Aromatase Inhibitors: Did you decide to go on them or not?
Nanaloves: I’m about to start arimidex and just feel that the contraindications , bone issues etc. are overwhelming. I’m 70 years old, dodged a bullet I feel with zero stage DCIS but the follow up is pretty much no different then if it was more aggressive. I’ve just done 33 treatments of radiation and now they advise arimidex as a preventative. I’m not sure with the beginnings of arthritis and lower back. sensitivity already that I should take it. Anyone not take it and not have a recurrence within the 5 years.
Interested in more discussions like this? Go to the Breast Cancer Support Group.
Again, my oncologist at Mass General, a top cancer treatment center, said alternate days or half dose was okay. I would try that, try a different manufacturer or brand name, and as others have said try a different AI, before giving up. Alternate days or half dose is more than enough. No need to have hormonal levels done since there were thorough studies done on effectiveness in inhibiting estrogen produced by the adrenal glands. Some posters here tried everything, I know. If your doc doesn't communicate, just go ahead and alternate days. It is in your control.
I'm not a current Mayo patient so am I allowed to just get into the portal without being a patient? I'm trying to get my initial patient visit set up!
100% agree. I have appointment w/ oncologist next Monday and will be discussing. Blessings to you.
@emeli13 I agree with what Cedar said. I also have been on Anastrozole since 2019. Right Mastectomy, no radiation or chemo. Mid October I stopped the Anastrozole because of the fog (brain fog?) that was over my entire body, and hip, knee, both feet & back pain were taking a toll on the quality my life. I felt many years older than what I am. I’ve been walking 2-3 miles at least 4 times a week. After about a week , maybe 2, the fogginess went away. The other pains are taking longer. Still shuffling around with sore feet when getting out if bed, but recovery time to tolerable discomfort in feet is shorter. The hip/knee pain is improving. Saturday & Sunday were a very noticeable improvement. Pain still there but improving. It’s been 6 weeks off of med. I’m feeling apprehensive about next week appointment w/ oncologist. I hope he listens to me. Only second appointment with him, as I quit the first oncologist after 2 yrs.
replied to wrong person 🙂
Oh sorry I thought you were at Mayo already. Yes you have to be a patient. Sometimes you need a code from the office.
Wherever I am a patient, I find communication works well on the portal and mine are all linked. Good luck!
You can also submit a request online at Mayo Clinic Phoenix. That may be the better route to take if you have gotten through by phone. The online request is also available on this page: http://mayocl.in/1mtmR63
I have been following this discussion with great interest. I'm most impressed that you are all critical thinkers who work with your health care teams, research information, and weigh risk and benefits for solutions that work for you. While you share your experiences and what you learn, you do not tell others what to do. Thank you!
That said, I would like to post some thoughts and cautions.
When considering complementary or alternative treatments, be open-minded yet skeptical. Learn about the potential benefits and risks. Here is an article from Mayo Clinic that might interest you about evaluating claims made by the producers and/or sellers of supplements, natural products and other alternative medicines. http://mayocl.in/2tGC0Jp
Always discuss any new treatment, changes in dosage or alternate possibilities with your oncologist.
A few things that many of you have already stated clearly that I would like to underline:
1. While you share the diagnosis of breast cancer, each person's journey is different. How a person responds to treatment will be unique to them.
2. What works for one person may not for someone else.
3. Not everyone experiences side effects from aromatase inhibitors and/or tamoxifen. The people who experience no or mild side effects are less likely to post to an online discussion like this one.
MOST IMPORTANT
Keep this disclaimer in mind https://connect.mayoclinic.org/blog/about-connect/tab/disclaimer/
"All information shared by members on the Mayo Clinic Connect, such as messages, images, advice, URLs, and any other material, is for informational purposes only and is not a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding your health. Never disregard professional medical advice or delay in seeking it because of something you have read on the community."
Thanks to all for this discussion
I hear what you’re saying !!! I had to stop tamoxifen after 9 mos. Oct 13 and I’m still dealing with side effects.