Muscular Dystrophy Charity | Muscle Help Foundation
Small national charity delivering life-changing, transformational experiences in the UK for children and young people with Muscular Dystrophy
Language: English
MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
FDMD are aggressively raising money for Duchenne Muscular Dystrophy research. Our hope is to find a cure for this horrible disease.
The mission of Grampy's Charities is to raise funds and support for children's organizations. It is our hope that by partnering with comfort and research based charities we will be able to make a difference in the lives of kids who need us most.
On this website, you can learn more about neurologists and their work by reading the many blog posts we share. Read on to learn more!
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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.
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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!
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
Pharmaceutical company in Switzerland committed to research & development of medicines for patients living with mitochondrial disorders & rare diseases.
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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
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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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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.
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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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