Annual campaign gives shoppers an opportunity to turn everyday purchases into meaningful impact for people living with muscular dystrophy, ALS and related neuromuscular diseases. NEW YORK – Wednesday, ...
The Muscular Dystrophy Association applauds the United States Senate for passing the House’s version of the ACT for ALS ...
A weekend to recharge, connect, and make memories—together. Family Getaways provide a unique recreation experience that promotes fun, independence, and adventure for individuals living with ...
MDA Virtual Summer camp provides an engaging and meaningful experience for kids and young adults who prefer to experience the joys of Camp from the comfort of their homes. Outfitted with a Supply Kit ...
The 26th Annual MDA Wings Over Wall Street Gala to Benefit ALS Research will take place on Thursday, June 4, hosted by Bill Ritter, ABC7 New York Eyewitness News. Dr. Merit Cudkowicz with Tim Green ...
The MDA Muscle Walk is an inspiring event that unites communities throughout the country behind the mission to empower people living with neuromuscular diseases to live life to the fullest potential.
Multidisciplinary care, including neuromuscular, cardiac, respiratory, endocrine, endocrinologic, nutritional, psychosocial, and orthopedic management, is recommended for people with DMD in order to ...
Join leading clinicians and researchers at MDA’s Clinical & Scientific Conference, March 8–11, 2026, in Orlando, FL. Learn more and register for the world’s most talked-about gathering of leading ...
Join us for a powerful and informative webinar focused on the unique needs and challenges of weight management with neuromuscular disease. Whether you're a patient, caregiver, or advocate, this ...
CHICAGO, August 20, 2017 — The Muscular Dystrophy Association is deeply saddened by the death of beloved comedian, performer, humanitarian and former MDA telethon star and national chairman Jerry ...
Transition from Pediatric to Adult Care in Muscular Dystrophies: DMD, LGMD, FSHD, Myotonic Dystrophy
The transition from pediatric to adult care is a challenging time for patients with neuromuscular disease and their families, as well as for providers. Increased use of disease-modifying treatments ...
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