Decode Duchenne Program
Decode Duchenne Program
Mar 28, 2024
parentprojectmd.org
Duchenne is a rare genetic condition that mostly affects boys. It’s progressive, and raising awareness is so important. Every day counts. We’re still learning what life with Duchenne looks like for Louie and we don’t have all the answers. We hope that by sharing our journey we can help other families get answers sooner than we did. Please share to spread awareness 💛 #duchennemusculardystrophy #duchenne #duchenneawareness #musculardystrophy #timeismuscle #makingmemoriesaccessible | Making Memori
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Duchenne is a rare genetic condition that mostly affects boys…
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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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