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

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

Advancements & Challenges in Muscular Dystrophy Treatment | AJMC