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Bottle o Tamoxifen

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Comments

  • Lomlin
    Lomlin Member Posts: 116
    edited October 2018

    So in reading about this tamoxifen, it sounds like it progressively gets worse with the side effects? I am only on my 3rd bottle, so 60 pills or 2 months new into this medication. I have pain in by breast where the surgery was and where the radiation was and keeps moving around, but just in that area.

  • beaverntx
    beaverntx Member Posts: 2,962
    edited October 2018

    Lin_lin, when I saw my BS about 8 months after my lx and told her my breast and axilla were sore she did a thorough exam and then said "that tissue has been through a lot over the last few months." I took this to mean the soreness was within the range of normal reactions as past experience has shown she moves quickly when something is of concern (as in my surgery was 6 days after my diagnosis). So I suspect your breast pain has more to do with your other treatments and the healing process than with Tamoxifen. As runor said it is a challenge to identify whether new aches and pains etc. are SEs, normal aging or something else. Hope your pain gets less and less.


  • runor
    runor Member Posts: 1,615
    edited October 2018

    Lin-Lin, I agree with Beaverntx, it is not likely that tamoxifen is causing breast pain. I also have pain in my breast, armpit (axilla), side, and ribs. It's lymphedema. Those tissues are flooded with fluid (lymph) and by the end of the day, I hurt. Sometimes my boob is hard as a rock and I have to massage and rub and stretch to get things flowing and overnight the swelling goes down a bit. But sometimes, overnight, the swelling gets worse. I never know which way it's going to go. But this problem existed before tamoxifen. This is lymphedema. It even shows on ultrasound. The tech commented "Wow, those tissues are loaded with fluid!" And it hurts.

    I suggest you look up some posts on lymphedema and I'd post a link to one but I am bad at knowing how to do that. Maybe someone else can.

    Thanks Catkin, I will give that a read!


  • rah2464
    rah2464 Member Posts: 1,192
    edited October 2018

    Runor you gave me such an "aha moment" this morning with the comment about how the foobs hurt and change throughout the day and with activity. I am seeing my medical massage therapist on Tuesday (I call her the foob massager) so I will discuss with her. Maybe she will have some ideas or techniques to use. I am going to her to try and loosen some of the surgery scar tissue in there but I just bet there is lymphedema as well. I am sorry for your first hand knowledge of this issue, but I am so thankful for your honesty in sharing what you know. The strength of the ladies on these forums humbles me.

  • rae7200
    rae7200 Member Posts: 23
    edited October 2018

    If it's lymphedema, you want to be seen by a PT/OT trained in lymphedema. There's a lot of info in the lymphedema section here in BCO. I was recently diagnosed with “edema" in the breast (caused by surgery and radiation), and the PT I spoke with on the phone said it's almost certainly lymphedema. She opined that even a lot of medical oncology personnel think lymphedema is in the arm, and it's edema every where else. My evaluation is this coming Thursday, 10/25. I've been doing some abdominal deep breathing 4-5x, a couple of times/day for the last couple of days, at the suggestion of one of the ladies here, and noticed an immediate improvement. Good luck to you!

  • Lomlin
    Lomlin Member Posts: 116
    edited October 2018

    Runor, thanks for this info about the lymphedema, so just this morning I massaged the area and boy did the pain reduce by almost 50%!! No doctor mentioned to do this, I am surprised, they are all worried about how much to lift to cause the lymphedema, which now from this forum is not limited to the arm, that they don't say to massage the area.

    Rah, yes share the techniques here from your massage therapist, I'm sure it would be help.

    Rae, thanks for your info too, I do the abdominal breathing as well, I read that somewhere probably somewhere on this website.

    Okay as far as the tamoxifen goes, and aside from the boob pain, it seemed I didn't word it right (I know the tamoxifen doesn't have anything to do with boob pain), does taking tamoxifen over time, do you get more and more SE's from it, or are you clear after a few months. It seems now I get anxious/ansty and the mind is all over the place, I jump on a stationary bike to work off the anxiousness/antsy.

    Thankful to have found this group!

    Heart

    Lin

  • GoKale4320
    GoKale4320 Member Posts: 580
    edited October 2018

    https://www.healthline.com/health/how-to-perform-l...

    Here's a link to manual lymphnode drainage (MLD). There is a lot of information online about this so if this link doesn't work for you, you can google other tips. I have lymphedema in my arm and I benefited greatly from a PT who specialized in breast cancer patients and lymphedema. She worked on my lumpectomy scar tissue and worked out the cording in my arm which reduced my pain to nothing - so really PT, exercises she assigned me, and time helped me.

