guaranteeing the safety and effectiveness, the reverence for nature, and the education. Current seminar development is happening in all of these countries; educating doctors in how to develop diagnostic protocol and healing therapeutic regimes for their patients, using these natural products. For the doctor who wants natural, homeopathic pharmaceuticals, Dr. Recommends is ready to serve with the highest level of quality and service all directed through the company pledge for safety, effectiveness, quality control, natural healing, reverence of nature, and education of both patient and doctor. Dr. Recommends welcomes you to a new standard and level of quality control and service.

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ORIENTAL HERBAL REMEDIES

ANTHELMINTIC (1 fl. oz.) Catalog No. 0127 Indication: Purgative for worms and intestinal parasites Ingredients: Meliae Toosendan Fructus, Quisqualis Fructus, Cucurbitae Semen, Torreyae Semen, Omphalia, 3x, 6x, 12x, 30x.

ANTI-ASTHMATIC (1 fl. oz.) Catalog No. 0135 Indication: Wind and cold effects, chills and fever, Exterior symptom complex, Regulates energy for lungs Ingredients: Perillae Folium, Astragali Radix, Ephedrae Herba, Cinnamomi Cortex, Armeniacae Semen, Glycyrrhizae Radix, Paeoniae Radix, Zizyphi Fructus 3x, 6x, 12x, 30x.

ANTI-PHLOGISTIC (1 fl. oz.) Catalog No. 0129 Indication: Protects body from wind, cold, dampness, Improves chi Ingredients: Schizonepetae Herba, Ledebouriellae Radix, Notopterygii Rhizoma, Angelicae Dahuricae Radix , Ligustici Rhizoma, Bupleuri Radix, Peucedani Radix, Platycodi Radix, Poria, Menthae Herba, Glycyrrhizae Radix, Aurantii Fructus 3x, 6x, 12x, 30x.

ANTI-PYRETIC (1 fl. oz.) Catalog No. 0137 Indication: Fever, Febrifugal, Expels toxic heat, wind, chills from exterior Ingredients: Forsythiae Fructus, Menthae Herba, Platycodi Radix, Lonicerae Flos, Schizonepetae Herba, Arctii Fructus 3x, 6x, 12x, 30x.

ANTI-RHEUMATIC (1 fl. oz.) Catalog No. 0138 Indication: Dispels wind, cold, dampness to improve rheumatic pain, Activates blood flow in collateral channels Ingredients: Aconiti Carmichaeli Preparata Radix, Angelicae Dahuricae Radix, Olibanum, Myrrha, Lumbricus, Clematidis Radix, Draconos Os 3x, 6x, 12x, 30x.

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BLOOD (1 fl. oz.) Catalog No. 0133 Indication: Replenishes blood, Restores vitality, Maximizes acupuncture system development of blood Ingredients: Ginseng Radix, Rehmanniae Radix, Angelicae Dahuricae Radix, Atractylodis Lanceae Rhizoma, Cinnamomi Cortex, Paeoniae Radix, Arctii Fructus, Trifolium pratense, Spinacea oleracea 3x, 6x, 12x, 30x.

BONE (1 fl. oz.) Catalog No. 0175 Indication: Degenerative conditions, Unstable chi Ingredients: Myrrha, Lonicerae Flos, Scutellaria lateriflora, Taraxacum officinale, Magnoliae Officinalis Cortex, Juglans nigra, Tang Kuei, Akebiae Caulis Fructus, Echinacea purpurea, Shark Cartilage, Sarcode: Bone/Bone Marrow, Equisetum arvense, Beta vulgaris 3x, 6x, 12x, 30x.

CARMINATIVE (1 fl. oz.) Catalog No. 0130 Indication: Relieves gas and stagnation of food, Dispels congestion of toxic energy from stomach and bowels Ingredients: Citri Immaturi Pericarpium, Magnoliae Liliflorae Flos, Linderae Radix, Rhei Rhizoma, Pharbitis Semen 3x, 6x, 12x, 30x.

COLD AND FLU (1 fl. oz.) Catalog No. 0162 Indication: Colds, Flu, Expels heat, cold and wind from interior Ingredients: Lonicerae Flos, Forsythiae Fructus, Arctii Fructus, Menthol, Glycerinum, Glycine, Schizonepetae Herba, Echinacea purpurea, Placenta, Zingiber officinale 3x, 6x, 12x, 30x.

DIGESTIVE STIMULATOR (1 fl. oz.) Catalog No. 0131 Indication: Invigorates stomach, spleen, lung, heart, Reinforces middle burner ngredients: Ginseng Radix, Codonopsis Pilosulae Radix, Astragali Radix, Glycyrrhizae Radix, Hordei Germinatus Fructus, Atractylodis Lanceae Rhizoma, Polygonati Rhizoma 3x, 6x, 12x, 30x.

ESOPHAGUS (1 fl. oz.) Catalog No. 0163 Indication: Degenerative conditions, Unstable chi, Balances upper warmer Ingredients: Salvia officinalis, Scutellaria Barbatae Herba , Zizyphi Fructus, Rhei Rhizoma, Achyranthis Radix, Zingiber officinale, Ammonium Nitricum 3x, 6x, 12x, 30x. 110

EXPECTORANT (1 fl. oz.) Catalog No. 0136 Indication: Clears lungs of mucous, Dispels heat in lungs Ingredients: Anemarrhenae Rhizoma, Mori Radicis Cortex, Trichosanthis Semen, Gardeniae Fructus, Poria, Citri Immaturi Pericarpium 3x, 6x, 12x, 30x.

FEMALE (1 fl. oz.) Catalog No. 0134 Indication: Regulates menstrual disturbances, Restores vitality and energy to blood of female Ingredients: Codonopsis Pilosulae Radix, Atractylodis Lanceae Rhizoma, Angelicae Dahuricae Radix, Rehmanniae Radix, Poria, Cyperi Rhizoma, Zizyphi Fructus, Ligustici Rhizoma, Glycyrrhizae Radix 3x, 6x, 12x, 30x.

HEPATIC (1 fl. oz.) Catalog No. 0128 Indication: Removes stagnant energy from liver, Restores liver chi Ingredients: Magnoliae Officinalis Cortex, Curcumae Rhizoma, Aquilariae Lignum, Verbena hastata, Bupleuri Radix, Corydalidis Tuber 3x, 6x, 12x, 30x.

HYPERTENSIVE (1 fl. oz.) Catalog No. 0140 Indication: Alleviates heat in liver, Corrects deficiency in yin of liver, Balances excess yang Ingredients: Haematitum, Pinellia Tuber, Achyranthis Radix, Rauwolfiae Verticillatae Radix 3x, 6x, 12x, 30x.

KIDNEY (1 fl. oz.) Catalog No. 0164 Indication: Degenerative conditions, Unstable chi, Removes toxic energy from ancestral meridians. Ingredients: Lobelia inflata, Imperatae Rhizoma, Dioscorea batatis Rhizoma, Lygodii Spora, Desmodii Herba, Haematitum, Cirsii Japonica 3x, 6x, 12x, 30x.

LARGE INTESTINE (1 fl. oz.) Catalog No. 0165 Indication: Degenerative conditions, Unstable chi, Removes wind from large intestine Ingredients: Oldenlandiae Herba, Lonicerae Flos, Scutellaria Barbatae Herba, Taraxacum officinale, Sophorae Flos, Sanguisorbae Radix, Magnoliae Officinalis Cortex, Akebiae Caulis, Citrus trifoliata, Salviae Miltorrhizae Radix 3x, 6x, 12x, 30x.

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LAXATIVE (1 fl. oz.) Catalog No. 0141 Indication: Relieves constipation due to spleen fluid deficiency, Dispels toxic energy from large intestine, Boosts liver chi Ingredients: Cannabis Semen, Rhei Rhizoma, Armeniacae Semen, Magnoliae Officinalis Cortex, Rhamnus purshiana , Capsicum frutescens, Rhei Rhizoma 3x, 6x, 12x, 30x.

LIVER (1 fl. oz.) Catalog No. 0166 Indication: Degenerative conditions, Unstable chi, Removes toxic energy liver Ingredients: Archangelica , Salviae Miltorrhizae Radix, Carathami Flos, Scutellariae Barbatae Herba, Echinopsis Radix, Akebiae Caulis, Paeoniae Radix, Gardeniae Fructus, Amoni Semen, Angelica Sinensis 3x, 6x, 12x, 30x.

LUNG (1 fl. oz.) Catalog No. 0167 Indication: Degenerative conditions, Unstable chi, Removes heat from lung Ingredients: Mori Folium, Coicis Semen, Trichosanthis Radix, Sargassum, Pumex, Houttuyniae Herba, Armeniacae Semen, Laminariae Thallus, Lepidii Semen, Stemonae Radix, Salviae Miltorrhizae Radix, Glycyrrhizae Radix, Imperatae Rhizoma 3x, 6x, 12x, 30x.

LYMPH (1 fl. oz.) Catalog No. 0168 Indication: Degenerative conditions, Unstable chi, Removes excess yin from interior Ingredients: Myrrha, Aconiti Carmichaeli Praeparata Radix, Angelicae Dahuricae Radix, Ephredrae Herba, Echinacea purpurea 3x, 6x, 12x, 30x.

MENTAL (1 fl. oz.) Catalog No. 0132 Indication: Invigorates kidney meridian, Senility, Old age, Balances excess yin Ingredients: Cornu Cervi, Hippocampus, Epimedii Herba, Ginseng Radix, Cynomorii Herba, Angelicae Dahuricae Radix 3x, 6x, 12x, 30x.

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PREVENTATIVE (1 fl. oz.) Catalog No. 0169 Indication: Tonifies and improves immunity, Balances yin and yang irregularities Ingredients: Wisteria chinensis, Trapa natans, Terminalia Chebulae Fructus, Coicis Semen 3x, 6x, 12x, 30x.

SEDATIVE (1 fl. oz.) Catalog No. 0139 Indication: Nourishes blood of liver, Expels heat from heart, Fatigue, Insomnia Ingredients: Coptidis Rhizoma, Cinnabaris, Valeriana officinalis, Zizyphi Fructus, Glycyrrhizae Radix, Zizyphi Spinosi Semen, Tritici Fructus 3x, 6x, 12x, 30x.

STOMACH (1 fl. oz.) Catalog No. 0170 Indication: Degenerative conditions, Unstable chi, Balances middle warmer Ingredients: Solanum nigrum, Salviae Miltorrhizae Radix, Scutellariae Barbatae Herba, Pteris Herba, Raphni Semen 3x, 6x, 12x, 30x.

UTERINE (1 fl. oz.) Catalog No. 0171 Indication: Degenerative conditions, Unstable chi Ingredients: Cinnamomi Cortex, Carthami Flos, Phellodendri Cortex, Ostraea Testa, Astragali Radix, Lonicerae Flos, Gentianae Scabrae Radix, Aconiti Carmichaeli Praeparata Radix, Linderae Radix, Violae Herba 3x, 6x, 12x, 30x.

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CHINESE-AMERICAN HERBALS

Achyranthes Laminaria Rhubarb Aconite (Processed) Leonurus Salvia Aconite (Roasted) Lepidium Sanguisorba Akebia Licorice Sargassum Anemone Lily Schizandra Angelica Lindera Schizonepeta Anteater Scales Lonicera Scute Apricot Seed Lotus Embryo Scute Herba Arctium Lotus Receptacles Smilax Areca Seed Lotus Seed Sophora Asparagus Lycium Fruit Stemona Astragalus Lygodium Sterculia Cardamon Magnolia Bark Tang-Kuei Carthamus Magnolia Flower Terminalia Centipeda Malt Thlaspi Chih-Shih Mentha Thymifolia Chrysanthemum Morus Bark Trichosanthes Fruit Cirsium Morus Branch Trichossanthes Seed Clematis Morus Leaves Tsao-ko Coix Myristicae Tsao-Tou-Kou Cyperus Myrrh Tussilago Cuttle Bone Oldenlandia Viola Dioscorea Omphalia Xanthium Dragon Bone Oryza Fennel Peony Forsythia Phellodendron Gardenia Placenta Gentiana Plantago Glehnia Pumice Haematite Pyrite Hoelen Raphanus Houttuynia Rauwolfia Imperta Jujube

This is a brief list of the most used Chinese herbal homeopathics. Others are available upon request made as homocords (3x, 6x, 12x, 30x) of the herbal.

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CHINESE HERBOLOGY AND HOMEOPATHY

In the chapter on the scientific explanation of homeopathy it was explained that there are several different pharmacological dynamics which allowed for homeopathy to occur at low-dose ratios; those of 12x or below. The Arndt-Schultz law indicated how poisons in certain compounds would have a paradoxical shift in activity as they were made more and more dilute. This means that whatever the effect of a poison is in raw dose, as it is made more and more dilute there is a paradoxical shift, or a reversal of what the compound does. As we have proved several times in the Quantum Biology, the Quantum Biology Workbook, and other publications, homeopathy is not just like treating like. Oftentimes homeopathy is treating via the pharmacological agent within the herb. Thus the indications of the homeopathic remedy are very similar, if not identical to the indications suggested by the active ingredients of the original herb. With this in mind, just what is homeopathy vs. allopathy? To offer a new definition for homeopathy which encompasses the old definition, we can see that a homeopath is truly trying to stimulate the organism of the human body to respond and heal itself. In allopathy, an outside intervention via a drug is meant to sedate, stimulate, block, deceive, or do some type of unnatural process. Thus, the organism becomes dependent on the outside stimulus, such as when an MAO inhibitor is used to stop depression; the person’s own development of monoamine oxidase becomes deficient. If we use an antihistamine to fight histamine release, then the person’s own development of histamine can be deficient. Allopathy seeks to build dependence. The key for the allopath is the hope that the allopathic medication will pick up some slack, and that the patient will heal himself while the allopathic medication is operating. In other words, he hopes that the patient can find his own biological 115 solution while the anti-histamine is working. But the anti-histamines and most of the allopathic synthetic medications, of course, do not cure; they only stimulate externally, relying on the forces of nature to cure the body in the interim. In homeopathy, there are many different principles at play that are trying to encourage the body to heal itself, rather than stimulating it to heal itself. This is the concept of the minimal dose which Hahnemann believed in; trying to find the smallest amount of a homeopathic or pharmacological agent that could gently nudge the patient back into the biological cybernetics of health. Using a “feather” to stimulate such a balance is the principle of homeopathy. In using the Arndt-Schultz law for poisons such as Belladonna, Apis mellifica, Hepar sulph, etc., we can see that this principle illustrates that what a poison does in raw dose is opposite to a homeopathic form of the poison. It can be observed in snake venoms and other biological poisons that they have the ability to mend and heal different enzyme pathways. In herbs which are not poisons, we can also see a homeopathic principle where a compound is used to apply a gentle nudge to the patient to return to health. In Chinese herbalism, if a patient had too much heat in the body, such as fever, the herbalist would use a refrigerant. If a patient had a problem with constipation, then an herbal laxative would be used. We see these different propositions as being akin to homeopathy in that we would try to use the least possible amount of refrigerant or whatever product to accomplish the job of bringing the patient back to stability, just as a homeopath might use Eyebright, or might use adrenal tissue to help in a weak adrenal case. This is also applied to the concept of Chinese herbalism. The new definition of homeopathy is one of gentle stimulation of the body to heal itself rather than to be dependent on an outside pharmacological intervention. This broader definition of homeopathy will 116 allow us to re-evaluate the different herbals and natural compounds that used to be in the natural compendium, and bring them back into the medical repertoire. In using the different compounds of the herbal repertoire we can see that this is much akin to a homeopathic philosophy. The dilution process is merely to seek a minimal dose of these items, so that we can accomplish the positive effects and minimize the negative effects of the herbs. Thus, homeopathy allows for many different factors: 1) Homeopathy can be nutritional supplementation. If we use a homeopathic compound such as Vitamin A or Vitamin B to supplement the body’s deficiency syndrome, then homeopathy can be used in a nutritional sense. If we were to take a concentrated source of B-12 and dilute it one part to ten, six times, to arrive at a 6x, we would see that this 6x is approximately equal to the RDA of B-12. Some of the minute doses of vitamins that people use can be reflected in the compounds of homeopathy. Such homeopathic compounds made for nutritional supplementation are in the Liquitrophic line made by Dr. Recommends. These different liquitrophic were developed for nutritional supplementation in using the minimal dose philosophy, and also using the highest quality of vitamins known to man; that of vitamins made by nature, not the synthetic vitamins made by man’s technology. This line was basically a variation of Royal Lee’s ideas of protomorphology and nutrition using natural compounds such as snow pea for kidney development, wheat grass for B Vitamins, natural wheat germ for Vitamin E, and the whole series of natural Vitamin C factors for Vitamin C. These compounds have been blended into natural liquids for vitamin supplementation, and are a superior line to some of the Standard Process Formulas. The Standard Process Formulas use different unnatural pills, as nature does not provide pill trees and capsule bushes. Using these liquids, we can increase the surface area over one million times. We can start the digestive process in the mouth with the help of 117 the brain and all the innervations that go into the nasal pharynx, so that the nervous system can properly prepare for absorption and utilization. By doing this, it has been possible to increase the effectiveness and the mode of delivery of the Standard Process Formulas while capturing an increase in the potency. 2) Homeopathy can be used to help stimulate the body. So if we use caffeine or Belladonna at low dose, we can achieve some of the low-dose pharmacological action; trying to trigger the body to do its own healing. The vast difference here between homeopathy and allopathy is that we do not try to incur dependence with homeopathy, but rather use the minimal dose, and gently shift the patient to being able to accomplish his own health. 3) Homeopathy can be used in many classic ways to help reverse symptoms, and stimulate the body to return to the balance of its cybernetic systems. This chapter is dedicated, however, to the idea of using herbs in high concentrations and low potencies of 2x, 3x, and 4x for pharmacological and homeopathic action. Let us return to the analysis of the Chinese herb philosophy. Belladonna contains atropine, and the pharmacological effects of it are that it makes us red as a beet, dry as a bone, and mad as a hatter. This is the anti-cholinergic effect of the pharmacology of the atropine in the Belladonna compound. Belladonna is a poison. If taken in large enough doses it will cause death. If we make the Belladonna solution more and more dilute, and more and more dilute, we will see, if we chart the pharmacological effects of Belladonna, that at a certain point it will cause a paradoxical shift, and it will reverse redness, reverse dryness, and reverse madness. Thus, if a patient were to come to us who was red as a beet, dry as a bone, and mad as a hatter, we might suggest a 6x, 9x, or possibly higher potencies of Belladonna to reverse these processes. The Arndt-Schultz law, as pointed out in the chapter on pharmacology, states that a compound that is a poison will always have a reversal. A 118

compound that is not a poison will follow Wilder’s Law of Initial Values. This tells us that as a nonpoisonous compound is made more dilute we might see an increase in its pharmacological activity of what the raw dose of the formula does, we might see an inverse, or we might see no effect whatsoever. An example of this would include most of the sarcodal tissues including thyroid and adrenal. Here we will see that the effect of these sarcodal tissues is stimulation or a hormonal effect. If we use raw adrenaline, we will see that it has a stimulating effect on the body. If we use a more and more dilute form of the adrenaline - 6x, 12x, etc., we will often see a similar increase in the same type of stimulation capacity. We rarely see reverses in the sarcodal formulas. Many herbs also follow this potentiation cycle, such as Eyebright, which if taken in raw doses makes the eyes bright; hence its name. It was named Eyebright because herbalists found that it helped conditions of the eye. As we make it more and more dilute we see that the homeopathic use of Eyebright, even in dilute quantities of 16x, 30x, and above, will help improve eyes and vision. If it were all reversal, we would only use Eybright when a patient came in whose vision was too good. If a patient said, “I see too well,” then homeopathic Eyebright would be used. But this is not the case; homeopathic Eyebright is used to improve vision. Many herbs have increased or equal health value in homeopathic form. It is wrong to merely value compounds by their dosages, as in synthetic pharmacology. Many Chinese herbs can have excellent effects in low-potency homeopathic form. As stated in the Law of Initial Values, some things will be reversal if they tend towards poisons, and some things will be potentiating of their original effects. Also, some items will have no effect at all as they are made more and more dilute. In the study of Chinese herbalism, we see a very profound description of an excellent natural pharmacology. We can see that the Chinese have studied the medicinal effects of herbs for thousands of years, and that 119 specific directions were developed in how to pick these herbs, preserve them, and then prepare certain remedies. Often these remedies were made in dilute quantities, sometimes as low as one part per trillion, which is equivalent to a 9x. The Chinese understood how certain items could be made more dilute and still achieve pharmacological effectiveness. To assume that the only active ingredients are chemical in these Chinese herbs is to make the same mistake the synthetic chemical companies make. Nature provides many energetic factors beyond mere chemistry. Subtle energetic effects, mineral balance, electrical regulation abilities, and more are stable in dilution. Dilution also offers safety in compliance with the minimal dose concept of medicine. The Chinese did not have a system of succussion, nor did they have a system of homeopathic dilution, but their pharmacology was much akin to some of these processes. Many herbs were diluted to find safer levels of activity. This titration allows for strong herbs to be used safely. One of the problems of the herbal industry in America is the lack of preciseness in how an herb should be picked and processed. In China, an herb is picked at precise times of the year using precise methods, so that the pharmacological activity of the herb is assured. In America, however, the herbal industry for the last fifty years has been much less precise. Without a precise pharmacopoeia, unknowing American distributors of herbs might pick them at non-pharmacologically active periods of their cycle. Without care for quality control, many companies pass on irregular or impotent products without safety or efficacy. This has led to the demise of the herbal industry in America; whereas, the fine quality control processes of the herbs in China has led to the high success of China’s sphere of medical influence. In 1962, the FDA abolished the natural compendium of herbs and natural remedies. We might look at several theories for its demise, but indeed, some of this lack of quality control is a factor.

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In developing an herbal protocol to mix with homeopathics, wise manufacturers including Dr. Recommends have had to develop severe, exacting quality control criteria for accepting different herbals ordered from American or other herbal suppliers. These types of quality control techniques include product surveys, product assays, and product determination in methods such as spectrophotometer, atomic absorption, chromatography, culture analysis, and other forms of chemical procedures to determine pharmacological activity. Dr. Recommends has been able to develop the finest quality control analysis protocol to assure the highest form of potency for the different herbs utilized. The Chinese literature is filled with herbal references, and information about how these herbs can be used medicinally to help patients in a wide variety of ways. It is Dr. Recommends’ idea that many of these herbs can also be put into homeopathic dilution, and used in a similar process. This is to insure safety first while guaranteeing effectiveness. We do not see this as contradictory to the homeopathic process in any way. In fact, Wilder’s Law of Initial Values tells us that many of these compounds, once understood, can be increased in energetic potency as we make them more and more dilute, while preserving activity. Dr. Recommends has developed a pilot study and statistical protocols to determine the absolute effectiveness and safety of the different compounds. Clinical trials are an important part of the Dr. Recommends’ quality control protocol. Dr. Recommends started with the idea that Chinese herbology and homeopathy were compatible in their format, and could be blended. The first type of blending in this technology was through a system of oriental herb formulas directed toward different organ systems, which were called “Oriental Herbs for Organs”. A list of these different products is included.

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These were taken from the book, Treating Cancer with Chinese Herbs, by Hong-Yen Hsu. In this book, several cancer treatment modalities were noted for a variety of different organ system types of cancer. These treatment modalities were developed by doctors in Shanghai, China. They used many different types of herbal therapies which Dr. Recommends sought to blend into formulas for treatment of similar degenerative problems. After twenty-five years of commerce with these products, the remarks by many doctors have confirmed that this is not only a safe system of treatment, it is a very effective one as well. The herbs in those different formulas were put into formulas at low potencies of 2x, 3x, and sometimes 4x, equivalent to the dilution methods used by the doctors in China. In fact, the dilutions are almost equivalent to the treatments used in China. The success of these formulas has led Dr. Recommends to develop other formulas following the Chinese herbal system. These are developed with the Chinese herbal acupuncture modality of treatment. In developing these herbal formulas, Dr. Recommends tries to use herbal remedies from all over the world, including those from the Amazon rain forest where certain herbs have been studied and used by Amazon tribes for years. In making up these formulas, Dr. Recommends has used herbal formulas from the Amazon, China, Korea, America, South America, Europe, Russia, and many other places.

Bibliography Lee, R. Hanson, W. Protomorphology. Lee Foundation for Nutritional Research, 1947. Milwaukee, Wisconsin.

Hsu, Hong-Yen. Treating Cancer with Chinese Herbs. The Oriental Healing Arts Institute, 1982. Long Beach, California.

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THE MIASM PHILOSOPHY

In classical homeopathy, a miasm is thought to be a tendency toward a disease pattern that is passed on from one generation to the next. Sometimes, these disease tendencies can produce a variety of conditions that can be inherited from our ancestors. Hahnemann found that miasms such as sycosis (a type of gonorrhea), syphilis, and psora, could be transmitted through genetic inheritance. We now know that there are other types of miasm links. Miasms work on very high vibrational levels; thus, the miasm formulas need to be in a very high homochord state to help in breaking up the miasm tendency in the patient. This is achieved through the QQCTM process. We caution the young initiate in homeopathy; using these remedies takes some degree of skill and training.

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MIASM REMEDIES

MIASM-ALLER (1 fl. oz.) Catalog No. 0154 Indication: Allergies Ingredients: Encephalitis, Typhus, Malaria, Anthrax, Toxoplasmosis, Venereum, Cold Virus, Allergic Reactivity Sarcodes: Adrenal, Pancreas, Liver 12x, 30x, 100x, 500x, 1000x.

MIASM-CAN (1 fl. oz.) Catalog No. 0155 Indication: Degenerative diseases Ingredients: Melanoma, Sarcoma, Myeloma, Neurofibroma, Carcinoma, Tumor 12x, 30x, 100x, 500x, 1000x.

MIASM-CF (1 fl. oz.) Catalog No. 0156 Indication: Chronic fatigue, Tiredness, Exhaustion Ingredients: Brucellosis, Epstein Barr, Mononucleosis, Cytomegalovirus, Tularemia, Streptococcus fecalis, Elephantiasis, Coxsackie, Neuromyasthenia, Candida albicans 12x, 30x, 100x, 500x, 1000x. Echovirus 12x, 17x, 30x, 100x, 500x, 1000x. Pseudomonas 12x, 17x, 30x, 100x, 500x, 1000x. Borrelia burgdorferi 13x, 30x, 100x, 500x, 1000x. Malaria, Pestinum 15x, 30x, 100x, 500x, 1000x. Spirillum minus 16x, 30x, 100x, 500x, 1000x.

MIASM-CHOL (1 fl. oz.) Catalog No. 0151 Indication: Cholera, Intestinal disorders Ingredients: Ameba 15c, 30c, 100c; Cholera, Dysentery (Bacillus dysenteriae), Pyrogenium, 20x, 30x, 100x, 500x, 1000x.

MIASM-FNG (1 fl. oz.) Catalog No. 0152 Indication: Fungus, Yeast sensitivity Ingredients: Amanita muscaria, Saccharomyces, Candida albicans, Molds, Epidermophyton, Chlamydia 12x, 30x, 100x, 500x, 1000x. Blastomyces 17x, 30x, 100x, 500x, 1000x. Candida parapsilosis 19x, 30x, 100x, 500x, 1000x.

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MIASM-LEP (1 fl. oz.) Catalog No. 0146 Indication: Leprosy, Skin disorders Ingredients: Leprosy, DNA, RNA, Myrrh, Verbascum thapsus 12x, 30x, 100x, 500x, 1000x.

MIASM-MEN (1 fl. oz.) Catalog No. 0153 Indication: Mental disorders Ingredients: Encephalitis, Nocardia, Bacteria, Virus, Imponderables: Guilt, Shame, Jealousy, Rage, Hatred, Prejudice, Incest, Greed, Judgmental, Obsession, Depression, Aggression 12x, 30x, 100x, 500x, 1000x. Meningitis, Trichinosis 15x, 30x, 100x, 500x, 1000x.

MIASM-MZL (1 fl. oz.) Catalog No. 0147 Indication: Measles, Dermatitis Ingredients: DNA, RNA, Chamomilla, Trifolium pretense, Pulsatilla 12x, 30x, 100x, 500x, 1000x; Morbillinum (Rubeola) 20x, 30x, 100x, 500x, 1000x.

MIASM-PSO (1 fl. oz.) Catalog No. 0143 Indication: Psora, Skin disturbances Ingredients: Psorinum, Staphylococcus, Streptococcus, Tuberculinum, DNA, RNA, Calcarea Carbonica, Medorrhinum, Kali Muriaticum, Pulsatilla, Bryonia 12x, 30x, 100x, 500x, 1000x.

MIASM-SYC (1 fl. oz.) Catalog No. 0144 Indication: Sycosis, Skin disorders Ingredients: Syphilinum, Nocardia, DNA, RNA, Natrum Muriaticum, Petroleum, Sulphur, Natrum Sulphuricum, Zincum Valerianicum, Apis mellifica 12x, 30x, 100x, 500x, 1000x. Medorrhinum, Chlamydia trachomatis 16x, 30x, 100x, 500x, 1000x.

MIASM-SYP (1 fl. oz.) Catalog No. 0142 Indication: Syphilis, Skin disorders, Sexual disturbances Ingredients: Syphillinum, DNA, RNA, Lymes, Antimonium Crudum, Kali Muriaticum, Mercurius Solubilis, Mercurius Vivus, Hepar Sulphuris Calcareum 12x, 30x, 100x, 500x, 1000x.

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MIASM-TB (1 fl. oz.) Catalog No. 0148 Indication: Tuberculosis Ingredients: Tuberculosis, Pneumonia, Bronchiecyasis, Pertussis, DNA, RNA, Natrum Sulphuricum, Aconitum napellus 12x, 30x, 100x, 500x, 1000x.

MIASM-TET (1 fl. oz.) Catalog No. 0145 Indication: Tetanus, TMJ disorders Ingredients: Tetanus, TMJ, DNA, RNA, Botulinum, Shigella, Calcarea Phosphorica, Calcarea Sulphurica 12x, 30x, 100x, 500x, 1000x.

MIASM-VAC (1 fl. oz.) Catalog No. 0149 Indication: Vaccine Ingredients: Vaccinotoxinum, Varicella, Parotitis, Polio, Grippe, Influenza, Diphtheria, Measles, Tetanus 12x, 30x, 100x, 500x, 1000x.

MIASM-VIR (1 fl. oz.) Catalog No. 0150 Indication: Virus sensitivity Ingredients: Apium Virus, Ichthyolum, Vaccinotoxinum, Morinum, Variolinum, Misc. Influenzinum, Vincetoxicum, Retrovirus 12x, 30x, 100x, 500x, 1000x. Psorinum 16x, 30x, 100x, 500x, 1000x.

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THE PSYCHOLOGICAL PHILOSOPHY

The Dr. Recommends’ psychological homeopathic formulas use a combination of homeopathic ingredients to help stabilize psychological conditions found in the patient population. These psychological conditions run the range of depression, anxiety, mania, etc. It must be pointed out that these patients’ systems are often complicated by other allopathic treatment that can diminish the homeopathic results. The Dr. Recommends’ psychological remedies are not complete therapy in and of themselves. Any type of psychological treatment should include a referral to a psychologist, counselor, or other professional trained in this area. These remedies are an adjunctive therapy and should never be used as a primary or a singular method of treatment.

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PSYCHOLOGICAL REMEDIES

PSY-ADJ (1 fl. oz.) Catalog No. 0301 Indication: Adjustment disorders Ingredients: Ustilago maidis, Antipyrine 2x. Caladium seguinum 3x. Digitalis purpurea, Arundo mauritanica, Glonoine, Xerophyllum asphodeloides 6x. Anhalonium 12x. Kreosotum 24x. Lachesis mutus 30x. Phosphorus, Nux vomica 30x, 60x, 100x.

PSY-ANX (1 fl. oz.) Catalog No. 0302 Indication: Anxiety Ingredients: Oxytropis lambertii 3x. Natrum Muriaticum, Borax 4x. Alumina 5x. Causticum 6x. Plumbum Metallicum 8x. Sepia 12x. Lilium tigrinum 30x. Chamomilla, Coffea tosta 30x, 60x, 100x.

PSY-DELR (1 fl. oz.) Catalog No. 0303 Indication: Delirium Ingredients: Chamomilla 1x. Helleborus, Chininum Sulphuricum, Passiflora incarnata, Scopolamine 2x. Datura stramonium 3x. Aconitum napellus 4x. Ranunculus bulbosus 4x, 30x, 60x, 100x. Rhus toxicodendron, Operculina, Kali Bromatum, Absinthium 6x. Lachesis mutus 8x. Belladonna 30x, 60x, 100x.

PSY-DEM (1 fl. oz.) Catalog No. 0159 Indication: Dementia Ingredients: Damiana 1x. Apium graveolens, Calcarea Phosphorica 3x, 1000x. Hyoscyamus niger 4x. Zincum Metallicum, Phosphoricum Acidum, Baryta Carbonica, Calcarea Carbonica 6x. Aurum Iodatum 8x. Picricum Acidum 10x. Lilium Tigrinum 12x, 30x. Phosphorus 12x, 30x, 60x, 100x. Stannum Metallicum, Alumina, Iodium, 30x, 60x, 100x. Sulphur, Plumbum Metallicum, Antimonium, Mercurius Vivus, Bismuthum Metallicum, Iodium 30x, 60x, 100x, 500x.

PSY-DEP (1 fl. oz.) Catalog No. 0158 Indication: Depression Ingredients: Vitamin B3, B5, B6 4x. Lithium Carbonicum, CCK 6x. Sarcode: Brain 6x, 12x. Caulophyllum thalictroides 12x, 30x. Ignatia amara 12x, 30x. Sepia 12x. Serotonin 16x. Mercurius Vivus, Silicea, Plumbum Metallicum, Iodium, Sulphur 60x, 100x, 1000x, 2000x.

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PSY-DEP/EX (1 fl. oz.) Catalog No. 0304 Indication: Depression (Extrovert) Ingredients: Pulsatilla 3x. Caulophyllum thalictroides 3x, 6x, 12x, 60x. Cimicifuga racemosa 6x. Natrum Muriaticum, Ferula asafoetida 12x. Lachesis mutus 16x. Sepia 16x, 30x, 60x. CCK 30x, 60x. Agaricus muscarius, Silicea 30x, 60x, 100x.

PSY-DEP/IN (1 fl. oz.) Catalog No. 0305 Indication: Depression (Introvert) Ingredients: Passiflora incarnata 2x. Pulsatilla 3x. Nux vomica 3x, 6x, 12x, 60x. Natrum Muriaticum 12x. CCK 12x, 30x. Sulphur, Petroleum 60x. Ruta graveolens, Causticum 30x, 60x, 100x, 200x.

PSY-DIS (1 fl. oz.) Catalog No. 0306 Indication: Dissociative disorders Ingredients: Cyclamen 3x. Thuja occidentalis, Sepia 6x, 12x. Datura stramonium 30x. Anacardium occidentale, Lachesis mutus, Nitricum Acidum, Hyoscyamus niger 200x. Cimicifuga racemosa, Gelsemium sempervirens 30x, 60x, 100x, 200x.

