Children’s Craniofacial Association is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions.

CCA’s mission is to empower and give hope to individuals and families affected by facial differences.
CCA envisions a world where all people are accepted for who they are, not how they look.

Each year, more than 100,000 children are born with a facial difference and other individuals may acquire one, through illness, accidents, or trauma. We stand ready to help all of these patients - from new parents with a baby in the NICU to an adult experiencing facial paralysis from due to illness. We help these individuals find much needed resources, support them with emotional and social connections, and help them become self-advocates, as we work towards facial equality together.

The majority of our program funding goes into three areas:

• Financial Assistance for Medical Travel
• Support Gatherings for our Families, notably our Annual Family Retreat & Educational Symposium
• Fostering acceptance and preventing bullying

Please join us in this important work, as we make the world a kinder, more inclusive, more accepting place for all.

If you prefer to donate via Zelle, you can do so by sending your donation to Donate@ccakids.com. Click here if you are interested in giving stocks or other types of donations.