Face to Face Portrait Project
The Face to Face Portrait Project creates portraits of children and adolescents with craniofacial conditions to help them see themselves in a different light.
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The Face to Face Portrait Project creates portraits of children and adolescents with craniofacial conditions to help them see themselves in a different light.
Important questions to ask potential providers when looking for a program to treat your child’s craniofacial difference.
Information and advice about how to ensure proper nutrition and manage feeding difficulties that affect many babies with cleft lip and palate.
Learn more about jaw surgery and how it's managed at CHOP.
Learn more about craniosynostosis and surgical treatment for the condition.
The Foundation provides medical, educational, psychosocial and local support resources for people with the 22q11.2 deletion syndrome and their families.
Philly Phaces provides peer support, advocacy, and resources to help Philadelphia-area children facing appearance differences from craniofacial abnormalities and cleft lip and palate.
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.
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
The Children's Craniofacial Association empowers and gives hope to individuals and families affected by facial differences.