CureDuchenne
We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community. Join us in our mission, help us save the lives of over 300,000 boys worldwide. CureDuchenne is committed to improving the lives of everyone affected by Duchenne muscular dystrophy (DMD) through accelerating research to find the cure, improving care and empowering the Duchenne community. From creating the first Duchenne-specific physical therapy education program and enabling human clinical trials for the first-ever FDA approved drug for these patients, to launching a supplemental newborn screening initiative, we believe in tackling Duchenne from every angle. Duchenne is a 100% fatal genetic disease and the most common form of muscular dystrophy, which affects mostly boys. There are over 300,000 patients worldwide and 15,000 in the US.
Founded
2003
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6274
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936710
Cure Duchenne Muscular Dystrophy – CureDuchenne No products in the cart. With a mission to cure Duchenne muscular dystrophy CureDuchenne breaks the traditional charitable mold and balances passion with business acumen. We will fulfill our mission to cure Duchenne muscular dystrophy with our innovative venture philanthropy model that funds groundbreaking research early diagnosis and treatment access. With pioneering education and support programs our organization drives real change for those with living with the disease and their loved ones.
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Promoting and funding research into the study and cure of Duchenne Muscular Dystrophy.
On the 4th February 2016, our beautiful son Connor was diagnosed with Duchenne Muscular Dystrophy.
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