Our vision is our name:
CureDuchenne

CureDuchenne was founded by Paul and Debra Miller in 2003 after their son was diagnosed with Duchenne muscular dystrophy. The Millers applied their professional backgrounds to create a fiscally responsible and strategically focused business model, and assembled a seasoned staff and an expert Scientific Advisory Board, to lead the charge for a cure. Today, our nonprofit is a national leader in affecting change worldwide.

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