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FACES: The National Craniofacial Association
(423) 266-1632
(800) 332-2373
P.O. Box 11082, Chattanooga, TN 37401





Kiall's Story

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Kiall's Story

Meet our little blessing, Kiall.
He was born with a rare condition called Apert Syndrome. He is a sweet and tough little guy who is great at doing what babies do best...
Bringing joy to our lives!

The surprise and struggle is real. I was scared hearing my son’s diagnosis shortly after he was born. What did this mean for our family? Is he going to be ok? What do I need to do? These questions were asked, but not answered. Finally, after turning to the internet for information, I found FACES and was able to call and get answers to my questions. I also found out that FACES could help financially! I felt an immeasurable relief for which I am SO appreciative!

Thank you to all the supporters of FACES!

Cori White & Family

Thank you, Our Friends, for helping Kiall and all the children of FACES. Your continued help is essential.

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