Morecambe schoolboy diagnosed with brain tumour after he draws his headache on an Etch A Sketch

A schoolboy used an Etch A Sketch to draw his 'headache that never went away' and helped doctors diagnose a life-threatening brain tumour.

By The Newsroom
Tuesday, 2nd May 2017, 10:00 am
Updated Tuesday, 2nd May 2017, 11:24 am
Emre Erulkeroglu in hospital.
Emre Erulkeroglu in hospital.

Months after medics told Emre Erulkeroglu’s family that there was nothing wrong with him, his drawing worried his mum Tiffani so much that she pushed again to get help.

It was only then that a fresh brain scan led to the diagnosis of a life-threatening brain tumour.

Emre’s first symptom came on Mother’s Day 2015 when he woke and told Tiffani he had a bad headache.

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Emre Erulkeroglu with his Etch A Sketch drawing.

“Within minutes he was lying in a drowsy state on the sofa but was screaming in pain every time he vomited,” she said.

“We took him to A&E where his headache disappeared due to the vomiting and we were told to go home as they thought it was just a migraine.”

Emre’s early morning headaches persisted for several weeks.

Following an online search Tiffani came across a HeadSmart campaign which lists symptoms and warning signs for brain tumours in children.

Emre Erulkeroglu with dad Huseyin, mum Tiffani, sister Esra and aunt Emine Cobanoglu and uncle Apo.

She said: “He was displaying red flag symptoms that were on the HeadSmart website so I went to the doctors on several occasions.”

Lancaster Road Primary School pupil Emre had a neurological examination after which doctors assured Tiffani that her son was fine.

“One doctor even told me to stop asking him daily if he had a headache as I could be making him think he had one,” she said, “so I relaxed slightly thinking I was making him worse and that it could be migraines.”

However, a few weeks later Emre drew a picture showing a black dot on his forehead and told Tiffani that it was “the headache that never went away.”

Emre Erulkeroglu with mum Tiffani and dad Huseyin.

Tiffani demanded an immediate referral and Emre was put on the four-month waiting list for an MRI scan as the paediatrician didn’t consider it an urgent case.

“Whilst we were waiting Emre was becoming difficult to handle,” Tiffani said.

“He would have rages over nothing that lasted for hours. I had no choice but to ring the MRI department every day for weeks until I managed to get in a cancellation.”

Following an MRI scan Tiffani was told that he had a benign cyst on his pineal gland and that it wasn’t the source of his problems.

Emre Erulkeroglu with mum Tiffani.

However, once he was home he quickly deteriorated, becoming sleepy, vomiting regularly and having severe headaches.

Tiffani took Emre back to hospital where, after further tests, she was told that the seven-year-old had a cystic tumour which was inoperable.

Emre, now seven, has since had a lumbar puncture, an endoscopic third ventriculostomy and has been placed on ‘watch and wait’. He has scans every six months to see if the tumour has progressed.

“It took three months of me pleading to get a diagnosis but he’s here, stable and getting on with life,” Tiffani said.

“He’s come on so well at school, a far cry from before diagnosis,” Tiffani said. “He is the funniest, most well-mannered boy and I wish he didn’t have to undergo everything.

“It’s scary being on ‘watch and wait’ but we are thankful that the tumour has stayed stable as the treatments are very disruptive and gruelling.

Emre Erulkeroglu with his Etch A Sketch drawing.

“Although everything is very frightening, we understand how lucky we have been to have caught things early.

“The prognosis is unknown but we are hoping and have everything crossed that he can stay stable as long as possible –that’s all we can ask at this stage.”

If the tumour starts to grow again, Emre will need 18 months of chemotherapy and possible surgery to ‘debulk’ the tumour – treatment which is high risk as the tumour is in the centre of the brain, on top of the brain stem.

Now the family, who live in Morecambe, are speaking out in support of HeadSmart, a campaign run by The Brain Tumour Charity, to raise awareness of the signs of childhood brain tumours.

HeadSmart has already helped cut the average diagnosis time for a childhood brain tumour in the UK from more than 13 weeks to 6.5.

A new drive has begun to bring that figure below four weeks, in order to save lives and reduce the long-term disability caused by childhood brain tumours.

It will focus closely on healthcare professionals, parents and teenagers in a bid to ensure young patients with possible brain tumour symptoms are referred for specialist help as quickly as possible.

Tiffani said: “We know from our own experience how important it is for doctors and parents to recognise when a child might have a brain tumour. There are still too many people out there who don’t spot the warning signs.

“I can’t thank the HeadSmart campaign enough for allowing me to push on with the diagnosis.”

The HeadSmart campaign, which includes pocket-sized symptoms cards and a website, lists the warning signs of a brain tumour in babies, children and teenagers.

These include vomiting, balance problems and unusual eye movements.

Newly-added symptoms, after a review of all of the evidence showing the most common signs of childhood brain tumours, include increasing head circumference in under-fives and loss of vision across all age groups.

The new campaign also includes an icon, nicknamed Sam.

Each of the ten key childhood brain tumour symptoms is represented by Sam in a different, easily-recognisable form.

Hayley Epps, campaign manager for The Brain Tumour Charity, said: “Brain tumours kill more children in the UK than any other type of cancer. HeadSmart has two aims: to save lives and reduce long-term disability by bringing down diagnosis times.

“Relaunching the campaign will help us to achieve those goals by alerting more healthcare professionals, parents and young people to the signs and symptoms of the disease.

“Emre’s story shows very clearly why HeadSmart is so important. We are very grateful to his family for their support.”

HeadSmart is run as a partnership between The Brain Tumour Charity, The Children’s Brain Tumour Research Centre and the Royal College of Paediatrics and Child Health.

Brain tumour warning signs:

The most typical symptoms of brain tumours in children and young people include:

· Persistent or recurring vomiting

· Persistent or recurring headaches

· Balance/co-ordination problems/walking problems

· Blurred or double vision

· Poor balance and co-ordination

· Abnormal eye movements

· Abnormal head position

· Fits or seizures

· Behavioural changes, especially tiredness

· Increasing head circumference in babies

· Delayed puberty in teenagers

Brain tumours in children and young people – the facts

· Brain tumours are the biggest cancer killer of children and young people.

· 500 children and young people are diagnosed each year with a primary brain tumour.

· A quarter of these children and young people will die – that’s one child every three days.

· Brain tumours are the largest cause of preventable or treatable blindness in children.

· Brain tumours reduce life expectancy by on average 20 years – the highest of any cancer.

· Childhood brain tumour survivors are 10 times more likely to suffer long term disability than well children. This accounts for 20,000 additional disabled life years for all the children who are diagnosed each year.

Emre Erulkeroglu with dad Huseyin, mum Tiffani, sister Esra and aunt Emine Cobanoglu and uncle Apo.
Emre Erulkeroglu with mum Tiffani and dad Huseyin.
Emre Erulkeroglu with mum Tiffani.