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We are always here for you.

Can only imagine how terrible it must be for you to be alone, especially when you are having a cholangitis attack. I dont know what brings them on but I am not ruling out stress as one of the factors. When my brother was dying had three in five days.

Just wish you were closer so I could give you a big hug.

My thoughts and prayers are with you and your daughter as the anniversary of your mother and s death draws near.

Take care

Leona

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,

I'm praying for you! I'm sorry that you've had to endure so much, and

in such a short period of time! No wonder your poor body is crying

out with pain. We are here any time you want to connect, vent or

otherwise express your feelings. Hang in there!

Oh, and if the transplant team wants to list you, I hope you will say

yes. I've found that being listed for three years has given me time

to get used to the idea of getting a transplant, and has given me the

transplant team to use as a resource. I'm still scared stiff about

having a transplant and all that can go wrong, but being listed has

been a good thing for me overall. I hope that offers you another

perspective to yet another overwhelming situation you face.

Peace in all you face,

Deb in VA

AIH 1997, PSC 1998, UC 1999, Listed Ltx 2001, MELD 19

> I also have concerns about seeing the tx team again in Oct. The

last

> time I had three cholangitis attacks in 6 mo. they were ready to

list me. This

> time I have had three, in just 5 mo. The talk about

immunosuppressants, after

> tx, and the risk of cancer is a little frightening, too. I have

already had

> precancerous cells removed from my face, as well as cervical

dysplasia (cryo

> took care of them). Don't misunderstand, I am not assuming the

worst, but

> these are things worth considering. And right now I'd give my

right arm to be

> able to sleep! I'm tired of hurting and tired of

thinking/feeling.

>

> Those of you who believe in the power of prayer, please send some

up for me

> and my family. >

> >

> Again, I'm sorry for carrying on, but I'm so glad there is a place

I can go

> and do just that when I need to! THANKS!!!

>

> Sincerely,

> (MO)

> PSC & UC dx '84, chronic pancreatis dx '97

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,

I am so glad that you were able to release or at least share some of your pain and anguish via the group. When I was going through a very lonely divorce I joined a divorce chat room that provided me with hours of comfort. I know ... sounds crazy, but it is a way to connect - in all hours of the night with all kinds of people. I am so sorry that you did not find the happiness, love and support we all hope for when we get married. You and your daughter will be in my prayers, there is an enormous amount of love and support in this world (why it's hidden sometimes is beyond me...). Your plans for Oct 6 sound like a great idea, I know that when I am feeling my daughters pain the best thing I can do (for myself) is to be near her, hopefully it helps her as well.

LINDA

(Mom of Suzanne, 15; UC 1/04, PSC 3/04)

(MO)

PSC & UC dx '84, chronic pancreatis dx '97

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EN

:

Of course you need to connect. We are always here. I do know the depth of

sadness you are experiencing and I likened it to being in a deep dark well. I

am SADD and I have bigger and brighter lights everywhere. This is not the magic

elixir for you I am sure but give it a try. You have almost everything you

loved come to an end and now fell unloved I am sure. The truth is: You are a

good mother, good daughter, good friend, good woman, that will find her way

back and be better than ever.

Love ya Baby, keep the faith and we send our prayers for comfort, strength and

lightening of the load you have been carrying forever. Time to turn over on

your back and float for a while. Enjoy the time with your daughter and try and

find some laughter in the day.

Fondly,

Dee in Peoria

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, You surely do not need to alologize; thanks for sharing

with me in a way that made me remember going though some tough times

myself when I was younger and how valuable my friends were. I think

you have a lot of concerned friends in this group that understand

and appreciate your problems. I hope that this is the low point and

it will be all up hill from here. Hang in there; it may get much

better soon. I am concerned that you are having chills and fever

and are home and not at the hospital. Are you having rebouts of the

same infection that they are just not knocking out? Sometimes when

that happened to me they would put me in the hospital for 10 full

days of IV alternating antibiotics and it would knock it out for a

long time. I assume you check in when you have an infection episode

and they monitor while you take orals?

My docs rule was if you have been on antibiotics more than two days

and you are still having chills head straight to the hospital cause

it's a bug that the antibiotic is not effective against.

How about those men, huh? Hard to live with 'em or without 'em.

You'll find the right one some day.

Tee

> I will apologize, THANKS!!!

>

> Sincerely,

> (MO)

> PSC & UC dx '84, chronic pancreatis dx '97

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