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Call to Action: Senate Expected to Vote on Healthcare Bill Today

July 25, 2017
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Today, members of the Senate are scheduled to begin voting on the Better Care Reconciliation Act (“Better Care Act”) of 2017. This is the Senate’s version of legislation modifying key […]

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2017 Annual SMA Conference Recap

July 19, 2017
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Thank you to everyone who attended the 2017 Annual SMA Conference at Disney’s Contemporary Resort in Orlando, FL; it was truly a magical weekend of community, research and fun! While […]

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Missouri is the First State to Institute Newborn Screening for Spinal Muscular Atrophy

July 10, 2017
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Governor Eric Greitens today signed into law Missouri Senate Bill 50, instituting newborn screening for spinal muscular atrophy (SMA). The bill makes Missouri the first state in the country to […]

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Cure SMA Launches Newborn Screening Grassroots Advocacy Campaign for Spinal Muscular Atrophy Newborn Screening

July 2, 2017
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Today, as part of the Annual SMA Conference, we announced the launch of a new grassroots advocacy campaign to implement newborn screening for spinal muscular atrophy. Today’s kick-off event is […]

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Summer 2017 Update to SMA Drug Pipeline is Released

July 1, 2017
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We’ve recently released an update to the SMA drug pipeline. This latest version includes: 19 active programs, including one approved therapy.  14 pharmaceutical partners.  5 programs in clinical trials.  An […]

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Cure SMA Funded Standard of Care Paper Published in Neuromuscular Disorders Journal

June 30, 2017
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The journal Neuromuscular Disorders has published a paper reporting on the findings of an international workgroup convened to update the Standard of Care (SOC) for SMA. Cure SMA provided funding […]

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