Als And Occupational Therapy

ALS and Occupational Therapy: Navigating Challenges and Maximizing Opportunities

Author: Dr. Emily Carter, OTR/L, PhD. (Registered Occupational Therapist, Licensed, Doctor of Philosophy in Rehabilitation Science)

Publisher: The American Occupational Therapy Association (AOTA) Press – A leading publisher of occupational therapy resources, known for its rigorous peer-review process and commitment to evidence-based practice.

Editor: Dr. Sarah Miller, OTR/L, CHT (Registered Occupational Therapist, Licensed, Certified Hand Therapist), with extensive experience in neurological rehabilitation.


Keywords: ALS and occupational therapy, amyotrophic lateral sclerosis, occupational therapy for ALS, ALS treatment, ALS management, occupational therapy interventions ALS, ALS rehabilitation, quality of life ALS, adaptive equipment ALS, assistive technology ALS


Abstract: Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease impacting daily living significantly. Occupational therapy plays a vital role in managing the progressive challenges posed by ALS, focusing on maximizing independence, participation, and quality of life. This article explores the unique challenges presented by ALS and highlights the diverse opportunities occupational therapy offers throughout the disease trajectory. We will delve into specific interventions, adaptive strategies, and the importance of a holistic approach in ALS and occupational therapy practice.


1. Understanding the Impact of ALS on Daily Living:

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, controlling voluntary muscle movement. This progressive muscle weakness and atrophy profoundly impact daily living activities, encompassing personal care, mobility, communication, and social participation. ALS and occupational therapy are inextricably linked because occupational therapists are uniquely positioned to address the functional limitations arising from this disease. The relentless progression of ALS demands a dynamic and adaptable approach from both the individual and the occupational therapy team. Early intervention is crucial in ALS and occupational therapy; it helps individuals maintain independence for as long as possible.

2. The Role of Occupational Therapy in ALS Management:

Occupational therapists working with individuals with ALS employ a holistic approach, considering the individual's physical, cognitive, emotional, and social needs. The primary goals of ALS and occupational therapy intervention are to:

Maintain Independence: Strategies focus on adapting tasks and environments to compensate for declining motor skills. This may involve assistive devices, adaptive equipment, and environmental modifications.
Enhance Participation: Occupational therapists help individuals participate in meaningful occupations, adapting activities to maintain social connections, work roles (if feasible), and hobbies.
Improve Quality of Life: Addressing the emotional and psychological challenges associated with ALS is crucial. Occupational therapy can facilitate coping strategies, stress management, and support systems.
Promote Comfort and Safety: As the disease progresses, strategies focus on managing pain, preventing falls, and ensuring safe mobility.


3. Specific Occupational Therapy Interventions in ALS:

ALS and occupational therapy interventions are highly individualized, tailored to the specific needs and stage of the disease. These interventions may include:

Assistive Technology: This encompasses a range of devices, from simple adaptive utensils to sophisticated communication aids and powered wheelchairs, enabling individuals to maintain independence in activities of daily living (ADLs).
Adaptive Equipment: Modifying existing equipment or using specialized tools (e.g., button hooks, zipper pulls, reachers) can facilitate self-care and maintain independence.
Environmental Modifications: Adapting the home environment, such as installing ramps, grab bars, and wider doorways, can enhance safety and mobility.
Energy Conservation Techniques: Teaching strategies to minimize energy expenditure during activities can help prolong independence and reduce fatigue.
Communication Strategies: As speech and swallowing difficulties arise, occupational therapists may collaborate with speech-language pathologists to implement augmentative and alternative communication (AAC) methods.
Splinting and Orthotics: These can support weakened limbs, reduce joint contractures, and improve hand function.
Therapeutic Exercise: While strength training is often limited, range-of-motion exercises and gentle stretching can help maintain joint mobility and prevent contractures.
Caregiver Training: Occupational therapists educate caregivers on safe handling techniques, energy conservation strategies for themselves, and adaptive strategies for assisting the individual.

4. Challenges in ALS and Occupational Therapy Practice:

Despite the significant benefits, occupational therapists face several challenges when working with individuals with ALS:

Rapid Disease Progression: The unpredictable and accelerating nature of ALS requires frequent reassessment and adaptation of intervention strategies.
Emotional and Psychological Impact: The diagnosis of ALS is emotionally devastating, and therapists must address the psychological needs of individuals and their families.
Caregiver Burden: Caregivers often experience significant stress and burnout, requiring support and education from occupational therapists.
Access to Resources: Access to assistive technology and adaptive equipment can be limited due to cost and availability.
Interprofessional Collaboration: Effective care requires seamless collaboration among multiple healthcare professionals (physicians, nurses, speech-language pathologists, respiratory therapists), which can sometimes be challenging.


5. Opportunities in ALS and Occupational Therapy Research:

ALS and occupational therapy research is crucial to improving the quality of life for individuals with ALS. Opportunities exist for research in:

Effectiveness of Specific Interventions: Rigorous studies are needed to evaluate the long-term effectiveness of various occupational therapy interventions.
Development of New Technologies: Research into innovative assistive technologies and adaptive equipment is crucial to enhancing independence.
Caregiver Support: Research focusing on effective strategies for supporting caregivers is essential in reducing burnout and improving outcomes for both the individual and caregiver.
Telehealth Applications: Exploring the use of telehealth for delivering occupational therapy services to individuals with ALS, particularly in rural areas, could greatly improve accessibility.


6. The Future of ALS and Occupational Therapy:

The future of ALS and occupational therapy is promising. Advances in technology, a growing body of research, and a heightened awareness of the importance of holistic care will continue to shape the field. Increased emphasis on early intervention, personalized care, and interprofessional collaboration will be crucial in maximizing the quality of life for individuals affected by ALS. The integration of technology into occupational therapy practice will offer innovative solutions for maintaining independence and participation.


Conclusion:

ALS and occupational therapy share a critical and evolving relationship. Occupational therapy plays a vital role in empowering individuals with ALS to maintain their independence, participate in meaningful activities, and improve their quality of life. By addressing the challenges and embracing the opportunities, occupational therapists can make a significant difference in the lives of individuals living with ALS and their families.


FAQs:

1. What is the typical length of occupational therapy treatment for someone with ALS? The duration varies depending on the individual's needs and disease progression. It could range from a few months to several years, with ongoing reassessment and adjustments to the plan.

2. How much does occupational therapy for ALS cost? Costs vary based on location, insurance coverage, and the intensity of services. It's recommended to check with your insurance provider and occupational therapist for a cost estimate.

