Hi there, and welcome to the forum. Somehow, we all manage to get through this somehow; even though sometimes it doesn’t work out like we wish it would.
As HCA mentioned, your viral load probably isn’t a significant reason by itself to treat; that decision is generally determined by biopsy, which tells you the amount of damage (fibrosis) sustained.
If you tried treatment previously, but only for two weeks; it might get better as time goes on. Many of us get quite a kick from the first one or two injections; after that, things quiet down for a bit.
Questions for your upcoming appointment can include:
HCV genotype?
Degree of existing fibrosis/inflammation?
Discuss the new protease inhibitor class drugs in trial; would it be worth waiting or them?
How are blood problems managed by the doctor? For instance, anemia, neutropenia, thrombocytopenia?
Duration of treatment?
Others will hopefully chime in with more thoughts; these are a few to digest for now. If you haven’t already, take a look at the following site:
http://janis7hepc.com/
You might begin by opening ‘newly diagnose’ at the top of the page, or by clicking on ‘other HCV information’, in the right-hand margin. This site can give you an excellent overview of basic information about this disease. Another page to review is the HCV acronym page here in Medhelp; it’ll help you understand some of the abbreviations used here:
http://www.medhelp.org/health_pages/Hepatitis/Common-Hepatitis-C-Acronyms/show/3?cid=64
That should be a good start; and continue to ask questions here as well as elsewhere; nothing like information to help you through this.
Best of luck to you—