Organizations Support Duchenne Muscular Dystrophy

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Directory of Duchenne Muscular Dystrophy Resources ...

    https://www.duchenne.com/resources
    The Duchenne community is inspiring and supportive. There are many helpful resources and organizations to support families living with Duchenne. Here are just a few to get you started. Sarepta does not endorse nor is responsible for the content of any of the listed websites or the services provided by these organizations. This is not a complete list of available websites.

Organizations: Are there good support groups for Duchenne ...

    https://www.thinkgenetic.com/diseases/duchenne-and-becker-muscular-dystrophy/organizations/7809
    There are many support groups or organizations for Duchenne muscular dystrophy that provide support, information, advice, referrals to physicians and medical centers, and up-to-date information on research and treatments. Many of these groups also fund research.

The Foundation to Eradicate Duchenne – Working for a Cure!

    https://duchennemd.org/
    Duchenne Muscular Dystrophy is a relentless, cruel disease. It is the world’s #1 lethal childhood genetic disorder. The Foundation to Eradicate Duchenne (FED) exists to fund scientific research for treatments for today’s generation of boys and young men who suffer from Duchenne.

Request Services Muscular Dystrophy Association

    https://www.mda.org/care/request-services
    To request services or support, please complete this short form and one of our trained MDA Resource Specialists will contact you. Or, call us directly at 1-833-ASK-MDA1 (1-833-275-6321). If you live outside the U.S., we may be able to connect you to muscular dystrophy groups in your area, but MDA services are only available in the U.S.

Duchenne Muscular Dystrophy - TREAT-NMD

    https://treat-nmd.org/treat-nmd-diseases/duchenne-muscular-dystrophy/
    Duchenne muscular dystrophy or DMD is the most common of the muscular dystrophies, affecting approximately 1 in every 3,500 newborn boys. It is caused by a fault in a gene called the dystrophin or DMD gene. A fault in this gene stops the body making a protein called dystrophin.



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