Craig's Success Story


Read Previous Read Next

Related News

Patient of the Month: Gabriela

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.

Patient of the Month: Theodore

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

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

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.