    Some on here have mentioned deep breathing, PT, MLD, stretches - all that really helps. Compression sleeves and other compression garments help. I am able to use KT tape on my arm to control it - thanks to my PT for showing me how to use it.

    Some can get it under control and can forget about it for a long time. Some have to stay on top of it always. I am one who has to keep working with stretches, MLD, KT tape and diet to keep it under control. Fingers crossed it continues to work.

  • Lomlin
    Lomlin Member Posts: 116
    edited October 2018

    Thanks GoKale, very helpful, nice that there were short videos. I wish my doctor would have advised me about doing these exercises.

  • MelanieK1111
    MelanieK1111 Member Posts: 1
    edited October 2018

    First time here. Diagnosed 6 weeks ago er/pr+her -. Had mastectomy 2 weeks ago. Oncologist said tamoxifen, 46, never been sick a day in my life. I’m reading all these side effects and scared as hell, wondering if it’s worth it, and realizing that my life as I knew it 6 weeks ago will never be again. WOW.

    I know I’m lucky, only stage one, no chemo but this still sucks. Scared to start taking it, and scared not to.

    Thank you all for your advice and posts. Been quietly reading since diagnosis. Good luck to us all

  • Skiboots42
    Skiboots42 Member Posts: 20
    edited October 2018

    Melanie1111: I am right there with you. Stage one and was told I did not even qualify for an onc score, 2 mm of invasive and the rest DCIS. I have been on tamoxifen for 4 months. I have not experienced any of the physical side effects, but feel more tired and short tempered. I am trying to change my perspective and be more positive in mind set. My husband and I have decided to give it a year, if it is difficult for my family to be around me than I will most likely stop, but am tying many different natural ways to increase serotonin and dopamine. Changed diet, more excercise, more outside time, and meditation. A lot of folks do just fine on the medication. I think those who have side effects are a little more verbal. It definitely is a personal decision and everyone’s perspective is different

  • runor
    runor Member Posts: 1,615
    edited October 2018

    Lin-Lin, I have been on tamoxifen 14 months now. Here is what I find: sometimes symptoms come in waves. I will have several weeks of terrible night sweats. Then none. I will have terrorizing leg cramps for three weeks. Then they quit. I'll be constipated randomly for a week, then I'm fine for a couple months until it happens again. My falling out hair and chin hairs like cables are pretty steady though. Honest, finding one of those chin hairs and giving it a twang with your fingernail is like plucking a guitar string! I never find them at home in the bathroom, either. No! I find them in the truck, just before I have to go see someone, that's when I feel one of those thick monsters sticking out like a big, black spider leg. And I never have a tweezer or a mirror. So you try burning it off with a lighter, which is a seriously bad idea. Then HUb asks what you're doing and you point at your chin hair all in a panic and he squints and looks and turns your face this way and that and says he can't see anything, you're imagining it, you look fine, wait, HOLY SHIT! will you look at the size of that thing! And then you cry.

    Yeah. Tamoxifen. You never know what's coming!

  • sm627
    sm627 Member Posts: 142
    edited October 2018

    thank you all for your support this past week with all my emotional ups and downs it means so much to me. Sending you all lots of hugs and love and hope you have a good week. Tamoxifen side effects took a backseat today because PMS was in the driver's seat. LOL

    So I met with a new gynecologist this past week. She asked how long I was on tamoxifen for she said that some of her patients are on it for their whole life. I thought to myself would want to be on this s*** for their whole life?? 5 years is long enough for me. Have any of your doctors mentioned taking tamoxifen for your entire life.

    Cheryl I couldn't find the gas mask. But I think I found something else that might keep the preschool kid germs off me. I plan to put this around every child that coughs on me.

    image


  • vl22
    vl22 Member Posts: 471
    edited October 2018

    sm627 - my onc said I should be on ten years - it’s been almost 8 months and I think of quitting every day! As I sit here now I am in a pool of sweat!

    As rumor said, I feel the side effects come in waves. I’ll have a day where I think that maybe I’m on the other side of them, but then BAM!

    I didn’t get an Oncotype score because I also had a TN tumor which automatically signed me up for chemo. When I plug my stats for the grade ER+ tumor in Predict, I get the results that in 15 years taking tamoxifen helps me by like 1%. But this only shows mortality rates, not recurrence. So why am I taking this crap? I struggle with it a lot.

