Muscular dystrophy, it's causes and treatment
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MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
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.
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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!
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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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The Neurology Muscular Dystrophy and Neuropathy Institute, headed by Doctor Natan Shaoulian, The Nerve MD. USC trained, Dr. Shaoulian is a board certified Neurologist subspecializing in neuromuscular disorders. Located in Beverly Hills California
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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Join the Muscular Diseases Awareness platform's fight against muscle diseases. What muscle diseases are there? Find out this & more inside.
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.
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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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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