Amyotrophic Lateral Sclerosis (ALS)
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46 L Nursing2015 L Volume 45, Number 10 46 L
46 l Nursing2015 l Volume 45, Number 10 www.Nursing2015.com Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. 2.0 ANCC ALCONTACT HOURSS Amyotrophic lateral sclerosis: What nurses need to know By Tamara L. Bellomo, MSN, RN-BC, and Lucille Cichminski, MSN, RN A MOTHER OF THREE teenage children, Mrs. is one of the most common neuromuscular dis- S, 49, presented to her healthcare provider eases in the world. This rapidly progressive, fatal with bilateral leg twitching and weakness, dif- neuromuscular disease involves the degeneration ficulty swallowing, and fatigue that’s worsened and death of the upper and lower motor neu- over the past few weeks. While she was on her rons.1 This article discusses the diagnosis and daily morning walk, she tripped and fell. She treatment of ALS and how nurses can help their experienced a small laceration to her leg, patients deal with the difficult diagnosis and find prompting her visit to the healthcare facility. the resources they and their families need. Her husband said that she’d had periods of slurred speech over the past few months as Who’s affected? well. She was alert and oriented, and her vital An estimated 20,000 to 30,000 Americans are signs were all within normal limits. living with ALS, and about 5,000 new cases After an exam, her healthcare provider are diagnosed each year in the United States.2 referred her to a neurologist who ordered This disease affects people of all ethnic, socio- magnetic resonance imaging (MRI), an electro- economic, and racial backgrounds.2,3 ALS most HOTOTAKE / P myogram, and a full bloodwork panel. -
2018 National ALS Registry Annual Meeting Executive Summary
ATSDR’s Annual ALS Surveillance Meeting Summary Report August 1-2, 2017 2018 National ALS Registry Annual Meeting Executive Summary The cause(s) of ALS (Amyotrophic Lateral Sclerosis) remain unknown for 90-95 percent of those diagnosed with the disease and there is still no cure. The Agency for Toxic Substances and Disease Registry (ATSDR) established the National ALS Registry to determine how many people in the US are living with ALS, to describe the demographics of ALS patients, and most importantly to examine the risk factors for ALS. Although the Registry’s primary purpose is to capture cases of ALS, the Registry does a lot more than just count cases. The Registry is also: Funding ALS research, Collecting specimens from Registry enrollees through the National ALS Biorepository, Connecting patients with researchers recruiting for ALS clinical trials or epidemiological studies, Obtaining etiologic data from Registry enrollees through 17 different online risk factor modules such as occupational history, military history, residential history, history of traumatic brain injury (TBI), Providing data and biospecimens to scientists to further ALS research. The National ALS Registry Annual Meeting was held in Atlanta on August 7-8, 2018. There were 51 attendees, including persons living with ALS, neurologists, researchers, representatives of national ALS organizations, representatives of pharmaceutical companies, Registry staff, and other ALS experts. Background, Methodology, and State of the Registry Because ALS is a non-notifiable condition, CDC does not receive reports from states of the occurrence of ALS, as it does for most communicable diseases. The novel methodology developed by ATSDR for identifying newly diagnosed ALS cases uses data from national administrative databases (i.e., Medicare and the Veterans Administration) in addition to the information entered into the online Registry web portal by persons living with ALS. -
Group Statement
May 25, 2021 ALS Organizations Double Down on Their Support for Reintroduced Legislation That Will Accelerate Research and Encourage Access to Critical Investigational Therapies for Those Living with ALS. Today, leaders in the House of Representatives and Senate reintroduced the Accelerating Access to Critical Therapies for ALS Act. The ALS Association, I AM ALS, and the Muscular Dystrophy Association (MDA) endorse the revised legislation with this statement: “The Accelerating Access to Critical Therapies (ACT) for ALS Act builds new pathways to fund early access to ALS investigational therapies, accelerates ALS and rare neurodegenerative disease therapeutic development through a public-private partnership, and increases research on, and development of, interventions for rare neurodegenerative diseases through a new Food and Drug Administration (FDA) research grants program. The ALS Association, I AM ALS, and the Muscular Dystrophy Association endorse this legislation that is a paradigm shift in how therapeutic development, access to treatments, and research has been approached in a fatal, fast- progressing disease like ALS. The ACT for ALS will authorize $100 million a year over a five-year period to: (1) create a new grant program that funds access to investigational ALS treatments currently in development from small biotechnology companies for those patients who cannot participate in clinical trials, while concurrently supporting a research objective on how these investigational treatments impact the disease; (2) establish a Health -
