Painful neuropathy in my feet up to mid-calf was my worst side effect. My cousin who also has pretty severe neuropathy got Hoka sandals. He swears by them. I’ve very poor so $150- for a pair of shoes is beyond my means.

The one thing that I did that has really help is that I bought slippers with memory foam soles and I always wear them at home. I have hard floors, not carpet, and I discovered that I was making it far worse by going barefoot on my hard floors.

I met a woman at our chemo center who told me that she got electromagnetic therapy from a chiropractor here and it worked wonders. I researched it and it sounds like it could be worth a try. The conclusion was mixed because they said that there isn’t a standard of practice being used. I haven’t tried it because of lack of funds. Here’s an article if you’re interested.
https://www.neuropathyreliefmiami.com/en/neuropathy/peripheral-neuropathy-pulsed-electromagnetic-field-therapy-pemf/
Good luck. 🍀 I will have to go through chemo again when my remaining tumors start growing again. Neuropathy and its pain is what worries me the most. I’m going to use far more supplements and ice even better to see if I can not get as much nerve damage the next time.
https://www.neuropathyreliefmiami.com/en/neuropathy/peripheral-neuropathy-pulsed-electromagnetic-field-therapy-pemf/