3. Can occupational therapy help with the emotional aspects of ALS? Yes, occupational therapists can provide support and coping strategies to address the emotional challenges associated with ALS. They may collaborate with other professionals, such as psychologists or social workers, as needed.

4. What types of assistive devices are commonly used in ALS and occupational therapy? These can range from simple adaptive utensils to complex communication aids, powered wheelchairs, and environmental control systems. The specific devices will depend on the individual's needs and functional limitations.

5. Is occupational therapy covered by insurance for ALS? Coverage varies depending on the individual's insurance plan and location. It's crucial to contact your insurance provider to determine your coverage.

6. How can I find an occupational therapist experienced in treating ALS? You can contact your physician, ALS Association chapter, or search online directories of occupational therapists, specifying experience in neurological rehabilitation or ALS care.

7. What is the difference between occupational therapy and physical therapy for ALS? While both are important, occupational therapy focuses on ADLs and adapting the environment, while physical therapy concentrates on improving strength, range of motion, and mobility. They often collaborate.

8. How can family members get involved in the occupational therapy process for ALS? Family members play a crucial role. Therapists actively involve them in the assessment, goal-setting, and implementation of strategies to support both the individual and the caregiver.

9. Is there research ongoing in ALS and occupational therapy? Yes, ongoing research focuses on improving interventions, developing new technologies, and understanding the effectiveness of various approaches. The ALS Association and other research organizations support such studies.


Related Articles:

1. "Adaptive Equipment for ALS: Enhancing Independence in Daily Living": Explores different adaptive equipment and its impact on maintaining independence in various activities.
2. "Assistive Technology in ALS: A Review of Current and Emerging Technologies": Provides an overview of available and emerging assistive technologies for individuals with ALS.
3. "The Role of Caregiver Support in ALS Management: An Occupational Therapy Perspective": Discusses strategies for supporting caregivers and reducing caregiver burden.
4. "Environmental Modifications for Individuals with ALS: Creating a Safe and Accessible Home": Details how to modify the home environment to improve safety and mobility.
5. "Communication Strategies in ALS: Augmentative and Alternative Communication Interventions": Explores methods to facilitate effective communication as the disease progresses.
6. "Energy Conservation Techniques for Individuals with ALS: Maximizing Function and Reducing Fatigue": Focuses on strategies to reduce energy expenditure during activities.
7. "The Psychological Impact of ALS: An Occupational Therapy Approach to Emotional Well-being": Explores the emotional impact and strategies for emotional support.
8. "Interprofessional Collaboration in ALS Care: Optimizing Outcomes Through Team-Based Approaches": Highlights the importance of collaboration amongst healthcare professionals.
9. "Telehealth in ALS: Expanding Access to Occupational Therapy Services": Discusses the benefits and challenges of using telehealth to deliver occupational therapy services.


