C.A.R.E.

Our Mission: To surprise kids with craniofacial difference (Newborn thru 20) as they face, sometimes numorous, procedures, test, or surgeries that can fill a child's life who has been born with craniosynostosis and/or other abnormality of the face or skull.
Fact is one in 50 children are born with a craniofacial defect that can sometimes require a lifetime of follow-up which can include numorous corrective procedures. As I found with my daughter's skull reconstruction when she was 10 yrs old one little card or a quick note from a stranger can be all it takes to help give a child an extra boost of courage.