We studied how common pain was thought to be due to muscle spasticity in the legs or arms is in children/adolescents with CP.
Jen Lyman provides a parent perspective on powered wheelchair standing devices as it relates to Dr. Lisa Kenyon's research article.
What do you do when you want to help your child but your local providers don't have the resources? You travel for treatment. In this personal story, Sophia's family describes their experiences traveling to Gillette Children's for treatment, including both neurosurgical and orthopedic surgeries.
The findings of this article demonstrate the need for improved screening rates in women with CP, and highlight areas for improving their screening experience.