logo
‘Fit and healthy' man, 31, given years to live reveals the first sign of killer that he blamed on ‘working long hours'

‘Fit and healthy' man, 31, given years to live reveals the first sign of killer that he blamed on ‘working long hours'

Scottish Sun16-05-2025
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
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

'I saw rainbows and forgot I was a mum - now I won't see son grow up'
'I saw rainbows and forgot I was a mum - now I won't see son grow up'

Daily Mirror

time6 hours ago

  • Daily Mirror

'I saw rainbows and forgot I was a mum - now I won't see son grow up'

Clare Smerdon, 37, was diagnosed son after her son Teddy's first birthday A woman has revealed how her brain tumour caused her to "forget" she was a mum, after experiencing flashing lights and rainbow-like patterns in her vision led to her diagnosis. Clare Smerdon, 37, was diagnosed with a grade 4 astrocytoma - just weeks after her son Teddy turned 13 months old. ‌ Doctors informed her that the aggressive tumour was life-limiting and Clare was terrified she would never get to see Teddy grow up. While awaiting surgery to remove the tumour, she confessed she was "acting completely out of character" and "forgot I was a mum". ‌ However, two years later, she has beaten the odds and proudly watched her four year old son don his uniform and enter the gates of Barton Hill Academy for his first day of school. ‌ Clare, from Torquay, Devon, said: "When I received my diagnosis, I didn't think I'd be alive today to see Teddy start school. This is such a huge milestone for us. I no longer feel like I am dying and feel incredibly lucky, but I know others may not get the same chance." Clare's symptoms first manifested in early 2022, when she began seeing flashing lights and rainbow-like patterns across her vision. She said: "I felt as though people didn't understand what I was going through. I was desperate to find out what was causing the immense pain in my head and changes in my vision." In July 2022, an MRI scan at Derriford Hospital in Plymouth revealed a 7cm brain tumour. She said: "When I got the diagnosis, I remember thinking that I'd just had a baby and I wanted to be around to watch my son grow up for as long as I could. Then the wait for surgery was horrendous. I was losing myself and acting completely out of character. "I even forgot I was a mum. Teddy spent more time with his dad and we drifted apart. That was heartbreaking." ‌ In August 2022, Clare underwent a gruelling six-hour operation at Derriford to remove the tumour, followed by an intense six weeks of radiotherapy and chemotherapy. She said: "Two weeks after surgery I returned home and doctors confirmed I had a grade 4 astrocytoma, which is also classified as a glioblastoma. On hearing the pathology results I knew my life was over. ‌ "The treatment made me sick, and I could only stomach a meal in the evening. At the same time, I got to spend more time with Teddy and we were both getting to know each other again." A routine scan in August 2023 delivered the devastating news that she had just two to three years to live. ‌ Clare said: "The thought of not being here to watch Teddy grow is destroying. I'm not sure if another operation is something I want due to the implications that come with it. "My eyesight is already compromised and my speech has been impacted, so now I just watch and wait. There are so few treatment options for brain tumour patients and the ones we do have are invasive and often life-changing. "I've looked into clinical trials abroad, but for most working-class families, the cost is impossible. I'm angry and frustrated at how little support and research funding there is." ‌ Clare has now teamed up with Brain Tumour Research and will participate in the charity's Walk of Hope this September. She said: "I want to do everything I can to help fund the research that will lead to better treatments and, ultimately, a cure. If sharing my story and taking part in fundraising encourages even one more person to join the cause, it will be worth it. That's why I'm calling on the government to increase funding for research into brain cancer, more must be done." Letty Greenfield, community development manager at Brain Tumour Research, said: "Clare's story is a powerful reminder of both the personal impact of a brain tumour diagnosis and the urgent need for change. We are so inspired by her strength and determination. Brain Tumour Research is committed to funding sustainable research at our dedicated Centres of Excellence, but we also campaign for the government to increase funding. It's only through increased investment that we can accelerate new treatments and, ultimately, find a cure." Brain Tumour Research is campaigning for an annual national expenditure of £35million to bring brain cancer funding in line with other cancers, such as breast cancer and leukaemia. A JustGiving page has been established by Clare to raise funds for Brain Tumour Research ahead of the Walk of Hope in September.

