So my liver went from decompensated to compensated. My 20% of good liver is doing 100% of my liver now. That’s fine but is it really compensated? I have banding for the GI bleeds, pills and a low liquid intake to stop the liquid retention. I take drugs to stop the HE. So is my liver really compensated or not? I feel more crap now and spend more time in hospital now than when I was decompensated.
Strange question?
Brett
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Brett11
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Damn I don;t know much about cirrhosis but reading this i am really praying i dont have it. fatty liver is enough to contend with I am sorry your in this situation but I did find this.
Haha. Cheers for looking though mate. I’ve got a doctors appointment on Friday. I will tell him to refer me to the liver transplant docs in both Sydney and brissie to see if I can get on the transplant list.
Fingers crossed. I bet he won’t though. Mean bloody doctors lol.
Hi Brett not an answer to your question but i have a question if that's ok? How do you know you have gone from decompensated to compensated? Do the doctors tell you from tests? I was just curious thanks
Hi Brett - i'm the same I've gone from decompensated to compensated, I did ask my consultant to confirm this about 6 months ago and he said basically the same as you - the remaining part of the liver that hasn't been affected is doing 100% of the work.
How regular are your blood tests? I get mine done every 3 months and an USS every 6 months - i did have a scare last week as i'd basically felt like cr*p for 3 weeks. The Dr agreed that it could possibly have gone back to a decompensated state however after blood tests it was my reaction to a very mild viral infection which having cirrhosis hit me a lot harder than those without this condition.
In terms of the transplant list i'm not sure how it works in Australia - Im in the UK and I was put on the transplant list initially but after 9 months I was removed as my condition was compensated. I think if your test results etc are saying you're compensated you will struggle to get added to the transplant list.
I don't know if thats helpful at all but it seemed like we are in a similar (ish) situation! 🙄
I get blood tests usually once a month and see my liver doctor every 3 months and see my GP almost every Friday. I get the camera down my gob every 6 months and the other scans every 6 months and every time I get admitted to hospital.
Phew! That’s a lot of tests and doing tests and waiting for results. I must have had some sort of life before cirrhosis? I can’t remember lol
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