Hi all - my poor Mum is currently in UCLH with HE. She has an autoimmune liver condition which first concurred 15 years ago and the original cause was never known, she has cirohssis (not sure how bad) and over the past 15 years she has been pretty well - 'flare ups' every year but with rest she would recover and get back to her normal. Her platele count ha she been about 50-60 over this time and she has seen her consultant every 6 months. About 3-4 weeks ago she started to get light bleeding from the nose and gums, and she got progressively worse and ended In A&E last Tuesday with a platelet count of 4. Took a while to get to th the diagnosis and we were rushed from local hospital to UCLH as they suspected TPP. This is now ruled out and they believe she has HE. She has deteriorated hugely since Sunday night when she was a little confused but could eat and drink and we had a chat last thing at night. Yesterday morning she did not really wake and could not drink or eat and the heptologist said she just needed laxatives to help her excrete the toxins. She would respond to nudges though and mutter one or two words, She is sadly worse again this morning and cannot say anything and we cannot stir her at all. We are waiting to see the liver team now but the treatment seems so passive when she has gone downhill so quickly. The ICU doc just said she has a GCS of six. She also has a blocked renal vein so we are not sure if a transplant is even an option. So many unknowns. Any advice from anyone please. So very sad.......
New to the forum - Mum is in UCLH with HE - British Liver Trust
New to the forum - Mum is in UCLH with HE
Written by
NeilR
To view profiles and participate in discussions please or .
Read more about...
3 Replies
•
I'm so sorry to hear about your mum, I can't give any advice I'm afraid but I'm sure some of the more knowledgeable people will reply, just wanted to say hope she gets better soon.
Thanks Gemma
Hi Neil,
We are really sorry to read how poorly your mum is.
You may find our publications on Hepatic Encephalopathy (HE) and also Cirrhosis of the liver useul to read for general understanding, prior to the meeting with the liver team.
britishlivertrust.org.uk/wp...
britishlivertrust.org.uk/wp...
We hope you find the forum a supportive place to visit and send you our very best wishes,
Trust1
Not what you're looking for?
You may also like...
Is HE always inevitable with severe chronic liver disease?
My daughter has been told there is nothing more the doctors can do for her multiple hepatic...
Hi I'm new. My mum has CIRRHOSIS and HE :'(
Hiya.
I'm just looking for some advice really.
My mum has been a heavy drinker for 10+ years and...
Fatty liver
Hi everyone im new to this. I have fatty liver doc dnt seem t be concerned i can never get a...
Help and advice please
This is my first time on here and it's probably going to be a bit long winded but I'm trying to get...
Gallstones
My Doctor,told me that gallstones cannot damage the liver,not sure if this is true.I Aways have...