Just a note you , would be better off starting your disscussion where it says "post a question" as this paticular thread started in july
Welcome to the forum, I am close to being at the same stage as you in treatment,actually a little shorter time . Just started wk.#3 . From what I understand side effects can vary all over the map and yours sound pretty standard. Good luck at you labs today and with your treatment. Will
hi my name is Diane i was diagnosed with hep c have been on therapy for five weeks now pegasys/ribaverin now have some side affects of fatigue /headaches/some diarrhea,emotional sometimes and boyfriend says a little lippier{imagine that} going to lab and doc today just looking to speak to people like myself.
Of course, welcome to the discussion group. You should start a new topic by going to the top of the page, and clicking on the 'post a question' button; this will open a new topic, you'll get more replies that way.
Bill
I would love to talk with others who are doing the peg reba treatment, is this possible.
HI Janice, you're doing fine. Just click on the 'post comment' button at the bottom of this page to add to this conversation. If you want to open a new thread (conversation on a nw topic, perhaps) click on the 'post question' button at the top of the page.
A link is just a website address; for instance a link to this page we're on now is:
http://www.medhelp.org/posts/Hepatitis-C/chat-with-other-herp-c-people/show/1287884
If this is typed or cut and pasted into the address bar at the top of the screen, it will take you to a page on the internet.
Feel free to ask questions; it's open game around here :o). There are hundreds of us here that have or are doing interferon therapy and some that choose to 'watch and wait' instead.
Where are you with your disease; have you been formally diagnosed, and if so, when? Do you know what genotype you are?
Bill
i really appreciate you taking the time to reply to my question. it is so hard for me to retain information or anything for that matter anymore. i dont even kno what a linkthanks again or a thread is. computer lingo is foreign to me. but, i will try to follow your instructions god, i sound so stupid.anyway if u hear from me again i figured it out. thanks guys. you all are so kind. hope to speak to u soon. Janice
also janis & friends has live chat rooms.
http://forums.delphiforums.com/friendship7/start
you can join:
http://hcvsupport.org/forum/index.php
they have a chat room.
This is more of a message board than a chat room; you're more than welcome to discuss issues here with us. Are you doing treatment for your HCV yet?
Bill