Advocacy Partner: Muscular Dystrophy Association
About the Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and over 300 related neuromuscular conditions. For nearly 75 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.
Muscular Dystrophy Association supports research, care, and advocacy for Friedreich’s ataxia.
For support, guidance, and resources please visit: MDA Resource Center
By Phone:Â 1-833-ASK-MDA1 (1-833-275-6321)
By Email:Â [email protected]
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About Advocacy Partners
The information above is provided by our partner. Learn more about our advocacy partners here.
Recent Posts
- There are many heroes in the FA community, and they all inspire me
- My message for other parents this National ‘FAmily’ Caregivers Month
- I’m Kendall, and I’m more than just my Friedreich’s ataxia diagnosis
- FA treatment shows potential to protect nerve cells
- Guest Voice: FA might slow me down, but my future is still bright
