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I have been on Femara for almost 5 years now. My oncologist says that Femara is the reason of my improvements. My tumors naturally stopped growing since I started taking this medication. And the only side effect that I have noticed was light migraine after taking the drug, but it is almost unnoticeable. Three of my friends (whom I met at the hospital when I was just starting visiting my oncologist regularly) also started taking Femara simultaneously with me. They report improvement in this or that degree, but still they are happy with the way Femara works. Some of them had noticed hair thinning during treatment, but sometimes you just have to choose.
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I have been on Femara for 3 months. After taking Tamoxifen for approximately 2 years, which I could not tolerate any longer, my oncologist put me on the Femara. While my hot flashes have pretty much disappeared, the joint and bone pain I am suffering is unbearable. My elbows, hands, fingers, knees, ankles and feet are the worse. In the mornings I cannot get out of bed. I take thyroid medicine in the morning and cannot open the bottle. It takes about 20 minutes before I can close my fingers or bend my toes. Nighttime is also bad. After sitting for short periods I cannot get up. I have never felt better in my life except for the constant agonizing pain. I am a very active 49 year old but feel like I am 90. This pain gets worse every day. I can only imagine what it will be like in 3 more months. I I am seeing my oncologist this week and am going to tell him I am stopping this drug. I believe the quality of my life is more important that the quantity.

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