Now it’s winter the tingling /numbness in my fingertips has got worse. Wearing gloves 24/7 in QLD.
Has anyone had any luck with some kind of hand therapy? Worried might have some nerve damage.
Massaging my own hands feel great, I’m sure it will feel better if I got someone else to do it .
I am on chemo ( round 9) and immunotherapy.
Hi! I had terrible foot pain and hand tingling after my first cycle, so I used cold therapy on hands and feet during second treatment - made a big difference (well I think it did - I guess there is no real way to measure but it was the only variable I changed).
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