PSY-HYS (1 fl. oz.) Catalog No. 0160 Indication: Hysteria Ingredients: Valeriana officinalis, Pulsatilla 2x. Castoreum, Picricum Acidum 5x. Asafoetida, Asterias rubens, Ignatia amara, Zincum Metallicum 6x. Mygale 9c. Moschus 12x. Alumina, Aurum Metallicum, Graphites, Sulphur 30x, 60x, 100x, 1000x

PSY-MANIA (1 fl. oz.) Catalog No. 0307 Indication: Mania Ingredients: Salix nigra 1x. Murex 3x, 30x. Atropinum 8x, 30x. Cantharis 12x. Belladonna 12x, 100x. Panax quinquefolium 20x. Absinthium, Aconitum, Baptisia tinctoria 30x. Natrum Muriaticum, Spongia tosta, Passiflora incarnata 30x, 60x, 100x, 200x.

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PSY-MOOD (1 fl. oz.) Catalog No. 0161 Indication: Mood disorders Ingredients: Chamomilla 1x. Aurum Muriaticum 2x. Borax, Aloe socotrina 3x. Capsicum annuum 4x. Agaricus, Baptisia tinctoria, Bryonia, Mancinella 6x. Phosphorus 9x. Sulphur, Aluminium Metallicum, Stannum Metallicum, Mercurius Vivus, Iodium 30x, 60x, 100x, 500x, 1000x.

PSY-PER (1 fl. oz.) Catalog No. 0308 Indication: Personality disorders Ingredients: Echinacea purpurea 3x. Rhus toxicodendron, Podophyllum peltatum 6x. Thuja occidentalis 6x, 12x, 30x. Sulphur 30x, 50x. Picricum Acidum 60x. Phosphorus, Natrum Muriaticum, Bryonia 30x, 60x, 100x.

PSY-SCHZ (1 fl. oz.) Catalog No. 0309 Indication: Schizophrenia Ingredients: Aesculus hippocastanum, Medicago sativa 2x. Helonias dioica 2x, 6x. Cypripedium pubescens 4x. Abrotanum, Aethusa cynapium 6x. Radium, Sepia 30x. Apis mellifica, Phosphorus, Belladonna, Nux vomica 30x, 60x, 100x.

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IMPONDERABLE HOMEOPATHY

Imponderable homeopathy is the science of using different vibrational entities and transferring them into a water and diatomaceous earth mixture. This mixture acts as a mother tincture, and can absorb negative or positive energies if exposed to them for fifteen minutes or longer. Thus, if the emotional vibrations of greed are exposed to diatomaceous earth and water, it can become a mother tincture of the imponderable known as greed. The most famous type of imponderable homeopathy is x-ray. X-rays are exposed to diatomaceous earth and alcohol, producing a mother tincture. This can then be utilized to detoxify a person who has been exposed to radiation. Within this range of imponderable homeopathics there is the potential to treat a wide range of intellectual, vibrational, and energetic problems. Included within this text is a long list of some vibrational homeopathics that are used by the Dr. Recommends’ pharmaceutical company. This range of imponderable homeopathics can be used with some exciting new perspectives on homeopathy. Another imponderable homeopathic series is the Bach remedies. These remedies were developed by Dr. Edward Bach in England, many years ago to help a wide spectrum of emotional issues. These remedies consist of flower essences derived from many plants and flowers. The science of Bach philosophy is extensive. The preparation of the remedies is of the homeopathic manner. The essences are diluted and then mixed with water and alcohol for patient consumption. For this reason, we have decided to add them to our Repertory and put them into this chapter; not because of the nature of their manufacture, but because of the nature of their use. These flower essences are made in a very rational, scientific way, but the process is not entirely comprehensible. Each entity seems to work on

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a variety of emotional and physiological functions within the patient. Thus, the pattern of work is “imponderable.” Aided by new biochemical techniques and a vastly expanded understanding of immunology and neurochemistry, researchers have recently conducted new scientific studies at leading universities, hospital, and research facilities throughout the country, clearly linking mental and emotional stress as a primary factor in nearly all physical disorders. These studies show that emotions, acting through the brain, can affect nervous system function, hormone levels, and immunological responses, thereby changing a person’s susceptibility to a host of organic illnesses. Source: http://query.nytimes.com/gst/fullpage.html?sec=health&res=9B06EFDA1E38F937A15 756C0A965948260&n=Top/News/Health/Diseases,%20Conditions,%20and%20Health %20Topics/Cancer

Stress and related disorders have grown to become a major concern to us all. However, stress in and of itself is not the problem. The problem is in just how well we handle stress. The more mentally and emotionally centered and balanced we are, the more effectively we are able to deal with stress in our lives. To this end, we chose to put these remedies and their repertory into this section of the book.

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BACH REMEDIES

Agrimony: For those not wishing to burden others with their troubles and who cover up their suffering behind a cheerful façade. They are distressed by argument or quarrel, and may seek escape from pain and worry through the use of drugs or alcohol.

Aspen: For those who experience vague fears and anxieties of unknown origin, they are often apprehensive.

Beech: For those who while desiring perfection, easily find fault with people and things. Critical and at times intolerant, they may overact to small annoyances or idiosyncrasies of others.

Centaury: For those who are over anxious to please, often weak willed and easily exploited or dominated by others. As a result they may neglect their own particular interests.

Cerato: For those who lack confidence in their own judgment and decisions. They constantly seek the advice of others and may often be misguided.

Cherry Plum: For fear of losing mental and physical control, of doing something desperate. May have impulses to do things thought or known to be wrong.

Chestnut Bud: For those who fail to learn from experience, repeating the same patterns or mistakes again and again.

Chicory: For those who are overfull of care for others and need to direct and control those close to them. Always finding something to correct or put right.

Clematis: For those who tend to live in the future, lack concentration; are daydreamers, drowsy or spacey, and have a halfhearted interest in their present circumstances.

Crab Apple: For those who may feel something is not quite clean about themselves, or have a fear of being contaminated. For feelings of shame or poor self image. For example, thinking oneself not attractive for one reason or another. When necessary, may be taken to assist in detoxification; for example, during a cold or while fasting.

Elm: For those who at times may experience momentary feelings of inadequacy, being overwhelmed by their responsibilities. 133

BACH REMEDIES, cont.

Gentian: For those who become easily discouraged by small delays or hindrances. This may cause self doubt.

Gorse: For feelings of hopelessness and futility. When there is little hope of relief.

Heather: For those who seek the companionship of anyone who will listen to their troubles. They are generally not good listeners and have difficulty being alone for any length of time.

Holly: To be used when troubled by negative feelings such as envy, jealousy, suspicion, revenge, vexations of the heart, and states indicating a need for more love.

Honeysuckle: For those dwelling in the past, nostalgia, homesickness; always talking about the good old days when things were better.

Hornbeam: For the Monday morning feeling of not being able to face the day. For those feeling that some part of the body or mind needs strengthening, and for constant fatigue and tiredness.

Impatiens: For those quick in thought and action who require all things to be done without delay. They are impatient with people who are slow and often prefer to work alone.

Larch: For those who despite being capable, lack self confidence or feel inferior. Anticipating failure, they refuse to make a real effort to succeed.

Mimulus: For fear of known things, such as heights, water, the dark, other people, or being alone, etc.

Mustard: For deep gloom which comes on for apparently no known reason; sudden melancholia or heavy sadness which lifts just as suddenly.

Oak: For those who struggle on despite despondency from hardships, even when ill and overworked; they never give up.

Olive: For mental and physical exhaustion, sapped vitality with no reserve. This may come after an illness or personal ordeal.

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BACH REMEDIES, cont.

Pine: For those who feel they should do or should have done better, who are self-reproachful or blame themselves for the mistakes of others. Hardworking people who suffer much from the faults they attach to themselves, they are never satisfied with their success.

Red Chestnut: For those who find it difficult not to be overly concerned or anxious for others, always fearing something wrong may happen to those they care for.

Rescue Remedy: The most well known formula in the Back Remedy system. It has a positive calming and stabilizing effect in an extremely broad range of stressful situations, which include nervousness, anxiety, accidents, bereavement, and times of great fright, anguish, and desperation. Even minor everyday stresses, such as arguments, taking exams, making speeches, job interviews or other similar stressful situations are reportedly greatly helped.

Rock Rose: For those who experience states of terror, panic and hysteria; also when troubled by nightmares.

Rock Water: For those who are very strict with themselves in their daily living. They are hard masters to themselves, struggling toward some ideal or to set an example for others. This would include strict adherence to a living style or to religious, personal, or social disciplines.

Scleranthus: For those unable to decide between two things, first one seeming right then the other. Often presenting extreme variations in energy or mood swings.

Star of Bethlehem: For grief, trauma, loss. For the mental and emotional effect during and after a trauma.

Sweet Chestnut: For those who feel they have reached the limits of their endurance. For those moments of deep despair when the anguish seems to be unbearable.

Vervain: For those who have strong opinions and who usually need to have the last word; always teaching or philosophizing. When taken to an extreme, they can be argumentative and overbearing.

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BACH REMEDIES, cont.

Vine: For those who are strong willed. Leaders in their own right who are unquestionably in charge. However, when taken to an extreme they may become dictatorial.

Walnut: Assists in stabilizing emotional upsets during transition periods, such as puberty, adolescence, and menopause. Also helps one to break past links and emotionally adjust to new beginnings such as moving, changing or taking a new job, beginning or ending a relationship.

Water Violet: For those who are gentle, independent, aloof, and self- reliant, who do not interfere in the affairs of others; and when ill or in trouble prefer to bear their difficulties alone.

White Chestnut: For constant and persistent unwanted thoughts, such as mental arguments, worries or repetitious thoughts that prevent peace of mind and disrupt concentration.

Wild Oat: For the dissatisfaction with not having succeeded in one’s career of life goal. When there is unfulfilled ambition, career uncertainty or, boredom with one’s present position or station in life.

Wild Rose: For those who, for no apparent reason, have resigned themselves to their circumstances. Having become indifferent, little effort is made to improve things or find joy.

Willow: For those who have suffered some circumstance or misfortune which they feel was unfair or unjust. As a result, they become resentful and bitter toward life or toward those who they feel were at fault.

Source: http://www.healingartsspa.com/bach_flower_remedies.htm http://bowentherapy.homestead.com/bachflowers.html

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VIBRATIONAL REACTANTS

AGGRESSION 2000-2500 HERTZ ANGER 2500-3000 HERTZ ANXIETY 3000-3500 HERTZ AUTISTIC 3500-4000 HERTZ AWARENESS 4000-4500 HERTZ BLUE 4500-5000 HERTZ CARELESS 5000-5500 HERTZ CHAKRA, BASE 5500-6000 HERTZ CHAKRA, BROW 6000-10000 HERTZ CHAKRA, CROWN HESITATION CHAKRA, HEART HYPER GAMMA RADIATION CHAKRA, STOMACH INDIGO CHAKRA, THROAT INFRARED CONFUSION JEALOUSY COSMOS JOY (EMOTION) 50 CYCLES LA 60 CYCLES VERTEBRAE 75 CYCLES LEFT SPIN 100 CYCLES LUST 150 CYCLES MI DELUSION MICROWAVE DEPRESSION NEGATIVE MAGNETIC 1ST DIMENSION NEGATIVE STATIC 2ND DIMENSION ORANGE 3RD DIMENSION PASSIVITY 4TH DIMENSION POSITIVE MAGNETIC 5TH DIMENSION POSITIVE STATIC 6TH DIMENSION POWER 7TH DIMENSION PROJECTION 8TH DIMENSION RADIO 9TH DIMENSION RATIONALIZATION 10TH DIMENSION RE DO RECKLESS EELF RED VISIBLE ELF RIGHT SPIN FA SADNESS FEAR SO GAMMA RAYS TI GRAVITATION ULTRAVIOLET GREED VIOLET GREEN VISIBLE 0-500 HERTZ WORRY 500-1000 HERTZ X-RAYS 1000-1500 HERTZ YELLOW 1500-2000 HERTZ

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ALLERSODES

In treating allergies, it was found that small amounts of allergy-causing agents can be used to help reverse the anti-body cascade and other allergic factors within the body. This type of desensitization can be used with oral antigens or injectibles. Modern medicine has used this type of allergy treatment for several decades. Dr. Recommends has developed a large range of allersodes including inhalant and food allersodes. Within the scope of allersodes there are also phenolics which help break up the sensitivities to different phenol rings; bodily secretions, including hyluronidase; natural anti-histamines, including adrenaline; and other liver enzymes that help the body to naturally reduce allergic reactivity. Dr. Nelson has developed a large list of allersodes included here. To see the research on the effectiveness of these allergy compounds we point the reader to The Experimental Data on Homeopathy. Within this text, it is possible to see proof of how allergy homeopathy can be used to desensitize our patients.

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ANIMAL HAIR (1 oz.) Catalog No. 0291 Oral Antigen Combination Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione 8x. Cat Hair, Dog Hair, Horse Hair 9x, 12x, 30x, 60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol.

DAIRY (1 oz.) Catalog No. 0292 Oral Antigen Combination Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione 8x. Cheeses, Cow's Milk, Goat's Milk, Ice Cream, Butter 9x, 12x, 30x, 60x, 100x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol.

GRAIN (1 oz.) Catalog No. 0293 Oral Antigen Combination Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione 8x. Wheat, Corn, Barley, Millet, Rice 9x, 12x, 30x, 60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol.

MOLD/HOUSE DUST (1 oz.) Catalog No. 0294 Oral Antigen Combination Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione 8x. Mildew, Molds, Household Dust 9x, 12x, 30x, 60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol. 139

OLFACTORY SENSITIVITY (1 oz.) Catalog No. 0295 Oral Antigen Combination Ingredients: Rosa canina flos, Taraxacum officinale, Solidago virgaurea, Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione, Formaldehyde 8x. Miscellaneous Synthetic Aromatic Compounds 8x, 12x, 30x, 100x, 1000x. Olfactaid 12x. Formaldehyde Dehydrogenase 16x, 30x, 60x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol.

POLLEN (1 oz.) Catalog No. 0296 Oral Antigen Combination Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione 8x. Flowers, Trees, Grasses 9x, 12x, 30x, 60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol.

SULFIDE SENSITIVITY (1 oz.) Catalog No. 0297 Oral Antigen Combination Ingredients: Trifolium pratense, Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3 Cyclohexanedione 6x. Salicylicum Acidum, Salicinum, Sodium Bisulfide, Tartrazine, Monosodium Gluconate 8x, 12x, 30x, 100x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of purified water and non-allergenic alcohol.

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INHALANT REACTANTS

ACACIA ACTINOMYCES ISRAELII AGARICUS MUSC. ALDER, RED, WHITE ALFALFA ALLSCALE ALERNARIA TENIUS ASH, ARIZONA, GREEN, OREGON, WHITE ASPEN, QUAKING ASPERGILLUS, FLAVUS, FUMIGATUS, GLAUCUS, NIGER, TERRUS BAHIA BARLEY, CULTIVATED BARLEY SMUT, LOOSE BAYBERRY BEEFWOOD BENT, CREEPING BERMUDA GRASS BIRCH, MIXED, RED, RIVER, WHITE BLASTOMYCES DERMATITIDIS BLUE, ANNUAL, CANADA, KENTUCKY BLUEGRASS BOTRYTIS BOX ELDER BROMEHUNG BROMWEED CANADA BLUEGRASS CANDIDA (MONILA) ALBICANS CARELESSWEED CEDAR, MOUNTAIN, PINCHOT, RED CEPHALOSPORIUM, COMMON, ROSEUM CHAETOMIU CHESS, SOUTHERN CHINESE ELM CLADOSPORIUM FULVUM CLAVICEPS, PASPALI, PURPUREA CLOVER, SWEET COCKLEBUR CORN, CULTIVATED, POLLEN CORN SMUT COSMOS COTTONWOOD COTTONWOOD, MIX, COMMON, ARIZONA, EASTERN, WESTERN CRAWLING INSECT

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INHALANT REACTANTS, cont.

CURVALIARIA SPICIFERA CYPRESS, BALD, ARIZONA DAHLIA DANDELION DERMATOPHILUS CONGOLENSIS DOCK, RUMEX MIX, SOUR, YELLOW ELM, AMERICAN, CEDAR, CHINESE, SLIPPERY EUCALYPTUS FIR, DOUGLAS FIREBUSH FIVE GRASS MIX FLOWER POLLEN FLYING INSECT FUSARIUM SOLANI GELASINOSPORA CEREALIS GEOTRICHUM CANDIDUM GLIOCLADIUM FIMBRIATUM GOLDERNROD GRAIN GRAMMA, BLUE GRASS, BERMUDA GRASS, BROME, CANARY, JOHNSON, JUNE, OAT, ORCHARD, QUACK GREASEWOOD GUM, BLACK, SWEET HACKBERRY HAY HAZELBERRY HAZELNUT, AMERICAN HELMINTHOSPORIUM SATIVUM HEMLOCK, WESTERN HEMP, COMMON HICKORY, MIXED, PIGNUS, SHELLBARK HISTOPLASMA, CAPSULATUM, FARCIMINOSUM HONEYSUCKLE HORMODENDRUM CLAD HOUSE IODINE BUSH IRIS VERSICOLOR JERUSALEM OAK JOHNSON GRASS SMUT JUNIPER LAMBSQUARTER LOMBARDY POPLAR MAGNOLIA 142

INHALANT REACTANTS, cont.

MAPLE, SOFT, HARD MARIGOLD MARSHELDER, BURWEED, NARROWLEAF, ROUGH MEADOW FESCUE MESQUITE MEXICAN TEA MICROSPORUM, AUDOUINII, CANIS, GYPSEUM MONOTOSPORA MUCOR, CORYMBIFERA, MUCEDO, PLUMBEUS MUGWART, COMMON MULBERRY, PAPER, RED, WHITE MYCOGONE ALBA NARCISSUS NASTRUTIUM NEUROSPORA, SITOPHILA NIGROSPORA, SPHAERICA NOCARDIA ASTEROIDES OAK, BLACK, BLACKJACK, BUR, LIVE, POST, RED, WHITE OAKBLACK OAT, CULTIVATED PAEONIA OFFICINALIS PENICILLUM, CHRYSOGENUM, NOTATUM, RUBRUM PIGWEED PLANTAIN, ENGLISH POVERTY WEED QUAILBUSH RABBITBUSH RAGWEED, DESERT, FALSE, GIANT, SHORT, SLENDER, WESTERN WOOLY, MIX REDTOP RHIZOPUS NIGRICANS RHODOTORULA MUCILAGINOSA RINKEL ROSE RUSSIAN THISTLE RYE, CULTIVATED RYE GRASS, COMMON, ITALIAN, PERENNIAL SAFE, DRAGON, PASTURE, PRAIRIE, MIX SAGEBRUSH, COMMON SALTBUSH, ANNUAL SCOPULARIOPSIS SHADSCALE SHEEP SORREL SORGHUM, GRAIN 143

INHALANT REACTANTS, cont.

SORGHUM, SMUT SPONDYLOCLANDIUM ATROVIRENS SPOROTRICHUM PRUINOSUM STACHYBOTRYS ATRA SUGAR BEET POLLEN SUNFLOWER SYNTHETIC FABRIC TOBACCO WEED POLLEN MIX WESTERN WATER HEMP WHEAT, CULTIVATED, GRASS WINGSCALE WINTERFAT WORMWOOD, ANNUAL, COMMON

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PHENOLS I ACC ACETALDEHYDE ACETIC ACID ACETONE ADENINE AFLATOXINS ALDEHYDE ALLYL BUTYRATE ALLYL TIGLATE AMSOLE AMYGDALIN ANETHOLE APIOL ARGININE ASPARAGINE d1-ALANINE BENZALDEHYDE BENZOIC ACID BENZOTHIAZOLE BENZYL BENZYL BUTYRATE BENZYL TIGLATE BHA BHT BIOFLAVENOIDS BRAIN SUBSTANCE BUTANOIC ACID BUTYRIC ACID d-BIOTIN CAFFEIC ACID CAFFEINE CALCIUM AMINO ACID CHELATE CALCIUM OROTATE CAMPHOR CANDIDA CAPSAICIN CAROTENE CARYOPHYLLENE CHALCONE CHLOROGENIC ACID CINEOL CINNAMALDEHYDE CINNAMIC ACID CONIFERYL ALCOHOL COUMARIN

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PHENOLS I, cont.

DECANOIC ACID DOPAMINE ELLAGIO ACID EPHEDRINE HCL ESTERS (30 TYPES) ESTROGEN ETHYL BUTYRATE ETHYL HEPTANOATE ETHYL HEXANOATE ETHYL OCTANOATE EHTYL PROPIONATE ETHYL PYRUVATE ETHYL VALERATE EUGENOL FD&C BLUE NO. 1 FD&C BLUE NO. 2 FD&C GREEN NO. 3 FD&C RED NO. 2 FD&C RED NO. 3 FD&C RED NO. 40 FD&C VIOLET NO. 1 FD&C YELLOW NO. 6 FOLIC ACID FORMALDEHYDE DEHYDROGENASE FURFURAL FURFURYL BUTYRATE FURFURYL HEPTANOATE FURFURYL HEXANOATE FURFURYL OCTANOATE FURFURYL PENTANOATE FURFURYL PROPIONATE GABA GALLIC ACID GENISTEIN (BIOCHANIN A) GERMANIUM GLUTIN GLYCINE 1-GLUTAMIC ACID HEART SUBSTANCE HEMOGLOBIN HESPERETIN HISTAMINE HYDROCINNAMIC ACID

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PHENOLS I, cont.

HYPOTHALAMUS SUBSTANCE n-HEXYL BUTYRATE n-HEXYL TIGLATE ICOLEUCINE INDOLE INOSINE INOSITOL ISOASCORBIC ACID ISOPROPYL BUTYRATE ISOPROPYL TIGLATE KIDNEY SUBSTANCE alpha-KETO GLUTARIC ACID L-CARNITINE HYDROCHLORIDE L-DOPA L-GLUTAMINE + GLUTAMIN ACID L-GLUTATHIONE L-LYSINE (PILL) LACTIC ACID LACTOSE LEUCINE LIMONEN LINALOOL LIPASE BLENDS LYMPHATIC SUBSTANCE MALIC ACID MALTOSE MALVIN MANGANESE AMINO ACID CHELATE MANNAN MENTHOL METHIONINE METHYL BUTYRATE METHYL SALICYLATE METHYL TIGLATE MINADIONE MOLYBDENUM AMINO ACID CHELATE MONO AMMONIUM GLYCYRRHIZINATE N, N-DIMETHYLGLYCINE HYDROCHLORIDE NARINGENIN NICOTINE NOREPINEPHRINE OCTACOSANOL OCTANOIC ACID OCTAPAMINE 147

PHENOLS I, cont.

ORCHIC SUBSTANCE OVARIAN SUBSTANCE PABA PANCREATIN PANCRELIPASE PENTOSE PHENETHYL 2-METHYLBUTYRATE PHENYLALANINE PHENYLISOTHIO PHLORIDZIN PINENE

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ALLERSODES ACC Acetaldehyde Acetic Acid Acetone Adenine Aflatoxins dl-Alanine Aldehyde Allyl Butyrate Allyl Tiglate Amygdalin Anethole Apiol Arginine Asparagine Benzaldehyde Benzoic Acid Benzothiazole Benzyl Benzyl Butyrate Benzyl Tiglate BHA BHT (Buylated Hydroxytoluene) d-Biotin Bioflavenoids Brain Substance Butanoic Acid Butyric Acid Caffeic Acid Caffeine Calcium Chelate Camphor Candida Capsaicin Carotene L-Carnitine Hydrochloride Caryophyllene Chalcone Chlorogenic Acid Cineol Cinnamic Acid Coniferyl Alcohol Coumarin Decanoic Acid

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ALLERSODES, cont. N, N-Dimethylglycine Hydrochloride L-Dopa Dopamine Ellagic Acid Ephedrine HCl Esters (30 types) Estrogen Ethyl Butyrate Ethyl Heptanoate Ethyl Hexanoate Ethyl Octanoate Ethyl Propionate Ethyl Pyruvate Ethyl Valerate Eugenol FD&C Blue No. 1 FD&C Blue No. 2 FD&C Green No. 3 FD&C Red No. 2 FD&C Red No. 3 FD&C Red No. 40 FD&C Yellow No. 5 FD&C Yellow No. 6 FD&C Violet No. 1 Folic Acid Formaldehyde Furfural Furfural Butyrate Furfural Heptanoate Furfural Hexanoate Furfural Octanoate Furfural Pentanoate Furfural Propionate GABA (Gamma-Amino Butyric Acid) Gallic Acid Genistein (Biochanin A) Germanium 1-Glutamic Acid 1-Glutamine L-Glutathione Glutin Glycine Glycyrrhizinate Heart Substance

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ALLERSODES, cont.

Hemoglobin Hesperetin Histamine Hydrocinnamic Acid Hypothalamus Substance Indole Inosine Inositol Isoascorbic Acid Isoleucine Isopropyl Butyrate Isopropyl Tiglate alpha-Keto Glutaric Acid Kidney Substance Lactic Acid Lactose Leucine Limonene Linalool Lipase Blends Lymphatic Substance Lysine Malic Acid Maltose Malvin Manganese Chelate Mannan Menadione Methionine Menthol Methyl Butyrate Methyl Salicylate Methyl Tiglate Molybdenum Chelate Naringenin Nicotine Norepinephrine Octacosanol Octanoic Acid Octopamine Orchic Substance Ovarian Substance PABA (Para Amino Benzoic Acid) Pancreatin 151

ALLERSODES, cont.

Pancrelipase Pentose Phenethyl 2-Methylbutyrate Phenylalanine Phenylisothio Phloridzin Pinene Piperine Piperonal Pituitary Substance Progesterone Propyl Butyrate Propyl Tiglate Putresine Pyrrole Pyridoxal-5-Phosphate Pyridoxine Hydrochloride (Vitamin B-6) Phytic Acid Pyruvic Quercetin Red Bone Marrow Riboflavin (Vitamin B-2) Rutin Safrole Salsolinol Serotonin Skatol Spleen Substance Succinic Acid Suprarenal/Adrenal Substance Suprarenal Cortex Taurine Thiamine Hydrochloride (Vitamin B-1) Thujone Thymol Thymine Thyroid Trypsin Tryptophan Tyramine Tyrosine Ubiquinone 50 Uric Acid Uterus Substance 152

ALLERSODES, cont.

Valeraldehyde Vanillin d-Xylose

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ALLERGINS, ANTIGENS, FOODS Almond Meal Angora (Goat Mohair) Apple Banana Bean Birch Mix Brewers Yeast Broccoli Cabbage Carrot Cat Cattle Cauliflower Celery Cheese Cheddar Mix Chicken Chocolate Citrus Coffee Corn Pollen Cotton Seed Cotton Wood Cucumber Dock Sorrel Dog Dust Mix (House) Dust Mix (Mattress) Dust Mix (Rug) Dust Mix (Upholstery) Eastern Oak Egg White (Chicken) Elm Mix Feathers (Chicken, Goose, Duck) Flax Seed Flower Pollen I Fruit Juice Garlic Grain Mill Dust (Corn) Grain Mill Dust (Wheat) Grass (Alfalfa) Grass (Golden Rod) Grass (Kentucky Blue) Grass (Meadow Fescue)

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ALLERGINS, ANTIGENS, FOODS, cont.

Grass (Orchard) Grass (Perennial Rye) Grass (Red Clover) Grass (Red Top) Grass (Sweet Vernal) Grass (Timothy) Green Pepper Hair Spray Hickory Mix Horse Juniper Kapok Kelp-Iodine Lemon Lettuce Maple Mix Milk Mold Mix Mulberry Mushroom Nut Mix (Almond) Nut Mix (Brazil) Nut Mix (Cashew) Nut Mix (Coconut) Nut Mix (English Walnut) Nut Mix (Peanut) Nut Mix (Pecan) Onion Orange Penicillium (Chrysogenum) Penicillium (Digitatum) Penicillium (Notatuer) Penicillium (Roquefort) Perfume Mix Pollen (Amaranthus) Pollen (Chenopodium) Pollen (Cockle Burr) Pollen (Daisy) Pollen (Dandelion) Pollen (Grass) Pollen (Honey Suckle) Pollen (Marsh Elder) Pollen (Mugwort) Pollen (White) 155

ALLERGINS, ANTIGENS, FOODS, cont.

Red Meat Rice Sage Salmon Scale Mix Sesame Sheep Wool Shellfish (Clam) Shellfish (Crab) Shellfish (Oyster) Shellfish (Scallop) Shellfish (Shrimp) Soybean Spinach Strawberry Tobacco Tomato Western Oak Mix

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THE DEHABITUATE PHILOSOPHY

In our society today, addictions have become a dramatic problem in the culture’s disease structure. Many people have addictive tendencies and can become addicted to a variety of things, not just illegal drugs, but caffeine, tobacco, alcohol, sugar, sex, stress, and other things. The Dr. Recommends’ dehabituate remedies have been designed for homeopathic stimulation of the organism to deal with the addictions and discharge them in simple, natural ways. The dehabituate remedies have been engineered for safety through the QQCTM techniques. These remedies are only designed as an adjunct therapy to a more complete addiction reduction system. We recommend Alcoholics Anonymous, Gamblers Anonymous, or any other twelve-step programs that help people deal with these addictive tendencies.

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DEHABITUATE REMEDIES

SMOKING DEHABITUATE 1 (1 fl. oz.) Catalog No. 0021 Indication: Systemic stimulation to help reduce smoking. Use during first 3 to 4 weeks as a nicotine supplement (Do not use beyond suggested dosage.) Ingredients: Nicotinum 3x. Calcarea Phosphorica, Zincum Metallicum 4x. Lobelia cardinalis, Selenium Metallicum 6x. Bladder 6x, 12x, 30x, 60x, 100x. Hypothalamus 6x, 12x, 30x, 60x, 100x. Lung 6x, 12x, 30x, 60x, 100x. Beta-Endorphin 6x, 30x. Coffea Tosta 6x, 30x, 100x. Nux vomica 12x. Tabacum 12x, 16x, 24x, 100x. Saccharinum 16x, 100x. Plumbum Metallicum 18x

SMOKING DEHABITUATE 2 (1 fl. oz.) Catalog No. 0022 Indication: Systemic stimulation to help reduce smoking. Use after first month as a detox and for relapse prevention. Ingredients: Zincum Metallicum, Calcarea Phosphorica 4x. Silicea, Lobelia inflata, Selenium Metallicum 6x. Sarcodes: Lung, Hypothalamus, Bladder 6x-12x, 30x, 60x, 100x. Endorphins 6x, 30x, 100x, 500x, 1000x. Coffea 6x, 30x, 100x. Nux vomica 12x. Tabacum 12x, 16x, 24x, 100x, 500x, 1000x. Saccharinum 16x, 50m. Plumbum Metallicum 18x, 100x, 1000x. Nicotinum 30x.

158

VITAMINS

The Dr. Recommends’ vitamin and mineral products can be used in a therapeutic practice. The sciences of nutritional medicine and orthomolecular biology have shown that compounds can be used to help patients in attaining balance. The science of nutritional deficiency and excess must be dealt with. The following products can be utilized to supplement patient’s diets, and also to help in orthomolecular ways through the stabilization of enzyme pathways, hormonal utilization, and vitamin integrity. These formulas are designed to work with the body naturally by assisting the nutritional intake of the patient and supplementing the needed vitamins and enzymes.

159

LIQUID VITAMINS

A-Z LIQUID (4 fl. oz.) Natural Source of Full-Range Essential Vitamins Ingredients: Aloe vera, Medicago sativa, Calcium Ascorbate, Panax quinquefolium 1x. Caryophyllus aromaticus, Ribes nigrum., Angelica archangelica 2x. Apis mellifica, Chromium, Selenium Metallicum 3x. In a tincture of water and non-allergenic alcohol.

DRINKER'S VITAMIN (4 fl. oz.) Supplies Vitamins and Minerals depleted by alcohol Ingredients: Magnesium, Calcium Gluconate, B-Complex, Eggshell, Saccharomyces cerevisiae, Bee Pollen, Angelica archangelica 2x. Liver Sarcode, Tang Kuei, Oldenlandia affinis, Baptisia tinctoria, Prunus armeniaca 3x. In a tincture of water and non-allergenic alcohol.

SMOKER'S VITAMIN (4 fl. oz.) Supplies Vitamins and Minerals depleted by smoking Ingredients: Ascorbic Acid, Beta Carotene 1x. Taraxacum officinale, Petroselinum sativum, Spinacia oleracea, Urtica dioica, Equisetum arvense 2x. Beta vulgaris, Paeonia officinalis, Carthamus tinctorius, Selenium Metallicum, Commiphora myrrha 3x. Ephedra sinica 4x. In a tincture of water and non-allergenic alcohol.

HOMEOPATHIC CATALYST WATER (4 fl. oz.) Increases osmotic capacity NOTE: Should NOT be used by diabetics. Ingredients: Purified water, Non-allergenic alcohol, Chlorophyll, Magnesium, Stearic Acid, Natural Organic Tree Sap, Equisetum.

160

VITAMINS

ADERMINE HCL ANEURINE ANEURINE PYRO PHOSPHATE ARACDONIC ACID p-AMINOBENZOIC ACID BETA-CAROTENE BIOFLAVINOIDS CALCIFEROL CAPROIC ACID COENZYME Q6 COENZYME Q7 COENZYME Q8 COENZYME Q9 COENZYME Q10 COLLAGEN CYTOCHROME CYTOCHROME FAD DESTHIOBIOTIN DICHLOROFOLIC ACID ELASTIN ERGO CALCIFEROL ERGOSTEROL FAD FERODOXIN GLUTATHIONE GSG GLUTATHIONE HYDROXO COBALAMINE LIBOAMIDE LINOLEIC ACID LINOLENIC ACID LIPOIC ACID NADP NAPATHO QUINONE NICOTINIC ACID ORTHO QUINONE PHYKO BIOTIN PORPHYRIN PTEROYLGLUTAMIC ACID PYCOCYANIN CYANIN RETINAL RETINOL RETINOL ACETATE RETINOL PALITATE THIOCTIC ACID 161

TOCOPHEROL TRIGONELLINE UBIQUINONE –ALL UBIQUINONE -30 UBIQUINONE-35 UBIQUINONE-40 UBIQUINONE-45 UBIQUINONE-50 VITAMIN A VITAMIN A2 VITAMIN A3 VITAMIN B1 VITAMIN B2 VITAMIN B3 VITAMIN B4 VITAMIN B5 VITAMIN B6 VITAMIN B7 VITAMIN B 8 VITAMIN B9 VITAMIN B10 VITAMIN B11 VITAMIN B12 VITAMIN B13 VITAMIN B14 VITAMIN B15 VITAMIN B16 VITAMIN B17 VITAMIN B18 VITAMIN B19 VITAMIN B20 VITAMIN C VITAMIN D VITAMIN D2 VITAMIN D3 VITAMIN E VITAMIN F-ALL VITAMIN K VITAMIN U

162

POWDERED PRODUCTS

In keeping with the Dr. Recommends’ philosophy which involves digestion starting in the mouth, there are various powdered products available that contain different minerals, vitamins, enzymes and other ingredients that are not easily made into liquids. They have long shelf lives in powdered form, and can be utilized by patients for detoxification and other things for long periods of time, safely and efficiently. Many of the powders can be stirred into juices or other liquids by the patient and taken as part of his/her daily regime. These must be used with the help of a trained practitioner or skilled professional to help the patient in treatment.

