Sep 03, 2009 - 11:11 pm
I'm wondering if anyone can give me some info and thoughts about neuropathy that happens during Taxol treatments. I've done 4 AC treatments and 2 taxol treatments with 2 more to go. Everything I heard made it sound like taxol was going to be a breeze and it is in a lot of ways, but I've got tingling in my right foot and my fingertips that seems like it's getting worse. I'm worried it's cumulative and I've read that it can be permanent. I'm taking vitamin B6 and glutamine as suggested by my nutritionist and it seemed to help my foot, but then my fingertips have started getting worse. Has anyone had this and seen it go away once chemo ended? Anyone have any other suggestions about how to handle it?