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HelpSAM.info - Help S.A.M. - The Struggle Against Muscular Dystrophy
Cure CMD is a nonprofit organization dedicated to curing Congenital Muscular Dystrophy by advancing research and empowering families.
Duchenne Muscular Dystrophy - Jesse's Journey - The Foundation for Gene and Cell Therapy provides funding for research into Duchenne Muscular Dystrophy. This charitable organization targets neuromuscular diseases like Duchenne MD through research in gene therapy, cell therapy and genetics.
Neuromuscular disease is rare compared with other disease s. Three or four persons in 100.000 inhabitants live for example with the muscle dystrophy
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5, 000 boys.
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.
The world's largest research-focused patient advocacy group for facioscapulohumeral muscular dystrophy (FSHD). Accelerating therapies and empowering individuals and families since 1991.
Stan Kearey, a Muscular Dystrophy sufferer, lives with his lovely wife Pauline, at the foot of Mount Ponoch outside the idyllic and ancient village of Polop de la Marina on the SE coast of Spain.
ALS, Motor Neuron disease, muscular dystrophy, muscular gravis, multiple sclerosis, syringomyelia, progressive spinal muscular atrophy(SMA), amyotrophic lateral sclerosis (ALS)
Circa 1988, Endless Pools is the world leader in swimming pools for exercise, therapy & fun, with thousands of swimming pools in over 100 countries.
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
Scoliosisspecialists.com scoliosis Care Centers offer non-surgical solutions for children and adults with scoliosis including Idiopathic Exercises, and the Spinecor Brace designed to help ease the pain of a curved spine.
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling 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.
We provide care and support for people affected by muscle-wasting conditions, fund vital research and campaign for better services
www.disableddatingonline.comDisabledDatingOnline.com - the ultimate singles club for disabled bodied singles to make dates and friends
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!
Parent Project Muscular Dystrophy's mission is to end Duchenne muscular dystrophy. We accelerate research, raise our voices in Washington, demand optimal care for all young men, and educate the global community.
WiViK on-screen keyboard (virtual keyboard) software is an assistive technology that can help persons such as those with spinal cord injuries, ALS, muscular dystrophy, and cerebral palsy who cannot use a standard computer keyboard.