Talia

Geordie Shore star Aaron Chalmers’ ex Talia shares post about ‘endless tears’ as son is admitted to hospital again

GEORDIE Shore star Aaron Chalmers’ ex Talia Oatway shared a heartbreaking post about their son Oakley.

The mum-of-three, who shares her kids with MTV reality star turned MMA fighter Aaron, has been giving fans regular updates on their youngest son’s health.

Talia Oatway shared a heartbreaking post about ‘endless tears’ in a new updateCredit: Instagram / @talia.oatway
The brave mum said it’s been 11 days since her little boy was admitted to hospital againCredit: Instagram / @talia.oatway
Geordie Shore star Aaron Chalmers’ ex Talia shared a tearful photo of herselfCredit: Instagram / @talia.oatway

Their son Oakley has Apert Syndrome, which is a genetic disorder that causes fusion of the skull, hands, and feet bones.

On Friday, Talia shared a series of photos of herself and Oakley at hospital.

One picture showed Talia looking exhausted and tearful following another difficult week after Oakley was admitted to hospital.

She wrote: “It’s been 11 days since we got admitted to hospital, a transfer to another hospital, another 2 GAs, more training for mumma, endless tears and another diagnosis for my Oakley boy. Road to recovery now.”

Love Island star Sophie Lee commented: “My strong girl and fighter of a little cherub! You got this!”

Charlotte Trippier posted: “You are something else you girl! Absolute supermum with a warrior of a boy. Love you so much.”

Hollyoaks actress Chelsee Healey added: “One strong mumma and boy, sending so much love always.”

Earlier this month, Talia gave fans an update, and said: “I know I haven’t been on it today. Um, so Oakley had a gemranosec earlier this morning to have a CT scans on his brain just to basically out rule a lot of stuff for the sickness.

“Um, so he had that and then had to wait obviously for the neurosurgeons to look at the scans.

“I mean I’ve still got no answers but they did tell me some bits that’s going on with Oakley’s brain which obviously has petrified me.

“Um, but I’m waiting until the surgeons at Newcastle obviously speak to the surgeons in Liverpool and then I’ll have more of an understanding about the situation that Oakley is in.

“Um, but yeah it’s just been a really shit day, very emotional day.”

In the summer, Talia shared another worrying post about Oakley.

Taking to her Instagram story, the concerned mum penned: “Oakley had the worst sickness last night, from 11ish till about 5am.

“Bath after bath, bed change after bed change.

“I feel so sorry for him. The fundo surgery he’s due to have soon (after his hands) is so needed.

“It will stop him being sick completely. Currently on a meds run for him.”

What is Apert syndrome?

APERT syndrome, also known as acrocephalosyndactyly, is a rare disorder that is named after the doctor who first discovered it in the early 20th century.

It is a genetic condition and is caused by a mutation of the FGFR2 gene.

This affects how cells in the body – namely bone cells – grow, divide and die.

Children born with Apert syndrome have a characteristic appearance, which is caused by the bones in the skull and face fusing and not growing in proportion, according to Great Ormond Street Hospital.

It can increase a child’s risk of hydrocephalus, which results in pressure building on the brain, and it can also cause Chiari malformation, where the base of the brain is squeezed.

Other complications include breathing difficulties and heart problems, which require life-long monitoring.

The condition is said to occurs in one in every 65,000 to 88,000 births and a child’s outlook can vary greatly depending on the severity of symptoms

Talia previously took to Instagram to post a video of her son taking his first steps and shared an update with her followers.

Alongside the clip, she wrote: “Oakley has been using a walking frame for a few months now.

“He’s had some shoes made for him as it’s impossible to get shoes that fit his feet.

“Which is common with Apert syndrome.

“Today we tried the shoes for the first time. We also had physio at home which we are doing every week.”

Aaron and Talia welcomed Oakley into the world in February 2022.

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They also share Romeo, four, and Maddox, three.

The former couple got together in 2017 but split just months after Oakley’s birth.

Oakley has Apert Syndrome, which is a genetic disorderCredit: instagram/@aaroncgshore

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Geordie Shore star’s ex Talia Oatway reveals ‘petrifying’ development as son Oakley returns to hospital

GEORDIE Shore star Aaron Chalmers’ ex Talia Oatway has revealed a “petrifying” development as their son Oakley returns to hospital.

The mum-of-three, who shares her kids with MTV reality star turned MMA fighter Aaron, has been giving fans regular updates on their youngest son’s health.

Geordie Shore star Aaron Chalmers’ ex Talia Oatway has given an update on her child’s healthCredit: Unknown
Oakley has the genetic disorder Apert SyndromeCredit: Instagram/talia.oatway
Talia said it had been an ’emotional day’Credit: Instagram
Geordie Shore’s Aaron and Talia welcomed son Oakley – his third child – back in 2022Credit: Instagram

Their son Oakley has Apert Syndrome, which is a genetic disorder that causes fusion of the skull, hands, and feet bones.

Today Talia gave fans an update, and said: “I know I haven’t been on it today. Um, so Oakley had a gemranosec earlier this morning to have a CT scans on his brain just to basically out rule a lot of stuff for the sickness.

“Um, so he had that and then had to wait obviously for the neurosurgeons to look at the scans.

“I mean I’ve still got no answers but they did tell me some bits that’s going on with Oakley’s brain which obviously has petrified me.

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Geordie Shore star Aaron Chalmers’ ex Talia reveals health update on son Oakley

“Um, but I’m waiting until the surgeons at Newcastle obviously speak to the surgeons in Liverpool and then I’ll have more of an understanding about the situation that Oakley is in.

“Um, but yeah it’s just been a really shit day, very emotional day.”

In the summer, Talia shared another worrying post about Oakley.

Taking to her Instagram story, the concerned mum penned: “Oakley had the worst sickness last night, from 11ish till about 5am.

“Bath after bath, bed change after bed change.

“I feel so sorry for him. The fundo surgery he’s due to have soon (after his hands) is so needed.

“It will stop him being sick completely. Currently on a meds run for him.”

Talia previously took to Instagram to post a video of her son taking his first steps and shared an update with her followers.

Alongside the clip, she wrote: “Oakley has been using a walking frame for a few months now.

“He’s had some shoes made for him as it’s impossible to get shoes that fit his feet.

Aaron and Talia split back in 2022Credit: Instagram

“Which is common with Apert syndrome.

“Today we tried the shoes for the first time. We also had physio at home which we are doing every week.”

Aaron and Talia welcomed Oakley into the world in February 2022.

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They also share Romeo, four, and Maddox, three.

The former couple got together in 2017 but split just months after Oakley’s birth.

What is Apert syndrome?

APERT syndrome, also known as acrocephalosyndactyly, is a rare disorder that is named after the doctor who first discovered it in the early 20th century.

It is a genetic condition and is caused by a mutation of the FGFR2 gene.

This affects how cells in the body – namely bone cells – grow, divide and die.

Children born with Apert syndrome have a characteristic appearance, which is caused by the bones in the skull and face fusing and not growing in proportion, according to Great Ormond Street Hospital.

It can increase a child’s risk of hydrocephalus, which results in pressure building on the brain, and it can also cause Chiari malformation, where the base of the brain is squeezed.

Other complications include breathing difficulties and heart problems, which require life-long monitoring.

The condition is said to occurs in one in every 65,000 to 88,000 births and a child’s outlook can vary greatly depending on the severity of symptoms

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