I must be missing something here.... Crackerjack, have you been here before then? Anyhows to catch up on previous replies, i did the interferon for the year but it didn't really decrease my VL enough for me to call it quits at the end of the year. I am now on combo-treatment (as you have read) and managed to sero-convert. The year is gruelling but i was more afraid of the needles than the side effects which tbh wasn't too bad for myself... Leeds huh? I wonder if you might go on the same tx procedure... How long you been on pega now?
what kind of pains are you having and are the pains from hep b or from the treatment medicine.
Good enough. So where's Ann8? I miss him.
Welcome back crackerjack230!
Not Ann8. See that's tricky, because Ann8 is male.
But I know who you are before. Not because of connection to MH, but because I am a NYer and NYers just knows stuff. So I'll just say welcome back crackjack230 and leave it at that.
I'm thinking this is jack1642...but wanted to make sure. no not jack1642, LOL ... this is fun
I'm thinking this is jack1642...but wanted to make sure.
LOL ...not telling but you were a friend in my past id... this could be funny
Good news!
Help me out, what was your old name?
just read your profile.... you are on ....Adevoir and Lumuduvine. I do wish you luck and hope you get a better outcome at the end of treatment.
you talking about pega interferon? ...Yeah course I am, Pegylated Interferon , just call it peggy in Leeds. Hi Peter nice to meet you. Are you on treatment or are you finished yet. It has been a journey indeed. I find it much more helpful to talk to others doing the jasus therapy as opposed to a hepatology nurse who comments.... that symptom is on "my list". I need to know I am understood and not talking to someone who hasn't a clue. I have been to my GP more times the past year, I found the treatment doable but frightening at time especially when I has awful symptoms and I did not understand what was happening. The hyperthyroidisim was the worst but it only lasted a few weeks and it has gone now. Hope you are ok and the therapy is been kind. I cannot believe some people actually continue working whilst on interferon, I must be very sensitive indeed.
Hi,
Noticed you are in the UK....
I'm also here matey so just thought it would be good to share our treatment experiences. When you mention therapy are you talking about pega interferon?