LCIS: should I take Tamoxifen?
LCIS diagnosis May 2017 followed immediately by lumpectomy. Since then go to Sloan Kettering 2x/year (mammo in Dec and June ultrasound). So far so good. Can’t decide if Tamoxifen is worth it - I do long (6+ hours) flights every three months so worry about blood clots and other side effects. And definitely worry about ten year outlook - docs tell me LCIS can mean cancer takes a long time to show up but if it’s lobular it’s harder to treat. Frustrating that so little known about LCIS. Thoughts on taking Tamoxifen? Anyone with an LCIS diagnosis more than five years ago? Thanks
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Cancer sucks! The disease itself is dreadful; and then we get to take medication that has dreadful side effects! Life is hard, but it’s better than the alternative…. Unfortunately there isn’t a cure yet and our only alternatives are medications with unpleasant side effects. In reality though, even with unpleasant side effects, these drugs are better than recurrence of breast cancer. There are many other diseases and difficulties that people must face.
I don’t know anybody who doesn’t have hard challenges. Thank you to everybody on this site for supporting one another!
I actually don’t get to see an oncologist. I am being followed by a oncologic surgeon who feels that after a double mastectomy for LCIS, the risks of tamoxifen is greater than the benefits. But the oncology Nurse Practitioner who I was finally given to see in the oncology department suggested tamoxifen at low dose as an extra layer of protection.
Hi! Are you finding good patches? These are my concerns as I will probably take tamoxifen in the future since my cancer was highly hormone related. I have a few months to 50 and was not yet menopausal, but just started chemo, and then will likely start hormone blockers after that. Not excited about all the possible issues due to eliminating estrogen. But, like you said, preferred over cancer. Thank you for sharing.
I was never able to take the hormone blocking drugs (tried 'em all) but I was post menopausal at the time of my bi lateral mastectomy and I do think that's a strong factor. I am close to 8 years from my surgery and no recurrence of cancer!! Very grateful. I will say that many of the drug side effects have happened over time anyway, gradually (joint pain, vaginal atrophy, hair loss, skin changes, etc). I guess those horrible maladies are inevitable? I spend a lot of my day patching up those conditions (sigh). I was also very lucky my cancer was Stage 1 when I found it the second time...so no chemo or radiation. It's a tough decision and a long road, but hang in there and take good care...........HUGS to you.
Hi
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