So glad I found this site where women can talk to women. My journey started over 30 years ago with a biopsy .. which I have had to date around a dozen .. most were clear, but ten years ago I was told that I was LCIS (Lobular Carcinoma in Situ). The lower outside quarter of my right breast was removed, and I was pronounced with clear borders. Having a routine annual mammogram, this year a small 1cm lump was noticed, and after further mammo's, an MRI & biopsy I was told I had invasive lobular and invasive ductal both in early stage in the right breast. I sat about to find an all female group of doctors .. so glad I did the work. My primary surgeon is the head of the breast center, plastic surgeon, and oncologist are also women. Had a bi-lateral mastectomy March 1st and I must say that I am one blessed woman .. early stage .. found ductal in situ in the left breast, also early stage (so happy I did both). The cancer had not gone in to the lymph glands .. now comes the decision to take or not to take Anastrozole. I am 71 years old .. in excellent health .. very active .. what do I do? After reading up on this medication, I am not sure I want to subject myself to the side effects, and possibly end up with problems. I am thinking 71, and if I can have a good 10 more years .. in good health .. I do not want to take Anastrozole. And do we really know if the medication gives us an advantage ....... any in put would be greatly appreciated.
Hi Mogal129
I'm similar to you, found in one breast early stage and have had double mx - no other treatment - but am now on Tamoxifen. I was told that I could take it or not, it doesn't increase my chances by more than 1% so I gave it a go. So far (I've been on it for nearly 4 months) I've not noticed any side effects. I'd already had a hysterectomy, so that's one side effect I couldn't get! I'm 48.
My suggestion would be to start taking it and see if you get any symptoms. If you don't, all well and good! If life becomes miserable on it, then you can make an informed choice to stop if you want to.
Hope this helps
Helen
Hi there
I had a WLE and sentinel node biopsy at the end of February. I am about to start radiotherapy tomorrow and started on Anastrozole last week. Its probably too early to say if there are any side effects for me but so far so good. The thing is not everyone does have side effects, it depends on the individual. I agree, why not give it a try because if you do suffer effects that are too bad you can always stop it. It may be the drug that gives you that extra ten years or even more. Anything is worth a try; life is precious. Try not to worry about it. sometimes when we sit waiting for aches, pains ect then they happen. It doesnt mean they are not real or that we bring them on. Its just that we are focusing our awareness on that instead of just being. Try this. Just focus your attention on your big toe for a few mins. What does it feel like? Is it warm or is it cold? Is is comfy or not? See, I bet a few minutes ago you did not even notice your big toe? So sometimes it can be like that with other things. Just see how you go.....you may be fine then it is worth taking it.
Huggs
Sue
Hi Sue,
Firstly good luck with your 1st radio tomorrow. I start mine April 23rd after a mastectomy in Nov followed by 6 chemo sessions which finished 2 weeks ago. I am due to start on Arimidex after chemo & would be interested to see if you have any side effects eventually. I know we are all different & I dont get "scared" into things I read but just like to have info so that if I do get S/E's its good to know if they are normal or not.
Good luck to you all & take care xx
hi Suzie.
Thanks for your good wishes. now had 2 sessions of radio therapy only 16 to go!! Not a problem apart from all the travelling. I will keep you posted on any side effects from Anastrozole.. I dont know how long it would be for any to materialise but perhaps thats a good thing not knowing because then Im not waiting for any. I think the meds and radio must be a doddle compared to the treatment you have had and so many ladies here on this site. You will be starting yours then the week after next. It feels like we are ticking boxes off but if it helps us get our life back on track, its all good stuff.
Best of wishes to you
sue x
hi all
I started on Anastrozole 4 weeks ago. The 2nd week I felt sick for 5 days and couldn't bear the thought of eating. However that soon passed. Since then I have a lot more aches and pains, especially in my hips when I walk. And a rash but it looks like it is slowly going now.
My body just feels like I've partied and danced the night away a bit too much lol
And I have to say it's far far easier then chemo ! :)
I've just sent off for the information pack on getting fit after treatment...don't know how I will get on but I have to try !
Ellen
Ellen .. what type & stage was your breast cancer? Mine was early stage, 1cm, lymph nodes clear. I am wondering with all the side effects that I have read about if it is worth it for me to take Anastrozole . I am 71, in good health except my cholesterol is on the high side (& I understand that Anastrozole can push it higher). I am still reading & blogging in hopes that I can make a decision within the next couple of weeks and tell my Oncologist. Thanks for your reply. Jene
Hi,
I am a little younger than you being 64 years old. I have been taking Anastrozole for about two and a half months and have not had any side affects.
If you do decide to take them eat a bowl of cereal or something before taking as this I think has kept away the my sickness . I have had the odd ache and pain but I put this down to age.
Best wishes
Christine
Thank you Christine, the more information I can gather the better for my decision .. what type cancer did you have?
Jene
Hi,
I had oestrogen receptor cancer hope this helps. Do remember when making up your mind that everyone is different when it comes to side effects of any drug.
Best wishes
Christine
Hi Jene
Mine was Invasive ductal carcinoma,ER and PR positive, grade 2, 30mm, no lymph node involvement.
But it's my second time around. I had it in 2003. So I'm taking all that's thrown at me. I don't want it to happen again ! I've had a masectomy and 6 x fec75. Can't have radiotherapy as had it on the same side first time around. I'm not menopausal ( well before chemo I wasn't !) so I'm having Zoladex and Anastrozole. Hope it works this time.
I had Tamoxifen last time but stopped it after 4 years. Maybe that's the reason of my recurrence. They don't seem to be able to tell me if ir's a new tumour or a recurrence so I will never know if it's because I stopped the Tamoxifen.
Everyone is different as reacts differently so not everyone has side effects. But it must be worth it to prevent it coming back :)
I'd say go for it...you can always change your mind instead of regretting it one day.
Ellen x
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2026 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007