POWDERS

ACTIVATED CHARCOAL POWDER (6 oz.)

Ingredients: Activated Charcoal Powder.

ANTACID POWDER (6 oz.)

Ingredients: Kali Bicarbonate, Natrum Bicarbonate, Calcium Carbonate, Magnesium Phosphorica, Natrum Muraticum, Kali Muraticum, Silicea.

CLEANSING & SKIN POULTICE (6 oz.)

Applied to skin to draw out toxins, Intestinal Cleanse Ingredients: Organic Bentonite, Activated Charcoal, Orsa Clay, Equisetum arvense, Symphytum officinale, Arnica montana, Myristica fragrans, Magnesia Sulphurica, Natrum Muriaticum, Capsicum annuum.

DISODIUM PHOSPHATE POWDER (6 oz.)

Ingredients: Disodium Phosphate, Magnesia Sulphurica.

MUSTARD POULTICE (6 oz.)

Ingredients: Bentonite, Brassica nigra, Brassica alba, Sanguinaria Canadensis, Symphytum officinale, Urtica dioica, Arctium lappa, Carica papaya, Activated Charcoal, Capsicum frutescens.

163 Screening Groups Used in the Academy of Applied Quantum Biotech Computer Programs

Listed here are some screening groups used in the Academy of Applied Quantum Biotech computer programs with biofeedback instrumentation for bio-computer analysis. These compounds can be used and purchased as homeopathics.

THE SCREENING GROUPS

Congenital 1 Syphilinum Syphlitic miasm Medorrhinum Gonococcinum Papilloma Virus

Congenital 2 Tuberculinum Kock Tuberculinum Bovinum Tuberculinum Avis Bacillinum Retrovirus

Congenital 3 Tuberculinum Klebs Tuberculinum Denys Tuberculinum Rosen Tuberculinum Marmoret Ricketsia

Upper Respiratory Bacteria 1 Staphlococcus Aureus Strept B haemolyticus Pneumococcus Haemophilus influenza Tersina Pestis

164 Bowel Nosodes 1 E. Coli Proteus Pseudomonas (Bac. pyocyanus) Klebsiella pneumoniae Thermal Baccilli

Bowel Nosodes 2 Staph abdominalis Strept faecalis Enterococcus Bacteroides Pseudomonas

Bowel Nosodes 3 Typhiodinum sp. Shigella dysenteriae Cholera Pasturella Giardia

Bowel Nosodes 4 Tularemia Clostridium welchii Shigella sonnei

Bowel Nosodes 5 Acidophilous Bifidus Bulgaricus Caucaucous Lacto Baccilus (All)

Upper Respiratory Viruses Adenovirus Rhinovirus Coronavirus Respiratory syncytial virus Retro Virus HLV 1-2 HLV 3-4-5 HLV 6-7-8 HLV 9-10-11-12 ARC

165 Influenzal Screen Influenza, all varieties Influenza A Influenza B Influenza current year (79/80)

Enteric Viruses Retrovirus Polio Coxackie Echo virus

Liver Viruses Hepatitis A Hepatitis B Hepatitis C Cytomegalovirus Epstein-Barr virus

Childhood Viruses Parotidinum Rubella Morbillinum Roseola infantum Herpes (All)

Protozoal Screen Malaria Toxoplasmosis Entamoeba histolytica Strongaloides Amoeba (All)

Fungal Screen #1 Tines Aspergillus Coccidiomycosis Histoplasmosis Blasto Hominus (Mycosis)

Fungal Screen #2 Cryptococcus Aspergillus Sacromyces Mycosis Tycosporon

166 Fungal Screen #3 Candida Albicans Candida Rugosa Candida Stellerata Candida Tropicalis Candida Krusei

Venereal Group Syphilinum Medorrhinum Chlamydia trachomitis Mycoplasma (All) Papiloma

Uric Acid Metabolic Group Acid uricum Hypoxanthine Kreatine Glutamine Oxalic Acidum

Lipid Group Screen Cholesterinum Blycerinum Acid acetessigsour- aethylester (acetic acid ethylester) Acetone Triglyceridus

Liver Miscellaneous Brucella abortus Listeria monocytogenes Leptospirosis Tularemia Glandular Fever

Urinary Tract Irritants Acid citricum Acid sorbicum Acid benzoicum Terebinthina Allergic Irritant

167 Nephrolithiasis Screen Acid oxalicum Acid uricum Calcarea phosphoricum Calcarea sulfuricum Acid Nitricum (Proteins)

Vaginitis Screen Candida albicans Trichomonus vaginalis Haemophilus vaginalis Strep faecalis Allergic Vaginitis

Accessory Lung Pathogens Chlamydia psittacosis Mycopolasma pneumoniae Parainfluenza viruses Actinomycosis Israeli Crypto Cystitis Aspergillus Histoplasmosis

Respiratory Tract Irritants Tobacco smoke Auto exhaust fumes Acid sulfurous Asbestos Allergic Irritant

Stimulant Screen #1 Coffee cruda Tobacco smoke Caffeine Tea (Thea Chinese) Sugar

168 Stimulant Screen #2 Salt Animal fat Theo-bromine Adrenal stress protein

Salicylate Screen Acid salicylicum Acid acetyl salicylicum Food dyes Sodium bisulfide

Heavy Metals 1 Arsenicum album Plumbum metallicum Cadmium met. Merc. sol. Molybdenum

Heavy Metals 2 Stannum met. Aluminum Cuprum metallicum (copper) Niccolum metallicum (nickel) Antimony

Heavy Metals #3 Barium Germanium Gold Vanadium Silver

Heavy Metals #4 Plutonium (Radioactive) Uranium Radium Radon Cesium

Parasite Screen #1 Giardia lambia Enterobius vermicularis Ascaris lumbriocoides Oxyures vermicularis Blastohominus

169 Parasite Screen #2 Ancylostoma Chilomastix Diphylidium Endolimax Necator Americanus

Parasite Screen #3 Fasciola hepatica Dicrocdelium lanceatum Hymenocepis Schistosoma Teania

Nerual Viruses Vaccininum Variolinum Varicella Herpes zoster Meningitis (Viral)

Neurotoxins 1 Tetanus Botulinum Q-fever Scarlatinum Salmonella

Neurotoxins 2 Hydrophobinum Distemperinum Arbovirus Tick fever Candida Albicanus

Herpes Group Herpes Simplex I Herpes Simplex II Herpes Simplex Herpes Progenitalis Herpes Zoster

Adrenal Screen Diptherinum Toxoplasmosis Tularemia Meningecoccinum Pseudomonas

170 Food Additive Screen Acid salycylicum Butylated hydroxyanasol Sodium nitrate Monosodium glutamate Synthetic Chemicals Addex

Dermatology Irritants Rhus tox Niccolum metallicum Petroleum Benzoin Hydro carbons (All)

Toxic Bowel Metabolites Indol Skatol Mercaptan Thioether Sulphur

Antibiotic Screen Penicillin Erythromycin Tetracycline Sulfanilimide Chemex Synthetic Chemicals

Epidermals House dust House dust mite Cat/Dog hair Feathers House dust scale

Pollen Mix Grass mix 1, 2, 3 Tree mix Weed mix Flower Pollen Grains

Mold Spore Mix Mold mix A Mold mix B T.O.E. Candida albicans FNG Fungifuge

171 Phenol Group Acid carbolicum Acid benzoicum Creosole Kreosotum Phenols (All)

Hydrocarbon Group Ethyl alcohol Petroleum Kerosene Diesel Envrox, Enviro. Industrial Pollutants

Miscellaneous Chemicals Formaldehyde Acetone Acid sulfurosum Benzenium Industriox Industrial pollutants

Mutagen/Carcinogen Group Methylcholanthrene Nitrosamine Benzene Chloroform Phosphorous compounds

Pesticides 1 – Halogenated Hydrocarbons D.D.T. Lindane Hexachlorbenzol Heptachlor Insecticides

Pesticide 2 – Organophosphates Malathion Parathion DDVP Diazanon Addex Insecticides

Pesticide 3 – Carbamates Dithiocarbamate Aldicarb

172 Pesticide 4 – Miscellaneous Paraquat 2, 4, 5, t-Ester Dinitrokresol Diquat

Dental Materials 1 Chrom Cobart Molybdenum Gold Silver amalgam Palladium Amalgam Dental Materials

Dental Materials 2 Phosphate cement Carboxylate cement Polymerisat Zinc oxydatum Phenol/Cresol

Gingival Screen Gingivitis Ulcer gingivitis Necrotic gingivitis Amoebic gingivitis

Periodontal Screen Zahnfleistasche Paradontose Zahnsacken Periodontitis Parulis (Strep muc.) Parulis (Staph aur.)

Pulpitis Screen Gangranose pulpa Acute pulpitis Chronic pulpitis Toxic pulpitis

Periapical Screen Odonton Fudus Root canal granuloma Gangran granuloma Radicular cyste

173 Jaw Lesion Screen Jaw ostitis Exudative ostitis Acute bacterial ostitis Chronic bacteria ostitis Infective ostitis Injury ostitis

Foci Screen #1 Foci in right lower jaw Foci in left lower jaw Foci in right upper jaw Foci in left upper jaw Foci in cranium

Foci Screen #2 Foci in cranial vertebrae Foci in cervical vertebrae Foci in thoracic vertebrae Foci in lumbar vertebrae Foci in sacral vertebrae

Foci Screen #3 Foci in palatine tonsils Foci in adenoids Foci in pharyngeal tonsils Foci in tubal tonsil Foci in laryngeal tonsil

Foci Screen #4 Foci in maxillary sinus Foci in cavernous sinus Foci in sphenoidal sinus Foci in ethmoid cell Foci in frontal sinus

Foci Screen #5 Lesions in body Foci in head area Foci in right upper quadrant Foci in left upper quadrant Foci in right lower quadrant Foci in left lower quadrant

174 Foci Screen #6 Right side brain Foci in frontal lobe Foci in temporal lobe Foci in parietal lobe Foci in occipital lobe Foci in midbrain

Foci Screen #7 Left side brain Foci in frontal lobe Foci in temporal lobe Foci in parietal lobe Foci in occipital lobe Foci in midbrain

Foci Screen #8 Neurological Foci in (Ans) parasympathetic nerves Foci in (Ans) sympathetic nerves Foci in (Cns) motor nerves Foci in (Cns) sensory nerves Foci in cranial nerves

Foci Screen #9 Digestive dist. Foci in stomach Foci in small intestine Foci in large intestine Foci in liver Foci in pancreas

175 INDICATED SCREENING GROUPS FOR THE MERIDIANS AND VESSELS OF ELECTROACUPUNCTURE ACCORDING TO DR. REINHOLD VOLL

SPLEEN

Sp4 Congenital 1, 2, 3 Liver viruses Enteric viruses Protozoan group Heavy metals 1, 2

Sp3 Hepatitis viruses Enteric viruses Dental materials Heavy metals 1, 2

PANCREAS

Pn1 Hepatitis viruses Enteric viruses Childhood viral illnesses Toxic bowel metabolites Bowel nosodes 1-4

Pn2 Upper respiratory bacteria 1 Uric acid metabolite group Pn3 Childhood viruses Hepatitis viruses Enteric viruses Bowel nosodes 1-4

Pn4 Lipid metabolic group Heavy metals 1, 2 Childhood viruses

176 STOMACH Congenital 1, 2, 3 Upper respiratory bacteria 1 Enteric viruses Heavy metals 1, 2 Dental materials 1

LIVER Liver viruses Enteric viruses Congenital 1, 2, 3 Protozoal group Bowel nosodes 1-4 Liver miscellaneous Fungal group Insecticide groups Salicylate combo Common antibiotics Stimulant screen

GALL BLADDER Bowel nosodes 1-4 Lipid metabolite group Protozoan group Intestinal parasites

KIDNEY

Ki1 & Ki2 Bowel nosodes 1, 2 Nephrolithiasis group Urinary tract irritants Congenital 1, 2, 3

Ki2a & Ki3 U.R.I. bacteria 1, 2 Congenital 1, 2, 3 Heavy metals 1, 2 Food testing Common stimulant group

177 UROGENITAL

B1 67 Bowel nosodes 1, 2 Congenital 1, 2, 3 Venereal screen Urinary tract irritants

B1 65, 64 (male) Congenital 1, 2, 3 Venereal screen Protozoan group Vaginitis group Bowel group 1, 2

B1 65, 64 (female) Congenital 1, 2, 3 Venereal screen Protozoan group Vaginitis group Bowel group 1, 2

LUNG Congenital 1, 2, 3 U.R.I. bacteria 1, 2 U.R.I. viruses Influenzal group Bowel nosodes 1, 2 Enteric viruses Accessory lung pathogens Respiratory tract irritants Salicylate screen Fungus screen

LARYNX/HYPOPHARYNX Use above nosode screen as for Lung

LARGE INTESTINE Parasite screen Protozoan screen Congenital 1, 2, 3 Bowel nosodes 1-4 Enteric viruses Liver viruses Mutagen/Carcinogen screen Heavy metals 1, 2 Toxic bowel metabolites

178 SMALL INTESTINE Congenital nosodes 1, 2, 3 Bowel nosodes 1-4 Enteric viruses Liver viruses Stimulant screen Parasite screen Protozoal screen

HEART Congenital 1, 2, 3 Influenzal screen Enteric viruses Liver viruses Upper respiratory viruses Upper respiratory bacteria 1, 2 Protozoal screen Neurotoxin screen Neural viruses Herpes group Heavy metals 1, 2 Common stimulants Insecticide screen Childhood viruses

NERVOUS SYSTEM Congenital1, 2, 3 Neural viruses Neurotoxins screen Childhood viruses Protozoal screen Enteric viruses Liver viruses Influenzal screen Upper respiratory viruses Heavy metals 1, 2 Insecticides

179 MENINGES

ND 1b Congenital 1, 2, 3 Upper respiratory viruses Upper respiratory bacteria 1, 2 Protozoal screen Bowel nosodes 1-4

ND 1a Basic autonomic screening protocol Hydrocarbon group Phenol group Miscellaneous group Food additive group Stimulant group Antibiotic group Respiratory irritant group Toxic bowel metabolites Dental materials 1, 2 Root canal group Heavy metal group 1, 2 Pesticide group 1-4 plus all nosode groups for Nervous System groups

CIRCULATION Congenital 1, 2, 3 Upper respiratory bacteria 2 Enteric viruses Liver viruses Heavy metals 1, 2 Dental materials Mutagen/Carcinogen screen Neurotoxins 1, 2

180 ENDOCRINE - Triple Warmer Meridian

Tw1 (adrenal) Congenital 1, 2, 3 Tw1 (gonads) Adrenal screen Refer to nosodes B1 65, 64 for male and female

Tw2 (Thyroid) Congenital 1, 2, 3 (Parathyroid) Upper respiratory (Thymus) viruses Enteric viruses Upper respiratory bacteria 1, 2 Heavy metals 1, 2 Dental materials 1

Tw3 (Pituitary) Congenital 1, 2, 3 (Pineal) Upper respiratory viruses Enteric viruses Influenzal screen Heavy metals 1, 2 Dental materials 1

ALLERGY VESSEL

Allergy 1 Food screens Urinary tract irritants Insecticide screens Food additive screen Dermatology irritants Stimulant screen Parasite screen

ADG 1a Basic autonomic screening protocol Heavy metals 1, 2 Dental materials 1, 2

ADG 2 Pollen screen Mold screen Epidermal screen Food screening

181 ADG 3 Pollen screen Mold screen Epidermal screen Insect stings Dental materials 1, 2

SKIN Congenital 1, 2 Childhood viruses Upper respiratory bacteria 1, 2 Refer to pancreas Refer to liver Dermatology irritant screen Mold screen Food screens Heavy metals 1, 2 Dental materials 1, 2 Toxic bowel metabolites

JOINT DEGENERATION & Congenital 1, 2, 3 FIBROID DEGENERATION Upper respiratory (Connective Tissue) bacteria 1, 2 Enteric viruses Liver viruses Bowel nosodes 1-4 Dental pure culture nosodes

LYMPHATIC VESSEL Congenital 1, 2, 3 Lyl, Lyl-La, Lyla (Tonsils, Pharynx, Middle Ear) viruses Upper respiratory bacteria 1, 2 Influenzal screen Dental materials 1, 2 Dental pure culture nosodes Bowel nosodes 1

182 Ly3 (Nose and Paranasal Sinuses) Congenital 1, 2, 3 U. R. I. viruses U. R. I. bacteria 1, 2 Influenza screen Bowel nosode group 1 Remember to refer to ADG 3, ND3a & Twla

Ly2a (Eyes) Congenital 1, 2, 3 U. R. I. viruses U. R. I. bacteria 1, 2 Bowel nosodes 1 Enteric viruses Protozoal screen Fungal screen

Ly2 (Dental) Dental materials 1, 2 Root canal screen Gingival screen Pulpitis screen Periodontal screen (remember Tw2) Periapical screen Upper respiratory bacteria 1 Dental pure culture nosodes Bowel nosodes 1 Jaw lesion screen

183 AN OPERANT DEFINITION OF HOMEOPATHY

Homeopathy has been cloaked in mystery and misunderstanding, in that there are many principles which have not fully done justice to the complete range of homeopathic action. Many proponents use homeopathy in vastly different ways making the field look confused and irregular. One of the misconceptions is that it is assumed that all things are reversal in homeopathy that what a substance causes in a large dose it will reverse in a minute dose. This is not always so, and we will dedicate this chapter to that topic. As is pointed out in the chapter on snake venoms, the Arndt-Schultz law allows for the principle that what a poison might do at a raw dose, an extreme dilution of that poison will often time produce a paradoxical reversal of activity. If a patient were having a heart arrhythmia or irregularity, rattle snake venom, which causes a proteolytic effect on tissues and also has a cardio toxic effect on the heart muscles, oftentimes in small quantities, can help reverse the arrhythmia and stabilize the heart. The chapter on venoms and poison goes into this in detail. Dr. James P. Isaacs, in his book entitled Complementarity in Biology: Quantization of Molecular Motion. (James P. Isaacs, John C. Lamb: John Hopkins Press: Baltimore, 1969), points out another law of pharmacology which is Wilder’s law of initial value. In Wilder’s law, if a substance is not a poison, as we make it more and more dilute, one of three things will happen: 1) it still could have a reversal, 2) there might be an increase in the original effect, or 3) nothing may happen at all. This is Wilder’s law of initial value. It is often used in pharmacology to chart out dose response curves. Many herbals, plants, glandulars, minerals, etc., are used in homeopathy and are not poisonous. Some of these will not always have

184 reversal effects. A classic example often noted in the literature is that of Eyebright. Eyebright is an herb used in homeopathy and herbal remedies. The name was coined because of the product’s positive effect on vision and the optic system. It helps make eyes bright. That is the herbal indication for Eyebright. The homeopathic indication for it is exactly the same. It is also used for vision problems, and to help patients with optical disturbances. If everything in homeopathy were truly all reversal, we would only use Eyebright on the patients who had vision that was too perfect, because then the reversal effect of Eyebright in homeopathic form would be that it would interfere with vision. This is not the case. It is also not the case in many types of sarcodal formulas. Thyroid tissue has been demonstrated to have positive effects on the thyroid system, and the thyroid hormone from the tissue can be utilized in cases of hypothyroidism to stabilize thyroid function. In homeopathic form this same thyroid tissue, as a sarcode, has the exact same indications. It can also be utilized in the hypothyroid condition in which the patient has a weak thyroid gland. Examples of sarcodal remedies abound in this non-reversal action. Adrenaline tissue, brain tissue, endocrine systems, heart tissue and the like, all have the same indications homeopathically as they do in glandular technology when used in raw dose. In all of these cases the glandulars (sarcodes) are used to stabilize function. Thus, they can be used in hyper or hypo cases. In the case of hyperthyroidism or hypothyroidism, the thyroid sarcode might be used which helps stabilize tissue. But it is not always reversal. The sarcodal remedies, as we proved in the chapter on sarcodes, will have a stabilizing effect in rejuvenating or increasing the probability that healthy tissues will ensue in the organism. As the organism produces new tissues in the thyroid, the cervical, the vertebrae, or wherever in the body, the homeopathic sarcodal therapy can help to insure that healthy

185 tissues will be built instead of unhealthy ones. The sarcodal forms of homeopathics do not follow what is thought about homeopathy; that it is all reversal of action. Another example in homeopathy is the indications of calendula. Calendula, which is taken from the marigold plant, has been used by herbalists for centuries, if not eons, for different injuries. The homeopathic indications for calendula are equivalent. Oftentimes homeopaths will find that the dilute form of calendula can, in certain cases, have increased activity in treatment of injuries, and trauma conditions. James Tyler Kent writes that homeopathic calendula cannot be denied its ability to help in accident or injury cases. Another example is Dioscoria villosa, known as wild yam. The herbal therapeutics of it is that it is hepatic, stomachic, atonic, expectorant, anti-spasmodic, a sedative, and an anti-asthmatic. Its herbal uses include colic, jaundice, hardening/blocking of the liver, nausea (in pregnant women), cholera, neuralgia, hiccups, whooping cough, bronchitis, etc. Homeopathic indications are for painful afflictions of the abdomen, pelvic viscera, feeble digestive powers, colic, gallstones, heart spasms, uterine colic, back pain, and cramps. There are almost identical indications for the homeopathic as for the herbal. We now look at the herb Caulophyllum also known as squawroot or blue cohosh. It is used as an anti-spasmodic, nervine tonic, diuretic, anti-rheumatic, and anti-inflammatory. It is known as “woman’s best friend” for the reason that it has a powerful effect on stabilizing women’s systems, and helping in the alleviation of cramps. This remedy is excellent for spasms, epilepsy, uterine inflammation, and the like. If everything worked in reversal, we would use the cohosh for the opposite indications of its herbal.

186 Let us now look at the homeopathic indications. Oscar E. Boericke’s repertory calls it Caulophyllum, and it is a woman’s remedy. During labor, when pains are present, the patient is exhausted and fretful. This remedy is excellent in its ability to help birthing pains. It is good for the stomach, dyspepsia, and all problems of the female system. It increases stability of menses and leucorrhea, and works for stiff joints, etc. Here is another example that the herbal recommendations are the same as the homeopathic. Even using this in dramatically dilute form, at 30x, and 40x, there is stability in its action. Another example is Blue Vervain, in Latin; Verbena. Its herbal indications are that of a nervine tonic, anti-spasmodic, diaphoretic, and beneficial for the stomach; astringent, fever-fugue, and antiseptic. Its uses are for dyspepsia, indigestion, all liver conditions, kidney/bladder complaints, amenorrhea, dysmenorrhea, hysteria, epilepsy, chorea, nervous exhaustion, insomnia, diarrhea, nervous system, nervous depression, weakness, spasms, and irritation. It promotes the absorption of blood, and helps in pain and bruises. It is tremendously helpful for the liver, insomnia, epilepsy, hallucinations, and mental exhaustion. Find below a list of some of the formulas in the HPUS (Homeopathic Pharmacopeia of the United States) which have similar indications herbally as well as homeopathically. As we go through the HPUS we will see that 65% or more of the HPUS has similar indications herbally and homeopathically, making the two modalities almost equal. By building this new definition into homeopathy we can utilize the best of homeopathy, as well as naturopathy and herbal therapy to help the American public demystify some of the homeopathic reactions. This will give needed publicity as well as simplicity to allow them to choose the system of homeopathy as a medical modality. As can be seen from the dose-response curve in Figures 1, 2, and 3, there are dramatic differences between the Arndt-Schultz principle of poisons and Wilder’s law of initial value.

187 LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Abelmoschus Aquilegi Abies Nigra Aquilegia Vulgaris Abrotanum Aralia Dispida Achyranthes Calea Aralia Quinquefolia Actae Spicata Arbutus Andrach Adamas Areca Catechu Adelheidsquelle Artemisia Vulgaris Adonis Virnalis Arum Dracontium Adrenaline Arum Italicum Aesculus Glabra Arum Maculatum Aesculus Hippocastanum Arum Triphyllum Agave Americana Arundo Mauritanica Agave Tequilana Asclepias Incarnata Agnus Castus Asclepias Syriaca Agrimonia Eupatoria Asimina Triloba Agrostemma Githago Asparagus Officin Aletris Farinosa Aspidosperma Alfalfa Asperula Odorata Alisma Plantago Avena Sativa Allium Sativum Barosma Alnus Glutinosa Bellis Perennis Aloe Socotrina Berberis Aquifolium Alstonia Constricta Berberis Vulgaris Alstonia Scholaris Berberis Vulgaris, Fructus Althaea Officinalis Beta Vulgaris Ammi Visnaga Bixa Orellana Ampelopsis Quinquefolia Boldo Amygdalus Persica Borago Officinalis Anagallis Arvensis Branca Ursina Ananassa Brassica Napus Anchusa Officinalis Buxus Sempervirens Anemone Nemorosa Cacao Anemopsis California Cactus Grande Anethum Graveolens Cahinca Angelica Archangelica Cajuputum Angelica Atropurpurea Calcarea Acetica Angophora Lanceolata Calcarea Lactica Anthenis Nobilis Calendula Officinalis Apium Graveolens Calotropis Gigantea Apocynum Andro Calthapalustris Aqua Marina Canlophylum

188 LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Canchalagua Clematis Vitalba, Folia Canna Anjustifolia Coccus Cacti Carduus Benedictus Cochlearia Armoracia Carduus Marianus Cochlearia Officinalis Carum Carvi Collinsonia Canadensis Cascara Comocladia Dentata Cascarilla Conchiolinum Castanea Vesca Condurango Castoreum Convolvulus Arvensis Catalpa Bignonioides Copaiva Officinalis Cataria Nepeta Cornus Alternifolia Ceanothus Cornus Circinata Ceanothus Americanus Cornus Florida Cedron Crocus Sativa Celtis Occidentalis Crataegus Cephalanthus Occidentalis Cucurbita Citrullus Cerasus Virginiana Cucurbita Pepo, Flos Cereus Bonplandii Cucurbita Pepo, Semen Cereus Serpentinus Cuphea petiolata Cetraria Islandica Cydonia Vulgaris Chamomilla Cynara Scolymus Cheiranthus Cheiri Cypripedium Pubescens Chelidonium Majus Cytisus Scoparius Chelidonium Majus, Radix Daphne Indica Chelone Glabra Dictamnus Albus Chenopodium Anthelminticum Dioscorea Villosa Chenopodim Vulvaria Dirca Palustris Chimaphila Maculata Dolichos Pruriens Chimaphila Umbellata Draba Verna Chionanthus Virginica Drosera Rotundifolia Chrysanthemum Leucanthemum Dulcamara, Flos Cicer Arietinum Echinacea Angustifolia Cichorium Intybus Elaeis Guineensis Cimicifuga Racemosa Elaterium Cineraria Maritima Epiiedra Vulgaris Cinnamomum Epigaea Repens Cistus Canadensis Epilobium Palustre Citrus Decumana Epiphegus Virginiana Citrus Limonum Equisetum Arvense Citrus Vulgaris Erechtites Hieracifolia Clematis Virginiana Erigeron Canadensis

189 LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Eriodictyon Californicum Glycerinum Erodium Glycogenum Eryngium Aquaticum Glycyrrhiza Glabra Eryngium Maritimum Gnaphalium Leontopodium Erythraea Centaurium Gossypium Herbaceum Ethylicum Granatum Eugenia Caryophyllata Gratiola Officinalis Eugenia Jambosa Grindelia Euonymus Atropurpureus Guaco Euonymus Europaeus Guaiacum Eupatorium Aromaticum Guatteria Gaumeri Eupatorium Cannabinum Gymnocladus Canadensis Eupatorium Perfoliatum Haematoxylon Campechianum Eupatorium Purpureum Hamamelis Virginiana Euphrasia Officinalis Haronga Madagascariensis Fagopyrum Esculentum Helianthus Annuus Fagus Sylvatica Heliotropium Peruvianum Ferula Glauca Helonias Dioica Ficus Religiosa Hedeoma Filix Mas Helleborus Foeniculum Vulgare Hepatica Triloba Fragaria Vesca Hoang-Nan Franciscea Uniflora Homarus Fraxinus Americana Hura Crepitans Fraxinus Excelsior Hydrangea Arborescens Fucus Vesiculosus Hydrastis Galanthus Nivalis Hydrastis Canadensis Galega Officinalis Hydrocotyle Galium Aparine Hydrocotyle Asiatica Galphimia Glauca Hydrophyllum Virginianum Gambogia Hypericum Gaultheria Procumbens Iberis Amara Genista Tinctoria Ilex Aquifolium Gentiana Lutea Ilex Paraguariensis Gentiana Quinquefolia Illicium Anisatum Geranium Maculatum Imperatoria Ostruthium Geranium Robertianum Inula Helenium Geum Rivale Iris Florentina Geum Urbanum Iris Foetidissima Ginkgo Biloba Iris Germanica Glechoma Hederacea Iris Tenax

190 LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Iris Versicolor Magnesia Grandiflora Jacaranda Caroba Mandragora Officinarum Jalapa Mangifera Indica Juglans Cinerea Marrubium Bulgare Juniperus Communis Matica Juniperus Virginiana Melissa Officinalis Justicia Adhatoda Menispermum Canadense Kamala Mentha Piperita Karaka Mentha Pulegium Kousso Mentha Viridis Laburnum Anagyroides Mentholum Lacerta Agilis Menyanthes Trifoliata Lachnanthes Tinctoria Mezereum Lamium Album Millefolium Lappa Major Mimosa Humilis Lathyrus Sativus Mitchella Repens Lecithin Momordica Balsamina Lemna Minor Musa Sapientum Leonurus Cardiaca Myosotis Lepidium Bonariense Myrica Cerifera Leptandra Virginica Myristica Sebifera Lespedeza Captiata Myrrha Levisticum Officinale Myrtus Communis Liatris Spicata Nabalus Serpentarius Lilium Tigrinum Narcissus Pseudo-Narcissus Linaria Vulgaris Nasturtium Aquaticum Linum Usitatissimum Negundo Lonicera Periclymenum Nepeta Cataria Lonicera Xylosteum Nux Moschata Lophophytum Leandri Nymphaea Odorata Luffa Operculata Ocimum Basilicum Lupulinum Ocimum Canum Lycopersicum Esculentum Oenothera Biennis Lycopodium Clavatum Oleander Lycopus Virginicus Oleum Carvi Lysimachia Nummularia Ononis Spinosa Macrotinum Onopurdum Magnesia Carbonica Opuntia Vulgaris Magnesia Muriatica Oreodaphne Magnesia Oxydata Origanum Majorana Magnesia Sulfurica Ornithogalum Umbellatum

191 LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Ostrya Primula Vulgaris Ovi Gallinae Pellicula Prunus Padus Oxalis Acetosella Prunus Spinosa Oxydendrum Arboreum Prunus Virginiana Paeonia Officinalis Ptelea Trifoliata Pareira Brava Pulsatilla Parietaria Officinalis Pulsatilla Nuttalliana Paronichia Illecebrum Pyrus Americana Parthenium Quassia Amara Passiflora Incarnata Quebracho Pastinaca Sativa Quercus Robur Paullinia Pinnata Ranunculus Paullinia Sorbilis Ratanhia Pecten Rap Hanns Pediculus Capitis Rhododenrom Penthorum Sedoides Rhus Aromatica Persea Americana Resina Laricis Petroselinum Sativum Rhamnus Californica Phaseolus Rhamnus Cathartica Phellandrium Aquaticum Rhamnus Purshiana Physalis Alkekengi Rheum Officinale Phytolacca Ricinus Communis Pichi Robinia Pseudoacacia Pimenta Officinalis Rosa Canina Pimpinella Saxifraga Rosa Damascena Pinus Lambertiana Rosmarinum Officinalis Pinus Sylvestris Rubia Tinctorum Piper Methysticum Rumex Acetosa Piper Nigrum Rumex Crispus Piscidia Erythrina Rumex Obtusifolius Plantago Major Russula Foetens Platanus Ruta Graveolens Plectranthus Fruticosus Sabadilla Plumbago Littoralis Sabal Serrulata Polygonum Punctatum Salix Alba Polygonum Sagittatum Salix Nigra Populus Candicans Salix Purpurea Potentilla Anserina Salvia Officinalis Pothos Foetidus Sambucus Canadensis Primula Obconica Sambucus Nigra Primula Veris Sambucus Nigra

192 LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Sanicula Thlaspi Bursa Pastoris Sarracenia Purpurea Thuja Occidentalis Sarsaparilla Tilia Europaea Sassafras Officinale Tormentilla Schinus Molle Torula Scolopensrium Vulgare Trifolium Pratense Scutellaria Lateriflora Trifolium Repens Sedum Acre Trillium Pendulum Semper Vivum Tectorum Triosteum Perfoliatum Senecio Aureus Triticum Repens Senecio Jacobaea Tropaeolum Majus Senega Officinalis Turnera Senna Tussilago Farfara Sepia Tussilago Petasites Sinapis Ulmus Fulva Sinapis Nigra Uricum Acidum Skookum Chuck Urtica Dioica Solanum Carolinense Urtica Urens Solanum Mammosum Usnea Barbata Solidago Virgaurea Uva Ursi Spartium Scoparium Valeriana Officinalis Spigelia Marilandica Verbascum Thapsus Spilanthes Oleracea Verbena Hastata Spinacia Verbena Officinalis Spiraea Ulmaria Viburnum Opulus Stellaria Media Viburnum Prunifolium Sterculia Acuminata Viola Odorata Sticta Pulmonaria Viola Tricolor Stigmata Maidis Wiesbaden Stillingia Sylvatica Wyethia Helenioides Sumbul Symphoricarpus Xanthoxylum Fraxineum Racemosus Symphytum Officinale Yucca Filamentosa Taraxacum Officinale, Radix Yohim Binum Taxus Baccata Zingiber Officinale Teucrium Marum Teucrium Scorodonia Thaspium Aureum Thymus Serryllum Thea Sinensis Theobrominum

193 SUMMARY

As can be seen from this brief list of examples, much of homeopathy is not always reversal; much of it is very similar to the action of herbal therapy. In herbal homeopathy, the minimal dose of an herb can achieve an effect. Herbology and homeopathy might join forces to become a more powerful form of medicine. In 1962, the FDA developed a new Food and Drug Cosmetic Act, which let homeopathy in the HPUS, as well as the USP (United States Pharmacopeia). In 1962, they did not include the Natural Compendium of Herbs which was supplied before 1962. This was because of an inability of herbalists to agree and to actively support themselves in the development of their Natural Compendium. Now we are going to provide a new description and definition of homeopathy which includes herbal precepts and reinstate herbalism under our new HPUS guidelines. Since homeopathy and herbalism share so much, and since the HPUS provides a legal backdrop for doctors to have NDC (National Drug Code) coded formulas within the HPUS, it is possible to include these different herbs and their activity within our guidelines. Homeopathy need not always involve using dramatically dilute substances. Mother tinctures, 1x, 2x, and 3x, are often high concentrations and yet this is still homeopathy. Let us explore the description of an opposite to homeopathy, which is allopathy. In allopathy we are working against the body, just as the allopath might use an antihistamine when the patient has a histamine response. By using an outside intervention the practitioner intervenes with the body so that the body will have time to heal itself. Thus, if there is a histamine response due to some causative factor, the allopath would use an antihistamine to help block the histamine, hoping that he/she

194 provides enough of a buffer to stall, so that the body can overcome the disease. Allopathy is not dealing with the true cause (rarely is the cause of the disease the fact that the person is deficient in the antihistamine or other drug). Oftentimes, histamine release is prompted by allergic activity, nutritional disturbances, chemical imbalances, and the like. The patient can sometimes build a dependence on these allopathic medications, as they will help the symptom, not the disease, and thus, will build dependence. This can often be beneficial to the synthetic chemical companies, but not to the patient. Allopathy seeks to provide an outside intervention from the smart doctor to the “stupid” patient’s body, to try to sedate, block, stimulate, trick or fool the system with a synthetic pharmacological agent. Allopathy can be seen as a heterogeneous type of medicine in which the intervention comes not from within the system, but from outside the system. In homeopathy, however, we provide the minimal dose of activity from our agents to allow the human system of the patient to achieve its balance through its own cybernetic feedback control. Homeopathy develops healing forces from within, or homogeneously, whereas allopathy does it from outside, or heterogeneously. The homeopath tries to work with the patient’s body to stimulate it towards healing and homeostasis balance. The principle of homeostasis implies that the body will seek to try to balance its activity along the lines of a certain degree of function. Thus, in maintaining calcium balance, the parathyroid and thyroid hormones will help to regulate calcium, oftentimes by taking calcium out of the bone to maintain serum calcium or by appetite control to drive the appetite toward different foods to balance our calcium intake. A very intricate sense of balance is needed for the extremely complex job of homeostasis. The whole principle of homeopathy relies on the study of homeostasis. In homeopathy, an herb is used only to provide the stimulus for the body to heal itself. The minimal dose is sought. Thus, Eyebright might help to

195 supply the needed nutrition and the needed pharmacological agents to help the patient’s body to rejuvenate its optical system, and achieve health. This implies a homogenous stimulation of homeostasis which is homeopathy. Our definition of homeopathy is: “Homeopathy is the medical art of gently stimulating the patient’s body toward balance and homeostasis.”

