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 !