Has anyone used ice packs for hands and feet during chemo to help with neuropathy? If so, how was it? My oncologist said maybe don’t do it first time so she can see if I develop it and the dose needs adjusting. I’m concerned if I do develop it the neuropathy won’t go away.
Also any other tips? Did ice cap work if anyone was able to use it?
Feelibg very nervous now treatment is coming up.
Hi Mundesley2
I had my chemo (paclitaxel and carboplatin) in 2022.
I have been left with peripheral neuropathy in my feet, legs and hands/wrists. I also have some sensations in my lower arms.
Mine started from the first infusion and despite reductions in doses it progressed.
I did not know about ice packs for hands and feet. If I did know, I would have tried them. From my understanding they would do no harm although could be a bit painful- like the cooling cap. However I would imagine they would go numb after a short time.
I did do scalp cooling. This link may help with info.
One thing that helped me- suggested by one of the chemo nurses- was to wear layers and bring a cosy blanket from home. With the scalp cooling you can feel pretty cold to start with.
Good Luck
Jane