Drug Development for Amyotrophic Lateral Sclerosis Guidance for Industry
Drug Development for Amyotrophic Lateral Sclerosis Guidance for Industry August 2017 Contents I. INTRODUCTION ................................................................................................................ 1 II. BACKGROUND ................................................................................................................... 2 III. BENEFIT RISK...................................................................................................................... 5 A. General comments .................................................................................................................. 5 B. Evidence of patient and caregiver preferences ....................................................................... 5 C. Implications of patient risk/benefit preferences in ALS ......................................................... 7 1. Alternative endpoints........................................................................................................... 7 2. Placebo control arm ............................................................................................................. 8 3. Threshold for statistical significance ................................................................................... 9 4. Method of delivery ............................................................................................................ 10 5. Role of expanded access and accelerated approval ........................................................... 11 6. Patient protection and need for informed -
2020-ALS-Mission-Toolkit Web.Pdf
OUR MISSION OUR MISSION TABLE OF CONTENTS OUR MISSION Our Case for Support . iv Annual Impact . v Our Vision and Mission . vi CHAPTER 1: RESEARCH The ALS Association Research Program The ALS Association Research Program . 1–1 Research . 1–5 Our Strategic Initiatives . 1–5 Infographics Current Projects . 1–13 Accelerating the Search for a Cure . 1–14 Research By the Numbers . 1–15 Research Strategy . 1–16 Funded Research . 1–17 Scientific Focus Areas . 1–18 Advances in ALS Research . 1–20 Research Initiatives The ALS Association’s ALS Roundtable Program . 1–22 ALS Voice of The Patient Report . 1–24 ALS Focus Survey Program . 1–26 Research Staff . 1–28 CHAPTER 2: CARE SERVICES How We Work Summary . 2–1 How We Work . 2–2 Chapter Membership . 2–4 ii How We Support Clinical Care Supporting Clinical Care . 2–11 Certified Centers . 2–14 Where We Support Care . 2–15 Impact & Resources Care Services Impact . 2–20 Filling the Gap . 2–21 Education — Living with ALS: General Scope . 2–22 Education — Living with ALS: Medical Resources . 2–24 Assistive Technology — Assistive Technology in the ALS Space . 2–26 Children’s Programs and Resources . 2–28 The Jane Calmes ALS Scholarship Fund . 2–32 ALS Association Care Connection . 2–33 Care Services Staff . 2–34 CHAPTER 3: ADVOCACY Introduction To ALS Advocacy Introduction . 3–1 History of ALS Advocacy . 3–2 History of ALS Advocacy: Timeline . 3–3 Advocacy Action Advocacy Guiding Principles . 3–5 How We Advocate . 3–6 Priorities, Impact, and Coalitions ALS Guidance . 3–10 Advocacy Impact . -
A Er the Wildly Successful Ice Bucket Challenge
RESEARCH FEBRUARY/MARCH 2015 BY GINA SHAW Azer the Wildly Successful Ice Bucket Challenge ~e Ice Bucket Challenge raised big bucks on social media. Now, the ALS Association tells us where that cold, hard cash is going. As snowstorms and icy winds batter much of the country, it's hard to imagine willingly pouring a bucket of ice water over your head for any reason. But last August—when temperatures were much more forgiving—that's exactly what about 3 million people did. In an astonishing example of the power of social media, a July 31 dare from former Boston College baseball player Pete Frates, who was diagnosed with amyotrophic lateral sclerosis (ALS) in 2012, quickly went viral. The dare? Dump ice water on your head within 24 hours of being challenged or donate $100 (or whatever amount you could afford) to the ALS Association or another organization supporting ALS research. Pretty soon, the Ice Bucket Challenge meant dumping ice on your head and donating money, and everyone from your neighbor's preschooler to Bill Gates (with a custom-built ice douser), Oprah Winfrey, Jon Bon Jovi, and entire casts of Broadway shows were doing it—and posting their videos online. Even 86-year-old Ethel Kennedy took the challenge. (President Obama donated but declined the ice; actor Patrick Stewart posted a video of himself writing a check.) In La Jolla, CA, prominent ALS researcher Don Cleveland, PhD, who pioneered a novel therapy that turns off the defective genes that contribute to neurodegenerative diseases, watched the online commotion with skepticism. -
Genetics and Genomics
