Early dementia from chemotherapy and radiation: Has anyone had it?
Breast Cancer hr+ her2 - 6 yrs ago
I went through chemotherapy, radiation and Anastrozole for breast cancer 5 yrs ago. I started losing my memory more and more recently.
It scares me to think I’m developing early dementia at 68. My mind goes blank , problems with names, past times and what’s worse not remembering my parents have passed many years ago but I talk like they’re still alive.!, Scares me is it Dementia or Alzheimer’s?
I’d appreciate any feed back and thoughts 🤔
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My doctor asked me a series of questions and then gave me some written instructions, it was pretty straightforward. He said if he thought I was even a little borderline he would have sent me to a specialist. Instead he said go home and be happy. This is probably from all the cancer treatments.
I did just that. My question is; if you were given a simple screening, could you accept the answer?
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2 ReactionsThis is my concern ,is my lack of memory due to chemo and if so will it only get worse? What type of doctor did you see for your memory? I will ask my pcp dr to lead me to a dr. Thank you for replying !😉
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1 ReactionI really appreciated your comments it made sense how some people react differently to medication specific to their disease. I am so grateful I found the Mayo Clinic site. It provides me with so much information and answers to questions I may not even thought of asking. It eases my mind me to hear of others’ conditions and how they resolve their issues. Thanks to All who replied to my post. ❤️
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5 ReactionsThank you very much for this article it was so informative It explained between dementia and cancer medicine that can mimic ea other. I am going to see my oncologist and hear what she has to say.
Thank you,Much appreciated❤️
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3 ReactionsHi 👋
Curious what type of testing was done to test your memory issues?
Sometimes I feel I may have “chemo brain” or the start of dementia driven by chemo n radiation I had in the past for my breast cancer It scares me either way of losing my memory more at every passing day. I mentioned before, I will be 69 in few months and fear idea of memory issues. I should be grateful my cancer hasn’t returned but it’s always in back of my mind there may come that day😢🤞
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3 ReactionsI have been on Anastrozole now 14 months - first up was brain fog and hot flushes - after 6 months it had not cleared - I had days where I would be crawling into bed by 11am - great in the morning, fun friendly (normal) shop etc. but then a blind would come down and felt I was not safe to drive home. Concentration plummeted I had days where I would be crawling into bed by 11am. The flushes didnt help either - living in the North of QLD - hard to tell if I was flushing or just getting an intolerance to the humidity. The oncologist suggested I take the tablet at night instead of the morning - this worked - still have days where i crash by lunch time but the brain fog is soooo much better - flush occasionally during the day but mostly now at night.
@rosy54
Thank you
I had Abracane, Hercepyin, Radiation and am now on Anestrol an aromatase inhibitor. All to eliminate the Estrogen that feeds my type of breast cancer HER 2 + All this then through you into menopause or back into it. Menopause causes some memory loss issues. Mine are tgat I am in middle of conversation every day and I lose the word I am trying to say it is so annoying and embarrassing because others have to wait for me to find the word or finish my sentence for me. You can see that they find it hard to talk to me and their forehead furrows I hate it so much but I don’t think it’s dementia. I do not have any of that kind of issues in any of my elder families on either side. And when I mention my issues to the doctor he does not seem concerned. And all of my Drs are top notch.
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1 ReactionIt is tough to discuss this because I don’t think anyone really knows if there’s a difference in early dementia and “brain fog”. Plus, doctors seem to have either the “it shouldn’t be a problem now” or the “talk to the other doctor” mentality. I had chemo 2 1/2 years ago along with the inherent brain fog. Started an Anastrazole and unsure if it contributed or if it was just residual from the chemo. Have now been on exemestane for about 1 1/2 years. Because of severe fatigue and insomnia (lucky to get 3 hours a night and suffering the consequences of that), he told me to stop for 4 weeks and call him. I’m on week 6 now because it took 4 weeks to even begin to recognize how bad I was. Still miss my words at times but 80% improvement in being able to remember what I came into this room to get! Less joint pain (guess it wasn’t just arthritis). So I’m torn between needing another 2+ years of meds (letrozole is next) or maybe better quality of life. Of course, is it really better if I don’t take meds and end up with another tumor and this starts all over again. It’s all so rock and hard place. PCP says discuss with oncologist or wants to put me on anti depressants. (But would I seem depressed if I wasn’t on these meds!!!). Oncologist seems all about the standard of care for dosing and length of treatment. Anyway, I’ll stop now before this becomes a disjointed pity party and call my oncologist to see what we need to do. But I do question every day if it’s worth it.