Hi there - it is all very frightening but I can assure you that cancer teams are so good - you always have someone to talk to are allocated a buddy nurse who you can ring or email anytime.
I had half my liver removed (the great thing is that it grows back) and although it was painful for the first week and I did not think I would be the same again - meaning couldnt get up from bed, walking to the toilet was slow and painful but within a month I was back to me again. I am, and am now receiving chemo for any cells that may have got away, in tablet form for 8 cycles and which you receive a 'red card' which you carry in case you are not well and which you can call 24/7. I am in my 4th cycle hands and feet sore but feeling 100% me again.
I hope this helps and if you need any further info or questions - just contact me again.
I understand how frightening it is - but there is a way back after surgery.
take care
I went to my local hospital for an appointment today 17th December, seen the liver specailist, He informed me that the transplant hospital had sent him an Email saying I was not going to have a liver transplant, I was a too high risk. which I understand. my normal liver doctor said he could not put a time limit on me having liver failure. could be two three months or a year. but he has said I need to put my affairs in order. I kind of knew this was going to be the outcome in the long run. but at least I know I'll be with my wife soon.
All I wish for is anyone having to go through the rigmarole of tests have a better outcome. and would like to thank everyone who has been suportive through the last year and wish everyone well. thank you all.
