Forum Discussion
LisaG
14 years agoMember
Femara
Hi Girls,
I am now five weeks post chemo and about to start radiation. I have had a review with my oncologist and he has changed his plan to put me on Tamoxifen due to the fact that I am a warfarin patient.
He now says I am to go on Femara. Of course I Googled it and now I'm scared ! Not only does it read like a checklist of chemo side effects but it can even cause more tumours! What's with THAT!?
Has anyone else been on this medication and if so - what were your side effects? I have had a bone density test but won't know the results till my next review in 5 weeks time but he's also talking about possible monthly needles to keep my bones healthy.....
I don't want another 5 years of crappy side effects!
15 Replies
- Mich_xMember
Hey Lisa
Reading your post about the Femara is sounding exactly how I feel.
I also found that around the 4 month mark of being on Femara the "real" pain and stiffness set in. Getting up from sitting or out of bed in the mornings I look and feel like I am 90.
I thought in the beginning I had got off lightly with the Femara but between the pain, stiffness, chills and then sweats straight after each other all day and night I now know I am taking the dreaded Femara.
My onco wants me to change to another AI (3rd one) but I am thinking I don't know whether that is a good thing to do because I am a good few months down the track on this one and starting a new one who knows it will be any different. When I go back to see him next month he will probably be annoyed at me but I guess I am scared to change now.
I agree with you that exercise definitely helps but doesn't quite take the pain away. I am on natural anti-inflams every day plus Panadol Osteo every 4 hours to get through the days at present along with Krill oil, Vit E, Vit D, glucosamine, B12, COQ10, orobiotic, multi, caltrate plus. Needless to say I rattle when I walk. I sometimes ask myself should I bother with taking all this as I still get all the symptoms. I have seen GP and Naturopath and shown my list to onco and they all agree I should stay on them..........The hormone clinic has now also added Clonodine to my tablet regime......
Sorry to say it but I do feel better knowing I am not the only poor bugger suffering from the Femara and I also remind myself there are sooooooo many people out there a lot worse off than me so I do count my blessings every day.
Lots of luv, Mich xoxo
- LisaGMember18 months!? O no! I know my onc said it could take anything up 2yrs to settle reactions but I have been praying for a shorter time. Thanks for the hints. Maybe I'll increase my dose of fish oil and see how that goes. I gave in and took an Endone last night but though it did ease the leg pain, it made my tummy feel yuck and I didn't get to sleep till 2am. I'm having a lie in today. Its nice to listen to the rain on the roof now the wet season is finally here. I think I'll make today a "gather my strength" day. Thank goodness for smart phones! I can chat online from here ;-)