Woman 'saw rainbows' and 'forgot' she was a mum before 'destroying diagnosis'
Woman 'saw rainbows' and 'forgot' she was a mum before 'destroying diagnosis'

Wales Online

time6 hours ago

  • Wales Online

Woman 'saw rainbows' and 'forgot' she was a mum before 'destroying diagnosis'

Woman 'saw rainbows' and 'forgot' she was a mum before 'destroying diagnosis' Clare Smerdon was given the news soon after her son's first birthday Clare Smerdon with Teddy (Image: Brain Tumour Research/SWNS) A woman says her brain tumour made her "forget" she was a mum - after flashing lights and rainbow-like patterns in her vision led to her diagnosis. Clare Smerdon, 37, was diagnosed with a grade 4 astrocytoma - just weeks after her son Teddy turned 13 months. ‌ Doctors told her the aggressive tumour was life-limiting and Clare feared she would never get to watch Teddy grow up. While waiting for surgery to remove the tumour, she said she was "acting completely out of character" and "forgot I was a mum". ‌ But two years on, she has defied the odds and proudly watched her son, now four, put on his uniform and walk through the gates of Barton Hill Academy for his first day of school. ‌ Clare from Torquay, Devon, said: 'When I received my diagnosis, I didn't think I'd be alive today to see Teddy start school. This is such a huge milestone for us. I no longer feel like I am dying and feel incredibly lucky, but I know others may not get the same chance." Clare's symptoms first appeared in early 2022, when she began experiencing flashing lights and rainbow-like patterns across her vision. She said: 'I felt as though people didn't understand what I was going through. I was desperate to find out what was causing the immense pain in my head and changes in my vision." Article continues below Clare had an MRI scan at Derriford Hospital in Plymouth, which revealed a 7cm brain tumour, in July 2022. She said: "When I got the diagnosis, I remember thinking that I'd just had a baby and I wanted to be around to watch my son grow up for as long as I could. Then the wait for surgery was horrendous. I was losing myself and acting completely out of character. "I even forgot I was a mum. Teddy spent more time with his dad and we drifted apart. That was heartbreaking.' ‌ Clare Smerdon with baby Teddy (Image: Brain Tumour Research/SWNS) In August 2022, Clare underwent a six-hour operation to remove the tumour at Derriford, followed by six weeks of radiotherapy and chemotherapy. She said: 'Two weeks after surgery I returned home and doctors confirmed I had a grade 4 astrocytoma, which is also classified as a glioblastoma. On hearing the pathology results I knew my life was over. ‌ "The treatment made me sick, and I could only stomach a meal in the evening. At the same time, I got to spend more time with Teddy and we were both getting to know each other again.' A routine scan in August 2023 revealed she had just two to three years to live. Clare said: 'The thought of not being here to watch Teddy grow is destroying. I'm not sure if another operation is something I want due to the implications that come with it. ‌ Clare Smerdon (Image: Brain Tumour Research/SWNS) "My eyesight is already compromised and my speech has been impacted, so now I just watch and wait. There are so few treatment options for brain tumour patients and the ones we do have are invasive and often life-changing. "I've looked into clinical trials abroad, but for most working-class families, the cost is impossible. I'm angry and frustrated at how little support and research funding there is.' ‌ Clare is now working with Brain Tumour Research and will take part in the charity's Walk of Hope in September. She said: 'I want to do everything I can to help fund the research that will lead to better treatments and, ultimately, a cure. If sharing my story and taking part in fundraising encourages even one more person to join the cause, it will be worth it. That's why I'm calling on the government to increase funding for research into brain cancer, more must be done.' Clare Smerdon taking part in Walk of Hope (Image: Brain Tumour Research/SWNS) Article continues below Letty Greenfield, community development manager at Brain Tumour Research, said: 'Clare's story is a powerful reminder of both the personal impact of a brain tumour diagnosis and the urgent need for change. We are so inspired by her strength and determination. Brain Tumour Research is committed to funding sustainable research at our dedicated Centres of Excellence, but we also campaign for the government to increase funding. It's only through increased investment that we can accelerate new treatments and, ultimately, find a cure.' Brain Tumour Research is calling for a national annual spend of £35million to bring brain cancer funding in line with other cancers, such as breast cancer and leukaemia. A JustGiving page has been set up by Clare to help raise money for Brain Tumour Research ahead of the Walk of Hope in September.

