Owen Dumm: Pediatric Muscular Dystrophy Patient Story | Cleveland Clinic
Owen Dumm: Pediatric Muscular Dystrophy Patient Story | Clevelan…
Mar 9, 2017
clevelandclinic.org
208 reactions · 558 shares | The family of a boy with life-limiting Duchenne muscular dystrophy have told ITV news they are devastated after being refused a breakthrough drug because it is not cost-effective. 10-year-old Archie Hill is one of 50 boys affected by the regulator's decision today. | ITV London | Facebook
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208 reactions · 558 shares | The family of a boy with life-limiting D…
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Today, the Food and Drug Administration approved the first gene therapy treatment for Duchenne Muscular Dystrophy. This groundbreaking treatment, developed here at Nationwide Children’s, is giving boys like Easton and Connor a future full of hope and possibilities. Watch their incredible stories. Learn more: https://bit.ly/3PzvLQK | Nationwide Children's Hospital
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Today, the Food and Drug Administration approved the first …
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Palm Beach County firefighters unite for marathon to support Duchenne Muscular Dystrophy
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Duchenne muscular dystrophy (DMD) is a devastating genetic condition that results in progressive muscle weakness, spinal deformities, heart failure and early mortality. While genetic therapies are being explored, current treatments only alleviate symptoms. However, MCW’s Dr. Brian Lin and his lab are researching a promising approach that examines a calcium channel which becomes hyperactive in DMD and how inhibiting that channel could counteract the leading cause of death in DMD patients. Learn m
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