Well, chemo has slowly dragged on. It hasn't made me feel bad particularly. I've been tired and not wanted to leap tall buildings in a single bound but the previous CHOP chemo made me feel worse. The rub here is that you are wired up 24/7. There are 4 lots of a drug called Cisplatin that you get for 96 hours, accompanied by loads of fluids (as it is a bit of a nasty sucker to your insides if let loose on its own). Now, the annoying thing about constantly getting fluids fed in, as I've gone on about before is that they start to bloat you out unless you can get rid of them. They give you some drugs to help get rid of them, but it's an ongoing drudge. Anyway, the 96 hours is getting near to an end and my grumpy mood (obviously noticeable as my wife has bought me a Mr. Grumpy t-shirt. Thanks love). Also, both a plus and a minus are the large steroid doses used on this chemo. Plus side, I've always responded well, so yay there. Downside, if they are given late they can stop you sleeping. Mine were given late, as the infusions were going on so long (on and on and on...! You can tell I'm not the most patient person in the world). So, first night, no sleep, just mad thoughts that wouldn't go away. You think of one thing and go off on a tangent and then another and then another, until you pull back and think "I WANT TO GO TO SLEEP!" and then a thought about sleep, e.g. a film that had sleep in the title comes to mind and away you go again. Thankfully, I seem to have adapted and was able to sleep okay last could of nights, apart from the regular wakings up to pee in bottles (all urine out has to be measured and compared to fluid in, to make sure it's not welcome to bloats-ville).
Saturday, 4 October 2008
No sleep till Brooklyn!
That's fluids aside, ooh, lovely fluids. Or so you'd think! That brings me to blood. Apparently my red count was getting low, which would help explain why I was getting tireder. Now, I really appreciate people who give blood (and I'm glad I got over my cowardice and did myself, before getting ill), as I have now been a recipient (sorry to upset any Jehovah's Witnesses that may have stumbled onto this page, but blood transfusions are the least you've got problems with! Wow! That was a bit harsh. A brief aside. Whilst at home, between treatments two 60+ year old JWs came round to convert me, after hearing their arguments I gave counter arguments to their claims and they were not very happy that I did not just gleefully accept their rather "intriguing" version of the way of the universe. Have a look at their beliefs, I was amused. Perhaps I'm over stepping the mark now and should get back to business). Anyway, I was told I would need a new little cannula poking into my hand as my other 2 lines were busy. Joy! A new hole and a hand I can't use properly. They said as soon as the blood is in we'll take the cannula out. Cool! I thought, so that's not so bad.
"How, long to put the blood in?", I asked.
"About 2 hours, 4 at max"
Blimey, I thought to myself, that's a fair while. My thoughts were interrupted though...
"Per pack and we're giving you 3"
Lordy! Upto 12 hours to shove some blood in! And it ended up taking longer. Man, this blog is turning into my personal rant zone. I'm sure earlier posts were all happy and positive and talking about flowers and trees and other crap. Rah! Mr. Grumpy is in town!
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3 comments:
Good idea about the jokes but I'm even worse than you Rich and either laugh before the punchline or forget it! I'll look for a good one next time. Don't forget we're all patiently waiting to hear the next 'hedge episode'. Hope you got some sleep last night.
Cheers and prayers
Peter
PS-try leaping small buildings first!
I used to give blood and it never freaked me out, indeed the promise of a cup of tea, chocolate biscuits and friendly nurses was positively alluring.
But then for some reason one day while lying in the church hall I looked down and saw my blood pumping out and it really did freak me out. I never went again.
What a wimp.
I promise to get back into the blood letting groove, and I urge everyone else to do the same.
Rich i find your blog interesting and so the more info in the blog the better.
I always check out your blog to see how your are doing and wish you well matey, so shoulders back (easier in bed anyways i supppose) chin up and keep positive and still keep that sense of humour and you my friend will get there.
Rgds thoughts
Mark
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