My RN Gail doing my Muscular Dystrophy shaving cream challenge! #musculardystrophyawarness #mdachallenge #duchennemusculardystrophy
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Joe was diagnosed with Duchenne (DMD) muscular dystrophy in 2014. On a day off, Susanne took Joe to the GP, unaware the doctor was assessing him for DMD. After observing his movements, the doctor mentioned muscle weakness. A quick Google search showed that Joe matched every symptom. They were asked if Joe wanted to take part in a clinical trial, they said yes because for the boys that came after Joe it was important. "Now he’s a little bit older we ask him how he feels. We’ve always been quite o
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Joe was diagnosed with Duchenne (DMD) muscular dystrophy in 2014…
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1.4K views | Duchenne muscular dystrophy (DMD) is one of the most severe types of muscular dystrophy. “John-John’s Journey” chronicles one family’s urgent move across the globe to get their toddler in our #genetherapy clinical trial in an effort to save his life. Watch the new, original documentary via the link in our bio! 喙 #Duchenne #musculardystrophy #DMD #Elevidys #raredisease | UC Davis Health | Facebook
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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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Take memories of the good days. #duchenne #dmd #musculardystrophy #findingjoy #makingmemories | Harrison & Duchenne - Raising Awareness of Duchenne Muscular Dystrophy
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