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When Daniel was born nine years ago with a cleft lip and palate, micrognathia, and almost no lower jawbone, he needed a tracheostomy to breathe and a feeding tube to survive. His parents, Robi-Lyn and John, faced not only the fear of his complex medical needs but also the overwhelming cost of getting him to life-saving care.

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For over 50 years, FACES: The National Craniofacial Association has been dedicated to assisting children and adults with craniofacial disorders resulting from birth, disease, or accident.

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Save the Date: FACES Camp
Mark your calendars for June 14–19, 2026!
FACES Camp is a week where kids and teens with craniofacial differences can connect, explore, and just be themselves in a supportive, joy-filled community. More details are coming soon—but for now, save the date and get ready for an unforgettable summer.

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The heart & the hub of the craniofacial community since 1969

FACES helps Blessing get to the craniofacial surgeries she desperately needs.

Whether you're looking for help for yourself, or for someone else, we can help you find the information and support you need.

 

Call Us Toll Free at 800-332-2373

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FACES: The National Craniofacial Association

5325 Old Hixson Pike | Hixson, TN 37343 | USA

(800) 332-2373

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50 Years of Serving Families
FACES is a member organization of America's Best Charities
FACES is a member organization of GuideStar Exchange
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A member organization of America's Best Charities

FACES The National Craniofacial Association is a 501(c)(3) nonprofit organization incorporated under the laws of the State of Tennessee.

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Since 1969, FACES: The National Craniofacial Association, has served children and adults throughout the United States with severe craniofacial disorders resulting from birth, injuries, or disease. There is never a charge for any service provided by FACES.
Our program services address three distinct areas:

Client Travel, Public Awareness and Understanding, and Information and Support.

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