  als and occupational therapy: Willard and Spackman's Occupational Therapy Barbara A. Schell, Glen Gillen, Marjorie Scaffa, Ellen S. Cohn, 2013-03-08 Willard and Spackman’s Occupational Therapy, Twelfth Edition, continues in the tradition of excellent coverage of critical concepts and practices that have long made this text the leading resource for Occupational Therapy students. Students using this text will learn how to apply client-centered, occupational, evidence based approach across the full spectrum of practice settings. Peppered with first-person narratives, which offer a unique perspective on the lives of those living with disease, this new edition has been fully updated with a visually enticing full color design, and even more photos and illustrations. Vital pedagogical features, including case studies, Practice Dilemmas, and Provocative questions, help position students in the real-world of occupational therapy practice to help prepare them to react appropriately.
  als and occupational therapy: Palliative Care in Amyotrophic Lateral Sclerosis David Oliver, Gian Domenico Borasio, Wendy Johnston, 2014-03-20 Amytrophic Lateral Sclerosis (ALS or motor neurone disease) is a progressive neurodegenerative disease that can cause profound suffering for both the patient and their family. Whilst new treatments for ALS are being developed, these are not curative and offer only the potential to slow its progression. Palliative care must therefore be integral to the clinical approach to the disease. Palliative Care in Amyotrophic Lateral Sclerosis: From diagnosis to bereavement reflects the wide scope of this care; it must cover not just the terminal phase, but support the patient and their family from the onset of the disease. Both the multidisciplinary palliative care team and the neurology team are essential in providing a high standard of care and allowing quality of life (both patient and carer) to be maintained. Clear guidelines are provided to address care throughout the disease process. Control of symptoms is covered alongside the psychosocial care of patients and their families. Case studies are used to emphasise the complexity of the care needs and involvement of the patient and family, culminating in discussion of bereavement. Different models of care are explored, and this new edition utilizes the increase in both the evidence-base and available literature on the subject. New topics discussed include complementary therapies, personal and family experiences of ALS, new genetics research, and updated guidelines for patient care, to ensure this new edition remains the essential guide to palliative care in ALS.
  als and occupational therapy: Occupational Therapy Practice Guidelines for Adults with Neurodegenerative Diseases Katharine Preissner, 2014-01-01
  als and occupational therapy: Conditions in Occupational Therapy Ben Atchison, Diane K. Dirette, 2007 This Third Edition focuses on chronic health problems and their impact on an individual's physical, cognitive, psychological, and social capabilities. Readers learn how the patient's age, life tasks, and living environment affect occupational therapy needs, and how to determine what occupational therapy services to provide. Chapters present the etiology, symptoms, prognosis, and progression of conditions frequently encountered in practice. Case studies at the end of every chapter help students apply the content to real-life clinical situations. This edition includes new chapters on anxiety disorders and cardiopulmonary disorders. The expanded art program includes more photos, drawings, charts, and graphs.
  als and occupational therapy: Current Therapy in Neurologic Disease Richard Tidball Johnson, John W. Griffin, Justin C. McArthur, 2006-01-01 Neurologists present their own experiences and step-by-step guidelines on the management and treatment of specific disorders affecting the nervous system. Diagnosis, epidemiology, and pathophysiology are discussed only when they affect treatment strategies and decisions. Treatment algorithms and patient resource information complement each chapter.
  als and occupational therapy: Pedretti's Occupational Therapy - E-Book Heidi McHugh Pendleton, Winifred Schultz-Krohn, 2024-03-25 Gain the knowledge and skills you need to treat clients/patients with physical disabilities! Pedretti's Occupational Therapy: Practice Skills for Physical Dysfunction, 9th Edition uses a case-based approach threaded through each chapter to provide a solid foundation in evaluation, intervention, and clinical reasoning. The text continues to support the entry-level occupational therapist and the experienced occupational therapist focused on expanding skills and knowledge. With the OT practice framework as a guide, you will focus on the core concepts and central goals of client care. And by studying threaded case studies, you will learn to apply theory to clinical practice. Written by a team of expert OT educators and professionals led by Heidi McHugh Pendleton and Winifred Schultz-Krohn, this edition includes an eBook free with each new print purchase, featuring a fully searchable version of the entire text. - UNIQUE! Threaded case studies begin and are woven through each chapter, helping you develop clinical reasoning and decision-making skills and to apply concepts to real-life clinical practice. - UNIQUE! Ethical Considerations boxes examine the obligation to collaborate with clients on their care, using evidence to select treatment options. - UNIQUE! OT Practice Notes convey important tips and insights into professional practice. - Illustrated, evidence-based content provides a foundation for practice, especially relating to evaluation and intervention. - Information on prevention — rather than simply intervention or treatment — shows how OTs can take a proactive role in client care. - Focus on health promotion and wellness addresses the role of the occupational therapist in what the AOTA has identified as a key practice area. - Content on cultural and ethnic diversity is included in every chapter, reflecting occupational therapy's commitment to this important issue. - Key terms, chapter outlines, and chapter objectives highlight the information you can expect to learn from each chapter. - NEW! Updated content reflects the new Occupational Therapy Practice Framework (OTPF) and the new Accreditation Council for Occupational Therapy Education (ACOTE) curriculum standards along with the new AOTA Code of Ethics. - NEW! Implementation of Occupational Therapy Services, Therapeutic Use of Self, Telehealth, and Lifestyle Redesign chapters are added to this edition. - NEW! Content on the role of the occupational therapist with clients/patients who experience long COVID. - NEW! Inside look at the lived experience of disability covers the intersection of disability perspectives and occupational justice, along with the implications for Occupational Therapy. - NEW! Updated Mindfulness chapter is expanded to cover the wide use of mindfulness in occupational therapy for those with physical disabilities. - NEW! eBook version – included with print purchase – allows you to access all of the text, figures, and references from the book on a variety of devices, and offers the ability to search, customize your content, make notes and highlights, and have the content read aloud.
  als and occupational therapy: Preparing for the Occupational Therapy National Board Exam: 45 Days and Counting Rosanne DiZazzo-Miller, Fredrick D. Pociask, 2016-10-14 Preparing for the Occupational Therapy National Board Exam: 45 Days and Counting, Second Edition is a comprehensive overview for occupational therapist students preparing to take the National Board for Certification in Occupational Therapy (NBCOT) OTR exam. It utilizes a well-received health and wellness focus and includes tips and self-assessment forms to develop effective study habits. Unlike other OTR examination review guides, this text chooses to provide a more structured and holistic approach, including a detailed calendar and plan of study for the 45 days leading up to the exam.
  als and occupational therapy: Amyotrophic Lateral Sclerosis Hiroshi Mitsumoto, 2010-04 ALS, also known as Lou Gehrig's disease, cannot be cured but it can be treated. A great deal can be done to treat the symptoms of ALS, to improve an individual's quality of life, and to help families, caregivers, and loved ones to cope with the disease. This extensively revised and rewritten new edition of the bestselling Amyotrophic Lateral Sclerosis: A Guide For Patients and Families addresses all of those needs, and brings up-to-date important information to those living with the reality of ALS. The book is completely revised throughout and contains NEW information on: Recently developed approaches to treating ALS symptoms Use of non-invasive ventilators Multidisciplinary team care New guidelines being developed by the American Academy of Neurology for patients with ALS The use of riluzole (Rilutek) to treat ALS Amyotrophic Lateral Sclerosis covers every aspect of the management of ALS, from clinical features of the disease, to diagnosis, to an overview of symptom management. Major sections deal with medical and rehabilitative management, living with ALS, managing advanced disease, end-of-life issues, and resources that can provide support and assistance in this time of need.
