As I sit here, writing these gentle prose to you, dear reader, this is the view I enjoy.
It's an old man's piss-bag.
Levels have been rising steadily all day, and I was tempted to try a time-lapse movie for your lurid enjoyment, but decided the moral line had to be drawn somewhere, and this is it.
The main purpose of this posting is to let you know how difficult it is to get pain relief in hospital.
At home, I had a nice combination of pain killers going which was genuinely helping me. Sure, they were strong, but they worked quite well.
When I came into hospital, the one doctor I did see promised me that I had nothing to fear, and that they would ensure I was as comfortable as possible. It was one of those nice, comforting speeches which invites trust.
Initially I got two of the three drugs I took, with a promise of the third later. It never came. Then I moved wards. Upon arrival at the new ward they informed me that one of the drugs had been stopped. The other two were supplied regularly.
Today I discover that the other drug has been stopped, leaving me with just paracetamol. I can requst the morphine, but it requires approval each time and they often cannot get it.
My question is this:
Who is making these decisions? Who is cancelling my medication without telling me? Someone is deciding my level of pain relief without examining me or speaking to me. I find this deeply troubling. Nor can I complain.
I must wait till a doctor chooses to visit this backwater. Since I don't belong on this ward, my doctor may never visit. Nor can I leave to seek him out.
The nurses can only give me what comes up on their computer, and they say they do not know who controls the computer.
Somewhere along the line, I am being told a tale.
Is it too much to ask that my pain is regularly and effectively relieved without me having to fight all the time?
On a similar theme, one of the advantages of being in hospital is that I can have my bandages changed more regularly - particularly on my left leg which is pouring with fluid.
I was told today that they did not have the staff to do the second change, so would have to wait till morning. They say they are too short staffed to do it.
I am glad that this is a public record of how I am being treated. I would guess that it is typical of the way patients can expect to be looked after if they have a condition like mine, which does not easily sit in a category.
The message from this side of the fence is that the NHS feels very second rate, overstretched, inefficient and, quite honestly, under skilled.
I am really sorry to be here, but I will tolerate it, as long as they are able to give me the IV antibiotics that I need.
I am sad, exhasperated and very very tired.
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