Scoliosis affects 1 in 40 children and up to 1 in 3 adults. Many individuals go undiagnosed for years. Increased awareness can lead to earlier detection, improved treatment options, and better quality of life.

In 2008, the National Scoliosis Foundation launched Scoliosis Awareness Month to educate the public, reduce stigma, and advocate for change. Since then, June has become a time of action, visibility, and hope.

Scoliosis is an abnormal curvature of the spine that most commonly develops in children aged 10 to 15 during growth spurts. In 80% of cases, the cause is idiopathic, meaning the cause is unknown. Treatment options vary depending on severity and include observation, bracing, or surgery for more serious cases.

This initiative was brought forward by one of my brave constituents, Ella, who was diagnosed with severe idiopathic scoliosis in middle school. In sixth grade, she attended her first annual well visit after COVID and was screened for scoliosis. Her pediatrician noticed a rib hump on her back. Upon meeting with a spine specialist, she learned that at the time of her diagnosis, her curve was around 50 degrees. She was initially treated with a brace that she had to wear at least 20 hours a day. Unfortunately, the brace did not prevent progression, and her curve worsened, leaving surgery as her only option. Ella underwent spinal fusion surgery on May 12, 2025, at the Children’s Hospital of Philadelphia. The surgery was successful, reducing her curve from nearly 60 degrees to less than 15 degrees. After surgery, she was able to return to her favorite sport, soccer, just 12 weeks post‑operation. She hopes to raise awareness about the importance of early scoliosis screening and to reassure individuals with severe scoliosis that, even if surgical correction is required, they can still continue doing the activities they love—including playing sports.

I respectfully invite you to join me in supporting this resolution designating June 2026 as “Scoliosis Awareness Month” in Pennsylvania.