welcome to DuchenneXchange- a positively charged Duchenne muscular dystrophy community.
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This is the first of a new series of interviews we’ll be sharing to help bring our readers closer to others involved in the Duchenne community.
I was honored to have the opportunity to ask Debra Miller a few questions about her experience as the President and CEO of CureDuchenne. She was very generous with her time and candid with her thoughts.
CureDuchenne’s mission is to save this generation of children and young adults with Duchenne muscular dystrophy. The organization has made a tremendous impact in the Duchenne community. I think their story is amazing and you’d like to know, how they have managed to obtain so much support for this cause.
Focus on What You Can Do Rather Than What You Can’tIn fifth grade, it was hard for me to gr...
Craig Teen With Muscular Dystrophy Inducted as Honorary FirefighterNearly 10 years ago, Craig’s JP Price ...
Duchenne Dash 2018https://www.youtube.com/watch?v=MBFm81-g...
The World of Duchenne: How to Support a Duchenne ParentThe World of Duchenne I live in two wor...
Champions to Cure Duchenne 2019https://www.youtube.com/watch?v=YQsB3prX...
Walking StrongWalking Strong is a 501c3 non-profit fou...