  • Lula73
    Lula73 Member Posts: 705
    edited October 2018

    VL22- you take it to keep the recurrence from happening because if it does recur it’s typically at a different stage which changes those mortality rates significantly. Tamoxifen reduces risk of recurrence by about 50% during the years you actively take it and by about 33% for the 5 years after you stop taking it. My MO recently upped my Wellbutrin from the 150 I’ve been taking for years to the 300 mg dose to help with libido and hot flashes. Hot flashes were worse for about 10 days then all of a sudden they decreased in number and severity. Ask your MO or PCP for help with the flashes. If you’re having mood swings or seem to have a shorter fuse of late he can help with that too.

  • Lomlin
    Lomlin Member Posts: 116
    edited October 2018

    Runor, ah that explains a few things, you just never know what side effect is going to pop up on you taking this medication. One day I feel like conquering the world and the next I just want to be left alone.

    I went to a Wellness House here in Illinois and joined a breast cancer group, a very nice bunch of ladies with lots of info to share, that helped and then got me sad.

    Anyone have any SEs from Tamoxifen with your eyes?

  • Nancy618
    Nancy618 Member Posts: 318
    edited October 2018

    I haven't been here in several weeks and I am terribly behind! I'll try to summarize where I am briefly , but I'm not promising.

    I was only on tamoxifen for 5 days before I started getting what felt like menstrual cramps. I'm post menopausal for many years. Each day they got worse. Finally, after 5 days of pain, called my mo. Nurse said to stop and scheduled me for an ultrasound. After about 10 days off, the cramps stopped. Ultrasound essentially normal, with upper limit of uterine lining thickness. Sent to a new gyn, who said she's never heard of cramping as a side effect of tamoxifen. Exam showed nothing abnormal. Advised to try the tamoxifen again and to try and tolerate the pain if it returned because sometimes the body will get used to it.

    Today is day 5 back on the tamoxifen. I didn't even realize it until... you guessed it... cramps started again. I am taking Advil and trying to suck it up. I don't think that daily all day pain should be part of the deal.

    Lin Lin, you asked about eyes. On the other AIs, I got dry eyes which resulted in double vision in one eye. Drops at night and a night mask helped some.

    I forgot who here, but they recommended calcium gluconate rather than calcium citrate. I actually did some research which said calcium malate is best for calcium absorption and osteoporosis as well as high BP and high cholesterol. I still have a bottle of liquid magnesium and calcium citrate that I have to use up. I don't have any intestinal problems on it. I saved the article I read explaining it all, but I can't find it. 😕

    I'll have to read all the posts and reply... Just wanted to update.

  • runor
    runor Member Posts: 1,615
    edited October 2018

    Lin-Lin my eyesight has gotten TERRIBLE! To be fair, prior to this cancer crap I had the typical after 40 decline in my vision. But the failing eyesight since taking tamox is like a runaway train. I remember eye doc saying not to get glasses yet, to ride it out with cheater glasses until the decline stopped - yeah, where? Total blindness? I have cheaters everywhere and hear myself asking people in grocery stores or drugstores, dear, can you read this for me? Oh my god.

  • shelabela
    shelabela Member Posts: 327
    edited October 2018

    my eyesight has gotten worse also.

  • Lomlin
    Lomlin Member Posts: 116
    edited October 2018

    So how soon do you see the decline in the eyes? I have been wearing glasses since the age of 10 and am farsighted, which typically people get as they age. Are cataracts part of some of the side effects? I went to a support group and a woman there had a different side effect from it, not dry or cataracts but something she got that ended up in the eye, and for the life of me I can't remember what it was, so not helpful here. LOL.

  • trvler
    trvler Member Posts: 931
    edited October 2018

    Ok, so I have a question. Let's say you start Tamoxifen 4 years before you would have gone through menopause. So as time passes and you get closer to menopause, should the side effects (hot flashes) wear off because the difference between your natural estrogen level and you tamoxifen induced estrogen level grows smaller? Does this make sense to ANYONE?

  • runor
    runor Member Posts: 1,615
    edited October 2018

    Trvler, I think I understand your question. I think.

    How to give you my non-scientific, unresearched, not valid opinion and make sense?

    I think that whether you are making lots of estrogen, or only a little estrogen, tamoxifen allows your body to use NO (or close to none) estrogen. Whether you produce estrogen or don't, tamox keeps you at the same usage level (zero).

    If that is the case then no, natural menopause is not going to lessen the side effects. Tamoxifen does not stop you from producing hormones, it blocks some cells ability to use that estrogen. So how much you make, or don't, is not the issue.

    Having said that, for reasons I am not clear on, postmenopausal women are often put on drugs other than tamoxifen. So maybe a reduction in estrogen production means that you change meds to a more effective one, but it does not mean that the side effects of tamoxifen become less.

    I have read this post. It makes no sense. Ignore it.

