I don’t think I have any photos of myself getting chemotherapy from the first time around. That was nearly a quarter of a century ago, in the pre-digital age, so any photos there are would be the old-fashioned type, buried in a folder somewhere. In any case, it didn’t feel like the sort of thing one would take photos of. It was too desperate, too morbid, too confusing—too close to the bone.
Now though? Well, we take photos of anything, don’t we?
In the photo above, I’m having my first session of chemotherapy in St. James’ Hospital, getting a combination of pemetrexed and carboplatin pumped into my veins. Pumped very carefully, of course. These are toxic chemicals, and if the needle isn’t positioned right, well … 25 years ago it was explained to me that it would be like a chemical burn under your skin. They didn’t go into the gruesome detail this time around, but the nurse was appropriately careful.
You might note that I’m smiling in the photo above. Does that seem odd? Wrong? I don’t know, but it is honest. As much of a shock as the lung cancer diagnosis was, I feel like I’ve adjusted well. This is what needs to be done for now, and compared to a lot of other people, I’m lucky. I had one of my best friends keeping me company through the first session and plenty of others asking after me. Plus—and this is no small thing—I’ve been through this (or a variation of this) before. I’m prepared.
(Or at least I think I am. Time will tell.)
Back in the 1990s, the experience was similar, though maybe a little less efficient. Chemotherapy for Hodgkins’ Lymphoma likewise involved a combination of drugs, the names of which have long since escaped me. Though I was, at the time, put on the less harsh regime of the two available, it wasn’t a fun experience. Beyond having a line inserted into the veins of my hand (more painful than the elbow, but I have decent veins, so it wasn’t a chore for most nurses), the several hours that I spent in the ward watching drugs drip into my feed usually saw the side effects kick off, in the form of nausea and lethargy.
Whether the combination of drugs have been refined, or it’s just early days and I’ve yet to be worn down, that’s not the case this time around. The initial session lasted just a couple of hours, and two days later I’ve yet to be hit with anything particularly bad as regards side effects. Inevitably, the bit that has dropped in has been my least favourite: constipation. Still, that’s not so bad—my prescription included a couple of hefty boxes of laxatives, and I’m not going to wait around to use them. Fecal impaction is one of the least fun experiences I’ve had over the course of my life.
It’s probably too early to be making much of a comparison between then and now. I need a few more runs around the chemo carousel to get a better idea of how things are different. Or I need to do more reading to get a better idea of how things have advanced in the last quarter century of anti-cancer efforts.
What I can say is that this treatment does feel more refined. Last time out, I was taking in cytotoxic drugs two weeks out of three and swallowing enough pills every morning to make me rattle. This time, it’s one week out of three, and the drug intake has been pared down to cover the treatment days and any side effects that might crop up. My body should have enough time to recover between sessions. Hopefully the cancer won’t.
The reassurance, then: I feel fine, right now. Walking and driving around, living the same life as before. Waiting for the hammer to fall, just a little, but not so much as to stop me living my life. It’s Christmas, after all. I’ve got people to see. The role of a cool uncle to play (current plans include introducing my nieces and nephews to Dungeons & Dragons). Chemo’s not going to get in the way of me doing that.