Letrazole

Hi mkitty
As 60% of bc diagnosis are hormone po 's itive there are many of us who are taking this AI therapy and lots have minimal side effects.myself i have been on for 15 months with min side effects. Joints ache cold weather..prickly heat hot weather ..but i 
Have Mets bc    so still working for me
Be proactivive with this drug to lessen side effects
Walking excellent
Reccomend getting b one density test to establish bone health
Add Calcium vitamin D 
Watch blood pressure ..im on low dose bp tab
Watch cholesterol..im on low dose statin
Also consider asprin for blood th I nner as SEcould be blood clots
Lots of hints from others to come 
All the best B

@brightspace thank you :-) 

My bp seems to be really good, usually it's lowish, so is around low-normal at the moment. He's ordering the bone density to be done soon, i'm already on calcium & vit D on his recommendation during chemo. My cholesterol is generally good, although it's not been checked lately. 

Walking i really need to get back to though, not hard as I have 2 young American Staffy's (2.5 & 4 years old) that need walking ;-) I haven't done much walking due to lethargy from chemo, but have started trying to get out there a bit with them. The 4 year old is new to my family, having only adopted him 4 weeks ago, but he's fitting in so well with us, but has needed some training, and as I am the definite Alpha with my dogs, and my partner has no real experience with larger dogs, it's been up to me. 

With doing dose dense chemo it's been one hell of a ride!
I am definitely wanting a reconstruction, and considering asking for the other side to be taken off with immediate recon at the same time. I had skin & nipple sparing mastectomy in May which went really well. 

I was lucky to have caught my bc before it became mets - I had 17 lymph nodes, all removed and all were + for bc, so i guess i dodged a bullet there. My tumours were also only 1mm from my chest wall. Who knows where it would have spread to. I feel very lucky indeed! 

Ive been on for quite a while at first cramps in legs so upped my magnesium and this worked a treat and very stiff for about a month but othetwise a great experience.

Hi MKitty68, 

i have been on Femara for four and a half years. I have had no aches, pains, flushes etc at all. It can have an effect on bone density so a test will be done to check your current levels before you start. Mine was extremely good before I started, there has been an impact but I should get through 5 years OK. My bone density will probably then be average for my age, but so be it. I have had no accidents or bone related injuries. Femara can also cause vaginal dryness. This is pretty variable and there are lubricants available, but worth discussing. My oncologist encourages me to keep up dairy - low fat milk, yoghurt seems OK. I have also taken Vitamin D and calcium. Best wishes.

@adean & @Afraser thanks for your replies.
I have bad vaginal dryness & lack of libido from Paclitaxel already, so hoping it's not too bad. 
I eat bananas, but may look at a magnesium supplement I think, I already have issues with my legs due to arthritis. I also take a Vitamin D & Calcium supplement, and a B group supplement. 

Oh my yes l forgot the libidio yep thats gone lol. I just love my bed   to sleep xx

Hiya. I've been on letrozole about 14 months now. Initially I had painful wrists and ankles but that has lessened. The odd day it's bad (and when I swim with just a kickboard my ankles kill me)
Initially my libido plummeted and the nether-region was teribbley dry. However my body seems to have adapted a bit. Only need lubricant now for the marital business and not all the time. Libido is back somewhat but of course not what it was pre menopause anyway. For some bizarre reason when fitter and have aching muscles I'm more interested... maybe its all the pain stimuli....haha. My post chemo and  pre letrozole bone density scan showed a dranatic drop. However 12 months on and I'm within normal bone loss and possibly even gained some back in hips. I'm now doing weights to try to increase my back bone density. Next test 2 years. I haven't had any more hot flushes than I had post menopause but have a fan handy just in case. Wine, coffee and cooking always results in a hot flush but I persist regardless. Kath x

@primek thanks for your reply, and a giggle re: wine, etc.. i'm allergic to sulfates, so a few drops in the bottle of food grade peroxide is needed for me, or i get bad leg cramps & flushes from wine. 
I've had hot flushes with Pacletaxel, and of course the neuropathy. 
I'm keen to get my libido back & try something for the vag dryness as it can be really uncomfortable during sex & needing lube all the time can be a bit of a put off, my relationship is only 6 months in. Luckily he's a very understanding guy with hormone issues of his own - he was born with a hormone disorder & needs regular Testosterone injections, so also has fluctuating hormones and all that come with that. 
Pre-cancer I was on HRT, and my libido was really high, which was pretty normal for me... to the point it scared some poor buggers off when I was casually dating LOL so the thought of living with a low to non-existent libido is a bit hard to handle for me. 

Taxol killed my libido. I did find a few months on the dryness improved a lot (which seemed to help the actual desire weirdly). My husband has testosterone injections too so we have our struggles. A netflex night of "outlander" can help.  :D

oooh i'm yet to start watching that.... may have to give that a try! *grin* 
I've had topical estrogen, which he's said I could use during chemo from time to time, but i've no used it at all as i'd need to time it between his T shots, his often weird work hours & my chemo.