OKLAHOMA COUNTY, Okla. (KFOR) – About two years ago, a family in a Midwest city was given the news that their son would have a spinal cord defect and that he might never walk, but now their daughter is running, climbing and leaning. .
“We thought on the day of the diagnosis three years ago that our world was going to be flipped upside down,” Megan Kershaw said.
The man, Robert, told KFOR doctors that his daughter was born with spina bifida.
Spina bifida is a spinal deformity that develops while in the womb, where the spinal cord does not form properly.
“That causes nerve damage, lower extremity weakness, and sometimes core weakness,” said Oklahoma Hospital OU Health Physical Therapist Assistant, Daryn Wauters.
Robert said that six out of 10 babies diagnosed with spina bifida are aborted.
“It was pretty hard to hear right out of the gate,” added Robert. “It was pretty scary.”
Their two-year-old daughter, Millie and Megan, underwent surgery before Millie was born to repair her spine while still in the womb.
“The experience of my life was awesome,” says Megan.
When Millie was born, her family told KFOR they decided to have her on her feet and walk.
Millie went through physical therapy for one year at another facility before transferring to OU Health Oklahoma Hospital.
Wauters is a very sensitive part of Millie’s body.
She has been doing physical therapy there for about a year now.
“It’s progressed so well that we’re taking it from just the physical level.” So now it’s just, you know, walking and playing like a normal kid,” Megan said.
When Megan and Robert saw Millie walk for the first time, they were all so moved that even some tears were shed.
“I feel really blessed that, you know, he’s walking,” Megan said.
The pain itself should be treated as pain.
“That’s what I do in my job. I always say that one of the best things in the world is that I get to meet some amazing kids and families and help them and their kids reach, you know, the highest role they can and it’s really rewarding,” Wauters said. my heart is so happy. I love them and their families. So when they reach those goals and I see their parents excited about that and for their son, being a mother himself, I know they’re excited to see what makes me happy and right.
Robert remembers when Millie broke out of her first bra, saying that she remembered him from the movie Forest Gump.
“I think it’s the next thing for him to run.” [Millie’s current braces]He had not unlike the first goats. It was kind of cool, kind of like the movie Forest Gump, when he’s running around, bucking the bucks. 1. That’s the kind of painting that he did,” explained Robert.
Before officially graduating from physical therapy, Wauters said he had a few more miles to go.
“We’re just perfecting balance and walking. He’s walking, he’s running, but it’s still a different kind of, you know, surface. We’re just trying to perfect that so he can run and keep up with his siblings and his peers,” Wauters said.
Megan told KFOR when Millie is five or six, she will undergo another surgery but this time on her legs.
The surgery aims to help straighten Millie’s legs.
Meanwhile, Megan and Robert said they are living a normal life together while loving their three kids unconditionally.