Click here if you are trapped in
someone's frames
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WIDE
SMILES | |||
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Got a question? Search Cleft Links for an
answer! Topics include: ·
Surgery ·
Causes? ·
Speech |
WELCOME! This website and other internet activities are maintained on a volunteer basis. Your financial support will help keep online and offline activities available for others. Thank you.
PLEASE NOTE: Information provided is not to be construed as medical advice, it is made available to you for informational purposes only. Check with your personal physician before embarking on any change in routine or in making decisions regarding your healthcare or that of your family. Don't forget to visit the Web Store All proceeds go to help WideSmiles | ||
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One child in
700 is born with a cleft. It is the fourth most common birth defect, and
the first most common facial birth defect. And yet so many parents feel so
alone. | |||
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Contact
Information | |||
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Postal
Address Wide Smiles Phone: 209-942-2812 Electronic
Mail: | |||
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Network With
Others: |
Who Has a Cleft? | ||
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·
Cleft-talk ·
View our Cleft Talk
Quilt ·
Check out Real
Time Chats in the Wide Smiles
Conference Room ·
Outreach: Reaching out to a
new family? Click here for Supportive
documents. |
KIDZ Club area is for kids, created by kids born with clefts. Stop by and have fun! Journey: For Adults Born with Clefts The People Side: Who Has A Cleft, Feelings on Birth, Surgery & More Pacific Cleft Prevention Program Fill our their survey here
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NEW! Lippy the Lion - A goodwill
ambassador for cleft lip and palate, all around the world. Lippy is a very special lion. He
was born with a cleft lip. Now that his lip is all stitched together,
Lippy has decided to travel the world, visiting girls and boys who
understand what it means to be born with a cleft lip and
palate. Watch his page and see all the
adventures Lippy has while he visits his friends all over the world. Add
your name to Lippy's itinerary and someday, before you know it, Lippy will
come visit YOU, too! | |||
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Medical
Resources | |||
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Clefts & Beyond: Related
Syndromes ·
Support section: Online
& offline support for various craniofacial
conditions ·
Information
concerning some Rare
Syndromes & related conditions ·
Looking For A
Doctor? Try Here: ·
Question and Answer Sessions
with Plastic Surgeons - View the logs of these informative
sessions! | |||
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More Resources - Not all Cleft
Related | |||
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Info on Military
Insurance ·
EIP: Early Intervention
Programs |
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Helpful Products
for Parents &
Kids ·
Resource Mall: Books, &
More
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NEW!
FaceUP! Educating the Media
about Cleft New! Jacob’s
Report on Cleft Lip and Palate! | |
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* FRIENDS OF WIDE SMILES
* | |||
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Our heartfelt thanks to our Wide Smiles
Volunteers |
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Joanne Green is Founding
Director of Wide Smiles. Winner of 1997 Parent-Patient Leadership
Award | |||
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Yahoo Medical Site of
Week, |
Sept 3, 1996 |
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Do you have a homepage? A webring links together homepages of a similar topic. This webring is open to any individual or family who is dealing with cleft lip and/or palate and/or other craniofacial anomalies.
To sign up for the ring, please
click here
.
You will be emailed the
code to put on your page
If you have any questions about
joining the ring, please email Joanne Green
.
WebRing
FAQ: WebRing HTML Code
Wide Smiles Circle of
Smiles
This Circle
of Smiles site is owned by Joanne Green. Want to join the Circle of Smiles ? |
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If you have questions about joining
the ring, please email CircleOfSmiles@yahoo.com.
Copyright © Wide Smiles,
Inc
Revised: July 07, 2008