Some dictums of homeopathy:

¾ The human body is complex beyond our understanding, so we must work reverently with it to encourage health and balance from within.

¾ Disease results from violation of natural law, and disease symptoms are a message from the body as it attempts to deal with the causative agent. Symptoms are beacons and traffic signals which point to cures. Symptoms are not the enemy as believed by allopaths.

¾ Cure must come from removing or reducing the cause of disease, and then stimulating balance and homeostasis.

¾ The healing of nations shall come from the leaves of the field. Only nature knows the intimate details of cure, and only nature can manufacture truly curative agents.

¾ Homeopathy, herbology, acupuncture, and naturopathy have more in common than originally believed. Together with other similar modalities they represent a new era in medicine.

Our broadened viewpoint of homeopathy lets the techniques of herbology to be used to their fullest proficiency. This allows the different herbal manufacturers to have a professional naturopathic and homeopathic philosophical governmental agency through the HPUS to guide them in quality control and legal direction. This broad-based definition of homeopathy has existed for years, and yet because of the mystery of homeopathy in like treating like, oftentimes it is categorized

196 as only like treating like. With this new, broader definition, and by utilizing the forces of different homeopathic practitioners and manufacturers to propagate this definition to the American public, they can get a better idea of how homeopaths are able to help in dramatic ways to stabilize and balance their bodies. Our herbal repertoire also will bring Chinese herbals into the system and let legally controlled manufacturers supply quality Chinese herbs with a proper national drug code to doctors. It is hoped that this chapter and the rest of this Natural Repertory will help to clear up some of the myths and misunderstandings in regard to homeopathy in its practical use. Homeopathy represents an inexpensive modality of medicine which is safe and effective in treating a wide variety of medical ills. In the 1990s, the American culture was severely threatened economically, and overburdened by a medical system that clung to allopathic synthetic pharmacology and surgery. These measures are not only drastically expensive and environmentally unsafe, but they are not cures. Allopathy is needed in medicine as a last resort in keeping some patients alive. The baby must not be thrown out with the bath water. Allopathy will always be a part of medicine. But allopaths should learn the fallacies of their techniques. They do not seek to bring patients to balance or cure. They only seek to develop dependency on different items in the lost hope that patients’ bodies can regain balance before the synthetic drugs do their damage to kidneys, liver, nerves and digestion. Allopaths treat symptoms. To this end, homeopathy offers economic solutions, the development of safe and effective modalities, and help in returning to a system of reverence for the natural process of our bodies and the natural process of the ecological system of the world. One day medicine might overcome its egocentric biases, and teach all techniques and philosophies together under one true medicine. A new day will dawn in which healers will learn to appreciate each other and help patients, rather than propagate egos.

197 AN ADVANCED TREATISE IN QUANTUM BIOLOGY The Quantic Link to DNA

The father of quantum theory was Erwin Schrödinger. He believed that there was a definite link between quantum theory and DNA. As we have reviewed several parts of biological literature in this book, we now would like to review a brief introduction on quantum theory and genetic coding. Here we see the best demonstration of a quantum biological function, as the formation of the DNA code does not utilize half-steps; it makes distance coding jumps. There are distinct patterns in the DNA code that allow for exacting patterns. In hereditary techniques we can see that there is a preciseness of transfer which yet has some degree of indeterminacy. As we have discussed in the Quantum Biology and in this workbook, there must be a metabolic side as well as a reproductive side to our matrix, so that the metabolism can respond to a wide variety of different types of environmental conditions. But the genetic coding would have to have very limited, predictable and distinct types of jumps. It would have to be a more precise and closed process. We have already discussed this in some detail (see Quantum Biology). Now, let us review some of the literature which has led to our understanding of DNA function. In the early days, there were three categories of food: oleaginous (fats), saccharinous (carbohydrates), and albuminous (protein). The development of protein was a key factor in the development of life. It is protein which is analyzed in our treatise on DNA. Jöns Jakob Berzelius proposed the names of cystein and glycine as he was doing research on amino acids. In 1838, he coined the word “protein”, which is Greek for primary substance. He found that this was the basic unit of all albuminous material. Gerardus Johannes Mulder, also working in the very early 1800s, continued some of the Berzelius work. He proposed a

198 basic albuminous substance with an empirical formula C40H62N10O12; this combined with many other formulas produced some of the basic proteins of life. In the 1890s, Emil Fischer, who was once a student of August Kekulé, found that there were dextro and levo types of polymers. He was the first to find that there was a chirality, or “handedness” to nature. He then found that this “handedness” also applied to protein compounds. In the 1850s, Thomas Graham found crystalloids and colloids, and studied their functions. Colla came from the Greek for glue. Theodor Svedberg contributed evidence to the theory that proteins were homogenous. Using Avogadro’s number and the weight of the large colloidal particles, he determined their diffusion rate and sedimentation as a constant in the earth’s gravitational field, producing up to 500 times the force of gravity. He then separated these colloidal factors, and helped to further the concept of homogeneity. By 1936, Linus Pauling and Alfred Mirsky put forth the idea that polypeptide chains of native proteins could be folded and held together between the N/h group and the oxygen atom of the C//O group of peptide bonds. Many different scientists, including Corey and Perutz, started working with these large chemicals and proposed some of the different fashions which led to the discovery of the helix. John Kendrew was the first to find the three-dimensional structure of myoglobin which has an approximate molecular weight of 17,500. He found that 75% of myoglobin has a helical polypeptide chain. Thus, the helix was further brought into science. The three-dimensional structure of insulin was discovered in 1969, by Dorothy Crowfoot Hodgkin, working at Oxford University. Other bio- molecules were found, such as cholesterol, calciferol, penicillin, and B- 12, using x-ray photographs of the diffusion patterns of the insulin crystal. Dorothy Hodgkin was able to propose the structure of this very complex molecule. Insulin was the first native protein to be synthesized.

199 In 1966, Robert Bruce Merrifield developed insulin by means of a machine which was designed to carry out polypeptide synthesis. Synthetic chemistry was well underway, and the precept of synthetic chemistry to this day has been that of placing the calcium, carbon, and hydrogen in the right spots. This was achieved by looking at the x-ray photographs and diffraction patterns, doing spectrographic analysis, and other different functions. But they were not able to discern the type of energy that existed in the quantic bonds, or of the electrons in their outer rings. Nature still has many secrets. Some of the different quantic energy patterns of the natural substances still were unknown to these synthetic developers. The synthetic developers sought to develop synthetic compounds but found that they were not as effective as natural entities. This did not hinder them in the least; they achieved extreme financial success through their synthesis. They were able to develop and manufacture compounds and live off rather rich royalties as these synthetic compounds were sold as medicines. As they reduced the complex world of natural biology into synthetic components they developed more and more compounds. Many were to follow after insulin. Let’s take a look at some of the first work that was done with insulin. It was founded to be only 3.4% effective at best in the early crystalline structure designed by Merrifield. Later, in the 1960s, scientists started to dispel the idea that organic substances were different from the synthetic matter which they were developing. Because of the limits of their thought and the limits of their techniques of measurement these compounds appeared to be equal. This is not the case in the 1990s. With our sophisticated energy equipment and methods of discerning the energy patterns and electrical responses of compounds, we now find that nature does indeed have some rather complex safeguards and complex secrets which the synthetic chemical companies have yet to divine.

200 In 1986, Carl Popper delivered an address to the Royal Society. In this address he told the attendees, who included many of the fathers of synthetic molecular biology, that biochemical organizations and processes could never be understood in chemical terms alone. Because of this, Popper proposed that organic evolution would never be explained by chemical or Darwinian Theory and that chemical reductionism for the environment proposed many different risks, as we put many of these synthetic chemicals into our environment and our bodies. In fact, due to the large number of chemicals which have been put into our bodies, perhaps Carl Popper’s warning has come too late. Many dramatic problems have resulted from iatrogenic poisoning of the planet and iatrogenic diseases which were caused by synthetic compounds. Dramatic damage has resulted from ignorance and profiteering. Man’s ability to understand is always limited by his ability to measure the results of his work. At every point in science the scientists assume that their measurements are complete, therefore their knowledge must be complete. As new discoveries are made and more sophisticated measurement techniques are developed this philosophy opens the door to deeper and deeper understanding. With the advent of quantum theory and the idea of the Heisenberg Uncertainty Principle we now realize that true knowledge cannot be attained, and that we cannot in any way manufacture the same compounds developed by nature. Our attempts at this are merely guesses, perhaps good guesses but still, nature holds secrets as we continue to explore biology to the end of our days. Only nature truly knows. In 1893, Albrecht Kossel, doing physiological research identified chromatin as a nucleoprotamine. This was found to be a nucleoprotein, and was some of the beginning work needed in looking at RNA and DNA function. Nucleic acid sugars and their phosphate-bonded brothers were written about by Phoebus Levene in 1905. Levene, working with Walter A.

201 Jacobs, classified sugar of yeast nucleic acids as D-Ribose. This is linked to the bases by a glycosidic bond. They termed these nucleosides. Adenosine, guanosine, cytidine, and uridine, when esterified by phosphates, became adenylic acid, guanylic acid, cytidylic acid, and uridylic acid. It was Levene who later found that this sugar is RNA and DNA was not a hexose, but a pentose. Early determinations of the molecular weight of DNA gave values of the order of 103. In 1938, Frederick Sanger proposed that its weight was 106. Levene also was able to confirm this new molecular weight in 1938. In 1944, at the Rockefeller Institute Hospital, Oswald Avery came up with the first strong evidence that DNA was really the key to transferring genetic characteristics in microbes. Avery also proposed some of the DNA enzymes, such as DNA depolymerase and deoxyribonuclease. These enzymes were found to deactivate DNA, but were later key in the process of unfolding and unwinding the DNA to set genetics in motion. In 1945, DNA was found to have light absorption in the area of 260 nanometers, and to have some mitogenic-like production of UV. These purines and pyrimidines were also found to have strong light relationships; both absorption and production. Erwin Chargaff in 1950 was able to show some of the strong light spectrophoto reaction of the different components of DNA and DNA itself. From this, the research finding adenine, guanine, cytosine, and thymine, or A, G, C, and T, led to the discovery of the different Chargaff rules. First, the total of purines and pyrimidines are quantitatively equi- molecular; that is, A + G = T + C. Second, the molecular quantities of adenine and thymine individually are equal: A = T. Third, the amounts of guanine and cytosine are molecularly equivalent; G = C. A relation of the preceding rules comes to the final rule in which A + C = G +T. Later, it was found that uracil took the place of thymine in the RNA components of the cell. These rules echo our quantum rules in many ways.

202 Many people around 1950 were struggling to find ways of understanding this. But it was Crick and Watson at Cambridge who best improved on Pauling’s research, using the Chargaff rules and developing a consensus idea of the structure of DNA. They proposed a double helix. This opened the door for dramatic understanding. The mechanics of this process could be easily understood by the mechanically-minded scientists of the time. Yet, this type of mechanical process did not appear in any other chemical process. Chemical processes were known to be statistical, or involving random development of compounds which were pushed and pulled apart through entropic or thermodynamic processes. This strand of DNA does not do this; it is not a randomized process. It pulls apart and pushes together in a very precise maze. The actual mechanisms of this push and pull were not studied by these scientists; they liked the idea of the chemistry involved. But now, we can ask the question: Through what processes is DNA pushed/pulled apart? The answer leads to quantum dynamics. Our quantic analysis matrix can be superimposed on the DNA action. Research blossomed into the concept of the mechanics of DNA. As Isaacs has told us, the E. coli is an example of a type of near vion from cells, meaning the base amount of matter needed to actually make up a living unit which could metabolize and reproduce on its own. Inside the E. coli is a double–stranded DNA chromosome which contains 4 x 106 base pairs. It will reproduce at maximum rate of 750 base pairs per second. This is at a given unwound replicating fork region. So it will take about forty minutes to reproduce a complete chromosome. If the conditions are right, E. coli will divide into two daughter cells every twenty minutes. This is the nature of vionic activity. In 1953, Paul Zamecnik, working at Harvard University, tried to put radioactive isotopes of different amino acids into a bacteria colony. This was an attempt to trace the radioactive polypeptides through the different ribosomes. The experiment was a failure because by putting in

203 the different radioactive isotopes the RNA functioning came to a halt. It could only be brought back by bringing in a fresh, natural selection of the amino acids. Thus, DNA has some ability to possibly ‘know” that the items involved are radioactive. This would be reinforced by our quantum theories; if a radioactive particle were put into this process, the biology would soon be able to “know” it and halt its progress. Biology and life operate on many levels including sub molecular. The process would be able to notice radioactivity as an irregularity. This makes us wonder about the different radioactive tracing experiments in which radioactive iodine was put into the body by experimenters who found that it goes to the thyroid; and then it was assumed that all iodine would go to the thyroid. All we know from that experiment is that radioactive iodine goes to the thyroid. We do not know where normal iodine goes. This is another limitation of quantic theory. Tracing experiments have led to many faulty conclusions in biology. Electron microscopists started to come up with ideas of transcription and translation of the ability to handle RNA and DNA. But basically, at the relative body temperature E. coli’s DNA is transcribed at a rate of around sixteen nucleotides per second into the messenger RNA strand. The messenger RNA strand has an average length of 2,000 to 3,000 nucleotides. The half-life of the messenger RNA strand is about 90 seconds. So the ten to fifteen ribosomes which are in the process of translating with a given messenger RNA and forming a polyribosome become attached to the strand during the period of transcription from the DNA. Polypeptides formed by each ribosome of a polyribosome system are the same. The formation time of a polypeptide is around ten seconds under certain prime conditions. The growing E. coli bacteria contain some 15,000 ribosomes. They make up 25% of the cell mass. The ribosome is approximately 20 nanometers across and has a molecular weight of 2.7 x 106.

204 By 1966, many of the details of the genetic code were worked out, 61 out of the total 64 triplet codons. From the late 1950s, the sequence of amino acids in proteins with a specific function, such as insulin, hemoglobin, or cytochrome c, were determined and catalogued by a range of organisms followed a decade later by corresponding determination of nucleic acid sequences. In analyzing the sequences then available, Zuckerkandl and Pauling (1965), pointed out that a present-day protein contains its own ancestral history in its quantic organization, and that similarities of homologous polypeptide chains along with the accepted fossil record provide evolutionary data of three types. ¾ The probable amino acid sequence of the ancestral polypeptide from which the chains compared had diverged.

¾ The approximate epoch at which the divergence started.

¾ The lines of descent through which the alterations in amino acid sequence proceeded.

The vast extent of data storage and processing that was proved in our quantic chapter easily allows for this process. Zuckerkandl and Pauling calculated a mean substitution rate for a hemoglobin polypeptide of one amino acid every 14.5 million years from the 18 residue differences attained in comparison of the horse and the human α−chain. It was known that the α− and the β−chains of the human hemoglobin tetramer (α2β2) show 78 differences so one can surmise that the two polypeptides originally split from a common origin by gene duplication at least 565 million years ago. Originally, the common point was monomeric hemoglobin consisting of a single polypeptide chain. This chain has a more modern representation in the blood of primitive jawless fish (the lamprey and the hagfish, which lack the advantage of cooperative oxygen uptake and release that emerged with the evolution of the hemoglobin tetramer).

205 A similar technique to that of Zuckerkandl and Pauling with their construct of a ‘molecular evolutionary clock’ was put forward by Motoo Kimura. They used a Poisson distribution. Thus, the events of low probability in a vast population like the decay of radioactive isotopes used to calibrate the geological evolutionary clock are mathematically calculated. Kimura posted that for two homologous polypeptides made of

n residues with varying amino acids at d sites due to bifurcation over a time t, the rate of evolutionary amino acid substitution per site per years,

kaa, is given by the relation

2tkaa = -1n(1 – d/n) - -2.31og(1 – d/n). This equation, applied to a series of sequenced polypeptides with a common biochemical role such as the α−chain of vertebrate hemoglobin

will result in a constant value of kaa of the order of 10-9 residue replacements per site per year, a unit that M. Kimura termed the pauling or the ‘molecular evolutionary unit’ (MEU). This is allowed for in our bioquantic matrix. Life must allow for some minute variations to occur in its reproduction accounting system. Varying slightly for a given type of

protein, the value of the kaa varies readily for proteins of contrasting functional types by three orders of magnitude. This ranges from the rapidly evolving fibrinopeptides (8.3 MEU) to the well conserved histone proteins (0.009 MEU). The fibrinopeptides are key in the formation of blood clots, and only a minuscule part of the polypeptide has an essential function. The amino acids of the other segments freely undergo substitution without the benefits of selective control. This process involved no drastic functional changes. Comparatively, histone polypeptides are essential in the conservation of the genetic material, making up the nucleosome particles where the double-stranded DNA supercoils in the eukaryote nucleus to provide the nucleoprotein chromatin whereby a ‘string of beads’ form.

206 The MEU, or one Pauling, is a definite quantic type of function. Our bioquantic matrix must tolerate some limited variations. These variations can result in genetic improvements from genetic bifurcation (see “Fractals” in Quantum Biology). But, for these variations to last they must result in increased productivity. Increased productivity comes from cooperation with the environment, not superiority. So Darwin was wrong about survival of the fittest. Now, we can say that there is survival of the adaptive and cooperative. The histone proteins are stabilized and conserved. They have only two differences out of about 100 amino acids in the H4 polypeptide between calf thymus and the pea plant even though animals and plants split apart some 1.2 billion years ago. Contrasts of the mRNA sequences coding for the histone H4 polypeptide in two sea urchin species demonstrates that the synonymous mutation rate in the DNA transcribed is as high as that of the fast evolving fibrinopeptides. The degeneracy of the genetic code is eminent for the third position (3’ –end) of the coding base triplets. Here the transitional mutations (U/C) or (A/G) are mostly inert. Comparison of the mRNA sequences coding for the α− and the β−polypeptide chains of mammalian haemoglobin demonstrate that natural selection has lowered the rates of surviving base changes in the first and second positions of the triplet codons which are approximately equal+ to one-quarter or less of the mutational rate found for the third codon position. Quantum theory is consistent with such processing. Schrödinger was right in assuming that genetics is a quantic activity. Genetics or reproduction requires an exacting and limited process. Metabolism requires vast responsiveness. The archaebacteria characteristically thrive in extreme environments, hot sulphurous vents, salt marshes, or anaerobic organic-rich muds. Archaebacteria are ancient, as the term archae implies. They have

207 heterogeneity of their 16S rRNA sequences due to divergence over aeons. As Isaacs points out jumps in species and genes also must follow quantic law. The indices of those 16s rRNA sequences distinguish three major divisions: ¾ The methanogens and halophiles ¾ Thermoplasma, a group containing a single organism ¾ A heterogeneous group of sulphur-dependent thermoacidophiles, probably the most ancient of the prokaryotes

These bacteria can live under acidic conditions (pH 1-6) and at elevated temperatures (60-95 ºC). Sulfolobus oxidizes sulphur to sulphate while others reduce sulphate to sulphide, like Archaeoglobus which develops small quantities of methane as well. These are some of the extremes of life, or conditions in which the matrix of life can operate. The 16S tRNA sequences of the eubacteria indicated that, while Gram positive organisms form a distinct group of related species, gram negative organisms are much more diverse. The break into nine groups is defined by a common coefficient of 0.2-0.3 within a group. Most Gram negative bacteria belong to the purple bacteria group which has not only the colored photosynthetic organisms but also many colorless analogues. Samples of these analogues are E. coli and other enteric bacteria. The green photosynthetic bacteria also go into two distinct groups ~ ¾ Sulphur (hydrogen sulphide substrate) ¾ Non-sulphur (organic substrate) types which are not closely related (SAB 0.18). The cyanobacteria consist of a coherent group, and they are similar to the chloroplast organelles of eukaryotic red and green algae, and green plants (SAB values of 0.25 – 0.30). If a quantum leap is performed in the genetic code of bacteria, then this will result in a new type of bacteria. The sulphate-reducing bacteria which use the oxygen of the sulphate for a primitive form of respiration comprise a Gram negative eubacterial

208 group. A type of bacteria in this group, Desulfovibrio sulfodismutans, can attain free energy from the disproportionation of sulphite or thiosulfate to sulphide and sulphate. This is an ‘inorganic fermentation’ process similar to the redox disproportionation of glucose to ethanol and carbon dioxide (Bak and Cypionka 1987). Thus, we can plot genetic changes on a hermitian matrix. This allows us to develop new energetic laws of biology. The eukaryote organelles, the mitochondrion, and the chloroplast all share a prokaryote size (1 μm). They are vions that contain their own DNA. These vions also have a circular double strand as in bacteria, and ribosomes of the bacterial type. The 165 rRNA sequences of the organelles tell us that the mitochondria belong to the purple group of eubacteria and the chloroplasts to the group of cyanobacteria. Indigenous DNA in the organelles and the sameness of their 16S rRNA sequences to those of extant eubacteria led to the theory that mitochondria and chloroplasts evolved by a process of endosymbiosis. This theory hypothesized that ancestral eukaryote with a vacuole nutrient method of securing nutrients into a membrane-bounded vacuole once engulfed a purple-group aerobic bacterium generating ATP through the respiratory chain. As the guest supplied ATP, the host archae- eukaryote provided back to the guest proto-mitochondrion the materials required for its maintenance and ATP production. So, mutual vionic patterns merged for symbiotic cooperation. The phagocytosis of a cyanobacterium into a vacuole led to the development of the chloroplast, which supplied carbohydrate to its host. In return, the cyanobacteria supplied a life-support system. The two membranes around the organelle are leftovers of the endosymbiotic beginnings. The inner membrane represents the cytoplasmic membrane of the eubacterial guest. The outer membrane corresponds to that lining supplied from the vacuole of the host eukaryote. In vionic coupling sometimes functions can be presented

209 dually. Quantum laws can still be obeyed. Backup systems are abounding in biology. Possible relatives of the ancestral eukaryote, as many as a thousand species, have no mitochondria or other organelles. These species split from vion tendency to form the archaezoa subdivision of the eukaryotes, just as the metakaryota, which contain mitochondria, is an example of a vion. Sequenced representatives of the archaezoa are minute parasites of the metamonada and the microsporidia. These vions contain bacterial – sized ribosomes with 16S rRNA in the smaller subunit. They don’t have the 18S rRNA found in the higher eukaryotes. The 16S rRNA sequences of a microsporidia and a metamonada species differ greatly from mitochondrion – containing eukaryotes, the metakaryota. This suggests an early vionic divergence. The archaezoa and the metakaryota split before the age (1.4 billion years) of the larger microfossils (10 μm) which, on account of their size probably represent the remains of organelle – equipped eukaryotes (Cavalier–Smith 1989). We can see this vionic divergence in our matrix. Biochemically, the eukaryotes share similarities with both the eubacteria and the archaebacteria. The translation of mRNA into a polypeptide starts with methionine in the eukaryotes as it does in the archaebacteria. But translation starts with N – formylmethionine in the eubacteria. Elongation of the polypeptide chain is stopped by dipthera toxin in the eukaryotes and the archaebacteria but not in the eubacteria. Chloramphenicol stops the elongation in eubacteria but not in eukaryotes or archaebacteria. The lipids of the cytoplasmic membrane in both eubacteria and eukaryotes contain the diesters of L- glycerophosphate with straight-chain fatty acids. In contrast, the archaebactrial lipids are composed of the diethers of D-glycerophosphate with phytanol and other branched-chain alcohols. The variance of vionic

210 technique in metabolism responsiveness is pointed out here. The quantic interchange of environmental forces can have a wide range of activity. The analysis of DNA and its function has received extreme scrutiny from the scientific community over the last twenty-five years. Many different abilities of DNA have been described and experimentally ascertained. One of the most recent advances in DNA is that of gene splicing, wherein genetic engineering can be accomplished by taking out a bad gene and splicing a healthy gene into the DNA. This dramatic new research offers great potential for medicine in correcting metabolic or genetic disorders. Modern medicine has also developed the technique of splicing the gene into a virus and allowing the virus to penetrate into the cell membrane, and to create a new gene code which will replace the diseased code with a healthy genetic code. But with all this dramatic research being done with DNA, scientists have done little to account for the phenomenon of how the transmission of genetic data can be accomplished. For this, we can go to Schrödinger and his description of the quantum abilities of DNA. This we have outlined in the chapters of his book to give a basic understanding. Our description of the quantum philosophy and the quantum dynamics will let us find and be predictive of the long range forces in biology that account for the function of DNA. The development of the matrices will also help explain some of the DNA functioning.

211 SUMMARY - THE QUANTIC LINK TO DNA

¾ We reviewed the literature and the thought processes which arrived at the different philosophical understanding of DNA, leading to today’s use of chromosomal therapy in medicine.

¾ We outlined the possible ways that Schrödinger was right about DNA working on quantum levels. Genetic transfer of the DNA is accomplished by quantum dynamics.

¾ We outlined a basic mathematical precept to understand this quantic link to DNA. Thus, we attempted to explain genetics through quantum theory.

¾ A proposition was outlined on how DNA function can be further analyzed, not just from the chemical dynamics, but also from an energetic, quantum dynamics to further understand how to correct these situations in the future. A possible new DNA therapy is hinted at by using chromosomal homeopathy.

Bibliography

Bak, F. Cypionka, H. A novel type of energy metabolism involving fermentation of inorganic sulphur compounds. Nature. 1987; 326:891- 892.

Cavalier-Smith, T. Molecular phylogeny. Archaebacteria and Archezoa. Nature. 1989; 339(6220):100-1.

Zuckerkandl, E. Pauling, L. Evolutionary divergence and convergence in proteins, 1965; 97-166 In: Evolving Genes and Proteins, edited by V. Bryson and H.J. Vogel. Academic Press, New York.

212 THE HUMAN GENOME How to interpret the index and map

Disorders that appear within square brackets [ ] represent “non-diseases” – mainly genetic variations that lead to apparently abnormal laboratory test values (e.g., dysalbuminemic euthyroidal hyperthyroxinemia). Disorders printed inside boxes in the map represent allelic disorders, which can result in multiple, quite dissimilar disorders from the various mutations in the same gene. Disorders printed within braces { } represent genetic mutations that make affected individuals susceptible to a specific disease, infection or other condition (e.g., coronary artery disease). A question mark ? before the disorder means that confirmation of a gene or locus is uncertain or in dispute. Although all known or suspected genetic disorders appear in the index, some do not appear on the map if their chromosomal location is particularly controversial. Moreover, on the ideogram of chromosome X, some disorders have been left out to conserve space. These excluded disorders are included in the index and marked with an asterisk *. Disorders printed in bold were added to the list in the past year. Those printed underlined have been changed in location on the chromosomes in the past year. Finally, each disorder in the index is followed by one of three numbers in parentheses that indicates whether the mutation was located by mapping (1) wild-type gene, (2) the disease phenotype, or (3) both approaches.

213

ALPHABETICAL INDEX OF HEALTH DISORDERS AND CHROMOSOME LOCATION

Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency (1) 8q21 Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency (3) 6p21.3 3-hydroxyacyl-CoA dehydrogenase deficiency (1) Chr.7 *46, XY female (2) xp22.2-p21.3 Aarskog-Scott syndrome (2) Xq13 ?Abetaa Lipoproteinemia 2p24 [Acanthocytosis 1 form] (1) 17q21-q22 Acatalasemia (1) 11p13 Acetyl-CoA carboxylase deficiency (1) 17q21 Acid-maltase deficiency, adult (1) 17q23 Acoustic neuroma (2) 22q11.21-q13.1 ?Acrokeratoelastoidosis (2) 2p ACTH deficiency (1) 2p25 Acute alcohol intolerance (1) 12q24.2 Acute Lymphoblastic Leukemia (2) 9p22-p21 Acute Promyelocytic Leukemia (1) 17q21.1 Acute Promyelocytic Leukemia (2) 15q22 Acyl-CoA Dehydrogenase, medium chain, deficiency of (1) 1p31 Acyl-CoA Dehydrogenase, short chain, deficiency of (1) 12q22-qter Adenylosuccinase deficiency (1) Chr.22 Adrenal hyperplasia II (1) 1p13 Adrenal hypoplasia, primary (2) Chr.10 Adrenocortical carcinoma (2) Xp21.3-p21.2 Adrenoleukodystrophy (2) 11p15.5 Adrenomyeloneruopathy (2) Xq28 [AFP deficiency, congenital] (1) Xq28 Agammaglobulinemia, type 2, X-linked (2) 4q11-q13 *Agammaglobulinemia, X-Linked (2) Xq21.3-q22 Aicardi syndrome (2) Xq22

214 Albinism (3) 11q14-q21 Albinism-deafness syndrome (2) Xq26.3-q27.1 ?Aldolase A deficiency (1) 16q22-q24 Allan-Herndon syndrome Xq21 Alpha-1-antichymotrypsin deficiency (1) 14q32.1 Alpha-NAGA deficiency (1) 22q11 Alport syndrome (3) Xq22 Alzheimer’s disease, type I (3) 21q21.3-q22.05 *Amelogenesis imperfecta (1) Xp22.3-p22.1 [AMP deaminase deficiency, erythrocyte] (1) 1p21-p13 Amyloid neuropathy, familial, several allelic types (3) 18q11.2-q12.1 Amyloidosis, cerebroaterial, Dutch type (1) 21q21.3-q22.05 Amyloidosis, Finnish type (1) 9q34 Amyloidosis, Iowa form (2) 11q23 {?Amyloidosis, secondary, susceptibility to} 1q12-q23 Amyotrophic Lateral Sclerosis (2) 21q21.1-q22.3 ?Anal canal carcinoma (2) 11q22-qter Analbuminemia (1) 4q11-q13 Anemia, congenital due to deficiency of gastric intrinsic factor (1) Chr.11 Anemia, sideroblastic/hypochromic (3) Xp21-q21 Aneurysm, familial (2) 2q31 Angelman syndrome (2) 15q11-q13 Angioedema, hereditary (1) 11q11-q13.1 Anhidrotic ectodermal dysplasia (2) Xq12.2-13.1 Aniridia of WAGR syndrome (2) 11p13 Aniridia-1 (2) 2p25 Aniridia-2 (2) 11p13 Anterior segment mesenchymal dysgenesis (2) 4q28-q31 Antithrombin III deficiency, (3) 1q23-q25 ApoA-I and apocC-III deficiency, combined (1) Chr.11 Apolipoprotein B-100, defective (1) 2p24 [Apoliproprotein H deficiency] (1) Chr.17 Argininemia (1) 6q23 Argininosuccinicaciduria (1) 7cen-q11.2 Arteriohepatic dysplasia (2) 20p11.2 Aspartylglucosaminuria (3) 4q23-q27 Ataxia-telangiectasia (2) 11q22-q23 Atopy (2) 11q12-q13 Atransferrinemia (1) 3q21 Atrial septal defect, secundum type (2) 6p21.3 Autonomic failure due to DBH deficiency (1) 9q34

215 ?Batten disease, 1 form (1) 15q24-q25 Batten disease (2) 16p11 Becker muscular dystrophy (3) Xp21.2 Beckwith-Wiedemann syndrome (2) 11pter-p15 Bernard-Soulier syndrome (1) 17pter-p12 ?Bloom syndrome (1) Chr.19 ?Bloom syndrome (2) Chr.12 *Borjeson-Forssman-Lehmann syndrome (2) Xp26-q27 ?Branchiootic syndrome (2) 8q13.3 ?Breast cancer (1) 17p13.3 Breast cancer, ductal (2) 1p36 Breast cancer, ductal (2) Chr.13 Breast cancer, early onset (2) 17q21 Brody myopathy (1) Chr.16 Burkitt’s Lymphoma 8q24.1 ?C1q deficiency (1) 1p ?C1q deficiency (1) 1p C1r/Cis deficiency, combined (1) 12p13 C1r/Cis deficiency, combined (1) 12p13 C2 deficiency (3) 6p21.3 C3 deficiency (1) 19p13.3-p13.2 C3b inactivator deficiency (1) 4p25 C4 deficiency (3) 6p21.3 C4 deficiency (3) 6p21.3 C5 deficiency (1) 9q34.1 C6 deficiency (1) 5p13 C7 deficiency (1) 5p13 C8 deficiency, type I (2) 1p22 C9 deficiency, type II (2) 1p22 C9 deficiency (1) 5p13 ?Campomelic dysplasia with sex reversal (2) 5q33.1 ?Campomelic dysplasia with sex reversal (2) 8q21.4 Carbamoylphosphate synthetase I deficiency (1) 2p [Carbonic anhydrase I deficiency] (1) 8q22 ?Cardiomyopathy (1) 2q35 ?Carotid body tumor-1 (2) 13q34 Cate eye syndrome (2) 22q11 ?Cataract, anterior polar (2) 14q24 ?Cataract, anterior polar (2) 2p25 Cataract, Coppock-Like (3) 2q33-q35 Cataract, Marner type (2) 16q22.1

