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The Muscular Dystrophy Association is proud to share that the recently passed FAA reauthorization law includes significant reforms aimed at improving the air travel experience for passengers with disabilities. These changes will help provide a safer and more dignified air travel experience, making air travel more inclusive for everyone. To celebrate this milestone, MDA reconnected with advocates Mindy Henderson and Madison Lawson to get their thoughts on what this legislation means for accessibl
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Today, on World Health Day, the Muscular Dystrophy Association reaffirms our commitment to ensuring that every person we serve who lives with a neuromuscular disease—has equitable access to healthcare. We believe that access to lifesaving treatments, specialized care, and groundbreaking research is not a privilege but a right. Together, we are driving real change, but there is more work to be done. Join us in making a difference: MDA.org/Advocacy | Muscular Dystrophy Association
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We are so grateful to Ethan LyBrand, who lives with Duchenne muscular dystrophy, for serving in his role as MDA National Ambassador for the last three years. Ethan has brought so much joy as he raised awareness and funds for MDA to empower all families living with neuromuscular disease. Let’s take a look back at some of the laughs he gave us along the way in his series “Joke of the Day for MDA”! Thank you, Ethan! | Muscular Dystrophy Association
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