This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
Online. Resource for educational materials, cleft/craniofacial team information, emotional support and more. Local and regional family networking for parents, kids, teens and adults. Hosts the North American Craniofacial Family Conference for individuals and families dealing with all craniofacial conditions, including acquired facial differences (trauma, illness and disease).
Online. Members 2100+. Founded 2000. Support for families who have, or want to, adopt children with cleft palate and/or cleft lip internationally.