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Community Spotlight: The Hoskin Family

December 16, 2020
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High school sweethearts, Steven and Amy Hoskin, and their 19-month-old son, Grayson, reside outside Sacramento, CA. Steven describes them as a goofy bunch, always playing practical jokes on each other. […]

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Cure SMA, Novartis Publish Economic Burden of SMA Analysis in Journal of Market Access & Health Policy

December 14, 2020
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Recently, Cure SMA and colleagues at Novartis Gene Therapies published a manuscript titled, “Economic burden of spinal muscular atrophy: an analysis of claims data” in the Journal of Market Access […]

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Answering Questions about COVID-19 Vaccination and SMA

December 13, 2020
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To the full spinal muscular atrophy (SMA) community, we want you to know that Cure SMA is continuing to support you with information and resources related to the COVID-19 pandemic. […]

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Cure SMA Shares Perspective on COVID-19 Vaccination

December 7, 2020
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Dear SMA Community, Although this year has brought with it many challenges, the SMA community continues to demonstrate its strength and resilience. Cure SMA remains committed to bringing you the […]

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Community Spotlight: Nikki McIntosh

November 25, 2020
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Nikki McIntosh is known as the founder of Rare Mamas, an online resource that supports and empowers mothers who have children with rare diseases. She and her husband, Tony, live […]

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Biogen SMA Q4 2020 Community Statement

November 20, 2020
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Dear Members of the SMA Community, As we celebrate National Family Caregivers Month this November, Biogen acknowledges the vital role caregivers have in our society, including within our spinal muscular […]

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