MDA Advocate John Gaudet shares his personal story about how inaccessible air travel affected his life and urges Congress to take action by passing the Air Carrier Access Amendments Act.…
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Muscular Dystrophy Association
MDA Advocate Amy Shinneman invites us home to show appreciation for her caregiver husband, Jamie. Thank you to all our caregivers at MDA #NationalCaregiversMonth #MuscularDystrophy #ALS #neuromuscular. Source Muscular Dystrophy…
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Award-winning singer-songwriter and host on the ABC hit “Rising Star” Brad Paisley introduces us to JoeJoe and Dominik Stoop, ages 5 and 3, of Los Angeles, have been diagnosed as…
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Justin Moy, 12, is from Concord, Mass., and enjoys singing, swimming, playing video games and collecting coins. He also loves studying science. He is affected with congenital muscular dystrophy (CMD).…
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Reagan Imhoff of New Berlin, Wis., has spinal muscular atrophy (SMA), a genetic disease affecting the part of the nervous system that controls voluntary muscle movement. Her spirit and enthusiasm…
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#MDA #Hill Day #AccessibleAirTravel – advocate to make air travel accessible at MDA.org/AirTravel Source Muscular Dystrophy Association YouTube
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MDA Team Momentum member Chris Benyo talks about his wife, Denise, who he honored while running the Chicago Bank of America Marathon in 2016. Learn more about Team Momentum at…
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#MDA #SummerCamp – Zach’s ‘Note to Self’ Source Muscular Dystrophy Association YouTube
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May is ALS Awareness Month and MDA’s funding of research and care is striving to unlock the cure for this disease. Hear from the leading experts in the United States…
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Meet Faith, a 7-year-old girl from Waco, TX, who lives with Spinal Muscular Atrophy (SMA) type 2 and is MDA’s National Ambassador. Today, Faith is currently receiving and benefitting from…
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