Cure Duchenne Muscular Dystrophy - CureDuchenne - CureDuchenne
CureDuchenne's mission - cure Duchenne muscular dystrophy (DMD). Our venture philanthropy model funds research, early diagnosis, treatment
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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.
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Duchenne San Diego :. Non-Profit Charity for the Benefit of Duchenne Muscular Dystrophy
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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.
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.
Cure CMD's mission is to advance research toward treatments for the congenital muscular dystrophies and improve the lives of those living with CMD through engagement and support of our community.
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
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FSH Muscular Dystrophy (FSHD) is a disease that causes the progressive deterioration of skeletal muscle, robbing people of the healthy, independent years of their lives. The main diagnostic features of the condition are loss of muscle in the Face, Scapula, and Humerus (arm). In the medical literature the disease is referred to as facioscapulohumeral muscular dystrophy; however, we simply refer to the disease as FSHD (sometimes shortened to FSH), since muscle loss is not limited to the face, scapula, and hu
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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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Families Supporting Families You are not alone. Whether you are dealing with a new diagnosis of Duchenne Muscular Dystrophy (DMD), or are further along in the journey, the Duchenne Family Support Group is here for you. Our helpline: 0800 121 4518 The DFSG is a UK national charity, run by families for families affected by
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