I start adjuvant capox next Wednesday after pan proctocolectomy with permanent iliostomy on 1st July. Just 2 positive lymph nodes so next step adjuvant capox for 3 cycles.
I had my new patient talk with the chemo nurse today and asked if I could try the oxaliplatin infusion hand and foot icing to try and lower risk of peripheral neuropathy. The hospital don’t offer this protocol.
The data I have seen looks good with statistical significance even in smaller studies. Looks like only a few hospitals in the UK have the electrical kit but I would be happy to buy the mitts and socks which use the gel packs. Logistical nightmare as we live an hour from the hospital and would need plenty of spare frozen gels to maintain low temps for the 2+ hours of infusion infusion. The hospital can’t offer any help with fridge or freezer space and really don’t support this protocol.
Looks like my stoma may misbehave during chemo so keeping my hands working and useful is really important to me. I have bought diclofenac and udderly smooth moisturiser to help with the capecitabine risk of palmar / plantar skin problems and would like to try icing if it might help lower the risk of oxaliplatin CIPN.
And advice please?