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Duchenne Muscular Dystrophy non Profit
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FDMD are aggressively raising money for Duchenne Muscular Dystrophy research. Our hope is to find a cure for this horrible disease.
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
Angels for Isaac works to educate the public about Duchenne Muscular Dystrophy and how they can help in our fight to find a cure. We have kicked off our 2014 RZR Raffle. Purchase your ticket to help us put an END to Duchenne Muscular Dystrophy, a terminal muscle wasting disease with no treatment and no cure!
Official Dwellingup 100 MTB & Mighty Jarrah Trail Run event website.
Associació Catalana de Persones amb Malalties Neuromusculars. Atenció individual i familiar a persones amb Duchenne, Atrofia Espinal, Steinert, Charcot Marie Tooth, Miastenia,
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Parent Project Muscular Dystrophy (PPMD) fights to end Duchenne muscular dystrophy. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
Pharmaceutical company in Switzerland committed to research & development of medicines for patients living with mitochondrial disorders & rare diseases.
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Harrison's Fund - The Duchenne Mental Health Charity and home of the Chrysalis Grant, giving potential access to private psychological and mental health support to newly diagnosed parents, patients and families living with Duchenne Muscular Dystrophy.
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