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What have you been doing today?

Stripping and painting skirting boards.

Why are paint tins (specifically, the lids) such a shoite design by the way?

Designed to get dried flecks into the paint :mad:
I’ve been told not to pour any unused paint back into the tin, and I always wipe the tin to remove excess paint.

But I feel your pain! We’ve got 12 inch skirts and they’ve been a labour of love.
 
Pointing my brick slips, last 3 courses then a welcome pot noodle break (chicken & mushroom) only as a celebration of my amazing chimney breast..
 
Long walk including across The Downs near suspension bridge. Perfect weather - warm but not roasting. Surprising how parched the grass is on The Downs - just dust in some areas. Not seen it like that for a long time. Part of the trouble is they keep holding concerts, Pride bowllux, shows, etc, etc which is destroying the turf. There's a concert on today and they're allowing cars to park on the grass. Looked more like the Serengeti with the clouds of dust thrown up by the cars' wheels. Anyway, had the roast beef when I got to my destination pub. Only £13 and a real plate full. Pub was dead, which is unusual for a Sunday lunch. Probably all away enjoying the sun in the M5 tailbacks. Landlady makes it - gravy is the high point. Made from scratch with bones. Three pints of Thatchers Gold and the walk home flew past.
 
An appointment call today, from my kidney consultant, with some bad, but long expected news. He wants me in next month, to get me sorted for home dialysis. I was warned to expect it within two years, five years ago, where they offered me the option of hospital, at home, but I've somehow managed to delay it. I agreed to home, and one of the spare bedrooms, we set up the room up back then, in readiness for the day, when.

Just last week, my GP prescribed iron tablets, for my anaemia, and low stamina, but the consultant has said to stop bothering to take them, they are no very effective. He said they will schedule me to have intravenous iron, in a month, in hospital. I've had it intravenous before, and last time I seem to remember it had an almost dramatic, and instant effect on my stamina.

I'm just confused now, about the methods of dialysis. One description mentioned inserting cannula, another, plus the dialysis nurse, and consultant, on about plumbing permanent access pipes into me somewhere.
My Dad had Peritoneal Dialysis (PD) for years. Had a tube through the abdominal wall.

Maybe that's what they were talking about?
 
Went with Mrs Mottie to see her mum in the care home yesterday. She has dementia. Mrs Mottie and her sister see her together at least once a week. They both live about 30 minutes away, her brother lives less than 10 minutes away and hardly goes at all. I’ve not seen her for about 2 months. God, how she has changed! I was shocked - she's gone from a very outgoing immaculate woman to a bumbling shell of her former self. The home are having to take over her personal care now as she can’t wash herself or even follow simple instructions such as 'sit down'. It’s heartbreaking to watch. She thought I’d dyed my hair grey - she swears it was black the last time she saw me. Only good thing about it, if there is such a thing, is that she knows nothing about it and seems perfectly happy - it’s not like a person that has a physical illness and is in pain or suffering. It’s a horrible, horrible disease.
 
Went with Mrs Mottie to see her mum in the care home yesterday. She has dementia. Mrs Mottie and her sister see her together at least once a week. They both live about 30 minutes away, her brother lives less than 10 minutes away and hardly goes at all. I’ve not seen her for about 2 months. God, how she has changed! I was shocked - she's gone from a very outgoing immaculate woman to a bumbling shell of her former self. The home are having to take over her personal care now as she can’t wash herself or even follow simple instructions such as 'sit down'. It’s heartbreaking to watch. She thought I’d dyed my hair grey - she swears it was black the last time she saw me. Only good thing about it, if there is such a thing, is that she knows nothing about it and seems perfectly happy - it’s not like a person that has a physical illness and is in pain or suffering. It’s a horrible, horrible disease.
We have the same with my step-father. He’s not as far along and Mrs Motties’ mum, but you can see the downward trend. My mum is basically his full time carer now.

Like you say, the only consolation is that he’s blissfully unaware of it all.
 
My Dad had Peritoneal Dialysis (PD) for years. Had a tube through the abdominal wall.

Maybe that's what they were talking about?

I suspect so, the specialist nurse during a call mentioned tubes, as did the consultant, the other day. All quite scary at the moment, despite all the years of warning, of what was to come eventually.

The frustrating part at the moment, is I can be sitting around, feeling perfectly fit, having the mental capacity to carry out jobs, but when I make a start - I soon need to sit down to recover, before doing a bit more. It would at least be good to know, why my stamina is so poor - the kidney people seem to be suggesting it's not due to my kidneys, the GP also seems at a loss. Luckily, Avril has been very understanding, and supportive.
 
I suspect so, the specialist nurse during a call mentioned tubes, as did the consultant, the other day. All quite scary at the moment, despite all the years of warning, of what was to come eventually.

The frustrating part at the moment, is I can be sitting around, feeling perfectly fit, having the mental capacity to carry out jobs, but when I make a start - I soon need to sit down to recover, before doing a bit more. It would at least be good to know, why my stamina is so poor - the kidney people seem to be suggesting it's not due to my kidneys, the GP also seems at a loss. Luckily, Avril has been very understanding, and supportive.
best of luck mate - hope it all works out well
 
I suspect so, the specialist nurse during a call mentioned tubes, as did the consultant, the other day. All quite scary at the moment, despite all the years of warning, of what was to come eventually.

