on tamoxifen 1 month, going crazy help
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Oh Robyn, I'm SO very sorry that you had the same symptoms too on Tamox. Just one awful medication as far as I'm concerned. You know what I found interesting and I don't know if it was coincidental, but the SE's happened right went I got my period one month after I started the Tamox. The SE's kept up after that. I think it definitely screws up the hormones BIG time. I wish you well in your recovery and please keep us posted too.
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So is there anyone out there taking tamoxifen and not having problems? I am suppose to start soon. What are the other options? I have appt with ongologist to get prescription and will talk to him too. All this is so scary! I hope those of you having problems find relief very soon!!!!
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I did it for 5 months, entertained suicide every other day, my relationship with my 9 year old daughter fell apart because the energy I emitted was horrible, I didn't know who I was, stopped taking it 3 weeks ago, and now feel incredible. Told my onco after arguing with him 3 times that I am done with this crap. I got a lupron shot yesterday, and I will start femara in a month. My butt hurts, I had a hot flash, big deal.
Don't take tamox if you feel that bad after 1 month(like me!) because it only gets worse.
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I took Tamox for 8 months. I was depressed, angry and anti-social. I had gained almost 40 lbs (since dx, surgery, chemo, etc...) and had absolutely no energy. I stopped taking tamox after my first post tx appointment (had finished 12 months of Herceptin) and started feeling better, emotionally, almost immediately. I was also able to think more clearly.
In Oct I was dx'd with a new cancer (Thyroid), had a partial thyroidectomy and started taking natural supplements. I am so tired of cancer and all the gifts that it brings,
I just saw my onc a few weeks ago and had to tell her I quit taking the tamox. She was very upset with me. The first thing she did was pull up the online tool and advise me that without tamox I had a 11% change of recurrence, with tamox my rate of recurrence would drop to 6%. I asked her if those figures included the fact that I had a year of Herceptin and she said 'no' we don't have statistics yet for early stage bc and Herceptin. I think she is more worried that I am going to skew the trial results for the clinial trial I am on then she is about my quality of life.
I do not believe that 5% decrease in recurrence is worth living with the depression, aches and weight issues. I am at peace with my decision to stop the tamox. My husband and family support me as well in this decision. I am now trying to lose weight, improve my diet and exercise as a way to fight recurrence. I am also researching bio identical hormones and finding a way to balance my hormones naturally rather then depriving my body of hormones that it needs to stay healthy.
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i have been on Tamoxifen since August. Other than a few hot flashes, I haven't noticed any SEs. My onco told me that most of her patients did not have SEs but that with those who did, it typically settled down after a month. If it were me, I think I would give it another month to see what happens.
I'm sorry you have having so many issues.
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crazykitties,
is femara an alternative to tamoxifen? i am so leery to take anything after my reaction to the tamox, reading the "s" word
in your post made me feel i was in good company. i remember before all of this thinking people who committed suicide were so selfish but i remember being in the midst of it thinking, people who love me would NOT want me to feel like this.......so crazy what it does to the wiring in our brains. please keep me posted with the se's on your femara and my best wishes to you!! xxoo robyn
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o2bhealthy!
it is so weird you mentioned bioidentical hormones.........i just bought suzanne somers BREAKTHROUGH and it's about bioidenical hormones, supplements, diet and more. i AM going to try it, looking for a dr. locally who can do the testing. there are so many success stories w/people going through a more natural treatment. my appt. w/my oncologist is next week and i'm anticipating him wanting me to go on ANOTHER cancer med but i'm leaning towards NO
there is a lot to be said about the QUALITY of life. thank you for your post and please keep us posted. my wishes and prayers to you! xxoo robyn
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3monstmomma,
i think you are in the majority and most people do not have such severe side effects but unfortunately i was in the minority here. i was literally incapacitated and could have have lasted another day on tamox. i am so happy you did not have those se's but i think, depending on the severity of the se's everyone has to make that individual choice. it is DEFINATELY not for me
i do think even if i were warned about the small percentage of people who experience these severe se's i would have tried it anyway, i would have thought "well that won't be me" but the odds were just against me in 2010! best wishes to you! xxoo robyn
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I AM in the minority, I have ADHD and FIBRO---I do not react well to many meds. I am not against treatment---in fact, I have been quite logical about the whole thing. I cannot stand to debate with stupid people who claim that doctors know nothing, blame them for lack of prevention, when clearly WE know what to do for prevention, many of us have done it, and we get sick anyway. I don't blame my docs for anything except the fact that most of them don't want to hear when treatments don't agree with us.
