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I was diagnosed with ulcerative colitis in 1994 and PSC in 1998.

Until today I didn't know there was any group that I could join.

Suddenly I don't feel so alone.

I have been lucky...they tell me. Normal liver functions...occasional

pain but all in all lucky. But I can't help feel like there is a bomb

ticking inside of me.

My first hospitalization was after an ERCP...pancreatitis. As I lay

there wondering what life had in store for me, the news of Walter

Payton's death came across the news. I have been scared ever

since...I function but inside i am afraid. Any suggestions?

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Bobbi,

I would feel like you too if I was not proactive in my care. Learn about your body and how diet, stress management, positive attitude, supplements and exercise play a BIG role in your continued well being.

Gema

Hello everyone

I was diagnosed with ulcerative colitis in 1994 and PSC in 1998. Until today I didn't know there was any group that I could join. Suddenly I don't feel so alone.I have been lucky...they tell me. Normal liver functions...occasional pain but all in all lucky. But I can't help feel like there is a bomb ticking inside of me.My first hospitalization was after an ERCP...pancreatitis. As I lay there wondering what life had in store for me, the news of Walter Payton's death came across the news. I have been scared ever since...I function but inside i am afraid. Any suggestions?

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Dr. Elta is my doc here. I think we are both in very good hands.

Small world isn't it?

> Bobbi,

>

> I live in Michigan and am treated at U of M Hospital by Dr.

!

>

> Gema

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Hi Bobbi,

I'll pipe in here and say ,hi, and welcome to the group. I live in

Grand Blanc and my DR at U of M is Fontana. Dr Rudich did my tx last

Aug. Tim Long

Tim Long UC / PSC 25+ yrs TX 8/2/02

married 36 yrs, 2 daughters & 2 grandkids

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  • 2 months later...

Hi Alice,

Welcome. Glad that you found us, sorry that you have PSC.

You probably are the youngest member. There are some parental

caretakers of kids and a few that joined while in high school, but the

years add on and most are no longer the young kids that first joined.

I'm sure that they will still have insights on your situation that

some of us oldsters may not.

I agree with that changing when you take your ursodiol may help

with the sick feeling. Another thing to consider is to gradually

increase the dose over several weeks so your body has time to adjust

to the change. Since you aren't feeling well after taking ursodiol you

should talk to your doctor about makeing some changes. Let us know how

it goes.

Tim R ltx 4/4/98 @ 51 yo; recurrance 2002

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Hello, Alice! Welcome to the group. Even though we may a bit older than you,

don't let that stop you from chatting with us any time you feel the need. You

will probably experience things we have, at one time or another, experienced, so

feel free to let us know how you feel. :-))

Janet from New Jersey

Janet E.

Saiber Schlesinger Satz & Goldstein, LLC

One Gateway Center, 13th Floor

Newark, New Jersey 07102

, Ext. 4892

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Hi Alice-

Welcome to the group. I'm sorry to hear about your recent diagnosis,

but you came to the right place for answers and support to any of

your questions. Feel free to ask anything. I am fairly young also I

am 19 now but I was diagnosed with PSC when I was 18. Once again,

welcome to the group,

Brett

(Doing well, 19 years old, dx. UC 3/01, dx. PSC 6/03)

> Hello everyone,

>

> I'm new to this group, and it looks like I am probably the only

kid here. I was diagnosed with Sclerosing Cholangitis about a year

ago. I had UC when I was young so they found out I had liver problems

when I had the regular blood tests. Then I had 2 ultrasounds, and an

MRI. I didn't have an ERCP because my doctor though it would be too

risky for me. I have had 3 colonoscopies in my life and it looks like

I will have to have one once every 3 years. I've been on

Ursodeoxycholic acid for a week now. I take the tablets 3 times a

day. They are OK, I feel less tired now, but I keep feeling like I'm

going to be sick all the time. My friends react funnily to me having

this disease, as if it's some sort of disability. But they are only

teenagers I suppose. I'm glad there's a support group for PSC, and

that I have people to talk to when I need to.

>

> Love from Alice

>

>

> ---------------------------------

> Want to chat instantly with your online friends? Get the FREE Yahoo!

Messenger

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  • 4 years later...
Guest guest

Hi Becky

Just saw your note sorry you are having such bad headaches. Are you having any

problems with your vision. re: double vision; blurred or losing vision in either

eye.Did they do a vision test? Did you hit your head a while back and forgot?

How is your blood pressure been and what was it like when you went to the ER?

Any ringing in your ears? Did they check to see if you could walk without

falling (with your eyes closed)? Did they check to see if you had a sinus

infection? I guess that is all I can think of for now.

Write me back please get well soon.

Toni

-

--- , " Becky " wrote:

>

> I have had an 8 day strong pounding headache. It apparantly has made

> friends with my body and doesn't want to leave. I have blacked out a

> total of 4 times now and almost blacked out a couple more. It's

> killing me and I've tried everything I know.

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