hello everyone

[Guest guest]

Thanks to the moderator for letting me join this most sort after liver

group.

I live in Chicago, I have hep c with cirrhosis, each 6 months I am very

scared of testing for tumor marking, etc., so far for the last 10 years

everything has been study.

Doctors says there is no need to be on the waiting list for donor because I

don't have none of the symptom that warrant me to be put on it. I am excited

and glad that their determination testing have proved such, however I am

worried that if the liver becomes worse, and God forbid it, it would be fatal

for me.

I think that each and every one of us should be worried about getting a

needed liver if things get worse. we must do and see that all that can be done

should be done on time not later.

I got hep c through a blood transfusion in the 80ty.

there are so many ways we can harm ourselves and not no it, by having hep c.

I read of the posts and I have to agree, no one really knows the pain we

suffers.

Along with hepc, I have diabetes type 2, so i have to be worried, but I

strong, I just don't want to let things happen medically that could have been

prevented.

That is why each and every one of us should be searching for the truth.

I plan to form a support group here in Chicago, for patients living with

cirrhosis. I am sure there are some but they are not visible.

Thanks to everyone for reading my article, please keep up the good works.

always, in Chicago

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