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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.
Our kids our nation is an exquisite coffee table book that features our Australian children. It is a unique fundraising project for Muscular Dystrophy Australia. Children from newborn to 15 years old will be professionally photographed by an accredited photographer. One of the images taken of your child will be guaranteed to appear in this book.
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.
We provide care and support for people affected by muscle-wasting conditions, fund vital research and campaign for better services
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.
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.
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.
Pharmaceutical company in Switzerland committed to research & development of medicines for patients living with mitochondrial disorders & rare diseases.
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
Medical, biomedical, disease, therapy, treatment, diagnosis, drug, clinical trial, pharmaceutical, biotechnology, medical devices, and life sciences research discoveries and news.
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.
UNIQUE assistive technology innovations EMPOWERING through INDEPENDENCE Quadriplegics, Muscular Dystrophy, Cerebral Palsy, ALS - Lou Gehrig's Disease, Multiple Sclerosis, Tramatic Brain Injury, & Stroke - disabled wheelchair users with limited dexterity or no use of their hands and arms
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
What is ALS Disease, ALS Symptoms, Amyotrophic Lateral Sclerosis, Motor Neuron Disease. ALS Disease Information, News and Facts. Find Symptoms and Cure for Motor Neuron Disorder, Autoimmune Disease that can cause Muscular Dystrophy.
ALS, Motor Neuron disease, muscular dystrophy, muscular gravis, multiple sclerosis, syringomyelia, progressive spinal muscular atrophy(SMA), amyotrophic lateral sclerosis (ALS)