Resources for Parents & Patients
Craniosynostosis and Positional Plagiocephaly Support
Craniosynostosis And Positional Plagiocephaly Support (CAPPS) is the pioneer and leader in supporting and educating families diagnosed with Craniosynostosis and/or Positional Plagiocephaly. CAPPS was started by parents, not physicians, who personally experienced the condition.
- Phone: 888.572.5526
- Email: Info@cappskids.org
- Website: https://www.facebook.com/Cappskids/www.cappskids.org
- Facebook: https://www.facebook.com/Cappskids/www.facebook.com/Cappskids/
The National Association for Plagiocephaly
The mission of The National Association for Plagiocephaly is to raise awareness, and educate parents and the general public about a common, treatable condition known as plagiocephaly.