In early 2022, I noticed strange bruises on my back. My GP did three separate rounds of blood tests, which came back clear. But the bruises kept getting worse.
After paying for more extensive private tests, my world was turned upside down when I was eventually referred back to the NHS and told I had blastic plasmacytoid dendritic cell neoplasm. Known as BPDCN, it's a very rare type of blood cancer normally only found in men over 60 and there are only around 10 cases every year in the UK.
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I know it may sound strange, but as I sat in the consulting room holding my mum Pauline's hand, hearing the "C word" was somehow a relief as well as a nightmare.
I'd finally get treated. I had no idea what my prognosis was and I'd certainly never heard of BPDCN before. Neither had my consultant, who handed me a leaflet. I read with horror that the average survival time was just 12 months
I had to stay strong. I told myself I didn't fit into the usual demographic for the disease and I refused to be that statistic.
I started a form of called immunotherapy tagraxofusp, followed by a high-strength chemotherapy. It meant staying alone in a hospital room for four weeks, away from Clare and Ben.
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I could only see them through a glass window into the corridor. We’d play noughts and crosses through the glass and I’d feel the warmth of their hands as we pressed on each side.
By then the aggressive cancer had spread to my lymph nodes, breasts, bone marrow, skin and ears. But the children were too young to take in what cancer meant – and I had to stay positive for their sake. I prepared for the worst and hoped for the best, because without hope I had nothing.
Over the following months I had a series of seemingly ineffective chemotherapies and each time they hit me harder.
I wrote my will to prepare for the worst, but I also started a gratitude journal, to create a positive mindset around the horrible situation. I also practised daily affirmations, such as, “I am cancer free. I am in remission. I am grateful for the treatment.”
I began meditating and even danced on my own in that prison of a hospital room to lift my spirits. I shared my journey on social media too, to show other people the gruelling reality of cancer treatment.
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STOPPING TREATMENT
Eventually, doctors found a combination of chemo drugs that worked, but then I ended up in the ICU with sepsis. My kidneys were failing, my blood pressure was seriously low and I developed steroid-induced diabetes. I had to stop the treatment because while it was killing the cancer, it was also killing me.
I was told a stem cell transplant could be my only hope. It would involve killing off my bone marrow and replacing it with donated stem cells, effectively giving me a whole new immune system. If that didn’t work, it might be the end of the road.
I had no idea then that my one final hope would be my sister, Sarah. When she proved to be a match she didn’t hesitate. We’ve always been close and she’s the ...