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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. CCA's mission is to empower and give hope to facially disfigured children and their families.
CCA envisions a world where all people are accepted for who they are, not how they look.
What is a craniofacial disorder?
A craniofacial disorder refers to an abnormality of the face and/or the head. Craniofacial differences can result from abnormal growth patterns of the face or skull, which involves soft tissue and bones. A craniofacial condition may include disfigurement brought about by birth defect, disease or trauma.
For more information on craniofacial disorders and CCA Kids, please visit their website - www.ccakids.com - or call 800.535.3643.
CCA Services
CCA provides the following services for children and famlies suffering from craniofacial conditions:
Doctor Referral
Financial Assistance
Qualified Centers
Family Networking
Toll-Free Hotline
Educational Booklets
Information and Support
Financial Assistance
CCA Newsletter
Chers Family Retreat
Public Awareness
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