Having polycystic kidney disease stage 4, I am often browsing the Internet for information which will help me with the numerous questions I have about my illness.
Many of these sites are quite medical in nature and often, that is just what I need.
Sometimes though, I need to hear it from the side of someone going through the same thing as me. I want to know what it feels like to have a fistula fitted, what the side effects to dialysis can be, what its like to live on a kidney diet and I want to understand how I can cope with everything that is inevitably ahead for me.
That is why this forum has been and continues to be so useful.
A few weeks ago I also came across this web page:
mylifeasapincushion.blogspo...
....it is one man's experiences of living with polycystic kidney disease. Upon reading it, I just had to buy his book. It is from a publisher that prints the book to order. As you can imagine, it has a select audience but I found it well worth waiting for.
Michael tells it like it is but uses humor to make it a really good read. I've only put the book down long enough to write this post as it might just be what many people on this forum might like to read too.
It's called 'Tell me if this hurts' and its by Mike Sullivan. (ISBN 978-1-291-068662-7)
Never give up
confused over GFR readings
Lab results after one year vegan
mum in hospital with kidney failure...new member
