Craniofacial Program Resources
ASHA is the national professional, scientific and credentialing association for audiologists; speech-language pathologists; speech, language and hearing scientists; audiology and speech-language support personnel; and students.
Jaw surgery surgery can correct problems with your jaws that cannot be fixed by orthodontics alone. Download this resource to understand more information about this surgery.
In this video, experts from Children’s Hospital of Philadelphia explain why highly specialized, comprehensive care is so important for children with Beckwith-Wiedemann syndrome.
In this video, clinicians and patient families talk about the diagnosis and treatment of craniofacial conditions, including craniosynostosis, hemifacial microsomia, and other syndromes.
AdoptCleft is a support group for parents wanting to adopt cleft children, parents that have cleft children (biological or adopted), and others that can contribute or learn from the conversations.
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
Changing Faces us a charity that helps improve the lives of people with craniofacial abnormalities and transform public attitudes toward people with an unusual appearance.
The Children's Craniofacial Association empowers and gives hope to individuals and families affected by facial differences.
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
CPF is a nonprofit organization that enhances the quality of life for individuals affected by cleft lip and palate and other craniofacial birth defects.
FACES: The National Craniofacial Association assists children and adults who have craniofacial disorders resulting from disease, accident or birth.
The Foundation provides medical, educational, psychosocial and local support resources for people with the 22q11.2 deletion syndrome and their families.
March of Dimes is an international organization that works to prevent birth defects, premature birth, and infant mortality and to support expectant and new parents.
PSHA advocates for the communicatively disabled and the professionals who serve them to insure that the integrity of services is maintained.
Philly Phaces provides peer support, advocacy, and resources to help Philadelphia-area children facing appearance differences from craniofacial abnormalities and cleft lip and palate.