Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
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.
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
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.
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.
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
Neuromuscular disease is rare compared with other disease s. Three or four persons in 100.000 inhabitants live for example with the muscle dystrophy
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
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.
Circa 1988, Endless Pools is the world leader in swimming pools for exercise, therapy & fun, with thousands of swimming pools in over 100 countries.
We provide care and support for people affected by muscle-wasting conditions, fund vital research and campaign for better services
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
Inspire connects patients, families, friends, caregivers and health professionals for health and wellness support. Connect with others who know what you're going through.