
‘Fit and healthy' man, 31, given years to live reveals the first sign of killer that he blamed on ‘working long hours'
Read on for a full list of symptoms of Scott's deadly condition - from headaches to memory issues and double vision
SUBTLE CLUES 'Fit and healthy' man, 31, given years to live reveals the first sign of killer that he blamed on 'working long hours'
A FIT and healthy weightlifter chalked up red flag symptoms to "working long hours" and "not drinking enough water" - but was given just years to live after a terrifying seizure landed him in a coma.
Scott Hinch, 31, led a fit and active lifestyle and had no significant health problems - aside from "experiencing a few headaches and nosebleeds".
Advertisement
10
Scott Hinch, 29, was fit and active when he started experiencing headaches and nosebleeds
Credit: SWNS
10
He chalked them up to working hard but a terrifying seizure led to him being diagnosed with a brain tumour
Credit: SWNS
10
Scott was given three to five years to live - he's pictured here after brain surgery
Credit: SWNS
But on his way to work on August 19, 2019, he suffered a seizure and was rushed to Nevill Hall Hospital in Abergavenny, Monmouthshire, Wales.
He was put in an induced four-day coma after the seizures continued for 45 minutes.
After waking up, an MRI revealed a grade 2 astrocytoma - a type of tumour that usually develops in the brain or spinal cord - and he was given just three to five years to live.
Scott realised the headaches and nosebleeds he'd experienced over the last few months were in fact warnings signs of the cancer.
Advertisement
On September 4, Scott underwent emergency surgery to partially remove the tumour and started aggressive radiotherapy and chemotherapy to keep the cancer at bay.
But despite its initial success, Scott's cancer returned two years later, at the end of 2023, and he began his second round of treatment - which involved 20 months' worth of intensive chemotherapy, condensed into 10.
He is now undergoing his third round of treatment for his tumour and says he suffers from "relentless fatigue" and that he is "dependent" on his mum, Fiona Lott, 51, because he "can't leave the house most days".
Scott, who worked as a solar engineer from Abergavenny, Wales, said: "Looking back, I now realise there were signs.
Advertisement
"Headaches, nosebleeds, things I chalked up to long work hours.
"Maybe heavy training at the gym and not drinking enough water.
A mum dismissed her twitching eye as stress until discovering it was a rare brain tumour
"I even went to the opticians, but nothing was picked up.
"Most days, I can't leave the house.
Advertisement
"But I'm still here, and that's something I'm grateful for."
Scott was diagnosed with a grade 2 astrocytoma after suffering a seizure on his way to work on August 19, 2019.
10
Scott's brain scan, revealing the grade 2 astrocytoma
Credit: SWNS
10
Scott recalls waking up from the coma terrified and not knowing what happened
Credit: SWNS
Advertisement
10
Scott during his gruelling treatment
Credit: SWNS
Although the general prognosis is good - people with a grade 1 have a 96 per cent chance of survival after five years - it can decrease to below 30 per cent for those with grade 3 or higher.
Scott woke from a four-day coma induced coma when a consultant told him the "devastating" news that he had three to five years to live.
"I had no memory of anything since leaving the house," he said.
Advertisement
"I had four days completely missing, I remember setting off for work and then waking up in the hospital with doctors and nurses over my bed.
"It was frightening.
"I was shocked and scared and didn't know what was going on."
Symptoms of astrocytoma
Astrocytoma is a common type of primary brain tumour, which means it starts in the brain instead of spreading there.
Astrocytomas start in stem cells, which eventually develop in to one of the different types of brain cells, such as astroctyes.
Astrocytes are brain cells that connect and support nerve cells in the brain and spinal cord.
As astrocytes are found throughout the brain, astrocytomas can occur in many different areas of the brain.
These tumours grow from cells that are vital in processing information in the brain, so they can disrupt the function of whichever area of the brain they are growing in.
Some of these tumours grow in the cerebellum, which controls balance.
They can also occur in the optic pathways, which are involved in sight.
