Yesterday I completed another long day in the chemo chair, emerged from it tired but happy (you are always happy when a session is over and there are congratulatory hugs shared all around). Slept well but dreamt – for some reason – of next season’s “Sons of Anarchy” episodes. It will be interesting to see if my dream pans out. If it does, then one un-anticipated side effects of chemo is prescience and maybe I can channel that skill into a lottery win. J
In my continuing work here, trying to write about my/our journey through Cancerland, I feel a need to “go deeper” into my experiences (San is keeping her own journal), at least deeper than the opening paragraph, which, without the bit about SOA and a lottery win, is the kind of illness gloss that is true but isn’t very helpful in showing you “what it is like to” live with cancer. So in the spirit of doing that, what follows is a chronicle of yesterday’s chemo treatment and today’s reflection on it. It is a longer piece but I hope you find it helpful.
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Doctor Robin’s assistant called us around ten o’clock to let us know that the Doc was a little backed up and needed to move our scheduled appointment from 11:40 to noon. No biggie, but nice of the Doc to call. Last time we had an appointment I had complained about sitting too long in one of the clinic’s hard chairs, but that was back when I was still experiencing pain in my back. That she…
I have not cut back on some of the meds. Other than that I’m fine.
I mean there’s nothing to worry about. I’m doing fine. I’m also doing fine with the drug dosages too. I still take the prescribed doses of long-term oxy twice a day, Advil every six hours, B-12 and ALA twice a day, Prilosec once a day, and depending on the state of my “regularity,” and whether or not I needed to rely…