I’ve had issues with the “hand and foot” side effect from Capecitabine this cycle. They’re red and I had a day where they were really red and sore. Hurt to walk. Fingerprints are almost non-existent and the touch feature on my phone and iPad don’t work all that well. So the drug is getting to be too much for my system. My GPO has said when the pain starts this cycle (she says when) to stop taking the drug until my next appointment and they’ll reduce the dosage.

I read on a fellow MBCer’s blog to keep a little notebook with me for a drug cycle and keep track of anything I experience related to my treatment. This will help me (and anyone around me who’s interested) in what I’m really dealing with. I have issues with giving myself a break or being kind to myself so hopefully this will help. My counsellor thinks it’s a good idea too.