Childrens Choanal Atresia Foundation
Children's Choanal Atresia Foundation mission is to support awareness thus improve diagnosis, research to improve treatment and care, and research to identify possible genetic links and possible long term developmental issues. Choanal atresia is a birth defect that impairs a newborn infant’s ability to breathe. According to the NIH/CDC each year over 750 newborn infants suffocate to death before they reach 27 days of age and are termed SIDS incidents. Some of these deaths may be due to undiagnosed CA. The Foundation also provides Parent-to-Parent support through our “Angel Network” which began in 1989.
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CCAF - Home An open letter to the Womens Congressional CaucusSaving Infant lives Childrens Choanal Atresia Foundation was founded in 1989 to improve the treatment and care for babies born with choanal atresia. The Foundation carries out this mission through programs of research parenttoparent outreach programs education and advocacy on behalf of babies touched by choanal atresia. The Foundation also acts as a catalyst to bring about much needed research to address the immediate treatment and care as well as the long term issues that may not be fully realized. Choanal atresia is a birth defect that truly test parents especially mothers who carry the burden of care.
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