Hi Adriana

I felt just the same when I was diagnosed. I think it's a sense of shock to realize that there is something wrong with you. There is such a lack of awareness and understanding that you feel alone with this virus. I felt I wanted to know everything about the disease and the exact state of my liver there and then, I soon learnt that it all takes time. Hep C is a slow moving disease so don't worry if things take time between tests.

Like I said, I felt just like you and here I am , virus free and well. Keep us posted on what's happening and if you ever need anyone to talk to feel free to send me a message.

Take care....Tracey

{{{Hi Adriana}}} I'm so sorry you're feeling so alone and frightened. I remember those feelings oh so well when I first found out. For me, it was from a form letter from the Blood Bank (in '96) after donating blood). I was shocked and devastated..sent me on at least a week-long crying jag, until I, like you, gave it time to sink in, get tests, do research and (very important) found others in the same boat for support. I'm glad you're feeling a bit better after realizing what a slow progressing disease it is...you've got time to sort it all out...and you know what? you are NOT alone...there are millions of us out here. (and I'm right next door to ya in louisiana :)

Hope you'll come back and share your lab results...be sure to find out your viral load and your genotype - Both of those, along with a biopsy will give you a better idea of how to proceed.

Sending you a big hug,
Denise