Children’s Craniofacial Association

Children’s Craniofacial Association (CCA) provides extensive support and resources for children and parents living with craniofacial conditions. Governed by a board of directors and a medical advisory committee, CCA empowers and gives hope to individuals and families affected by facial differences.

Some services they provide include:

• A toll-free support line with a list of experienced and qualified craniofacial reconstructive surgeons, teams, and centers
• CCA Network, a quarterly newsletter highlighting patient stories and advice from healthcare professionals
• Family networking by connecting those who are interested in sharing their experiences and talking with others in similar situations
• A blog (ccakidsblog.org) as a platform for advocacy, awareness, and updated resources
• The Annual Family Retreat and Educational Symposium, held in June to educate and connect craniofacial individuals and their families
• Annual weekend retreats
• Financial assistance for transportation and accommodation when travelling for surgery

For more information, contact program director Annie Reeves or find out more at
www.CCAkids.org !
Phone 214-670-9099
Fax 214-570-8811
Toll-Free 800-535-3643
Email AReeves@CCA.kids