I had my first chemotherapy session yesterday. An initial check found fluid had accumulated around the lung, which I've been suspecting since I've quite short of breath for the past week, but which was too little to order a drain at the moment. The idea being that if the chemo checks the activity rate of the cancer cells, the fluid may be reabsorbed naturally.
I was half expecting an attack of rls while I lay on the bed with an intravenous needle in the back of my left hand, but it was obviously asleep at the wheel, and failed to grasp its opportunity. Not so later in the day, however, from about 4 pm when I sat in my easy (non-easy) chair/recliner before mowing the lawn in the back, and afterwards. Rls taking revenge. I tried my whole-back massager for about 20-30 minutes with little immediate effect, then tried sitting on it to massage buttocks and upper thighs, with the same lack of immediate effect. I also did some of the leg exercises, taught me by my osteopath, for the first time since dropping off my perch with the collapsed lung. With no effect there either, I got so frustrated I took a pramipexole (sifrol), and rls abated somewhat, though whether it was due to the massaging, leg exercises or pramipexole I wouldn't know.
When you're given chemotherapy - as I expect some of you know better than I - you're medicines to counter the side effects. These pills have their own side effects of course, one of which they highlight in particular being constipation. Being forwarned and forearmed I started drinking from Wednesday copious amounts of the lovely versions of cultured milk they have in Norway (kefir, kulturmelk, biola, yoghurt with prunes etc.).
I'd also decided this time to park in a street a km or so from the hospital to avoid the exorbitant parking fees, and walk the distance. One of the side effects of the pills they didn't mention however was the opposite of constipation, i.e. diarrhoea, and I only just managed to get to the loo in the hospital before exploding. That was the first of five aftershocks in that department, by which time my backside was red as a traffic light stuck on stop.
Things seem calmer so far today though.
Another side effect, which is more humorous than annoying or even much use at my age and situation in life is also one they didn't mention. The viagra-like effect. I've never taken viagra so haven't a clue how it works. But the pills (or the chemotherapy drugs) certainly increased the blood flow to the nether regions. Just thought I'd mention it as a way of smuggling in viagra through the back door, so to speak.
The actual infusion of the drugs took about an hour, and apart from wanting to go to the loo most of the time - you get so much liquid into the blood stream, you're bladder gets full to overflowing - there was no discomfort and I was very relieved to get started on the course.
I did get a hot flush back at home around 2 pm (or are they called hot flashes?). Bit scary, but it didn't last more than a minute or two. Perhaps my body thought it was going through a belated menopause, poor thing.
The doctor prescribed vival to help me sleep (which has been a constant pain in the neck for years). I said I wasn't too keen on taking sleeping pills, and that last two I took, one at the hospital a week or two ago, and one back home, had the opposite of the intended effect, but she said don't be a sissy, your body is undergoing major changes and you need to get a good night's sleep.
I didn't collect the vival on the way home, believing that all the excitement of the day would knock me out, but was sorely disappointed not to sleep until 4 am and wake up at 7.30 am, just in time , however, to hear the roundup of the week's Farming Today programmes on BBC Radio 4 (7.30 here being 6.30 in the UK).
So I'll probably go to the chemist's today and get the vival. I'll start on half a tablet. Do not want to get addicted.
I have tried herbal sleep inducers, the last one is made in Denmark I believe, and it tastes so foul it almost acts as an emetic. No noticeable effect in the sleep department though.
I'll keep you updated if anything happens which may be of interest.
best,
Chris