Well, dear Constant Reader, normal service isn’t being resumed as soon as I’d like, I’m simply too ill and, not to mince words, trying very hard not to die. And no, I don’t do hyperbole, sadly.
As some of you know, I have pneumonia – so much for that bloody vaccine ! – and pleural empyema. Basically, my left lung is – or was, it’s improving now – a huge abscess (for those familiar with the condition, don’t get picky, that’s a good enough description for those who aren’t). In addition , the allegedly minor COPD-related heart failure that’s been lurking around the fringes for years appears to be working quite hard to polish me off. Stern words needed with my GP on that one – why, for example, was it never monitored?
And I’m quite heavily drugged at present, which is preventing me writing the article about Arrowe Park Hospital, Wirral, that needs to be written, because the place is a chaotic hell-hole.
So, assuming I can get past the current crisis, and that’s by no means totally certain at this stage, though it’s looking more promising, then some lifestyle changes are needed if I’m actually going to have a life to change, and taking things extremely easy is the first step. Bloody-mindedness and a refusal to just quit can take you only so far – sometimes you just have to give way a little. Or a lot, even. Life might be crap, but it’s mine and I’m kind of attached to it!
In the interests of taking it easy, I’ve just bought a power chair – a remarkable bargain, too – £849 delivered and set up. I just lucked into their sale, it’s normally £1299 http://www.betterlifehealthcare.com/view_product.php?prodID=7619
It’s a folder, which I don’t really like as they tend to creak, but hell, right now I’m in no position to be picky. And I know how to fix that, anyway.
That I have no more beer is a given – heart failure and large doses of fluid just aren’t compatible, never mind the alcohol, and with the money I’ll save, come summer, I can load my chair into a taxi and go out for the day somewhere – Ness Botanical Gardens, over on the Dee side of Wirral, will cost around £40 in fares, for example, but it’s not as if I’ll be doing it every day, just a few times a year. Closer to home, the lake, with birds to photograph, and a nice pub for a (beerless), lunch nearby, is about £20 in fares, and that I could do every week. (Royden Park, Roodee Mere, and the Farmer’s Arms, for those familiar with the area.)
All I have to do is get through this current mess. I am getting better, but as I discovered today when my Sainsbury’s order arrived, there’s still an awfully long way to go (now the empyema is improving, the pneumonia is making its presence felt more – I simply couldn’t breathe well enough for it to be a factor before, now I can breathe somewhat better, but not well enough to speak above a whisper – I have almost no voice at all), and I’m sure I’ll feel better psychologically, at least, once I have my chair (next week sometime), and I can get out of here for a bit of fresh air.
In addition, it’ll allow me to do things like my laundry, and taking out rubbish, on a regular basis, not just when I’m able to, which is often no more than every couple of weeks (luckily I’m not short of clothes or bedding). Festering rubbish is no fun, though. As some of you know, I live in a supported flat – still, after 14 years, trying to figure out exactly where the support is!
I’ll sell my scooter, it just didn’t work out and I’ve no real idea why – it really should have been perfect for me. Actually, with the benefit of that wonderful thing hindsight, it’s clear I’ve been incubating the empyema for at least a year, or more (night sweats are a major symptom, and I’ve been sleeping on towels for well over a year – that’s now stopped, which is a little seed of hope), which may explain the overwhelming apathy and tiredness that’s affected me for so long. It also explains why my need for antibiotics has been so much higher during that time.
Back with the scooter, and now, of course, manhandling it into my flat is quite impossible. I can ride it out easily enough, but it’s proven impossible to ride back in, I have to lever it sideways first, with a pickaxe handle, before it’ll fit through the door. Just can’t do that ever again.
Ah well…
Bottom line, I’m dying; I was, by all accounts, extremely lucky to survive last weekend (not to mention 4 totally sleepless days and nights that had me on the ragged edge, and got me a negotiated early discharge on the grounds that my chances were better at home than amid the chaos there), and there’s a lot of that hill still to climb. That, I’m afraid, people, is the unavoidable crux of the matter, but I intend to do all I humanly can to try to make sure it’s not just yet (insofar as I have any control over it at all). To be fair, I’ve done well to get to 66 (at 17, I was expected to be dead by 40).
