Hi Guys, first post here in Hep C land...I am 55 male, who was diagnosed with Hep C in 2002...How long I had been infected before that, who knows? so at least7 yrs...I didnt do anything about it. Because I was invunerable, and I didnt, and still dont have any symtoms.. 3 yrs ago, I had a disabling stroke (clot). talk funny and wak funny. On both LTD and SSA disability (thank God). My point, my gen practicioner said I should go see a interal med specialist for the Hep C (after he looked at blood tests. I was/am type 1A genotype, Specialist did a biopsi 1 month ago.. Got results today and said "Well, good news is, you dont have cirrosis, yet." He said it was stage 2, whatever that means. He wanted me to do the MEDS but advised of the rate of success vs side effects of medicine etc, And I said well what will happen if I dont take meds. He said that I would/could have cirrosis or liver cancer anytime within the next 5 yrs... I dont know how he can know that, but I do trust doctors.. My question(s) is/are: does anyone here have experience of how long it takes to go from stage 2 to cirrossis. I dont even know how long I've been at stage 2. I read somewhere if you have stroke or heart conditions, you shouldnt take the meds. Is that true. My doc says if I'm not having seizures, I should be fine to take the meds, IF I can handle the side effects.. If you do get cirrosis, is that a death sentence? or at least a slow walk to death? Sorry for all of the questions and rambling on.. but I feel great now, he also said there was a chance (type 1A) the meds wont work..
what to do.. Help!!! he is sending me to classes. Classes just for the interferon etc meds..to have a "class" just for med taken, it must be brutal.. and I'm a big sissy, just when I get a cold..
thanks
Mike