Last summer, in her 18th week of pregnancy, Kerres was shocked to learn that the fetus she was carrying had spina bifida, a neural tube defect in which the spinal column doesn't close completely.
"It was potentially devastating," said husband Adam Kerres, 29.
Though she now thinks the doctor was using "very outdated information" about the defect, "it felt like our hearts were breaking," said Johnna Kerres
, also 29.
The cause of spina bifida
is unknown, and it can have a lifetime of effects on the brain, bowel and bladder function, mobility and learning abilities. However, the severity of those complications varies widely.
The best-known type of spina bifida involves an opening in the back through which the spinal nerves bulge out. These lesions are repaired either immediately after birth or, increasingly, before birth through a 3- to 4-inch cut in the uterus. But that in-utero procedure causes scarring and means the mother can never have a full-term vaginal delivery.
Despite their initial diagnosis, doctors gave the Kerreses a list of hospitals across the country that offered treatment options.
After contacting several of them, the couple got a life-changing call: Drs. Michael Belfort and William Whitehead of Texas Children's Hospital in Houston were calling from Whitehead's kitchen to share more information about the defect and offer hope in the form of treatment.
The doctors developed a method of in-utero surgery involving only two tiny incisions, bringing a much smaller risk of problems for both mother and fetus.
"They gave us a lot more positive outlook, and they gave us a lot of hope," Johnna Kerres said. "Just hearing that [Everett] was going to be OK was a huge, uplifting thing."
The procedure took only a few hours and "went beautifully," said Belfort
, obstetrician/gynecologist-in-chief at Texas Children's Pavilion for Women. Kerres was able to carry to full term, and in September, baby Everett was born.
Less than two weeks later, the whole family was back home in Illinois, celebrating their "very healthy" addition with a photo shoot. For one picture, Johnna Kerres held Everett belly-to-belly in order to show off their scars from the surgery.
"When I look at it, I just think of the journey to get there," Johnna Kerres said of the photo. "I think of the powerful love I have for my son, and I see his strength and resilience.
"We've been so, so blessed. ... The results have been really fantastic."
Everett is now growing normally, Belfort said, with normal neurologic function. He doesn't have the shunt that spina bifida patients often require to drain fluid from the brain, and a clubfoot is being treated with orthotics. He's even getting advanced ratings in some development metrics such as core strength and ability to push himself upright.
"We don't know what the very long-term outcomes are going to be," Belfort said, so the team will continue to monitor his development for at least five years. "This is a lifelong disease. Spina bifida is not something you fix with a single surgery."
In the meantime, he and the Texas Children's team continue to develop their new fetal surgery method for other issues beyond spina bifida and are sharing its lessons with health care centers around the world.
The Kerreses hope to use their picture of Everett and Johnna to raise awareness of spina bifida and the medical advances around it.
"People should know that just because someone has spina bifida doesn't mean they can't have a good quality of life," Johnna Kerres said. "Whether they have fetal surgery or not, they really can do amazing things."