I blamed stomach pain on a dodgy BBQ but then I was told I have just months to live
I blamed stomach pain on a dodgy BBQ but then I was told I have just months to live

Scottish Sun

time9 hours ago

  • Scottish Sun

I blamed stomach pain on a dodgy BBQ but then I was told I have just months to live

Dad Matt Eamer was diagnosed with one of the most common cancers in the UK - find out symptoms of the disease to look out for below SHOCK TWIST I blamed stomach pain on a dodgy BBQ but then I was told I have just months to live Click to share on X/Twitter (Opens in new window) Click to share on Facebook (Opens in new window) WHEN Matt Eamer began experiencing stomach pain he put it down to eating "a dodgy sausage" at a family BBQ. But when the pain persisted, doctors discovered a "big blockage" in his intestine, which turned out to be stage 4 cancer. Sign up for Scottish Sun newsletter Sign up 6 Matt had been celebrating his son's birthday when he began experiencing stomach pain Credit: SWNS 6 When the pain persisted, doctors discovered a big blockage in his intestine, which turned out to be bowel cancer Credit: SWNS Matt, 44, had been celebrating his son Alex's second birthday in September 2020 when "spiky" pain began. The dad-of-two was rushed to hospital and was given Buscopan - an over the counter medication that helps stomach cramps - and sent home. But he continued to feel awful. His wife Sarah, 41, a doula, took him to East Surrey Hospital, Surrey, where tests confirmed the blockage in his large intestine. Just days later, following surgery to remove the mass, it was confirmed as stage four bowel cancer. Matt underwent six months of intense chemotherapy, but during surgery to cut away part of his liver, in March 2021, surgeons told him it had spread to his peritoneum - the lining of the abdominal wall. It was also discovered Matt had a BRAF mutation - a genetic alteration that can lead to uncontrolled cell growth - and his "cancer had formed and grown very quickly". Matt was "looking at months" left to live when he began taking newly approved immunotherapy drugs called Cetuximab infusion and pills called Emcorafenib. But he responded well, and five years on has no signs of cancer, and still takes the medicine. Matt, from Redhill, Surrey, who runs a design agency, said: "I was speaking to work colleagues over the first week or two and thought I'd cooked a dodgy sausage on the BBQ. "My pain escalated quickly. I thought my sore knee was a drunken injury but it was cancer at 27 "I can still remember the person's voice when she phoned and said 'the plan for your diagnosis has changed'. "They said 'we're talking months not years from a survival point of view'. "Hitting five years with stage four is a rarity. "You're not on your death bed but you're forced to think about how you spend your time". He said doctors initially thought the mass might be benign. "They took out two thirds of my large intestine," he said. "A few days later they confirmed it was active cancer." New life-extending drugs After chemotherapy, Matt was informed on his 40th birthday by doctors that his treatment plan had changed Matt has been taking four Encorafenib pills every evening since and has fortnightly infusions of Cetuximab - designed to extend his life by three to six months. "It was a very dramatic movie like point," he said. "It was a pivotal change, they said, 'we've gone in, it's gone further, we're going to try these new drugs. "My wife Sarah collapsed to the floor." He began the new drugs approved just a few months earlier, which target rapid growth of cancer cells. Matt had an "unusual response" to the drugs - with scans after six months not showing "any cancer"- and now has fortnightly infusions. Despite needing a 14-hour surgery in December 2024 to remove tissue in his ribcage that had the BRAF mutation and HIPEC chemotherapy, Matt says doctors are back to the view of not seeing anything, with scans showing things are clear. I'm never going to know what my future really looks like Matt Eamer "I'm never going to know what my future really looks like," he said. "I continue to run my own business and the family. "I remember four or five months ago listening to Virgin Radio and Chris Evans was interviewing Chris Hoy. "He's really trying to challenge the perception of stage four. "The reality is younger people are able to deal with treatments better and liver longer better lives even if it is stage four. "The book he's written highlighting things like being presented with things like a devastating life ending diagnosis, the cliche is you go for big bucket list of swimming dolphins and all that stuff. 6 Matt was told he had months to live because his cancer was stage 4 Credit: SWNS 6 He underwent 14-hour surgery, as well as chemotherapy, before doctors decided to try new drugs to prolong his life Credit: SWNS 6 Matt had an "unusual response" to the drugs and six months later scans showed things were clear Credit: SWNS 6 He's now taking part in a charity cycle to raise funds for Bowel Cancer UK Credit: SWNS "The reality is the 'bucket and spade things', the little moments. "I spend more time looking at my kids faces taking them to a show or swimming in the sea, they are heightened. "It means your ability to be present and focus upon what matters is heightened". He is now set to take part in a charity cycle set up by Sir Chris Hoy in Glasgow on September 7 raising funds for Bowel Cancer UK. It will mark five years since he was diagnosed. "It's marking a milestone in a meaningful positive way," he said. To donate, visit his GoFundMe.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store