This site is dedicated to our daughter Jaimeson, who was born with Treacher Collins Syndrome, and to our son, Anderson, who was born with Goldenhar Syndrome.
We hope that this Web site will be helpful to those caring for a child with a facial difference, or to anyone seeking to learn more about various types of craniofacial conditions. We also hope to facilitate parent-to-parent networking and support, and to spread understanding and acceptance of individuals with facial differences.
Our mission is to provide support via information and inspiration. We want to let individuals and families know that they are not alone.
The information and resources provided here are for educational purposes only. This site is not engaged in rendering any professional services or medical, pharmaceutical, or therapeutic advice. The information provided in these pages—or any links from this Web site—should not be used as a substitute for direct professional advice by qualified doctors and/or other healthcare professionals.
Friendly Faces is an interactive resource—we welcome your feedback.