Children’s 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, parent-to-parent 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. There is nothing more frustrating for a mother than to have provided every comfort possible to her child, yet still feel completely inadequate in her care. The loving act of breastfeeding for example, can be a daunting if not impossible act. With your help, Children’s Choanal Atresia Foundation can fund research to improve treatment and care, like the nasal stent project, and continue to provide resources through information, special needs programs, and services such as our parent-to-parent program.

Children’s Choanal Atresia Foundation is the only private source for funding in support of research for choanal atresia.