Latest news with #BartonHillAcademy
New York Post
2 days ago
- Health
- New York Post
Mom's brain tumor caused her to ‘forget' she had a son: ‘That was heartbreaking'
A UK woman says her brain tumor made her 'forget' she was a mom — 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. Advertisement Doctors told her the aggressive tumor was life-limiting, and Clare feared she would never get to watch Teddy grow up. While waiting for surgery to remove the tumor she says she was 'acting completely out of character' and 'forgot I was a mum.' 5 UK mom Clare Smerdon was diagnosed with a brain tumor just 13 months after giving brith to her son Teddy. Brain Tumour Research / SWNS 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. Advertisement 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.' 5 Clare's scar from her brain tumor surgery. Brain Tumour Research / SWNS Advertisement 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.' Clare had an MRI scan at Derriford Hospital in Plymouth which revealed a 2.75 inch brain tumor 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. Advertisement 5 The tumor caused Clare to see flashing lights and even forget that she was a mother. Brain Tumour Research / SWNS '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 six-hour operation to remove the tumor 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. 5 Clare was told in 2023 that she would only have two to three years to live. Brain Tumour Research / SWNS 'At the same time, I got to spend more time with Teddy, and we were both getting to know each other again.' Advertisement 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 comes 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 tumor patients, and the ones we do have are invasive and often life changing. Advertisement 5 Clare participating in a charity walk to raise money for brain tumor research. Brain Tumour Research / SWNS '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. Advertisement Start your day with all you need to know Morning Report delivers the latest news, videos, photos and more. Thanks for signing up! Enter your email address Please provide a valid email address. By clicking above you agree to the Terms of Use and Privacy Policy. Never miss a story. Check out more newsletters '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 tumor diagnosis and the urgent need for change. Advertisement '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 $47.2 million to bring brain cancer funding in line with other cancers such as breast cancer and leukemia. 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.
Daily Mirror
3 days ago
- Health
- 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.
Wales Online
3 days ago
- Health
- 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.
