A Cumbrian toddler has left medical experts amazed after his brain function dramatically increased.
Three-year-old Noah Wall from Abbeytown, who has spina bifida, had just two per cent brain function at birth.
But scans have now revealed that his brain is almost fully functioning - a development doctors had not expected.
The scans were taken at Newcastle's Royal Victoria Infirmary where Noah had operations on the arches of both his feet on Friday to help him stand.
Parents Michelle and Rob Wall were warned their unborn son was unlikely to survive birth, after it became apparent he was missing a back quarter of his brain and were told to expect him to be paralysed from the chest down.
However, Noah defied the odds from birth and has continued to defy them ever since.
The scans of his brain will now be used by medical researchers to help increase understanding about spina bifida.
Claire Nicholson, the consultant treating Noah, believes the pressure of fluid effectively squashing his brain at birth was so severe that he appeared to have little brain function but this function has increased as the pressure's reduced.
She's in no doubt however about what a remarkable little boy he is.
A Cumbrian toddler has left medical experts dumfounded after going from just two per cent of brain function at birth to it now being almost fully functional.
Noah Wall, three, from Abbeytown, who has Spina Bifida, had operations on the arches of both of his feet on Friday, at hospital in Newcastle.
He also had an MRI scan of his brain, which will be used by medical researchers.
The brain scan showed a dramatic increase in Noah's brain function, which doctors had not expected.
Noah's mum, Shelly, sent ITV Border this video, showing the toddler after the operations, and scan:
A three-year-old boy from West Cumbria, whose parents were told he would be lucky to survive being born, has won a modelling contract.
Noah Wall is from Abbeytown, and has signed a deal with a well known agency.
He has Spina Bifida and other serious conditions.
If you want to hear Noah singing then watch Ryan Dollard's report from Sunday.
International businessman Duncan Bannatyne has been speaking to ITV Border about 'inspirational' Cumbrian boy, Noah Wall.
Noah, from Abbeytown, was born with spina bifida. Despite doctors warning he was unlikely to survive birth, he has just turned two years old. He's now received a national bravery award.
Duncan Bannatyne said: "I met Noah, Shelly and Rob in the Lake District and have been friends ever since, Noah is an inspirational little boy who has fought the odds to survive. I am an Ambassador for the Scottish Spina Bifida Association and seeing Noah doing so well is an absolute delight.
" I am ecstatic that Noah has won the 'Baby Against All Odds' award from Mother and Baby magazine's and would like to wish Noah, Shelly and Rob a very happy and bright future and long may our friendship last."
Noah will be appearing on tonight's Lookaround programme on ITV Border from 6pm, showing off his new award.
A little boy from our region has been celebrating a very special birthday.
Noah Wall, from Abbeytown, was born with spina bifida - and just two per cent of his brain was working.
Despite doctors warning he was unlikely to survive birth, Noah has just turned two years old.
And it has been another special day for the family, as Noah received a national bravery award.
Finola Miles reports.
Two year old Noah Wall received a belated birthday present today as he was named Mother and Baby magazine's 'Baby Against All Odds'.
Noah along with his mum Shelly and dad Rob made the journey to the Dorchester in London from their Abbeytown home.
Little Noah has been dubbed a 'miracle' baby by his parents after he was born with just two per cent of his brain working and they were told to plan his funeral before his birth. Despite ongoing health problems he is now a happy smiling little boy.
More than 800,000 people have now visited the web page his mother Shelly set up to share his story.
Her aim has been to raise awareness of spina bifida and what prospective parents can do to decrease the chances of their baby being born with it.