Find all needed information about Organizations Support Muscular Dystrophy. Below you can see links where you can find everything you want to know about Organizations Support Muscular Dystrophy.
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
https://lgmd-info.org/organizations/
The Clifton R. Lewis Good Life Foundation is a non-profit organization which provides support and assistance to better the lives of people with Muscular Dystrophy. Through accessibility assistance, special equipment, funding for research and the Dream Creator the foundation will strive to improve the lives of people with MD.
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 …
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:
https://musculardystrophynews.com/2017/04/20/5-ways-help-fund-sma-muscular-dystrophy-charities/
Apr 20, 2017 · Organizations such as the Muscular Dystrophy Association and Cure SMA regularly hold fundraising events. These events are fun and participants can either pay to enter or have their friends and family sponsor them to take part. Events include gala dinners, fun walks, golf days, full- and half-marathons, and other sporting events.
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
Direct support services include annual social events and other equipment and services that enable those with Muscular Dystrophy to enjoy greater mobility and independence. MDFF is a qualified 501(c)(3) non profit tax-exempt charity organization under federal tax guidelines.
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