Introducing Cure SMA’s new advocacy update video series! We hope this monthly series will help you learn more about ways you can take action and make a difference for the SMA community. Links included below💜🧡 Cure SMA Advocacy Page: https://www.curesma.org/cure-sma-advocacy/ Cure SMA Advocacy Action Center: https://www.votervoice.net/mobile/CureSMA/Home Cure SMA Advocacy Blog: https://www.votervoice.net/iframes/CureSMA/News | Cure SMA
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Introducing Cure SMA’s new advocacy update video series! W…
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FacebookCure SMA
With the support of friends, adults living with spinal muscular atrophy (SMA) can achieve extraordinary things. Kevan, who’s living with Type 2 SMA, shares how his friends are the best part of him and his life. This #SMAAwarenessMonth, help us share these incredible stories of adults living with #SMA. https://bit.ly/2MygS1D | Genentech
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With the support of friends, adults living with spinal muscular atroph…
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FacebookGenentech
Cure SMA: New treatment for genetic muscular disease in children gives hope to parents
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35K views · 21 reactions | Some people may think spinal muscular atrophy (SMA) is always a fatal disease. Advances in SMA screening and innovation aim to improve outcomes in those diagnosed early in life, with the more rapidly progressing types of SMA. Watch to learn about #UnderstandingSMA. | Biogen | Facebook
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