We have one goal: to make the world a better place for kids with facial differences.
Each year approximately 50,000 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.
