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The Jett Foundation aims to increase worldwide awareness of Duchenne Muscular Dystrophy (DMD) by raising funds for programs, education, research and advocacy to fund treatments, realize a cure and ensure all affected by Duchenne have the opportunity to enjoy a full life.
In 2001, Christine and Stephen McSherry started the Jett Foundation after receiving devastating news their then five-year-old son Jett had DMD, the most common and lethal childhood genetic disorder in the world, affecting one in every 3,500 male births.
For over 15 years, Christine has been a tireless advocate to find a cure. Donate here.
– Tara Frier, Goodwin Group PR