"Good luck to you Harry. Incidentally, just took my last shot (#48) 10 minutes ago.
r4"
r4c7's Profile
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About Me: Male, 70, Denver, CO, member since Feb 2007
Its July 13, 2008, my last day of treatment. Pegasys and Copegus. UND before week 12, still UND today. Started at 22 million viral load, geno 1b. The first 20 weeks were very difficult, horrible anemia, fatigue, rash, gout, forgetfulness, hair loss. The next 18 weeks
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have not been so bad, some anemia, fatigue, gout. Recently I've had a hard time waking up. Its like your mind wants to wake up but your body doesn't...crazy. Had a recent spike in LFT's from normal levels, but they are starting to come back down slowly. At the present time I feel like a complete zombie,don't sleep well, can't really work, but am also optomistic about achieving an SVR. Now...the 6 month waiting game...
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Interests:
Getting through treatment
You haven't updated your status yet!
Jun 29, 2008
" The information you sight from HALT-C raises a lot of questions. For example, I would doubt that minor or infrequent dose reductions of ribavirin would have only a negligible effect on rapid and early viral responders. Also, ribaviri..."
Jun 25, 2008
"Having almost completed treatment (in week 46 of 48) and now having firsthand experience as to what its like to live in a living hell, if I were a stage 1 or 2, I would wait as long as I could. Who knows, with technology advancing like ..."
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04/10
My name is Miss loveling i saw your profile to day when i am in sache here in the site i became intrested in you ,i will also like to know you more,and if you dont mind. i will like you to send an email to my email address so i can give you my picture for you to know whom i am.Here is my privte email address ( l o v e l i n g m b o o @ y a h o o .c o m) believe we can move from here!I am waiting for your mail to my email address above.grace.(Remeber the distance or colour does not matter even our age difrent because i have something very IMPORTANT to tell you,but love matters alot in life)
thanks and your
friends to be,
loveling mbogo
07/08
Well I'm glad for the rest of us that you stay attached to this site :-); It's you who we learn from. In 1993 when dx my Specialist told me to tell no-one. My boy was 1 and he knows about blood alerts . He's now 16 and I haven't had him tested; waiting for this year to finish &it's heavy exams; I know it's unlikely that he's positive but don't want the stress right now. And if he doesn't know, well, I just can't share it with the rest of the world now can I; he is my family and family come first. So, I've made things a little complicated over the years to continue with a bit of denial - No point in denial now and am warming up to being an honest camper again. Thanks for the note :-); really appreciated.
07/08
I don't know how you managed to keep your job!!!! If all the people on this site got rid of HVC and formed a World Government I think we'd fix the planet!!! Everyone is so much stronger than they think in here - it blows me away. I've got 3 months leave without pay which my employers will review to see whether they'll let me have another 3 months (and whether I want it depending on what type of payrise I get - will find out in August :-)... You may not get this note for a while (if i was you, I'd be recovering well and truly and not checking this site out toooooo much), but best wishes anyway.
07/08
Hey R4C7 - I saw an earlier post of yours and see that tomorrow is your LAST SHOT date!!!! I'll be celebrating the milestone for you congratulations and you're in my prayers for SVR. Your posts have really helped me and others; thanks and good luck :-0
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