Each year approximately 100,000 children in the United States are born with or develop some form of facial anomaly. In many cases, reconstructive surgeons can correct these problems early—often while the child is still an infant. However, many children must undergo dozens of surgeries and procedures throughout their life, and face isolation and teasing from their peers. Throughout childhood and into adulthood, CCA helps families navigate, prepare for, and thrive on the craniofacial journey. Children's Craniofacial Association is the premier organization that supports these children and CCA offers programs and services including Financial Assistance for Medical Travel, hosting the Annual Family Retreat & Educational Symposium, and presenting kindness education and bullying prevention resources in schools across the country, through our #ChooseKind program.
13140 Coit Road • Suite 517 • Dallas, TX 75240 | Toll-free 800.535.3643 • Phone 214.570.9099 • Fax 214.570.8811 | Email contactCCA@ccakids.com
Children's Craniofacial Association
is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas. CCA's mission is to empower and give hope to individuals and families affected by facial differences. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions.
© 2016 Children's Craniofacial Association