The month of August marks not only SMA Awareness Month but the start of our fall event season. SMA Day with the Chicago Cubs, the Colorado Walk-n-Roll, and the Texas Bowl-a-Thon are just a few events that kicked off the season within the first weeks of August. Over the next few months our dedicated event […]
Cure SMA Fall Event Season Kicks Off Read More »
Last night, Governor Bruce Rauner of Illinois signed SB 456, adding spinal muscular atrophy (SMA) to the state’s newborn screening panel. The bill adds Illinois to a number of states who have already adopted permanent SMA screening, including Missouri, Utah, Minnesota and Indiana. The legislation was sponsored by Senators Julie Morrison, Michael Connelly and Thomas
Illinois Adopts Permanent SMA Screening Read More »
The guest blog post below was written by Heather Tomko, sharing her experience in the Ms. Wheelchair USA 2018 pageant. She is the reigning Ms. Wheelchair USA in addition to being a public health researcher and masters student. Heather is a lifelong Pittsburgh resident and lives with SMA Type II. Being in a pageant is
Heather Tomko Crowned as Ms. Wheelchair USA 2018 Read More »
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the largest research meeting in the world specifically focused on SMA and seeks to create open communication of early, unpublished data to accelerate the pace of research. The meeting also furthers research by building collaborations—including cross-disciplinary dialogue, partnerships, integration of new researchers and drug companies, and educational opportunities for junior
2018 SMA Researcher Meeting Summary: SMA Therapy Development Read More »
At 10 years old, Brynne Willis knew something was wrong; it was time for the Presidential Fitness Test required by public schools and she kept falling behind her peers. “I kept falling every time I tried to run and was the last to complete the one-mile run,” said Brynne. Worried about the cause of her
Community Spotlight: Brynne Willis Read More »