  • Lula73
    Lula73 Member Posts: 705
    edited October 2018

    runor, you did a good job on that explanation! I’ll clarify the fuzzy parts... tamoxifen attaches to the estrogen receptor on specific cells in your body preventing estrogen from accessing the receptor and entering the cell. It does not do this on all cells in the body, just specific ones (that’s why the uterine lining thing is an issue). And because it’s blocking that estrogen, you likely will find that your blood estrogen levels will rise as it’s not being utilized at the same rate anymore. This rise does not overcome the action of tamoxifen but may make your blood stickier and in a handful of cases result in blood clots (hence the blood clot warning in the label). With the blocking you will get some side effects of menopause but not all of them because of the cell specific way it works. Bone loss seen in menopause is a prime example as tamoxifen does not promote bone loss. So in the end some symptoms may pear at menopause that weren’t there before, some may disappear, and some may stay the same.

    The difference between tamoxifen and AIs: First we have to understand where the estrogen comes from - 80% of our estrogen comes from our ovaries, 20% of our estrogen comes from a process of androgens (released by our adrenal glands) being converted to estrogen in our fat cells by an enzyme called aromatase. Now we look at how each medication class works: tamoxifen blocks estrogen receptors; AIs inhibit/prevent aromatase from working to convert the androgens to estrogen. Since AIs only stop androgen conversion and does not impact ovarian release or action of ovarian estrogen, it is only effective in post-menopausal women.

    Why use an AI vs tamoxifen? In several head to head clinical trials, AIs were shown to be significantly more effective than tamoxifen by about 13% in post-menopausal women. This was duplicated in a subsequent study in ladies who had their ovarian action suppressed who took an AI as well. With new data showing 10 year use of tamoxifen/AI to be more effective than 5years, these studies will be relevant to more and more women. Hope this helps!

  • sm627
    sm627 Member Posts: 142
    edited October 2018

    Okay so today Tamoxifen wasn't to bad. I hope it is on its best behavior for tomorrow morning when I go in for my breast MRI and then the following week when I have my pelvic exam.

    Oh joy these tests sure are fun NOT LOL

    Please send good thoughts to the boob gods for me.

    Hope you all are doing well.

    Hugs and Love to all,

    Sara

    Heart

  • vampeyes
    vampeyes Member Posts: 523
    edited October 2018

    Hey Sara, so glad that the big T was behaving for once, fingers crossed that this turns into a pattern for you. Good thoughts have been sent! xxx

    Runor you crack me up! Do you have a blog, if not you should start one. ;)

  • rah2464
    rah2464 Member Posts: 1,192
    edited October 2018

    Lula73 thank you for your great explanation of how our little white pills works! I know I am counting down each bottle of 30 I finish.

    Sm627 sending up a little prayer that the boob gods are kind. Wonder what that boob god looks like? Hmmm

  • scrafgal
    scrafgal Member Posts: 413
    edited October 2018

    just to add to the excellent AI and T doscussion, because of how AIs work vs T, taking an AI before menopause actually increases BC risk. I might switch to an AI in December after one more hormone test for menopause. I had a partial hysterectomy a few years ago but I still have ovaries and was nowhere near meno when I was diagnosed at 50. Just turned 52 and have been trending toward meno since chemo ended. We need to be sure about my meno status and before making the switch. Some o c assume that all 50 year olds should go on an AI but it's all about meno status not age.

  • Dmoore39
    Dmoore39 Member Posts: 5
    edited October 2018

    That's interesting about the decline in eyesight. I just had my eye exam and my right eye has really gotten worse goi g from 1.5 last year to 2.0. My lef eye has stayed the same at 1.25. I have been on T for a year. So strange that it's just the right eye though. I'm 41. Oh, and I've noticed reading on my phone is a little blurry. Dr said it's not quite bad enough to correct it unless it really bothers me. I told her I probably just need a new phone ; )

  • princessbuttercup
    princessbuttercup Member Posts: 161
    edited October 2018

    Has anyone had tamoxifen joint pain decrease from exercise? I have been walking most days in the hope that my joint pain will improve, but it seems to be getting worse. I started tamoxifen in June. I was advised to add vitamin D3, which I have, and I also take Gabapentin at night.

    Buttercup

  • trvler
    trvler Member Posts: 931
    edited October 2018

    Runor: Lol. No that makes sense. Sooooo.....hotflashes would not be a symptom caused by reduction of estrogen, but estrogen somehow attaching somewhere which would have previously prevented hotflashes?

  • trvler
    trvler Member Posts: 931
    edited October 2018

    Thanks, Lula!