Search Results: spinraza

Community Spotlight: The Jankowski Family

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It has been a little over two years since doctors told Chris and Kelly Jankowski that their first-born son, William, had spinal muscular atrophy (SMA) […]

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December Webinar on SMA Treatments and Clinical Trials Now Available Online

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A recording of the December 13th webinar updating the community on SMA treatments and clinical trials is now available online. A PDF of the webinar […]

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2018 Research Year-in-Review

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Over our past fiscal year—from July 1, 2017, to June 30, 2018—Cure SMA has funded over $5 million in new research funding. This funding will be […]

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Community Spotlight: The Berkovits Family

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When Milo Berkovits was seven months old, his daycare teacher noticed he was not reaching his milestones. What followed from there on were visits to […]

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Register for Cure SMA’s Webinar on SMA Treatments and Clinical Trials

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On Wednesday, December 12th, at 12:00pm CST (10:00am PST/11:00am MST/1:00pm EST) Cure SMA will hold a webinar updating the community on the latest information on […]

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Cure SMA Launches “SMArt Moves” for Early Diagnosis and Treatment

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Cure SMA today launches SMArt Moves, a new disease awareness and educational campaign to empower parents, pediatricians and other healthcare professionals to swiftly recognize and […]

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Community Spotlight: Allyson Henkel

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My son Pete and I began advocating to have SMA added to the newborn screening panel in Pennsylvania in December of 2017. Pete was 13-years […]

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Community Spotlight: The Lasko Family

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After Max began receiving Spinraza in 2017, we wanted to do our part to help ensure that children born with SMA would be diagnosed as […]

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Updated 2018 SMA Standards of Care Statements Available Online

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The 2018 SMA Standards of Care recommendations were published in Neuromuscular Disorders in February 2018 and March 2018 and are available online through Open Access […]

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2018 SMA Researcher Meeting Summary: SMA Therapy Development

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The SMA Researcher Meeting is the largest research meeting in the world specifically focused on SMA and seeks to create open communication of early, unpublished […]

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