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Books About Duchenne For Children and Parents
Enjoy this hand-picked selection of books about Duchenne muscular dystrophy for children and parents. This list was shared at the 2022 FUTURES National Conference in Orlando, FL. (Duchenne Community Bookstore […]
NEW CHIEF OF STAFF AND NATIONAL DIRECTOR OF DEVELOPMENT
Kent Mora and Nancy Young Bring Experience in Organizational Leadership and Strategic Fundraising to Rare Disease Nonprofit Newport Beach, Calif. – April 6, 2022 – CureDuchenne, a leading global nonprofit […]
Protected: Pfizer expands their gene therapy clinical trial to include boys living with Duchenne who are non-ambulatory
There is no excerpt because this is a protected post.
Physical Therapist Karin Gorman is a Glimpse of Hope for Local Duchenne Community
After her 10-month-old nephew was diagnosed with Duchenne muscular dystrophy, Karin Gorman was inspired to learn more about the disease and find a way to make a difference in the […]
Showing Nepal’s Duchenne Community our Southern California Hospitality
To turn away from any member of the global Duchenne community would be to turn away from our own here at home. That’s why we at CureDuchenne, the non-profit […]
Passion Meets Courage
To say I have witnessed young men and boys with Duchenne face heartbreaking challenges is an understatement. Duchenne is one of the toughest diseases in the world. That’s why […]
CureDuchenne’s Debra Miller Wins OCBJ Women in Business Award
On behalf of team CureDuchenne, we are ecstatic to announce that our co-founder and our daily inspiration Debra Miller was presented with the esteemed Women in Business Award to […]
Mack Brown, Jack Ingram, Matthew McConaughey, Vince Young…and The Revell Family, Champions Fighting to Cure Duchenne
For some people it takes a trophy or medal to denote a champion. For those in the fight against Duchenne Muscular Dystrophy, there are all kinds of champions and […]