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Re: Me Again...

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Hi. Welcome to the group. I have hep c and It is looking like I am a non responder to the medication. Doctor warned me about that so it is not a total shock. Just a set back. He is saying that new medicine should be available in 2-3 years. I have a bit to sort through in regards to medical insurance and financial issues. Anyone out there have any suggestions? Where is a good place to start.

Subject: Me Again...To: HepatitisCSupportGroupForDummies Date: Wednesday, November 26, 2008, 6:14 PM

I've been reading thru a few posts and it all makes my head spin trying to figure out what it all means. I've done a lot of research on the HC and so much of it contradicts itself. One thing I read said that Hep C is much like Russian Roulette. There's just no way of knowing how things are going to go. I try to understand what I can but then feel totally overwhelmed. I read about the transplants and it makes me cry and scares me to death at the same time. I'm so sorry for ALL of us here...

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In our files

are drug company CARE programs where they will supply the drugs for free but you

have to verify to them by sending statements of income,bills,rent ,etc and if they

see that you can’t pay for the meds,they will send them to you or your treating

doctor to give to you. That is how I got treatment.

Gail

-----Original

Message-----

From:

HepatitisCSupportGroupForDummies

[mailto:HepatitisCSupportGroupForDummies ]On Behalf Of Stens

Sent: November 26, 2008 7:24 PM

To:

HepatitisCSupportGroupForDummies

Subject: Re:

Me Again...

Hi. Welcome to the

group. I have hep c and It is looking like I am a non responder to the

medication. Doctor warned me about that so it is not a total shock. Just a

set back. He is saying that new medicine should be available in 2-3 years. I

have a bit to sort through in regards to medical insurance and financial

issues. Anyone out there have any suggestions? Where is a good place to

start.

From:

pita54me

Subject: Me Again...

To: HepatitisCSupportGroupForDummies

Date: Wednesday, November 26, 2008, 6:14 PM

I've been reading thru a few posts and it all makes my

head spin trying

to figure out what it all means. I've done a lot of research on the HC

and so much of it contradicts itself. One thing I read said that Hep C

is much like Russian Roulette. There's just no way of knowing how

things are going to go. I try to understand what I can but then feel

totally overwhelmed. I read about the transplants and it makes me cry

and scares me to death at the same time. I'm so sorry for ALL of us

here...

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