The crazy thing about tamox is I lost 20 pounds and my sex drive came back. I also wanted to die. That is NOT ME. I have always had medium depression---I was and still am in treatment for it, 10 mg lexapro, 15 mg buspar at nite. But this was over the top, so horrible, I could not see how I would survive 5 years, let alone, I could not live with hurting my daughter emotionally. THAT ISN'T ME, and I am so glad I stood up FOR ME, MY FAMILY, and for the greater good. You will find your way, all of you!!!
I NEED to go into menopause---my mom had her period until age 60! I will be 50 next week. These SOB ovaries are not going down easily. I feel like this is the right thing to do. Also, Femara does not have depression as a side effect. I can live with physical pain, but depression is worse than anything.
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robyn - I had heard an interview by the author of 'Hormone Harmony' on one of my FB support group forums. I was really intrigued by what she had to say about bio identical hormones and BC. I looked up a physician through a website she recommended http://www.bodylogicmd.com/
I am saving up for the initial consult and lab work (they run saliva, urine and blood tests to determine where you are hormonally and have a compound pharmacy on site). The initial appointment in my area is....gulp...$395 and it is not covered by insurance. I was never real big on alternative medicine (my mom is very 'alternative' and had really turned me off). However I am now more open. We actually found my thyroid cancer through thermography since I wanted some kind of scan to verify my onc's NED dx and she would not order a PET or CT scan.
I think the dx of thyroid cancer immediately after finishing BC tx really made me sit up and take notice that maybe I should be looking at a more natural approach, I'll let you know how it goes. My 40th birthday is next week and I plan on being around another 40+ years
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o2bhealthy,
why isn't the appt. covered by insurance? i hadn't even thought of that........argh more $$. i'm going to have to check out if it is covered on my policy. i am like you, in that i was never into "alternatives", my mantra was, if a pill will fix it give it to me! the more i read the more i like it but it's easy to get overwhelmed with the all natural approach, makeup, fillings, organic everything. i really don't think i can do all of it but i'm going to do what i can, baby steps. i dooooo like a glass of wine a night and most of what i've read says a glass of red is okay, thank GOD!
i had gone to a place in torrance, california that was into natural meds and they had a pharmacy on site, i kind of felt like they pushed a lot of VERY expensive items on me and i stopped going there, i just think i would be leery of that??? please keep us posted on your progress, thank you! xxoo robyn
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crazykitties,
i totally agree w/everything you just said! i WAS on paxil for about 7 years? went off of it 2 years ago and lost 20 lbs immediately but i was on it for anxiety, not depression. i'm trying to get off all meds, besides the armour thyroid i've been on for 20 years........please keep us posted on your meds and progress, thank you so much for responding! xxoo robyn
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I've been on Femara since August 2010, now on Jan 23 stopped because of intolerance: strong non-stop headache, impossible to bend, no sleep, loosing memory, loosing vision, weakness, hypertherios, start feeling of depression, felt very unhappy. Though, hot flashes were tolerable, no muscls or bon pain. Just stopped - the headache reduced and my mood is up. I called to my dr, he prescribed Tamoxifen! Not started yet, very scared by your experience. But yesterday went for the first time for the acupuncture. After one treatment felt rather happy and very active, laughed a lot with naturopat, but couldn't fall asleep that night.
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Best wishes to you on Tamox, I have an appt. w/acupuncturist next week also but I'm going off all cancer meds, I feel great. Well a little sore today after getting TE's yesterday but nothing compated to the SE of all those meds. Best wishes to you!
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Goodness I am supposed to start Tamoxifen probably in April. These posts have petrified me!
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Hi Letlet: I'm so sorry that this board scared you but please know that the SE's we have experienced happen to a very small % of women. Please give the medication a chance...the odds are on your side that the med won't be a problem for you. If it is, you can always decide to stop taking it or try taking a med to counteract the SE's.
Crazykitties, I completely related to your comment about menopause going on forever. I'm 53, going to be 54 next month, and I'm still getting my periods regularly. My ovaries are just chugging along and don't want to stop. Like you, I know someone who got her period til she was 58. My goodness though...60! That's a long time.
Di
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Robyn I just found this thread again, I'm SO SO pleased to know you're on the mend, I thought Something Awful might have happened. You sound so much happier and with your mind made up now, stick with it and good luck!
