FEMARA
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cakes- How long did you take it just every other night before you went to every night?
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just saw your edit. Thanks
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Peaches, Please check with your doctor to see if it might help you to ease on into the Femara. I just know it worked for me.
Good luck and please keep us posted.
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Peaches,
My onc said the same thing, take every other day for 2 weeks then go to every day. As I initially reported, I was taking it at night but just couldn't sleep so my husband suggested daytime and it worked! Good luck -
Amy
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Thanks, Amy and Cakes. I'm going to do every other night for the 2 weeks starting tonight without even asking my onc because it makes sense, especially since she told me to wait several weeks to start Femara after my body adapted to Lexipro, which I have done. Since I had sleep problems with Lexapro till I switched to mornings I'll do the same if it happens with Femara. I'm going to text my doctor son right now and get the ok from him. Thanks again. (-:
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I take my letrozole in the morning, otherwise I'd forget. Think I've had every SE--hot flashes, joint pain, neuropathy, continued chemo brain, weight gain, hair loss, vertigo, deeper depression, sleep problems, etc. My onc has put me on gabapentin for the hot flashes and neuropathy, and meclizine for the vertigo. I was already on Cymbalta and wellbutrin. I told her I feel like I'm turning into a druggie, but she assures me these drugs are ok. SEs started about two months into the drug, and are getting worse. I just don't want to take any more drugs. Has anyone had success with other treatments for these SEs? I'm so tired of feeling so bad. Can't work, don't feel like doing much around the house. A dear friend told me he thought I was "spinning out of control," because my house was in disarray (I used to put Felix Unger to shame) and I can't handle bill paying and the medical bills. (Getting them organized, fighting insurance, etc.)
I appreciate his willingness to tell me what he truly thinks, but just feel like no one who is not part of "our club" understands what the treatment does to me. I started letrozole in Feb. 2013 right after finishing chemo.
Sorry for the pity party. I would like to know how people have handled these symptoms, though. I've read most of the posts on this topic, but want some specific suggestions if you have any. Many thanks.
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Adnerb - How are you feeling today?
DivePuppy - I am SO sorry you're so miserable on Femara. Have you asked your MO about possibly trying another AI? I didn't have chemo, but I had such significant SEs on Arimidex (anastrozole), and had to switch. It's amazing, Anastrozole and Letrozole are ALMOST the same drug... yet women can react so differently to each of them. Perhaps a different drug wouldn't give you so many issues. Hope you find some solutions!
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I have a question for my Canadian ladies on board. Has anyone stayed on the Femera more than five years? I have
completed the five years of Femara and my oncologist said there are no studies that show any advantage of staying
on this medication longer. However I have seen on the Her2 forum and this forum that many of the women in the
U.S. are being kept on the medication up to 10 years. I of course have faith in his care but am a little scared to go off. Thanks ladies
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have no idea how I did that typing double spaced
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I am almost at the five year mark. Both the oncologist and my GP say five years is enough. Both of them also say that constant vigilance will be necessary ever after. I'm OK with keeping up with various check ups and paying attention to my body - really, that is happening now anyway.
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I've been told I will be on the Letrozole for 10 yrs. I had micomets in my one sentinel lymph node that was removed but will ask the Onc why 10yrs vs. 5 when I see her next month. The more info the better.
Stay Strong Sisters
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I'm told that I'll be on it until it stops working and we move on to something else...I have no real SEs, so I am ok with that.
Michele
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cakes, I too am going to be taking the pill for 10 years. My MO said that he used to recommend 5 years but because of research and studies he now recommends 10 years to his patients. I did not press him for more info but I will the next time I see him in May.
