Our Patient Support Committee (PSC) offers long‑term scoliosis patients a meaningful way to support newly diagnosed patients who are just beginning their own journey to recovery. This group is made up of individuals who were diagnosed young, completed treatment, and are now living full, active lives. While they don’t always provide direct one‑on‑one communication, they share valuable insight, encouragement, and guidance through written messages or short digital recordings—helping families feel less alone as they navigate treatment and healing.

Space in this committee is limited, but if you’re interested in joining, please fill out our sign‑up form. We’ll review your submission and let you know as soon as a spot becomes available.

Requirements:

  1. Be at least 10 years post-treatment and willing to share your long-term perspective
  2. Have strong communication skills
  3. Be comfortable writing letters and making phone calls when needed
  4. Be willing to record short video clips for educational and awareness initiatives
  5. Have experience with writing, proofreading, or content editing
  6. Be able to participate in bi-monthly virtual meetings and collaborative discussions

Current PSC Members

  • Dickie Davis

  • Jeanne Loo

  • Traci Miele

  • Noel Anderson

Patient Research Advisory Committee

Patient Volunteer Committee

Patient Support Committee

Scoliosis Ambassador Committee