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Welcome Jerry

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Jerry,

Welcome to the Group. As Darin

mentioned, I’m one of several retreads here, having had 2 Tx’s virtually back-to-back in 1985. I’m also

one of the Group who has been diagnosed with recurrent

PSC, after 17 years of excellent post-tx health. Yes,

Darin, I’m at L+18 (eighteen days after being Listed). I finally beat the

medical bureaucrats into submission in the last week of April. There were not

very many people ahead of me when I was listed, so every time the phone rings

now, I jump, and I don’t even go across the street to pick up the mail

without my cellphone.

Jerry, it’s good to have another experienced voice in

the group. I’m glad you found your way here.

Steve

Rahn

L Tx 9/6 & 9/8 '85. (Wash. U-STL)

Listed for Re - Tx (U of Iowa)

" Do

not go gentle into that good night

Rage,

rage against the dying of the light "

(Dylan

)

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Glad you found this group, Jerry. It's good to have another

experienced voice. I'm one of the other " two-timers " but I got mine

within a three-day period. I can't imagine having to start all over

dealing with tx issues after several years. All my doctors were more

or less convinced I had PSC, right up until my formal tx evaluation

when suddenly they just weren't sure, so they backed off to a " We

don't really know " diagnosis.

Today is the second anniversary of my " rebirthday #1 " but haven't

had too much chance to sit and ponder the " what ifs? " Lots of

relatives will be arriving by evening for my daughter's h.s.

graduation on Sunday, so yesterday and today I've been home making

my way down one very long " honey-do " list. Well, brisket's in the

oven now--one more thing to check off. House painters are finishing

up this morning, just in time (thought we needed a little more

stress this week). I'm really looking forward to being back in my

office Tuesday morning--and getting some rest!

Rich in KC

Crohns, cryptogenic cirrhosis, liver txs 5/23 & 26/2001

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Thank you for the welcome. Yes it was difficult going through liver failure

twice. My first transplant worked very well for about five years (from Oct

1993). My alk phosphatase went haywire after about 3 years. The last year was

tough. I had fully expected not to see two grandchildren who were born that

last year (I now have seven). But the new liver did become available.

I guess the message is - don't give up.

Jerry

> Glad you found this group, Jerry. It's good to have another

> experienced voice. I'm one of the other " two-timers " but I got mine

> within a three-day period. I can't imagine having to start all over

> dealing with tx issues after several years. All my doctors were more

> or less convinced I had PSC, right up until my formal tx evaluation

> when suddenly they just weren't sure, so they backed off to a " We

> don't really know " diagnosis.

>

> Today is the second anniversary of my " rebirthday #1 " but haven't

> had too much chance to sit and ponder the " what ifs? " Lots of

> relatives will be arriving by evening for my daughter's h.s.

> graduation on Sunday, so yesterday and today I've been home making

> my way down one very long " honey-do " list. Well, brisket's in the

> oven now--one more thing to check off. House painters are finishing

> up this morning, just in time (thought we needed a little more

> stress this week). I'm really looking forward to being back in my

> office Tuesday morning--and getting some rest!

>

> Rich in KC

> Crohns, cryptogenic cirrhosis, liver txs 5/23 & 26/2001

>

>

>

>

>

>

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