216 Cataract, zonular pulverulent (2) 1q22 *?Cataracts, congenital total (2) Xp Central core disease of muscle (2) 19q12-q13.2 Cerebral amyloid angiopathy (1) Chr.20 Cerebrotendinous xanthomatosis (2) 2q33-qter [CEPT-deficiency] (1) 16q21 Charcot-Marie-Tooth disease, slow nerve conduction type Ia (2) 17p11.2 Charcot-Marie-Tooth disease, slow nerve conduction type Ib (2) 1q21.2-q23 Charcot-Marie-Tooth disease, X-linked dominant (2) Xq13 Charcot-Marie Tooth disease X-linked recessive 1 (2) Xq22.2 ?Chediak-Higashi syndrome (2) 1q43 Cholesteryl ester storage disease (1) 10q24-q25 *Chondrodysplasia punctata, X-Linked dominant (2) Xq28 Chondrodysplasia punctata, X-Linked recessive (2) Xpter-p22.32 Choroideremia (2) Xq21.2 Chronic granulomatous disease due to deficiency of NCF-1 (1) 7q11.23 Chronic granulomatous disease due to deficiency of NCF-2 (1) 1q25 Chronic infections (1) 10q11.2-q21 Citrullinemia (1) 9q34 Cleft palate, X-linked (2) Xq21 CMO II deficiency (1) 8q21 *Coffin-Lowry syndrome (2) Xp22.2-p22.1 ?Coloboma of iris (2) 2pter-p25.1 Colorblindness, blue monochromatic (3) Xq28 Colorblindness, blue monochromatic (3) Xq28 Colorblindness, blue monochromatic (3 Xq28 Colorblindness, deutan (3) Xq28 Colorblindness, protan (3) Xq28 Colorblindness, tritan (2) 7q22-qter Colorectal adenoma (1) 12p12.1 ?Colorectal cancer (1) 12p12.1 Colorectal cancer (1) 18q23.3 Colorectal cancer (3) 17p13.1 Colorectal cancer, familial (2) 5q22-q23 Combined C6/C7 deficiency (1) 5p13 ?Combined variable hypogammaglobulinemia (1) 14q32.33 Conductive deafness with stapes fixation (2) Xq13-q21.1 Coproporphyria (1) Chr.9 {Coronary artery disease, susceptibility to} (1) 6q27 Cortisol resistance (1) 5q31 CR1 deficiency (1) 1q32

217 Craniosynostosis (2) 7p21.3-p21.2 [Creatine kinase, brain type, ectopic expression of] (2) 14q32 Creutzfeldt-Jakob disease (2) 20pter-p12 ?Cryptorchidism (2) Xp21 [Cystathioninuria] (1) Chr.16 Cystic fibrosis (2) 7q31.3-q32 Debrisoquine sensitivity (1) 22q11.2-q12.2 Dentinogeneis imperfecta-1 (2) 4q13-q21 Diabetes insipidus, nephrogenic (3) Xq28 Diabetes insipidus, neurohypophyseal (1) 20pter-p12.21 ?Diabetes mellitus, insulin dependent (2) 6p21.3 Diabetes mellitus, insulin-resistant, with acanthosis nigricans (1) 19p13.3-p13.2 Diabetes mellitus, rare form (1) 11p15.5 ?Diaphragmatic hernia (2) 1q32.3-q42.3 Diastrophic dysplasia (2) 5q22-q34 DiGeorge syndrome (2) 22q11 Diphenylhydatoin toxicity (1) 1q22-qter [Diphtheria, susceptibility to} (1) 5q23 ?Dubin-Johnson syndrome (2) 13q34 Duchenne muscular dystrophy (3) Xp21.2 [Dysalbuminemic hyperthyroxinemia] (1) 4q11-q13 [Dysalbuminemic hyperzincemia] (1) 4q11-q13 Dysfibrinogenemia, alpha types (1) 4q28 Dysfibrinogenemia, beta types (1) 4q28 Dysfibrinogenemia, gamma types (1) 4q28 Dyskeratosis congenital (2) Xq28 ?Dyslexia-1 (2) 15q11 Dysplasminogenemic thrombophilia (1) 6q26-q27 Dysprothrombinemia (1) 11p11-q12 [Dystransthyretinemic hyperthyroxinemia] (1) 18q11.2-q12.1 Ehlers-Danlos syndrome, type IV (3) 2q31 Ehlers-Danlos syndrome, type VIIA1 (3) 17q21.3-q22.05 Ehlers-Danlos syndrome, type VIIA2 (3) 7q21.3-q22.1 ?Ehlers-Danlos syndrome, type X (3) 2q34-q36 [Elliptocytosis, Malaysian-Melanesian type] (1) 17q21-q22 Elliptocytosis-1 (3) 1p36.2-p34 Elliptocytosis-2 (2) 1q21 Elliptocytosis-3 (2) 14q22-q23.2 Emery-Dreifuss muscular dystrophy (2) Xq28 Emphysema (1) 14q32.1 Emphysema due to alpha-2-macroglobulin deficiency (1) 12p13.3-p12.3

218 Emphysema-cirrhosis (1) 14q32.1 Enolase deficiency (1) 1pter-p36.13 ?Eosinophilic myeloproliferative disorder (2) 12p13 Epidermolysis bullosa dystrophica, recessive (3) 11q11-q23 Epidermolysis bullosa Ogna type (2) 8q24 Epidermolysis bullosa progressiva (2) Unassigned Link ?Epidermolysis bullosa simplex, Koebner type 1q21-q24 Epilepsy, juvenile myoclonic (2) 6p21.3 Epilepsy, progressive myoclonic (2) 21q22.3 ?Erythremia (1) 7q21-q22 Erythremias, alpha- (1) 16pter-p13.3 Erythremias, beta- (1) 11p15.5 Erythroblastosis fetalis (1) 1p36.2-p34 Erythrokeratodermia variabilis (2) 1p36.2-p34 *[Euthyroidal hyper- and hypothyroxinemia] (1) Xq21-q22 Ewing Sarcoma (2) 22q12 Exertional myoglobinuria due to deficiency of LDH-A (1) 11p15.4 Fabry disease (3) Xq22 Facioscapulohumeral muscular dystrophy (2) 4q34-qter Factor H deficiency (1) 1q32 Factor V deficiency (1) 1q23 Factor VII deficiency (1) 13q34 Factor X deficiency (1) 13q34 Factor XI deficiency (1) 4q35 Factor XII deficiency (1) 5q33-qter Factor XIIIA deficiency 6p25-p24 Factor XIIIB deficiency 1q31-q32.1 ?Familial Mediterranean fever (1) 9q32-q33 ?Fanconi anemia (1) 1q41-q42 Fanconi anemia-1 (2) 20Q Favism (1) Xq28 ?Fetal alcohol syndrome (1) 12q24.2 ?Fetal hydantoin syndrome (1) 1p22-qter Fletcher factor deficiency (1) 4q35 *Focal dermal hypoplasia (2) Xp22.31 Fragile X syndrome/Martin-Bell syndrome (2) Xq27.3 Friedreich ataxia (2) 9q13-q21.1 Fructose Intolerance (1) 9q22 ?Fryns syndrome (2) 1q24-q31.2 Fucosidosis (1) 1p34 Fumarase deficiency (1) 1q42.1

219 G6PD deficiency (1) Xq28 Galactokinase deficiency (1) 17q21-q22 Galactose epimerase deficiency (1) 1pter-p32 Galactosemia (1) 9p13 Galactosialidosis (1) 20q13.1 Gardner syndrome (2) 5q22-q23 Gaucher disease (1) 1q21 Gerstmann-Straussler disease (2) 10q21-q22 Glanzmann thrombasthenia, type A (1) 20pter-p12 Glanzmann thrombasthenia, type B (1) 17q21.32 Glaucoma, congenital (2) 17q21.1-q21.3 Glioblastoma multiforme (2) Chr.11 Glutaricaciduria, type II (1) 10p12-q23.2 Glutaricaciduria, type IIc (1) 15q23-q25 Glutathioninuria (1) Chr.19 Glycerol kinase deficiency (2) 22q11.1-q11.2 Glycogen storage disease VII (1) Xp21.3-p21.2 *Glycogen storage disease, X-Linked hepatic (2) Xp22 [Glyoxalase II deficiency] (1) 16p13 GM1-Gangliosidosis (1) 3p21-p14.2 GM2-Gangliosidosis, juvenile, adult (1) 15q22-q25.1 GM2- Gangliosidosis, AB variant (1) Chr.5 Goeminne TKCR syndrome (2) Xq28 Goiter, adolescent multinodular (1) 8q24.2-q24.3 ?Goldenhar syndrome (2) 7p *Gonadal dysgenesis, XY female type F (2) Xp22-p21 Gonadoblastoma (2) 11p13 *?Gonadotropin deficiency (2) Xp21 Granulomatous disease, autosomal, due to deficiency of CYBA 16q24 Granulomatous disease, chronic, X-Linked (2) Xp21.1 Greig craniopolysyndactyly syndrome (2) 7p13 *?Growth hormone deficiency, X-Linked (2) Xq21.3-q22 ?Gynecomastia, familial, due to increased aromatase activity (1) 15q21.1 Gyrate atrophy of choroids and retina with ornithinemia, B6 responsive or unresponsive (1) 10q26 Harderoporphyria (1) Chr9 Hb H mental retardation syndrome (2) 16pter-p13.3 Heinz body anemias, alpha- (1) 16pter-p13.3 Heinz body anemias, beta- (1) 11p15.5 Hemochromatosis (2) 6p21.3 Hemodialysis-related amyloidosis (1) 15q21-q22

220

Hemolytic anemia due to ADA excess (1) 20q13.11 Hemolytic anemia due to adenylate kinase deficiency (1) 9q34.1 Hemolytic anemia due to bisphosphoglycerate mutase deficiency (1) 7q31-q34 Hemolytic anemia due to G6PD deficiency (1) Xq28 Hemolytic anemia due to glucosephosphate isomerase deficiency (1) 19cen-q12 Hemolytic anemia due to glutathione peroxidase deficiency (1) 11-q12 Hemolytic anemia due to glutathione reductase deficiency (1) 8p21.1 Hemolytic anemia due to hexokinase deficiency (1) 10p11.2 Hemolytic anemia due to PGK deficiency (1) Xq13 Hemolytic anemia due to phosphofructokinase deficiency (1) 21q22.3 Hemolytic anemia due to triosephosphate isomerase deficiency (1) 12p13 Hemophilia A (3) Xq28 Hemophilia B (3) Xq27.1-q27.2 Hemorrhagic diathesis due to “antithrombin” Pittsburgh (1) 14q32.1 Hemorrhagic diathesis due to PAI1 deficiency (1) 7q21.3-q22 ?Hepatic lipase deficiency (1) 15q21-q23 ?Hepatocarcinoma (2) 2q14-q21 Hepatocellular carcinoma (3) 4q32.1 [Hereditary persistence of alpha-fetoprotein] (3) 4q11-q13 ?Hereditary persistence of fetal hemoglobin (3) 11p15.5 *[Hereditary persistence of fetal hemoglobin, Swiss type (2) Xp11.23 Hers disease, or glycogen storage disease VI (1) Chr.14 Heterocellular hereditary persistence of fetal hemoglobin (2) 11p15 *?Heterocellular hereditary persistence of fetal hemoglobin (2) Xq28 !Hex A pseudodeficiency! (1) 15q22-q25.1 ?H syndrome (2) 13q34 [Histidinemia] (1) 12q22-q23 ?Holoprosencephaly (2) 2p21 ?Holoprosencephaly (2) 21q22.3 ?Holoprosencephaly (2) 7q36 ?Holt-Oram syndrome (2) 14q23-q24.2 ?Holt-Oram syndrome (2) 20p13 Homocystinuria, B6-responsive and nonresponsive types (1) 21q22.3 HPFH, deletion type (1) 11p15.5 HPFH, nondeletion type A (1) 11p15.5 HPFH, nondeletion type G (1) 11p15.5 HPRT-related gout (1) Xq26-q27.2 Huntington’s disease (2) 4p16.3 Hurler syndrome (1) 4p16.3 Hurler-Scheie syndrome (1) 4p16.3

221 Hydrocephalus, X-Linked (2) Xq28 Hydrops fetalis, 1 form (1) 19cen-q12 Hyperammonemia due to CTPase deficiency (1) 1pter-q12 Hyperbetalipoproteinemia (1) 2p24 Hypercholesterolemia, familial (3) 19p13.2-p13.1 ?Hyperglycinemia, isolated nonketotic, type I (2) 9p22 ?Hypergonadotropic hypogonadism (1) 19q13.32 ?Hyperimmunoglobulin G1syndrome (2) 14q32.33 Hyperkalemic periodic paralysi (3) 17q23.1-q25.3 ?Hyperleucinemia-isoleucinemia or hypervalinemia (1) 12pter-q12 Hyperlipoproteinemia I (1) 8p22 Hyperlipoproteinemia, type Ib (1) 19q13.1 Hyperlipoproteinemia, type III (1) 19q13.1 [Hyperphenylalaninemia, mild] (3) 12p24.1 [?Hyperproglucagonemia] (1) 2q36-q37 Hyperproinsulinemia, familial (1) 11p15.3 Hypertriglyceridemia, 1 form (1) 11q23 Hypertrophic cardiomyopathy, 1 form (3) 14q12 ?Hypervalinemia or hyperleucine-isoleucinemia (1) Chr.19 Hypobetalipoproteinemia 11q23 Hypobetalipoproteinemia (1) 2p24 [Hypoceruloplasminemia, hereditary] (1) 3q21-q24 Hypofibrinogenemia, gamma types (1) 4q28 ?Hypogonadotropic hypogonadism due to GNRH deficiency (1) 8p21-q11.2 Hypomagnesemia, X-Linked primary (2) Xp22 ?Hypomelanosis of Ito (2) 15q11-q13 ?Hypomelanosis of Ito (2) 9q33-qter Hypoparathyroidism, familial (1) 11p15.3-p15.1 *Hypoparathyroidism, X-Linked (2) Xq26-q27 ?Hypophosphatasia, adult (1) 1p36.1-p34 Hypophosphatasia, infantile (3) 1p36.1-p34 Hypophosphatemia, hereditary (2) Xp22.2-p22.1 ?Hypophosphatemia with deafness (2) Xp22 Hypoprothrombinemia (1) 11p11-q12 Hypothyroidism, hereditary congenital, 1 or more types (1) 8q24.224.3 Hypothyroidism, nongoitrous (1) 1p22 Hypothyroidism, nongoitrous, due to TSH resistance (1) 14q31 ?Ichthyosis vulgaris (1) 1q21 Ichthyosis, X-Linked (3) Xpter-p22.32 Immunodeficiency, X-Linked, with hyperIgM (2) Xq24-q27 *Incontinentia pigmenti, familial (2) Xq27-q28

222 Incontinentia pigmenti, sporadic type (2) Xp11.21 Infertile male syndrome (1) Xcen-q13 [Inosinie triphosphatase deficiency] (1) 20p Interferon, alpha, deficiency (1) 9p21 Interferon, immune, deficiency (1) 12q24.1 ?Isolated growth hormone deficiency due to defect in GHRF (1) 20p11.23qter Isolated growth hormone deficiency, Illig type with absent GH and Kowarski type with bioinactive GH (3) 17q22-q24 Isovalericacidemia (1) 15q14-q15 ?Jacobsen syndrome 11q Kallmann syndrome X22.3 Kennedy disease (2) Xq21.3-q22 ?Kniest dysplasia (1) 12q13.11-q13.2 ?Kostmann agranulocytosis (2) 6p21.3 Krabbe disease (1) 14q21-q31 ?Lactase deficiency, adult (1) Chr.2 ?Lactase deficiency, congenital (1) Chr.2 ?Lactoferrin-deficient neutrophils 3q21-q23 Langer-Giedon syndrome (2) 8q24.11-q13.2 Langer-Saldino achondrogenesis-hypochondrogenesis (1) 12q13.11-q13.2 Laron dwarfism (1) 5p13-p12 ?Laryngeal adductor paralysis (2) 6p21.3—p21.2 {Lead poisoning, susceptibility to} (1) 9q34 ?Leiomyomata, multiple hereditary cutaneous (2) 18p11.32 Leprechaunism (1) 19p13.3-p13.2 Lesch-Nyhan syndrome (3) Xq26-27.2 ?Letterer-Siwe disease (2) 13q14-q31 Leukemia, acute lymphoblastic (1) 19p13.3.-p13.2 ?Leukemia, acute lymphocytic, with 4/11 translocation (3) 4q21 Leukemia, acute myeloid, M2 type (1) Xpter-p21 Leukemia, acute T-cell (2) 11p13 Leukemia, chronic myeloid (3) 22q11.21 Leukemia, chronic myeloid (3) 9q34.1 Leukemia, T-cell acute lymphocytic (2) 10q24 Leukemia/Lymphoma, B-cell, 1 (2) 11q13.3 Leukemia/Lymphoma, B-cell, 2 (2) 18q21.3 Leukemia/Lymphoma, B-cell, 3 (2) 19q13 Leukemia/Lymphoma, T-cell, (2) 1p32 Leukemia/Lymphoma, T-cell, (2) 14q32.1 Leukemia/Lymphoma, T-cell, (2) 2q34 Leukemia/Lymphoma, T-cell, (3) 14q11.2

223 Leukocyte adhesion deficiency (2) 21q22.3 Li-Fraumeni syndrome (1) 17p13.1 Lipoamide dehydrogenase deficiency (1) 7q31-q32 Lipoid adrenal hyperplasia, congenital (1) Chr.15 Lipoma (2) 12q13-q14 Liver cell carcinoma (1) 11p14-p13 Long QT syndrome (2) 11p15.5 Lowe’s syndrome Xq25 Lupus erythematosus, systemic (1) 1q23-q24 Lymphoproliferative syndrome, X-linked (2) Xq25 ?Lynch cancer family syndrome II (2) 18q11-q12 ?Lysosomal acid phosphatase deficiency (1) 11p12-p11 Macrocytic anemia of 5q syndrome II (2) 5q12-q32 Macular dystrophy, atypical vitelliform (2) 8q24 Macular dystrophy,?vitelline type (2) 6p25-qter ?Major mental illness (2) 11p21-q22 ?Male infertility due to acrosin deficiency (2) 22q13-qter ?Male infertility, familial 11p13 ?Male pseudohermaphroditism due to defective LH (1) 19q13.32 Malignant hyperthermia (2) 19q13.1-q13.3 Malignant melanoma, cutaneous (2) 1p36 Manic-depressive illness, X-Linked (2) Xq28 Mannosidosis (1) 19p13.2-q12 Maple syrup urine disease (1) 19q13.1-q13.2 Maple syrup urine disease, type II (1) 1p31 Maple syrup urine disease, type III (3) 6p22-p21 Marfan syndrome (2) 15q-q21.3 Maroteaux-Lamy syndrome (1) 5q11-q13 Martin-Bell syndrome/Fragile X syndrome (2) Xq27.3 NASA syndrome (2) Xq28 McArdle disease (1) 11q13 *[McLeod phenotype] (2) Xp21.2-p21.1 Medullary thyroid carcinoma (2) 10q21.1 ?Megacolon (2) 13q22.1-q32.1 ?Megaloblastic anemia 5q11.1-q13.2 ?Megalocomea, X-Linked (2) Xq21.3-q22 Meningioma (2) 22q12.3-qter Meningioma (3) 22q12.3-q13.1 Menkes disease (2) Xq12-q13 Mental retardation of WAGR (2) 11p13 *Mental retardation, X-Linked nonspecific, I (2) Xp22

224 *Mental retardation, X-Linked nonspecific, II (2) Xq11-q12 *Mental retardation-skeletal dysplasia (2) Xq28 Metachromatic Leukodystrophy (1) 22q13.31-qter Metachromatic Leukodystrophy due to deficiency of SAP-1 (1) 16pter-p13.3 Methemoglobinemia, enzymopathic (1) 11p15.5 Methylmalonicaciduria, mutase deficiency type (1) 6p21 ?Microcephaly, true (2) 1q31-q32.1 Miller-Dieker Lissencephaly syndrome (2) 17p13.3 MODY, 1 form (3) 11p15.5 Mucolipidosis II (1) 4q21-q23 Mucolipidosis III (1) 4q21-q23 Mucopolysaccharidosis I (1) 4p16.3 *Mucopolysaccharidosis II (2) Xq28.1 Mucopolysaccharidosis IVB (1) 3p21-p14.2 Mucopolysaccharidosis VII (1) 7q22 Multiple endocrine neoplasia II (2) 11q13 Multiple endocrine neoplasia II (2) 10q21.1 Multiple endocrine neoplasia III (2) 10q21.1 ?Multiple exostoses (2) 8q23-q24.1 ?Multiple Lipomatosis (2) 12q13-q14 ?Muscle glycogenosis (1) Xq12-q13 Myeloperoxidase deficiency (1) 17q21.3-q23 Myoadenylate deaminase deficiency (1) 1p21-p13 Myopathy due to CTPase deficiency (1) 1pter-q12 Myopathy due to phosphoglycerate mutase deficiency 7p13-p12.3 Myotonic dystrophy (2) 19q13.2-q13.3 Myotubular myopathy, X-Linked (2) Xq28 Myxoid Liposarcoma (2) 12q13-q14 *?N syndrome Xp23.3-p21.1 Nail-patella syndrome (2) 9q34 *Nance-Horan syndrome (2) Xp22.3-p21.1 Neuroblastoma (2) 1p32 Neuroepithelioma (2) 22q12 Neurofibromatosis, von Recklinghausen (2) 17q11.2 Neutropenia, immune (2) 1q23-q24 ?Nevoid basal cell carcinoma syndrome (2) 1p Niemann-Pick disease (1) 11p15.4-15.1 *Nightblindness, congenital stationary, type I (2) Xp11.3 Norrie’s disease (2) Xp11.4 Norum disease (3) 16q22.1 Nucleoside phosphorylase deficiency, immunodeficiency due to (2) 14q13.1

225 *Ocular albinism, Forsius-Eriksson type (2) Xp11-q11 Ocular albinism, Nettleship-Falls type (2) Xp22.3 ?Optic atrophy, Kjer type (2) 2p Ornithine transcarbamylase deficiency (3) Xp21.1 Orofacial cleft (2) 6pter-p23 Oroticaciduria (1) 3q13 Osteoartrosis, precocious (3) 12q13.11-q13.2 Osteogenesis imperfecta, 2 or more clinical forms (3) 17q21.31-q22.05 Osteogenesis, retinoblastoma-related (2) 7q21.3-q22.1 Osteosarcoma, retinoblastoma-related (2) 13q14.1 Ovarian carcinoma (2) 9p24 *Ovarian failure, premature (2) Xq26-q27 Oxalosis I (1) 2q36-q37 ?Paget disease of bone (2) 6p21.3 {?Parkinsonism, susceptibility to} (1) 22q11.2q12.2 Paroxysmal nocturnal hemoglobinuria (1) 11p14-p13 Pelizaeus-Merzbacher disease (3) Xq22 ?Pendred syndrome (2) 8q24 Periodontitis, juvenile (2) 4q11-q13 Persistent Mullerian duct syndrome (1) 19p13.3-p13.2 Phenylketonuria (3) 12q24.1 Phenylketonuria due to dihydropteridine reductase deficiency (1) 4p15.31 *Phosphoribosylpyrophosphate synthetase-related gout (1) Xq22-q24 ?Phosphorylase kinase deficiency of liver and muscle (2) 16q12-q13.1 ?Piebaldism (2) 4q12 PK deficiency hemolytic anemia (1) 1q21-q22 [Placental lactogen deficiency] (1) 17q22-q24 Placental steroid sulfatase deficiency (3) Xpter-p22.32 Plasmin inhibitor deficiency (1) 18p11.1-q112 Plasminogen activator deficiency (1) 8p12 Plasminogen deficiency, types I and II (1) 6q26-q27 Plasminogen Tochigi disease (1) 6q26-q27 Platelet alpha/delta storage pool deficiency (1) 1q21-q24 {Polio, susceptibility to} (2) 19q12-q13.2 Polycystic kidney disease (2) 16p13.31-p13.12 Polycystic ovarian disease (1) 17q11-q12 Polyposis coli, familial (2) 5q22-q23 Pompe disease (1) 17q23 Porphyria, acute hepatic (1) 9q34 Porphyria, acute intermittent (1) 11q23.2-qter Porphyria, congenital erythropoietic (1) 10q25.2-q26.3

226 Porphyria, cutanea tarda (1) 1p34 Porphyria, hepatoerythropoietic (1) 1p34 Porphyria variegata (2) 14q32 Postanesthetic apnea (1) 3q25.2 Prader-Willi syndrome (2) 15q11 *Progressive cone dystrophy (2) p21.1-p11.3 Prolidase deficiency (1) 19cen-q13.11 *Properdin deficiency, X-Linked (3) Xp11.4 Propionicacidemia, type I or pccA type (1) 13q32 Propionicacidemia, type II or pccB type (1) 3q13.3-q22 Protein C deficiency (1) 2q13-q14 Protein S deficiency (1) 3p11.1-q11.2 Pseudohermaphroditism, male, with gynecomastia (1) 17q11-q12 Pseudohypoaldosteronism (1) 4q31.1 Pseudohypoparathyroidism, type Ia (1) 2oq13.2-q13.3 Pseudo-Zellweger syndrome (1) 3p23-p22 ?Pyridoxine dependency with seizures (1) 2q Pyropoikilocytosis (1) 1q21 Pyruvate carboxylase deficiency (1) 11q *Pyruvate dehydrogenase deficiency (1) Xp22.2-p22.1 ?Rabson-Mendenhall syndrome (1) 19p13.3-p13.2 ?Ragweed sensitivity (2) 6p21.3 Reifenstein syndrome (1) Xcen-q13 Renal cell carcinoma (2) 3p14.2 [Renal glucosuria] (2) 6p21.3 ?Retinal cone dystrophy-1 (2) 6p25-q25 ?Retinal cone-rod dystrophy (2) 18q21-q22.2 Retinitis pigmentosa, autosomal dominant (3) 3q21-q24 Retinitis pigmentosa-2 (2) Xp11.3 Retinitis pigmentosa-3 (2) Xp21.3 Retinoblastoma (2) 13q14.1-q14.2 ?Retinol binding protein, deficiency of (1) 10q23-q24 Retinoschisis (2) Xp22.3-p22.1 *?Rett syndrome (2) Xp Rhabdomyosarcoma (2) 11p15.5 Rhabdomyosarcoma, alveolar (2) 2q37 Rh-null disease (1) 3cen-q22 ?Rh-null hemolytic anemia (1) 1p36.2-p34 Rieger syndrome (2) 4q23-q27 ?Rothmund-Thomson syndrome (2) Chr.18 Salivary gland pleomorphic adenoma (2) 8q12

227 Sandhoff disease (1) 5q13 Sanfilippo syndrome D (1) 12q14 *Sarcoma, synovial (2) Xp11.2 Scheie syndrome (1) 4p16.3 *SCID, X-Linked (2) Xq13.1-q21.1 Sclerotylosis (2) 4q28-q31 Seizures, benign neonatal (2) Chr.20 Severe combined immunodeficiency due to ADA deficiency (1) 20q13.11 Severe combined immunodeficiency due to IL-2 deficiency (1) 4q26-q27 Severe combined immunodeficiency (SCID), HLA class II-negative type (1) 19p13 ?Sialidosis (1) Chr.10 ?Sialidosis (2) 6p21.3 Sicle cell anemia (1) 11p15.5 ?Situs inversus viscerum (2) 14q32 ?SLE (1) 1q32 Small-cell cancer of lung (2) 3p23-p21 ?Smith-Lemli-Opitz syndrome (2) 7q23-qter Smith-Magenis syndrome (2) 17p11.2 Spastic paraplegia, X-Linked, uncomplicated (2) Xq21-q22 Spherocytosis, recessive (1) 1q21 Spherocytosis-1 (3) 14q22-q23.2 Spherocytosis-2 (3) 8p11.2 Spinal muscular atrophy II (2) 5q11.2-q13.3 Spinal muscular atrophy III (2) 5q11.2-q13.3 Spinocerebellar-ataxia 6p21.3-p21.2 Spondyloepiphyseal dysplasia congenital (3) 12q13.11-q13.2 *Spondyloepiphyseal dysplasia tarda (2) Xp22 Stickler syndrome (3) 12q13.11-q13.2 Sucrose intolerance (1) 3q25-q26 ?Susceptibility to amyloid in FMF (1) 11pter-p12 Tay-Sachs disease (1) 15q22-q25.1 Testicular feminization (1) Xcen-q13 Thalassemias, alpha- (1) 16pter-p13.3 Thalassemias, beta- (1) 11p15.5 Thrombocytopenia, X-Linked (2) Xp21-p11 Thrombophilia due to elevated HRG (2) 3p14-qter Thrombophilia due to excessive plasminogen activator inhibitor (1) 7q21.3-q22 Thrombophilia due to heparin cofactor II deficiency (1) Chr.22 Thyroid hormone resistance (3) 3p24.3 Thyroid iodine peroxidase deficiency (1) 2pter-p12 Thyroid papillary carcinoma (1) 10q11-q12

228 Thyrotropin-releasing hormone deficiency (2) Chr.3 Torsion dystonia (2) 9q32-q34 Torsion dystonia-parkinsonism, Filipino type (2) Xq21 ?Tourette syndrome (2) 18q22.1 Transcobalamin II deficiency (1) 22q11.2-qter [Transcortin deficiency](1) 14q31-q32.1 ?Treacher Collins mandibulofacial dysostosis 5q11 Trichorhinophalangeal syndrome, type I (2) 8q24.2 Trypsinogen deficiency (1) 7q32-qter Tuberous sclerosis-1 (2) 9q33-q34 Tuberous sclerosis-2 (2) 11q23 Tyrosinemia, type I (1) 15q23-q25 Tyrosinemia, type II (1) 16q22.1-q22.3 Urolithiasis, 2,8-dihydroxyadenine (1) 16q24 Usher syndrome, type-2 (2) 1q32 van der Woude syndrome (2) 1q32 Vitamin D dependency, type I (2) 12q14 {Vivax malaria, susceptibility to} (1) 1q21-q22 von Hippel-Lindau syndrome (2) 3p26-p25 von Willebrand disease (1) 12pter-p12 Waardenburg syndrome, type I (2) 2q37.3 ?Watson syndrome (2) 17q11.2 Werdnig-Hoffmann disease (2) 5q11.2-q13.3 *Wieacker-Wolff syndrome (2) Xq13-q21 Wilms tumor (2) 11p13 Wilms tumor, type 2 (2) 11p15.5 Wilson disease (2) 13q14-q21 Wiskott-Aldrich syndrome (2) Xp11.3-p11.2 Wolf-Hirschhorn syndrome (3) 4p16.1 Wolman disease (1) 10q24-q25 ?Xeroderma pigmentosum (1) 1q41-q42 ?Xeroderma pigmentosum, 1 form (1) 19q13.2-q13.3 Xeroderma pigmentosum, group A (1) 9q34.1 Xeroderma pigmentosum, group B (1) 2q21 Xeroderma pigmentosum, group F (2) Chr.15 ?Xeroderma pigmentosum, one type (1) Chr.13 Zellweger syndrome (2) 7q11.23

229

DR. RECOMMENDS METABOLIC 1 A CHROMOSOME HOMEOPATHIC

Chromosome No.

RNA Control 13 Nerval Disease 1A RNA Control 13A Nerval Disease 2 RNA Control 14 Nerval Disease 2A RNA Control (Tactile) 14A Nerval Disease 3 RNA Control (Vision) 15 Nerval Disease 3A RNA Control (Hearing) 15A Nerval Disease 4 RNA Control 16 MS 4A RNA Control 16A MD 5 RNA Control 17 Digestive 5A RNA Control 17A Kidney Problems 6 Bone Disturbance 18 Kidney Problems 6A Bone Disturbance 18A Kidney Problems 7 Skin Disturbance 19 Liver Problems 7A Skin Disturbance 19A Liver Problems 8 Lipid Metabolism 20 Liver Problems 8A Cholesterol Control 20A Pancreas 9 Cholesterol Control 21 Pancreas 9A Cholesterol Control 21A Pancreas 10 Blood Disturbance 22 Brain 10A Blood Disturbance 22A Brain 11 Downs Syndrome (Alzheimers) 23 Sex System 11A Downs Syndrome (Alzheimers) 23A Addiction 12 Immune System 24 Extra Chromosome (Sociopath) 12A Immune System

230

LECTINS

Lectins are proteins or glycoproteins of non-immune origin that agglutinate cells and/or precipitate complex carbohydrates. The agglutination activity of these highly specific carbohydrate-binding molecules is usually inhibited by a simple monosaccharide, but for some lectins di, tri, and even polysaccharides are required. Lectins are isolated from a wide variety of natural sources, including seeds, plant roots and bark, fungi, bacteria, seaweed and sponges, mollusks, fish eggs, body fluids of invertebrates and lower vertebrates and from mammalian cell membranes. The precise physiological role of lectins in nature is still unknown, but they have proved to be very valuable in a wide variety of applications in vitro, including:

¾ Blood groupings and erythrocyte poly agglutination studies ¾ Mitogenic stimulation of lymphocytes ¾ Lymphocyte subpopulation studies ¾ Fractionation of cells and other particles ¾ Isolation, purification and structural studies of carbohydrate containing molecules ¾ Histochemical studies of normal and pathological conditions

Source: http://www.answers.com/topic/lectin?cat=health / http://books.google.com/books?id=9xWhUBTdDqgC&pg=PA30&lpg=PA30&dq=lectins +are+proteins+or+glycoproteins+of+%22non+immune%22+origin+that+agglutinate+cell s&source=web&ots=5zlpr6hyyU&sig=nCH_vu506zeDKX5XEuwc_LyXXgQ

231 Common Name

Asparagus Pea Limulin Avocado Mung Bean Black Locust Mushroom Broad Bean Osage Orange Camels Foot Tree Pagoda Tree Chick Pea Pea, Garden Concanavalin A Peanut Coral Tree (Israel) Pokeweed Eel Potato Elder Red Kidney Bean False Acacia Red Marine Algae Fava Bean Roman Snail Furze Scarlet Runner Bean Gorse Siberian Pea Tree Green Marine Algae Snail, Garden Hairy Vetch Soybean Horse Gram Spindle Tree Horseshoe Crab Sweet Pea Jack Bean Thorn Apple Japanese Wisteria Tomato Jimson Weed Wheat Germ Laburnum, Scotch Winged Bean Lentil Winged Pea Lima Bean

232 OLIGO ELEMENTS

FIRE DIATHESIS III Manganese-Cobalt

EARTH DIATHESIS V Zinc-Nickel-Cobalt, Zinc-Copper

METAL DIATHESIS II Manganese-Copper

WATER DIATHESIS IV Copper-Gold-Silver

WOOD DIATHESIS I Manganese

IODINE LITHIUM MAGNESIUM SULPHUR ZINC

OLIGO DEOXYRIBONUCLEOTIDE

URACIL CYTOSINE ADENINE THYMINE INOSINE GUANINE

233 MINERALS ALUMINUM BORON CALCIUM CARBON CHLORINE CHROMIUM BOCALT COPPER HYDROGEN IODINE IRON MAGNESIUM MANGANESE MOLYBDENUM NICKEL NITROGEN OXYGEN PHOSPHOROUS POTASSIUM SELENIUM SILICON SODIUM SULPHER TIN VANADIUM ZINC

234 METALLIC ELEMENTS

ALUMINUM MERCURY AMERICUM MOLYB ANTIMONY NEODYMIUM ARGON NEON ARSENIC NIOBIUM BARIUM OSMIUM BERYLLIUM PLATINUM BISMUTH PLUTONIUM BROMINE POLONIUM CADMIUM POTASSIUM CALCIUM RADIUM CERIUM RADON CESIUM RUBIDIUM CHROMIUM SB COBALT SCANADIUM COPPER SELENIUM FLOURINE SILVER GALANIUM SODIUM GALLIUM STRONTIUM GERMANIUM TECHNETIUM GOLD TELLURIUM HAFNIUM THORIUM HELIUM TIN IODINE TITANIUM IRIDIUM TUNGSTEN IRON URANIUM KRYPTON VANADIUM LANTHANUM W LEAD XENON LITHIUM YTTRIUM MAGNESIUM ZINC MANGANESE ZIRCONIUM MENDELEVIUM

235 PHENOLICS

Acetaldehyde: Petrochemical sensitivity, (perfumes, flavors, dyes, plastics, synthetic rubber), alcoholism, spreading phenomenon of allergies to foods, sugar, metabolism, and yeast.

