UK mom’s brain tumor caused her to ‘forget’ she had a son


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.

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.”

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.

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 scar from her brain tumor surgery. Brain Tumour Research / SWNS

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.

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.

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.”

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.

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.

“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.

“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.



Source link

Credit to Nypost AND Peoples

Related Articles

Leave a Reply

Your email address will not be published. Required fields are marked *

Adblock Detected

  • Please deactivate your VPN or ad-blocking software to continue