Just curious to know: are you on SOC or taking triple therapy? I started a clinical trial in Vancouver July 8 and found each progressive week was different. Now that I have started week 9 I look back and think week 1-4 wasn't so bad but if you had asked me during those first few weeks I'm sure I thought I was dying. We are doing battle with a highly evolved virus and our weapons are powerful drugs with collateral damage no matter what you do. The interferon was worst the 1st week but now I feel like a cancer patient doing chemo when I take the protease inhibitor. This week I was ready to quit but I want to beat this thing and this is the only option. You need to see your MD and tell him/her everything you are feeling so they can help you sort it all out. Your situation sounds really complicated but you can get through it. Hang in there girl!
Pauline
Call your doctor NOW and tell him/her how you're feeling. If you're not already on antidepressants you may need to take them. How I feel on treatment varies from day to day. Some days I'm a hair's breadth away from tears all day. Some days are OK. Some days I'm tired. Some days I'm jittery. But each and every day I'm doing everything I can to clear my HCV. Hang in there, talk to your doc and take care.
Sherry
You've got a really special set of circumstances. Is your treating Dr. a liver specialist? Let him know what you're going through. I have a friend w/ lupus and her depression is hard to deal with. The depression from the tx is temporary and will end when tx stops. I think that is easier to endure. That's kind of contradicting, but I've never personally experience depression like my friend w/ lupus.
I hope ur Dr. can give you some advice n you'll get relief. Karen :)