DT .. I'm in the Hoffman LaRoche R1626 trial, it's another PI, only a polymerase inhibitor whereas Telaprevir is a protease inhibitor.
The thread I referred to is here:
http://www.medhelp.org/posts/show/465519 - we've been sharing results and info about our trial experiences with each other as we go along and it's been a great help to sort through things as they come up.
So no .. I'm not on regular treatment. I'm taking Peg but not sure if it's at half dose or full. I'm taking ribavirin and it's at full dose. Then there's the trial drug, and however much of that I'm on. All will be revealed to us at the end.
Alternative tx's .. by that if you mean are there alternatives to interferon and ribavirin, that's the main treatment. If you were going to treat, that's your core. Then there are ways of approaching that treatment and then there are other things people are starting to add to the mix and ways to tweak your traditional treatment to a certain extent depending on your own circumstances and the attitude of the docs taking care of you.
Trials are another matter. There are trial drugs being tested at the moment and others coming along that we're hoping will improve treatment regimens and outcomes for all of us and those coming after us.
I hope some of that helps?
Thanks for the kind words ... with treatment, we deal with the cards we're dealt and I've been dealt a reasonably good hand so far. I'm able to keep working and keep pushing through a number of other things. I have my bad days too like everyone else and this forum and the people in it are a good support.
Good luck to you starting treatment in June. You're a 2a I see so short(er) treatment regimen for you .. although treatment is treatment! How are you doing with getting all the information you need from your doctors? Keep posting and asking questions. :)
Take care.
Trish