Hi guys n gals, how’s everyone?
I’ve just started a 8 week program on 3 Maviret daily for my hep c, I was just wandering how everyone is getting on with side effects and basically how they are feeling day to day
I done the first treatment they took out, the injection and tablets, I can’t remember the names of them, but my treatment worked, my hep was gone after 4 weeks, the treatment was ment to be for 12 months but they dropped it to six months but it basically came straight back, that treatment made me so ill , I ended up 7 stone in weight, sick all the time and my hair was falling out, all for nothing so I’m a bit worried that this might happen to me again but the hospital said it wouldn’t be nothing like my last time so that’s why I want to hear from people who are actually going through it and them who’ve done it