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where r u on treatment

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I am the mom of the pediatric pt here on the group. I know this group doesn't specifically deal with the peds population but there is not a group that does, and I find you all so wonderful and the info is amazing and helpful and most of all supportive. So thanks from the bottom of my heart for letting me join. My daughter will turn 3 next month and we have an appointment for the liver biopsy and hope to start the Pegasys treatment this summer. we are scared yet very hopeful in her situation. She is Genotype 6 which is rare here in the US but a good success rate with treatment. My daughter contracted Hep C from her birthmom in Vietnam, who was coinfected with HIV, apparently this increases the rate of transmission from mom to baby. Thanks Again and I'm

sure I'll have lots of questions when we get closer. jamie

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