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Inspirational boy with ‘no brain’ named children’s charity ambassador after parents refuse abortion 5 times

An eight-year-old, born with spina bifida and only 2% of his brain, has been named as the newest Young Ambassador for Variety children’s charity, a group which supports disabled and disadvantaged children.

Doctors did not expect Noah Wall to live more than a few days and advised his parents, Shelley and Rob Wall, to consider abortion on five separate occasions.

But they refused, wanting to give their baby boy the chance of a healthy life, and Noah has been defying expectations ever since.

He’s starting to read, loves numbers, and, determined to fulfil his dreams, has already ticked off an impressive range of adventurous activities like horse riding, surfing and skydiving.

Speaking about his new role, Noah said: “I’m so excited to be a Variety Young Ambassador! It will be a pleasure to help raise lots of money for all the children who are disabled – because it’s good to give.”

Miracle baby

Describing the day Noah was born Shelly told the Mail: “The day he was born was amazing. We waited with baited breath.”

The couple were admitted to hospital a week before Noah was due to be born because the pressure on his brain was becoming dangerous.

There were twelve doctors in the operating theatre as experts performed a caesarean section and as Noah came into the world, he gave the doctors a sign.

Rob said: “He let out this amazing scream. We knew there was power there.”

Scans of Noah’s brain shortly after his birth show he had just 2% of his brain.

Miraculously, he kept on growing and so did his brain.

Medical professionals stunned

By the age of three, his brain had grown to a remarkable 80 percent of what it should be and is now nearly fully-functional, leaving medical professionals stunned.

Last year, Noah, who is paralysed from the waist down, moved his foot for the first time after undergoing pioneering therapy designed to alter the way the brain sends messages to his limbs.

Now the family sends regular updates to the doctors who told them Noah wouldn’t make it.

Shelly said: “He’s extraordinary. We send them emails and pictures and we take them presents at Christmas time.”

Every year, Noah gives out hundreds of Christmas presents to staff and patients at Great North Children’s Hospital in Newcastle – the hospital he was born in. With more therapy, it is hopeful he will one day deliver gifts on foot.

Rob said on the documentary, The Boy Without a Brain: “We were offered termination five times. It was never an option for us. To me, we wanted to give Noah that chance of life.”

“To hear his brain’s almost back to normal is beyond belief,” Shelly added.

“Rob and I broke down when we heard the news. It was like a dream. I’ve never known anything like it. Even the consultants were in tears. Every time we see the doctors, they just shake their head. They’re just amazed at what he can do.”

Claire Nicholson, Noah’s consultant neurosurgeon, said in 2016: “He has surprised us through his life so far. He’s completely remarkable.”

She added that Noah teaches the medical profession that “you can’t ever know, doesn’t matter how many statistics you throw at something”.

Noah is just one of many babies who have defied the odds. 

Estimates have predicted that 80 percent of unborn babies diagnosed with spina bifida, each year, are aborted.

However, pro-life campaigners are hopeful that now the surgery has been made routinely available on the NHS the number of unborn babies terminated each year will fall.

Help stop abortion up to birth for babies with disabilities including Down's syndrome & club foot

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Dear reader

In 2020, the UK Government imposed an extreme abortion regime on Northern Ireland, which included a provision that legalised abortion right up to birth for disabilties including Down’s syndrome, cleft lip and club foot.

A new Bill has been launched at the Northern Ireland assembly that will remove the current provision that allows abortion for ‘severe fetal impairment’.

It is under these grounds in the regulations that babies with disabilities including Down’s syndrome, cleft lip and club foot can currently be singled out for abortion in Northern Ireland because of their disability and can be aborted right up to birth.

Before the new abortion regime was imposed on Northern Ireland in 2020, disability-selective abortion for conditions such as Down’s syndrome, cleft lip and club foot was not legal and there was a culture of welcoming and supporting people with these disabilities rather than eliminating them.

This is reflected directly in the latest figures (2016) from the Department of Health in Northern Ireland, which show that while there were 52 children born with Down’s syndrome in Northern Ireland, in the same year only 1 child from Northern Ireland with Down’s syndrome was aborted in England and Wales. 

This contrasts with the situation in the rest of the United Kingdom where disability-selective abortion has been legal since 1967.

The latest available figures show that 90% of children diagnosed with Down’s syndrome before birth are aborted in England and Wales.

We are, therefore, asking people like you to take 30 seconds of your time and add your support to the campaign to stop abortion up to birth for disabilities including Down’s syndrome, cleft lip and club foot in Northern Ireland.

If you live in Northern Ireland: 
Ask your MLAs to vote to stop abortion up to birth for disabilities including Down’s syndrome, cleft lip and club foot:

If you live outside Northern Ireland: 
Show your support by signing this petition in support of the Bill:

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Help stop abortion up to birth for babies with disabilities including Down's syndrome & club foot

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