Day 3 now since starting chemo last Thursday and all going well. The infusion procedure was better than expected - no pain / discomfort and a good lunch whilst it took place. A great hospital team - I'm using a private hospital for chemo. The pre-warned side effects of tingly fingers when touching cold objects (I've been wearing thin cotton gloves) and a strange momentary jaw / throat spasm when eating / drinking coolish foods / drinks, which soon goes after a few deep warm breaths.
Now into serious pill popping each day - 3 tablets of Xeloda twice a day + steroids + anti-sickness pills. The steroids run out today and so I might well be on a steroid high at the moment!
I think exercise is all important. My target is 3,000 steps a day, achieved Friday but not yesterday, all done indoors because it's still -2C here where we live in the UK and I've been told not to take gulps of cold air as this will trigger the jaw / throat spasms. I've also just taken delivery of an exercise bike!
Yes, a good family / friend support group is essential too and I'm lucky in that respect. I hope the same goes for you and that you have a joyous Christmas.