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At PPMD, I get to be part of a fraternity that none of us signed...
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At PPMD, I get to be part of a fraternity that none of us signed...
Each year, I attend at least one national gathering of people living with muscular dystrophy. In addition to learning about the most updated care standards, treatment strategies, and research initiatives, I’m able to bond with those who share a similar diagnosis, and have made some dear friends. The upcoming Parent Project Muscular Dystrophy (PPMD) 2026 Annual Conference, which is held each year in June, continues to expand its outreach, and as …
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