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Jett Foundation – LinkedIn

While we were founded out of one family’s desperate need to save their son, we have transformed dramatically. Once a non-profit dedicated to raising money for biomedical research, today we are meeting our families and young people where they are with direct service and educational programs that improve and enrich the lives of individuals impacted by Duchenne. Through our direct service programs, such as Camp Promise – which is open to young people with any neuromuscular disorder, we provide children and young adults with a fun-filled week of traditional camp activities where kids get to “just be kids” while parents and caregivers are given a much-needed week of respite.