Searching for Duchenne Muscular Dystrophy Support Services information? Find all needed info by using official links provided below.
https://www.jessesjourney.com/family-support-resources/
Duchenne Muscular Dystrophy Treatment & Support Josh and Amy Cavalier, with their sons Liam and Kaleb If someone in your family has been diagnosed with Duchenne muscular dystrophy your first instinct will likely be to seek out information on available treatments and other available support services.
https://www.mda.org/services
Our trained specialists are here to provide one-on-one support for every part of your journey. Send a message below or call us 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 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.
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.
https://www.duchenne.com/about-duchenne
Duchenne muscular dystrophy, sometimes shortened to DMD or just Duchenne, is a rare genetic disease. It primarily affects males, but, in rare cases, can also affect females. Duchenne causes the muscles in the body to become weak and damaged over time, and is eventually fatal.
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