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 ... see all
All of you warriors suffering with pain, tell your oncologist to put you on Tomoxifen. Life changing
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I have been on Anastrozole which caused severe memory/cognitive issues, along with the aches and pains. Then my doctor put me on Tomoxifin, that was better but some brain fog continued. It seems I can choose between the possibility of cancer returning, or not being able to think clearly.
We are all different so our reactions are not the same . After 3 1/2 months anastrozole destroyed my joints , bones and muscles . Stoped taking it 7 months ago and working at getting my body to function like it did before that horrible medicine. I have an 87 chance cancer won’t come back with
Out further treatment so why did they do this to me ? Money that’s why
I personally don't think AIs are being prescribed from a monetary gain standpoint. Rather, I believe it is because the risk of recurrence climbs over time. AIs keep the risk low during the first five years. This is a good subject to discuss with your oncologist.
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@francine6829 Hi Francine, How long have you been on Tomoxifen and what dosage. Thanks
I've taken anastrozole for 9 months – but my hands hurt SO much!! Oncologist is stopping my drugs for 2 weeks. I think she will be switching me to Exemestane. Said the joints won't hurt as much. Anyone have any experience with Exemestane?
Took Femura then exemestane- both Same joint pain. Am on Tomoxifen now- no pain
Liked by trixie1313, kathyomaha55
@francine6829 Hi Francine – I'm hoping I do ok on the exemestane..I get 3 weeks off from the Femara and how nice it is. My left knee is hurting less and my hands hurt less. Ankles still a problem but not as bad. If exemestane doesn't work, it's on to Tamoxifen, but doctor is hesitant as my mother had clots in lungs twice in her lifetime so would need to be followed closely. Sounds like many people on Tamoxifen do well.
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@kathyomaha55 I began exemestane no muscle or bone problems at all. But my blood pressure took off. I was on 3 weeks only.
@gwinter I'm sorry that you had BP elevation. I'll be sure to keep an eye on mine when I start. But must have been nice for no bone aches..ugh…makes me feel 50 years older! What are they putting you on next?
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@kathyomaha55 believe it or not NOTHING! New oncologist
gwinter – why is your oncologist not putting you on a new medication to prevent the cancer from returning?
I wondered that, too, Francine.
I have been taking arimidex for 8 months since dx of lobular carcinoma. I have many side effects, including hair thinning. Has anyone else experienced this? Will I eventually lose it all?
I’ve been on Arimidex (aka Anastrozole) 5 yrs and hair loss is issue for me. There is plenty of regrowth and did not lose it all! The quality of my hair changed overall. It’s very thin where parted. Good beautician with cuts and style has helped me feel better.
Yoga & exercise helped for joint pains.
Liked by Colleen Young, Connect Director, trixie1313, lisman1408, sparklegram
Thank you for this @newgranny ! Encouraging to hear someone is out there getting some regrowth. Feels so vain to be worried about hair, but it's upsetting to lose it to chemo, get it all back, and then start losing it again. Take care.
Liked by newgranny
My Dr. suggested Rogaine for bald spots on the scalp. You need to take it for about 4 months to see if it works though.
Has anyone tried going on a gluten free diet to reduce the joint inflammation in their body? I just started 3 days ago to give it a try.
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