Our Impact

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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Biogen and Ionis Enter Into New Collaboration to Identify Novel Therapies for the Treatment of Spinal Muscular Atrophy

December 29, 2017
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Biogen and Ionis Pharmaceuticals announced that they have entered into a new collaboration agreement to identify new antisense oligonucleotide drug candidates for the treatment of […]

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Cure SMA Assists Hundreds of Families in 2017

December 27, 2017
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Each year, Cure SMA provides thousands of families with vital support and resources to help them live active, engaged and hopeful lives. Our programs provide […]

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2017 Research Year-in-Review

December 19, 2017
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Over our past fiscal year—from July 1, 2016, to June 30, 2017—Cure SMA has funded 28 projects with over $2.5 million in new research funding. […]

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Cure SMA-Funded Research Results in 21 Published Journal Articles

December 12, 2017
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An important goal of our research funding strategy is to share scientific findings with the broader scientific community. To help accomplish this goal, scientists who […]

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