TALIA Oatway sparked concern after revealing her and Aaron Chalmers’ son Oakley can’t stop being sick ahead of crucical surgery.
She found fame thanks to her relationship with MTV reality star turned MMA fighter Aaron – but the pair split shortly after welcoming their third child.
Geordie Shore’s Aaron Chalmers welcomed son Oakley – his third child – back in 2022[/caption]
Oakley has the genetic disorder Apert Syndrome[/caption]
Aaron and Talia split back in 2022[/caption]
Their son Oakley has Apert Syndrome, a genetic disorder that causes fusion of the skull, hands, and feet bones.
Taking to her Instagram story, Talia 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.”
Proud mum 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.#
Talia added: “Using an object to hold on so Oakley feels safe. I’m so proud of how far he’s come.”
Fans rushed to comment on the upload, with one writing: “He’s a legend. Well done Oakley.”
Another said: “So emotional, what a little beauty, well done Oakley and to mummy!”
And a third added: “What an inspiration you both are.”
Aaron and Talia welcomed Oakley into the world in February 2022.
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
