Mayo Clinic Connect
I completed all treatments for breast cancer but now I am supposed to take hormone blocker, named anastrozole. im concerned about the side effects. Has anyone here taken it and did anyone have hair loss?
Liked by coquimti, Molly MIller, farmgirl1556, kathyomaha55
I’ve been on anastrozole for 5 months and so far my only major symptom has been insomnia. I am up to an average of 5 hours sleep a night at this point. I am also having chronic mild headaches but not sure if that is related to my chronic migraines or the anestrozole. I will see my neurologist in Sept and discuss with him. I did lose some of my hair after my first surgery (8 hours) but that has pretty much stopped now. I had IDC, Mucinous type, 2 tumors, Stage 1 and Stage 2. I elected for bilateral mastectomy with natural reconstruction using my own fatty tissue. I am the most blessed woman as I did not need Chemo or radiation but anestrozole is wreaking havoc with my emotions and depression. Good luck and blessings to you.
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❤️ your comments about wreaking havoc with your emotions! This has been my story as well! I am hopeful the anxiety issues will stop once I’m off Anastrozole….awaiting Oncology appointment next week to discuss. I have been on drug for 5 years (but who’s counting?)
Oh, you are not alone! Almost 2.5 years on this drug and anxiety & depression are significant side effects… you begin to feel like "why can't I just pull it together?" but it is very real. Not sleeping soundly doesn't help either. I try to meditate but I'm not that good at it. I also use an essential oil diffuser at home and find that some of the anti-anxiety blends help a little. Worth a try and diffusers are inexpensive. All the best to you.
All of you warriors suffering with pain, tell your oncologist to put you on Tomoxifen. Life changing
Francine6829, sooooo pleased for you that Tomoxifin is working!!! I was on Tomoxifin for a few months and the side effects were better than when I was on Anastrozole, but I still had some nasty side effects. My oncologist has let me be on a break from meds for a few months as my cancer was a very slow growing type. It’s been heaven to have the break!! But I’m supposed to go back on Tomoxifin when I see her at my next appointment in late September. Not looking forward to it!
What side effects ?
Just wanted to let everyone in the Breast Cancer group know that this week's Mayo Clinic Connect member spotlight highlights a member who has been active in this discussion and often supports others in the group. Get to know more about @cindylb, her Connect experiences and how getting support from all of you helps. Get a glimpse of Cindy and what she enjoys offline, too.
– Sustained on Her Journey by Connect Members: Meet @cindylb https://connect.mayoclinic.org/page/about-connect/newsfeed-post/sustained-on-her-journey-by-connect-members-meet-cindylb/
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This is just slightly off topic but I had to share………..I had Stage 1 Lobular BC, no lymph node involvement and low risk of recurrence BUT I wanted to try the AI's and tried them all. I couldn't tolerate any of them due to the usual side effects and some relatively serious. I had my hormone levels checked by my oncologist multiple times and my levels of Estrogen were low (ER positive BC for me). Here's the next saga……I have been having some vaginal atrophy over the past few years and it finally became so bad that I had to start using vaginal estrogen. I have worked so hard to reduce my estrogen so my breast cancer won't recur (a goal we all share in a big way) and although this cream is low dose and doing the trick for me, I'm feeling all sorry for myself because it seems the hormone woes just never end. Sigh…..
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