I'm one of those who could maybe have predicted bad results from a hormone treatment, as i had very bad postnatal experience needing five weeks in hospital. They warned me then to consider my little family complete, avoid the Pill and HRT and to expect further disturbances at menopause - which I never quite got to yet, as they didn't predict the BC! But i'm going to have to let it run naturally even if it does raise the BC recurrence risk, life has to be tolerable in the meantime.
Travelgal, yes my mom went on til 56 but she had the benefit of HRT to get through the worst, I can't now go that route. And she got osteoporosis anyhow. I'm also not keen in the removal of non-tumourous bits and deciding to find out more about bio-identical hormones, not sure whether they are available over here. Doctor, healthfood store??
Sheri56: No, many women get along fine on Tamoxifen, (or adequately, or their onco's have scared them into it) what you see on this thread is a gathering of those of us who didnt, sharing bad times and looking together for workable alternatives.
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Letlet- My SE's from the tamox were not 'horrible' I am just choosing to look at alternatives since I have been dx'd with a 2nd cancer (thyroid). The thyroid and our hormones work in a delicate balance and I feel that I would benefit from looking at a more balanced approach. There are many, many women who have little to no SE's on Tamoxifen. I think that on this thread you will find more negativity as we come here to commiserate and talk about alternatives.
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Few things: for starters, I stuck with Tamox and am on month 3. My SEs settled out, no more issues with depression, or TMJ. I am sober about the long term effects, though.
I'm confused, and would love some feedback. I understood that the Oncotype score can be doubled without Tamox/AI. I had 8%, without Tamox, my recurrence over 10 is 16%. This is markedly different from the 4 or 5% advantage I see with gals with similar profiles whose doctors have told them these numbers.
Who is right? 16% is not 5%. There are HUGE differences in risk and choices with that margin for me. It also means different choices if it turns out I'm in menopause and they want to put me on an AI (I feel pretty firm that 40 is not the age to begin an AI, but if we are talking 16% advantage, it's another story).
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MHP70 - I am not sure what your specific markers/dx is however many statistics come directly from the research provided by the manufacturer of Tamoxifen. So if anything, it may exaggerate the benefit and downplay side effects.
You can go to this site http://breastcancerchoices.org/tamoxifen which explains how the manufacturer's studies came up with the numbers.
or here where they just give you the numbers http://www.druginfonet.com/tamoxfen.htm
I found both to be helpful in making my decisions regarding risk/benefit re Tamoxifen
edited to thank and acknowledge mathteacher for the links to these studies
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Thanks o2bhealthy and travelgal...I will cross my fingers then
)
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Thanks for those links, they were interesting. These findings pre-date Oncotype, which is a good thing for some of us, and not so good for others. The survival reviews were everyone lumped in, regardless of genetic idiosyncrasies revealed now by Oncotype for ER+ patients. How Oncotype arrives at a "50% reduction in recurrence" by taking adjuvant hormonals is a mystery to me. It's also totally odd to me that it would be straight across the board--equally effective in those with high and low Oncotype scores.
If we use some common sense, the answer is probably somewhere in the middle. Tamoxifen probably gives me somewhere between 3.5 and 8% advantage over 10 years. But there is another factor, and that is Tamox/AIs also are preventative in new primaries. And unfortunately, BC patients have a whopping cumulative 1% a year risk of a new primary. Everyone's so focused on recurrence they often overlook that little secret.
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My SE's went away w/in 2 weeks of stopping it too but in retrospect 2 weeks doesn't sound that long but it was the longest 2 weeks of my life. I just wish I was given the opportunity to know the SE's, all I was told was I might experience "mood swings and/or hot flashes" I'm 50 and haven't gone through menopause yet. I was only on tamox for one month. My next appt. w/my oncol. is next week, I'll let you all know what he suggests.
Had TE's put in Thursday, sore and keep hearing this liquid squish around in my breast area, very strange
I definately don't want them bigger than they area already, wondering if he can take out some of this liquid. I started out with DD's and now would prefer a full B, no neck pain, dented shoulders from straps, I LOVE my little boobs!! Best wishes to all of you here, don't know what I would have done w/out this board some days! xxoo Robyn
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Robyn to give you a pointer what to research before you meet the oncologist next week, the likely alternatives to tamoxifen which the onc may suggest in combatting oestrogen, are Arimidex or other Aromatase Inhibitors (AI's) combined with a monthly injection to suppress your ovaries temporarily I think that's called Zoladex, or else knocking out the ovaries permanently either by surgical removal (oopherectomy) or destructive radiotherapy (ablation). I willing to bet a silver sixpence he won't mention any natural ways to reduce your oestrogen, but that's the course I personally have chosen - diet & exercise. My feeling is that any synthetic way to reduce my body chemistry, will have the same effect that Tamox had on my brain. Even if i get a recurrence doing this i still won't regret having fought to get my brain and my quality of life back. But that's just my pig-headed choice. If you're interested, have a look at the Natural Girls thread and the Alternatives & Complementaries area. Also if I do now get a recurrence, i figure it's likely to be ER+ again, whereas any recurrence you get while on oestregen blockers is much more likely to be ER- and harder to treat. Just my disordered thinking!
