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AARON Chalmers' ex Talia Oatway has shared the affectional infinitesimal their lad Oakley walked for the archetypal clip aft his gruelling wellness battle.
Oakley, two, has Apert Syndrome, a familial upset that causes fusion of the skull, hands, and feet bones.
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Proud mum Talia took to Instagram to station a video of their lad taking his archetypal steps and shared an update with her followers.
Alongside the clip, she wrote: "Oakley has been utilizing a walking framework for a fewer months now.
"He’s had immoderate shoes made for him arsenic it’s intolerable to get shoes that acceptable his feet. Which is communal with Apert syndrome.
"Today we tried the shoes for the archetypal time. We besides had physio astatine location which we are doing each week.
Talia added: "Using an entity to clasp connected truthful Oakley feels safe. I’m truthful arrogant of however acold he’s come."
Fans rushed to remark connected the upload, with 1 writing: "He's a legend. Well done Oakley."
Another said: "So emotional, what a small beauty, good done Oakley and to mummy!"
And a 3rd added: "What an inspiration you some are."
In June past twelvemonth Oakley underwent exigency surgery aft a spread was recovered successful his skull, causing encephalon fluid to leak out.
He was forced to enactment successful infirmary for much than 5 weeks and Talia aboriginal revealed the country had suffered complications.
Geordie Shore’s Aaron Chalmers gives fans immense update connected earnestly sick son’s information aft terrifying wellness battle
She said astatine the time: "He has had a batch of complications. CSF leaks, CSF corruption which pb to sepsis shock.
"Two lumbar drains, a EVD drain (in the head), IV fluids and antibiotics, 4 surgeries successful full (on this admission).
He was successful an induced coma for astir six days to assistance his assemblage portion helium was warring the infection."
Talia and Geordie Shore prima Aaron besides stock Romeo, four, and Maddox, three.
The erstwhile mates got unneurotic successful 2017 but split conscionable months aft Oakley's birth.
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What is Apert Syndrome?
APERT syndrome, besides known arsenic acrocephalosyndactyly, is simply a uncommon upset that is named aft the doc who archetypal discovered it successful the aboriginal 20th century.
It is simply a familial information and is caused by a mutation of the FGFR2 gene.
This affects however cells successful the assemblage - namely bony cells - grow, disagreement and die.
Children calved with Apert syndrome person a diagnostic appearance, which is caused by the bones successful the skull and look fusing and not increasing in
proportion, according to Great Ormond Street Hospital.
It tin summation a child's hazard of hydrocephalus, which results successful unit gathering connected the brain, and it tin besides origin Chiari malformation, wherever the basal of the encephalon is squeezed.
Other complications see breathing difficulties and bosom problems, which necessitate life-long monitoring.
The information is said to occurs successful 1 successful each 65,000 to 88,000 births and a child's outlook tin alteration greatly depending connected the severity of symptoms
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