In case that title sounds confusing, don't worry, there is some sort of system that the hospital uses to count the chemos and I don't get it. When I think I do, it always leads to some sort of confusion with the oncologist, nurse, nurse practitioner, or maybe just everyone.
Everything when super extra smoothly yesterday. SO, so nice. My sister Jenny went with me to the treatment to "watch" me. The planes were on time, there were no lasting side effect issues to talk about, the schedule went pretty much on time, so I was so happy. Plus we learned something very important. The patient has their own tv (see how important) and they recently changed the format which has been nice, but we discovered that they have movies on there that you can choose and watch. Well neither of us got into that Twilight craze, but were interested because of the amount of people who said how awesome it was, so that is what we did for a bit of the time. It was pretty good. Now they need to get the sequels on there so we can watch those. :) It really is nice to be in a routine.
The only thing that is sort of weird is that I was taking a drug that I am not taking anymore because I have had a lasting side effect from that. It is to do with the kidneys. Nothing seems to be breaking down, nothing hurts, everything works, but I wish it would get better. It may be a time taking thing. Oh well. Plus I am trying to help that mess out with some homeopathic supports.
So things are well. I am getting well-er. One more treatment in this round. A week off, then the moment of truth! It will be here in a minute!
And Jenny and I are going to breakfast this morning and a little shopping! That is going to be awesome!
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