31st International Symposium on ALS/MND Theme 02 – Genetics and Genomics GEN-01: An Interval Look at Early outcomes of strength (ATLIS), bulbar function (quantitative speech analysis and IOPI), and disease Markers of Disease in Familial ALS progression (change in ALSFRS-R total score over time). Isabel Anez-Brunzual1, Austin Lewis, Katherine Burke1, Multiple measures of strength (ATLIS, HHD) and Diane Lucente1, Jennifer Jockel-Balsarotti2, Margaret cognition (NIH examiner, ALS-CBS) will be evaluated in all participants over time. Clapp2, Amber Malcolm2, Taylor Stirrat1, Stephanie Berry1, Tania Gendron3, Mercedes Prudencio3, Kathryn Results to date: Connaghan4, James Chan5, Jordan Green4, Leonard Petrucelli3, James Berry1, Timothy Miller2, Dr Katharine Interval analysis will be shown for 86 participants Nicholson1 enrolled in the DIALS Network. Forty-one of 86 1Massachusetts General Hospital, Boston, United States, participants are positive for an ALS causative mutation 2Washington University, Saint Louis, United States, 3Mayo (33 C9orf72, 5 SOD1, 1 TARDBP, 1 VAPB, and 1 FIG4). Clinic, Jacksonville, United States, 4MGH Institute of Health Peri-conversion data will be shown for the 4 C9orf72 Professions, Boston, United States, 5Biostatistics Center, MGH, carriers (3 ALS, 1 FTD) who have developed symptoms. Boston, United States Longitudinal strength, bulbar, and cognitive outcome data as well as direct biomarker comparison will be Live Poster Session A, December 9, 2020, 5:10 PM - 5:50 shown. DIALS enrollment and follow-up visits are PM ongoing. Background: Discussion: The validation of sensitive biofluid markers of inciting The DIALS Network dataset is composed of a growing disease pathology and clinical outcomes is crucial to number of pre-symptomatic ALS gene carriers, now detecting early disease, and to understanding the onset including several symptom converters. -
The Ice Bucket Challenge Chatter the Campaign Went Viral Who's Talking
TREATO: AFTER THE ALS ICE BUCKET CHALLENGE, WHAT IS THE HEALTH CONSUMER SAYING? Last summer’s ALS Ice Bucket Challenge was one of the most successful social media campaigns of all-time. Millions dumped a bucket of ice water on their head to promote awareness of the disease amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's Disease) and encourage donations to the ALS Association. Round Rock High School Dragon Band - photo by Henry Huey The campaign went viral More than 1billion 2.4 views million + videos posted to Watch Bill Gates ice #donate bucket challenge! $220 #ALS @alsassociation million raised Promoting awareness & AUGUST So what did the health consumer really think of such a grand campaign? With August creeping closer, will we see the same social virality that 1 2015 consumed YouTube and Facebook a year earlier? Online activity Discussions about ALS over time % Posts Monthly Although campaign sustainability was short, conversations still remain stead- ily higher than a year ago. 4/1/2014 7/1/2014 10/1/2014 1/1/2015 4/1/2015 ALS discussions grew by close to 6x the normal activity from July through August, a reflection the effectiveness of the ALS campaign Discussions about ice bucket challenge and ALS over time 35% Almost 30% of the ALS 30% discussions last August were 25% 20% about the ice bucket challenge. 15% The conversations then dropped 10% but we are beginning to see a 5% rise again this June. 0% Who's talking? 44% of all patients discussing ALS The percentage of caregivers are within the 30-49 age group, in talking about ALS is considerably contrast to a disease that is most higher than with other conditions prominent in the 50+ age group. -
Join the Fight Against Lou Gehrig's Disease! the ALS Association
The ALS Association Greater New York Chapter Join the fight against Lou Gehrig’s Disease! Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Eventually, people with ALS lose the ability to initiate and control muscle movement, which often leads to total paralysis and death within two to five years of diagnosis. There is no cure, and only one drug approved by the U.S. Food and Drug Administration (FDA) modestly Nerve Cells extends life expectancy. Cell Body axon axon atrophied muscle muscle Normal nerve cell ALS and muscle -affected nerve cell and muscle About The ALS Association Greater New York Chapter The ALS Association is the only national, 501(c)(3) not-for-profit voluntary health organization whose mission is to lead the fight to cure and treat ALS through global cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to lead fuller lives by providing them with compassionate care and support. The Greater New York Chapter provides a full range of essential patient and family services in all five boroughs of New York City, Long Island, Westchester County, the Hudson Valley, and northern and central New Jersey. 2 Students Challenge ALS • 2015 is a school-based program supported by The ALS Association Greater New York Chapter that provides students with the tools to become advocates for the ALS community by encouraging and emphasizing community activism. The goal of this program is to increase support for those living with Lou Gehrig’s disease by raising funds and awareness to improve the lives of ALS patients and their families. -
