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The AmeriFace Circle of Smiles - Welcome to the AmeriFace Circle of Smiles©! In conjunction with the AmeriFace, cleftAdvocate, Goldenhar Syndrome S

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The AmeriFace Circle of Smiles

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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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   Tori's Web Site Preview Go
Tori bas born 1/8/03 with a unilaterial cleft of the lip and palate.
   Home page of Riley Forth and family Preview Go
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 Preview Go
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


   Introducing Ilona Preview Go
Starring this site is my daughter Ilona who was born in February 2005 with bilateral cleft lip and palate. This is her story so far, more updates on life in our hometown Helsinki, Finland will follow...
   Jenny's Story: My Life with Crouzon Syndrome Preview Go
This website has a lot of information about Crouzon Syndrome. It is written by a mother who has Crouzon Syndrome and describes her experiences with growing up with the syndrome and the experiences she is going through with her two children who also have Crouzon Syndrome. The aim of the site is to educate and inspire.
   Zachary's Journey Preview Go
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.
   Emily's Story Preview Go
This is a blog about how we are dealing with the news that our unborn baby, Emily Rose, will have bilateral cleft lip and palate. The blog will continue after her birth with pictures of Emily before and after surgery and lots of info on how we are dealing with our new little miracle.
   Cleft Lip & Palate Website Preview Go
This site is mantained through Parents Place Cleft Lip and Palate Message Board Leader. We have pictures of our cuties, a page of our many surgery stories and many other pages that we feel will be useful. Also will link you to our support group on iVillage.
   Langer Loksh Preview Go
An honest blog about what it feels like when your kid comes out healthy but crooked.
   Cleft Notes Preview Go
Alex from birth (27 July 1996)to present. Bilateral Cleft lip w/submucous palate. Lots of pictures showing his progression. Little bits of information to help others.






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