Imagine a world where all people are accepted for who they are, not how they look. This is the vision for the Children's Craniofacial Association.

Both Connor (left) and Francis (right) have Treacher Collins syndrome. Connor has taken a liking to Francis since they met at CCA's Annual Family Retreat. When Francis was a baby, his adoptive parents were told by the doctors he should be institutionalized because he would not be functional in society. Thank goodness they did not listen. Today you may call him Dr. Francis Smith!

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. To learn more about CCA Click Here!