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I have something to say. There are all kinds of people in our group who are on treatment or post transplant or thinking about TX. Peop[le have questions and many have not heard the answers. Please read what toy see and remember this is an HCV Support Group.

Getting to know one another is special and is how our group has formed.

But if you have something to say to a specific person....write them.

We are here to help all HCV and family members.

One more thing..... For those who get dail;y digests, it is hard for them to keep up without new mail.

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