Last night's radio marked the half way point of the treatment :)
We had our training on how to use the food pump yesterday and I'm now on continuous feed, which takes about 10 hours, though the pump is portable so it isn't overly inconvenient. Having more calories is making me feel a whole lot better, as is not trying to force down food through a throat that is just too sore. I can't begin to imagine how people manage through this without the PEG (much as I hate the thing).
My two day's of anti-sickness (post chemo) is almost over again, which is a relief as I suffer from hiccups as a side effect of the Zofran. Having hiccups for two days a week seems a cruel and unnecessary additional thing to deal with.
I'm now eager to get another week out of the way.
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