Acetylcholine Chloride: Parasympathetic stimulant (neurotransmitter) lowers blood pressure; chronic fatigue, depression, phobias, schizophrenia.

Apiol: PHS, obesity, infertility, gout, arthritis, hypothalamus-pituitary axis, homosexuals.

Ascorbic Acid: Allergic shiners, antioxidant, anxiety, bleeding gums and gum disease, cataracts, chemical sensitivity, collagen disease, dental caries, diarrhea, easy bruising, edema, fatigue, frequent infections, fruit intolerance, high cholesterol level, hyperactivity, hypertension, light sensitivity, loss of appetite, mental problems, muscle soreness, open angle glaucoma, premature aging, slow wound healing, stiff and tender joints, weakness in connective tissue.

Butylatedhydroxytoluene (BHT): Aggression, belligerence, depression, hyperactivity, temper outbursts.

Caffeic Acid: Constricts capillary walls, stimulates ACTH release (decreasing thymus weight), allergic rhinitis, pharyngeal drainage, otitis, asthma.

Chlorogenic Acid: Allergies to pollens, dust, molds; skin rashes, congestion and headaches, asthma, hay fever.

Cinnamic Acid: Bladder dysfunction, cystitis, enuresis, skin problems, (acne, eczema, psoriasis), congestion, asthma, chronic fatigue, hypoglycemia, cravings for fruit.

Coniferyl Alcohol: Allergies to evergreens, headaches.

Coumarin: Constricts capillary walls, inhibits clotting, estrogen effect asthma, hay fever, digestive problems, low back and cervical neck pain, chronic fatigue.

Dopamine: Neurotransmitter, arrhythmia, Parkinsonism, anxiety, depression, dyslexia, autism, schizophrenia.

Estrogen: PMS, cyclic changes, (closely associated with Vitamin D), effeminate traits in males.

236 PHENOLICS, cont.

Gaba: Lowers blood pressure, inhibitory transmitter in brain, anger, hostility.

Gallic Acid: Related to racing heart, anti-cancer (in 80% foods-universal reactor), chronic sinusitis, rhinitis, craving sweets, musculo-skeletal problems (low back pain), chronic fatigue, hyper-activity.

Histamine: Released from injured cells, increases pore size, dilates capillaries, hay fever, vertigo.

Indole: Bloating, constipation, asthma, allergic rhinitis, sinus congestion, chronic fatigue, common in milk drinkers and children.

L-Dopa: Arrhythmia, stimulates ACTH release (decreasing thymus weight), Parkinsonism, chronic anxiety, depression.

Malvin: Red to purple coloring in food, arthritis, psoriasis, asthma, epilepsy, MS, dyslexia, autism, hyperactivity.

Mannan: Constitutes 30-50% of yeast cell wall, suppresses T-lymphocyte production, chronic hives, angio-edema.

Menadione: Related to Vitamin K production, liver dysfunction, fatigue, easy bruising, chronic nosebleeds, chronic colitis, diarrhea, varicose veins, arthritis.

Norepinephrine: Stimulates sympathetic nervous system (fight or flight), raises blood pressure, maintains freedom from depression, agoraphobia.

Octopamine: Petrochemical sensitivities.

Phenylalanine: Building block for dopamine, cinnamic acid, caffeic acid, coumarin and coniferyl alcohol, headaches, blurred vision, poor appetite, depression, sleep disorders.

Phenylisothiocyanate: MD, diarrhea, chronic arrhythmia, hypertension, thyroid dysfunction.

Phloridzin: Strengthens vascular system, blocks absorption of glucose in kidneys (glucosuria), sugar cravings, collagen diseases.

Piperine: Stomach disorders.

237 Progesterone: PMS, menopausal stress, temporarily raises cholesterol levels.

Pyrole: Gas, bloating, anxiety, depression, mauve factor in schizophrenia.

Quercetin: In 78% of foods. Hay fever, suppresses histamine release, chelates with metals to prevent oxidation of Vitamin C and adrenaline, decreases vascular fragility, stimulates adrenaline release, decreasing thymus weight, reduces overall metabolism, reduces temperature and oxygen consumption, suppresses thyroid activity, linked with male impotence.

Rutin: Increases vascular strength, hay fever, rhinitis, reduces permeability of capillary walls.

Salsolinol: Alcoholism, chocoholism, headaches, throat discomfort, general weakness, mental fog, obsessive-compulsive behavior.

Serotonin: Neurotransmitter, sensory perception, temperature regulation, decreases bleeding, increases peristaltic motion, insomnia, memory loss, depression, dyslexia, mental retardation, obsessive, compulsive, aggressive, suicidal (lower serotonin level, higher aggression, and more violent suicide).

Taurine: Stimulates liver function and bile flow, related to viruses in liver and environmental toxicity.

Tryptophan: Antidepressant, sleep disorders, bloating, constipation, increases peristalsis, decreases bleeding, skin inflammations.

Phenylpropanolamine: Aids in the elimination of environmental sensitivities.

238 VENOMS

Many different types of venom have been used historically in different medicines by many cultures. Snake venom in particular has gotten much attention throughout the ages. The snake was thought to represent death but also to represent aspects of life. It has been part of mythology in almost every culture. The symbol for healing, the staff with the snake around it, is used by the American Medical Association as its signature. Many aspects of healing are connected to snakes. Venoms were found to have many different effects for both medicine and biology. As early as 1737, Geoffroy and Hunault observed that the blood from cats and dogs bitten by vipers did not coagulate. In 1787, Felice Fontana found that when he injected a rabbit in the jugular vein with a small quantity of the same venom, this caused immediate death. On opening the vessels he found that the blood was coagulated. This was later solved in 1899, by M. Phisalix, who found that there were two distinct types of activity in this viper venom. One was an anti- coagulant at high doses, and the other a coagulant at low doses. This was part of the first evidence that some compounds could have various effects at different potencies. The amount of dilution could sometimes accomplish an influx or a distinct difference of action in potencies or dilutions. This was later developed as the Arndt-Schultz law of pharmacology which states that what a poison does at a raw dose, a dilute form of that poison will affect inversely, or paradoxically. Dr. Isaacs remarks that the effect between alpha receptors and beta receptors in the body is not a factor of different compounds that stimulate results, but different amounts of the same compound. Different dilutions can have different effects on neural transmitter points within the body which is key to the understanding of homeopathy, especially when looking at different snake and insect venoms.

239 In 1854, Brainard found that venom in blood taken from animals bitten by crotalidae did not cause coagulation. In 1860, Mitchell found that the toxic secretion of the Crotalus adamanteus prevented blood from clotting in vitro. In 1893, Martin cited that the venom of elapidae (an example of which is the Pseudechis porphyriacus and the Notechis scutatus) coagulated blood in the vessels when injected at high doses; but at low doses it rendered the blood unable to coagulate. The venom of an Indian cobra when tested at any dose was found to inhibit blood coagulation in vivo and in vitro. This was found to be true in 1895, by D. D. Cunningham, in 1898, by Stephens and Meyers, in 1904, by Rogers. In 1901, George Lamb classified a dissertation of venoms according to their action on plasma. He noted in his article that Russell’s pit viper venom coagulated citrated plasma. This plasma does not in itself spontaneously coagulate. F. Noc confirmed these findings, and discovered that the venom of Asian and African elepidae prevented the coagulation of citrated plasma to which calcium chloride had been added for protection. In 1904, Paul Morawitz proposed that there was an essential element of the transformation of fibrinogen to fibrin which allows for the formation of different blood clots. The serozyme of serum acting on the cytozyme from the platelets caused thrombin to form. Thrombin was found to be the factor reacting on fibrinogen. In 1910, Noc presumed that some venom induced coagulation by the contribution of active thrombin to the blood. J. Mellanby found that coagulation of these venoms was increased by the addition of calcium. In 1912, Maurice Arthus put forth the idea that crotalidae acted as if it contained thrombin, whereas Russell’s pit viper venom accelerated the transformation of prothrombin to thrombin. In 1905, C. J. Martin was able to demonstrate that the coagulating factors of venoms did not pass through dialysis membranes.

240 In 1904, Paul Morawitz introduced the idea of the enzyme capacities of these different venoms, and their ability to act very similarly to the digestive juices. The capacity of these venoms to have enzymatic action in the body was then determined. These venoms could be deadly if the enzyme activity was too intense such as in the case of Russell’s pit viper which causes thrombosis. Cortalus was a very strong enzyme; whereas elapidae was found to be weak proteolytically, but strong in its other enzyme activity. In 1912, C. Delezenne claimed that the venom of Lachesis contained akinase which activated pancreatic juice. Later in 1919, he observed in experiments that the toxic secretion of snakes was able to cause catalytic breakdown of nucleic acids. By the beginning of the twentieth century, classification of the different distinguishing properties of snake venoms was possible. Some acted as if they had ferments, or protein enzyme-like substances. Some were toxic. Some had diastases. In 1887, Henry Seawall, at the University of Michigan, Ann Arbor, was the first one in the United States to observe that a type of venom serum could be developed. He injected pigeons with small amounts of venom; not enough to cause death. Weeks later, the same pigeons, when injected with a larger quantity of the venom were able to resist the venom’s effects. Hahneman’s work with some snake venoms pointed out their reversal functions. This brief document is an attempt to discuss some of these venoms and their use in medicine today. Snakes can use their venom in many different ways. Often, the purpose of venom is to hunt and digest. People bitten by a snake usually have respiratory, circulatory, neurological, cardiac and coagulation problems. The enzymes in the venom will start digestion of the tissues of

241 the victim so that the digestive system of the snake, which is not extremely strong, can get a head start on the digestive process. These venoms have strong pharmacological activity with a highly specific mode of action. Most of the contents of these venoms are proteins. Low molecular weight compounds such as peptides, nucleotides and metal ion are also often present.

CLASSICS OF NEUROTOXINS

In the neurotoxin development there are two pharmacological classes of neurotoxins: 1) those which are post-synaptic, and 2) those which are pre-synaptic. Curare is an example of a post-synaptic neurotoxin. It binds to the nicotinic acetylcholine receptors, and prevents the depolarizing action of acetylcholine. These toxins are usually referred to as curare-like toxins. Pre-synaptic toxins inhibit the release of acetylcholine, and their toxicity is much higher than that of the post- synaptic toxins. Another type of toxin is the membrane toxins which change the permeability of the membrane. They are often cardio-toxins, lytic factors, cytotoxins, etc. These names indicate the types of membranes they affect. Membrane toxins have been isolated only from elapid venoms. These membrane toxins work by penetrating into the hydrophobic layer of the membrane. Many of these toxins have phospholipase types of structures. A secondary hypothesis is that the membrane might be disrupted by the interaction of the disulfides in the toxin and the sulpha-hydro groups in the membrane. These toxin-induced permeability changes can have many biochemical and pharmacological activities. They might be hemolytic which would allow for the disruption of red blood cells; or cytotoxic, where they might induce a type of leukemia or lymphocytoma. There is a depolarizing effect of the different membranes which can cause peripheral nerve problems, contracture, paralysis, ventricular fibrillation

242 and systolic arrest of the heart muscle. They might interfere with transport mechanisms such as inhibition of the accumulation of anions, amino acids, or glucose into the tissues of thyroid, kidney, small intestine, etc. There can be effects on membrane activity and membrane enzymes. This might provide inactivation of magnesium, sodium, potassium, and possibly even ATPase. All of these require intact membranes in order to function properly. Certain of these toxins can liberate calcium from muscle fibers and produce tetany. Some plants share some of these membrane toxins. An example is mistletoe which is a parasitic plant of the family Loranthaceae. Mistletoe toxins are very basic, and they have an isoelectric point of about pH11.

They are very stable, and heating an ocular solution to 100 °C for thirty minutes has no influence on their toxicity. This mistletoe toxin consists of 46 amino acids in the peptide chain, cross-linked by three disulfides. These toxins in low concentration of ten micrograms per milliliter will produce depolarization and contraction in rabbit papillary and frog skeletal muscles, and the effects can be reversed by calcium. So it is suggested that the toxins bind to the cell membrane, and thus displace calcium. Let us proceed to analyze some of the different toxins provided by different venoms. One is crotoxin which is the main neurotoxin of the South American rattlesnake Crotalus durissus terrificus. This is a very powerful toxin which affects certain neurons and muscular structure. Specifically, the toxin from this snake produces problems in the neck and can contribute to nuchal rigidity. This has caused the South American rattlesnake to be called the “neck breaker,” because of its effect on neck muscles. Homeopathic crotoxin has been used quite successfully on neck and cervical conditions. The Australian tiapan, Oxyuranus scutellatus has extremely potent venom. It exhibits a low phospholipase activity, and has an effect similar

243 to curare. The Australian tiger snake venom has strong effects in being able to bind calcium, and it is inactivated in the presence of bromine. Enhydrina schistosa, known as the common sea snake, has venom which produces myoglobinuria and muscle movement pains. Mice die rapidly of respiratory failure at high doses; whereas, at low doses, respiratory conditions can be treated. The venom of the Bungarus multicinctus has three different neurotoxic reactions, all of which produce a post-synaptic type of neuromuscular block. This bungaro toxin has a huge ability to inhibit choline uptake in the synaptic cleft, blocking the synthesis of acetylcholine which leads one to believe that it could be important in the homeopathic treatment of cholinergic diseases such as Alzheimer’s. The venom of different rattlesnakes contains a convulxin which induces convulsions in the intended victim. An example of a cardiotoxin comes from the Mohave rattlesnake venom. A compound known as Mohave is known to have dramatic cardiological effects. It is thought that this venom is also a phospholipase type of toxin. All types of Crotalus, especially the western diamond back rattlesnake, contain myocardial depressor proteins which suppress and produce a myocardial anesthesia or a myocardial depression in the animal. Some of the different rattlesnakes have a potent hypotensive peptide known as hypotensin which can dramatically reduce arterial pressure. Another interesting compound often found in snake venoms is that of NGF (nerve growth factor). NGF is an agent which regulates growth and differentiation of neurons in the sympathetic and in some cases sensory neural tissue. There are three principal characteristics of NGF: 1) the holofiber outgrowth from dorsal root or sympathetic ganglia; 2) the sympathetic ganglion enlargement in neonatal mice characterized by hyperplasia and hypertrophy; and 3) the immuno-sympathectomy, the destruction of sympathetic chain ganglia by the in vivo injection of anti- serum to NGF.

244

Snake Venoms Containing NGF

Viperidae Bothrops jararaca Bitis gabonica Crotalus adamanteus Echis carinatus Crotalus atrox Echis coloatus Crotalus horridus Vipera ammodytes Crotalus terrificus Vipera aspis Elapidae Vipera russellii Dendroaspis viridis Crotalidae Naja melanoleuca Agkistrodon piscivorus Naja naja Ancistrodon contortrix Naja nigrocollis lactocinctus Ancistrodon rhodostoma Sepedon haemachatus

Oftentimes, this nerve growth factor occurs in the cobra family. Cobra venom seems to contain the highest amount of NGF of all the snake venoms. The venom of the Black Mamba, Dendroaspiaspsis jamesoni, causes marked depolarization of membranes and inhibits the excitability of skeletal muscles. This can effect cardiac and respiratory function; whereas, the cobra venom is primarily neuro-toxic and causes degenerative tissue to form. The venom of the families of the viper and rattlesnake are primarily related to hemorrhages and coagulation disturbances. The enzyme effect of these different venoms can start lysis in red cells as well as other cells of the body. This is to prepare the intended victim for digestion. Cobra venom lowers the red blood cell count in victims, but this alone does not seem to produce lethal effects. The most powerful hemolytic snake is the Pseudechis papuans, also known as the Papuan black snake. People bitten by this snake often produce red or black urine which results from the breakup of red blood cells. The hemolysis effects are profoundly proteolytic, and this venom offers homeopathy some interesting challenges.

245 Venoms of the viper family are potent in their ability to digest different cells. In fat, small tears in the blood vessels can occur as a result of this venom. The action of the proteolytic enzyme in the venom can also produce necrosis. The venoms of the rattlesnake viper family can have strong necrotizing effects. Oftentimes necrosis is seen at the site of the bite in the human victims who survive these snake bites. The proteolytic effects kill cells homeopathically. It can restore life to necrotized areas, as in peripheral circulatory disease. Edema and swelling occur after many different snake bites because they start histamine cascades. A chart on some of the hemorrhagic and proteolytic effects of snake venom is shown below.

246 Distribution of Hemorrhagic, Lethal and Proteolytic Activities in Snake Venoms

(Ohsaka, A. et al., 1960)

Hemorrhagic Lethal Proteolytic LD50 Snake Venom activity activity activity / MHD(μg) LD50(μg) (units/mg) MHD

A. contortrix 1.90 200 33.7 105 contortrix A. contortrix mokasen 1.20 125 48.1 104 A. piscivorus 0.80 60.0 41.5 75 piscivorus A. halys 0.14 16.0 35.8 114 Bothrops atrox 2.11 5.6 44.5 2.7 Bothrops jararaca 0.75 18.5 74.0 25 C. adamanteus 0.04 18.5 9.76 462 C. atrox 0.43 45.0 83.6 105 C. durissus terrificus 18.0 3.6 39.2 0.2 C. viridis viridis 0.56 21.0 39.5 38 T. flavoviridis 0.20 54.0 33.0 270 T. flavoviridis 1.15 160 37.8 139 tokarensis T. elegans 0.30 71.0 13.0 237 T. okinavensis 1.38 140 69.0 102 Vipera russellii 21.0 2.2 5.56 0.1 Vipera ammodytes 0.47 7.4 41.7 16 Vipera palestinae 0.54 7.1 4.96 13 Cuasus rhombeatus 0.81 › 250 0.26 › 309 Bitis arietans 0.15 15.0 18.7 100 Bitis gabonica 0.04 13.5 11.7 338 Ophiophagus hannah 0.84 54.0 12.0 64 Bungarus fasciatus › 100a 18.5 0.06 ‹ 0.18 Naja melanoleuca 100 6.0 7.00 ‹ 0.06 Naja naja atra › 100a 8.0 0.12 ‹ 0.08 Naja naja 100 5.6 2.85 ‹ 0.06

Key: A: Agkistrodon C: Crotalus T: Trimeresurus

247

This type of histamine release is compounded by other toxins. Many rattlesnakes have strong histamine releasing proteins which help to complicate the involvement of their venoms. A list of the different venoms and their effect on histamine and serotonin content is shown below.

Effect of Venoms from Different Species of Snakes on the Histamine (H) and Serotonin (S) Content of Isolated Rabbit Platelets

(Markwardt, F. et al., 1966)

Venom Concentration Effect a Effect a

(μg/ml H S

Naja flava, N. haje 100 0 0

N. naja, N. n. oxiana N. nigricollis 100 ++ ++ Bungarus fasciatus 100 0 0

Dendroaspis viridis 100 0 0 Bitis arietans 100 0 0

Echis carinatus 100 0 0 Vipera ammodytes V. berus, V. russellii 100 0 0 Agkistrodon piscivorus 100 0 0 A. contortrix 100 + 0 Bothrops alternate 100 0 0 B. neuwiedii 100 0 0 B. cotiara, B. insularis 10 + 0

B. jararacussu 10 + + B. jararaca 10 ++ + Crotalus adamanteus

C. atrox, C. viridis 100 0 0 Lachesis muta Sistrurus catenatus ++ ++ 100 Crotalus horridus 10 ++ ++ C. durissus terrificus 10 + + ++ ++ C. durissus terrificus 1 C. durissus terrificus 0.1 + +

a 0 = no release: ++ = over 50% release: + = less than 50% release.

248 Another area to explore is the liberation of pharmacologically active substances by different snake venoms. Snake venoms can activate and release histamine, serotonin (five-hydroxytryptamine), and bradykinin. Some slow-reacting substances can be released such as prostaglandins and lysophosphatides, catecholamines such as adrenaline, chetosteroids, and finally, anaphylatoxin. Anaphylaxis can also be stimulated by certain venoms, or treated with dilute forms of same. Another dangerous fact about snake venoms is their nephrotoxicity. The kidney is affected in almost all types of snake bites. Venom can produce renal lesions including glomerulitis, glomeronephritis, arthritis, interstitial nephritis, tubular necrosis, cortical necrosis, and renal infarct. Renal failure is oftentimes the most common result, as well as hematuria, myoglobinuria, hemoglobinuria, and proteinuria. Probably the most frequently used remedy in homeopathy from snake venom is Lachesis. This venom comes from Lachesis trigonocephalous, a large South American snake from three to fourteen feet long. Its poisonous venom was first used by Dr. Constantine Hering of Philadelphia. The Lachesis is prepared at 6x and higher; proportions below 6x may be dangerously toxic. In its raw form this can produce a poisonous condition of the blood which causes hypersensitivity in the body. The patient usually reports that he cannot bear anything tight around the throat. This is known as a left-sided remedy, as it usually affects the left side in its raw form. There is a general aggravation of conditions after sleep which indicates Lachesis must be used. Blueness of the skin and eruptions can appear. Some of the other homeopathic indications are loquacity where the patient jumps from one subject to another; jealousy, fear of being poisoned, and sometimes the patient imagines that he is under some superhuman control. Headache over the left eye accompanying a cold, with the headache worsening in the heat of the sun might also indicate that Lachesis may be needed.

249 Facial erysipelas that first appear as red and then dark bluish or purplish, with more on the left side, can also indicate the need for Lachesis. Watery discharge from the left nostril, throbbing headache relieved when the discharge appears; dry tongue protruded with difficulty, cracked tongue at the tip which is brown on the dorsum, great difficulty in swallowing, high fever, exhaustion, a craving for oysters, horribly offensive diarrhea, ovarian trouble (often pain in the left ovary), menses which are scanty, feeble, black or offensive; and pain in the hips (bearing down on the left ovary, better when flow is established) are some of the conditions which can indicate that Lachesis is needed. Crotalus, the rattlesnake venom, is a classic homeopathic which Dr. Hering also wrote about. Its homeopathic indications are often a yellowness of the skin from disintegration of the blood and a tendency to hemorrhage. In yellow fever, crotalus is often indicated in the stage of black vomit when there is low delirium, yellow skin, and oozing of blood from every orifice. Naja is aother classic homeopathic venom found in the cobra Naja tripudians. It is often used in degenerative diseases as well as in valvular diseases of the heart, with a dry, teasing cough present. Another is the elaps, a type of Elaps corallinus. This is the coral snake venom which was first introduced homeopathically by Dr. Benoît Jules Mure of Brazil. Some initial homeopathic indications for elaps are: sniffles in children, stuffed up nose, and a great sense of coldness in the stomach from cold water. Another type of venom used in classical homeopathy is the Bufo rana, or the South American toad. Many South American toads have sweat that contains neurotoxins. These are noted to affect the sexual system, and Bufo rana has been used widely for sexual deviance and for many other types of cases as well. Bufo rana has been used to help encourage sexuality and to treat cases of frigidity. Its usual dose in those cases is 100x or above.

250 The Colorado River toad venom is known to cause epilepsy, as many of the different toad venoms do. Homeopathic treatment of epileptic conditions consists of different toad venoms. Sepia succus is an inky secretion released by the cuddle fish when it is pursued by its enemies. The cuddle fish releases it as a “dummy target,” allowing the cuddle fish to go unnoticed. This Sepia product has been widely used in homeopathy for many kinds of conditions. The five general characteristics of sepia are: 1) weakness, 2) yellow complexion, 3) bearing-down sensation, 4) violent motion that relieves the symptoms 5) the amelioration of symptoms at midday. The mental symptoms of sepia include weak memory, helplessness, susceptibility to excitement, susceptibility to terror, despair, fear of being alone (the person wants company desperately), and headaches (more common in the morning), increasing as the day goes by, relieved by sleep or violent motion. The patient who is sad and tearful with headache feels better in open air. Menstrual headache can also be noted. Blue Octopus venom produces blood disorders similar to leukemia. It is powerful homeopathically in the treatment of leukemia Many spider venoms are of value for homeopathic use. The tarantula venom, known as Tarantula hispaña, helps in cases of restlessness. The patient needing this will always be in constant motion, even though motion aggravates most of the symptoms. The person must be doing something all the time. This venom becomes very useful with patients who are hysterical. Tarantula cubensis relieves the atrocious pain that accompanies a sloughing carbuncle. Black Spider venom, also known as Mygale lasiodora, is used in chorea where there is twitching of the facial muscles, irregular convulsive movements of one side of the body, words are jerked out, and the movements cease during sleep but return more violently in the morning.

251 Theridion, spider venom from Theridion curassavicum or the orange spider is found in the West Indies. This venom can produce throbbing pains over the left eye which is aggravated in the heat of the sun. Noise aggravates it as well. This pain is associated with vertigo, and often times, nausea. It is worsened by closing the eyes, motion or jarring, or walking across the floor. There is extreme sensitivity to noise. This venom is very good for conditions of cardiac anxiety. The cross spider, known as Aranea diadema, is a large black spider of the central United States. Two particular symptoms directing one to aranea are numbness of the parts of the body supplied by the ulnar nerve, and boring, digging pain in the oscalcis. Black widow venom gives dramatic help for many neurological conditions, especially peripheral neuropathy. Scorpion venoms are powerful in homeopathy. They usually cause paralysis, pains and weakness, and can be used to reverse some of those same conditions. Even the venom from the ant can have homeopathic effects. Ant venom is very rich in formic acid, and this causes inflammation and irritation; thus, ant venom can help reverse such conditions. The venom of the honey bee, Apis mellifica, is highly important in homeopathy as it produces certain types of conditions. The characteristic symptoms of Apis are: 1) drowsiness, 2) edema, 3) thirst, 4) intolerance of heat, 5) stinging pains, 6) aggravation in the afternoon (between 4:00 and 6:00) and 7) bruised sensations. Meningitis can often be treated with Apis. Oftentimes the patient is fidgety, awkward, clumsy, and silly; laughs, drops things, and is often very jealous. Wasp venom can have very powerful implications in homeopathy, as can the Spanish fly or cantharis. With this brief review of venoms that nature offers, some intriguing protein compounds can be utilized. Many of these venoms follow the Arndt-Schultz principle and have reverse action in small, dilute

252 homeopathic forms, whereas many of these venoms can be utilized in low doses to accomplish other tasks. There are hundreds of thousands of insects, spiders, snakes, and animals that carry different venoms. These venoms have had dramatic potential in shaping medicine. They offer medicine profound techniques in treating the myriad of diseases found in the human being. This is another reason why it is such a tragedy to destroy our rain forests. Many of the people going to the rain forests are looking just for plants, herbs, and fungi that might be used in pharmaceuticals, not realizing that some of the most potent pharmacological acting agents in the rain forests come from the venoms of these different insects and animals which are becoming extinct. We must stop cutting down the rain forests and look in as many different places as we can to find ways to let nature heal. Nature can heal, and man can destroy. This short treatise has been only a brief introduction to some of the pharmacological ways that venoms can be used in homeopathy.

253

Summary of Immunopathology, Histopathology, and Electron-microscopic findings of the Kidney in Snakebite

Immunopathology Histopathology Electron-microscopy Location of deposits

Type of Glomerular Arteriolar Arterial Proliferation Tubular Necrotizing Thrombophlebitis Glomerular Glomerular Tubular capillary wall wall of glomerular necrosis and arteritis electron- basement degeneration, Snake mesangial regeneration dense membrane necrosis and cells deposits alteration regeneration Russell’s 1gM C3(=) C3(+) + ++ + + + - + viper (+ to ++) C3(=) Green 1gM (trace to C3(=) No + to ++ + - + +b - + +) deposit pit viper C3(=) Fibrin a Cobra 1gM (+) C3 (=) No + - - - + + - C3 deposit (+ to ++)

- = Negative + = Mild ++ = Moderate a = Focal deposition b = With deposition of fibrin

255 Renal Failure with Known Lesions in Various Snakebites

Snake Renal Lesion

Crotalus terrificus Tubular necrosis

Cryptophis nigrescens Tubular necrosis

Sea snake Tubular necrosis

Russell’s viper Tubular necrosis Echis carinatus Cortical necrosis

Borthrops jararaca Cortical necrosis Agkistrodon hypnale Cortical necrosis

Bitis arietans Proliferative glomerulonephritis

Cases with renal failure without known snake or renal lesions are not included.

255 Bibliography

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Angeletti RH. Studies on the nerve growth factor (NGF) from snake venom molecular heterogeneity. J Chromatogr 1968b; 37 (1):62-9.

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258 GEMMOTHERAPY

Gemmotherapy consists of making herbal remedies from the buds or shoots of young plants. These remedies cleanse cells of toxins through digestion, urinary tract, lung, and skin. Some of the remedies can be found below.

Abies Pectinata: Decalcification and rickets, dental caries Acer Campestres: Sequelly of poliomyelitis and paralysis, Herpes Zoster Aesculus Hippocastanum: Hemorrhoids Alnus Glutinosa: Sequelly of cerebral hemorrhage, cerebral infarction, chronic rhinitis Alnus Incana: Arthritis Ampelopsis Weitchii: Chronic rheumatism, rheumatoid arthritis Betula Pubescens: Intellectual overwork, psych-asthenia Carpinus Betulus: Spasmodic and chronic rhino-pharyngitis, spasmodic cough Castanea Vesca: Venous congestion Cedrus Libani: Dry eczema, ichthyosis, pruritus Cercis Siliquastrum: Improves arterial circulation Citrus Limonum: In the presence of an increase in blood fibrinogen levels Cornus Sanguinea: Enhanced coagulation Corylus Avellana: Emphysema and pulmonary fibrosis Crataegus Oxyacantha: Cardiac insufficiency, precordial pain, tachycardia, sequelly of infarction Fagus Sylavaatica: Renal insufficiency, renal lithiasis Ficus Carica: Obsessional and anxiety neurosis, gastric and peptic ulcers Fraxinum Excelsior: Acute and chronic gout Ilex Aquifolium: Gout or urethema

259

GEMMOTHERAPY, cont.

