welcome to DuchenneXchange- a positively charged Duchenne muscular dystrophy community.
- join today!
Best Day Ever Foundation, founded by Laura McLinn, is working aggressively to raise awareness and help extinguish Duchenne muscular dystrophy. Laura McLinn’s 8 year old son, Jordan McLinn, is one of about 200,000 boys in the world with this disease, and she wants help to Jordan and other children like him live out their dreams … one BEST DAY EVER at a time!
The home base of the Foundation is Central Indiana but it still encourages people to register even if they are located elswhere.
Here is the registration link: Register with Best Day Ever Foundation.
Best Day Ever Foundation is a non-profit 501(c)(3), and all donations are tax deductible.
Duchenne UK – LinkedInDuchenne UK is a lean, ambitious and hig...
La Force DMDThe Force Foundation’s mission is to u...
Romito FoundationIn 2007, Dominic Romito was diagnosed wi...
joinourboysThe Join Our Boys Trust’s ultimate aim...
Hope for Gus FoundationHope For Gus Foundation was founded by p...
@CureDuchenneDuchenne is the most common muscle disea...