Concerned about the side effects of anastrozole

Thanks Cindy and Canada
I appreciate your input. Canada, I can't believe you're still losing your hair that's so unfair. My texture is changing and my hair is drying out but my hairdresser says it's not thinning like it was when I was on Tamoxifen- fingers crossed! I'm disappointed to hear your docs said your hair was falling out due to age. I'm 54 and I agree with you we shouldn't be losing our hair in our 50's. There must be other things we all can do to prevent or repair hair loss. Does anyone else in this site have specific suggestions to mitigate the loss.
Hugs to you both!

Hi Cindy.....I am 72, so I am thinking cancer, drugs...which do I choose.....but somehow quality of life looms large in my books...I also hate the weight gain since I have been on Anastrozole. I do aerobics three times a week, and lift 5lb weights 3 times a week for 10 minutes....that seems to help with the joint pain, but the hair that is another story....it is thinning and doesn't look right....but I think your hair loss is due to stress....you should check the blood in the stool to make sure it is not colon related.....I had colon cancer 10 years ago, but they tell me the breast cancer is not related in any way. Keep me posted.

I am also stage I, no lymph node involvement but I had a bi lateral mastectomy (due to my cancer type, lobular - which was in one breast 4 years ago and then the other breast two years ago). I chose to remove the whole thing to avoid the constant worry and subsequent surgeries. Imagine my surprise following surgery when I found out follow up with an aromatase drug was recommended. Heck, I thought I was done. I tried Letrozole and had depression, joint pain and brain fog that was severe. I switched to Arimidex and had blood in my stools, got Shingles twice in a 3 month period (perhaps these are unrelated, don't know) and then went back to Letrozole. All in all I've only taken these drugs a total of 4 weeks in the past year and a half. The dilemma is.......do I want the side effects or cancer? I haven't worked this out yet for myself. I am not taking the drugs and am coming up on my 2 year check up. My quality of life on the drugs is very poor but if the cancer returns with no breasts, I'm in trouble. I wish I could offer more clarity to support you but I'm still on the fence. And to all posting here......I'm NOT on the drugs and I'm losing all my hair anyway. I am 59 years old and the only reason I've been given for hair loss is old age. I am supplementing for it with biotin and using the best products I can find on my hair and have quit dying my hair but it's falling out daily. Also, no support or clarity there. You can naturally reduce estrogen by losing weight, eating a cancer diet, etc. (if your cancer is hormone positive) but you see healthy, thin women with cancer all the time. I wish I could take the drugs with less severe side effects and am not opposed but so far I can't function on them.

I had stage 1 breast cancer, no lymph nodes involved, decided not to have radiation, and am now on Anastrozole since March. I don't like the pill....have hair thinning, joint pain, mood swings, bone lost...and I do wonder what percentage of women stop the pill, and get cancer again.....has anyone out there stopped the pill, and is still fine? Also, I thought I would wait for my mammogram in October and make a decision then....that would mean I was on the pill for only 7 months. Any thoughts....Suzie

Joint pain seems to be the most consistent side effect of Anastrozole. It was my experience that the body starts to level out on the many side effects after being on it for +4 months. Among the joint pain almost exclusively in my wrists and fingers, i have numbness and tingling in my hands. I have, however, feel that my hair is thinning, but I'm more paranoid about that, so I'm taking a hard look at this. Continued good health and good luck!

My switch to letrozole eliminated the aches and pains, bit the hair thinning and weight struggles continue after 2 years. It is working though because i just got the all clear at regular 6 mo. check. Has anyone found a way to reduce the weight gain?

Fifteen months on the Arimidex. Gained twenty pounds - but really starting to fight back now. Assorted other side effects that come and go - I can deal with that. Major concern is hair thinning. Everyone (husband included) keeps telling me it's my imagination. It's not, but I could live with this level of hair loss if it stops here. Some are indicating that things seem to level off after six months or so on Arimidex. If this is my new normal, I guess I'm okay with that. I enjoy the feedback on this site. I wish everyone here the best of luck as they go forward.

Hi @wandering
Which oncologist did you choose in PH? I'm in that area.

I needed to switch to letrozole because of the aches and pains. I dont have them any more, but still have hair thinning, insomnia, weight struggles, flaky fingernails. Ive been on it about a year. You adapt to a new normal!

Shenriq ~ Thank you! It is through the experiences of others that I gather my strength and take an optimistic stance. I have several friends who are a number of years ahead of me ~ Diagnosis/surgeries/chemo or not/radiation and then Arimidex. These women have all done so well with all aspects of treatment.They are active and happy and living the good life...Some of them very mindfully. I am trying to live in the moment, deal with the side effects of whatever happens next....Hoping it will be sunny days and happy thoughts when possible. Sending peaceful thoughts ~ Molly