24Th Annual Meeting Sunday and Monday, 4-‐5 December 2016
24th Annual Meeting Sunday and Monday, 4-5 December 2016 Liffey Hall 2, Convention Centre Dublin AGENDA SUNDAY, 4 DECEMBER 2016 08:45 1 Welcome & Introduction (30 min) 09:15 Annual General Meeting (45 min) 10:00 2 Opening Remarks from the General Manager (15 min) 10:15 Morning Refreshments (30 min) 10:45 3 Welcoming Our NeW Members (15 min) 11:00 Programming for PALS/CALS (60 min) 4 Beyond Awareness Gaps Hiroki Okabe, Japan ALS Association 5 The Cost of Achieving Your Goals: Assistive Technology Program in Israel Efrat Carmi, IsrALS 6 A Comprehensive Information and Education Resource for People with MND, their Carers, Health and Community Care Providers Gina Svolos, MND Australia 7 New Challenges to Our Association Alessandra Dorca, ALS Pro-Cura Association 12:00 Lunch (60 min) 13:00 Programming for PALS/CALS Continued (30 min) 8 ACELA: A Vision of Hope Rocio Reyes, ACELA, Colombia 9 Life Is Now Gudjon Sigurdsson, MND Iceland 13:30 Partnerships and Collaborations (90 min) 10 A Phased Shift in MND Care in Scotland Craig Stockton, MND Scotland 11 Victories and Partnerships Tatiana Mesquita e Silva, ABrELA 12 Local Fundraising for Project MinE Gorrit-Jan Blonk, ALS Netherlands 13 Using the MND Association’s Experience to Promote Optimal Care and Support in Russia Anna Kassianova, Martha-Mary Medical Centre “Miloserdie” 14 The South African MND Caregiving Experience: Lessons Learned from a Cross-Country Collaboration Melinda Kavanaugh, University of Wisconsin-MilWaukee 15 First Ever ALS Student Exchange Jodi O’Donnell, Hope Loves Company -
Real Or Perceived Amyotrophic Lateral Sclerosis (ALS) Objectives
10/11/2019 Nursing Care and Considerations of Patients with Amyotrophic Lateral Sclerosis (ALS) 40th Annual Neurorehabilitation Conference on Traumatic Brain Injury, Stroke and Other Neurological Disorders Saturday & Sunday, November 16 & 17, 2019 Hyatt Regency Cambridge 575 Memorial Drive • Cambridge, MA encompasshealth.com/braintreerehab Vincent M. Vacca, Jr., MSN, RN 1 Conflicts of interest – Real or Perceived • NONE 2 Amyotrophic Lateral Sclerosis (ALS) Objectives: 1. Following this presentation the learner will be able to list three signs and symptoms of motor neuron dysfunction found in ALS. 2. Following this presentation the learner will be able to explain three diagnostic tests utilized to establish diagnosis of ALS. 3. Following this presentation the learner will be able to describe three essential nursing interventions guided by best practices and care of patients with ALS. 3 1 10/11/2019 The median age of ALS onset is 55 years • ALS affects about one in every 300 people. • About 30,000 currently with 5,000 new cases per year. • ALS is sporadic in 90% of cases and show familial inheritance in the remaining 10%. • Estimates of the median survival of people with ALS vary between 27 and 64 months. • Death from ALS is primarily pulmonary. 4 ALS is the most frequent motor neuron disorder in adults • Due to degeneration of upper and lower motor neurons in spinal and bulbar myotomes. • Most studies show male predominance with a gender ratio of 3:2, but gender differences are age related. • Age of onset tends to be later in females than in males (68.4 years vs. 61.5 years). -
Amyotrophic Lateral Sclerosis (ALS)?
Amyotrophic Lateral Sclerosis U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Amyotrophic Lateral Sclerosis What is amyotrophic lateral sclerosis (ALS)? myotrophic lateral sclerosis (ALS) is a A rare neurological disease that affects nerve cells (neurons) in the brain and spinal cord that control voluntary muscle movement. Voluntary muscles produce movements like chewing, walking, breathing and talking. The disease is progressive, meaning the symptoms get worse over time. Currently, there is no cure for ALS and no effective treatment to halt, or reverse, the progression of the disease. ALS belongs to a wider group of disorders known as motor neuron diseases, which are caused by gradual deterioration (degeneration) and death of motor neurons. Motor neurons are nerve cells that extend from the brain to the spinal cord and to muscles throughout the body. These motor neurons initiate and provide vital communication links between the brain and the voluntary muscles. Messages from motor neurons in the brain (called upper motor neurons) are transmitted to motor neurons in the spinal cord and to motor nuclei of brain (called lower motor neurons) and from the spinal cord and motor nuclei of brain to a particular muscle or muscles. 1 In ALS, both the upper motor neurons and the lower motor neurons degenerate or die, and stop sending messages to the muscles. Unable to function, the muscles gradually weaken, start to twitch (called fasciculations), and waste away (atrophy). Eventually, the brain loses its ability to initiate and control voluntary movements. Early symptoms of ALS usually include muscle weakness or stiffness. Gradually all muscles under voluntary control are affected, and individuals lose their strength and the ability to speak, eat, move, and even breathe.