In a startling turn of events, Kerry Brown, a 54-year-old production manager from Yorkshire, discovered that her seemingly innocuous symptoms were indicators of a serious health condition. What she initially perceived as menopause-related experiences, including hot flashes and tingling sensations, were later revealed to be the result of multiple brain tumours.
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The onset of Kerry’s symptoms began in 2017 when she started feeling hot flushes and inexplicable tingling throughout her body, symptoms she attributed to hormonal changes typical of menopause. Over the next two years, her condition deteriorated, and she began grappling with extreme fatigue and occasional slurred speech. However, it was not until she started to experience vision problems that she sought medical advice.
Reflecting on those early signs, Kerry stated, “I thought it was just the menopause, but then I’d go pale, start slurring my words, and feel overwhelmingly tired. I didn’t think it was anything serious.” She then described a concerning incident where her vision in her right eye felt obstructed, akin to a “thumbprint” covering her sight.

In 2019, following a visit to an optician who detected swelling behind her eye, Kerry was referred for an MRI scan at her local hospital. The results triggered immediate concern; her doctor instructed her to come to the hospital without delay. “I remember walking in and seeing pictures of brains on the wall and thinking, ‘This can’t be good,’” she recalled.
Upon receiving her MRI results, Kerry was informed that she had four brain tumours, and what she had believed to be menopausal hot flashes were, in fact, seizures. “I was completely stunned,” she admitted. Further examination revealed that the tumours were meningiomas, which are the most common type of brain tumor, resulting from the abnormal growth of cells in the membranes surrounding the brain and spinal cord.

During the surgery which followed, doctors discovered an alarming number of tumours. Instead of the four they had originally identified, Kerry awoke to the news that they had found ten tumours. “When I woke up after the surgery, they told me they hadn’t found four tumours – they’d found 10,” she recounted. “I remember joking, ‘Every time I speak to you, you find more.’ But inside, I was terrified.”
While medical professionals succeeded in surgically removing five of the tumours, the remaining growths required ongoing monitoring. Despite the initial surgical success, Kerry continued to experience seizures and would later suffer the loss of vision in her right eye, attributed to one of the tumours pressing on her optic nerve.
“The biggest impact was on my sight because the tumour at the front of my head had been pressing on my optic nerve,” she explained. Although doctors had hoped that removing the tumour would alleviate the pressure, the damage had already been done, leading to her blindness in that eye.
In a recent follow-up appointment, Kerry was informed that two of the remaining tumours had begun to grow, necessitating further radiation treatment. As she confronts this challenging journey, she has taken on the important role of advocate, sharing her experiences to raise awareness and secure funds for brain tumour research.
Kerry believes that her firsthand experience compels her to act. “Knowing how underfunded research into brain tumours is, and having experienced this first-hand, really motivated me,” she stated. “I know what it’s like to go through this. I’ve lived it. If sharing my story helps raise awareness or helps someone else feel less alone, then it’s worth it.”
Kerry Brown’s harrowing story emphasises the complexities and often misinterpreted symptoms associated with brain tumours. As she continues her fight against the malignancy, her determination to raise consciousness surrounding this critical health issue serves as a beacon of hope, illuminating the path toward necessary research and support in an often-overlooked field of medicine.
