Craniosynostosis and Positional Plagiocephaly Support Inc.
The information on this website should not be used for medical advice. Medical or health advice should be provided only by medical or health professionals.
Our mission is to spread awareness, educate and offer support and guidance to families affected by Craniosynostosis and/or Positional Plagiocephaly.
WELCOME TO CAPPS!
Welcome to our community. We are here to provide you with information and strength. Browse our photo gallery - watch our videos - call or email a CAPPS friend.
cappskids001029.jpg cappskids001028.jpg cappskids001027.jpg cappskids001026.jpg cappskids001025.jpg cappskids001024.jpg
Email Syddesi2@aol.com / Phone (516) 232-7015
Have you ever heard of CRANIOSYNOSTOSIS?
cappskids001023.jpg cappskids001022.jpg cappskids001021.jpg cappskids001020.jpg cappskids001019.jpg cappskids001018.jpg
(Click on suture type for info)
CAPPS is a 501(c)(3) Registered Corporation
Amy Galm
President
İCraniosynostosis and Positional Plagiocephaly Support, Inc. 2001-2010
Make an on-line slide show at www.OneTrueMedia.com
cappskids001015.jpg cappskids001014.jpg cappskids001013.jpg cappskids001012.jpg cappskids001010.jpg
What the
doctor said
Cranio Kid
of the month
Our Stories
Our Surgeons
LINKS
Message
Board
CranioKids
cappskids001007.jpg
Board
Message
Capps
cappskids001006.jpg
The Jorge Posada Foundation
If you get lost the
will take you home.
 Insurance Help
cappskids001003.jpg
Home
cappskids001002.jpg
FACEBOOK
cappskids001001.jpg
(Click the flower to learn more)
Donate via Guidestar