Juglans Regia: Varicose ulcers, skin infections (impetigo, infected eczema) Juniperus Communis: Major hepatic insufficiency and cirrhotic syndromes Olea Europaea: Hypertension, arteriosclerosis, hypercholesterolemia Pinus Montana: Chronic rheumatism, vertebral osteoarthrosis, osteroarthrosis of the hips and knees Platanus Orientalis: Urticaria with accompanying inflammation, itching, and discomfort Pulus Nigra: Obliterative arterial disease of the lower limbs and associated trophic disturbances Prunus Amygdalus: Vascular sclerosis, hypertension Quercus Pedonculata: Increases the bodily defense mechanisms Ribes Nigrum: Allergic problems, chronic coryza, hay fever, migraine Rosa Canina: Migraine and headache Rosmarinus Officinalis: Hepatic insufficiency, biliary colic, biliary dyskinesia Rubus Fructicosus: Female problems, menstrual disturbances, pelvic pain, metritis and vaginitis Secale Cereale: Hepatic insufficiency Sequoia Gigantea: Prostatic hypertrophy and adenoma, uterine fibroids Sorbus Domestica: Venous problems, sequelly of phlebitis, haemogliasis Syringa Vulgaris: Arterial sclerosis or improved arterial circulation Tamaris Gallica: Various types of hypercholesterolemia Tilia Tomentosa: Nerve sedative, tranquilizer, insomnia, neuralgia Ulmus Campestris: Weeping eczema, acne and impetigo

260 GEMMOTHERAPY, cont.

Vaccinium Vitis: Intestinal syndromes, chronic E. coli infections Viburnum Lantana: Simple and complicated asthma Vitus Vinifera: Bone metabolism and inhibits proliferative deformities such as osteophytes Zea Mais: Favors post infarction healing of cardiac tissue and produces a fall in blood transaminase levels Source: http://homeoinfo.com/08_non- classical_topics/is_it_homeopathy/gemmotherapy.php

261 CLASSICAL HAHNEMANIAN SINGULARS

Acetonum Cactus Grande Acetyl Choline Chloride Caulophyllum Acid Cic-Aconite Cell Salts (All) Acid Citricum Chamomilla Acid Fumaricum Cehlidonium Acid Glutaminicum Chlorcamphor Menthol Acid Malic Chlormphenicol Acid Pyruvicum Chloroformium Acid Succinicum Chlortetracycline Adipinic Acid Cholesterinum Allergy Malus Chromium Oxide Aloe Cina Alpha-Ketoglutaaric Acid Cinchona Alumina Congo Red Ammonium Carb. Cortisone Ammonium Phos. Crataegus Anacardium Cysteinum Apis Mel. Cystinum Arnica Digitalis Arsenicum Alb. Dimethyl terephthalate Bar. Oxalsusccinicum Diphenylamine Belladonna Diphenylhydantoin Bentonite Di-Sodium Phosphate Benzinum Crudum DNA Benzpyrene Echinacea Berberis Estradiolbenzoate Bilirubinum Ethylene Glycol Bryonia Ethylene Oxide Bufo Rana Evening Primrose Butter Yellow Formaldehyde Dehydrogenase Calendula Formaldehyde Sol. Cantharis Formic Acid Caprolactam Fumaria Caprylic Acid Fucus Vesiculosus Capsicum Germanium Carbo An. Glutaminum Carbo Veg. Glycerinum Carboneum Tetrachloratum Glycocollum Cardus Mar. Glycogen Carrageenan (Type 1, Glyoxal Lycopodium) Graphites Carrageenan (Type 5, Hamamelis Virginica Lycopodium) Harnsaure (Acid. Uric)

262 Classical Hahnemanian Singulars, cont.

Hepa Sulph. Petroleum Hexamethylentetramin Phenacetinum Hirudinum Phenylalanine Histidinum Phosphorous Hyaluronidase Phytolacca Hydrangea Plasma (Horse) Prophlthiouracil Hypoxanthinum Pulsatilla Ignatia Rauwolfia Indican Rhus Tox. Indolum Ruta Grav. Insulinum Sepia Interferon Serotonin Ipeca Silicae (Equisetum) Iris Versicolor SolidagoSpigelia Isoniazide Spongia Isotonic Plasma Staphisagria Jodoformium Sulfanilamidum Juglans Sulfur Kali Carb. Superheated Vegetable Fat Kreatinum Tetracycline Lachesis Thioacetamid Lithium Nitrate Thuj Lycopodium Tryptophanum Macrodantin Ubiquinone Mag Phos. Urea Mercurius Urtica Methylethylketon Vaccinnum Naja Viscum Album (Gr. on Abies Natrum Muriaticum Alba) Natrum Sulph. Viscum Album (Gr. on Acer Nux Vomica Camp.) Oleander Viscum Album (Gr. on Populus) Paraffinum Viscum Album (All) Penicillinum Vitamin D Peptonum

263 A NEW PERSPECTIVE ON RESEARCH

In 1991, U.S. News and World Report published a series of articles about alternatives to medical techniques, and how they are getting more and more attention by doctors throughout America. More doctors were turning to alternative techniques in light of the inability to get lasting results via synthetic allopathy and surgical intervention. As the populace starts to look for more natural techniques with fewer side effects, alternative medicine practitioners have been developing natural types of therapies, and improving their skills with these natural modalities. This underground medical group has developed some wonderful techniques to deal with a wide variety of medical problems. It is important to note that every field of endeavor in society will have evolution in its thought and philosophies. There can be no eternal stagnation in the philosophy or psychology of any group. Through the years medical philosophy has created many different foundations which have yielded over time. Medicine started with very natural philosophies and became more statistical and analytical after the development of statistics by Poincare. Synthetic chemistry came along and offered its processes, and the dramatic amount of profitability which could be incurred from patenting such items further helped to develop the synthetic cause, thus leading to an allopathic philosophy primarily based on synthetic chemistry and surgical intervention. This is the basic mind set which has developed in medicine over the last fifty years and which is now starting to yield to other fields of endeavor. Some of them are electronics, physics, energetics, naturopathy, and homeopathy. There is a new psychology of medicine which will develop over the next five to ten years, and will have a softer philosophy, making up for some of the mistakes made in the past due to synthetic allopathy. As we observe this process of the psychological evolution in medical philosophy, it is important to note that it parallels the psychological

264 evolution of the minds of men. This chapter is dedicated to a new concept of medical psychology and philosophy. The opponents of this development will try to cling to old style ideations, and they will also secure themselves in the arrogant, obstinate stance of being judgmental. This attitude might stop them from reading and getting the benefits that this treatise has to offer. We hope that they can soften their hearts and minds to allow a new psychology and philosophy to develop freely. In this U.S. News and World Report article, several different modalities were addressed: acupuncture, biofeedback, homeopathy, nutrition, naturopathy and others. Please see full-text article below.

BIG CLAIMS, NO PROOF

A look at farther-out cures, from aromas to reflexology

Mainstream doctors may wonder why anyone with heart disease would take herbs instead of a beta blocker. Yet the claims for alternative healing are intriguing, if largely unproven. Here's a guide to six treatments.

HOMEOPATHY

WHAT IT IS. A medical system based on the teachings of Samuel Hahnemann, a German doctor who in the 1800s believed that symptoms such as fevers should not be suppressed because they represent the body's efforts to repel disease.

THE CLAIM. Diseases can be cured only by using drugs that echo the symptoms. A feverish person, for example, would be given a drug that would raise body temperature. And the drugs should be administered in doses so diluted they are practically undetectable.

THE EVIDENCE. An analysis of 105 controlled though sometimes poorly executed studies published worldwide found ''positive'' results for homeopathy treatments in 81 trials, according to a report in last February's British Medical Journal. The results provide a basis for continued research, the authors conclude -- with better- done trials.

265 HERBALISM

WHAT IT IS. An ancient system of medicine in which preparations of leaves, stems, seeds and roots are consumed or rubbed on the body.

THE CLAIM. Herbal remedies contain natural ingredients as potent as synthetic drugs but often safer.

THE EVIDENCE. Plant extracts can indeed be valuable; researchers constantly seek out new possibilities. May's Proceedings of the Society for Experimental Biology and Medicine, for example, reports that Andrographis paniculata, an herb used in China to cure hepatitis, dysentery and meningitis, also hampers reproduction in lab tests of the human immunodeficiency virus, which causes AIDS. But a report in Allergy last year found that herbal treatments for rashes made symptoms worse.

NATUROPATHY

WHAT IT IS. A therapy dating to 19th-century Germany that relies on air, sunshine, water, heat, massage and herbs to cure both the body and the mind.

THE CLAIM. Illnesses from colds to typhoid can be cured by purging the body of poisons, accomplished through fasting, salt-water baths, breathing and relaxation exercises -- even psychotherapy.

THE EVIDENCE. Few controlled trials have produced conclusive results.

AROMATHERAPY

WHAT IT IS. An ancient Chinese form of herbal medicine that seeks to cure illnesses with the aromatic oils of plants.

THE CLAIM. Plant essences are massaged into the skin, used as bath oils, inhaled and, in very rare cases, even ingested.

THE EVIDENCE. Scents can indeed evoke strong emotions. Recent studies also show that certain scents, like peppermint, can increase workers' productivity and

266 vanilla's aroma can be relaxing. But whether scents can cure diseases like gastrointestinal disorders, as is claimed, is as yet unproven.

MAHARISHI AYUR-VEDA

WHAT IT IS. A form of natural healing based on ancient Indian texts recently translated for Westerners by Maharishi Mahesh Yogi, who introduced the world to transcendental meditation.

THE CLAIM. All illness results from ''imbalances'' in such functions as respiration, circulation and metabolism and can be treated through meditation, massage and herbal medicines.

THE EVIDENCE. In May, the Journal of the American Medical Association ran a three-page letter -- not a study -- from proponents citing positive findings from a range of investigations. One U.S. study found that so- called Ayurvedic herbal compounds reduced the incidence of breast cancers in ''up to 88 percent'' of experimental animals. It will take many solid studies to make doctors overlook Ayur-Veda's mystical precepts.

REFLEXOLOGY

WHAT IT IS. A massage technique that attempts to treat diseases and keep the ''life force'' in balance. Its origins can be traced to ancient China.

THE CLAIM. Areas on the soles and sides of the feet govern ''energy channels'' that extend throughout the body. By massaging specific spots on the foot, a reflexologist can sense and unblock clogged channels.

THE EVIDENCE. No controlled clinical trials are described in medical journals.

Reference

Podolsky, Doug. U.S. News & World Report. Big Claims, No Proof. 23 September 1991. Vol. 111, Issue 13, p77.

267 The critique of homeopathy was that there were not enough apparent clinical trials. It is the purpose of this article to question the very foundation of clinical trials as the end all deciding factor in whether procedure or medical belief is acceptable or worthwhile in medicine. The factor of clinical trials means that once an item or drug is chosen it can be put to a clinical test in the patient population to see if it really does that for which it was originally designed. To do a clinical trial, a randomly selected group of patients, possessing whatever traits we would be looking for (such as diabetes, high blood pressure, or any other type of medical illness) would be selected. Then, a controlled population or group is selected. We now give the substance, the therapy, to a certain number, known as the “effect group”, and the control group would get a placebo, or some other type of comparative therapy regime. We now do a statistical manipulation at the end of this study, whatever time line it might be, to see if the purported remedy would work better than placebo in the study. Comparative statistics would be used to evaluate whether the substance performed well versus the placebo or control group. This is an over-simplification of a statistical clinical trial. The purpose and the basis of our study is to challenge the Null hypothesis. The Null hypothesis: the two groups which are being statistically challenged will be equivalent, and will not show any difference. If the Null hypothesis is disproved, and the two groups are different, then we can assume that there is statistical evidence that one group outperforms the other by some criteria. The problem with modern medical statistical analysis is that if the two groups are proved equal, and the Null hypothesis is not disproved, then the assumption is that the two therapies are equivalent. This is not what the Null hypothesis states, as it was originally set up for analysis. The true conclusion is that the groups differed, but the difference in the two groups could not be detected by the limitations of our measurements.

268 Thus, in determining that synthetic vitamins are equivalent to natural vitamins in the statistical studies we must clarify that the Null hypothesis does not state that the two groups are equivalent; just that the sophistication of our measurement skills is not sufficient to measure the difference. This is the true conclusion which can be achieved from the Null hypothesis. But oftentimes in science the Null hypothesis is abused as in assuming that two groups are equivalent, when actually there might be a problem with accuracy skills. As we have pointed out, reductionism is often a problem in science, not the solution. In doing these types of studies we see the errors of reductionism at their finest.

269 PROBLEMS WITH CLINICAL TRIALS

¾ Reductionism. Reducing the complex patient to simple measurements. This makes attained information suspect and weak. Medicine becomes cold, impersonal, and statistical. Compassion cannot be reflected by statistics.

¾ Never long enough. Effects of a synthetic medication can result in genetic damage generations later.

¾ Overconfidence and misinterpretation of the Null hypothesis. If a study of natural vs. synthetic vitamins shows no difference in results, it does not occur to researchers that they or their ability to measure could be in error.

¾ Most always benefits the one who can afford to fund the study. Experimenter effect.

¾ Trials will always reward and reinforce the philosophy of those performing them. Allopathy is preferred; homeopathy and naturopathy are ignored.

¾ Quantity does not dispel quantity. Publish or perish rule pushes paper out of educational institutions which just perpetuates the allopathic delusion.

¾ Inability to accept the truth that allopathy is hurting patients in vast numbers. Iatrogenic malpractice suits resulting from synthetic drugs top fifteen billion dollars a year. We must realize that our clinical trial process is a failure, and replace it.

These errors of reductionism result in errors of decision-making within the medical establishment. As we take these individuals with rampant, variant problems, different conditions of liver function, kidney function, skin conditions, ethnic backgrounds, and the like, we then take these populations and reduce them to one type of criteria. We reduce the complexity of their human diversity to a simple variable of blood pressure, hormone level in the blood, range of motion, or whatever type of statistical measurement technique we use.

270 There are possibly millions, if not millions of millions of variables which can be measured in the human body. The body is vastly complex. No known study has ever measured all of the variables possible to achieve a total analysis. Every known study has been reductionistic in some way. It is necessary to realize the inadequacy of statistical information, and not revere them or put them on the pedestal created by modern science.

SOLUTIONS TO CLINICAL TRIAL PROTOCOLS

¾ Realization of the inadequacy of any clinical trial to give perfect conclusions. Incorporate compassion, education, and love back into medicine.

¾ Nature has designed chemicals and complex compounds such as herbs and glandulars for millions and millions of years. Naturopathy comes with its own long-term background study.

¾ Realize that the Null hypothesis only says that this study showed, not proved, no effect.

¾ Reduce restrictions on orphan drug funding and encourage more natural drug testing by reducing philosophical criticisms.

¾ Broaden our philosophy of medicine to revere the natural process and acknowledge the unknown in biology.

¾ Give equal funding to studies on homeopathy and naturopathy at educational institutions.

¾ Broaden our medical philosophy to include quantum theory, energetics, homeopathy and naturopathy. Teach doctors that there is a safer and more compassionate way to do medicine. “First don’t hurt” must be brought back into medicine. Clinical trials should only be a small part of medical consideration, and not deified.

As has been stated several times, the concept of reductionism is the fallacy, the error of science. Not that reductionism is totally bad; it must be a part of our decision-making process. But to make it the only part, the pinnacle, the demigod of medicine, is where the error lies. Using

271 reductionistic studies to shape medical protocol has resulted in a medical establishment which is about to collapse under the weight of iatrogenic diseases and malpractice payments. In science, the Null hypothesis is often talked about, meaning that we try to prove an experiment with the Null hypothesis. As an example, our hypothesis might be that digitalis can help heart patients. The Null hypothesis is that digitalis does nothing, and actually is no different from a placebo. To test our Null hypothesis we work up a random-sample group, wherein two populations will receive different treatments. One will get digitalis and one will get a placebo. If both groups experience equal results, then the Null hypothesis is proven; there is no difference between the groups or the interventions. This basic assumption is incorrect in the true management of science. In the true management of experimental science and statistical management we will find that all that we know from this study is that the study could not prove any difference between these two materials. It is wrong to assume that the two materials are the same just because this study did not prove them to be different. In 1982, the Journal of the American Medical Association published an article about hyperactive children. (Consensus Conf: Defined diets and childhood hyperactivity. JAMA 1982; 248(3)290-292.) One group was given lemonade made with a processed white sugar and the other was given lemonade made with saccharin. It was found that there was no basic difference between the two groups, and that the Null hypothesis was achieved. Many of the medical doctors who reported on this study and who were quoted on Lifetime Medical Network said that from this study they could conclude that there were no problems regarding hyperactivity generated by sugar. That was an irregular conclusion. The actual conclusion is that there is no difference between saccharin and processed sugar, but the study did not involve any natural sugars or fruit sweeteners.

272 Just because the study tells us that there are no differences does not mean that differences do not exist. One such example of bad science has happened over the last fifty years: during this time scientists have found from their studies that there is no difference between natural and synthetic compounds. Thus, a natural vitamin was found to have the same effect as a synthetic in that the two did not prove different in studies performed. These studies were reductionistic and flawed. Just because their studies could not find any difference does not mean that there were no differences. The basic misuse of the Null hypothesis has generated a tremendous income for synthetic pharmaceutical companies who develop synthetic compounds by the train-car load. Studies that do show differences between the natural and synthetic compounds are quickly discounted by the chemical companies. This brings us to a political ideation of who can make a true judgment on the correctness of a study, and oftentimes the philosophy of the judge will affect his decision. In America, it is complicated by the issue of freedom of choice. If a person truly wishes to have natural entities, and only natural entities put into his/her body, this is his/her choice. These natural compounds are dispensed under the same guidance of the Food and Drug Administration to guarantee safety and efficacy. Yet, synthetic chemical companies wish to inhibit the choice of the population and force on it synthetic compounds. Many drugs get through clinical trials and later are found to cause sickness in the patient population. Every year, ten to twenty medications, on the average, are taken off the shelves of pharmacists because the clinical trials were not thorough enough in finding out some of the different problems. Prozac was released into the medical system, and now much evidence is pointing to the fact that people taking Prozac

273 might develop unstable thinking. Prozac might possibly even contribute to provoking a user to kill other people in fits of anger. Thalidomide was made available after clinical trials proved its success in handling morning sickness. But thalidomide produced babies born with flipper like appendages, and other gross genetic defects. One of my professors remarked at that time that it was a “blessing” that thalidomide caused these deformed flippers and great aberrant dysfunctions of genetic material. I inquired what he meant by “blessing.” He said that the blessing was that it was a violent enough reaction that it got taken off the market quickly. What if the effect of thalidomide was that it just lowered one’s I.Q. five or ten points? We might not have discovered that until several generations later. Thalidomide was taken off the market, altered, and released back on the market as Benedictine. Benedictine had just that effect, it lowered the IQ ten points, and was later taken off the market in the late 1980s because of its ability to alter genetic functioning and cause a wide variety of learning disabilities and other disturbances. The thalidomide problems were horrible, but were not pervasive throughout the population. The Benedictine problems were much less horrible, but were much more pervasive, as it affected literally millions of children in America. The following is a list of drugs that were taken off the market after it was found that their original clinical trials were not thorough enough to indicate some of the problems with them. Perhaps this list will convince the reader that clinical trials are not sufficient to protect the public.

274 Acetazolamide Acetyldigitoxin Alkavervir Allopurinol Alseroxylon Aminophylline Aminosalicylate Sodium Amitriptyline Hydrochloride Amodiaquine Hydrochloride Ampicillin/Ampicillin Trihydrate Anileridine Hydrochloride Anisotropine Methylbromide Atropine Sulfate Azathioprine Bacampicillin Hydrochloride Bendroflumethiazide Benzthiazide Benztropine Mesylate Betazole Hydrochloride Bethanechol Chloride Bretylium Tosylate Bromodiphenhydramine Hydrochloride Brompheniramine Maleate Butabarbital Sodium Calcium; Meglumine; Metrizoic Acid Calcium Metrizoate Captopril Carphenazine Maleate Carprofen Cefadroxil Cephalexin Cephradine Ceruletide Diethylamine Chlophedianol Hydrochloride Chloramphenicol Chloramphenicol; Polymyxin B Sulfate Chloramphenicol; Prednisolone Chlordiazepoxide Hydrochloride Chlorhexidine Bluconate Chlormerodrin, HG-197 Chloroquine Phosphate Chloroquine Phosphate; Primaquine phosphate Chlorothiazide Chlorpheniramine Maleate Chlorphentermine Hydrochloride Chlorpromazine Hydrochloride

275 Chlorpropamide Chlorthalidone Chlorzoxazone Chymopapain Cisplatin Clindamycin Hydrochloride Clorazepate Dipotassium Codeine Phosphate; *Multiple* Colchicine; probenecid Cortisone Acetate Cryptenamine Acetates Cryptenamine Tannates Cyclobenzaprine Hydrochloride Cyclothiazide Cycrimine Hydrochloride Cyproheptadine Hydrochloride Cysteine Hydrochloride Decamethonium Bromide Demeclocycline Hydrochloride Deserpidine Desoximetasone Desoxycorticosterone Acetate Dexamethasone Dexamethasone Sodium Phosphate Dexbrompheniramine Maleate Dexbrompheniramine Maleate; Pseudoephedrine Sulfate Dextroamphetamine Sulfate Diatrizoate Meglumine Diazepam Diazoxide Dibucaines Hydrochloride Dicloxacillin Sodium Dicumarol Diethylpropion Hydrochloride Diethylstilbestrol Difenoxin Hydrochloride: *Multiple* Diflorasone Diacetate Digitoxin Digoxin Dihydroergotamine Mesylate; Heparin Sodium; Licocaine Hydrochloride Dimenhydrinate Dinoprost Tromethamine Diphemanil Methylsulfate Diphenhydramine Hydrochloride Disulfiram

276 Dopamine Hydrochloride Doxepin Hydrochloride Doxyclycine Hyclate Dromostanolone Propionate Dydrogesterone Dyphylline Epinephrine; Etidocaine Hydrochloride Epinephrine; Lidocaine Hydrochloride Ergocalciferol Ergoloid Mesylates Erythromycin Estradiol Valerate; Testosterone Enanthate Estrogens, Conjugated Estrogens, Esterified Estrone Ethchlorvynol Ethinyl Estradiol Ethinyl Estradiol; Norethindrone Ethoxzolamide Ethylestrenol Ethynodiol Diacetate; Mestranol Etidocaine Hydrochloride Ferrous Citrate, FE-59 Fluocinolone Acetonide Fluorometholone Fluphenazine Hydrochloride Fluprednisolone Folic Acid 1 mg Gallium Citrate, GA-67 Gemfibrozil Blutethimide Glycopyrrolate Gonadorelin Hydrochloride Gonadotropin Chorionic Guanabenz Acetate Halcinonide Haloperidol Heparin Sodium Hetacillin Hetacillin Potassium Hexachlorophene Hexocyclium Methysulfate Hexylcaine Hydrochloride

277 Homatropine Methylbromide Hydralazine Hydrochloride Hydrochlorothiazide Hydrochlorothiazide; Labetalol Hydrochloride Hydrochlorothiazide; Methyldopa Hydrochlorothiazide; Pindolol Hydrochlorothiazide; Reserpine Hydrochlorothiazide; Spironolactone Hydrochlorothiazide; Triamterene Hydrocodone Bitartrate; *Multiple* Hydroflumethiazide Hydroxocobalamin Hydroxystilbamidine Isethionate Hydroxyzine Hydrochloride Hydroxyzine Pamoate Ifosfamide Imipramine Hydrochloride Indocyanine Green Indomethacin Insulin Suspisophane Purified Pork Insulin Susp Protamine Zinc Purified Pork Insulin Zinc Susp, Extended Biosynthetic Human Iodipamide Sodium Iodoxamate Meglumine Isoetharine Hydrochloride Isoniazid Isoproterenol Hydrochloride Isoproterenol Sulfate Isosorbide Dinitrate Lactulose Levallorphan Tartrate Levodopa Levopropoxyphene Napsylate, Anhydrous Lidocaine Hydrochloride; Oxytetracycline Liothyronine Sodium Liotrix (T4; T3) Lithium Carbonate Loperamide Hydrochloride Loxapine Succinate Mannitol Mazindol Mebutamate

278 Meclizine Hydrochloride Meclofenamate Sodium Mefenamic Acid Mefloquine Hydrochloride Menadiol Sodium Diphosphate Menadione Mepenzolate Bromide Meperidine Hydrochloride Meprednisone Meprobamate Mestranol; Norethindrone Mestranol; Norethynodrel Metharbital Methicillin Sodium Methixene Hydrochloride Methocarbamol Methotrexate Sodium Methoxsalen Methyclothiazide Methylprednisolone Methylprednisolone; Neomycin Sulfate Methyltestosterone Methyprylon Metoclopramide Hydrochloride Metrizamide Minocycline Hydrochloride Minoxidil Molindone Hydrochloride Naloxone hydrochloride Netilmicin Sulfate Niacin 500 mg. Nitrofurantoin Nitrofurantoin Sodium Nystatin 500,000 IU. Orphenadrine Citrate Oxandrolone Oxazepam Oxybutynin Chloride Oxyphenbutazone Oxyphenonium Bromide Oxytetracycline Hydrochloride Oxytocin Paramethadione Pargyline Hydrochloride Paramomycin Sulfate Penbutololl Sulfate

279 Penicillin G Benzathine Penicillin G Potassium Penicillin G Procaine Penicillin G Sodium Penicillin V Potassium Pentazocine hydrochloride Pentobarbital Sodium Pentolinium Tartrate Perphenazine Phendimetrazine Tartrate Phenindoine Phenmetrazine Hydrochloride Phenprocoumon Phentermine Hydrochloride Phentermine Resin Complex Phenyl Aminosalicylate Phenylpropanolamine Hydrochloride; *Multiple* Phenytoin Sodium Phytonadione Piperacetazine Piperazine Citrate Pipobroman Potassium Aminosalicylate Potassium Chloride Pralidoxime Chloride Prednisolone Prednisolone Acetate Prednisolone Sodium Phosphate Prednisone Prilocaine Hydrochloride Procainamide hydrochloride Procaine Hydrochloride Procaine Merethoxylline; Theophylline Prochlorperazine Edisylate Prochlorperazine Maleate Progesterone Promazine Hydrochloride Promethazine Hydrochloride Propantheline Bromide Propoxyphene Hydrochloride Propoxyphene Hydrochloride; *Multiple* Propranolol Hydrochloride Propyliodone Propylthiouracil Protamine Sulfate Pseudoephedrine Hydrochloride

280 Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride Pyridoxine Hydrochloride Pyrvinium Pamoate Quinestrol Quinidine Gluconate Quinidine Sulfate Rescinnamine Reserpine Saralsin Acetate Secobarbital Sodium Selenomethionine, SE-75 Sodium Iodide, I-123 Sodium Iodide, I-131 Sodium Monofluorophosphate Sodium Succinate Somatropin, Biosynthetic Streptomycin Sulfate Succinylcholine Chloride Sulfabenzamide; Sulfacetamide; Sulfathiazole Sulfadiazine Sulfameter Sulfamethizole Sulfamethoxazole Sulfaphenazole Sulfasalazine Sulfinpyrazone Sulfisoxazole Diolamine Sulfoxone Sodium Suprofen Technetium TC-99M Albumin Aggregated Technetium TC-99M Sodium Pertechnetate Temazepam Testolactone Testosterone Propionate Tetracycline Hydrochloride Thalidamide Theophylline Thioridazine Hydrochloride Thyroglobulin Timolol Maleate Tioconazole Tolazamide Tolbutamide Trazodone Hydrochloride Triamcinolone Acetonide

281 Triazolam Trichlormethiazide Triclofos Sodium Tridihexethyl Chloride Triflupromazine Hydrochloride Trihexyphenidyl Hydrochloride Trimeprazine Tartrate Trimethoprum Trimipramine Maleate Tripelennamine Hydrochloride Triprolidine Hydrochloride Trisulfapyrimidines Troleandomycin Ursodiol Verapamil Hydrochloride Veratrum Viride Vinblastine Sulfate Fincristine Sulfate Viomycin Sulfate Warfarin Potassium Warfarin Sodium Xenon, XE-133

Some forms of these compounds were restricted after clinical trails showed them to be safe. There has been tremendous iatrogenic (doctor- induced) damage done to the people of the United States. Clinical drug trials are not at fault here, but the medical establishment’s worshipping of these clinical drug trials are. Every drug on this list went through the same clinical trials that the medical establishment uses as its criteria. This decision-making process of taking clinical trials and making them the demigod of the industry is at fault. People are being hurt because of faulty logic in medicine. These trials are expensive and can be purchased by rich patent-seeking synthetic chemical companies. This author realizes that challenging the establishment’s heart will not be taken lightly, and will not be without violent attacks. If the legal damages that have been incurred by these iatrogenic compounds are looked at, it is possible to see that there are literally billions of dollars every year paid out by drug companies in medical

282 malpractice and iatrogenic damage suits. The vast amount of damage caused by this industry is incredible; an industry which takes in approximately one hundred billion dollars of income pays out literally ten to twenty billion dollars a year in malpractice settlements. This still leaves an eighty billion dollar profit margin in an industry which spends very little in actual product manufacturing. The largest amount of expenditure by any drug company is that of research, development, and clinical trials of laboratory studies. It is this very research and development of the whole cognitive plan of allopathic medication that is being challenged. The allopathic medication philosophy is one that works against the body, or develops a compound to sedate a symptom. If the person has a histamine response, an antihistamine is given; if the person has depression, an MAO inhibitor may be given. In every case of allopathic utilization, it is assumed that the body’s function is irregular and foolish, and some type of synthetic irregularity which can upset the cybernetic balancing system of the body develops. The legal issues of medical practice are also stacked against alternative practitioners. In 1990, of the 570,000 doctors in the United States, 1,437 were put on probation, or had their licenses suspended or revoked. That represents .3% of the doctor population. In 1989, there were 1,500, and 9 practitioners who were likewise reprimanded. Very few of these practitioners were actually prosecuted for unprofessional conduct by aligning themselves with alternative practices. The majority of these medical doctors were dealt with because of alcohol abuse, drug abuse, and sexual abuse of patients; some of them for allopathic malpractice. Very few of them were actually dealt with because of alternative theories. In most states, a medical doctor is bound to perform therapies and diagnostic techniques which are medically accepted. In 1990, the Alaska State Medical Board “may not base a finding of professional incompetence solely on the basis that a licensee’s practice is

283 unconventional or experimental in the absence of demonstrable physical harm to the patient.” Source: www.healthy.net/public/legal- lg/regulations/MPA.HTM) If the doctor is not hurting anybody with an experimental or unconventional technique, he/she would not have his license revoked. Strong evidence would have to be found that the patient had been harmed in order to challenge the doctor. Many of these so-called unconventional therapies are accepted by a vast majority of doctors, and there is no one form of medicine that is accepted above all others. Medicine abounds with many techniques that are not fully, scientifically evaluated or properly challenged. Oftentimes, doctors who use these unconventional techniques are challenged by traditional medical doctors on the basis of only one or two cases. Many doctors have had their practices disrupted because of one or two cases where unconventional therapy did not quite abate the patient’s complaint. Doctors see patients dying every day. Hospitals abound with patients whose therapies and diagnostic accuracy have led to their demise. Robert S. Mendelsohn, in his book, Confessions of a Medical Heretic, (Chicago: Contemporary Books. 1979), wrote that when the doctors in a group of hospitals in a certain local community went on strike, there was a major change in the death rate – it dropped dramatically. Fewer people died when doctors stopped practicing some accepted medical techniques. In another case in Denver, Colorado, the state charged parents for not using traditional medicine when their child died from a disease that was assumed to be treatable at a local hospital. The parent was a Christian Scientist who believed more in prayer than in drugs. If the ratio of children who survive with Christian Scientist parents vs. the ratio of children who survive overall in hospitals is looked at, there is a tremendous degree of variance. Children died at a greater rate in hospitals than they did from having Christian Scientist parents. In the world today, The United States is fifteenth overall in birth mortality,

284 meaning that there are fourteen countries where newborns have a better chance of survival than in the United States. These countries are those that depend more on natural medicine, homeopathy, and prevention techniques. Perhaps these types of analyses can open up the closed minds of the so-called traditional statisticians to realize that perhaps there is an alternative. Legal judgments can be based on incomplete scientific ideas. It must be accepted that the science of medicine is a pseudo-science; it is not an exact philosophy. With this in mind, we should be slow to write laws that prohibit or discourage different philosophies of medicine. Practitioners and patients have the right to make choices. Medical boards and peer groups are not needed to challenge practitioners who try to take philosophies and practices and push them into areas where they do not have strong scientific validity. The laws of each state for the practice of medicine are vital, and medical board inquiries are essential in developing better and better qualities of medicine. Yet in the proof that a doctor is doing something wrong with unconventional techniques, as in the case of Warren Levin, who was challenged because of two separate instances, it should become quickly apparent that one should not jump to conclusions on one or two cases of impropriety. No doctor in the land could withstand such a shifted bias. Whereas one or two cases out of the thousands seen over a ten-year period should put a person’s practice on the line. Statistics must be looked at as well, and looked at for a certain percentage, wherein a doctor might be brought out in front of a peer group, and the peer group also should be able to express different opinions. Many people with medical minds are firmly entrenched in reductionism, synthetic chemistry and surgery, who make tremendous amounts of money for the industries that they promote. Yet people die every day of iatrogenic diseases resulting from surgery and synthetic drugs. Society has found a way to let these doctors off the hook, and yet

285 they put doctors who do unconventional therapies on the hook. It is possible that this challenge might be directed to help destroy a natural medicine industry which would challenge the incomes of the synthetic drug companies. Investigative books, including: Murder by Injection: The Story of the Medical Conspiracy against America, by Eustace Mullins (P.O. Box 1105, Staunton, Virginia 24401: National Council for Medical Research, 1988). Off the Pedestal: New women in the Art of Homer, Chase, and Sargent, edited by Holly Pyne Connor. New Brunswick, N.J.: Rutgers University Press, 2006, Mendelsohn’s series, and many others, are bringing to light the vast medical cover-up that has been promulgated by allopathic minds seeking to tyrannize and influence the minds of men. We need to deepen our philosophy of medicine, get into quantum physics, and try to understand biology at many different levels. These levels will include the ideas of statistical analysis, peer group philosophies, and scientific development of energetic phenomena. In the Quantum Biology Workbook, a heavy-duty physics statement is made using the highest levels of mathematics, physics and science known to our society. We conclude that allopathy is an irregular choice, and that the factors of clinical trials in reductionistic science are incomplete in their ability to protect the people using pharmaceutical products. We can see from this advanced physics and this upper level science that homeopathy and naturopathy are much more logical choices to use in developing medical techniques. As we go through different clinical trials that have been done in this book, we also review the literature of other research that has been done in naturopathy and homeopathy. We can see that in almost every attempt to utilize naturopathic and homeopathic techniques success is achieved. It is very rare in the literature to find a homeopathic or naturopathic study that failed to show a large degree of efficacy and safety.

286 Jos Kleijnen, Paul Knipschild, and Gerben ter Riet, in their article in the British Medical Journal, Clinical Trials of Homeopathy, (BMJ 1991; 302(6772), 316-323), assayed over 105 clinical trials of homeopathy from around the world. They concluded that 81 of the trials showed positive scientific undeniable results; 24 of them could be challenged. They concluded that there was a legitimate case for further evaluation. Full text article can be found at: www.pubmedcentral.nih.gov/picrender.fcgi?artid=1668980&blobtype=pdf According to the Null hypothesis in the case of homeopathy there is dramatic evidence of efficacy. Homeopathy works according to the scientific literature. With this type of data contained in these books and in this type of report it would seem that the use of homeopathy not only should be warranted, but that using an allopathic drug, which could produce a side effect or risk, might become a case of medical impropriety. I don’t believe that medicine can wait for homeopathy to be challenged over twenty years time. Homeopathy and naturopathy as an industry throughout the world outsell allopathic medications by almost three to one. This is because of the large amount of sales that are done in India, Pakistan, Bangladesh, China, etc. Out of this entire world market, which amounts to perhaps ten billion dollars in sales (it costs much less to manufacture and sell homeopathic products than allopathic ones), malpractice and different settlements measure in the thousands of dollars throughout the entire world. There are hardly any suits against naturopathic and homeopathic doctors, although when this does happen they are usually very small. Out of a ten billion dollar industry, less than one percent of one percent of one percent of one percent of its total capital generation is paid out in malpractice, compared to our allopathic counterparts, who pay in the neighborhood of fifteen to twenty percent a year in settlements. The justification for homeopathy need not come completely from clinical trials. Without using clinical trials it’s possible to look at the

287 world market and see that homeopathy works. It makes sense. One can look at the returns on malpractice insurance which shows how many people were hurt, and see that homeopathy works, whereas synthetic chemistry hurts. The statistics bear this out. One can look at these statistics and see that allopathy needs to be challenged, and that the process of using clinical trials and revering the publication/print process as the end all answer must be challenged in order to proceed any further with medicine. Reductionistic clinical trials are the problem, not the solution. It must be realized that the mind of the observer interferes with the experiment. This is a basic premise of quantum theory which allopathy is not putting into use. The basic treatise of this book has proven that quantum theory must be considered as a meaningful step into biology. In quantum theory, the mind state of the observer will influence the outcome. In the preparation of clinical trials, the power of mental philosophy and the mind state of the person behind them must be recognized. The development of modern chemistry, which pinnacled in synthetic processes, gave these people a severe mind set, a mind set based on chemical analysis, not energy, physics, and other sciences. This predominantly chemical-based philosophy will interfere with their observational ability. Hence, it is possible to see the action of this philosophical backdrop in their pursuit of medical truth. This has led to chemical solutions, surgical solutions, and allopathic ideation. Another philosophical and psychological problem behind this medical juggernaut is the idea of allopathic superiority to nature. As was pointed out in Quantum Biology, it is basically akin to the philosophy of allopathy and synthetic chemicals that the observer knows more than the situation he or she observes, in that the medical doctor knows more about biology than the patient’s body. The patient’s body, thus, becomes flawed and stupid in the eyes of the experimenter. If there is a histamine reaction, an anti-histamine is given to the “stupid body”; if there is depression, the

288 “stupid body” is given an MAO inhibitor; if there is fever, the “stupid body” is given an anti-pyretic. In other words, the concept of allopathy is that something is wrong with the body and that outside intervention from a superior intellectual source will help correct the problem. This also is a seriously flawed philosophy and psychological backdrop to which all of the medical experiments are then interred. With homeopathy and naturopathy as a basis in medicine, we can develop a different foundation. Our foundation will revere the natural process, and realize our inability to know intimately such a process. We would want to intervene on the process very little, and try to stimulate the process back to its own natural balance using natural mechanisms and gentle nudges to help stimulate the organism to achieve its own balance. The organism has the superior knowledge of biology. If we take such a philosophy, and reevaluate the last hundred years of medical research, we can see that some of the conclusions drawn from allopathy were severely flawed. An overview of the medical research will show us that many of the experiments performed were reductionistic and philosophically inadequate. Part of this book has been written with the idea that there is an evolution in human thought, and that human thought has evolved from many different states. It is wrong for us to think that human thought and social conditions have stayed the same through the years. The early tribes and societies had very weak ideas of philosophy and the ideation of a king becoming part god showed some of the limitations of their thinking. Early societies did not have the ideation of spatial organization to allow them to do proper art perspectives. This was a developmental process. There was a developmental process in the ideas of psychology and philosophy, in the idea of science, and in the concepts of religion and theology. Every form of human thought will evolve and change through the ages, just as medicine will evolve and change through the impact of this book

289 and thousands more like it. They will challenge the ideas behind medical thought and philosophy and bring about new ones that include a soft approach, and a gentleness and humility toward what is not known. As we develop and achieve this new type of mental thought we will be able to embrace an old philosophy of medicine. We will be able to find this old philosophy, ignored by technology and achieve a new way. The thesis and the antithesis will blend into a new form of truth. The thesis is that of naturopathy and homeopathy; the antithesis is allopathy and surgery. These two will blend to achieve a new form of thought in which the doctor, being educated and knowledgeable in all of these different philosophies will have more directed choices, and will be able to affect more safety and efficacy with his patients. It is this author’s purpose to challenge the conclusion of the article in the U.S. News and World Report. Perhaps more long-term studies need to be adapted to allopathic thought (long-term meaning over a period of ten generations). To say that more clinical trials need to be done in homeopathy is to state a truth, but to say that before homeopathy should be used by the masses, this needs to be done is to state an untruth. Grossly incorrect is this proposition to make homeopathy spend massive amounts of money on ridiculous reductionistic trials. Homeopathy is a legal entity in America and should not be forced into major expenditures in clinical trials which would do nothing to increase safety or efficacy. It is the opinion of these synthetic drug companies that if they could force homeopathy into such trials, they could perhaps destroy homeopathy, because it does not make the large amounts of money that allopathy does. Homeopathy would not have the money to afford such trials. Homeopathy by definition is not a money-making proposition. It is, however, curative. These trials are irregular with modern mathematics and modern medicine, and they will not give us the complete results we thought they would. Statistics lie, and statisticians deceive.

