Duchenne Muscular Dystrophy ❤️
2:57
YouTubebodikaidenandi
Duchenne Muscular Dystrophy ❤️
Duchenne Muscular Dystrophy is a rare, genetic, progressive muscle wasting disease. If is severe and fatal, there is no cure. My son Kaiden is 10, Autistic level 2 and he has Duchenne Muscular Dystrophy. ️ ️ ️ #duchennemusculardystrophy #musculardystrophy #disability #specialneeds #raredisease
1.1K views1 month ago
Duchenne Muscular Dystrophy Explained
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What parents need to know about Duchenne muscular dystrophy
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99. Duchenne & Becker Muscular Dystrophy Explained | Clinical Features, Diagnosis & Management.
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99. Duchenne & Becker Muscular Dystrophy Explained | Clinical Features, Diagnosis & Management.
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Top videos
Gene replacement therapy for Duchenne Muscular Dystrophy (DMD): New documentary from UC Davis Health
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💪 Day 26 of My 30-Day Challenge 🔥 I have Duchenne muscular dystrophy (DMD) — a rare genetic disease that affects my muscles and makes them weaker over time. I'm getting closer and closer to the end of this challenge, but this is not the end of my journey. I will continue training, and there will be more challenges in the future. What you see in these videos is only the biggest moments. Behind every video, there is much more work and effort than you can see. See you tomorrow ❤️ Join me on this
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TikTokbodikaidenandi
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One of our many trips to the ER. RC wasn’t able to keep anything down, and I couldn’t get his fever to break. When your child has Duchenne Muscular Dystrophy, you don’t take chances. Vomiting and fevers can be serious because long-term steroid use can put him at risk for adrenal insufficiency. Dad was completely wiped out once RC started feeling better. 😂 Meanwhile, RC bounced right back, bright-eyed and bushy-tailed. And me? I stayed in full mom mode the entire time, watching every symptom, ev
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