Hi Ray, welcome to the forum.  You will definitely get great support here.  No question is silly, so post any question you have.  All the best.  Caroline

Ray,

Welcome again! I spoke to you recently and am glad you've introduced yourself. As you've read, we've got a great support network and an abundance of current information on beating this disease. The new treatments are opening a new window of successful options, so your chances have never been better! As suggested, if you can provide some history and lab report data, we can provide better informed opinions. We're glad you're here! Good luck...

Tig

Hi and welcome, Ray.

Tell us your story and some lab. results, and we'll be happy to help with any questions. Cheers.

Hi Ray,

Welcome to the group. There are many of us on treatment - new and old, recently diagnosed, on trials, non-responders/partial responders, and those waiting for better options. Here is a wealth of knowledge and a great support system in place.

It is always daunting when you are first diagnosed and there is so much information to absorb, but take your time and get used to the change in your situation. It becomes very normal and unscary very quickly.

Have  lovely day, L

Hi Ray, welcome!  You`ve come to the right place for support, this is a very friendly group so please feel free to tell us some more about your situation and diagnosis, for example your genotype and latest viral load results, which will help us give you any information you need. 

If  you look through the `sticky` threads at the top of this section you`ll find lots of information which you might find very useful for finding out more about Hep C and your current treatment options. 

Looking forward to hearing from you!