We are all so different - Teva was the worse for me & Accord the best, but thanks I will certainly keep an eye out for ovary problems - something else I could do without!!
Hello my name is Ruth,
i had been on letrozole for 6 weeks and I was a crying sweating angry mess, since I already had mobility issues and muscle pain and stiffness I didn't know if my worsening mobility was because of the letrozole.
After a meeting with my oncologist she agreed I should stop using them until my next appointment on the 29th of July.that was on the 10th , I already feel so much better. No weeping,sweating,yelling and fuming.
i am hoping that on the 29th she can help me find an alternative to letrozole .or it looks like me and my family are going to be going thru hell for the next 5 years. If that's so then what quality of life is that. I would seriously consider just taking my chances. All my best wishes to all you super brave lady's out there xxxx
Hi rubycat many thanks for your response xx I've been on teva and have another months supply but will ask for another brand and see if that changes things. It is very hard to unpick what is post treatment, what is the drug SE and what is just life now!!! I'll see if things improve and if not, will get to the GP again x thx
Hello Jets, don't know whether you've already tried this route, but I found an enormous difference in side effects with the various brands of anastrozole that I had. Have had lots of bone aches & pains, hair thinning, but found the Accord brand the best of a bad lot! Dr has now asked chemist that I'm only given that brand and it is helping. It's worth trying a variety of brands for a couple of months each to weigh up any pros and cons. My onc really understood that people's reactions to s/e vary enormously and what suits one person does not suit another. On the dizzy front, before being diagnosed last year I was taking tabs for high blood pressure, lost a lot of weight, (thanks to Slimming World), then started really getting dizzy and spaced out. Found that I didn't need the blood pressure tabs any more, hooray a tablet I didn't need to take. We never know where these s/e come from, or whether it's connected at all, very frustrating. Don't tolerate feeling dizzy and out of sorts, I'm sure there is some explanation so get to the Docs!!! Wishing you well and let us know how you get on.
Hi - not been on here for a very long time but am really hoping that someone can give me some solutions! bilateral mx/chemo/7 months tamoxifen but was having a mare so moved to anastrozole 2 months ago. bone pain better except for weird pain in feet in morning and digit pain (sometimes cramping at night), some lower back pain which can be bad on some days. lots of headaches and nausea. I've been experiencing some thinning of hair as have lost eyelashes and keep finding hairs - this is really making me sad as its only just grown back from chemo. But my big problem is dizziness - its causing me to feel like Im floating or on a roller coaster - I sit in meetings at work and feel completely out of control. I dont know whether this will go/subside? Has anyone else had this? tbh Im getting to the point where I dont think I can carry on with the hormone treatments - might go back on tamoxifen as thinking that the dizziness is honestly worse than the bone pain and maybe that could be more treatable. However, i also got severe depression on tamoxifen. Anyways, Im rambling but wondered if people had experience of this drug getting better with time?