Cure CMD is a U.S. registered 501(c)(3) nonprofit organization founded in 2008 by three parents with a mission to advance research and empower those living with congenital muscular dystrophies. They focus on supporting the community through engagement, research funding, and optimizing medical care for individuals with CMD.
With a commitment to advancing treatments for rare genetic disorders, Cure CMD has funded over $4 million in research and operates the Congenital Muscle Disease International Registry to support researchers and participants. Their impact includes providing resources, care guidelines, and advocacy for those affected by CMD.
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