Hi everyone I’m new to this group, I got diagnosed last week with secondary liver and bone mets, I’m trying to keep as positive as possible and hearing some really good experiences from people who are living well for a good amount of years after diagnosis. I’ve said to my consultant that I don’t want to know anything about prognosis etc because it’ll make me panic!
Hi, I read you’re having hand and feet issues. I’m on Capecitabine too and use MooGoo lotion. I’ve had amazing results. As soon as I feel that stinging of a possible blister I cover my feet in it. I also buy extra thick shoe liners. Hope that helps. My chemo nurse prescribed vitamin b6. That really helps prevent blisters.
