Websites using duchenne muscular dystrophy (dmd) as a keyword

Duchenne Muscular Dystrophy non Profit

Enter the website of the Nash Avery Foundation. Committed to the destruction of Duchenne Muscular Dystrophy.

Learn about Duchenne Muscular Dystrophy and stay connected with the DMD community. Understanding the signs, symptoms & diagnosis is difficult. Learn more here.

The Duchenne Family Support Group (DFSG) exists to provide support for families with children diagnosed as having Duchenne Muscular Dystrophy (DMD). The DFSG is a national charity run by families for families affected by DMD. It provides a positive national support network of parents, their families and professionals. The DFSG helps bring families together for mutual support, sharing of information and experience, and social activities and has been doing so since 1987.

FDMD are aggressively raising money for Duchenne Muscular Dystrophy research. Our hope is to find a cure for this horrible disease.

Learn more about what DMD is, and understand why lung function is important for people living with DMD, including respiratory symptoms, management & care.

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.

Jack has Duchenne Muscular Dystrophy, DMD. There is no cure at the moment. We're raising money to fund research to find effective treatments

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Duchenne Muscular Dystrophy (DMD) – A degenerative disease of the muscles for which there is no treatment. The Force DMD Foundation’s are here to help.