Escape Pain Dear All I wanted to share an initiative that I have only recently heard of called “Escape Pain”. This has got a web site at https:\\escape-pain.org It is a brilliant rehabilitation programme for people with chronic joint pain, usually arthritis of the knees and/or hips. What it has been really good at,[…]
My daughter asked me an interesting question the other day. “Is your glass half full or half empty mum?”. I thought about this and started reflecting on my life. Do I think that I’ve been dealt some unlucky cards? Well yes if I consider that not long after I separated from my daughter’s father[…]
Hello hello, haven’t been here for a while.. Whats happening?..well dialysis is still a struggle (nothing new there!) no two days are ever the same. If an ‘ok day’ could be had two days on the trot, I’d be laughing! Plummeting Bp and flaking out..yay go me! 🙁 Anyone else encounter that!? Wobbly legs after[…]
I think this may be useful to anyone researching kidney failure.
When I was first diagnosed with CKD back in 2005 I didn’t feel any difference in my ability to work or do the things I’ve always done, or so I thought. Changes in me was noticed by my wife and work colleagues, people would ask if I was well, “why are you asking that” was my reply, “because you look off colour a little pasty with a bit of yellowing in the eye” was the answer. The other thing my wife noticed was that I would fall asleep quite often. As the years rolled by these comments became more frequent even my work colleagues would see me nod off at my desk. Other things started to affect me (which I now know as symptoms), night cramps, itchy legs and feet usually at night when in bed with the itching getting worse as the CKD got worse.
Three months before the acute failure my skin stated to be more yellow/orange and the white of my eyes also became yellowish. The change that I noticed most was my taste, food stated to taste different it didn’t taste nice and certain foods that I really like became unpalatable, it drove my wife mad because it got to a point were I was picking and leaving good food and never knew what I wanted. I would make sandwiches and smother the contents with a hot relish and thats all I would eat right up to the acute kidney failure. Even after starting dialysis food didn’t taste as it should have done and it was several weeks before I could taste some foods and over a year before my taste was something like normal.
Hope this is of some help to new patients. Victor […]
Well dear friends, I have a serious confession to make which is an indictment to how Chronic Fatigue can affect someone. It affected my concentration so much that I made the simple mistake of thinking that I had only been transplanted three and a half years instead of four and a half years. Please add[…]
I had a blood test just one week following my infusion of Cosmofer on the morning when I have my injection of EPO. The week following that, I was referred to an Endocrinologist in the diabetics department. She reviewed my blood test results and informed me that I was still anaemic. This confirmed what I[…]