Baby's Rare Genetic Condition Caused Skull to Form Abnormally: 'I Think She's Beautiful,' Mom Says
Amber Thibault's daughter, Halle Cosgrove, has a rare genetic condition called Pfeiffer syndrome
Amber Thibault and Floyd “Ray” Cosgrove were thrilled last year when they found out Thibault was pregnant with their second child. But they never expected that their lives would be turned upside down the day she was born.
Thibault says there was nothing out of the ordinary about her pregnancy with her little girl, Halle Cosgrove. But doctors whisked the baby away after her birth and, four hours later, delivered shocking news.
“[Doctors] didn’t know what it was at first,” Thibault, of Redding, California, tells PEOPLE. “They told me she had really low-set ears and that her head was cone-shaped. They started feeling around and realized it was her skull. Then they said they were pretty sure it’s Pfeiffer syndrome.”
Pfeiffer syndrome is a rare, genetic disorder in which some skull bones fuse together and grow abnormally, according to the National Institute of Health. The growth usually leaves children with high foreheads, wide-set eyes, an underdeveloped jaw and an altered nose. The illness affects one in 100,000 people, the NIH reported.
Thibault, 27, says the condition is so rare that doctors never thought to check for any signs during her pregnancy. She was “in shock” when they receieved the diagnosis.
“When I saw her, [her appearance] didn’t change my mind about anything. I just held her and she was just the cutest little baby,” the mom of two tells PEOPLE. “When I first saw her and held her, she was my perfect little baby so I tried to block out any negative things. I said, ‘There’s nothing wrong with her.’ I didn’t want to believe she had that.”
Still, the mom had to come to terms with her daughter’s syndrome. And Thibault says she cried in her hospital bed as she researched Pfeiffer online — and learned that the late singer, Prince‘s, son had the syndrome and lived for just six days.
Thibault — first shared her story with Love What Matters — says she was devastated by what she read, and was relieved when doctors cleared up some misconceptions about the illness.
“Her surgeon told us that as long as [children] get the surgeries and procedures that they need on time, they should have a normal life expectancy,” Thibault says. “That made me really excited. I was so scared every night that I’d wake up and she wouldn’t be here anymore, so that just made our day.”
When Halle was five weeks old, she underwent a dangerous surgery in which her skull was removed to reduce swelling. Now five months old, she’ll need to undergo several more surgeries in the future “to make room for her brain.” She will undergo Chiari decompression surgery in November, which doctors say will help with any speech delays and sleep apnea.
Despite the invasive surgeries, Thibault says the family has been adjusting well to life with Halle.
“We thought it would be a huge struggle, but I think it’s brought our family closer together,” Thibault tells PEOPLE, noting that her toddler son Sawyer loves being a big brother. “He loves her. He’s constantly trying to pick her up out of her swing. He loves having a sister.
Thibault has spoken openly about Halle’s illness, never hesitating to share photos of the baby girl online.
“When she grows up, people with disabilities are always gonna have some insecurities,” she tells PEOPLE. “I want her to know that I think she’s beautiful and I’m not afraid to show her off.”