  als and occupational therapy: Early's Physical Dysfunction Practice Skills for the Occupational Therapy Assistant E-Book Mary Beth Patnaude, 2021-01-15 - NEW! Intervention Principles for Feeding and Eating chapter is added to this edition. - NEW! Reorganization of all chapters aligns content more closely with the Occupational Therapy Practice Framework. - NEW! Combined chapters make the material more concise and easier to navigate.
  als and occupational therapy: Occupational Therapy Practice Guidelines for Adults with Neurodegenerative Diseases , 1999
  als and occupational therapy: Preparing for The Occupational Therapy Assistant National Board Exam: 45 Days and Counting Rosanne DiZazzo-Miller, Fredrick D. Pociask, 2017-08-30 Preparing for the Occupational Therapy Assistant Board Exam: 45 Days and Counting provides a comprehensive overview for occupational therapy assistant students preparing to take the Certified Occupational Therapy Assistant (COTA) exam. Each new print copy includes Navigate 2 Preferred Access that unlocks a complete eBook, Study Center, Homework and Assessment Center, Navigate 2 TestPrep with over 500 practice questions.
  als and occupational therapy: Amyotrophic Lateral Sclerosis Richard S. Bedlack, MD, Hiroshi Mitsumoto, MD, 2013 Amyotrophic Lateral Sclerosis: A Patient Care Guide for Clinicians is intended as a practical reference for clinicians caring for ALS patients, and will bring together the collective wisdom of those at the forefront of patient-oriented research and practice. This will be an official project of the ALS Research Group (founded by Dr. Mitsumoto and currently headed by Dr. Bedlack), and provides both an evidence-based and experience-based guide to multidisciplinary ALS care. The book will begin with a brief review of current concepts of ALS including diagnostic criteria, genetic and sporadic subty.
  als and occupational therapy: Living Under the Sword Harold B. Haley, 2004 An investigative documentary examining the crucial issues of food production and food distribution in the world economy--Case-slip.
  als and occupational therapy: Primary Care Occupational Therapy Sue Dahl-Popolizio, Katie Smith, Mackenzie Day, Sherry Muir, William Manard, 2023-05-15 Healthcare is shifting towards a holistic, whole person approach to improve population health, decrease cost of care, and improve patient, and provider experiences. To achieve this, the primary care sector is adopting an integrated, interprofessional care team model which addresses both biomedical and behavioral health, and includes preventative care, population health management, technology, and innovative strategies to increase access to care. Occupational therapy (OT) is uniquely positioned to add their distinct whole person mental/behavioral health and medical care scope and skill to these teams to address patient needs. As this is an emerging practice area for OT, and no guidelines specific to primary care exist, this book will be a first of its kind text for occupational therapy practitioners (OTP) in primary care settings. As OTPs work with habits, roles, and routines that affect health, OT in primary care promotes health and improves patient self-management of medical conditions and lifestyles, reducing patient dependence on costly health care services. This timely clinical manual guides best practices for primary care OT. It helps OTPs fit into the quick paced primary care practice model. In traditional OT settings, intervention sessions are longer, and focus on acute rehabilitation or mental/behavioral health conditions. In primary care, visits are brief, and address patient needs in the context of their presenting issue. No other published guide meets the unique needs of this emerging practice area. Authors provide administrative information specific to OT in primary care, and interventions for specific health conditions, including chronic conditions, common to this setting. Written by experts in the field, Primary Care Occupational Therapy is the definitive resource for all primary care OTPs or those interested in lifestyle-based interventions for conditions frequently seen in primary care. It is also a useful guide for behavioral health care providers and administrators of general medical practices.
  als and occupational therapy: Strong Girls, Stronger Together: A Guide to ALS Awareness Laurence Donelson lll, 2024-05-17 Discover the strength of unity and empowerment in 'Strong Girls, Stronger Together: A Guide to ALS Awareness'. This guidebook offers a comprehensive journey through understanding ALS, sharing courageous stories, navigating support systems, and advocating for change. From fostering a deeper understanding of ALS research to empowering girls in science, each chapter inspires action and amplifies voices in the fight against ALS. With a focus on building support networks and envisioning a future free from ALS, this guide serves as a powerful tool for those committed to making a difference in ALS awareness and advocacy.
  als and occupational therapy: Amyotrophic Lateral Sclerosis Lina Machtoub, Yu Kasugai, 2016-01-05 Recently, the implication of biocompatible nanotechnologies has set the stage for an evolutionary leap in diagnostic imaging and therapy. In this scope, the book presents a comprehensive overview of the possible causes, diagnostic criteria, and treatment assessments of amyotrophic lateral sclerosis, and presents the recent findings using innovative
  als and occupational therapy: Occupational Therapy for Physical Dysfunction Diane Dirette, 2019-12-17 Designed to help students become effective, reflective practitioners, this fully updated edition of the most widely used occupational therapy text for the course continues to emphasize the “whys” as well as the “how-tos” of holistic assessment and treatment. Now in striking full color and co-edited by renowned educators and authors Diane Powers Dirette and Sharon Gutman, Occupational Therapy for Physical Dysfunction, Eighth Edition features expert coverage of the latest assessment techniques and most recent trends in clinical practice. In addition, the book now explicitly integrates “Frames of Reference” to help students connect theories to practice and features a new six-part organization, thirteen all-new chapters, new pedagogy, and more.
  als and occupational therapy: Dying Well Ira Byock, 1998-03-01 From Ira Byock, prominent palliative care physician and expert in end of life decisions, a lesson in Dying Well. Nobody should have to die in pain. Nobody should have to die alone. This is Ira Byock's dream, and he is dedicating his life to making it come true. Dying Well brings us to the homes and bedsides of families with whom Dr. Byock has worked, telling stories of love and reconciliation in the face of tragedy, pain, medical drama, and conflict. Through the true stories of patients, he shows us that a lot of important emotional work can be accomplished in the final months, weeks, and even days of life. It is a companion for families, showing them how to deal with doctors, how to talk to loved ones—and how to make the end of life as meaningful and enriching as the beginning. Ira Byock is also the author of The Best Care Possible: A Physician's Quest to Transform Care Through the End of Life.
  als and occupational therapy: Amyotrophic Lateral Sclerosis Robert G. Miller, 2010-05 ALS is not a curable disease, but it is a treatable one. Treatments are now available that can make a major difference in prolonging life and enhancing the quality of life for people with the disease, and there are treatments for many of the symptoms of ALS that can help ease its burden. Multidisciplinary teams in specialized ALS centers are providing top quality care and comprehensive rehabilitation for persons with ALS. In spite of the progressive nature of this disease and its clear tendency to shorten life, the momentum of research in this disease is expanding dramatically and numerous clinical trials are testing promising new therapies. Our understanding of the basic causes of ALS is expanding gradually. The substantial resources of patient advocacy groups such as the Amyotrophic Lateral Sclerosis Association and Muscular Dystrophy Association provide tremendous help and support for people with ALS and their families. Although the diagnosis of ALS can initially be devastating, the vast majority of people discovering new courage from within to battle this disease and live life with vigor and enthusiasm. The information in this book will prove useful to people with ALS and their families both in managing the disease and living within its limitations. ''
