February 2013 |
At the beginning of 2013, I'd not long turned 18, so was enjoying nights out and looking forward to becoming more independent. I was studying for my A-Levels, and I was probably the fittest I'd ever been in my life, with my daily routine including bodyweight circuits, a 3-mile walk to and from school, and running throughout the warmer months.
A week before I was diagnosed |
Things started getting worse, I saw a woman drop her ID, and found myself unable to run the short distance to give it back to her. I also started getting headaches, and people were commenting that I was looking visibly more pale. I didn't know what was wrong with me, but I was pretty sure it was something to do with my blood. My headaches got progressively worse and were accompanied by dark patches in my vision, so I went to see my GP. He thought it this was a "migrainoid" and prescribed some migraine tablets.
That afternoon was the first sunny day of the year, so I dusted off a pair of shorts for the first time. That's when I noticed my ankles were covered in tiny marks, which looked like small freckles. When I went back to see my GP the next day, he thought this was an allergic reaction to the migraine tablets, but luckily took a blood test anyway.
My first overnight stay in hospital 2nd May 2013 |
When I got to the hospital, I was escorted into a great newly-furbished private room, where I was asked a load of questions and had "an armful of blood" taken off me. I was told that I would need to have a bonemarrow biopsy the next day. I knew that this was a diagnostic test for cancer, but I thought that it was being done to rule cancer out as a possibility, before finding out what was really wrong with me.
I was worried about the notorious pain of bonemarrow biopsies, but my main concern at this point was that I hadn't printed off my final draft of my Media Studies coursework, and that I didn't have my phone charger with me.
It was explained to me that my excessive tiredness, lack of energy and pallour was because of my low red blood cells. The marks on my ankles were pinprick bruises which hadn't been able to clot due to my low platelets, and the patches in my vision were caused by similar bruises occurring on the retina of my eyes.
The next day, my mum and auntie came to visit, who were shortly followed by a group of doctors. They turned off the TV and told everbody to sit down before breaking the news. They said that they had looked at my white blood cells under a microscope, and had identified them as cancerous, and told me that I had acute lymphoblastic leukaemia.
I was a little shocked, but my first reaction was the pragmatic one: "okay, this is what I've got, what can we do about it?". They asked if I had any questions, so I asked the obvious one whenever cancer is brought up: "how early have you caught it?". Apparently this doesn't make much of a difference with ALL, as symptoms only present when the bonemarrow is roughly 100% leukaemia, and therefore every patient is diagnosed at around the same point.
Overnight drip in Bristol 3rd May 2013 |
This meant that we needed to leave straight away and drive to Bristol, in what was an emotional whirlwind, and I needed to tell most of my family members and friends about my diagnosis over the phone...
I guess that was chapter 1 of my cancer journey throwback, I'm sure I'll post more in time.
Pete
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