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Biogen Releases Statement on CHERISH Data and Plans for New Clinical Research

February 14, 2018
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Biogen has provided the following community statement on the final results from CHERISH, a Phase 3 study of SPINRAZA.  Dear Members of the SMA community, This past December marked one […]

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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 capacity at SMA treatment centers […]

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Cure SMA Announces Local Educational Symposiums in 16 US Locations

February 12, 2018
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Cure SMA is pleased to announce a slate of one-day local symposiums, beginning late spring and continuing into fall 2018. The symposiums will be held in 16 locations across 15 […]

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Winter 2018 Compass Now Available Online

February 9, 2018
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The winter 2018 issue of Compass is now available online. This issue covers Cure SMA’s community survey, and reviews how data is used to improve research, care and coverage in […]

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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 is an important step toward […]

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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 announcement makes Utah the first […]

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