I had trigger thumb surgeries on both thumbs the first year. I've gained 7 pounds.

To get the problem corrected, find out and correct the primary cause. (done in June!) All the drugs can do is limit chance of recurrence. And cholesterol shot way up which is apparently another side effect. I was 100% estrogen positive and 90% progesterone positive. My oncologist said he never heard of this, (and he must be in his 70s.) For the last 1 1/2 yrs.

This is a tough journey to endure.Carolyn you are not crazy. We comply with the HONcode standard for trustworthy health information - I started getting short of breath almost immediately after starting the arimidex, but now I can't even do light housework for 5 minutes without breathing hard. Some women go through it with few side effects and cope very well. I feel like the onco poopooed me off.I had the same experience. However, I do feel fortunate that there is a drug available that may slow down/avoid a recurrence"Welcome @cautiousoptimism. Within the first 6 months on it I broke 3 toes and every one of my top teeth and 4 of my bottom teeth cracked off. My hands hurt, walking is tough because of my feet and hips. Again the horrible hot flushes but this time I would get so hot I would pass out. You can find out more about them and what to expect here It would be nice to get a first-hand experience for someone who has taken hormone therapy. Piece of cake I thought. I've also started gaining weight this is after only being on this for 2 months this is so hard to believe but I honestly think I I'm going to stop taking this med” I've Just read the info on my new prescription Exemestane.....it states I shouldn't take herbs or vitamins.I was thinking I'd do both to hedge my bets. This is no way to live life. Lumpectomy Now and overnight, my thumbs have almost “locked up” and are popping like in trigger finger. God bless you all. Keep telling myself "just a bad day", "too much moving around", "it will get better" or "I can take it". “Breast Cancer Stage 1 Anastrozole and side effects...hair loss/thinning and hair regrowth. I lost my hair, it’s not coming back very well, my last treatment was in April 2015.I have been taking arimidex for 8 months since dx of lobular carcinoma.
it has stayed in my bones. Which is weird because I’ve never been very sensitive to drugs / pain killers.

It will be 8 years this year cancer free. But I went in to my family doctor because the depression was scaring me. I finally had to have surgery to correct a trigger finger on my dominant hand. I am now taking letrozole and so far no problems. My Dr took me off it for two weeks and I restarted it in September. I just wasn’t one of them. I was experiencing bone/ joint pain, hair loss, memory problems, dry itchy skin just to name a few. According to my oncologist this new tumor was totally unrelated to the first one in 2016; it was a “new” cancer. My hair is very thin.

Arimidex (anastrozole): “The first year of taking anastrozole, I experienced hair loss, weight gain even though I was having difficulty keeping food down. Joint pain back to the near intolerable stage. I see my onc in July and may pursue a change. I had Invasive Ductile Carconima (Stage 1) and had surgery to remove the tumor in August of this year and then went through 16 treatments of Radiation Therapy. I think OTs are great.I took that drug, it made my knees and joints hurt so bad that I could not walk, I had to change drugs, I am now on Letrolzole, it has side effects too but so far nothing like the anastrozole. My hands are so sore at night that I can sometimes not sleep. I am going to investigate this further with one of their reps. I took that drug, it made my knees and joints hurt so bad that I could not walk, I had to change drugs, I am now on Letrolzole, it has side effects too but so far nothing like the anastrozole. I refused the anastrozole, at first, but since I have been taking one pill every other day. Again I told my oncologist & surgeon and like other people I was made to feel like I was exaggerating. Some enlightened oncologists have studied how to mange the side effects and found acupuncture and exercise (moving the joints to keep them lubricated and flexible) work the best. But don't think I can. I never went through anything like this when I went through menopause. It’s incredible: I have the latter two different docs but my surgeon argues with them!) I am grateful for this forum because in reading other experiences, I see that I am not alone. I just finished my five years and it's not necessary for me to continue on with it. I still have ongoing issues from the 12 months that I did take them, but they are minor and I can cope with them. However, if anyone knows how to help the knee pain, please share.” So, hang in there Ladies! If you do decide to take them eat a bowl of cereal or something before taking as this I think has kept away the my sickness . The surgeon performing the surgery noted he has an endless line of patients needing the surgical procedure, all of whom took ai’s post chemo and radiation.

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