After Tx (Alpha 2A and Ribavirin yearly treatment)

[Guest guest]

Hi everyone... I started treatment in mid-October of 2007. Even though I have many issues related to HEP-C, I have been virus clear since 12 weeks (3months). I was at 443 when I started treatment. Classified as severe inflammation (4), portal/central bridging (4), and advanced Liver fibrosis (3). I will finish my treatment in mid-October (basically 1 year). I have a few questions, see below. My doctor has told me his opinion, but I was curious what others plans were after treatment is completed. A. What is the average length of the ongoing blood tests after treatment is completed. (Monthly? Quarterly? and how far in the future will they do the blood work.) B. What are the odds it may come back after treatment? C. Is there a healthy diet plan that is set up for HEP-C patients after treatment? D. Any other changes to help the

Liver after treatment that your doctors recommend? E. Any other comments for someone in this position? **Good Luck to everyone going through this hell...Have a good day!!