So, symptoms can be very different between people affected by these tumours. That being said, common astrocytoma symptoms could include: Headaches
Difficulty speaking
Change in vision, like double vision or blurriness
Cognitive difficulties, like trouble thinking or remembering
Seizures (epilepsy)
Source: The Brain Tumour Charity
The consultant at the University Hospital of Wales, in Cardiff, Wales, explained to Scott and his family that due to the tumour's diffused nature, only part of it could be safely removed.
Advertisement
The procedure took place on September 4 and Scott recalled being "terrified".
"But I woke up a couple of hours later, cracked a joke, and asked for a cup of tea," he said.
"It was a relief to know my brain function was intact."
'Relentless fatigue'
After the surgery, Scott went through 16 "gruelling" months of therapy - including seven weeks of radiotherapy and 12 cycles of chemotherapy - which kept things stable for two years.
Advertisement
But a routine scan towards the end of 2023 revealed the tumour was active again and Scott started his second round of treatment with intensive chemotherapy - with no success in curing the cancer.
"I take it one month at a time," he said.
"The fatigue is relentless and most days I can't leave the house."
His mum, Fiona, became his full-time carer and was "dependent on her" for everything.
Advertisement
During this time, the 31-year-old had lost his driving licence as a result of his seizures and sold his car.
"I felt like losing my independence," he said.
"I couldn't visit friends, and the risk of infection meant limited visitors.
"I felt incredibly isolated."
Advertisement
10
Scott before his diagnosis
Credit: SWNS
10
Scott with his dog Toby - he struggles with deep fatigue and is taking one day at a time
Credit: SWNS
'Still here'
Five years later, Scott is still battling cancer and is now undergoing his third round of treatment.
But he remains determined.
Advertisement
"I'm still here, and that's something I'm grateful for," he said.
To help raise awareness, his mum, Fiona, and auntie, Lyndsey, are taking on the 200k in May Your Way challenge to raise money for the Brain Tumour Research Charity.
Fiona said: "Watching my son go through the trauma of surgery and three rounds of treatment for brain cancer has been heartbreaking.
"No family should have to experience the fear, uncertainty and pain that we have.
Advertisement
"We need better outcomes, kinder treatments, and ultimately a cure.
"If our efforts can help spare just one family from this suffering, then every step will be worth it."
You can support Fiona and Lyndsey's 200k In May Your Way challenge here.
10
Fiona, Scott and and his two sisters celebrating Scott ringing the bell for the second time
Credit: SWNS
Advertisement
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles

Leader Live
21 hours ago
- Leader Live
Terminally ill Wrexham toddler visited by Peppa Pig
Earlier this year, Callie Shaw was tragically diagnosed, aged just 10 months, with a rhabdoid tumour - a rare and aggressive form of childhood cancer. She spent the next few months in Alder Hey to receive treatment. After undergoing four months of chemotherapy - things appeared to be going well and the tumour was shrinking in size. Callie Shaw and mum, Sarah (Image: Sarah Shaw) However, her family was given the devastating news last month following an MRI scan that Callie's cancer has spread to her lungs - and is now terminal. Callie was given a prognosis of four-six weeks. A GoFundMe page set up to support Callie's family at this very difficult time has raised over £7,000. With her first birthday spent during her time at Alder Hey, family and friends recently organised a party so she could celebrate properly. And on Monday (June 9), she received a surprise visit from Peppa Pig and Chase from Paw Petrol - her and her brother's favourite characters. (Image: Sarah Shaw) The visit was organised by Mold-based Blue Duo Events - which also donated 50 bags of candy floss for Callie's party. Blue Duo Events said on its Facebook page: "As a business, we felt there was more we could do – and this evening, we did just that. We surprised Callie with a visit from her two favourite characters, bringing smiles and joy to her and her family. One of our playful pups also joined in to surprise her little brother, making sure he felt just as special. (Image: Blue Duo Events) "Thank you, Sarah (Callie's mum) for allowing us to visit Callie at home and letting us be part of these precious moments. MORE NEWS: "The Blue Duo team are thinking of you all and sending love during this incredibly difficult time." Sarah Shaw said: "It was amazing to have Peppa Pig come and visit Callie. She absolutely adores Peppa Pig and it was really special. "I want to say a massive thank you to Blue Duo Events - you made memories that will last forever. It means so much to us."


