856K views · 8.4K reactions | If Hannah has the SMA gene, there is a chance our kids will have SMA. If she doesn't, there's no chance. 溺 | Squirmy and Grubs | Facebook
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856K views · 8.4K reactions | If Hannah has the SMA gene, there i…
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FacebookSquirmy and Grubs
Today, the Food and Drug Administration approved a new gene therapy for Spinal Muscular Atrophy. SMA Type 1 is the number one genetic killer of children 2 and under. This first-time gene therapy, developed here at Nationwide Children's, is allowing kids like Evelyn to have a bright future. Watch her incredible story. | Nationwide Children's Hospital
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Today, the Food and Drug Administration approved a new ge…
321.6K viewsMay 15, 2019
FacebookNationwide Children's Hospital
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Nris_Adda on Instagram: "A baby needs ₹16 crore for a life-saving treatment because the baby is suffering from a rare genetic disorder called Spinal Muscular Atrophy (SMA), which causes severe muscle weakness and breathing difficulties, and requires a one-time gene therapy injection (Zolgensma) that can stop the disease and save the baby’s life. I have done my part by contributing ₹27,000—if you could help in whatever way you can, it would be greatly appreciated."
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Nris_Adda on Instagram: "A baby needs ₹16 crore for a life-saving tr…
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Gene therapy offers a new chapter for families facing spinal muscular atrophy. Hope shines brighter every year. #GeneTherapy #SMA #MedicalBreakthrough #Hope #Science #Innovation
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