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Description:
In 1999, the national non-profit organization Craniosynostosis And Parent Support, Inc. was established by a mother whose child had Craniosynostosis to offer support and information to other families who had a child with Craniosynostosis.
Headquartered in Fredericksburg, VA, Craniosynostosis And Positional Plagiocephaly Support, better known as CAPPS, is dedicated to offering support and providing information to families who have a child with either condition.