Uraemia - CKD/statins

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I think I may at last, have diagnosed the cause of the issues I have been suffering increasingly over the past year or so...

  • anxiety or panic-like sensations
  • nighttime restlessness
  • cognitive fog / confusion
  • hot–cold swings
  • heavy limbs or muscle weirdness
  • inability to get comfortable
  • episodes lasting an hour to an entire night
I, at first blamed it on the statins, I had been prescribed, not knowing any better, and getting no diagnosis from medical professionals. I stopped the statins, and the episodes appeared to decline, which sort of confirmed statins were the cause, but since then, the weird episodes have returned. I suffered episodes, both last night, and the night before.

The past week, I've been doing some research, and finally came across the word 'Uraemia', which seems to cause some sort of poisoning of the brain, due to the kidneys, failing to adequately filter the poisons from the blood, but I was unable to find any symptoms, to confirm it. I also got in touch with the National Kidney Foundation UK, describing some of the symptoms, inviting their comments, and they responded, at length, agreeing they were common symptoms of Uraemia affecting the brain's function.

I have an face to face appointment tomorrow, with my kidney specialist, so I will attend, armed with a copy of my episode log, and a printout from the NKF, and the word 'Uraemia'.
 
You might also like to consider neuropathy as a possible cause.

And not wishing to jump to conclusions, but especially if alcohol has been an issue in the past.
 
They'll draw your blood and rule it in/out as soon as the results are back. Hopefully it's something else, while having a diagnosis is good having kidney failure is not. Good luck.
 
You might also like to consider neuropathy as a possible cause.

And not wishing to jump to conclusions, but especially if alcohol has been an issue in the past.

No, I only rarely drink.

They'll draw your blood and rule it in/out as soon as the results are back. Hopefully it's something else, while having a diagnosis is good having kidney failure is not. Good luck.

There is no doubt about the kidney failure, I'm CKD5, in the care of PD. I have numerous times mentioned the episodes I have been suffering, to both the PD team, and my own doctor. None have even hinted that the problems could be due to my CKD.
 
No! Have you read and understood what has been posted?
I'm not a doctor, I read it, not sure I understood it. It's just that some of your symptoms are common with another type of mens health issue, so I wondered if you had an enlarged prostate that you were taking testosterone meds for.
 
I'm not a doctor, I read it, not sure I understood it. It's just that some of your symptoms are common with another type of mens health issue, so I wondered if you had an enlarged prostate that you were taking testosterone meds for.

Oh got you now, and no - my meds are mostly for lowering blood pressure, amongst them statins originally.

The past almost a year, I've been suffering some really frightening effects, mostly during the night hours, with no actual physically traceable cause. I managed to match, and read of similar symptoms, from several people, where they traced it to taking statins. I was already suffering many of the reported physical symptoms of statins. Having stopped the statins, the physical symptoms cleared up, and the mental issues seemed to improve, so I convinced myself it had all been due to statins. Then the mental issues returned recently, and so back to trying to find the cause....

I tried to describe what I felt like, during the weird episodes, to someone at the Kidney Foundation. The bulleted points, were symptoms, they suggested I might suffer - I was suffering all of them, during an episode. The reply I received back, listed exactly what I was suffering, and is one of the symptoms of failing kidney function, and a result of uraemia. I think I've understood it, in that it's nitrogen poisoning of the brain.

This was the first I'd heard of it being due to my CKD. I've numerous times mentioned the episodes to the medical professionals, and none suggested it might be a result of my CKD.
 
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I hope you feel better - are there any lifestyle adjustments you can make?

I don't know. I have an appointment to attend tomorrow, with the kidney specialist, so I will be walking in once more with my log of the episodes, and at last - my own diagnosis, of the cause, to see what they say.

When I first showed them my log, and described the episodes, they said it might just be my panicking, worried about the forthcoming catheter installation operation.
 
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