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I have been on letrozole for 4 years and 3 months. After about the first 3 months I switched to 1/2 a pill a day and have continued that until the present. I did that due to severe joint pain, trigger finger and changes in my personality that I noticed, but noone else really did, or at least didn't say anything. The above mentioned side effects got much better....however I have still been plagued by fatigue, some hair thinning, extreme vaginal dryness and pain and atrophy. I cannot wait to finish this drug. My Onc said there are no studies showing a benefit to taking longer,unless you are Stage 4. Disclaimer: I went to 1/2 pill a day on my own. My Onc did not recommend it, but he knew quality of life was a big deal to me. It was either that or go off the drug completely! Hang in there ladies!!
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I had such problems with Aromasin and Arimidex that I had few expectations that Femara would be any better. So, on my own and without my MO's knowledge, I split my dose and took 1/2 in the morning and 1/2 in the evening. After a couple of months with no SE's to speak of, I started taking the full dose in the morning. I still have some joint pain, drowsiness, and brain fog but to far less a degree than with the other drugs. A new SE with Femara is hair thinning but only my hairdresser and I have noticed it. All-in-all, Femara is treating me much better than either of the other drugs. But I will not hesitate to go back to splitting my dose if I need to.
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Has anyone had any intestinal problems with Femara?
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No more Femara for me!!! Though I am looking forward to no more se's from this evil, tiny pill, I need to go back to chemo. Latest scan shows progression. I wish you all less se's and lots of good luck!!!
Love,
Brenda
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Brenda, yes it is an evil, tiny pill. But we have to be thankful for the entire list of treatments that are available, however difficult the side effects. I wish you minimal side effects with your new treatment and NED. I hope we all will get to benefit soon from some of the treatments that are poking their heads out. Every night, I pray that there are more and more breakthroughs.
MsP
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(((((Brenda)))))
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((((((((((Brenda))))))))))). Hope the chemo kicks cancers butt!
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((((BRENDA))))
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Today has been a better day, if only because it was 75 degrees and sunny! That helps! However, the side effects continue. I have an appointment with my onc next month, and I'm going to ask her about other options. Everyone is so different when it comes to the side effects. Thanks for asking! Kathy
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Thanks, All! I wish you minimal or no side effects and the best of luck in this cancer journey!!! Maybe one day (hopefully in our lifetime) the fear of recurrence will be a thing of the past!!!
Love and hugs,
Brenda
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Brenda, I wish you all the best with your new treatment.......❤️
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Brenda, (((hugs))).....
For those who think they'll forget to take their meds at night, here's my tip....I leave them under my pillow...it's saved me a number of times...
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Another tip ladies.....I leave my box right under my bedside lamp so before I turn out my light for the night! I pop that little devil.....lol
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But what if you don't have a glass of water there as well? The logistics at night are always more difficult than in the morning. Kudos to everyone who can manage night time pills!
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lassie11.......I always have water by my bedside and I believe many others do too. I can NEVER forget to take it because I see the pack as I am about to turn out the light.
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I can never use those pill organizers because I take a different cocktail of drugs every night, depending on how I feel!
So I do the next best thing... I line up ALL my possible drug containers out on my bathroom counter.... just like I used to bug my mom about doing! (I hide them all in a drawer if company comes over...)
At least then I can pick and choose, and each time I remove a pill from the container I put it in a little pile on the counter. Then I review my symptoms, make sure I've got everything I need (letrozole is a regular) and THEN I swallow my pills before I go to bed.
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Hi Ladies. I'm new to this board, starting Femara today - I think tonight after reading a lot of your posts. I just feel like this is all a bad dream that we need to wake up from. But no, this is my life. : ) I would love to hear more from those who have not experienced bad SE's. I know we are all different but it helps to read the positive as well as the negative. I already have joint pain from the oopherectomy and forced menopause, my fingers are a bit stiff, and I have mild hot flashes. I can manage all of these, just worried about new SE's. I am going to ease into the Femara by taking 1 pill every other night for two weeks.
I do believe diet and exercise play a big part in how we manage these symptoms. After chemo, radiation, oopherectomy, my sister's wedding, and a long vacation with my family, I am now settling into an everyday workout and healthy eating routine. Hoping that helps. Would love to hear if anyone else feels better after eating well or working out?
Thanks for being there.
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