Positive Experience with Aromatase Inhibitors
Comments
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The raisins looked done & DH started them last Wednesday. It will take at least a couple weeks (or more) to see if he feels any different.
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I've been taking them this week, but not much difference that I can tell.... In truth, my joints have been pretty painful with the change of weather, so I will be happy if these golden babies do something! Best to both of your DHs wih our exoeriment!
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Haven't needed to try the raisins (although I have read about them for years) but appreciate hearing about dried plums for bone density, since mine's been a little on the low side for a few years.
I've been on Femara for just a few weeks so who knows what I might experience down the road but so far I have had NO discernible side effects. I started taking it at bed time in case it did make me drowsy and it might but it could just be that I'm tired at the end of the day, too.
I usually turn into a carb-seeking monster with the closing in of dark, wet weather and this year has been no exception. I don't think it's been any worse on Femara.
I've had no loss of energy, no stiffness, no mental fog, no digestive issues, etc. In time I'll probably notice drier skin, etc., since lack of estrogen would logically have that effect, but so far so good. On top of that, my co-pay is only $10. I can definitely live with that.
I've not checked out any of the other conversations regarding SE of Femara because I've made up my mind that it's going to work out well for me. However, I think I'm one of the fortunates who's doing well on it. And I thoroughly agree with Ruth - knowing that there are alternatives is great.
Good luck Lacey - I hope you do find one that you can live with comfortably.
Happy Hallowe'en, all!
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Thanks for your positive post, Hopeful!
It is so good to hear from folks who are doing well. Are you just thinking about eating the prunes as a preventative measure or did your bone scan indicate a need to work to ward off osteoporosis. It's an easy enough idea....
So Halloween is now over and we had a record low number of kids when I thought Friday would bring out a lot. Guess our cold temps affected motivation! The leftover candy will need to find another home.....;)
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My DH likes them, he is very crippled....Dr. Just shake their head & say sorry, nothing we can do.
DH has a guilt free snack....I am not a raisin fan, but they are growing on me.
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I have been on Arimidex for 8 years and the symptoms have been minimal.
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Aug2422007.....good to know and thanks for sharing. Hope to be able to say the same thing once I start. Just wondering if you can attribute anything like exercise and diet to your good fortune or are you just lucky?
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I am starting on year 6 of arimidex therapy with very few problems and I plan to continue for the immediate future. My side effects have been minimal. My primary complaints are it does seem to affect my memory [difficulty recalling names etc,], some hair thinning and I find it easer to gain weight and harder to lose it. These are all things that also happen with age so it's difficult to know if it's the drug that is wholly responsible. My bones are doing fine as well. So I decided to continue for a while to see if any new studies come out which confirm benefits to staying on longer than 5 years.
One caveat; I once switched to the generic Anastrozole and almost immediately noticed significant side effects--joint pain, nausea, fatigue. It took me a couple months to make the connection. Once my onco switched me back to the name brand, these effects disappeared in a few days. I understand many women do quite well on the generics, but I have met others who had the same experience I did.
But in my case I feel that arimidex really has been very well tolerated.
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I am starting on year 6 of arimidex therapy with very few problems and I plan to continue for the immediate future. My side effects have been minimal. My primary complaints are it does seem to affect my memory [difficulty recalling names etc,], some hair thinning and I find it easer to gain weight and harder to lose it. These are all things that also happen with age so it's difficult to know if it's the drug that is wholly responsible. My bones are doing fine as well. So I decided to continue for a while to see if any new studies come out which confirm benefits to staying on longer than 5 years.
One caveat; I once switched to the generic Anastrozole and almost immediately noticed significant side effects--joint pain, nausea, fatigue. It took me a couple months to make the connection. Once my onco switched me back to the name brand, these effects disappeared in a few days. I understand many women do quite well on the generics, but I have met others who had the same experience I did.
But in my case I feel that arimidex really has been very well tolerated.
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I have been successfully taking anastrozole for 8.5 months. During the first couple of months I had many and pretty severe night sweats nightly and some hot flashes daily, but they steadily decreased until it is now no worse then it was before cancer (I am 12 year post menopause, but have never been completely free of night sweats). The only really difficult side effect was a couple of months early on I suffered a very strange depression: I lost almost all joy in anything and was beginning to think "what's the point," but it did not interfere with my living my life as usual (just joylessly). Overnight, literally from one one day to the next, it disappeared and I wokeup feeling completely normal, as I have ever since. My MO said it was my body reacting to the loss of estrogen, but that eventually the body adapts. I have had no joint or muscle pains different than the usual ones of being 67. I walk 3-5 miles pretty briskly every day, do strength training three days a week, and also have taken glucosamine/chrondroitin prophylactically for at least 10 years. My mother suffered from severe arthritis, but I have none that I am aware of. Anastrozole costs me $4 a month, and I regard that $48 a year as the cheapest insurance I can buy for preventing recurrence!
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Thanks Lindissima and Aug! Your experiences are certainly encouraging to those just starting. That is what i was hoping to hear about on this thread since it doesn't seem to be prevalent elsewhere.
By the way, ladies, I have been pretty faithful with downing nine raisins a day....not sure if it is doing anything yet....but I guess it takes some time. Holeinone, I dohope it brings relief to your DH!
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I agree with Lindissima. The generic Arimidex was much harder on me than the non-generic. Try to get the real Arimidex if possible. I had to really work with my health plan to get them to pay but it was worth it.
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Well, ladies, I am still early in the process, I guess, three weeks in, but I have to write to report that in the past five days, I have felt amazing relief from my typical joint pain! I have been doing things that I feel would offer a challenge to particularly inflamed joints (shoulder and wrists) like doing the more difficult poses in stretching class earlier this week, and today adding extra weights to my workout. Good news....no pain! Also our very cold weather usually sets off lots of joint pain for me.
What a happy improvement! So glad I tried this, and it will be wonderful if this result continues.
Anyone else started the raisins yet?
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My DH has been eating them faithfully and ran last week for the first time in months. He is pretty excited!! Go Team Raisins!
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Yay for you and DH, Ruth! I also saw on the internet today that the effect is even better with the addition of high quality cinnamon and honey. Not sure if I'll bother to change things up yet. Just enjoying the ride.
Thanks for sharing the recipe!
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Doing ok on exemestane. 2 more years I can do it. Seems to be working NED for 3 yearsm
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Don't do the cinnamon and honey....or at least not the cinnamon in big doses. I tried that 'cure' for a cold & the cinnamon made me really sick to my stomach!
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I have now started 8 years on AIs. My major problem has been GERD which is managed with meds. I have normal bone density, normal cholesterol, normal weight and blood pressure. My onc gave me the option of continuing on the AIs after studies in Europe started to point toward continuing the AIs gave longer no recurrence.
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