  als and occupational therapy: Amyotrophic Lateral Sclerosis V. Cosi, 2013-03-09 An International Conference on Therapeutic. Psychological and Research Aspects of Amyotrophic Lateral Sclerosis was held in Varese. Italy from the 27th to the 31st March 1985. Health care professionals. scientists. patients and their families from twenty countries around the world participated in this meeting. The objectives of the Varese conference were the following: a. To provide a forum for the proponents of the various paths of research into ALS. b. To correlate the useful therapies employed regionally. for the purpose of developing a common guide for patients, families, and supporting professionals. c. To encourage self-examination by the health care professionals into the psychological barriers imposed by a diagnosis of terminal illness for which there is no known cause or cure. Not surprisingly, there were no announcements of breakthroughs or miracle cures, which are nonetheless hoped for in the confrontation of a disease such as ALS. It is fair to say, however, that Varese provided the context for a thorough review of what is known about ALS and we hope that the papers will renew some of the enthusiasm which has characterized this conference. The book contains six sections: Basic Research Aspects, Diagnostic Tools, Clinical Management, Therapeutic Trials, Psychological Aspects and the Epidemiology of ALS. Certain aspects, such as pathological studies and animal models, have not been covered; these subjects were partially treated during the informal sessions. Nevertheless, the large number of papers bears evidence to the growing interest in ALS and to the success of the Varese meeting.
  als and occupational therapy: Nerve Disease ALS and Gradual Loss of Muscle Function Mary E. Miller, 2016-10-14 Amyotrophic lateral sclerosis, ALS, is a common form of motor neuron disease that involves a loss of function in upper and lower motor neurons. ALS causes a progressive loss of muscle function that frequently initiates in the limbs, called limb-onset ALS, or initiates in facial muscles, called bulbar-onset ALS. This book describes the current understanding of ALS symptoms, diagnosis, causes, and treatments. Initial symptoms vary in type of muscle dysfunction, intensity of symptoms, and speed of disease progression. Diagnosis requires loss of function in both upper and lower motor neurons for limb- and bulbar-onset ALS, distinguishing ALS from other neuromuscular diseases. Although no cause or initial trigger has been determined for ALS, eventually both limb and bulbar muscles will show dysfunction as the disease progresses. In later stages of the disease, muscle dysfunction typically leads to respiratory failure and death. Management of neurotransmitter levels in patients can prolong life by months, but no cure exits for the disease. Other treatments exist that can help patients manage muscle weakness or spasms as the disease progresses. The book concludes by considering future detection, treatment, and diagnostic approaches with the goal of preventing disease initiation or progression.
  als and occupational therapy: Occupational Therapy Lorraine Williams Pedretti, 1996 -- The new 5th ed. has been completely revised and updated.-- New features include, a new appendix providing case studies and treatment plans, plus Key terms and learning objectives.-- New chapters on treatment contexts, infection control and safety, functional motion assessment, pain management, plus many more.
  als and occupational therapy: Navigating Life with Amyotrophic Lateral Sclerosis Mark B. Bromberg, Diane Banks Bromberg, 2017 Navigating Life with Amyotrophic Lateral Sclerosis provides accessible, comprehensive, and up-to-date information about the challenges patients, family members, and caregivers face when confronted by ALS. This guide covers all aspects of managing ALS, from the onset of symptoms, diagnosis, treatments, and coping strategies, to the use of home health care or hospice, and new research in the field. The book also sheds lights on difficult topics, such as end-of-life care and managing legal affairs. Formatted in a question-and-answer style, peppered throughout with patient stories, and with sections devoted to family members and caregivers, this compassionate resource provides guidance to those seeking to understand how to live with this disease.
  als and occupational therapy: Noninvasive Mechanical Ventilation John R. Bach, 2002 In addition, patients with neuromuscular and lung disorders prefer noninvasive means over tracheal intubation and tracheostomy for ventilatory support and secretion management. This book presents the various noninvasive inspiratory and expiratory muscle aids and the outcomes of their use in patients with respiratory muscle dysfunction. It describes treatment and rehabilitation interventions specific for patients with these conditions.--BOOK JACKET.
  als and occupational therapy: Motor Neuron Disease Research Progress Raffaele L. Mancini, 2008 The motor neuron diseases (or motor neuron diseases) (MND) are a group of progressive neurological disorders that destroy motor neurons, the cells that control voluntary muscle activity such as speaking, walking, breathing, and swallowing. Neurological examination presents specific signs associated with upper and lower motor neuron degeneration. Signs of upper motor neuron damage include spasticity, brisk reflexes and the Babinski sign. Signs of lower motor neuron damage include weakness and muscle atrophy. Every muscle group in the body requires both upper and lower motor neurons to function. It is a common misconception that upper motor neurons control the arms, while lower motor neurons control the legs. The signs described above can occur in any muscle group, including the arms, legs, torso, and bulbar region. Symptoms usually present between the ages of 50-70, and include progressive weakness, muscle wasting, and muscle fasciculations; spasticity or stiffness in the arms and legs; and overactive tendon reflexes. Patients may present with symptoms as diverse as a dragging foot, unilateral muscle wasting in the hands, or slurred speech. This new book presents the latest research from around the globe.
  als and occupational therapy: Amyotrophic Lateral Sclerosis, Lou Gehrig's Disease , 1983
  als and occupational therapy: Adult Physical Conditions Amy J. Mahle, Amber L. Ward, 2022-03-01 The go-to resource for class, clinical, and practice…now in full color! A team of noted OTA and OT leaders and educators deliver practical, in-depth coverage of the most common adult physical conditions and the corresponding evidence-based occupational therapy interventions. The authors blend theory and foundational knowledge with practical applications to OTA interventions and client-centered practice. This approach helps students develop the critical-thinking and clinical-reasoning skills that are the foundation for professional, knowledgeable, creative, and competent practitioners. New & Updated! Content that incorporates language from the 4th Edition of the Occupational Therapy Practice Framework and aligns with the latest ACOTE standards New & Updated! Full-color, contemporary photographs that reflect real clients and OT practitioners in diverse practice settings New Chapters! Occupational Justice for Diverse and Marginalized Populations, Motor Control and Neurotherapeutic Approaches, Sexual Activity and Intimacy, Dementia: Understanding and Management, and The Influence of Aging on Occupational Performance “Evidence-Based Practice,” highlights recent research articles relevant to topics in each chapter, reinforcing the evidence-based perspective presented throughout the text. “Putting It All Together: Sample Treatment and Documentation” uses evaluation, treatment, and documentation based on one relevant case from each diagnosis chapter to connect what students are learning in the classroom and the lab to real-world, skilled, client-centered care. “Technology & Trends” highlights new and relevant technology or treatment trends and also shows how common technologies may be used in unique ways. Client examples provide context for how the conditions impact function and how to consider the person when doing an intervention. “Case Studies” based on real-life examples illustrate important learning points and feature questions to develop critical-thinking and problem-solving skills. Review questions at the end of each chapter assess progress, knowledge, and critical thinking while offering practice with certification-style questions.
  als and occupational therapy: Rheumatology E-Book Krysia Dziedzic, Alison Hammond, 2010-02-22 Rheumatology is an indispensable resource for physiotherapists, occupational therapists and other health professionals, offering practical approaches to the treatment and management of rheumatic musculoskeletal conditions. The text focuses on applying evidence-based understanding of these conditions to clinical context. The specific disease chapters cover: incidence and prevalence of the condition; clinical presentation and diagnosis; red flags; clinical assessment; important first treatments, early intermediate and long term management; prognosis and long term outcomes. Supporting case histories of increasing complexity and study activities illustrate the clinical relevance of the treatment and management approaches. • Multidisciplinary team approach • Practical solutions to management of conditions supported by the latest research • Case histories of increasing complexity consolidate understanding and develop clinical reasoning • Highlighted boxes throughout contain study tasks and key messages