290 The FDA was formed by Dr. Clayton to protect homeopathy. He lobbied for years and years for a federal organization that could protect the American people in their choices of food and drugs. He sought to help in protecting the philosophy of homeopathy. Within two weeks after founding the FDA, Dr. Clayton died. The FDA has acknowledged the Homeopathic Pharmacopeia of the United States, and it is a legally accepted in America. The Homeopathic Pharmacopeia of the United States (HPUS) has never commanded enough money to generate popularity. Allopathic philosophy and its use of clinical trials have sought to tyrannize people’s minds and change their perspectives. It has hoped that doctors would make allopathic choices of drugs, rather than homeopathic choices. This type of tyranny over the minds of people is what the founders of our country sought to defend against. In 1991, President George W. Bush developed a thyroid condition which produced heart palpitations. This author wrote him a letter. In that letter, I said (in paraphrase):

Mr. President:

As President of the United States, I recognize that you have a lot of pressure to choose an allopathic therapy for your condition. At this time of war, (written just after the Gulf War), I can imagine the tremendous amount of stress and tension that you were going through, and I can also fathom how it has probably produced a hyperthyroid condition that has now gone out of control. In your choice of therapy, Mr. President, you as an American citizen have the right to choose many different types of medicines.

Your can choose chiropractic treatment for your condition, and perhaps adjustment of the nerves might provide a balance to the thyroid and alleviate stress. You can choose acupuncture treatment, and an acupuncturist might try to balance the meridian flow and help to sedate the irritation of the nerves of the heart, and sedate the body and balance its energies. You can choose nutrition, and seek a diet to help relax and balance

291 your metabolism. You can also choose homeopathic therapy, and take a homeopathic which we have shown to be not only safe, but also effective in many cases of treating hyperthyroid conditions. You could choose naturopathy in the District of Columbia, and seek natural therapies for your condition. You also can choose allopathic medicine, which works against the body. I realize, Mr. President, the tremendous amount of pressure on you to choose allopathic medication. Because of your position as United States President, if you were to choose a chiropractor, acupuncturist, homeopath, or other doctor, you might rock a very large economic boat, and threaten an entrenched philosophy of medicine.

The Queen of England, in a very similar position, has made the choice of homeopathy, Mr. President. She, The Queen of England and her family are only treated by homeopathic physicians; they are not treated in allopathic ways at all. They have rocked the big boat for many, many years. Even in light of extreme pressure, the logic and success of homeopathy outweighs the finances of allopathy.

Along with this letter, I send two bottles of Hyperthyro-1 homeopathic which we were able to blend. We did some pilot studies and found that it was safe and effective in these cases. Many similar cases of hyperthyroidism have been cured by this remedy.

So, Mr. President, you as an American citizen have the freedom of choice, to choose any of these different endeavors. I, as an American citizen have the freedom of choice, to write this letter, and to voice what type of therapy I might have chosen. Had I been in your position, Mr. President, I would have chosen homeopathy and alternative natural therapies. [President Bush could also have chosen naturopathic treatment, since naturopathy is legal within the confines of Washington, D.C.]

But also, Mr. President, as an American citizen I will fight for you to have the right to choose. If you choose allopathy, even if I don’t agree or approve, I will fight to protect that choice. I hope, Mr. President that you will also fight to protect my choice. There are several forces in the allopathic community who so value clinical trails, and so value their process and their philosophy that they seek to tyrannize the minds of men. And Mr. President, you can walk down to the Jefferson Memorial, where written around the top of the inside of the memorial, in big letters carved in stone, is a quote by Thomas Jefferson: “I have

292 sworn on the altar to oppose any tyranny over the minds of men.” Mr. President, freedom of choice has never been more threatened than it is now by allopathic mental tyranny.

Homeopathy entered into 1992 with some baggage as well. The people doing homeopathy in the United States were, most of the time, unable and unwilling to do highly sophisticated quality control. Oftentimes, the manufacturers did not comply with legal regulations set out by the FDA. Even the 211 CFRs (Code of Federal Regulations) were not utilized by unregistered homeopathic companies. Homeopathy must build quality control techniques such as those used at Dr. Recommends; pilot studies, clinical trials, safety and effectiveness analysis, culture techniques, and chromatography. Quality control techniques of the energetic process must be done as well, such as the REGAE (Rare Electron Gas Allopathic Evaluation) capacitance rating, inductance rating, conductance rating, and polymorphic shaping studies to understand the crystalline effects. These are some of the techniques that must be done in a true quality control way, as well as total legal compliance. As yet, the homeopathy industry as a whole does neither. To meet the challenge of our new thinking, and to direct homeopathy back into the medical mainstay, it will have to meet these challenges head on, change, and bring itself into reputability. As we have seen from our exploration, reductionism was probably more of a problem than a solution in science. We need to use our reductionistic trials; we also need to develop holistic, individualized concepts of medicine for more safety and effectiveness without just using short-term clinical trials. Nature knows protection. We only hope that the freedom of choice be kept alive in America. Many people I have known have left America in search of freedom of medical choice. We can only hope that freedom of choice be reestablished as the basic tenet of the American justice system. Our capitalistic philosophy has produced a successful past for our patentable, synthetic, chemical brethren. But

293 now the logic and reason of homeopathy and naturopathy must earn at least the freedom of choice. Perhaps this philosophy will earn more. As Victor Hugo once said, “There is only one thing more powerful than all the armies of the world, and that is an idea whose time has come.” Natural medicine’s time has come. Watch out, allopathy. Deepak Chopra’s book, Quantum Healing: Exploring the Frontiers of Mind/Body Medicine, New York: Bantam Books, 1989, offers supportive information for what is discussed here. He speaks of the idea of quantum healing which must involve compassion, and a new form of understanding that goes beyond the physical area into quantic dimensions. This is very important for us to realize. In his book, he makes a point about how a certain patient was “picnic-deficient,” and needed to have nice, enjoyable picnics to restore him to health. Chopra puts into view a mystical connection with another world, and explains it in different Asian terms. These terms he later relates to as quantum factors of types of energy. In our treatise, we also find that there is something that affects this indeterminacy, or quantic principle. We have called it a “God Consciousness,” a nature within Quantum Biology. We truly believe that Chopra’s referral to a God Consciousness and a quantic understanding is the same as what we are implying. There must be some type of greater power that dictates the precision with which biology pursues. Chopra puts some of our scientific perspectives into more human terms as he relates different cases, and how the cases go beyond classic medical understanding. Many other researchers of late have followed a similar path, and found challenging ways of critiquing modern medicine’s statistical type of logic. We must point out in this document that if there is a God Consciousness, an ability of will, happiness, joy, compassion, caring, sharing and touch to help people, it will not fit into any model that could be measured with statistical pre-test/post-test, clinical, drug trial data. Clinical trials need to be part of our concept, but not deified.

294 We need to use them to help determine safety and help to interpret our range of effectiveness, but they still should be within the guidelines of nature.

PROBLEMS BEHIND THE MEDICAL DILEMMA

¾ Arrogance; a belief in superiority over biology

¾ Persecution for the belief in nature and homeopathy

¾ Judgmentalism; psychological over-reaction against other natural philosophies. Preferred doctors of high influence are almost always allopaths who are ignorant of homeopathy

¾ Greed; synthetic companies profit mostly from patented unnatural compounds

¾ Lack of personal responsibility in healthcare

¾ Belief that medical technology will save someone after years of an unhealthy lifestyle

¾ Crisis philosophy; seeking medical help only after all else fails

¾ Insurance costs

¾ Malpractice costs and medical fears

¾ Lack of a true biology and no philosophical base

¾ Quantity based medicine, not quality based

295 SOLUTIONS TO THE MEDICAL DILEMMA

¾ Humility, reverence for nature’s process, understanding of quantic philosophy

¾ Proper study will show homeopathic and naturopathic credibility

¾ Proper peer group process: allowing a group of like-minded doctors to evaluate the amount of harm done, if any

¾ Protecting natural formulas with more strict copyrights that allow natural based pharmaceutical companies to benefit from their research

¾ Building personal responsibility into medical education at every level

¾ Educating for prevention and early treatment procedures

¾ Building a low-cost system of wellness counselors who can intervene and help in early and simple health care problems, reserving doctors and hospitals for crisis care

¾ Reducing insurance costs by using homeopathy and naturopathy and also escalating insurance costs for:

Obesity Smoking Alcohol abuse Drug addiction

Letting the ones who incur the most medical costs pay them. This will discourage bad health habits.

¾ Malpractice results mostly from synthetic allopathic drugs and surgery. Changing to homeopathy and naturopathy will show dramatic results.

¾ Appreciation and reverence for the unknown builds a quantum philosophy for medicine.

¾ Building everything for quality, not quantity. This will take more cash initially, but will be cheaper in the long run.

296 Now, let us be more specific as to what might be needed to actually set the criteria of how to approve new combination homeopathics, or new combination drugs. First, we will need to depend on safety as our primary goal. We need to look for safety first, or as Hippocrates said, “First, don’t hurt.” This needs to be our absolute guideline for everything we do. We have to imagine that everything we do could get to the youth of our society, as I think that everything could get to my five year old daughter. The thought of anything happening to this small child is absolutely, totally intolerable. First don’t hurt. Safety first is an absolute guideline. It is unfortunate that in the late 1950s the president of the American Medical Association (AMA), said in a public address that the AMA no longer had to guarantee safety first; they had to biopsy, x-ray, sedate, stimulate, stab, cut, and otherwise defame the body in order to do medicine. This idea will be intolerable in our new medicine as it forms. Safety first must be insured every step of the way. In a recent report, it was said that there is a possibility that the plankton at the South Pole might be in a condition of iron deficiency, and that if the plankton had an exposure to iron, they might be able to develop the ozone needed to compensate for the ozone deficiency of the South Pole. His treatise makes very sound, scientific sense, and all the science regarding the plankton around the South Pole has been done in a superior manifest way. But yet, the scientific community is hesitant to make such a maneuver, fearing the consequences of what one tanker- load of iron might do at the South Pole. This same type of fear of what this might do to the ecology of the entire world is not shared by the synthetic chemical companies, as they engage ever increasing numbers of synthetic chemicals that do not exist in the world, and they are putting these into the exosphere of our planet. This has been happening for over fifty years. Our new medicine will absolutely insist on proof that safety within the smallest amount of parameters must be guaranteed before we can proceed. We should no longer dump

297 synthetic, never-occurring un-natural compounds into the environment in the percentage that they have been in the past. We must set policies as to what we are going to do, and this policy has to be geared through the idea that only nature knows. Only through such humility can science actually address the issues of biology and medicine. The arrogant idea that if, “we do not know its function we should cut it out”, allowed for the destruction of adenoids, tonsils, appendix, spleen, thymus, etc. This type of arrogance must cease. Nature knows, and nature had a plan for the adenoids, tonsils and appendix, even though we did not know it. To assume that it is not needed because we do not understand it, is the absolute arrogance of science. We must have humility and a reverence towards science to be able to proceed in any way, shape or form. Clinical trials are not enough; we must have a guaranteed policy of understanding nature and nature’s own in order to proceed into the new dimensions of medicine and biology The alternative industry has done very little to offer any type of scientific inquiry regarding statistics as its guideline. We will need to develop pilot studies that guarantee effectiveness in safety, primarily. These types of statistical endeavors will have to be replicated by many different doctors in many different ways; not with the same criteria as drug trial studies, but in something similar that will guarantee the world’s safety and the world’s effectiveness of such remedies. These pilot studies need to use the statistics of the day, and will have to be at a razor-sharp edge to prove safe and effective. As we continue to revere nature, and understand that only nature truly knows, we will have to develop this into a hallmark of our biology. This will allow homeopathy and all its nosodes, allersodes isodes, sarcodes, etc., to explode into the scene of medicine. We also need to have the philosophy and the psychology to understand that behavioral medicine, psychological intervention, the psycho-immunological link and other factors are also very much needed for us to have a true medicine. We

298 need to take Chopra’s advice, and develop a science and a medicine of compassion, caring, sharing, touch, and healing to carry us into the new era of medicine. We will need to have a constant field input to allow doctors who are using such medications to critique their actions in an ever changing environment, realizing that what the action of any homoeopathic or drug might be might change as the population evolves, in light of an ever changing reactivity to the environment. Statistics will play an ever larger part, but yet will not be deified in light of philosophy. The philosophy that nature knows must be revered, not the statistics of clinical trials. We must realize what nature and God Consciousness can do in the field of biology and medicine. Only then, can we truly shape a new medicine through these different guidelines, concentrating on safety at all costs. We need effectiveness, but never at the cost of safety; revering nature and education, so that the doctors, the populace, the society at large can share in our appreciation and harmony of the natural flow of medicine. To this end this book is written.

299 SUMMARY

¾ A review of the insurance literature and true success stories on naturopathy and homeopathy vs. synthetic allopathy have conclusively proven that there is a severe problem in the field of synthetic allopathy. Synthetic allopathy pays billions of dollars in damages each year. Millions more are hurt by this technology who do not seek damages. Those who are helped do not outweigh the damages. The solution for this could be the new wave of homeopathy and naturopathy into general areas of medicine.

¾ There were profiteering issues behind the surge of synthetic allopathy that were spearheaded by reductionism as a mechanism of directing research. Now with the skills developed through mathematics and quantum theory, it is possible to see that the field of reductionistic research leaves dramatic problems for medicine.

¾ A new system of research must be developed for medicine. Some ideas for a new system were presented within this chapter.

¾ Medicine must learn not to deify statistical reductionistic papers, and must learn to develop a reverence for the natural process rather than synthetic dynamics.

¾ Freedom of choice must return to the world system of medicine.

¾ Systems of medicine such as chiropractic, naturopathy, homeopathy, acupuncture, behavioral medicine and biofeedback are legal systems.

¾ Synthetic allopathy seeks to tyrannize the minds of men against these other medical beliefs.

¾ We must oppose any such tyranny over the minds of men.

300 METABOLIC PATHWAYS

This section includes a list of the cellular energy components utilized in cellular metabolism and energy regulation. Sometimes an irregularity of function can be corrected with a homeopathic of the enzyme or component.

Alcohol dehydrogenase Glycerol-3-phosphate dehydrogenase D-Xylulose reductase L-Xylulose reductase D-Iditol dehydrogenase Glucuronate reductase UDP glucose dehydrogenase Histidinol dehydrogenase Shikimate dehydrogenase Lactate dehydrogenase D-Lactate dehydrogenase Glycerate dehydrogenase 3-Hydroxybutyrate dehydrogenase 3-Hydroxyisobutyrate dehydrogenase Mevaldate reductase Hydroxyethylglutaryl-CoA reductase (NADPH) 3-Hydroxyacyl-CoA dehydrogenase Malate dehydrogenase Malate dehydrogenase (oxaloacetate-decarboxylating) Malate dehydrogenase (decarboxylating) Isocitrate dehydrogenase (NAD+) Phosphogluconate dehydrogenase Phosphogluconate dehydrogenase (decarboxylating) L-Gulonate dehydrogenase Glucose-6-phosphate dehydrogenase Ribitol dehydrogenase 3-Hydroxpropionate dehydrogenase Tartronate-semialdehyde reductase Glyoxylate reductase (NADP+) Hydroxypyruvate reductase Malate dehydrogenase (NAPD+) Phosphoglycerate dehydrogenase 3-Oxo-[acyl-carrier-protein] reductase Retinol dehydrogenase IMP:NAD+oxidoreductase

301 L-Gulonolactone oxidase Choline dehydrogenase Glycerol-3-phosphate dehydrogenase Aldehyde dehydrogenase Benzaldehyde dehydrogenase (NADP+) Betaine-aldehyde dehydrogenase Aspartate-semialdehyde dehydrogenase Glyceraldehyde-phosphate dehydrogenase IMP dehydrogenase Succinate-semialdehyde dehydrogenase (NAD (P) +) Malonate semialdehyde dehydrogenase (acetylating) Glycoadehyde dehydrogenase Succinate-semialdehyde dehydrogenase 2-Oxiosovalerate dehydrogenase Benzaldahyde dehydrogenase (NAD+) Aminoadipate-demialdehyde dehydrogenase Aminomuconate-semialdehyde dehydrogenase Retinal dehydrogenase Xanthine dehydrogenase Glutamate-semialdehyde dehydrogenase Xanthine oxidase Pyruvate dehydrogenase (lipoamide) 2-Oxobutyrate synthase Dihydrouracil dehydrogenase (NAD+) Dihydrouracil dehydrogenase (NADP+) Acyl-CoA dehydrogenase (NADP+) Enoyl-[acyl-carrier-protein] reductase Enoyl-[acyl-carrier-protein] reductase (NADPH) Prephenate dehydrogenase (NADP+) Orotate reductase Coproporphyrinogen oxidase Succinate dehydrogenase Butryl-CoA dehydrogenase Acyl-CoA dehydrogenase Glutaryl-CoA dehydrogenase Alanine dehydrogenase Glutamate dehydrogenase Serine dehydrogenase Valine dehydrogenase (NADP+) Leucine dehydrogenase D-aspertate oxidase L-amino acid oxidase Glycine dehydrogenase Amine oxidase (pyridoxal-containing) Ethanolamine oxidase Pyrroline-2-carboxylate reductase

302 Pyrroline-5-carboxylate reductase Saccaropine dehydrogenase (NAD+, lysine-forming) Saccharopine dehydrogenase L-Pyrroline-5-carboxylate dehydrogenase Sarcosine oxidase Sarcosine dehydrogenase Dimethyglycine dehydrogenase L-Pipecolate dehydrogenase Cystine reductase (NADH) Dihydrolipoamide reductase (NAD+) Hypotaurine dehydrogenase Sulphite oxidase Sulphite reductase (ferredoxin) L-Ascorbate-cytochrome b5 reductase Ascorbate oxidase Catechol 1, 2-dioxygenase Catechol 2, 3-dioxygenase Homogentisare 1, 2-dioxygenase 3-Hydroxyanthranilate 3, 4-dioxygenase Tryptophan 2, 3-dioxygenase Cycsteine dioxygenase B-Carotene 15, 15’ –dioxygenase 4-Hydroxphenylpyruvate dioxygenase myo-Inositol oxygenase Benzoate 1, 2-dioxygenase Y-Butyrobetaine-2-oxogluterate dioxygenase Proline, 2-oxogluterate dioxygenase Trimethylysine, 2-oxogluterate dioxygenase Anthranilate 1, 2-dioxygenase (deaminating, decarboxylating) Imidazoleacetate 4-monooxygenase Kynurenine 3-monooxygenase Phenylalanine 4-monooxygenase Tyrosine 3-monooxygenase Monophenol monooxygenase Prostaglandin synthase Acyl-CoA desaturase Squalene monoxyenase (2, 3-epoxidising) Ribonucleoside-diphosphate reductase Nicotinamide methyltransferase Guanidinoacetate methyltransferase Dimethylthetin-homocysteine methyltransferase Acetylserotonin methyltransterase Betaine-homocysteine methyltransferase Homocysteine methyltransferase Tetrahydropteroyltriglutamate methyltransferase Phosphatidylethanolamine methyltransderase

303 Glycine methyltransferase Noradrenaline N-methyltransferase Thymidylate synthase Serine hydroxymithyltransferase Phosphoribosyglycinamide formyltransferase Phosphoribosylaminoimidazole-carboxamie formyltransferase Glutamate formiminotransferase Methylmalonyl-CoA carboxyltransferase Aspartate carboamoyltransferase Ornithine carbamoyltransferase Glycine amidinotransferase Transketolase Transaldolase Amino-acid acetyltransferase Glucosaminephosphate acetyltransferase Arylamine acetyltransferase Choline acetyltransferase Phosphate acetyltransferase Acetyl-CoA acetyltransferase Dihydrolipoamide acetyltransferase Glycerophosphate acyltransferase Acetyl-CoA acyltransferase Diacylglycerol acyltransferase Carnitine palmitoyltransferase Lysolecithin acetyltransferase Sphingosine acyltransferase Lysine acetyltransferase Glutamate acetyltransferase S-Aminolaivulinate synthase [Acyl-carrier-protein] acetyltransferase [Acyl-carrier-protein] malonytransferase 3-Oxoacyl-[acyl-carrier-protein] synthase Serine palmitoyltransferase 1-Acylglycerolphosphate acyltransferase Phosphorylase Amylosucrase Glycogen (starch) synthase Sucrose synthase Glucuranosyl-transferase Starch synthase Lactose synthase Sphingosine B-galactosyltransferase Cellulose synthase (GDP-forming) Glucomannan 4-B-D-mannosyltransferase UDP galactose-N-acylsphingosine galactosyltransferase UDP-N-Acetylglucosamine glycoprotein N-acetyl-glucosaminyltransferase

304 UDP galactose-ceramide galactosyltransferase GDP-fucose-lactose fucosyltransferase Purine nucleoside phosphorylase Pryimidine-nucleoside phosphorylase Thumidine phosphorylase Hypoxanthine phosphoribosyltransferase Uracil phosphoribosyltransferase Orotate phosphoribosyltransferase Nicotinate phosphoribosyltransferase Amidophosphoribosyltransferase ATPP-phosphoribosyltransferase Anthranilate phosphoribosyltransferase Nocotinatemonomucleotide pyrophosphorylase (carboxylating) Dimethyltransferase Methionine adenosyltransferase Geranyltransferase Amonopropyltransferase Farnesyltransferase Spermine synthase Aminotransferase Aspartate aminotransferase Alanini aminotransferase Glycine aminotransferase Tyrosine aminotransferase Leucine aminotransferase Histidinol-phosphate aminotransferase Acetylornithine aminotransferase Ornithine-oxo-acid aminotransferase Glutamine fructose 6-phosphate aminotransferase Succinyl-diaminopimelate aminotransferase B-Alanine-pyruvate aminotransferase Aminobutyrate aminotransferase L-3-Aminoisobutyrate aminotransferase 4-Hydroxyglutamate transaminase Tryptophan aminotransferase Valine-isoleucine aminotransferase L-Lysine 6-aminotransferase 2-Aminoadipate aminotransferase Branched-chain-amino-acid aminotransferase Serine-pyruvate aminotransferase Phosphoserine aminotransferase Glutamate synthase Glucokinase Ketohexokinase Fructokinase Galactokinase

305 Mannokinase 6-Phosphofructokinase Ribokinase Ribulodinase Xylulokinase NAD+kinase Dephospho-CoA kinase Triokinase Glycerol kinase Glycerate kinase Choline kinase Pantothenate kinase Pantetheine kinase Mevalonate kinase Homoserine kinase Pyruvate kinase D-Ribulokinase L-Xylulokinase N-Acylmannosamine kinase myo-Inositol-kinase Shikimate kinase Pyrophosphate-serine phosphotransferase Acetate kinase Phosphoglycerate kinase Aspartate kinase Formate kinase Carbamoyl-phosphate synthase (glutamine) Creatine kinase Phosphomevalonate kinase Nucleoside-phosphate kinase Nucleosidediphosphate kinase dTMP kinase Cytidylate kinase Phosphoglucomutase Acetylglucosamine phosphomutase Phosphoglycerosmutase Ribosephosphat pyrophosphokinase Pantetheinephosphate adenylyltransferase RNA nucleotidyltransferase DNA nucleotidyltrnasferase Glucose-1-phosphate guanylyltransferase Ethanolaminephosphate cytidylyltransferase Galactose-1-phosphate uridylyltransferase Hexose-1-phosphate guanylyltransferase GTP-mannose-1-phosphate guanylyltransferase Ethanolaminephosphate cytidylyltransferase

306 Cholinephosphate cytidylyltransferase Nicotinatemononucleotide adenylyltransferase Mannose-1-phosphate guanylyltransferase UDP acetylglucosamine pyrophosphorylase Glucose-1-phosphate thyidylyltransferase Glucose-1-phosphate guanylyltransferase Phosphatidate cytidylyltransferase Acylmeuraminate cytidylyltransferase Ethanolaminephosphotransferase Cholinephosphotransferase Ceramide cholinephosphotransferase Blycerophosphate phosphatidyltransferase CDP diglyceride-serine o-phosphatidyltransferase CDP diglyceride-inositol phosphatidyltransferase Phospho-N-acetylmuramoyl-pentapeptide transferase Propionate CoA-transferase 3-Oxoacid CoA-transferase 3-Oxoadipate CoA-transferase Triacylglycerol lipase Phospholipase A2 Lysophospholipase Acetylcholinesterase Aldonolactonase 3-Oxoadipate enol-lactotase Acylcarnitine hydrolase 6-Phosphogluconolactotase Phospholipase A1 Acetyl-CoA hydrolase 3-Hydroxyisobutyryl-CoA hydrolase Phosphoserine phosphatase Phosphatidate phosphatase 5’ –Nucleotidase Glucose-6-phosphatase Hexosediphosphatase Histidinolphosphatase 1L-myo-Inositol-1-phosphatase Phosphatidylglycerophospatase N-Acylneuraminate-9-phosphatase Nucleotidase Glycerophosphinicochopane diesterase Phospholipase C Phospholipase D Phosphatidylinositol phosphodieterase Sphingomyelin phosphosphesterase B-galactosidase B-fructofuranosidase

307 Adenosylhomocysteinase Asparaginase Glutaminase Ureidosuccinase Formylaspartate deformatase Aryl-formamidase Acetylornithine deacetylase Glutaminase Ureidosuccinase Formylaspartate deformatase Aryl-formamidase Succinyl-diaminopimelatase desuccinylase Citrullinase Pantothensase Acylsphingosine deacylase Hippurate hydrolase Dihydropyrimidinase Dinydor-orotase Allantoinase Imidazolonepropionase Arginase Formiminoaspartate deiminase Arginine deiminase AMP deaminase IMP cyclohydrolase dCMP deaminase Phosphoribosyl-AMP cyclohydrolase Adenosinetriphosphatase Nucleoside triphosphatase Fumarylaetoacetase Kynureninase Phosphoamidase Carboxylyase Pyruvate decarboxylase Oxaloacetate decarboxylase Acetoacetate decarboxylase Aspartate 4-decarboxylase Glutamate decarboxylase Ornithine decarboxylase Diaminopimelate decarboxylase Phosphoribosylaminoimidazole carboxylase Histidine decarboxylase Orotidine-5’ –phosphate decarboxylase Aromatic –L-amino-acid decarboxylase Cysteine sulphinate decarboxylase Phosphoenolpyruvate carboxylase

308 Di-phosphomevalonate decarboxylase Keto-L-glutonate decarboxylase Phosphopantothenoyl-cysteine decarboxylase Uroporphyrinogen decarboxylase Phosphoenolpyruvate carboxykinase (pyrophosphate) Ribulosebisphosphate carboxylase Propionyl-CoA carboxylase Phenylpyruvate decarboxylase Aminocarboxymuconate-semialdehyde decarboxylase Tartronate-semialdehyde synthase Indole-3-glycerol-phosphate synthase Phosphoenolpyruvate carboxykinase (ATP) Phosphatidylserine decarboxylase Aldehyde lyase Phosphoketolase Ketopantoaldolase Fructose-bisphosphate aldolase Phospho-2-keto-3-deoxy-heptonate aldolase Isocitrate lysase Malate synthase Hydroxymithylglutaryl-CoA lyase Citrate (si) –synthase ATP citrate (pro-3S)-lyase 4-Hydroxy-2-oxoglutarate aldolase Acetolactate synthase N-Acylneuraminate-9-phosphate synthase Homocirtate synthase Anthranlate synthase Tryptophanase Fumarate hydratase Aconitate hydratase Citrate dehydratase Dihydroxyacid dehydratase 5-Dehydroquinate dehydratase Enolase Phosphogluconate dehydratase L-Serine dehydratase Threonine dehydratase Enoyl-CoA hydratase Methylglutaconyl-CoA hydratase Imidazoleglycerolphosphate dehydratase Tryptophan synthase Cystathionine B-synthase Porphobilinogen synthase Mesaconate hydratase dTDP glucose 4, 6-dehydratase

309 GDP-manose 4,6-dehydratase Urocanate hydratase Prophenate dehydratase Dihydrodipicolinate synthase 3-Hydroxyoctanoyl-[acyl-carrier-protein] dehydratase D-3-Hydroxydecanoyl-[acyl-carrier-protein] dehydratase Threonine synthase Cystathionine Y-synthase Aspartate ammonia-lyase Methylaspartate ammonia-lyase Histidine ammonia-lyase Uroporphyrinogen I synthase Argininosuccinate lyase Adenylosuccinate lyase Cystathionine Y-lyase Cystathionine B-lyase Adenylate-cyclase Ribulosephosphate 3-epimerase UDP-glucose 4-epimerase L-Ribulosephosphate 4-epimerase UDP-glucinonate epimerase UDP-acetylglucosamine 4-epimerase UDP-acetylglucosamine 2-epimerase Methylmalonyl-CoA racemase Maleylacetoacetate isomerase Retinal isomerase Triosephosphate isomerase Arabinose isomerase L-Arabinose isomerase Xylose isomerase Ribosephosphate isomerase Mannosephosphate isomerase Glucosephosphate isomerase D-Lyxose ketol-isomerase N-(5’ –Phospho-D-ribosylformimino)-5-amino-1-(5’ –phosphoribosyl)-4- imidazolecarboxamide isomerase Glucose isomerase Glucosaminephosphate isomerase (glutamine-forming) Isopentenyldiphosphate isomerase Muconolactone isomerase Phosphoglycerate phosphomutase Phosphoacetylglucosamine mutase Phosphomannomutase Methylasartate mutase Methylmalonyl-CoA mutase Chorismate mutase Lanosterol-cyclase

310 Muconate cycloisomerase myo-Inositol-1-phosphate synthase Succinyl-CoA-synthase Asparagine synthetase Glutamine synthetase Asparagine synthetase NAD+synthetase Pantothenate synthetase Y-Glutamylcysteine synthetase Glutathione synthase Phosphopantothenoyl-cysteine synthetase Phosphoribosylaminoimidazole-succinocarboxamide synthase UDP-N-acetylmuramoylalilne synthetase UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-D-alanyl-D-alanine synthetase Phosphoribosylaminoimidazole synthetase GMP synthetase CTP synthetase Adenylosuccinate synthase Argininosuccinate synthase 5’-Phosphoribosylamine synthetase Phosphoribosylglycinamide synthetase NAD+synthetase (glutamine-hydrolysing) GMP synthetase (glutamine-hydrolysing) Phosphoribosylformylglycinamidine synthetase Carbomoyl phosphate synthetase Pyruvate carboxylase Acetyl-CoA carboxylase Propionyl-CoA carboxylase Propionyl-CoA carboxylase Methylcrotonoyl-CoA carboxylase

See metabolic pathways below.

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313 314 315 316 317 318 319 320 321 322 323 324 325 326 327 For more on Metabolic Pathways: http://www.sigmaaldrich.com/Area_of_Interest/Life_Science/Metabolom ics/Key_Resources/Metabolic_Pathways.html?cm_mmc_o=TBBTkwCjCF wfz_BkBFbglCjC55gCjCFwfz_Bkbg%205zftczYl http://www.expasy.ch/cgi-bin/show_thumbnails.pl http://www.gwu.edu/~mpb/

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Dr. Recommends is dedicated to developing statistical data banks to prove the efficacy of homeopathy to standard medicine and the world. Many studies have been done by Dr. Nelson in developing experimental and clinical proof for the efficacy and safety of homeopathy.

DISCLAIMER

If conditions persist, and are not responding properly to the homeopathic program, we encourage the doctor to make other referrals so that the condition will not deteriorate. Allopathic medicine has some dramatic benefits that can help with different disease structure in their crisis stages. Many patients do not go to doctors until they are in a crisis stage. Homeopathy might be too slow in working. We usually suggest that the patient use the remedies for two to four weeks if the condition allows. If results are not attained, the doctor should make a referral for more dramatic therapies. These should be discussed with a bio-physician who has an appreciation for the rules of nature. Homeopathic remedies are designed to work as an adjunct and support to standard medical therapies. They are not meant as a replacement. If symptoms persist, consult a medical doctor. If pregnant or lactating consult your physician.

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Continuing Education Units

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that you spent in hours reading the book.

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