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.
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.
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
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
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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.
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.
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5, 000 boys.
Misty Vanderweele grows premium Dahlias, Sweetpeas, Sunflowers/ other cut flower varieties. Dedicated to providing long-lasting vibrant arrangements & bouquets.
Neuromuscular disease is rare compared with other disease s. Three or four persons in 100.000 inhabitants live for example with the muscle dystrophy
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.
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
Circa 1988, Endless Pools is the world leader in swimming pools for exercise, therapy & fun, with thousands of swimming pools in over 100 countries.
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.
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