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 Listed in: 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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Debra Shiveley Welch
My site is for the promotion of my books, but more importantly, there are essays and poems relating to craniofacial differences.
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cleftAdvocate
cleftAdvocate is your one-stop resource for education and inspiration! Insurance and advocacy information included. Visit the Photo Gallery and enroll with the Family-To-Family Connection, our on-line support network!
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Rowan's Odyssey
Rowan's site about his bilateral cleft lip and palate.
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Elijah Ashby's Story
Elijah Ashby was born with Nasal Aplasia, Frontonasal Dysplasia, Mid Facial Cleft, Bilateral Choanal atresia, Lipoma of the corpus callosum, Hypogenesis of the corpus callosum and a cleft lip. He has a GJ Tube, G tube for feeding.
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The Ort Family
Our family blog, including the story of our 12 year old son who was born with a cleft lip and palate.
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Camille
Camille is a young French girl suffering of Crouzon and Chiari syndroms.
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Langer Loksh
An honest blog about what it feels like when your kid comes out healthy but crooked.
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Cora Chin
Site tells about Cora's life from birth(6/3/04) to present. She was born with cleft lip and palate and other issues due to Amniotic Band Syndrome in addition to hydrocephalus. Her website contains many updates and pictures of how she has changed. It also contains many links to websites we have found helpful
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Cassandra Jane
Cassie's site. Cassie was born with a unilateral cleft lip and cleft soft palate.
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Faceforward
Faceforward forums are self-run and are the place for adults and parents of children with cleft lip and palate to share experiences, get advice, chat, arrange meetings, and provide support. All welcome.
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