The mission of the Jett Foundation is to increase worldwide awareness of Duchenne muscular dystrophy with the purpose of raising and appropriating funds for research that will realize a cure for this fatal disease and programming that will ensure children with Duchenne have the opportunity to enjoy a full life.
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All are welcome to attend Jett Foundation’s FREE roundtables that bring resources and information on treatment options and clinical trials directly to families affected by Duchenne. Jett’s next two roundtables are on Feb. 11th in Long Island, NY and on March 4th in New Orleans, LA. Check out our website for more dates and locations!
February 2, 2017
This sold-out event was filled with families, friends, advocates, industry partners, and corporate sponsors, and we could not be more grateful. Click here for photos of this special evening. Our honorees of the evening, Cindy Quitzau, Bill Brett and The Flatley Foundation were acknowledged for their ability to inspire those around them, their hearts of gold, and their […]