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Cure SMA and Parent Project Muscular Dystrophy Announce Collaboration

March 19, 2019
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Today, Cure SMA and Parent Project Muscular Dystrophy (PPMD) announced their strategic collaboration to collect real-world data to improve the lives of those affected by spinal muscular atrophy (SMA) and […]

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Cure SMA Launches Third Annual Community Survey to Address Important Issues in SMA Treatment

March 14, 2019
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For the past several years, we’ve been working to collect data and information on our community’s experiences, goals, hopes, and challenges. We know that the voice of our community is […]

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Recording of Genentech/Roche and Cure SMA Webinar Now Available Online

March 14, 2019
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A recording of this week’s webinar with Genentech/Roche is now available online. During the webinar, Genentech/Roche shared their history working with the SMA community, and their investigational medicine risdiplam. Updates […]

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Cure SMA Advocates for SMA Community at ICER Hearing

March 8, 2019
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On Thursday, March 7, Cure SMA testified on behalf of the SMA community at a meeting of the Institute for Clinical and Economic Review (ICER). ICER is an independent health […]

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Biogen Provides 2019 Community Update on Spinraza

March 5, 2019
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Dear members of the SMA community, As we celebrate Rare Disease Day 2019, we are honored to continue supporting the spinal muscular atrophy (SMA) community. In recent weeks and months, […]

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Genentech/Roche and Cure SMA to Co-Host Webinar

March 1, 2019
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On Monday, March 11th, at 12pm CST (10am PST/11am MST/1pm EST) Genentech/Roche and Cure SMA will co-host a webinar for the SMA community. During the webinar, you’ll hear from Genentech/Roche […]

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