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, I was " listed " for Tx way before I needed it. Not all centers list at

the last minute......many like mine do it early and just keep an eye on you with

visits often. I went from going every 3 months to every month then at the end

every week. When my MELD hit 18 I was put on the top of the list. I too had a

not very common blood type and they said the same to me.......... In my case

there wasn't anyone else on list with my blood type. ; - ) I was walking

about and doing things.......slowly but doing them.....eating

normal.etc.although I did fall asleep often (encephalophy). I too didn't think

I needed one yet..........although everyone else knew. I think we go into a

sort of denial. Then at the very end I knew I was dying.you can feel yourself

start to slip away.Your can feel your organs slow down. Then my edema was so

bad that I actually leaked fluids from my skin. Even as ill as I was that made

me sick to see. I ended up having to toss all my clothes away after my

transplant as they were all stained yellow from the fluids leaking.

BTW.You did join the Post Tx group.right? If not let me know and I will send

the link so you two can learn all about what to expect. Joanne

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