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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May 3, 2016
My name is Christine McSherry. You heard from me this morning when I presented the Patient Reported Outcomes Report. Now, I’d like to speak with you as a mother and an advocate. My son Jett was diagnosed when he was five years old. Today he is 20. Jett took his last steps at the age […]