Aromasin and joint stiffness

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Hi

I've been on Aromasin and Zoladex shots from the beginning of this year and I'm now incredibly stiff. The body of a 90 year old. I've also developed trigger finger. I walk over 10,000 steps and swim about 500 m a day and it doesn't make any difference. What do other people do. What supplements do you take. Any help would be appreciated.

Thank you.

Comments

  • Meow13
    Meow13 Member Posts: 4,859
    edited December 2018

    The only thing that helped me was to stop taking it. After 4 years I completely gave it up. Like you I was exercising everyday, I switched to exemestane still had joint pain and developed other issues.

  • Hiphiphoray
    Hiphiphoray Member Posts: 18
    edited December 2018

    Meow13, I really don’t want to give up. I just wanted to ask ask you, did the stiffness disappear when you gave up? At the moment I feel that I’ll be like this forever. Is there a light at the end of the tunnel

  • Meow13
    Meow13 Member Posts: 4,859
    edited December 2018

    Most of it disappeared. You might want to change to another drug and see if it helps. For me each had their issues but anastrozole had the worse joint pain for me.

  • love2paint
    love2paint Member Posts: 1
    edited December 2018

    I was on anastrozole and the pain in my hips was awful, I also felt like I was 90 (I'm 40). The onc changed me to Letrozole and its better but not perfect. I still joke that I'm an old lady but it's tolerable. Hoping I'll go back to normal when my treatment is done.

  • Murfy
    Murfy Member Posts: 342
    edited December 2018

    Hi Hip, I've discovered that temporarily lowering my dose of exemestane to 1/4 pill for about a week relieved me of my trigger thumbs. When I slowly increased my dose back to normal, that SE never returned. I am currently back on a lower dose for a different set of SEs and after only 3 days they are greatly relieved. In a couple of days I will resume upping my dose. Can't promise it will work for you, but lowering my dose for a few days sure works for me!

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited December 2018

    hiphiphoray—. My joint pain is lessened (but not gone) by taking glucosamine with chondrotin and Omega 3 (omega 3 I take 3 times a day

  • Hiphiphoray
    Hiphiphoray Member Posts: 18
    edited December 2018

    Thanks for replies. I’ll speak to my oncologist at my next appointment. I definitely have the body of someone 90+. It can be very frustrating.

    Dodgersgirl, I’ll try adding in those supplements. I’ll give everything a try.

    Thanks

  • Meow13
    Meow13 Member Posts: 4,859
    edited December 2018

    I still have some amount of residual pain years after taking anastrozole and exemestane.

  • Runrcrb
    Runrcrb Member Posts: 577
    edited December 2018

    hiphiphray,

    I had immediate side effects on arimidex (tired all the time) that went away upon stopping. I switched to aromasin with much better results. Some joint pain (knees, shoulders and hands/knuckles) but manageable. Worse on the right but everyone says that isn’t a true side effect - must be bilateral to be due to the AI. whatever. I run 3x and swim 2x per week. Strength train 2x. I take Loratadine 10mg (Claritin), Caltrate 600mg calcium, 800 IU vitamin D3 (2xday), Magnesium 400mg, and Tumeric 500 mg (2x day) all with the blessing of my oncologist.

    Talk to your oncologist about trying another AI if you haven’t already and also about supplements. Hopefully you can find some combination that balances quality of life with recurrence prevention.


  • Newy
    Newy Member Posts: 3
    edited January 2019

    Hi Runcrb, would you mind running me through what each supplement targets. I'm experiencing some challenging side effects at present and interested in understanding how supplements my help.


  • Runrcrb
    Runrcrb Member Posts: 577
    edited January 2019

    Newy - the magnesium and caltrate support bone health. The body can only take in so much calcium at a time so I take it morning and night to get the full recommended dose. The D is in the caltrate, supporting absorption. I also eat yogurt most days.

    https://ods.od.nih.gov/factsheets/Magnesium-Health...

    There is less evidence on tumeric for joint pain but it's not hurting me so I'm trying it.

    https://nccih.nih.gov/health/turmeric/ataglance.ht...

    Despite regular exercise and targeted strengthening for the alleged root cause of knee pain on the right, it hasn't gone away so I will attribute it to aromasin although everyone says AI-caused joint pain would be bilateral and everywhere. I rarely take pain med (ibuprofen, etc) choosing to ignore/live with the low level (2-3 on the 1-10 scale).

    I find that regular exercise helps with all breast cancer issues - recovery from procedures, side effects of meds, emotional health, etc.

    (The claritin is for general allergies - been taking that for 5+ years)

  • marim
    marim Member Posts: 1
    edited January 2019

    Hi, I'm brand new and technology challenged. Diagnosed with breast cancer 2017. tumors in both breasts removed, early stage (don't remember if 1 or 2) clear margins "the good cancer" as in hormone driven (sorry not totally up on the lingo) Radiation and genomic testing. Did not have chemo due to positive genomic test results of a 10 year window. Prescribed femora. Many side effects. After trying it our for a while I've been taking it every other day to good effect as far as the side effects go, just don't know how this effects the cancer itself. As in does it keep it in check for now. i know this isn't really what your post was about, but I couldn't find the one that was talking about this after i signed up for an account so you were my best choice. Sorry. Do you have any idea if femora taken every other day is of any benefit? What I saw in the original posts regarding this didn't have people saying they had been cancer free for any significant amount of time, so i was curious if anyone had any long range results. I have recently started to try taking it 2 days on 1 off, in the hopes of building up tolerance, but I can already feel the side effects beginning-hence my curiosity. Thank you for your time I appreciate any input you might have or direction you can point me.

  • Runrcrb
    Runrcrb Member Posts: 577
    edited January 2019

    Marim - do you mean Femara? Also referred to as letrozole, the chemical name? If so, it's one of three primary aromatase inhibitors (https://www.breastcancer.org/treatment/hormonal/ar...) - read this article as it might help you connect the dots for its purpose.

    None of us can advise you on taking it less often than prescribed. I can advise you to talk to your oncologist if the side effects are making it hard for you take it as prescribed. He/she may switch you to one of the other two aromatase inhibitors (AI) in hopes of finding you one that you can tolerate. This was how I ended up on aromasin - the arimidex that I started on made me feel tired and lethargic. Switching was a game changer.


  • Moderators
    Moderators Member Posts: 25,912
    edited January 2019

    Hi marim, We welcome you warmly to Breastcancer.org and hope that you find the answers and support here with us.

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