Welcome to the forum.
Firstly, don't worry. You now know you have HCV, and now you will learn as much as you can about your disease, treatment options and side effects. Knowledge is power, and you need to own your disease and be in control of the treatment.
Secondly, make a list of questions you want to ask your doctor. You will need to find out what type of virus you carry; the genotype will tell you all about what treatment options are available.
You mention that you have liver fibrosis Stage 2. What test did you do? A liver biopsy? A fibroscan?
Like Orphanedhawk mentioned, depending on your genotype, there are new meds on the way with less sx and a shorter treatment times.
Good luck, and remember, ask away.
You are young. That is in your favor. All you have to do is take care of yourself and get ready to treat. I was stage 4 and am still going. You have a long life ahead of you. This is a great place to learn and find support. Some sites are depressing. This group will stand by you no matter what your emotional state.
It's a scary time for you, I know. Take care and you will be around for those kiddos. xo Karen:)
Emotionally~ well remind yourself that you have time, these things move slowly.
There are things you can do, the first being to not drink any alcohol.
Drinking alcohol with hep C is like pouring gasoline on a fire.
You might decide to wait for the newer meds that doing great in clinical trials rather than taking on doing interferon treatment while caring for very young children.
Or you might be able to participate in a trial.
Don't make any decisions to begin treatment until you are fully educated about the virus and the options available to you.