Aromatase Inhibitors & carpal tunnel and trigger finger: Anyone?
14 mos of “AI” meds, I’m coping with daily hand-wrist-finger pain. I’m on my 3rd drug, having taken Anastrozole & Aromasin-each for 6 mos and now on Letrezol since January. Any advice to deal with this, besides using hand braces&finger splints and daily exercise? I need to be on this for 5 yrs total and can’t take Tamoxifin. Help!
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Same here. Tendon release surgery. He didn’t know anything but then I needed gel injections in my knee because I had no synovial (?) fluid…but I did a full 5 years and this all came down on me in the 4th to 5th year.
Appreciate that!
Thank you very much!
I am aware of the link between anastrozole and carpal tunnel syndrome. Four months after I started anastrozole, I had severe pain in my feet which was initially diagnosed as plantar fasciitis but became more severe and now is diagnosed as tarpal tunnel syndrome which is the same type of inflammation but in the tendons of the feet. Has anyone else had this happen? What did you do?
Thank you for your concern. I find that when I use my hands for longer periods of time such as computer work or sewing the pain level not only increases, it also remains for longer periods of time post hand use.
Someone in one of the posts on this site, mentioned doing hand exercises that they said helped them reduce pain. Unfortunately, I’m unable to locate the instructions for those exercises. Does anyone know who posted the hand exercises? Thank you.
Yes, was thinking I had a case of painful plantar fasciitis in my left foot.
Now I’m wondering if it’s not more likely what described as tarpal tunnel syndrome, same type of inflammation, but in the tendons of the feet!
Have been taking anastrozole for ten months now.
Also have varying frequency and degrees of pain my thumbs, hands, and wrist.
What medical specialist did you see for your foot problem diagnosis snd treatment? Thank you.
I saw a local podiatrist. It did not dawn on me that this could have happened because of the anastrozole. I went a whole year with pain and having to wear clunky tennis shoes before I started to question how this was happening. My podiatrist didn't think there was a link but after I talked to my oncologist she said there definitely was a link. She changed my medication to Exemestane. Unfortunately there are areas in my foot that have now started to calcify and I am seeing a foot surgeon in 2 weeks. I'll let you know how it goes. Lesson learned is to discuss any change in any part of your body with your oncologist. I didn't want to bother her with my foot problem and that was a big mistake.
I asked the poster about it but haven't got any responses yet.
@mrsmary ?
Well, guess I just learned another thing about 4 yrs of exemestane - trigger thumb for the last year; very painful and unexplained sudden appearance. No one - ortho, Onco or primary suggests side effect of the drug. So much they don’t seem to know; unsure they care - it’s always ‘just be glad’….Also now debilitating pain in hips, toes - though I remain active not sedentary. Long for the day they listen, connect the dots, do research related to one size fits all dosage of these drugs.
Cortisone shot helped my thumb, but only for 2 months. Then stiff again. Then when j took two weeks off to switch from anastrozole to exemestane and started that early April my thumb is loosening up again..not perfect but a lot better. Weird