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I was diagnosed as non-A/non-B in 1985 and diagnosed as Hep C+ in

2005, just turned 51 a few weeks back and finally made it into a

doctor I trusted - just got a blood work phone call back yesterday,

said I looked great for a 51 y/o with a hep c background for this

long, however my viral load was just under 4 million and well within

his guidelines for discussing PegaSys - which we're going to do next week.

Here's the questions I've posed to my local community who have gone

through treatment:

What was your viral load when you started Rx?

On a 1-10 scale, what was your health/quality of life?

How long was your treatment?

On that same 1-10 scale, how sick/miserable were you during treatment?

1-10, How do you feel now?

Given what you know now, would you do it as readily/quicker/with more

thought again?

I'm a local title holder and very active in community service so I'm

concerned about down time, however if I can feel better more often,

contributing to a better quality of life overall than I have now, I

think I'm ready to find out ;)!

Thanks for sharing,

" Mr. Mike " - Mike Little

Mr. San Diego Eagle 2008

1st Runner Up Mr. San Diego Leather 2007

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