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Hello,

I have had Hep C for years and am just now about to start treatment

after finally getting insurance, going through finding out what

genotype I have and talking it over with the doc. I've heard from

famly and friends (so many of the people I grew up with have this)

some of what to expect over the course of treatment but imagine that

I won't experience this in quite the same way that anyone else I know

has.

I'm also starting back in school (I " m 46 and returning after many

years) Monday and am not sure how that will go. I work a very active

job in which I walk about 8miles a day, five days a week and have to

be on my toes, so that's a concern for me also.

I quit getting high about two years ago and have taken so many

measures to improve my life. I hope that this is just one more of

those efforts and after the six months of treatment will be healtier,

happier and wiser.

I appreciate having a forum to discuss these experiences with others

in the same boat and look forward to meeting you all.

Thanks,

Mike

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