  als and occupational therapy: Public Policy in ALS/MND Care Robert H. Blank, Jerome E. Kurent, David Oliver, 2020 Anyone interested in ALS/MND-physician, patient, or healthcare policy director -should read this book and learn from it. -Walter G. Bradley D.M., F.R.C.P., Professor and Chairman Emeritus, Miller School of Medicine, University of Miami, USA This book illustrates the inequities in the accessibility of quality neurological care existing globally and which forms a major target for redress by the World Federation of Neurology and the World Health Organisation. -William M Carroll AM, MBBS, MD, FRACP, FRCP(E), President, World Federation of Neurology This book focuses on the public policy and political/ethical dimensions of ALS/MND across a wide selection of countries and argues for the need of a multidisciplinary and international approach. Policy issues addressed include adequacy of funding for research and care, payment policy and regulatory functions of public and private insurers, long-term services and caregiver support, public health and prevention efforts, access to genetic testing and assisted technologies, ensuring a competent and adequate workforce especially for hands-on caregivers, and the challenging issues of providing palliative and hospice care for ALS/MND patients, advance directives and assisted suicide that face policy makers in all political jurisdictions. Robert H. Blank, PhD, (University of Maryland) is an adjunct Professor of Political Science at the University of Canterbury in Christchurch, New Zealand. He has been a frequent guest professor at Aarhus University in Denmark and at National Taiwan University in Taipei, Taiwan, and a Research Scholar at New College Florida. Jerome E. Kurent received his MD from the University of Cincinnati College of Medicine and completed residencies in Neurology and Internal Medicine at the Johns Hopkins Hospital. He completed fellowships in neuromuscular diseases and electromyography at the National Institutes of Health, followed by a Geriatrics Medicine fellowship at Harvard where he also received his MPH. Dr. Kurent joined the Medical University of South Carolina faculty in 1984, and is Professor of Neurology, Medicine and Psychiatry and Behavioral Sciences. David Oliver, MD., recently retired as Consultant Physician in Palliative Medicine at the Wisdom Hospice in Rochester, Kent where he developed an integrated service over 32 years. He is an Honorary Professor at the Tizard Centre at the University of Kent, where he supervises students and is involved in research
  als and occupational therapy: Physical Dysfunction Practice Skills for the Occupational Therapy Assistant - E-Book Mary Beth Early, 2012-03-30 - New content on the latest advances in OT assessment and intervention includes prosthetics and assistive technologies, and updated assessment and interventions of TBI (traumatic brain injury) problems related to cognitive and visual perception.
  als and occupational therapy: Neuromuscular Disorders E-Book Tulio E. Bertorini, 2021-06-29 Offering an authoritative, multidisciplinary approach to the complex issues associated with neuromuscular disease, Neuromuscular Disorders, 2nd Edition, provides the latest tools and strategies for minimizing disability and maximizing quality of life. Dr. Tulio Bertorini, an expert in clinical neuromuscular care, and a team of world-renowned contributors cover all management and therapeutic considerations regarding the full range of neuromuscular disorders and resulting complications. - Provides comprehensive coverage of evaluation and diagnosis, treatments, and outcomes, including the latest management tools and targeted therapeutic strategies. - Includes the latest updates in the field: genetic causes of hereditary disease, new autoimmune diseases, promising new therapies such as antisense oligonucleotides and gene therapies, and more. - Features numerous drug tables, treatment algorithms, and clinical images throughout to aid in diagnosis and treatment. - Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices.
  als and occupational therapy: Adult Physical Conditions Amy J Mahle, Amber L Ward, 2018-04-17 The go-to text/reference for class, clinical, and practice! A who’s who of experts and educators brings you practical, in-depth coverage of the most common adult conditions and the corresponding evidence-based occupational therapy interventions. Written for OTAs to meet their unique needs, this approach combines theory with the practical, evidence-based functional content that develops the critical-thinking and clinical-reasoning skills that are the foundation for professional, knowledgeable, creative, and competent practice.
  als and occupational therapy: Amyotrophic Lateral Sclerosis Dr. Robert G. Miller, MD, Deborah Faith Gelinas, Dr. Deborah Gelinas, Patricia O'Connor, RN, 2004-10 Annotation Chapters cover nutrition and swallowing; speech, communication, and computer access; mobility; breathing and sleeping; end-of-life care; and much more, including insurance issues and practical tips. Chapters from leading ALS organizations offer useful lists of- support services- publications- websites and other resources.
  als and occupational therapy: Physical Therapy for Children - E-Book Robert J. Palisano, Suzann K. Campbell, Margo Orlin, 2014-04-25 Used as both a core textbook in PT programs and as a clinical reference, Physical Therapy for Children, 4th Edition, provides the essential information needed by PTs, both student and professional, when working with children. Like the previous bestselling editions, the 4th edition follows the practice pattern categories of the Guide to Physical Therapist Practice and uses the IFC model of the disabling process as it presents up-to-date evidence-based coverage of treatment. In this latest edition, Suzann Campbell DeLapp, Robert J. Palisano, and Margo N. Orlin have added more case studies and video clips, additional chapters and Medline-linked references online, and Evidence to Practice boxes to make it easy to find and remember important information. Provides comprehensive foundational knowledge in decision making, screening, development, motor control, and motor learning, the impairments of body function and structure, and the PT management of pediatric disorders. Reflects a family-centered care model throughout to help you understand how to involve children and their caregivers in developing and implementing intervention plans. Emphasizes an evidence-based approach that incorporates the latest research for the best outcomes. Follows the practice pattern guidelines of the Guide to Physical Therapist Practice, 2nd Edition which sets the standard for physical therapy practice. Features the International Classification of Function, Disability, and Health (ICF) of the World Health Organization (WHO) as the model for the disabling process, emphasizing activity rather than functional limitations and participation rather than disability in keeping with the book’s focus on prevention of disability. Provides extensive case studies that show the practical application of material covered in the text and are often accompanied by online video clips illustrating the condition and its management. Makes it easy to access key information with plenty of tables and boxes that organize and summarize important points. Clearly demonstrates important concepts and clinical conditions you’ll encounter in practice with over 800 illustrations. Takes learning to a deeper level with additional resources on the Evolve website featuring: Over 40 video clips that correspond to case studies and demonstrate conditions found in each chapter Helpful resources, including web links Questions and exercises you’ll find helpful when preparing for the pediatric specialist certification exam
  als and occupational therapy: Amyotrophic Lateral Sclerosis Julie Sørensen, 2020 Amyotrophic Lateral Sclerosis: From Diagnosis to Treatment focuses on two aspects of neuroimaging related to amyotrophic lateral sclerosis that have greatly evolved in the last decades: the development of optical tools in the biology field and advances in the field of magnetic resonance imaging. Therapeutic writing and expressive disclosure interventions have been demonstrated to facilitate the emotional processing of thoughts and feelings about the amyotrophic lateral sclerosis experience, with relevant implications for illness adjustment. Based on these premises, the authors explore the linguistic patterns in the cognitive-affective processing of illness experience in people with amyotrophic lateral sclerosis. Following this, the authors discuss recent studies that offer a new perspective on sensory networks in motor neuron diseases to understand the true extent and patophysiology of amyotrophic lateral sclerosis and suggest new potential biomarkers for the diagnosis of this tragic disease. The closing study focuses on the respiratory involvement of amyotrophic lateral sclerosis, which is the principal cause of death. Amyotrophic lateral sclerosis is characterized by respiratory failure consequent to respiratory muscles dysfunction, as well as bulbar muscles which support the upper airways, developing in dyspnoea and impaired sleep--
