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OUR CLIENTS

Callan

Callan - Courage Wears a Smile

Callan’s mom Jennifer says, “Dealing with the stress and burden of everything else during an emergency or surgery is heavy enough, but knowing that help is there when we need it is an amazing relief.

Callan was born with Complex Multi-Suture Syndromic Non-Specific Craniosynostosis. In addition, he also has a genetic component with overactive osteoblasts that causes his skull bones to fuse back together rapidly, which puts a lot of pressure on his brain.

Thank you, Our Friends, for helping Callan and all the children of FACES throughout the years.

Your continued help is essential.

Kiall

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As a parent, I vividly recall the questions that filled my mind when Kiall was born – Will he be okay? What should I do? What does this mean for his future? 

Kiall was born with Apert Syndrome, the premature closing of the skull sutures, underdeveloped mid-face region, large forehead, webbed fingers and toes.

Mary & Wesley

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"...Gwen and Paul weren’t aware they were having twins until 37 weeks pregnant — much less, twins with a complex medical journey called Pfeiffer syndrome.”

Mary and Wesley were born with Pfeiffer syndrome, (Premature closing of the skull sutures, underdeveloped mid-face region, bulging, wide-set eyes)

Braeleigh

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"...without FACES I am not sure how we would be able to get Braeleigh to the quality care she needs and deserves.”

Braeleigh was born with Apert Syndrome, the premature closing of the skull sutures, underdeveloped mid-face region, large forehead, webbed fingers and toes.

Gracie

Gracie

"...it was a blessing and an honor to be part of something as extraordinary as FACES Camp...I’m definitely going to be a counselor again!”

Gracie was born with Crouzon Syndrome, the premature closing of the skull sutures and underdeveloped mid-face region.

Zane

Zane

"There aren’t enough ‘Thank yous’ in the world that I could give to FACES and those who work there... You have been our light in some stressful times!"

Zane was born with Apert Syndrome, the premature closing of the skull sutures, underdeveloped mid-face region, large forehead, webbed fingers and toes.

Elena

Elena

"To be honest, when Elena was born, we never could have foreseen the brilliance that has greeted us in her team of doctors, nor the kindness of people we don’t even know helping us with all the expenses we’d never imagined."

Elena was born with Goldenhar Syndrome, abnormalities to one side of the face that affect the eye, jaw, and ear.

Kayden

Kayden

"...Kayden was born on June 9, 2014. We were caught by surprise when he was born with a bilateral cleft lip and palate. ”

Kayden was born with Cleft Lip & Palate, the incomplete closure of the lip and palate.

Lemuel

Lemuel

"FACES has been with our family every long car ride...up early in the morning, car loaded, Lemuel and Bronwyn in PJs, and leaving our small town to drive 12 hours to meet with a craniofacial team."

Lemuel was born with Treacher Collins Syndrome, underdevelopment of the eye sockets, cheek bones, lower jaw and ears.

Cammi

Cammi

"I was 21 weeks pregnant when I had the ultrasound that showed my little girl had a cleft lip and possibly a cleft palate. My husband insisted that I terminate the pregnancy, and when I refused, he left us."

Cammi was born with Cleft Lip & Palate, the incomplete closure of the lip and palate.

Wes

Wes

"With all the challenges, pain, fear... that fills this journey, it is all faced with strength that is fueled by kindness and the support of caring individuals like you."

Wes was born with Cleft Lip & Palate, the incomplete closure of the lip and palate.

Karson

Karson

"He is now a smiling eight-year-old little boy who has the confidence to tackle the world."

Karson was born with a facial hemangioma, a non-cancerous tumor that is reddish in color.

FACES: The National Craniofacial Association
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