Davia Jones said it took seven years for her son, Kyrie, to be diagnosed with Duchenne Muscular Dystrophy, a progressive ...
"My medicine is making me stronger," 7-year-old Hudson Sanford says after receiving a breakthrough gene therapy for Duchenne Muscular Dystrophy Cara Lynn Shultz is a writer-reporter at PEOPLE. Her ...
The U.S. Food and Drug Administration has given the green light for the first gene therapy that treats a rare form of muscular dystrophy to be used in most people who have the disease and a certain ...
A charity transforms a garden in Brierley Hill for two brothers with Duchenne Muscular Dystrophy.
Duchenne is a fatal genetic disorder that causes progressive and irreversible muscle loss. The Sapp family pose for a photo while on a family vacation. Amber Sapp, a St. Petersburg resident, is a ...
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SRPT stock surges on promising early results from siRNA programs
Shares of Sarepta Therapeutics SRPT rose 35% on Wednesday after the company announced early clinical data on two experimental ...
The Muscular Dystrophy Association trusts the decision of the FDA, which weighs the risks and benefits of the drug The Muscular Dystrophy Association trusts the decision of the FDA, which weighs the ...
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