I’ve had this blog three-quarters written for the last few days, so I figure I really ought to finish it off and publish it. By way of a change, having built that excitement and anticipation, this week you are getting an educational blog. No groaning at the back…
Following on from chatting to a few people, I thought I’d do an educational blog that gives a bit more detail about what my chemotherapy process actually involves.
Despite all the statistics there are about how many people’s lives are touched by cancer, I bet there are relatively few people who know that there are so many different kinds of chemo, or ways of administering it. Two years ago, I certainly didn’t. I suppose if asked I’d have said that chemo was given on drips, in hospital wards, to people whose hair fell out and whose skin turned yellow. It’s nothing I’d given any real thought to, but thinking back that was how I thought of it.
Turns out I was wrong. My first experience of chemotherapy, when I was first diagnosed back in summer 2009, was tablets. A tablet with your breakfast and one with your tea each day for a month or two and that was your chemo done. It all seemed slightly unreal. As I was having radiotherapy at the same time it was hard to tell what the side effects of that form of chemo actually were, but it was a type of treatment I never realised existed.
To be honest, and this will probably sound a bit bizarre, having had chemo by way of tablets I felt a bit of a fraud saying afterwards that I’d had chemotherapy. Surely that was a light touch, not the ‘proper’ stuff?
Anyway, this time round, there’s no tablets, and to start off with there is a hospital ward and a drip, so I guess it must be the proper stuff! Every two weeks, initially for three months, I go into hospital for a morning’s worth of treatment. Having had blood tests the day before to check I’m OK for the treatment to go ahead, the first drug is rigged up and pumped straight into me through a Hickman line. This is planted somewhere under my collar bone, taking the drugs straight into my bloodstream.
In the half hour that first drug (irinotecan, if you’re interested) is being administered, I’ll generally feel pretty tired or sick. Then it’s onto 2 hours worth of something else – not an actual drug this time, and to be honest I can’t remember what it is (which kind of dilutes the educational value of this blog, but there you go…). Anyway, it must be needed to set things up for the final drug.
This one, which goes by the catchy name of 5FU, takes the next 48 hours to administer. The hospital start off the process, and I get given a pot to take home with me (important use of the word ‘a’ there – they might be drug pushers, but there is a line to draw…). As you’ll see from the photo below, in the pot there’s a balloon, which at the point the picture was taken had pretty much fully deflated. The drugs are in the balloon and by some form of air pressure are passed on into the Hickman line. I have that attached for 2 days and once its gone, that’s it, job done for the next two weeks.
So that’s it. A few hours sat in hospital with a dripstand, but most of the time while I’m having chemo I can carry the stuff round with me and carry on as normal. Not really what I expected again but there you go.
So that’s two different kinds of chemo that I’ve had. No doubt there are endless more – you see people on the ward who are there for much shorter, and much longer times. But hopefully that gives you a bit more of an insight into what the chemotherapy process (or one of them) is.
Final educational thing – my Tour Down Under prediction last week. No shootout between the big sprinters, just as I said, but a couple of great results for South Yorkshire’s Ben Swift. A great way to start the season!