If it was me and it was on offer I would give it a go. If it’s too cold then you can stop and say you have tried. My unit didn’t offer cooling for peripheral body or able to keep things frozen for you. I bought some frozen slippers and cool packs for my hands and used them after I had returned home and the next day as I would told chemo is more active for 48 hours after infusion. I had minimal neuropathy but can’t say for definite the cold helped or the chemo didn’t affect me as much in that way.
Good luck with the cold cap, it worked for me. It’s not easy.
As you are HER2+ you, and anyone else on the thread, may be interest in joint the HER2+ and need some buddies which is a very popular and supportive thread that’s be going for over a year.
