Tamoxifen

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CL7
CL7 Member Posts: 2

Hi! Looking for woman with similar diagnosis. First stage BC had bilateral mastectomy with immediate diep flap reconstruction. Did not spread to my lymph nodes. Did four rounds of chemo. My oncologist suggested tamoxifen, but I’m not sold on it. Anyone with similar experiences? Thanks!!

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  • NotVeryBrave
    NotVeryBrave Member Posts: 1,287
    edited March 2018

    Pretty much anyone who is diagnosed as hormone positive is suggested to take Tamoxifen or an AI to reduce the risk of recurrence. For those of us who've already done chemo and BMX - it's a big question of benefit vs risk. Your doctors would be the best people to discuss your personal residual risk for BC.

    I took Tamoxifen for 3 months because - even though I had a great response to chemo and should have very little breast tissue remaining - I was afraid of not following through. Even more than the dread of hearing a cancer diagnosis again - the worry of how I would handle it is forefront in my mind.

    I quit due to unmanageable SE's. But many people do well and therefore are rarely posting on here. I would recommend trying it and seeing how you do. We are all so different and you never know unless you try.


  • gb2115
    gb2115 Member Posts: 1,894
    edited March 2018

    Do you know what % your estrogen receptors were? I am a year into taking Tamoxifen and hanging in there. It's not without side effects but I find it tolerable and worth it for metastatic recurrence prevention. I was 100% estrogen receptor positive.

  • beach2beach
    beach2beach Member Posts: 996
    edited March 2018

    Cl,

    I was stage 1, grade 1. No chemo or rads. Straight to implants. Been almost 6 months on tamoxifen. Side effect for me is minimal, dryness effect. No hot flashes like others have, which is usually a top side effect. For me, I see it as another thing I can do to hopefully prevent a recurrence. No guarantees but not many things have. For many, like the op above, the se's are intolerable. If that's what is worrying you, you won't know how your body reacts to it, until you try. You may have none.

  • EastcoastTS
    EastcoastTS Member Posts: 864
    edited March 2018

    I've been on Tamox since May. Few SEs. Mild in any case.

    Try it and see. Some have issues, some not so much. I was nervous and waited a little to take it -- wish I had not waited any. It's my security blanket. (maybe)

    Good luck!

  • edwards750
    edwards750 Member Posts: 3,761
    edited March 2018

    I took Tamoxifen for 4 years and Arimidex for 1 year. Oncologist switched me because Arimidex attacks the bones and I was borderline osteoporosis. I am 6 years out last August. I was Stage 1b, Grade 1 IDC. I had a lumpectomy and 33 radiation treatments.

    I had occasional hot flashes, lack of concentration and joint pain. Tolerable but at times the joint pain was brutal.

    I too was afraid not to take it plus it was my extra insurance policy. Admittedly, if the SEs had beenintolerable I probably would have stopped or maybe tried another drug.

    I didn't want to look back and say what if...

    Diane


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