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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 and shortly there after he was diagnosed with bicoronal and metopic craniosynostosis. After doing research on the internet, they noticed there were few places online for family networking 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, friendships, and fun. Come on in to our support forum, we would love to meet you and hear about your journey! |
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