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A sampling from our Member Sites(s) Use the link above to review/visit
Tori's Web Site
Tori bas born 1/8/03 with a unilaterial cleft of the lip and palate.
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
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
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.
Click here to preview and visit the member sites in
The AmeriFace Circle of Smiles ©.