We transform the lives of people living with muscular dystrophy, ALS and related neuromuscular diseases.
What We Do
腾博网址Since 1950, we've spearheaded efforts to transform the lives of people with muscular dystrophy, ALS, and related neuromuscular diseases. We fund groundbreaking research for promising treatments and provide families with the highest quality care from the best doctors in the country.
The freedom to walk, to talk, to run and play. To laugh, to hug, to eat — even breathe.
Each day these freedoms are taken away from kids and adults with muscular dystrophy, ALS and related diseases that weaken muscle strength and limit mobility. Together we can change that.About Neuromuscular Diseases
How You Can Help
Whether you’re looking to volunteer at a camp or a local office, organize a group of friends to fundraise, run a marathon, or advocate for the cause, the ways to get involved are endless.Ways to Get Involved
For the latest happenings in the MDA community and to read inspiring stories, browse the MDA blog.
Researchers Look to Treat Genetic Disease at its SourceRead More
Register Now to Attend MDA’s Public Policy and Advocacy ConferenceRead More
US House Passes Newborn Screening ReauthorizationRead More
Burn Boot Camp Bands Together for MDARead More
Meet Our Partners
腾博网址These friends are helping give strength to MDA families.
腾博网址Sign up to receive email updates on volunteer opportunities and the impact you’re making for families.
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 services are only available in the U.S.