I haven't visited this page in more than a week even though this is really the time for updates. The problem is my brain doesn't seem to work on chemo. So, it's begun. Now that I am feeling better, manageable is the word I would use to describe my first round - wholly unpleasant, but manageable. There were moments when I became despondent thinking that I did not want to continue like that until November. Obviously, there is a lot to learn about how I will respond to continued treatment but I need not live in November nor any point between now and then. I'm learning that most of all. In the end I felt less than great for a matter of days, not months. Manageable.
I went in on May 12th as Zebib's (nurse) first patient of the day and left as her last. So, it took a while. There was trouble accessing a vein, a mild reaction to the drugs (forcing them to put the brakes on for a period of time and begin again more slowly), and the delays I imposed by asking too many questions.
Luckily, my time wasn't spent in a facility that met any of my expectations. Because of the dread that is so often associated with chemotherapy I envisioned a sad little room painted institution green, with a series of worn out recliners occupied by some very sick looking people. That place may exist but it is not at Seattle Cancer Care Alliance. I did feel like I was in a medical facility, almost like a hospital, but it was far more private and comfortable than I anticipated. We, like most of the patients there, had a small room to ourselves, tricked out like a standard hospital room with a third the space. Comfortable as it was I couldn't wait to get out of there and head out to yoga for a little normalcy. A nap and some steroids made that possible.
1 comments:
We will plan the best party or trip in November to celebrate...but like all things worth doing, time, love and care will shrink this thing so you will look back on this in 1, 5, 10, 20 years and say - I did this! I am strong and I am loved! Love, Lori
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