Yesterday, before my last chemo, I saw Dr. Blue and Brown. His
opening was, “I heard you were a bad girl in Florida,” (because I hadn’t seen a
doctor about my fever. I could just imagine father-daughter rooms next to each
other in the hospital. No thanks. I survived without doctors.) We then took
stock of where things stand at this quarter way through my treatment. He had sent
me to a breast surgeon, whom I just met before going to Florida. There are
pictures of her in her office from the beginning of her practice, and Robert
and I did double takes to recognize her. I was glad she has lots of experience.
As she gave me my surgery lecture, I
wondered if it got boring for her. I had to stop and ask her to repeat some
things because her voice was soft and without modulation. I doubt doctors
take speech lessons in med school any more than they get handwriting classes.
Her competence and compassion are what matter.
Defenses |
Dr. Blue and Brown pshawed Dr. Soft-Spoken’s assessment. He said it was unlikely the lymph nodes were unaffected, and he poked around to double check. He said if I wanted, he could order another CAT scan to check for metastasis, but he didn’t recommend it because it was rare for cancer to spread during chemo, especially chemo like mine that was working, and if the test showed “hot spots,” all he would do is cancel surgery because there is no cure for metastasized cancer, so what would be the point? The cancer was out the gate. But he thinks so far so good (no guarantees).
So I realize after these four months of chemo that yes, the
cancer has probably been stalled, but it’s still capable of spreading, and surgery
is my next line of defense. I will live without lymph nodes on the right side after
Sept 1 and move on to radiation once things have healed, the third line of
defense.
What’s crazy to me is the silence of the battle. I know it’s
a life and death struggle, and all I feel are the effects of the chemo, nothing
of what’s happening inside. I take these good doctor’s words that my defenses
are holding, but I really won’t know for years. I sit in that chemo chair with that
final potion going in my arm, and I look at the five other people in my pod
connected to IV’s and most of us have care-givers like I do, and most of us are
silent. The couple to my left asks our petite nurse Lisa questions about what
the drugs do and how the PICC line works, and he has all his hair, so I realize
he’s new, but after 4 months, I have no questions for Lisa. At the end of my 6
hours, she takes out my PICC line, making my arm vibrate slightly, but no pain.
For the rest of this year, I’ll have an IV put in every three weeks to finish
out my treatments. When they offered me the gong, I said I’d wait until all that stabbing was over. Seemed premature right now to ring it when I have all that still
ahead of me. Surgery. Radiation. 13 stabs, which they beguilingly call pokes. (My chemo brain calculated 40. But it's NOT 40. It's only 13! Host Dad caught that one. Yay!) More prayer.
Robert said I should practice the gong. One battle down. But I was still thinking about the
uncertainty and the invisibility. My guess is that with teamwork
like this, it’s always that way, you trusting other people to help you see,
help you judge. So little of reality is accessible. Trust, waiting, underscores
everything.
Notice the melting ice, the bird trap. You've seen this before: Peter Bruegel the Elder |
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