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.
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.
In this episode of Pediatric & Congenital Heart Talks, Meryl Cohen, MD, reviews variations in AVC defects and how valvar imbalance impacts strategies of care.
Learn more about craniosynostosis and surgical treatment for the condition.
Learn more about jaw surgery and how it's managed at CHOP.
Here are some common questions parents have when they think about holding their baby in intensive care. Your care team is here to support you ever step of the way.
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.