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.
Showing 1 - 10 of 16 results
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.
Congenital Adrenal Hyperplasia: A Parents’ Guide is a comprehensive guide for parents of children with CAH, written in plain English by an endocrinologist and a mother of a child with CAH.
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.
Researchers at Children's Hospital of Philadelphia are working to create a non-invasive device to measure brain oxygenation during CPR and critical care, with the goal to reduce brain injury and death.
Learn more about craniosynostosis and surgical treatment for the condition.
Learn more about jaw surgery and how it's managed at CHOP.
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
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.