Abraham's Journey With Prenatal Cleft Lip and Palate

Young Abraham smiling for the camera.
Read Previous Read Next

Related News

A New Smile and Bright Tomorrow for Michelle

July 14, 2023 – Michelle’s journey started at  Nicklaus Children’s Hospital  before she was even born. We found out that Michelle was going to be born with a cleft lip and palate at my 20-week anatomy scan. The news was unexpected and was difficult to understand but I was assured that everything was going to be fine and that the pediatric craniofacial team at Nicklaus Children’s was one of the best.

Patient of the Month: Gabriela

October 01, 2018 – Following an emergency C-section, Gabriela’s mother, Katherine, was shocked to see that her new baby was missing part of her face. Gabriela was born with a cleft lip and palate. Katherine researched for hours to find the best doctors to fix her daughter’s condition and came upon the craniofacial team at Nicklaus Children’s Hospital.

Speak Now for Kids Family Advocacy: Tad's Story

August 10, 2020 – Over the last two years, Theodore “Tad” Hartrick has spent months at a time at Nicklaus Children’s Hospital. Like Tad, there are many children in the state and in the nation who rely on access to pediatric care and Medicaid funding. Here is a message from the Hartrick family in support of this year’s Speak Now For Kids Family Advocacy Week campaign.

South Florida hospital is leader in treating apert syndrome

September 07, 2018 – Dr. Chad Perlyn and Dr. Mislen Bauer from the Nicklaus Children's Craniofacial Center are committed to helping families and children with apert syndrome. Check out this segment featured on WPLG Local 10.