Scottish Sun
2 days ago
- Scottish Sun
Dad-of-two placed into coma after Turkey holiday as chef, 55, ‘caught rare disease from dirty 4-star hotel'
The dad began suffering severe flu-like symptoms and was rushed to hospital HOLS HORROR Dad-of-two placed into coma after Turkey holiday as chef, 55, 'caught rare disease from dirty 4-star hotel' A DAD-OF-TWO has claimed he nearly died after contracting a rare disease from a "dirty" 4-star hotel. Richard Moore, 55, began to suffer from a fever and chest pains after returning from a holiday in Turkey with partner Julie, 50. 6 Richard's family was told he may not survive the harrowing ordeal Credit: SWNS 6 Richard had to be placed into an induced coma Credit: SWNS Richard, a chef, became so ill that he had to be rushed to hospital and placed into an induced coma. His wife and kids were told by medical staff that he may not survive the ordeal. Doctors confirmed he was suffering from potentially deadly Legionnaires' disease, Richard needed five days of intense hospital treatment which included antibiotics and an IV drip. Richard, of Blyth, Northumberland, said: "This holiday was meant to be a short break before I started a new job as an executive chef. "Instead, it cost me my dream job, my health and very nearly my life. "As a result of the memory loss, I can't recall much of my time in hospital, but when I was admitted, I remember the fear and not knowing what was wrong. "I'm lucky to be alive but it's so upsetting to think my family were told I might not live. "I never realised Legionnaires' disease was so serious and I want to tell my story to make other people aware of the symptoms and the dangers. "I wouldn't want to think that other people were going off on a holiday unaware of what they could be walking into. "If there are issues with the hotel then that needs looking at urgently. Mum who nearly died after falling sick in Spain issues warning after anti-sickness pills left her 'acting possessed' "I feel fortunate to have pulled through. However, I do worry that someone else might not be as lucky as I was." Richard and his family paid £2,000 to stay at the four-star Champion Holiday Village in Kemer, Turkey. After arriving at the hotel on August 18 last year, Richard said he thought the hotel was dirty, old and dated. He also noticed that the room felt damp and had a grim fusty smell. 6 He suffered serious flu-like symptoms after returning from his holiday Credit: SWNS 6 Richard was unable to start at a new job because of the illness Credit: SWNS He said: "I can't specifically pinpoint to one thing but the water temperature fluctuated a lot in the shower. "The bathroom and hotel generally looked run down and the sofa in hotel room beneath the air con felt damp throughout the holiday which made me think it was leaking." Days after returning to the UK, Richard began suffering from severe flu-like symptoms. On August 30 he developed chest pains, a shortness of breath and a fever and was rushed to hospital for treatment. He spent a whole month in hospital and has been unable to start at his new job as an executive chef. Richard still struggles with lethargy, weakness and mobility issues linked to Legionnaires' disease. He has now instructed travel illness lawyers at Irwin Mitchell to investigate the cause of his Legionnaires' disease. 6 Richard visited Champion Holiday Village in Kemer, Turkey Credit: Champion Holiday Village 6 Richard is now having lawyers investigate the cause of his illness Credit: SWNS Jennifer Hodgson, representing Richard, said: "Richard's first-hand account of his experience at the hotel and contracting his illness is deeply disturbing. "Legionnaires' disease is an incredibly serious condition, and it can take several days from coming into contact with Legionella bacteria before symptoms of the illness start to appear. "As Richard has since discovered, the effects of the disease can be long-term. "Nothing can make up for the impact the illness has had and continues to have on Richard, but we're determined to provide him with the answers and specialist support he deserves. "Public buildings, such as hotels and offices, can have complex water systems, so it's vital that all precautions are taken to prevent the bacteria that causes Legionnaires' disease developing. "As part of our work and to assist with our investigations, we would be keen to hear from anyone else who may also have been affected by illness whilst staying at the Champion Holiday Village Hotel, Turkey."


