I tx'd in 1994, responded then relapsed and it was pretty rough going. I absolutely dreaded treating again but have done so (started in June 2008 for 6 months Genotype 3A). I knew I would have to again sometime and am glad I didn't earlier as I would've been given standard ribaviron. My specialist put me on a high dose for my weight, and while I started getting anemic, I managed to stabilise. Feel free to check my journal and posts.
Because I knew my condition had deteriorated I arranged for time off work, and stocked up on all the things I thought I may need, and read and re-read this site for tips on supplements etc. Without the handy hints I got here I would not have managed the tx, but I was also pretty determined to give it my best shot so did everything in my power to assist myself in getting there.
I did find the tx a little more difficult, but I'm a lot older, and a lot less healthy. I have met two people who fared better than me and know of many who continue to work.
However, in 1994 I didn't know that I had to keep myself hydrated (drink lots of water!!!), what vitamins may assist, that B-complex was important. And by 2008 I did have a better idea of what foods were liver-friendly.
I suggest you spend a good night on the PC searching this site and the Janice & Friends site so that you can co-manage your treatment. Get copies of all of your blood tests and check when they will do PCR's during tx.
I do wish you the very best of luck; tx'g such a long time ago, and having this hanging around your neck for so many years is a real drag. Have you had a biopsy done? There are new drugs around the corner, but it would certainly depend on whether you feel you are able to wait. Good luck.
Just bumping your thread to the top. I'm sure someone will respond.