I am very glad to have found this forum! :)
I was diagnosed Grade 2 Stage 2 last month and start on the treatments probably in the next week (as soon as my insurance company gets into gear).
I've been really fearful about every single aspect of this whole HCV thing and finding you all in here is a God send.
I will pray for all of you as I pray for me (which is pretty much constant now).
Thanks for being here!
Hey everyone, I just want to thank you for your support and your comments. My appt. is this Wednesday and so I need your expertise to help me ask questions. Is it o.k. to take a low dose of interferon everyday, not combination therapy, like I said I can't handle that. I get really, really sick and my white blood cell count dives even more than my normal low. Has anyone done daily treatment??? The other thing it can anyone please tell me what your physical symptoms of cirrhosis are? I am sick to my stomack, I sleep 12 hours a day now are there because of cirrhosis? I have lost weight about 10 lbs in the last year as well. My mental attitude is great though, I can help any of you with having hope and stuff like that. I am not afraid, I have been through 3 and one half treatments and during that time I have been so blessed with the things that have happened in my life that I never thought I would live to see when I was diagnosed in 1983.
Deb
Hi, I don't post much but read alot. Your question touched me cause I know how scared you must be. I too have stage 4, cirhosis. I have hep c type 2 stage 4 grade 1. my liver and spleen was very enlarged and blood platelets was in the 70's, when I started treatment. I have had it for 20 to 25 years. And just found out last year I had it. So all these years I drank on weekends. Anyway, what I wanted to say was Good luck to you and don't ever give up. I was lucky to respond and I take my last shot next week, so far I am clear. I will always have cirhosis, and need to keep an eye on it. Good luck to you and God bless!!!
Just to clarify,Knodell is cirrohsis at stage 4-It's Ishak that has 6 stages of measurement.
I am stage 3 Ishak-occasional bi-portal bridging,stage 1 (mild) inflammation
Thanks for praying for me. You know the last time I was treated they told me that it was probably the cause for my lupus diagnosis and also I now have a permanent low white blood cell count. I would be taking nupegen or however you spell it along with the interferon. Like I said I have been through 3 and 1/2 treatments, it does do some damage. I don't know if my body can take anymore. My appt. is Sept. 7. My ALT and AST went down to around 100's the first few months then rebound to around the 3-400 range which is what they are now. I am so glad to have found this forum. It really helps. Someone else asked what scale they used for the biopsy's and the last 3 just say stage 1-4 and grade - 1-4 in their grading. Like when I was grade 2 it says grade 2 of 4. So that must be their scale range.
Sorry, I meant I am a Grade 5 on Knodell scale, not stage 5.