Hello! Reaching out here looking for hope regarding my dad with HCV. He received his transplant from my, at the time, 23 year old boyfriend in June of 2011. He is now at grade 1:6 scarring from the HCV and will be starting treatment this coming Monday, March 25th. He will be taking the Pegasus (spelling?) shot once per week and the Riboviron pills three times daily. The doctors gave him about a 65% chance to clear, and say that there are not really any options available if the treatment doesn't work. He is genotype 2, and responded to treatment very well before transplant but needed to stop due to liver failure. I know that the way the body responds to treatment post transplant can change. He has had no issues with rejection, just bile duct complications. He still has small exterior tubes. My question are these:
Is there a lot of hope that he can clear this virus on treatment post-transplant and still have many years ahead?
Is there a lot of danger for him to be doing treatment post-transplant?
If he does not respond to treatment, what other options might be other there for us?
I am feeling pretty overwhelmed and anxious about the situation and am looking for anything anyone has to offer.
Thanks!!!