7.4K views · 60 reactions | Alfie's story puts a spotlight on Duchenne muscular dystrophy - his dad spells out what the condition means for people like his son | Stephen Nolan | Facebook
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FacebookStephen Nolan
7.4K views · 60 reactions | Alfie's story puts a spotlight on Duchenne muscular dystrophy - his dad spells out what the condition means for people like his son | Stephen Nolan |
Stephen Nolan. . Alfie's story puts a spotlight on Duchenne muscular dystrophy - his dad spells out what the condition means for people like his son
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345 reactions · 126 shares | Donate today to help change lives forever: bit.ly/MDAdonateRFS Ethan lives with Duchenne and frequently visits MDA’s Care Centers. Watch Ethan’s story to learn about how your donations go toward providing the best in innovations in research and care for kids just like Ethan. #RideForStrength | Muscular Dystrophy Association | Facebook
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345 reactions · 126 shares | Donate today to help change lives forever: bit.ly/MDAdonateRFS Ethan lives with Duchenne and frequently visits MDA’s Care Centers. Watch Ethan’s story to learn about how your donations go toward providing the best in innovations in research and care for kids just like Ethan. #RideForStrength | Muscular Dystrophy Association | Facebook
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Muscular Dystrophy Treatment
Doctors are studying a boy whose muscles are 40% larger than expected, despite normal myostatin levels. Research could lead to breakthroughs in muscular dystrophy treatment, potentially helping patients gain muscle and strength. A fascinating case! #MuscleGrowth #MedicalMystery #MuscularDystrophy #GeneticResearch #HealthScience From: The World's Strongest Toddler | Real Stories
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Doctors are studying a boy whose muscles are 40% larger than expected, despite normal myostatin levels. Research could lead to breakthroughs in muscular dystrophy treatment, potentially helping patients gain muscle and strength. A fascinating case! #MuscleGrowth #MedicalMystery #MuscularDystrophy #GeneticResearch #HealthScience From: The World's Strongest Toddler | Real Stories
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345 reactions · 126 shares | Donate today to help change lives forever: bit.ly/MDAdonateRFS Ethan lives with Duchenne and frequently visits MDA’s Care Centers. Watch Ethan’s story to learn about how your donations go toward providing the best in innovations in research and care for kids just like Ethan. #RideForStrength | Muscular Dystrophy Association | Facebook
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345 reactions · 126 shares | Donate today to help change lives forever…
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"The GPs unfortunately don't have enough knowledge about Duchenne." Satish's son Vinny lives with Duchenne muscular dystrophy. Together, they've felt the impact of a lack of understanding about the condition across healthcare professionals. This includes poor communication between hospitals and GPs, medical equipment not suitable for Vinny's wheelchair, and inaccessible transport between appointments. Learn more about Satish & Vinny's story 👇 | Muscular Dystrophy UK
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2.4K views · 35 reactions | Our new Muscles Matter podcast is out now️ Guests Charlotte Hardwick and Stewart Ross, both living with a muscle wasting condition, discuss their experiences of diagnosis and the support made available following this. The episode explores what an ideal diagnosis and support scenario might look like, and the support they’ve found most useful. Listen here: https://loom.ly/Byk3gyA | Muscular Dystrophy UK | Facebook
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