Our Mission:
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CHOPS Syndrome Global is dedicated
to our mission of building a better tomorrow for CHOPS Syndrome patients and their families through research, awareness and advocacy. The Foundation was launched in 2019 by Lainey Moseley whose daughter, Leta Moseley, was the first child in the world diagnosed with CHOPS Syndrome. We hope to achieve these goals by fundraising to support medical research that leads to a more informed CHOPS Syndrome body of knowledge, better patient treatment options and an eventual cure. |