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The AmeriFace Circle of Smiles ©Health & Wellness > Support
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Welcome to the AmeriFace Circle of Smiles©! In conjunction with the AmeriFace, cleftAdvocate, Goldenhar Syndrome Support Network, Crouzon Support Network and Treacher Collins Syndrome Support Network websites, as well as the Family-To-Family Connection listserv, the Circle of Smiles© brings families together...families whose lives have been touched by cleft lip and palate and other craniofacial anomalies, including acquired facial differences. Come meet these beautiful children, teens, and adults and share their experiences. Everybody...SMILE! © AmeriFace





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Zachary's Journey
Zachary is baby B of a set of fraternal twins. His twin sister was not born with a cleft. We knew prenatally that Zachary would have a complete bilateral cleft lip and palate. Our despair has been replaced by hope and complete bliss that Zachary, his twin, and their older brother bring.
Tori's Web Site
Tori bas born 1/8/03 with a unilaterial cleft of the lip and palate.
Raising a Child with a Cleft Lip and Palate
Finding out that your child is going to be born with a cleft lip or palate is not the end of the world. We were very surprised when we found out that our youngest child has a bilateral cleft and palate.A child with a cleft lip or cleft palate is no different than any other child they just have a correctable situation if you have access to proper medical care.
Home page of Riley Forth and family
Riley was born 01/24/98 with a complete unilateral cleft lip/palate. He has undergone lip repair surgery which was very successful.. The surgery was done at "Sick Kids" in Toronto . He now wears a nasal splint taped into his nostrils that is removed for feedings. Riley's a loveable, cheerful and beautiful little boy who is much loved by Daddy, Mommy and big brother Darby
Abigail Celeste Hunter
This website shows my family which include my husband, Tony, myself (Becki), my #1 daughter, Ashlee Lannette, and our newest addition, #2 daughter, Abigail Celeste. This website is dedicated to our baby girl, Abigail, as she was born with cleft lip and we want her to know that this birth defect is not a set back in life, but a gift given to her by God to make her a s

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· Community Created 05/18/1998
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