Woke up at about 11am today. Had normal type of sleep on and off. Took a sleeping pill which helped. It seems that being on dialysis has a major effect on the ability to sleep. Many of us find this - I think the doctors should pay a bit more attention to these types of things. Normally they say see your GP - I am not sure this approach works with renal patients. Perhaps they need to make the communication better. I am lucky and I have an amazing GP and consultant who I can talk to openly and understand what is going on. But some of the reports I here from other patients is not as good.
Had some sad news yesterday - one of my fellow dialysis patients died on Sunday. I had been dialysing in the same slot as him for the past 18 months. So that is sad - he had major heart problems. Not much more I can say really, I tend not to get emotional over death - unless that person is very close to me. I feel that death comes to us all and have accepted that fact. When you have accepted that it actually makes living easier!
Dialysis in a couple of hours first time I would have dialysed on a tuesday - the television is shit as well which makes it boring. Probably take a dvd.
I am now on a full regime of antirejection drug in preparation for the transplant. I cant imagine what is happening inside my body at the moment. yesterday literally blasted all my white blood cells apart leaving with little immunity.
Showing posts with label gp. Show all posts
Showing posts with label gp. Show all posts
Tuesday, 4 September 2007
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