Young man receives devastating diagnosis after noticing change to his eye

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Jack Carter and girlfriend Lucy
Jack Carter and girlfriend Lucy

A young man has been diagnosed with an inoperable brain tumour after an eye specialist sent him for a precautionary scan.

Doctors thought Jack Carter was experiencing palsy in one eye but a specialist at Derriford Hospital in Plymouth decided to send the 23 year old for an MRI scan as a precaution. He was diagnosed with a meningioma brain tumour in December 2023.

Mum Charlotte Carter, from Kingsbridge, said: “It was a bit of a shock to say the least to find out Jack had a brain tumour. Since then, thankfully, the tumour has remained stable, but because it’s pressing on Jack’s optic nerve and is right by his pituitary gland and carotid artery, surgeons can’t risk removing it.”

Last Friday, Jack and Charlotte were invited to the Brain Tumour Research Centre of Excellence at the University of Plymouth, to learn about research that explores new ways to diagnose and treat meningioma – the most common low-grade brain tumour affecting adults – to help patients like Jack in the future. They were among supporters given the opportunity to tour the labs, led by principal investigator Professor Oliver Hanemann,.

While there, they heard about recent breakthroughs from the Centre which have included an innovative blood test which could be used to diagnose and monitor meningioma brain tumours, and the development of a new technique to grow tumour cells in the lab, which could improve the success of future clinical trials.

Baby boy has spent his life in hospital as doctors are 'scared' to discharge him qhiddeidqzikqinvBaby boy has spent his life in hospital as doctors are 'scared' to discharge him

Charlotte added: “Jack has been amazing, with fantastic support from his lovely girlfriend Lucy, and his father and I are incredibly proud of how he has dealt with the situation. The tumour is not going to go away – there’s nothing we can do. He is continuing to learn to adjust to the changes in his life, including regular scans to monitor the tumour for growth. If that happens, there’s the option of radiotherapy treatment.

Young man receives devastating diagnosis after noticing change to his eyeJack with his family

“Nevertheless, he’s totally focused on finding work in film & TV production.” Coincidentally, long before Jack’s diagnosis, Charlotte has been a trustee of The Misses Barrie Charitable Trust which has been awarding grants since 2009 to Brain Tumour Research. The charity has four Centres of Excellence across the UK working to find a cure, including one at the University of Plymouth."

She said: “Since suddenly finding myself in the position of mum to a brain tumour patient, I am proud to say The Misses Barrie Charitable Trust, which had already granted more than £12,000 to Brain Tumour Research over the years, has committed to awarding the charity with £7,500 each year for the next three years to fund vital research.”

After touring the lab, Charlotte and Jack placed tiles on the Wall of Hope, recognising the fundraising support granted by the Misses Barrie Charitable Trust, as well as honouring Jack’s diagnosis and life with a brain tumour. Charlotte said: “It was heartening to hear from the scientists about the work being done in their quest to find a cure, which can’t come soon enough. I hope the grants awarded by the Trust are life-changing and that the amazing work being conducted at the Plymouth Centre of Excellence leads to a cure for Jack.”

Katrina Jones, head of community fundraising for Brain Tumour Research, said: “We’re really grateful to The Misses Barrie Charitable Trust and hope that Charlotte and Jack’s visit to our Centre of Excellence at Plymouth offered a useful insight into all we’re doing to improve treatment options for patients and, ultimately, find a cure. Brain tumours kill more children and adults under the age of 40 than any other cancer, yet just 1% of the national spend on cancer research has been allocated to this devastating disease since records began in 2002. This has to change.”

Kelly-Ann Mills

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