Parent Project Muscular Dystrophy (PPMD) | Fighting to End Duchenne
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.
Neuromuscular disease is rare compared with other disease s. Three or four persons in 100.000 inhabitants live for example with the muscle dystrophy
Pharmaceutical company in Switzerland committed to research & development of medicines for patients living with mitochondrial disorders & rare diseases.
We provide care and support for people affected by muscle-wasting conditions, fund vital research and campaign for better services
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.
A one-day, nationwide event designed to raise awareness about Duchenne muscular dystrophy . We need your help to stop this devastating disorder.
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.
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Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5, 000 boys.
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
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.
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
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.
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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
Children's Dentist Sacramento Carmichael Citrus Heights Fair Oaks is a pediatric dentist in Sacramento, California, dedicated to serving the special needs
ALS, Motor Neuron disease, muscular dystrophy, muscular gravis, multiple sclerosis, syringomyelia, progressive spinal muscular atrophy(SMA), amyotrophic lateral sclerosis (ALS)
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.