Somehow, that’s no consolation. Not at all…
Well, dear Constant Reader, normal service isn’t being resumed as soon as I’d like, I’m simply too ill and, not to mince words, trying very hard not to die. And no, I don’t do hyperbole, sadly.
As some of you know, I have pneumonia – so much for that bloody vaccine ! – and pleural empyema. Basically, my left lung is – or was, it’s improving now – a huge abscess (for those familiar with the condition, don’t get picky, that’s a good enough description for those who aren’t). In addition , the allegedly minor COPD-related heart failure that’s been lurking around the fringes for years appears to be working quite hard to polish me off. Stern words needed with my GP on that one – why, for example, was it never monitored?
And I’m quite heavily drugged at present, which is preventing me writing the article about Arrowe Park Hospital, Wirral, that needs to be written, because the place is a chaotic hell-hole.
So, assuming I can get past the current crisis, and that’s by no means totally certain at this stage, though it’s looking more promising, then some lifestyle changes are needed if I’m actually going to have a life to change, and taking things extremely easy is the first step. Bloody-mindedness and a refusal to just quit can take you only so far – sometimes you just have to give way a little. Or a lot, even. Life might be crap, but it’s mine and I’m kind of attached to it!
In the interests of taking it easy, I’ve just bought a power chair – a remarkable bargain, too – £849 delivered and set up. I just lucked into their sale, it’s normally £1299 http://www.betterlifehealthcare.com/view_product.php?prodID=7619
It’s a folder, which I don’t really like as they tend to creak, but hell, right now I’m in no position to be picky. And I know how to fix that, anyway.
That I have no more beer is a given – heart failure and large doses of fluid just aren’t compatible, never mind the alcohol, and with the money I’ll save, come summer, I can load my chair into a taxi and go out for the day somewhere – Ness Botanical Gardens, over on the Dee side of Wirral, will cost around £40 in fares, for example, but it’s not as if I’ll be doing it every day, just a few times a year. Closer to home, the lake, with birds to photograph, and a nice pub for a (beerless), lunch nearby, is about £20 in fares, and that I could do every week. (Royden Park, Roodee Mere, and the Farmer’s Arms, for those familiar with the area.)
All I have to do is get through this current mess. I am getting better, but as I discovered today when my Sainsbury’s order arrived, there’s still an awfully long way to go (now the empyema is improving, the pneumonia is making its presence felt more – I simply couldn’t breathe well enough for it to be a factor before, now I can breathe somewhat better, but not well enough to speak above a whisper – I have almost no voice at all), and I’m sure I’ll feel better psychologically, at least, once I have my chair (next week sometime), and I can get out of here for a bit of fresh air.
In addition, it’ll allow me to do things like my laundry, and taking out rubbish, on a regular basis, not just when I’m able to, which is often no more than every couple of weeks (luckily I’m not short of clothes or bedding). Festering rubbish is no fun, though. As some of you know, I live in a supported flat – still, after 14 years, trying to figure out exactly where the support is!
I’ll sell my scooter, it just didn’t work out and I’ve no real idea why – it really should have been perfect for me. Actually, with the benefit of that wonderful thing hindsight, it’s clear I’ve been incubating the empyema for at least a year, or more (night sweats are a major symptom, and I’ve been sleeping on towels for well over a year – that’s now stopped, which is a little seed of hope), which may explain the overwhelming apathy and tiredness that’s affected me for so long. It also explains why my need for antibiotics has been so much higher during that time.
Back with the scooter, and now, of course, manhandling it into my flat is quite impossible. I can ride it out easily enough, but it’s proven impossible to ride back in, I have to lever it sideways first, with a pickaxe handle, before it’ll fit through the door. Just can’t do that ever again.
Ah well…
Bottom line, I’m dying; I was, by all accounts, extremely lucky to survive last weekend (not to mention 4 totally sleepless days and nights that had me on the ragged edge, and got me a negotiated early discharge on the grounds that my chances were better at home than amid the chaos there), and there’s a lot of that hill still to climb. That, I’m afraid, people, is the unavoidable crux of the matter, but I intend to do all I humanly can to try to make sure it’s not just yet (insofar as I have any control over it at all). To be fair, I’ve done well to get to 66 (at 17, I was expected to be dead by 40).
Somehow, that’s no consolation. Not at all…