Devastated mum pays tribute to baby girl who defied medics by living for nine months


Nancy Jo Anne Rogers was born with Smith-Lemli-Opitz syndrome which is a condition which affects multiple body systems, including the internal organs, growth and intellectual development

Lisa said Nancy developed her own little character and was always laughing despite her rare condition

A heartbroken mum is paying tribute to her “perfect” baby daughter who defied medics by living for nine months after being diagnosed with a rare genetic condition.

Nancy Jo Anne Rogers was born with Smith-Lemli-Opitz syndrome – a condition which affects multiple body systems, including the internal organs, growth and intellectual development, facial features, fingers and toes.

Nancy defied medics’ expectations time and time again, going on to live for months after her parents were told she “wouldn’t be here in 48 hours”, Teesside Live reports.

Her mum Lisa Rogers, from Thornaby, is telling her daughter’s story to raise awareness of the rare genetic condition.

“She had a perfect life. We were told she would never smile or get head support and that she would never sit on her own – she managed all those things,” Lisa said.







Lisa has raised and donated money, along with blankets and clothing, to the special care baby unit at the University Hospital of North Tees
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“She laughed constantly, she started waving and smiling. She developed her own little character from her.

“All the things we thought she would never do, she did. And more. For a baby that was so poorly, she accomplished more in her nine months of life than most of us do in a year.”

After a normal pregnancy, Lisa was concerned about her baby’s movements and made her way to the University Hospital of North Tees in September 2020 – when days later she was induced. On Friday, September 25, the health care assistant welcomed her daughter into the world via caesarean section.

But it was only upon Nancy’s arrival that she and her midwifery team recognized something was out of the ordinary. Nancy was taken straight to the special care baby unit which cares for premature or seriously ill newborns.







Nancy Rogers pictured as a newborn
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Lisa, 40, said: “When she was born, she didn’t cry. She had difficulty breathing – she had a wheeze.

“The only thing I remember saying was that she only had four fingers – she didn’t have her little finger on her left hand.”

Medics found that Nancy had problems with her heart and kidneys, slanted eyes, webbed toes, a missing finger and she could not suck or swallow. The newborn was transferred from the University Hospital of North Tees to the pediatric intensive care unit at the Freeman Hospital.

Lisa continued: “Two days after giving birth by C-section, I was traveling to Newcastle. I needed time to heal but Nancy came first. I was allowed to change her and hold her but she was so poorly. A doctor there asked me if I understood how poorly she was.

“He told me to take her home to meet her family because she won’t be here in 48 hours. They’d done all they could and we just had to wait and see now.”

But three weeks later, on October 23, 2020, Nancy came home. The following month, she was diagnosed with Smith-Lemli-Opitz syndrome (SLOS). Symptoms of SLOS differ from person to person. Some people may have more symptoms than others and symptoms can range from mild to severe.

Those with the syndrome also have abnormally low levels of cholesterol in their blood. Lisa knows of only two other individuals in the North East with this condition – one of whom sadly died.

Despite being given just 48 hours to live, Nancy challenged doctors’ expectations, continuing to grow and develop. Although she remained under the care of several hospitals and specialists across the North East, Nancy lived a full life, Lisa said.

She enjoyed her first Christmas at home, went on three holidays and laughed as she spent time in the water. But on July 5, 2021, Nancy was taken to the University Hospital of North Tees by ambulance where she received treatment after Lisa noticed she was struggling to breathe.

She sadly died on the children’s ward two days later of heart failure and sepsis.

Lisa continued: “I was sat with her the whole time and one minute she was quiet and not moving much, then a few hours later she was lively and kicking her legs, playing. I was holding her in my arms and when I thought she’d gone to sleep, I put her back to bed and put her oxygen mask back on her and she just flopped to one side and was gone. She’d died in my arms.

“Doctors and nurses worked on her for 57 minutes. But she was ready to go – she was tired and she’d had enough. We say now that she didn’t want me to have to make that decision to give her open heart surgery which only has a 10% survival rate.

“Nancy made her own decision.”

Since Nancy’s passing in July last year, Lisa and her family have dedicated themselves to raising awareness of SLOS and raising money for the organizations who helped Nancy. She has raised and donated money, along with blankets and clothing, to the special care baby unit at the University Hospital of North Tees.

Lisa said: “I can’t describe how thankful I am to everyone in the special care baby unit at North Tees – to Zoe Kitching and Jayne Jobling especially.

“Jayne came to Nancy’s funeral and continues to be a great support to me, as are a lot of other nurses. Nancy simply would not have had her nine and a half months without the NHS. ”

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George Holan

George Holan is chief editor at Plainsmen Post and has articles published in many notable publications in the last decade.

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