The frustrating part at the moment, is I can be sitting around, feeling perfectly fit, having the mental capacity to carry out jobs, but when I make a start - I soon need to sit down to recover, before doing a bit more. It would at least be good to know, why my stamina is so poor - the kidney people seem to be suggesting it's not due to my kidneys, the GP also seems at a loss. Luckily, Avril has been very understanding, and supportive.
Chin up Harry, we all need to slow down eventually.
 
I suspect so, the specialist nurse during a call mentioned tubes, as did the consultant, the other day. All quite scary at the moment, despite all the years of warning, of what was to come eventually.

The frustrating part at the moment, is I can be sitting around, feeling perfectly fit, having the mental capacity to carry out jobs, but when I make a start - I soon need to sit down to recover, before doing a bit more. It would at least be good to know, why my stamina is so poor - the kidney people seem to be suggesting it's not due to my kidneys, the GP also seems at a loss. Luckily, Avril has been very understanding, and supportive.

I have copies of notes given to my Dad somewhere, who had poor kidney function.

From memory, he was told poor stamina can be a symptom of poor kidney function. The nurse said the build up of waste products in the blood was one cause. The second was that a hormone produced by the kidney does not get made when they are not running full whack. This hormone stimulates red blood cell production and with fewer RBCs, this causes weakness due to anaemia.

Have you had the doc check your haemoglobin levels?
Do you have sleep apnoea? This won't help the situation.

Have you got an exercise plan from your consultant, IE appropriate exercise?

And diet? A healthy diet plan that gives you the correct nutritional value without straining your kidneys?
 
An appointment call today, from my kidney consultant, with some bad, but long expected news. He wants me in next month, to get me sorted for home dialysis. I was warned to expect it within two years, five years ago, where they offered me the option of hospital, at home, but I've somehow managed to delay it. I agreed to home, and one of the spare bedrooms, we set up the room up back then, in readiness for the day, when.

Just last week, my GP prescribed iron tablets, for my anaemia, and low stamina, but the consultant has said to stop bothering to take them, they are no very effective. He said they will schedule me to have intravenous iron, in a month, in hospital. I've had it intravenous before, and last time I seem to remember it had an almost dramatic, and instant effect on my stamina.

I'm just confused now, about the methods of dialysis. One description mentioned inserting cannula, another, plus the dialysis nurse, and consultant, on about plumbing permanent access pipes into me somewhere.

Sorry to hear that Harry. My answer would be the same for all sorts of problems:
Download Grok and ChatGPT5 to your phone and ask them. They know a heck of a lot of medical stuff, and don't get tired explaining it, and all around it.
 
From memory, he was told poor stamina can be a symptom of poor kidney function. The nurse said the build up of waste products in the blood was one cause. The second was that a hormone produced by the kidney does not get made when they are not running full whack. This hormone stimulates red blood cell production and with fewer RBCs, this causes weakness due to anaemia.

The answers, from the professionals on this, seem to constantly vary.

Have you had the doc check your haemoglobin levels?

My original GP did recent blood samples, but said nowt, or failed to notice. The new GP, I have just moved to. Immediately spotted from those previous blood tests, Quote 'Note anaemia- likely chronic- but check haematinics.'

She put me on iron tablets, and scheduled me for an ECG and another blood test, for next week. That blood test, is also to make a decision on the statin problem.

Since when, my kidney hospital consultant rang on his appointment, to discuss my progress and yet another blood test, done specially for them. He had also noted my anaemia, I told him my GP had started me on iron tablets, just three days before. He said they were a waste of time, stop taking them, he would send me an appointment for an iron infusion.

Do you have sleep apnoea? This won't help the situation.

Not that I am aware of, I have always been a very sound sleeper, until recently. Recently, I seem to be waking more and more in the middle of the night, unable to get back to sleep, I usually get up and find something to occupy me.

Oh, and I suffered what seemed to be one of those panicking episodes, which I was blaming on the statins. Quite brief, and not nearly as troubling as the worst of the previous ones.

Have you got an exercise plan from your consultant, IE appropriate exercise?

No, none.
 
Your waking in the night may contribute to fatigue.

Do you get accused of snoring?
Could be of value to eliminate sleep apnoea.
It may be worth doing a Epworth test.

Epworth-Sleepiness-Scale.pdf https://share.google/7kfKebWUEXERLaquR

Don't look at the scoring at the bottom and answer all questions truthfully!

If course, you could be dog tired for reasons other than sleep apnoea (like the anaemia), but if you have it undiagnosed, you'd have a double whammy hitting your stamina and getting the SA sorted will make the world of difference.

If you can, print off the sheet, fill it in and if it is a high score, take it to the Quack and see what they say.

As for statins, not all cholesterol is bad. LDL is bad, HDL is good.
 
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