They have to give me these shots (neupogen) to keep my white blood count up. I've been getting them twice a week without too much problem. The one side effect is you can get a lot of aches and pain in your joints. I've had a little bit of it before, but it was almost debilitating yesterday. I hurt all over. It was a real bummer. I was in bed by 8:40.
Dr. Kaplan said we'll only do one shot next week, on Thursday, the day before my last Taxol/herceptin infusion.
We talked about what to expect when I switch to A/C, (stronger drugs) July 1. Everyone is different, but he said I might experience more fatigue (great), and nausea. I haven't thrown up once on the Taxol, or needed the anti-nausea drugs, thank God. A/C will be every other week, so I will be done with chemo by the end of August, pretty much on schedule. I just hope I don't spend the rest of the summer hugging the big white bowl. I don't know. He thinks I'll endure it pretty good since I've done so well so far. This whole thing seems to have gone by so fast. It seems like I was just diagnosed - but that was in January. What a way to spend a year.
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