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.
What to Expect at Your First Visit
Your child’s first visit to Texas Children’s Craniofacial Program will include a complete exam of the child’s head shape by a neurosurgeon and/or plastic surgeon. Our team has access to state-of-the-art technology, such as the 3DMD imaging system and the laser STAR scanner, and a wide range of resources to properly and accurately diagnose craniofacial issues.
