Patient of the Month: Gabriela


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Abraham's Journey With Prenatal Cleft Lip and Palate

July 19, 2021 – Abraham's mother was seven months pregnant when she found out her son was diagnosed prenatally with cleft lip and palate. Worried about her baby's future, she began a search for answers that led her to the Craniofacial Center at Nicklaus Children's Hospital, where she became the first parent to consult with the program about a prenatal patient. At 6 months of age, Abraham underwent the first of many surgeries.

Patient of the Month: Theodore

March 15, 2018 – When she was just 18 weeks pregnant, Micheleen, learned that her baby would be born with a congenital heart defect called hypoplastic left heart syndrome (HLHS), in which the left side of the heart is severely underdeveloped, as well as a cleft palate and cleft lip.

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.