Hepatitis C Support Group
Hepatitis C is a blood-borne viral disease which can cause liver inflammation, fibrosis, cirrhosis and liver cancer. The hepatitis C virus (HCV) is spread by blood-to-blood contact with an infected person's blood. Many people with HCV infection have no symptoms and are unaware of the need to seek treatment. Hepatitis C infects an estimated 150-200 million people worldwide.
Knowing all of this and the fact that Abvvie is fast tracked, I am waiting. I do not want to do interferon unless all else fails.
So Call me W...the Hepper. LOL W is for waiting.
For me, waiting is the plan. NEVER NEVER Interferon for this pussycat. And I'd just as soon leave Riba out of the mix too - which may be possible. SO MUCH is happening right now, Clay. The pharma "big guns" are all lined up, locked and loaded. They want a return on their investments - good thing they have to get FDA approval - for our safety. I salute the warriors who did all these trials. Yes, they wanted to CURE - but bottom line is the drugs are still experimental. If not for those brave guys and gals, all this GREAT STUFF on the NEAR horizon would not be so near. The timeline for Gen 1's has been pushed up a YEAR - to 2014 - since a few months ago. Trials still ongoing - final data being gathered and submitted. I am sure that in my case waiting is the right thing to do - can't speak for you, but with a Stage 2, you have plenty of time.
I have dwelt mentally - and emotionally - on my HCV for the past year, when the tests and images and that damn messed up bx forced me to realize I DO HAVE HCV. For 10 years after dx, all tests and labs looked great. So I never even thought about it unless I was going in for my six-month check-ups. I am TIRED of having to think about this full-time - but I can't help it either. It means so much to me to be part of this forum where the information, thanks mainly to Kramer, is being posted about the incredible fast tracking of these drugs - and that they WORK - and very few sides - Riba will give most people some - but maybe you and I and others won't have to take it. If I do, fine - my doc. will start me off as low a dosage as he thinks will be needed - and provide rescue drugs or take me down more or even OFF it if warranted.
We're gonna be okay. Yepper, hepper.
Forgive me, please. I am so sorry. I hate the fact that we can't change our posts on this forum.
LOVE THIS AVIE of yours today!
Ya comin' to Ozzie's party? It's getting started! Early - as we have a lot of places to go. Lear jet is going across the country right now picking up all the attendees. Be there or be square! Check the thread - gonna start a new one in a few hours once we have everyone on board the plane and land in Miami.
If the biopsy on May 3 and the tests in July, by some miracle, should show no signicant changes since last year, maybe I could wait for new drugs in trial after all, if they are going to be given to post-transplant patients. Just maybe it's a blessing in disguise that my kidney functions are holding up treatments. But my Hep C is more aggressive since my transplant 3 years ago.
Keep us posted of your results.