Visit MDA.org/Vote for essential information on polling place accessibility, voting options, and voter rights for people living with disabilities.

Mission Statement

Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and related neuromuscular diseases. For over 70 years, MDA has led the way in accelerating research, advancing care, and advocating for the support of our families.

MDA's mission is to empower the people we serve to live longer, more independent lives.

Our History

Connect. Support. Empower.

Since 1950, MDA has been the leading philanthropic organization in advancing understanding and treatment of neuromuscular diseases, driving breakthroughs in genetics, diagnostics, and therapies. Our legacy includes ensuring that people living with neuromuscular disease have access to exceptional care from day one of their diagnosis onward, advocating for inclusion, autonomy, and supporting our community through comprehensive educational resources. Through vibrant community programs, we foster deep connections and empower people living with neuromuscular disease to experience the world in the way that they want to, turning challenges into triumphs. Read more about MDA's journey and the progress we've helped make possible.

Your Impact

 

Your Impact

 

Your Impact

 

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Be In the Know

MDA uses every dollar we raise wisely to ensure it has the greatest impact in the fight to end muscular dystrophy. We strive to provide you with transparency and clarity around how contributions make a difference and how MDA is supporting your community. Learn more below.

MDA Resource Center: We’re Here For You

Our trained specialists are here to provide one-on-one support for every part of your journey. Send a message below or call us at 1-833-ASK-MDA1 (1-833-275-6321). If you live outside the U.S., we may be able to connect you to muscular dystrophy groups in your area, but MDA programs are only available in the U.S.

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