Fatigue worse after radiation: And still have fatigue, what helps?
Hi
In march I will be going into eleven months post radiation. I feel since winter hit my radiation Fatigue and fibro has gotten worse. I am struggling horribly with this fatigue and now i'm getting depressed. I live alone.It has been a very. Difficult. I did not think the fatigue would be this debiltating this far out. I am sure my fibromyalgia Is playing a big part also. My fibro has been very much under control with the odd flare but nothing like this. I will be starting counseling at the end of March and I will be starting grief counseling at the beginning of march which i've been waiting ten months for. I am hoping some of this makes a difference. I had four deaths during my treatment, Plus having to care for my mother when I was finished in April quite a few nights a week.Finally got her in a nursing home in August.She has alzheimer's , that also has been brutal. Wonder if others with fibro have had this much trouble recovering from radiation.
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I’m right there with you. Finished treatment December 2023 (surgery, chemo and radiation) and put on Anastrazole. Because of problems with bloodwork, further diagnostics (and stress) up till brain MRI and Petscan in July 2024 (both negative). Because of side effects (muscle and bone pain), switched to exemestane in November of last year. At that point, while tired, I was holding my own. Now, I am constantly tired to the point of nodding off mid day and for the last month or so now I can’t sleep - lucky to get 4 hours a night. I do high protein/fiber, low fat diet. Do 5000+ steps daily with strength training and cardio (not overdoing it, 30-45 minutes a day, 6 days a week). Oncologist did tests for possible causes and of course I’m “completely healthy” except for mild low white count and low lymph count that’s been persistent since the chemo. So of course, there is no treatment and I’m told I’m just depressed. I feel it’s from the exemestane just exacerbating the effects still present from treatment but that’s not really recognized and I am a bit afraid to come off the meds. I’ve avoided antidepressants because the side effects run pretty close to those from exemestane and I’m concerned it may worsen the problem instead of correcting it. (And I will admit a personal psychological feeling that taking these is a sign of my own weakness and inability to manage life) But may not have a choice as this particular sleep pattern is not sustainable.
Hi
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Hi
I did not have chemo but I had radiation and yes my radiologist told me that low RBC might be my new normal
Hi
Sorry you're struggling so bad. It definitely is from your exemestane .I did not take the hormone therapy drugs they give you. I just did not feel it was necessary for me because I was stage zero and I had dcis and I already have osteoporosis I did not want to make things 100% worse because what I researched on those medications they do a lot of bad things as far as I'm concerned everyone has to make their own decision of course. I did go on Zoloft 3 months ago 25 mg and I can tell you it's really helping me a lot. I too did not want to take something but I belong to a zoom breast cancer group and most of the women are on an antidepressant because when they take away your estrogen it's very normal to have severe depression and anxiety. I had tried four other antidepressants and they were horrible this one so far has been very good. I did have a rough three weeks when I first started it just increases your anxiety but then it leveled out and it's been good. So don't let yourself suffer. I was on HRT for 14 years so the day I was diagnosed with breast cancer my GP made me stop it. And within 3 months the anxiety and crying was just horrible.
Thank you so much for the reply. I see a lot of responses on this site of women who say they wouldn’t have made it this far without something to help but it doesn’t seem to be the majority. I tell myself it is side effect of the medication and I’ve always hated the idea of taking yet another pill to try to solve side effects of the other pill I’m taking. Then what about side effects of the new one needing yet another medication etc, etc. but as I said, this isn’t a sustainable lifestyle. I’ve been thinking heavily on calling the doctor and accepting the med - he’s just talking low dose Zoloft - to see if it helps. Your reply has helped that mental discussion in many ways. Again, thank you.
Thank you for sharing!!!
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Can you change your exemestane? I have heard different ladies in my zoom breast cancer group talk about changing the med and whatever they've decided to take instead has helped less side effects. I wouldn't be worried about Zoloft honestly 25 mg is what I'm on it's the lowest dose although in the states I think you guys have a pill not a capsule so you could do 12.5 mg if it's a pill. I hope you get some relief soon.
Already been on Anastrazole and moved to exemestane because of the side effects. This is better - helps me be more mobile and less painful. Only other option is Letrezole and it seems about the same (if not a little worse) in a lot of cases. I’ll call Doctor Monday and see about Zoloft. If it doesn’t help, then will have an in depth with oncologist.
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Is tamoxifen not an option I know some ladies in my breast cancer group that switch to that medication. Even though they are in menopause. That is the one my oncologist wanted me to take I took it for one week and said no thanks just because I'm so sensitive to medication I Get Wicked side effects to everything. He was okay with me not taking anything. I wish you luck I hope you get feeling more like yourself.
Hi,
Thank you again for your information. May I ask what brand of magnesium glycinate you use?
Thanks!