Aromatase Inhibitors causing pain
Not sure if this is the correct forum but since I'm stage III thought I'd start here. I was on Anastrozole from Feb. 2012 til August 2014. Took a 2 week break and started Exemestane. While on the Anastrozole I had very bad back, hip and leg pain. This didn't start until about 1 1/2 years after being on it. My onc really didn't think this was causing my pain but after ordering a bone scan and CT and both were clear he took me off of the Anastrozole for the 2 weeks. About day 12 of being off of it the pain lessened. Then started the Exemestane. For about 6 weeks all was well but now the pain is back. I can't sleep at night and I'm just miserable. I have to take an AI as I'm 100% estrogen positive plus stage IIIC. My onc prescribed Celebrex but at a very low dose. I "think" it may help in the day time but by evening the pain sets in with more intensity. I am going to see if I can take Celebrex twice a day instead of one to see if that would help. Does anyone have any suggestions as to what may help alleviate the pain?
Comments
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Unfortunately the AI's are notorious for causing serious joint pain for many women, at the same time they are well documented as being effective in keeping our cancer at bay. I had tremendous pain and eventually my shoulders and knees ripped apart due to inflammation. But, before that happened I found that moving, exercising really did help, which sometimes seemed counter-intuitive. Also acupuncture, Aleve, sitting for hours in my hot tub at about 101 degrees. Every few months my onc allowed me to take a vacation from the AI's. Sometimes I took them every other day or half a pill each day. I kept monitoring my estradiol level with a sensitive assay test, and tried to keep in under ten. If I got it under a ten, I would stop taking the AI until my estradiol level crept up again.
Make sure you read up on some of the side effects of Celebrex--sounds like you are taking a lot of it. I have read that estrogen depletion creates a particular form of arthritis, but fortunately when I stopped them for good I became pain free rather quickly.
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Hopeful56 - I took Arimidex for a year, and experienced severe enough side effects that my MO took me off it completely for two months. ALL the SEs went away (and they were serious ones.) I was thrilled!
But at the end of my drug holiday, I was shocked to hear her tell me to go pick up my Rx for Femara as I left her office. Even though I am Stage 1A, the MO still wanted me on an AI, as I am 100% ER+.
Since one of the SEs of the Arimidex had been severe joint pain, the MO referred me to an Acupuncturist for treatments after I started taking the Femara. I have to admit they helped!!! I went once a week, and Kaiser paid for it. (There have been clinical studies that have shown Acupuncture alleviates joint pain caused by AIs.)
I also second what weesa said about warm baths (I'm fortunate to have a jacuzzi bath at home) and Aleve. And, hard as it is to think of exercising, I do take a water aerobics class at the local Rehabilitation hospital, where the pool is heated to 94 degrees..... soooo soothing on painful joints!
Hope you find relief soon.....
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