The World Craniofacial Foundation is the primary source of voluntary support and advocacy for children with craniofacial abnormalities. We help some of the half million children who have acquired and are born each year with deformities so severe that they endure lives of isolation and shame. Many abnormalities are so extreme that children have difficulty eating, breathing, hearing and seeing. Media attention surrounding the successful separation of the Egyptian twin boys brought the Foundation’s efforts into public attention. 

WCF is dedicated to helping children with craniofacial abnormalities gain access to life-changing medical procedures. All people with craniofacial abnormalities will receive excellent craniofacial care regardless of geography or socio-economic class. As an organization, the World Craniofacial Foundation strives to be the global leader in advocacy for superb craniofacial patient care, education and research, as well as the primary resource of philanthropic support.