The Muscular Dystrophy Association is proud to celebrate 75 years of groundbreaking progress in research, care, and advocacy for people living with neuromuscular diseases. 💙💛 Watch our new PSA, Legacy. Impact. Momentum., honoring the families, researchers, clinicians, advocates, volunteers, partners and donors who’ve made these achievements possible. Learn more at MDA75.org #MDA75 #RareDiseaseDay #MuscularDystrophy #ALS #Neuromuscular
MDA is dedicated to advocating for policies and programs that empower families living with neuromuscular diseases by accelerating the development of therapies and treatments, facilitating early diagnosis, ensuring access to critical support, and urging lawmakers to pass policies that increase independence for people living with disabilities. Join us and raise your voice today at: https://www.votervoice.net/MDA/home
MDA is dedicated to advocating for policies and programs that empower families living with neuromuscular diseases by accelerating the development of therapies and treatments, facilitating early diagnosis, ensuring access to critical support, and urging lawmakers to pass policies that increase independence for people living with disabilities. Join us and raise your voice today at: https://www.votervoice.net/MDA/home

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