Childrens Craniofacial Association

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Childrens Craniofacial Association

Children's Craniofacial Association (CCA) was founded in 1989 to meet the unmet needs of families across the United States who has been affected by craniofacial differences. (CCA) is a non-profit organization based in the United States whose mission is to empower and give hope to individuals and families with facial anomalies. CCA is a family support organization recognized by government, educational and medical across the United States health care organizations. Children Craniofacial Association is dedicated to the empowerment and to give hope to individuals and families affected by facial differences. CCA is headquartered in Dallas, Texas. Nationally and internationally, the ACC meets the medical concerns, financial, psychological, emotional and educational for craniofacial conditions. The mission of the ACC is to empower and give hope to individuals and families affected by facial differences. In June 1990, the family holiday of the first Cher was held in Orlando, Florida so that families could come together to share resources and support. CCA has provided families with a list of the International Society of Craniofacial surgeons so they can achieve quality care. The funding program was launched to help families with travel and lodging when it was necessary to visit the relatively few US centers. CCA has printed the first two booklets syndrome, and the first bulletin in 1993.In 1991, the organization's name was changed to children Craniofacial Association to reflect the need to bring families on board for their children are young so they can enjoy  programs and services during every stage of their life. Now, 25 years later, it was brought to a whole generation of CCA children, many continue to attend the retreat each year, and young adults are now role models and mentors for younger. And 25 years later, although the technology has changed dramatically, many basic needs for families affected by craniofacial conditions remain the same, and the CCA continues to provide these needs. CCA now has 14 books published syndrome, added 14 an overview page that describe syndromes and related topics having craniofacial conditions and newsletter went from a 4 pager in 1993, with distribution from a few thousand to 24 pages today with a distribution of about 14,000. CCA continues to provide a list of craniofacial surgeons who are members of the International Society of Craniofacial Surgeons, but an extensive list, and continue to provide financial assistance for families who must travel for their care. Today, more than 7,000 families are treated under Craniofacial Association CCA.

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