My chemo has been reduced because they thought my hands were so bad. They don't seem that bad to me and my feet are fine. They are a bit red and are now peeling. I took ice and freezer packs with me to chemo yesterday as they said they couldn't provide that in the unit. I've got loads of hand cream but the doc recommended one with oatmeal. He's also given me vitamin B6 which I'd asked them about before for peripheral neuropathy but had to get myself. I asked them not to reduce the caelyx but he said if it got worse I'd need a complete break so this is the best option. I just wondered if anyone else had experience of this. Yesterday was my 3rd dose and the CA 125 has started to fall though it's still 1600. I've read that it takes a while to come down on caelyx so I was pleased that it has started to fall as it went up between 1 and 2.