Our Impact

Cure SMA Awards $150,000 Grant to Umrao Monani, PhD, Columbia University

March 13, 2018
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Cure SMA has awarded a $150,000 research grant to Umrao Monani, PhD, at Columbia University, for his project, “SMA modulators as a means to revealing […]

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Cure SMA Awards $150,000 Grant to Allison Ebert, PhD, Medical College of Wisconsin

March 7, 2018
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Cure SMA has awarded a $150,000 research grant to Allison Ebert, PhD, at the Medical College of Wisconsin, for her project, “Role of astrocyte-produced miR-146a […]

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Awareness is Best Raised When We Work Together

March 6, 2018
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When a loved one is affected by spinal muscular atrophy, whether recently diagnosed or living with SMA for a while, you want to make a […]

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Additional Funding for SMA Care Centers Announced

February 14, 2018
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Cure SMA is pleased to announce the second round of grants from $450,000 in funding, awarded to a total of 9 sites to help increase […]

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Advisory Committee on Heritable Disorders in Newborns and Children Recommends Nationwide Newborn Screening for Spinal Muscular Atrophy

February 8, 2018
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The Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC) today recommended that newborn screening for spinal muscular atrophy be implemented nationwide. This decision […]

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Utah Becomes First State to Implement Permanent Screening for SMA

February 6, 2018
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The Utah Department of Public Health has announced that, effective immediately, all newborns born in the state will be screened for spinal muscular atrophy. This […]

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Federal Committee to Vote on Spinal Muscular Atrophy Newborn Screening on Thursday

February 2, 2018
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On Thursday, February 8, the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC), a federal committee that oversees newborn screening, will vote on […]

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SMA Industry Collaboration Releases Spinal Muscular Atrophy Voice of the Patient (VoP) Report

January 19, 2018
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Cure SMA and our partners in the SMA Industry Collaboration are pleased to announce the release of the Spinal Muscular Atrophy Voice of the Patient […]

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Cure SMA Launches Advocacy Action Network

January 5, 2018
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Working together, we’ve achieved tremendous success in advocating for ourselves, our families, and our whole community, particularly in the past few years. Today, we’re building […]

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Minnesota Becomes Second State to Adopt Newborn Screening for SMA

January 4, 2018
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On December 27, the Minnesota Commissioner of Health accepted the recommendation of the state’s Advisory Committee on Heritable and Congenital Disorders to add SMA to […]

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