Hi All, I have started this new thread because I am worried. I am 2 months out of chemo (Dose Dense 4xAC 4xPaclitaxol) and the neuropathy in my feet is getting worse. From the balls of my feet to m...
I read a five year old report suggesting it was timely to look at other side effects of PN as well as pain. Pain is pain and needs to be alleviated but the report seemed to confirm that many with long lasting PN symptoms aren’t experiencing pain but a whole range of other sensations with their own limitations and challenges. But to be honest, I can find very little more on this aspect. Be interested if anyone else has.