Spinal stimulation restored muscles wasted by rare genetic disorder
Spinal stimulation restored muscles wasted by rare genetic disorder
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August is Spinal Muscular Atrophy (SMA) Awareness Month, and on this occasion, we'll be sharing voices from the SMA community. Danielle shares her family’s journey - from her own late diagnosis to raising two young children also living with SMA. Her story is one of resilience, progress, and hope for a better future. #SMAAwarenessMonth #BreakingDownBarriers #spinalmuscularatrophy | Muscular Dystrophy Canada
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José Flores lives with spinal muscular atrophy, but he’s never let it define him. With a powerful mind and an even stronger voice, he’s inspiring thousands to rise above their circumstances — and to speak up for those who can’t. As we honor 75 years of progress with the Muscular Dystrophy Association, José’s story reminds us that our limitations don’t have to become our standards. ✨ He has SMA, but SMA doesn’t have him. ✨ And your struggle doesn’t have to have you. Let’s be the voice for the voi
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