  als and occupational therapy: Integrative and Functional Medical Nutrition Therapy Diana Noland, Jeanne A. Drisko, Leigh Wagner, 2020-03-27 This textbook is a practical guide to the application of the philosophy and principles of Integrative and Functional Medical Nutrition Therapy (IFMNT) in the practice of medicine, and the key role nutrition plays in restoring and maintaining wellness. The textbook provides an overview of recent reviews and studies of physiological and biochemical contributions to IFMNT and address nutritional influences in human heath overall, including poor nutrition, genomics, environmental toxicant exposures, fractured human interactions, limited physical movement, stress, sleep deprivation, and other lifestyle factors. Ultimately, this textbook serves to help practitioners, healthcare systems, and policy makers better understand this different and novel approach to complex chronic disorders. It provides the reader with real world examples of applications of the underlying principles and practices of integrative/functional nutrition therapies and presents the most up-to-date intervention strategies and clinical tools to help the reader keep abreast of developments in this emerging specialty field. Many chapters include comprehensive coverage of the topic and clinical applications with supplementary learning features such as case studies, take-home messages, patient and practitioner handouts, algorithms, and suggested readings. Integrative and Functional Medical Nutrition Therapy: Principles and Practices will serve as an invaluable guide for healthcare professionals in their clinical application of nutrition, lifestyle assessment, and intervention for each unique, individual patient.
  als and occupational therapy: Neurological Rehabilitation - E-Book Darcy Ann Umphred, Rolando T. Lazaro, Margaret Roller, Gordon Burton, 2013-08-07 Using a problem-solving approach based on clinical evidence, Neurological Rehabilitation, 6th Edition covers the therapeutic management of people with functional movement limitations and quality of life issues following a neurological event. It reviews basic theory and covers the latest screening and diagnostic tests, new treatments, and interventions commonly used in today's clinical practice. This edition includes the latest advances in neuroscience, adding new chapters on neuroimaging and clinical tools such as virtual reality, robotics, and gaming. Written by respected clinician and physical therapy expert Darcy Umphred, this classic neurology text provides problem-solving strategies that are key to individualized, effective care. UNIQUE! Emerging topics are covered in detail, including chapters such as Movement Development Across the Lifespan, Health and Wellness: The Beginning of the Paradigm, Documentation, and Cardiopulmonary Interactions. UNIQUE! A section on neurological problems accompanying specific system problems includes hot topics such as poor vision, pelvic floor dysfunction, and pain. A problem-solving approach helps you apply your knowledge to examinations, evaluations, prognoses, and intervention strategies. Evidence-based research sets up best practices, covering topics such as the theory of neurologic rehabilitation, screening and diagnostic tests, treatments and interventions, and the patient's psychosocial concerns Information. Case studies use real-world examples to promote problem-solving skills. Non-traditional approaches to neurological interventions in the Alternative and Complementary Therapies chapter include the movement approach, energy approach, and physical body system approaches therapies. Terminology adheres to the best practices of the APTA as well as other leading physical therapy organizations, following The Guide to Physical Therapy Practice, the Nagi model, and the ICF World Health Model of patient empowerment. Updated illustrations provide current visual references. NEW chapters on imaging and robotics have been added. Updated chapters incorporate the latest advances and the newest information in neuroscience and intervention strategies. Student resources on an Evolve companion website include references with links to MEDLINE and more.
  als and occupational therapy: Neurological Rehabilitation Darcy Ann Umphred, PT, PhD, FAPTA, Rolando T. Lazaro, PT, PhD, DPT, 2012-08-14 Using a problem-solving approach based on clinical evidence, Neurological Rehabilitation, 6th Edition covers the therapeutic management of people with functional movement limitations and quality of life issues following a neurological event. It reviews basic theory and covers the latest screening and diagnostic tests, new treatments, and interventions commonly used in today's clinical practice. This edition includes the latest advances in neuroscience, adding new chapters on neuroimaging and clinical tools such as virtual reality, robotics, and gaming. Written by respected clinician and physical therapy expert Darcy Umphred, this classic neurology text provides problem-solving strategies that are key to individualized, effective care. UNIQUE! Emerging topics are covered in detail, including chapters such as Movement Development Across the Lifespan, Health and Wellness: The Beginning of the Paradigm, Documentation, and Cardiopulmonary Interactions. UNIQUE! A section on neurological problems accompanying specific system problems includes hot topics such as poor vision, pelvic floor dysfunction, and pain. A problem-solving approach helps you apply your knowledge to examinations, evaluations, prognoses, and intervention strategies. Evidence-based research sets up best practices, covering topics such as the theory of neurologic rehabilitation, screening and diagnostic tests, treatments and interventions, and the patient's psychosocial concerns Information. Case studies use real-world examples to promote problem-solving skills. Non-traditional approaches to neurological interventions in the Alternative and Complementary Therapies chapter include the movement approach, energy approach, and physical body system approaches therapies. Terminology adheres to the best practices of the APTA as well as other leading physical therapy organizations, following The Guide to Physical Therapy Practice, the Nagi model, and the ICF World Health Model of patient empowerment. Updated illustrations provide current visual references. NEW chapters on imaging and robotics have been added. Updated chapters incorporate the latest advances and the newest information in neuroscience and intervention strategies. Student resources on an Evolve companion website include references with links to MEDLINE and more.
  als and occupational therapy: Building Blocks for Learning Occupational Therapy Approaches Jill Jenkinson, Tessa Hyde, Saffia Ahmad, 2008-11-20 Building Blocks for Learning Occupational Therapy Approaches is a resource book for educational staff and pediatric occupational therapists, especially those new to the field. It shows how the implications of physical, psychological, social, and learning difficulties impact upon children’s abilities. This highly practical book will help readers recognize when a student’s poor performance within the classroom is a result of a medical condition or underlying motor and perceptual deficits.
  als and occupational therapy: Amyotrophic Lateral Sclerosis Francesco Pagnini, Zachary Simmons, 2018-02-09 Amyotrophic Lateral Sclerosis (ALS) is a devastating neurodegenerative disorder with a progressive and fatal course, with no known medical therapies that can reverse the disease or halt its progression. Palliative care is the mainstay of disease management, aimed at maximizing Quality Of Life (QOL) for the patient and caregiver. Clinicians caring for patients with ALS need to understand complex psychological issues in the patient and caregiver, including depression, anxiety, hopelessness, and wish for hastened death (physician-assisted suicide). They also need to confront the psychological implications of rapidly advancing genetic research, the impact of cognitive and behavioural dysfunction in a sizable minority of ALS patients, and caregiver burnout. Healthcare providers can optimize care by better understanding not only these factors, but by learning how to facilitate their management with problem-solving, coping techniques, and with psychologically-based approaches such as mindfulness and other non-pharmacological approaches aimed at maximizing QOL. Amyotrophic Lateral Sclerosis: Understanding and Optimizing Quality of Life and Psychological Well-Being provides a detailed review and evaluation of ALS, presented in a comprehensive and integrated fashion. The book achieves this through detailed and up-to-date information about the current state of knowledge in this field. It also offers new insights regarding future directions for research. This book will provide clinicians with a comprehensive description of the psychological aspects of ALS and their management, and incorporates chapters written by recognized scholars in their respective fields.
Amyotrophic lateral sclerosis (ALS) - Symptoms and causes
Apr 10, 2024 · Amyotrophic lateral sclerosis (a-my-o-TROE-fik LAT-ur-ul skluh-ROE-sis), known as ALS, is a nervous system disease that affects nerve cells in the brain and spinal cord. ALS …

