Re: new here, & Anne

[Guest guest]

Hi Ray,

It's nice to meet you, although I'm sorry it's

via HCV!

I am a non-responder (53 weeks combo), genotype

1b, only stage 1 fibrosis 3 years ago when I was

diagnosed. My sides during combo were not too

terrible, but I've 'met' many who absolutely could not

take it. For those, like you, there isn't much

available except the 'alternatives'. I hope you share

with all of us what you are taking. Even those who

tolerate and choose medical treatment can often

benefit from complimentary herbs and supplements. I

never thought I'd see the day, but even NIH and

doctors are starting to realize there might be

something to this! Right now I am taking Milk Thistle

(Maximum Milk Thistle), Vit. C (1000mg) and Vit. E

(800IU) for my liver, St. s Wort for my family ,

and Flax Seed Oil, Calcium w/D, and Magnesium for the

bones and joints since I have early osteoporosis.

(Common in those with liver disease.) I also take a

multi without iron, and B-complex. (Anne - you say you

have trouble with the milk thistle - have you tried

changing brands, to a higher quality product?) I think

we could use more info on alternatives, so whatever

you can share will be appreciated.

This is a great group. I think you will like it

here.

Happy New Year Everyone!!!!

Claudine

__________________________________________________

[Guest guest]

In a message dated 1/1/01 9:25:07 PM !!!First Boot!!!,

claudineintexas@... writes:

<< Anne - you say you

have trouble with the milk thistle - have you tried

changing brands, to a higher quality product?) I thin >>

Dear Claudine, No I hadn't thought about that, but I will and will let you

know how it works. Thanks for putting my brain on a new path. Anne