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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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"The GPs unfortunately don't have enough knowledge about Duchenne." Satish's son Vinny lives with Duchenne muscular dystrophy. Together, they've felt the impact of a lack of understanding about the condition across healthcare professionals. This includes poor communication between hospitals and GPs, medical equipment not suitable for Vinny's wheelchair, and inaccessible transport between appointments. Learn more about Satish & Vinny's story 👇 | Muscular Dystrophy UK
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