Hi everyone, I had my bc treatment 3 years ago - mastectomy, chemo and rads and been on anastrazole since then. I haven’t been online for two years as I was never really aware I had any problems connected with my treatment. I have had really bad arthritic fingers and thumbs for years but much worse in the last couple of years. I thought this was just the normal progression of arthritis, until I saw my surgeon for my regular annual checkup recently. For the first time I was asked if I had any joint pain. When I mentioned the pain in my hands, which is really severe now, he said it could be the anastrazole making it worse. I had also had cortisone injections into my thumbs a few months ago which had no effect at all, and the surgeon said the anastrazole could prevent the cortisone from taking effect. He suggested I talk to the oncologist about changing to something else.
Im now wondering whether or not to ask to change. It seems from this forum that all the hormone blocking drugs have some side effects. I do also feel tired and have hot flushes, mainly in the form of awful night sweats. But my hands are so bad, I’m taking paracetamol and Tramadol but there isn’t a lot of relief even from that. I’m afraid if I talk to the oncologist he will say (as I’ve heard others were told) that anastrazole is the best insurance against recurring bc, and I will have to choose between recurrent breast cancer and arthritis. A rock and a hard place!