Daily Mirror
2 days ago
- Daily Mirror
Girl, 12, dies after doctors mistook fatal tumour for 'tummy bug'
Jackie Dunlop has urged parents to "trust their gut" after losing her daughter Ava Nelson from a condition which GPs initially dismissed as something minor A mum is urging parents to trust their instincts after her daughter's tummy bug turned out to be an inoperable brain tumour. Jackie Dunlop from North Ayrshire became concerned when her daughter Ava Nelson, then aged 10, suffered with severe headaches and sickness for three weeks. Following visits to the GP and her local hospital, the young girl was a viral infection or a gastric bug. However, after the fourth week of Ava feeling unwell, Jackie pushed for more testing and what followed shocked the 38-year-old to the core. An MRI revealed a pressure of Ava's brain, caused by a large mass, and she was rushed up to the Royal Hospital for Children in Glasgow. She had to have an emergency operation to relieve the pressure and a biopsy a week later revealed Ava had a high-grade glioblastoma. The family were told she had just six to 12 months to live, but Ava outlived that prediction and passed away nearly two years later in April 2024, aged 12. Now Jackie, from Kilwinning, who previously worked as a carer, is telling parents not to ignore their own suspicions regarding their child's health. She said: "We thought it was a sickness bug. But going into week three I started to worry. Everyone put it down to a viral sickness bug. Four weeks I had been fighting with doctors. The surgeon told us if we didn't fight she'd have been dead within a week because the pressure was that bad." She continued: "I always say to any mother go with your gut instinct if you feel that something is wrong with your child. If you feel something is wrong then go get them checked. If you aren't getting anywhere stand your ground and make sure you get the help and support you need until you have the right answers. Mothers know their child best." Ava began experiencing headaches, dizziness, and balance issues in May 2022. Despite numerous GP appointments and hospital visits, her symptoms were dismissed as just a viral illness, reports Glasgow Live. Growing concerned about her daughter's health, Jackie refused to accept this and persevered for further medical attention at Crosshouse Hospital's children's ward. Jackie recounted: "To look at her you wouldn't know anything was wrong. They agreed to do blood tests – Ava then started vomiting. She started declining but the blood tests came back fine. I pushed for a scan." The persistence paid off when an MRI scan showed a brain tumour. Ava was rushed to the Royal Hospital for Children in Glasgow on May 31, 2022. Jackie said: "They told us Ava has severe pressure on her brain. They found a tumour. The pressure was caused by the tumour." Ava underwent emergency surgery the following day; however, doctors couldn't fully remove the tumour due to its location. The biopsy results returned on June 8, 2022, confirming Ava's diagnosis with cancer. Jackie revealed: "The hardest part for me was that wasn't going to survive. They gave us six to 12 months." Ava bravely endured 12 weeks of simultaneous radiotherapy and chemotherapy, which resulted in her needing a feeding tube after the treatment caused a rupture in her stomach. Her parents, Jackie and Roland, made the heart-wrenching decision not to disclose Ava's terminal prognosis, choosing instead to create cherished memories. Jackie shared: "We were trying to normalise life." The family dedicated themselves to ensuring their beloved "wee warrior" had as many joyous moments as possible, despite their own sorrow. Jackie said: "As a family we did everything in our willpower to make sure that the time we had left with our wee warrior was full of fun filled memories as much as it was killing us inside." In spring 2023, Ava was admitted to Robin House Children's Hospice, where she fought for another year before passing away on April 16, 2024, with her loving parents and sisters, aged nine and 17, by her side. Jackie recalled: "They moved her into the rainbow room. It was the most peaceful room." Jackie now aims to inspire other parents to trust their instincts about their children's health. She added: "Ava was quiet as a mouse. She was quite shy and timid. But she was sweet and loving. She was the best."