There was nothing unusual about Natasha Himes’s seventh pregnancy or delivery. Like her previous six, this one was easy and uncomplicated. While all of her other children were born in a hospital, the Ephrata woman wanted to have this baby at home.
Dec. 19, 2018, started out as any ordinary day. Himes’ children, ranging in age from 2 to 13, completed their homeschool lessons, and the midwife visited. The baby wasn’t due until Christmas, but he had other plans.
At 3:53 p.m., Knoxley came into the world, weighing 8 pounds, 8 ounces, and 21 inches long. “I was in labor just 53 minutes,” Himes said. “The midwife walked in as I was pushing.”
When the midwife saw Knoxley had a cleft palate, he was transferred to the neonatal intensive care unit at WellSpan Ephrata Community Hospital where he was diagnosed with Pierre Robin syndrome. According to the National Institutes of Health, the rare condition occurs in about 1 per 8,500 births.
Children born with this condition have a smaller-than-normal lower jaw and a larger-than-normal tongue for the size of the jaw. The tongue falls back in the throat and obstructs the airway, making it difficult for the child to breathe. In many cases, the child also has a cleft palate, like Knoxley.
Five days after being admitted to the Ephrata hospital, Knoxley was transferred to Penn State Children’s Hospital.
“His breathing was really noisy because his airflow was obstructed,” said Dr. Jeffrey Kaiser, chief of Neonatal-Perinatal Medicine at the Children’s Hospital. “We kept him on his belly so that his tongue would fall forward, and his airway would remain open.”
“The doctors were amazing,” Himes said. “You could tell they really cared about Knoxley and wanted what was best for him.”