Advice for aching wrists, joints

@Nina75 - welcome to the blog - to the club that NO-ONE wants to join!! grrr   Feel free to fill us in on the rest of your story .... and ask any questions on ANYTHING - as there will be some of us who've experienced what you've experienced & good to bounce ideas off each other!! xx    As @Cath62 says - it CAN settle down over time. 

Tamoxifen is the only Hormone Tablet that I HAVEN'T tried just yet - so give it a good 6 weeks and then, if you are still in pain & discomfort - don't be afraid to ask your Onc for a change if you aren't coping with the Tamoxifen ........  I hope your Onc is 'understanding' of the side effects of AIs .... as some 'pooh pooh' the notion - when it is a very REAL source of angst and discomfort to us!!  I actually swapped Oncs too, as my first Onc was VERY unsympathetic to my plight!!!   My current Onc is lovely & really takes on board what I say!

Are you pre menopausal?  Tamoxifen is often given to women who haven't started menopause yet - but some are also put onto the other AIs too.

I am currently on Arimidex and going 'ok' (3 years now) - after starting on Letrozole (6 weeks), then Exemestane (6. months) .... and my fingers, hands, wrists & joints were also quite painful - but I am going 'ok' just now!  Stiff fingers ... but not too much pain.

take care, and all the best xx

Hi lovely ladies!!! I had a very long day at work and when I checked just now was  delighted to receive so many responses, feel so supported!  Thank you one and all! 

Hi @Nina75,

I have been on tamoxifen for just over 12 months now. All the side effects I experienced initially seem to have settled except fatigue off and on. I experienced the side effects for a few months. Fingers crossed it settles for you too.

 I had the choice of tamoxifen or other AIs but tamoxifen had less joint pain associated with it so hence my choice with tamoxifen. I didn't want the joint pain because I love walking. 

You can always discuss with your oncologist or breast care nurse if it all gets too much. Best wishes 💐

Hi lovely. Not good to hear your having struggles. Does appear everyone's journey on HT is different but if it gives you any hope I have been on Tamoxifen for 11 months now and the side effects have settled dramatically,  almost like the body has got used to taking it. But it did take a good 6-8 months to get to that point. The first few months there wasn't a joint in my body that didn't ache, some days it felt like I'd got into an argument with a truck and come off more than 2nd best, got the hot flushes, night and day sweats etc, pretty much every side effect you could read about... but I pushed thru and now whilst there are definitely still side effects, particularly insomnia, they are absolutely manageable.. mind you, wait till the mood swings hit, lol... oh my goodness my poor family don't know whether to hug me, or go hide all the knifes 😊... its great tho, you can just blame the meds and get away with it. !!  HT is shitty, its pushing your body to do something it doesn't want to do, but its also giving you a better chance of that blasted cancer not coming back, a good thing to focus on when the days are particularly brutal. Hope it settles for you soon, give it time. All the best in your journey... 🤗

I was on Letrozole for 3 months when I developed carpal tunnel syndrome. I still have it but have since switched AI and I wear wrist splints every night. Keep an eye on it as if it’s carpal tunnel syndrome, your hand muscles start to waste away. 

I wrote about my situation with joint pain a few years ago, and it still applies. I've been on Letrozole since mid 2017 and also have joint issues. What does muddy the waters somewhat is that I have three other connective tissue autoimmune conditions which affect the connective tissue throughout my body, joints, tendons and muscles in particular. What helps me most, is to keep joints straight. When I'm in bed, and on my side. the wrist of the hand on the bed side, tends to drop in an extended position, so I prop one of those little crescent shaped neck pillows you get from the two dollar shop (filled with small polystyrene beads)under the wrist to keep it straight. The wrist on the upper side tends to drop the other way, towards my arm, curved inwards. This one I straighten with a similar cushion perched on my hip where the arm is resting. If I move that upper arm for the wrist to rest nearer my head on the mattress, I position the cushion so it keeps that wrist straight. For my hip and knee pain, I sleep with a memory foam pillow between my knees so that the upper leg isn't pulling the hip in a squiff position. It all sounds very complicated, but I become used to turning with my pillows and that is the only way I'm not in agony with the joint feeling as if hot lead has been poured into them.

I’m on Letrozole too. Joint pain seems to be part of the hormone therapy life from what I can work out. I’m taking glucosamine at suggestion of,oncologist but can’t say it makes any difference .I’ve now got bone metastases so guess down track it may be pain from that rather than hormone tabs . Can’t win !  . Im just trying to ignore it and get on with activities but I’ll be watching this post to,see if anyone’s got ideas or thoughts on how to combat it 

I'm on letrozole and I'm struggling with knee and ankle pain.  Makes walking and bending down hard and painful.  Feel like I've aged 25 years.