I had to finish my chemo 2 sessions early at the end of last year due to peripheral neuropathy after my first session of paclitaxel and we ended on a last session of Ec. I'm awaiting to hear the dates of my radiotherapy but I need some advice on what I think I've now got is hand foot syndrome.
I have no contact details for the oncologist and I don't want to bother the chemo helpline folks as I think I actually need someone to look at it.
I'm unsure whether the gp is best or will they just say can't help, talk to the oncologist! It's weird being in this in between phase to get advice.
Doesn't help it's flared up the eczema on my feet either so I'm m not sure if I can buy creams or if I'm still not allowed to use certain things in case the drugs are still floating about in my system.
Any advice on hand foot syndrome (particularly the feet rather than hands) or someone hopefully telling me the pins and needles etc do disappear eventually would be music to my ears!
