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Welcome to Cranio Kids!
We are glad you found us and hope that you find the resources and support you are seeking here. Cranio Kids was started by a mother and father looking for information on craniosynostosis. In June of 2004 their son Dillon was born with bicoronal and metopic craniosynostosis. After doing research on the condition, they noticed there were few places for information and support. They decided to do something about it, and Cranio Kids was born. The goal of Cranio Kids is to create a caring and educational environment where families can come for support, and to raise awareness on this virtually unheard of condition. Come on in to our support forums, we would love to meet you and hear about your journey!
Cranio Care Bears
Cranio Angel Network
Childrens Craniofacial Association

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