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.
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