A message from Donald S. Wood, PhD, President and CEO
Rare neuromuscular diseases stand as some of the most challenging puzzles in science and medicine today. The rare nature of progressive muscle disease like muscular dystrophies, spinal muscular atrophy, ALS, and Pompe, coupled with corresponding gaps in public awareness and scientific investment, can present obstacles to research and access to treatments. But at the Muscular Dystrophy Association (MDA), thanks to your support, we're tackling these challenges head-on and we’re seeing results!
Our work has led to historic advancements in genetic research, improved diagnostic methods, multidisciplinary care, and the development of groundbreaking therapies that once seemed beyond reach. These scientific discoveries have wide-reaching applications for other more commonplace diseases and conditions, affecting millions of people across the globe.
Together, we can surge past the limits of yesterday's understanding and treatments. It’s your commitment, involvement, and support that are the forces that drive us forward. Thank you for your dedication to people living with neuromuscular diseases and to MDA’s mission.
Mission Statement
The Muscular Dystrophy Association’s mission is to empower the people we serve to live longer, more independent lives.
MDA is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and over 300 other neuromuscular conditions. For 75 years, MDA has led the way in accelerating research, advancing care, and advocating support and inclusion of families living with neuromuscular disease.
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Accelerating Scientific Discovery and Breakthroughs
Transforming research into real world treatment and therapies.
Explore the Science -
Access to Comprehensive Care and Resources
Redefining what it means to live with neuromuscular disease.
Experience the Care -
75 Years
of Progress and ImpactOne community. A world of impact.
Our History
75 years and counting.
Neuromuscular diseases take away abilities many of us take for granted— moving, speaking, eating, even breathing.
At MDA, we’re funding innovative research that leads to real world treatments, changing the landscape for people living with these conditions. We also provide access to expert care, trusted resources and a supportive community, empowering people living with neuromuscular disease to live longer, stronger and on their own terms.
About Neuromuscular DiseasesGet Involved
There are many ways to get involved with MDA. Whether you’re looking to create a fundraiser, host a game night, volunteer at a camp, run a marathon, or advocate for the cause, the ways to get involved are endless.
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Start a Fundraiser
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Become a Volunteer
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Start Your Monthly Gift of $19 today
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MDA Let's Play
for a Cure -
Advocate for MDA
Latest Stories
For the latest happenings in the MDA community and to read inspiring stories, browse the MDA blog.
Press Releases
Meet Our Partners
These partners are empowering lives through science and care for MDA families.
Join Us
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 programs are only available in the U.S.
