Searching for Organizations That Support Duchenne Muscular Dystrophy information? Find all needed info by using official links provided below.
https://www.duchenne.com/resources
A national nonprofit organization that raises awareness and funds to find a cure for Duchenne muscular dystrophy. The funds raised support the most promising research programs aimed at treating and curing the disease.
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. Support groups for Duchenne and Becker muscular dystrophies, include:
Foundation to Eradicate Duchenne, is a 501c(3) organization established in 2002 with the goal of finding treatments and an ultimate cure for Duchenne Muscular Dystrophy, the world’s leading lethal childhood genetic disease. Contact Our Team
https://www.cureduchenne.org/
Our innovative venture philanthropy model funds groundbreaking research, early diagnosis and treatment access. With pioneering education and support programs, our organization drives real change for those with Duchenne muscular dystrophy and their loved ones.
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.
https://www.christopherreeve.org/living-with-paralysis/health/causes-of-paralysis/muscular-dystrophy
Muscular Dystrophy Association is dedicated to assisting people living with neuromuscular disease. Muscular Dystrophy Family Foundation provides a myriad of support services including supplying adaptive equipment. Parent Project Muscular Dystrophy, parents of children with Duchenne and Becker Muscular Dystrophy founded this not-for-profit organization to advance research and advocacy efforts.
How to find Organizations That Support Duchenne Muscular Dystrophy information?
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