Our mission is to spread awareness, educate, offer support and
guidance to families affected by Craniosynostosis and/or Positional
Plagiocephaly. Please use this site to educate yourself and arm yourself with the knowledge to advocate for your child. CAPPS was started in 1999 by our founder, Jennifer Pitchke. Jennifer saw a need for education and awareness and brought to life the group CAPPS. Click on the window to see our
FACES OF CRANIOSYNOSTOSIS video
AMY GALM
President and Executive Director of Craniosynostosis and Positional Plagiocephaly Support Inc. Mother of four including, Maxwell DOB 04/18/00 - life experience with Craniofacial surgery and Cranial Molding Band. Has sponsored and counseled hundreds of families worldwide facing a diagnosis of Craniosynostosis and Positional Plagiocephaly. Initiated "Blankets for Babies Program". Coordinated efforts to bring a baby born with Apert Syndrome from the Philippines to Medical City Dallas for a series of pro bono surgeries that included; syndactyly release of fingers and toes, a cranial vault expansion, ear tubes and a Cranial Vault Reconstruction. Coordinated, sponsored and helped secure the Medical Visa, airline tickets, food and a host family for the 6 months the family would be in the USA. Continuously educate pediatricians and non-medical persons regarding early diagnosis and management of Craniosynostosis and Positional Plagiocephaly by setting up meetings, distribution of educational materials printed by fund raising and educational/medical advocacy. Contact Amy - CAPPSKIDS1@aol.com
