Leiden Muscular Dystrophy Pages
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.
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.
Leading experts in cardiovascular care Rush offers comprehensive, multispecialty care for adults with cardiovascular disease, including the following conditions: Our experts, including cardiologists, cardiac surgeons, interventional cardiologists, electrophysiologists and nurse practitioners, specialize in providing accurate diagnosis and personalized cardiovascular disease treatment. They offer a full range of treatment options, including the following: And thanks to Rush's commitment to advancing cardiov
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
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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.
Children's Dentist Sacramento Carmichael Citrus Heights Fair Oaks is a pediatric dentist in Sacramento, California, dedicated to serving the special needs
Pharmaceutical company in Switzerland committed to research & development of medicines for patients living with mitochondrial disorders & rare diseases.
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.
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 - 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.
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
We provide care and support for people affected by muscle-wasting conditions, fund vital research and campaign for better services
Circa 1988, Endless Pools is the world leader in swimming pools for exercise, therapy & fun, with thousands of swimming pools in over 100 countries.
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.
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