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>

> I was dx. two months ago, had first dr. visit today. I am having a

cat

> scan done thus. and massive blood tests saturday. I am glad to be a

> part of the group. I am nervous because I think I had this for 25

> years or more. Do not feel sick though. I am however over whelmed

> already with copayments. I now have two drs. because of other issues

> unrelated and four visits in one month. any time I bring the hcv up

to

> talk to anyone about it I start crying so maybe this will help.Hope

to

> make some friends and give and receive support. brzynite

>

Welcome brzynite,

I am also just recently diagnosed with hep c and cirhosis of the liver.

And I understand just where you are... Cause I'm right there also..I

joined this group a couple of months ago, and I have found out so much

I didnt know about both hep c and treatments and also on cirhosis.

There are alot of links on the left that are very informative. Come on

in and sit a spell and let your thoughts flow... We are all here to

listen and lend moral support.... I also have had the virus 25+ years.

Only found out in march, and found out in july after biopsy I have

cirhosis too. I begin treatment soon I hope still waiting for

financial assistance on co- pay for the pegasas and ribiviron... Peace

out marsha

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