Hi all
Just wondering if anyone has been on this medication and if so how did you get on with it?
Thanks
Hi Rach_E. If you type Anastrozole into the search bar at the top of this page you'll get some answers. Click on the field "anywhere"
Symptoms vary from joint pain to fatigue. You could also chat to a nurse on the Macmillan Support helpline, freephone number below.
Also have a chat with your CNS if you've concerns.
Sending hugs, Barb xx
Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
"Never lose hope. Storms make people stronger and never last forever” - Roy T Bennett
Hi Rach_E,
I was diagnosed as having stage 3 incurable endometrial cancer 4 years ago. For the last 3 years I’ve been taking a hormone inhibitor since my ER assay showed that my cancer was oestrogen receptive. I took Megace for the first 2.5 years and had a good response (despite the weight gain). When it stopped working, I started taking Anastrozole. Unfortunately that didn’t work either as my tumours have become resistant. The way I look at it, I’ve had a good 3 yrs on the hormone medication and initially the medication did stop my cancer from growing.
Regarding the side effects, I only suffered with finger and toe joint pain when taking Anastrozole. All I did was flex my fingers and toes and the pain would ease. My suggestion would be to take your tablet around 6/7pm as the peak time for any medication side effects is around 6 hrs from taking the tablet. You might as well be asleep if you’re going to have any side effects.
I completely understand your concerns about taking the medication. When you read the drug information leaflet provided with cancer meds, it’s scary as hell. Just remember that you won’t get every side effect and your oncologist would not have prescribed them if you were at risk of developing some of the more serious side effects.
I’ve got everything crossed that the meds work for you. Look after yourself.
Liz x
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