Is it me?

[Guest guest]

Hiya Everyone, Is it me or is everyone in some type of cloud lately? I know most realize that all different genotypes are treated in different ways, ie length of prescriptions, amounts of the drugs, weights, etc. In most cases of Hep C, every patient is taken and treated on an individual basis, it's a preference amongst some to try alternative medicine, but lately it seems when someone asks questions about treatments there is a constant banter of confusion. Most of the research we read and find is based also on the length of time you've had this disease. Everyone's liver reacts differently, everyone's body reacts different with this disease. I've found reading the posts lately it's become very opinionated. Perhaps I am interpreting them wrong and forgive me if I am. It just seems as of late the material posted by reasearch and developement is not being read

throughly. Kindly rememeber these are facts along with statisitcs. My husband along with many others that cross our paths here have experienced many many years of damage, not only to their livers but to their lives. Let's stop the insensitivity to one another ...this is a forum, and it's a positive one for information, freindships and support for one another...can we kindly put aside opinions and get back on the track of support. Like I said previously, perhaps it's me reading this all wrong...but someone please reply if I've beaten off the track here about what this web site is here for and about!! Hugs to all you Mom's & Dad's on Mother's Day!!

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