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Daily Mirror
Daily Mirror
World
Fiona Jackson & John Bett

Toddler born with spinal condition defies the odds by learning to walk

A toddler born with a spinal condition has defied the doctors who said she wouldn't be able to use her legs properly - by learning how to walk.

Lacey Grace Bower has spina bifida and when her condition was discovered her parents, Michelle and Michael, were urged to terminate the pregnancy, but they refused.

The youngster had an operation on her back while she was still inside her mum's womb, but even with that they were told to prepare for the worst.

But now Lacey has defied the doctors who said she'd never be able to walk, and at 19-months-old she's starting to get around on her own, even learning how to manoeuvre a custom wheelchair.

Lacey was born with spina bifida (Michelle Bower / SWNS)
Lacey needed an operation before she was born (Michelle Bower / SWNS)

What do you think about Lacey's incredible accomplishment? Let us know in the comments...

Michelle, 37, from West Lafayette, Indiana, said she first found out about Lacey's diagnosis after her 20-week scan.

She said: "We had just found out that we were having a girl the day before. We wanted a girl. We went from the highest of highs to the lowest of lows in under 24 hours.

"It was a complete and utter nightmare, but we still had hope.

"We hoped it was the less severe form of the condition until we got more testing done."

Lacey in hospital with her dad, Michael (Michelle Bower / SWNS)
The Bower had to pull together (Michelle Bower / SWNS)

After refusing to lose their daughter, Lacey’s parents opted for a risky three-and-a-half hour surgery to fix the hole in her spine while she was still in the womb.

“It sounded completely insane and unfathomable for our financial circumstances and obligations at home," said Michelle.

"I thought it was crazy!”

The mum-of-one said: “The rest of the pregnancy was riddled with fear and uncertainty. It was beyond difficult to just enjoy being pregnant.

“However, from the copious amount of research we did, we knew that the foetal surgery would be her greatest chance at walking one day and her only chance of reversing her Arnold Chiari II malformation.”

She underwent the foetal surgery on April 27, 2020 at St. Louis Children’s Hospital, Missouri, with more than 35 medical professionals in the operating room.

Lacey's scar (Michelle Bower / SWNS)

She said: “It was quite literally the single most horrifying experience of my life.

“It was my first time in the hospital and my first surgery. Knowing my unborn baby was having surgery with me made it utterly terrifying.”

The procedure was three-and-a-half hours long and both Lacey, who weighed 1.8 pounds that day, and Michelle had their own team of doctors looking after them.

They made a ten-inch-long incision across her abdomen, and despite having to spend five days in recovery and waiting a week before she could walk, the procedure was deemed a success.

To ensure Lacey’s safety, Michelle had strict orders of bed rest for the next three months until she was due to give birth.

She said: “I stressed counting baby movements and strictly monitored my aches and pains.

“We got a calendar and counted down each day.”

Lacey Grace Bower in hospital (Michelle Bower / SWNS)

She was given a caesarean section on July 20, 2020 at 12:42pm, Lacey was born weighing 6lbs 9oz, and was immediately taken to the NICU.

Special education teacher Michelle said: “The first time I saw her was on a screen in the delivery room while they were giving her oxygen and getting her breathing started.

“I saw that something was seriously wrong with her legs. Her knees were hyperextended to where her feet were up by her face.

“She was stiffened in a fixed position from her positioning in the womb.

“I was so sad for her and afraid.”

Michelle and Michael Bower were over the moon when they learned they were expecting (Michelle Bower / SWNS)
Lacey had now defied the odds by learning how to walk (Michelle Bower / SWNS)

Lacey started to move her ankles and big toe early on, but it took her a long time to be able to feed on her own meaning she stayed in the NICU for 18 days.

She was monitored three times a week for the first three months, but now at 19 months she is speaking at the level of a three-year-old and is learning to walk.

Lacey is partially paralysed from the waist down and this means she still needs help with going to the toilet.

However the tot learned to sit, roll and pull herself along the ground ahead of schedule, and loves nothing more than climbing on things and cuddling her mum and dad.

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Michelle said: “Prior to birth, we were told she would have a ‘poor quality of life’.

“The doctor said there was a good chance she would never be able to eat, breathe, talk, stand or walk.

“She does more than that doctor ever imagined!

“She can climb up onto the couch and go to town on her rocking horse.

“The little things that others might somewhat take for granted are the things that dreams are made of for us - that is one of the many blessings that come with SB life.

“Life with a disabled person is a life worth living.”

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