By Jacob Gapko Jacob Gapko is 46 years old and has Duchenne muscular dystrophy. He uses a power wheelchair and non-invasive ventilation 24/7. He has a B.S. in physics and minors […]
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CureDuchenne Cares had its inaugural visit to San Juan, Puerto Rico, on June 10 for a workshop on current standards of care for Duchenne, research and clinical trials, family support, […]
Doug Levine, PT, a physical therapist instructor with CureDuchenne, and Kerry Johnson, senior director of community engagement, visited India in February to educate physical therapists, doctors, physical and occupational therapy […]
There’s plenty of times in life where plans fall apart. That’s especially the case if you have Duchenne muscular dystrophy like me. A building you were expecting to enter might […]
Consistent and frequent physical therapy is one of the few currently available treatments that’s been proven to provide benefits at all ages with the potential to delay disease progression. However, traditional […]
Community. Support. Knowledge. These are the things families and professionals worldwide seek – especially when faced with a rare disease like Duchenne. That’s why, in partnership with Duchenne Hungary, CureDuchenne […]
Leading Global Nonprofit Expands Professional Training Program to Meet Specialized Needs of Individuals with the Neuromuscular Disease NEWPORT BEACH, Calif., (October 10, 2022) – CureDuchenne, a global leader in research, […]
CureDuchenne firmly believes in working together to help any child with Duchenne muscular dystrophy find the support they need. Duchenne is a disorder which knows no cultural, economic, or social […]
