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“I’m sure five days with an infuser pump will be OK. I’m going to hang it on the bed head and see how it goes”
I may have spoken a little too soon. The hanging the pump on the bedhead worked, in general, quite well. However, as a plan it does require a certain amount of concentration. There were quite a few typos in my last post, so you may be able to deduce that I wasn’t concentrating well, and that an anecdote is about to be launched on the world.
Imagine it’s 4am, you need the bathroom (again), it’s half light . . .
(This is the reality of life as an older man, my dreams of yachts, sports cars and trophy wives have all been replaced with a genuine desire to simply sleep through the night.)
Then, as your left arm suddenly jerks , and your entire body judders to a halt, you realise the pump is still hanging on the bedhead. This can be even worse when they change the arm for the cannula, as all your coping strategies change sides.
Generally I am OK in the night, but in the day (when I hang the pump from my reading lamp) I am often thinking of other things as I walk away. The reading lamp has fallen over several times but is till working.
I am currently grey. Apart from my hair. I shaved that off a few mornings ago. While I was doing that I noticed my skin is grey and my eyes were grey – the whites that is, the iris is normally grey. To be honest, I was expecting them to be bloodshot. Grey was a bit of a shock.
The trips to hospital have generally been uneventful. A bit of waiting, some measurements, a lot more waiting. It tends to take about 45 minutes on average. I could get it down to ten minutes. The expiry date on the drugs is years off so you could get a load racked up the fridge. When the patient comes in, take them through, do the temperature, blood pressure, heart rate and that oxygen thing with the finger tip. Nod wisely, fill in the paperwork. Check the cannula, connect the pump, rewrap and done. ten minutes easy. If the cannula has closed up you need to insert a new one, but even that needn’t take too long.
They have changed my cannula several times over the last four days – once because it had started leaking (though it was still working) once because it blocked blocked and once because they rewrapped a perfectly good cannula badly and I had to go back, in pain, two hours after the insertion. The swelling meant they had to remove it and try the other arm.
I don’t really enjoy cannulas.
I also think that anyone who inserts one should be made to wear one for a week so they get the feel of it. I made that suggestion on the comments form this morning. I also said that the section that recorded my age, sexuality and religion was irrelevant to my care and they would be better concentrating on providing better parking. Julia says I’m getting better.


























