Be a light of hope this holiday season. Ignite more progress, restore more freedom, and inspire more hope for families living with neuromuscular disease.

About Us

Our mission is to empower people living with neuromuscular diseases to live longer, more independent lives.

Honors and Awards

Muscular Dystrophy Association (MDA) is proud to be at the forefront of research, care, and advocacy for people living with muscular dystrophy, ALS (aka Lou Gehrig’s disease) and over 300 related neuromuscular diseases. Our ongoing commitment for nearly 75 years includes accelerating scientific breakthroughs, advancing care, and advocating for access for people living with disabilities. From the MDA Resource Center and Gene Therapy Support Network, to over 150 MDA Care Center’s at the nation’s top healthcare institutions, to MDA Summer Camp, and recreational and educational programming for professionals and families, MDA has earned awards and recognition in all areas of our organization.

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