Resources for Families

Parents with children who have been diagnosed with a craniofacial condition often seek educational resources and information on local support groups. Our experts have collected a list of helpful online resources for patients and their families.

Children's Craniofacial Association 

Children's Craniofacial Association is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas, dedicated to improving the quality of life for people with facial differences and their families. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions. The CCA website offers information for children and parents touched by a craniofacial diagnosis.