40K views · 320 reactions | Meet some of the brave children and families living with Duchenne Muscular Dystrophy. Their courage fuels a movement, and their stories ignite a powerful call for change. Together, we can bring hope, and work towards a cure. Every step we take brings us closer to a future where Duchenne is no longer a battle. Let’s unite for a world of possibility!  #SaveOurSons #SOSDuchenneFoundation #EndDuchenne #HopeForACure | Save Our Sons Duchenne Foundation | Facebook
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40K views · 320 reactions | Meet some of the brave children and fa…
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Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophy
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sarepta.com
Duchenne Muscular Dystrophy - Young Adult Case Study
Duchenne Muscular Dystrophy - Young Adult Case Study
Oct 12, 2010
physio-pedia.com
When it comes to Duchenne Muscular Dystrophy, what a parent sees is more than just the diagnosis, it’s the quiet courage behind every struggle. She sees her child endure long stretches when he’d rather be playing. She watches lose a little physical strength every day and try to find solutions to find other ways to continue with his favourite activities, if possible, or invest time into other or new interests. Parents help their child get ready for therapies when he’d rather just stay home and be
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Duchenne muscular dystrophy is a progressive muscle wasting disease. It causes muscles to weaken over time because the body cannot produce dystrophin, a protein muscles need to stay strong. Duchenne affects every muscle in the body, including the heart and lungs. Despite the challenges, we choose faith, resilience, and joy. He has already surpassed what doctors once said was possible. Sharing our journey to spread Duchenne awareness and hope. If you’d like to support Duchenne awareness, drop a g
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Duchenne muscular dystrophy is a progressive muscle wasting disea…
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52K views · 510 reactions | 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 | Facebook
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52K views · 510 reactions | Today, the Food and Drug Administration …
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FacebookNationwide Children's Hospital
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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13 reactions | Here’s to the other Duchenne families doing the same…
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