Amyotrophic lateral sclerosis (ALS) - Diagnosis and treatment
Apr 10, 2024 · Amyotrophic lateral sclerosis, known as ALS, can be hard to diagnose early because it can have symptoms similar to other diseases. Tests to rule out other conditions or …

Esclerosis lateral amiotrófica - Síntomas y causas - Mayo Clinic
Apr 10, 2024 · Amyotrophic lateral sclerosis (ALS) fact sheet. National Institute of Neurological Disorders and Stroke. https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact …

肌萎缩侧索硬化症（ALS） - 症状与病因 - 妙佑医疗国际
Apr 10, 2024 · 肌萎缩侧索硬化症（简称 als）是一种神经系统疾病，可累及大脑和脊髓中的神经细胞。als 会导致肌肉失去控制。这种疾病会日渐恶化。 als 也常被称为卢贾里格症，卢·贾里格 …

التصلب الجانبي الضموري (ALS) - Mayo Clinic
أثناء تفاقم المرض، يتسبب التصلب الجانبي الضموري als في حدوث مضاعفات، مثل: مشكلات التنفس. يؤدي التصلب الجانبي الضموري مع مرور الوقت إلى ضعف العضلات التي يستخدمها الجسم في التنفس.

Amyotrophic Lateral Sclerosis - Overview - Mayo Clinic
Mar 22, 2025 · People who seek diagnosis or treatment with the doctors of the amyotrophic lateral sclerosis, also called ALS, specialty group receive comprehensive care. Your care team might …

Science Saturday: How regenerative medicine is advancing ALS …
May 29, 2021 · May is ALS Awareness Month, a time to reflect on the role of regenerative medicine research in advancing understanding and treatment of amyotrophic lateral sclerosis …

Amyotrophic lateral sclerosis (ALS) - Care at Mayo Clinic
Apr 10, 2024 · ALS clinics are part of all three Mayo Clinic campuses in Arizona, Florida and Minnesota. They have all been designated Certified Treatment Centers of Excellence by the …

Amyotrophic lateral sclerosis (ALS) - Doctors and departments
Apr 10, 2024 · Mayo Clinic is on the forefront of researching a cure for ALS. Researchers at Mayo Clinic study the possible causes of ALS . This includes identifying biomarkers in blood and …

Mayo Clinic awarded federal grant to study experimental ALS drug
Sep 24, 2024 · Mayo Clinic in Florida has received a grant to begin an innovative study that will provide hundreds of patients with amyotrophic lateral sclerosis (ALS) access to an …

Amyotrophic lateral sclerosis (ALS) - Symptoms and causes
Apr 10, 2024 · Amyotrophic lateral sclerosis (a-my-o-TROE-fik LAT-ur-ul skluh-ROE-sis), known as ALS, is a nervous system disease that affects nerve cells in the brain and spinal cord. ALS …

Amyotrophic lateral sclerosis (ALS) - Diagnosis and treatment
Apr 10, 2024 · Amyotrophic lateral sclerosis, known as ALS, can be hard to diagnose early because it can have symptoms similar to other diseases. Tests to rule out other conditions or …

Esclerosis lateral amiotrófica - Síntomas y causas - Mayo Clinic
Apr 10, 2024 · Amyotrophic lateral sclerosis (ALS) fact sheet. National Institute of Neurological Disorders and Stroke. https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact …

肌萎缩侧索硬化症（ALS） - 症状与病因 - 妙佑医疗国际
Apr 10, 2024 · 肌萎缩侧索硬化症（简称 als）是一种神经系统疾病，可累及大脑和脊髓中的神经细胞。als 会导致肌肉失去控制。这种疾病会日渐恶化。 als 也常被称为卢贾里格症，卢·贾里格 …

التصلب الجانبي الضموري (ALS) - Mayo Clinic
أثناء تفاقم المرض، يتسبب التصلب الجانبي الضموري als في حدوث مضاعفات، مثل: مشكلات التنفس. يؤدي التصلب الجانبي الضموري مع مرور الوقت إلى ضعف العضلات التي يستخدمها الجسم في التنفس.

Amyotrophic Lateral Sclerosis - Overview - Mayo Clinic
Mar 22, 2025 · People who seek diagnosis or treatment with the doctors of the amyotrophic lateral sclerosis, also called ALS, specialty group receive comprehensive care. Your care team might …

Science Saturday: How regenerative medicine is advancing ALS …
May 29, 2021 · May is ALS Awareness Month, a time to reflect on the role of regenerative medicine research in advancing understanding and treatment of amyotrophic lateral sclerosis …

Amyotrophic lateral sclerosis (ALS) - Care at Mayo Clinic
Apr 10, 2024 · ALS clinics are part of all three Mayo Clinic campuses in Arizona, Florida and Minnesota. They have all been designated Certified Treatment Centers of Excellence by the …

Amyotrophic lateral sclerosis (ALS) - Doctors and departments
Apr 10, 2024 · Mayo Clinic is on the forefront of researching a cure for ALS. Researchers at Mayo Clinic study the possible causes of ALS . This includes identifying biomarkers in blood and …

Mayo Clinic awarded federal grant to study experimental ALS drug
Sep 24, 2024 · Mayo Clinic in Florida has received a grant to begin an innovative study that will provide hundreds of patients with amyotrophic lateral sclerosis (ALS) access to an …