Guest guest Posted December 22, 2003 Report Share Posted December 22, 2003 Welcome and Happy Holiday's to You !!!!! We celebrate them all. Some people do relapse after treatment and some very soon. We do have medical articles stored with that info and Liz or I will try to find that info for you. Hang in there and NEVER give up or give in or you have lost the war against HCV. A positive attitude and outlook on life is our best defense along with prayers and support from others. We have a great bunch of family here. We consider ourselves an online family and not just members of a support group. It's very informal open to any subject or discussion and stress free as possible. So happy you posted so soon and wanted to let you know Tues.'s are our scheduled Chat sessions and I was just about to post a reminder. Chat and other options are at group site box to the left on every page. Just click Chat and you are there. Please join us tomorrow night. I'm almost 3 years post transplant and in chronic HCV stage again and a failed responder prior to transplant with the old trmt. meds. Liz is off trmt. meds but didn't finish full dosage and trying to start trmt. again with different meds. Many of us here have tried different forms of trmt. and some 2 or 3 times. Gotta run but looking forward to talking to you soon. Take Care and God Bless. Deb and Liz (by proxy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2003 Report Share Posted December 22, 2003 Chat!!!! Tuesday @ 5 pacific time. We'd love to have you. Be good to yourself,LizSome day's you're the dog, and some days you're the hydrantAttitude determines altitude. - unknown Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2003 Report Share Posted December 22, 2003 Thanks for the warm welcome. What time do you all chat. which timezone? I am really intrested in what treatments there are avalible to me like I said the Doctor that I was with the first time doesn't want to treat again until the protese I guess that is what it is called. I just can't let it take me over. I knew that the viral load was back becuase of the symtoms. headaches, tireness, forgetfulness, pain. I seem to have them all. He says he is consered that the peg will flare my lupus. It didn't the first time around. I have been on Plaqunil for years and it works great at keeping the lupus under control. mmerry x-mas everyone Quote Link to comment Share on other sites More sharing options...
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