Cure SMA is excited to announce that 12 new Panthera pediatric lightweight wheelchairs have been purchased thanks to generous funding from Sweet Baby Zane. These specific chairs are normally a large out-of-pocket expense for many families, as they cost over $6,000 each and are not usually covered by insurance because they are not manufactured in […]
Sweet Baby Zane Funds New Equipment Pool Item Read More »
Cure SMA would like to thank the Cash Scanlon-Philips Foundation for their generous donation to fund a years’ worth of type II newly diagnosed care packages. These care packages are sent to every newly diagnosed SMA family, within the US after connecting with Cure SMA. These care packages include toys and helpful items for children with
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In a recent paper titled, “Patient Reported Impact of Symptoms in Spinal Muscular Atrophy (PRISM-SMA)” Dr. Chad Heatwole and others describe a cross-sectional study of 359 adults with SMA using the International SMA Patient Registry. The goal of the study was to determine the frequency and relative importance of symptoms experienced by adults with spinal
Quinn Anton Jensen was diagnosed with spinal muscular atrophy (SMA) type II on March 2007 in Iowa City. Quinn’s mom, Nancy, recalls the genetic testing process took over a month. It was a stressful and frightening time and the Anton Jensens wish the diagnosis process was faster. Nancy recalls feeling devasted as there was still
Community Spotlight: The Anton Jensen Family Read More »
Mary was 4 months old when her parents, Ryan and Kate Nelson, suspected something wasn’t quite right with their daughter; she wasn’t bearing weight on her legs nor was she lifting her head like their friends’ babies. Mary’s pediatrician referred them to a neurologist who presumed Mary had a stroke in utero, so he ordered
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At 7 months old, Sarah Zmaczynski’s parents, Jill and John, noticed their daughter couldn’t bear weight on her legs. Sarah’s pediatrician responded with the “kids develop at different rates” speech. As John has a family history of late walkers, the Zmaczynski’s thought maybe their worries were unfounded. Although one in 50 people carry the genetic
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In 2014, Doug McCullough gave a TEDx talk at a Johnson & Johnson event in New Jersey that focused on disability inclusion in the workplace. His speech, A Billion People in the Shadows, represents the 1 Billion people worldwide who are affected by a disability. Cure SMA recently spoke with Doug about his TEDx talk
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The 2018 Cure SMA Concert for a Cure raised $210,000 on April 21, 2018. After combining many years of fundraising and hard work, the 18th Annual Concert for a Cure reached a very exciting milestone of $2 Million. “We are still in awe of the dedication, support and commitment that our families have received. Our
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In this Community Spotlight, Victoria Colone delves into the complexities of early diagnosis and treatment as a mom navigating the world of healthcare for her child with SMA. Victoria Colone was 22 weeks pregnant when she learned through an amniocentesis test that her son, Jaxon, had SMA Type I. Despite her OB/GYN and genetic counselor
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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 for families and healthcare providers. These documents are updates of the Standard of Care document issued in 2007. The 2018 recommendations emphasize that “a multidisciplinary approach is the key element
Updated 2018 SMA Standards of Care Statements Available Online Read More »
