Guest guest Posted May 30, 2010 Report Share Posted May 30, 2010 Hello. I'm Lion & Serpent93 and a newbie on your list. I have been lurking a few days here now and thought that perhaps I should introduce myself. I really don't know how to begin other than to give a brief biographical sketch so that you will understand why I joined this group. I was born in the 50s, grew up in the 60's and 70's and was pretty wild, mostly smoking alot of pot and taking alot of psychedelics well into the 80's. But I dabbled in what ever came by. I straightened up my act and graduated from Cal with a degree in Molecular Biology in the late 80's and went on to get a PhD in Microbiology from UC in the early 90s. I am a bona fide virologist having spent a significant number of academic years working with retroviruses and their role in cancer and AIDS pathogenesis. Throughout the 70's to the 90's, I was a big pothead and a die-hard 6-pack a day beer drinker. Weekends would be worse with hard liquor thrown in to get the good buzz going. I was a hard working functional drunk. Around 1992, I was just not feeling very well and it is hard to describe what I mean, just sort of off. It was after a hard weekend of drinking whiskey in the mountains of California. I went to the doctor and he did some blood work. He called me a couple of days later and said my ALT and AST were pretty elevated and he wanted to test me for antibodies to Hep B and C. I told him I would test positive for B because I had been vaccinated immediately after the Hep B vaccine became available because I worked with human blood and wanted the protection. Well, I got the call that I was Hep C positive and asked him what did that really mean. He said, " Probably nothing, we don't know much about the virus. But your drinking days are over. " So, being the very smart (ass) scientist I am, I drank as if he had never said that to me, never passed up a shot of whiskey or a beer, and continued with life as `normal'. I really never felt sick, so why change? On a routine visit to the same doctor, he said he wanted to test me again because he knew a GI doc who was " curing " people with Hep C using interferon and ribavirin. It had just come out and I said let's go for it. My viral loads were about 2 mil, my genotype was 3, and my liver enzymes were in the low 100's, not terribly bad. So, I hook up with this GI doc and he says he doesn't think that it's worth even treating me because my VLoad was low, my liver enzymes weren't terribly high, and I had a relatively passive genotype 3. I told him I had insurance and two sons and that I wanted to do whatever it took to prolong my life so that I could be there for them. I insisted he treat me and he agreed. Prior to treatment, he performed a liver biopsy and he was very encouraged. There was some minimal lymphocytic infiltration and very minor, almost insignificant, fibrosis. So I started the treatment. From day one, I felt like death. I had extreme flu-like symptoms: body aches, chills, fevers, malaise, weight loss, thinning hair…you name it. There was no pegylated IFN then (I believe this was in 1996 or 97), so I had to tough it out 3 times a week. Within 4 weeks, my liver enzymes were normal and I was virus-free by PCR…very encouraging. So, I continued on and to combat the severe depression, I drank even more. Very wise move there! Mr. PhD! I completed my 24 weeks in hell and was still virus-negative by PCR with normal liver enzyme levels and even 2 months post treatment. Hey!! I was home free! My regular doctor had me follow up with him 6 months post-therapy and did a blood test. VLoad was 4 mil and my liver enzymes were 4x above normal. My GI doc and my PCP were shocked, but it is what it is. My PCP said to just get a blood test every 6 months and a biopsy every 5 years so that we could track the progression, but not to worry because I would probably be okay. Quote Link to comment Share on other sites More sharing options...
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