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Hello everyone,

I'm new to this, thought it's about time I joined because I live alone and not

in a support group.I scare myself silly sometimes with what I read so hopefully

someone will be able to reassure me from time to time.

I've known about this hep c for 15 years but have had it 25 years from a blood

transfusion...I've chosen to go down the alternative route...but it's scary not

having a doc telling me what I should do next! Don't feel too good at the

moment.

Also I've never found good info on diet and recipes...the blandness of steamed

fish and chicken puts me right off food.

Bye for now

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