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This is a place where you can write your worries, while waiting for the test results.

Here, I am starting first: this morning I had a biopsy of a thyroid nodule that showed up 3 months ago. I went to do the biopsy all optimistic and I asked the doctor who performed the biopsy what his thoughts were. He said it looks 50-50!!! He seems very nice and knowledgeable from one of the well known hospitals with many years of experience. Right now I am seeing the glass half-empty. Waiting for pathology tests is the worst! Well, the worst are bad news but this one is close to the worst. Anyone had a thyroid cancer after she was diagnosed with BC?

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  • AliceBastable
    AliceBastable Member Posts: 3,461
    edited July 2020

    I haven't, but from what I've heard, it's one of the most easily treated cancers. You might check the thread for cancer with comorbidities - sorry, I can't think of the exact thread title right now.

  • GlobalGal
    GlobalGal Member Posts: 63
    edited July 2020

    Dear Lilly Was Here,

    I ended up with synchronous thyroid cancer and breast cancer.

    Initially, after a nodule biopsy showed papillary thyroid cancer, I had surgery to remove the thyroid along with some central neck lymph nodes. The 3 lymph nodes did not have thyroid cancer, but breast cancer instead. Because of the high position of the lymph nodes in the neck, I am considered de novo stage 4 for breast cancer (no evidence, so far, of breast cancer anywhere else in my body, including my breasts).

    For me, the papillary thyroid cancer diagnosis was not as big a deal compared to the breast cancer diagnosis. The thyroid was removed, I had radioactive iodine treatment a few months after surgery, and take daily levothyroxine. It was all very manageable.

    At first, I saw my ENT surgeon every 2 months, but not since Covid-19 as I have no current issues. My endocrinologist handles the prescription for levothyroxine and associated blood work. We chat by phone, usually every six months.

    Good luck with your results.

    Kind regards,

    GlobalGal

  • LillyIsHere
    LillyIsHere Member Posts: 830
    edited July 2020

    Thank you Ladies!

    GlobalGal, what a story! Do you take anything for breast cancer?

  • GlobalGal
    GlobalGal Member Posts: 63
    edited July 2020

    Dear Lilly Was Here,

    Yes, I take Anastrozole.

    This month I am scheduled for another PET scan, my third. The other two PET scans were clear —as were my breast MRIs, breast ultrasounds, and mammograms.

    GlobalGal

  • LillyIsHere
    LillyIsHere Member Posts: 830
    edited July 2020

    I wish you clear PET scans. What type of BC was found in your nodes? How did doctor explain it? Is it a possibility that your body's immune system killed the BC cells?

  • wallycat
    wallycat Member Posts: 3,227
    edited November 2021

    Lilyishere, I have not seen you update here so thought I would check in. I hope you are doing well.

    I just did a whole panel of labs and will do a urine collection on Sunday to make sure my MGUS is still "just hanging out." Scared is an understatement. The worry never ends. I read someone's post here that we need to get a handle on this since aging is going to bring on a host of "new" things...but I have not managed to figure out a way yet.

  • LillyIsHere
    LillyIsHere Member Posts: 830
    edited November 2021

    Wallycat, thank you for asking. Probably, I wrote it somewhere else that biopsy was negative for cancer and now I am on yearly screening of the nodule to make sure it is not growing or changing shape.

    When did you start having problems with MGUS? Let us know what the test shows and I hope to be just a benign condition.

  • wallycat
    wallycat Member Posts: 3,227
    edited November 2021

    I'm so happy to hear all is well with you, Lillyishere.

    MGUS was an incidental finding on routine annual preventive care labs...so this ick just started in February. Thanks for the good wishes.

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