Wise Cleft Center

04/07/2025

You're Invited!

Join us at 4th Annual Cleft & Craniofacial Family Retreat — the largest gathering of cleft and craniofacial families in Utah!

Bring your whole family for an unforgettable afternoon of connection, laughter, and fun. This is a special opportunity to meet other families who share your journey, exchange stories, and build lasting friendships.

🗓️: August 16, 2025

⏰: 2pm-6pm

📍: Summerhouse Farms, Heber, Utah

Register for your free tickets through the link in our bio or in our stories.

We can't wait to see you!

24/04/2025

We are proud to say we have created the nations first Cleft Center of Excellence. This amazing clinic is a dedicated space to the cleft community, especially pediatric care. We hope the patients who have received care from us so far have experienced the difference in our team’s approach and will recommend us in the years to come.

07/11/2024

"Today is Nayvie Kates' three year Smileversary! We went to her preschool and read "Jacks new smile" to her class, and showed them pictures of Nayvie with her cleft. We even made smiley face party favors bags for all her friends to celebrate the day. She very proudly showed them a picture, and said,
"This is me and my doctor, he fixed my lip." -Nayvie's mom

01/11/2024

"Eli has had a great year this year. He worked through something tough each race and powered through to get 13 out of 85 in his last race. He has all A’s and maintains at least a 3.8. He has wonderful friends. He goes to church and has strong convictions. As a mom with a cleft affected child, we often struggle to see how life might be for our kids. Eli has struggles but 99% aren’t from his cleft. He is 13 so still a long way to go in these teen years, but he is handsome, strong, smart, athletic, and has good morals/beliefs. Sometimes I feel like telling those just starting out, that you will make it. These kids are built tough," Megan, Eli's mom

01/11/2024

"Eli has had a great year this year. He worked through something tough each race and powered through to get 13 out of 85 in his last race. He has all A’s and maintains at least a 3.8. He has wonderful friends. He goes to church and has strong convictions. As a mom with a cleft affected child, we often struggle to see how life might be for our kids. Eli has struggles but 99% aren’t from his cleft. He is 13 so still a long way to go in these teen years, but he is handsome, strong, smart, athletic, and has good morals/beliefs. Sometimes I feel like telling those just starting out, that you will make it. These kids are built tough," Megan, Eli's Mom

14/09/2024

We are excited to welcome our VIP Gaten Matazarro to Cleft & Craniofacial Family Retreat tomorrow September 14, 2024! Gaten is no stranger to craniofacial conditions. He was born with Cleidocranial Dysplasia and is so excited to meet so many of you as we come together to support one another tomorrow!

If you don't have your free tickets to this retreat, there is still time to register! Link is in the bio or our stories. We can't wait to see you tomorrow!

13/08/2024

It's time again for Annual Cleft & Craniofacial Family Event! We look forward to this event all year long. It will be a day filled with support, connection, and fun activities for families impacted by cleft & craniofacial conditions. Click the link in the below for more details and to get your FREE tickets!

https://www.eventbrite.com/e/3rd-annual-cleft-craniofacial-family-retreat-tickets-989997287537?utm-campaign=social&utm-content=attendeeshare&utm-medium=discovery&utm-term=listing&utm-source=cp&aff=ebdsshcopyurl

Join us for an amazing event filled with fun activities, support, and connection for families affected by cleft and craniofacial conditions.

30/07/2024

Care for cleft and craniofacial patients is best managed by a team of specialists who work together to optimize patient outcomes. A comprehensive, multidisciplinary team is a defining characteristic of the accreditation, which we are proud to hold. Our team consists of a pediatric craniofacial surgeon, ENT, audiologists, oral & maxillofacial surgeon, orthodontists, pedodontists, speech and language pathologist, and a team coordinator.

Have you met our team? What’s your experience?

👩🏼‍⚕️

25/07/2024

26/06/2024

Do you know about the ? This vital organization is a non-profit 501(3)c with a mission to support children born with cleft lip/palates and other facial abnormalities. Founded by our very own pediatric craniofacial surgeon Dr. Devan Griner, works tirelessly to ensure that every child born with a cleft or craniofacial condition can receive optimal care & support. The makes our monthly cleft clinic meetings possible. In addition, the foundation holds various events throughout the year offer cleft children and their family’s care, resources, education & support. Jump over to the and give them a follow! You won't want to miss what they have in store this year.

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