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hymil,
i like your way of thinking, a LOT more than all the dr's i've talked to
i will tell him what you said, i definately want to go the natural route. thank you for the information and i will def check out the natural girls thread, i've been there before and it makes a lot of sense. i need to get my hormones checked next since all of my out of pocket $$ is spent this year, the rest of the year is free for medical, yeah!
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While I'm generally of the mind that diet can't keep us from getting cancer in and of itself, I do believe exercise is super-important. I'm trying to do physical activity every day, has anyone else found fitting it in difficult? I am really trying. 1/2 hour a day, nothing crazy. Just something: walking, swimming,running, biking, weights, pilates. The studies seem to indicate that cardio (that usually won't include things like yoga and pilates) regulates hormones. It also does a million other great things.
If I had to step off Tamoxifen, I would feel like I was doing something protective with exercise. I'm not convinced that cutting all sugar and alcohol, for instance, is going to cut it. I was a long-term vegetarian who ate pretty incredibly for 20+ years. Sadlly, that didn't seem to help when compared to the life I've lead (exposure to 9/11; grew up in worst toxic landfill nationally--perhaps these were part of the trigger).
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Trying really hard with the daily exercise. It is hard to fit it on top of work, cooking and the other necessaries of life. I think we need to re-align that as part of the new normal, this now Is one of those necessaries. At the end of the day, anyone can take the clothes to the launderette for me or get my groceries if I made a list, but only I can do my own exercises.
I got under the weather with a winter bug and missed two whole weeks at the gym and now Yuk, how sluggish I feel without those endorphins! Even the feeling of empowerment and control you get is a kick. Just waiting for the catarrh to clear up, I can't seem to roll from side to side to clear the sinuses the way I used to and still get the lymphoedema to drain the right way - Argh. Apparently this will get better once the exercise has me breathing deeper again...
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and Robyn, good luck with the onco. The cynic in me says they push pills because there is profit in them and because they don't beleive you will stick with the exercise diet thing. Feels like If it works for more than 50% of patients they prescribe it for nearly all and maybe 40+% of us might be really struggling for no benefit.. Well, if I know that I personally will struggle to a level that stops me personally from functioning the way I need to (and he hasn't seen the dire state of my house, had to live with my moods and outbursts or heard the latest opinions of my boss!) then I can make a choice for the one that matters to me, which is me! I see mine again in a few weeks and I just KNOW he will say, And now lets talk about stamping out these hormones of yours....,. Well i decided i don't want to be part of their big experiment, I know how i felt before and Im not going there again. But do give it a fair lookover before you reject a drug that does work for some poeple.
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Hi Gals....I've been posting on another thread...."Bottle O'Tamoxifen for over a year, and maybe if you check on that thread, you will find a lot of answers....It's like this thread, all about Tamoxifen & all the SE's or lack of...
Or just click my name, & follow the Tamoxifen thread....
I've been taking it for over a year, & doing good! And it IS supposed to help keep us safe. The Al's are a lot harder on our bones & joints than Tamoxifen. The T pill works differently than the Als, so we still have our hormones running around in there, where-as the Al's block your Estrogen.
There are also a lot of different ages taking Tamoxifen...I'm probably older than most of you, but I ASKED to take Tamoxifen, instead of Femara or Arimidex, & so far, so good....
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Hallo Chevyboy! Yeah, I found the other thread and it's 348 pages long, I can't even find my own posts there! Glad to see there are so many women over there doing so well on this drug though, we may well be in the minority, struggling here. Tamoxifen doesn't have the same effects on all of us, and for some the mental side-effects of knocking out the natural hormones is just unbearable. Maybe the AI's woudl be less bad in this respect who knows, but Robyn and I and several others here are too young for them without additional messing around; you can come back to tamoxifen but we can't get forward to the AI's. Tamoxifen may feel gentler for older ladies and I respect that and am very glad to hear it, but it runs chaos through your hormones if you are premenstrual. That's partly why I take my approach that if i do get an ER+ recurrence well i will probably be post-men by then and less upset by tamoxifen.
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