Foster Family

Family Story Foster

Our son was diagnosed April 1, 2019. We have spent the past 2 years doing research, completing a clinical trial and being an advocate for our son and Duchenne Muscular Dystrophy. In 2020, we started NBF Cure44, a business focusing on spreading awareness about Duchenne and donating a portion of profits to CureDuchenne for research into a cure. 

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You can advance the care, treatment and cure for Duchenne muscular dystrophy. Contributions in any amount can truly make a difference and can be credited to a fundraiser or event from the list below.