I had my second chemotherapy session. It’s at the doctor’s office in a small room with four handsome leather recliners in a loose circle. I chose the one with bright window behind it to make reading more pleasant during the three-hour intravenous drip. The chairs were occupied intermittently by ladies who had smaller procedures, although another lady who had a companion with her had a lengthy session, too. We didn’t engage each other even with eye contact. It surprised chatty me, but even I chose to behave as if we each were involved in a private act. Although I did banter with my nurse each time she checked the drip bag. Art was with me until he went to the deli to get me a salmon salad on a bagel -- quite a departure from my usual rehab lunch. I read, ate, but mostly dozed.
Dr. Gidron visited with me before the drip session and was so excited to see me get out of my wheel chair on to his examining table clutching the rail without his touching me. He congratulated me on my progress. I was enormously pleased, I am driving myself.
He explained the chemo process again. That it is a three-week curve. You feel fine, then slip down until you hit bottom, feel awful, and then come up strong again which is where I am now.
I said, “I want all the support I couldn’t get in my first session. I want painkillers, I want sleeping pills.” He said: “Absolutely. And I will offer nausea pills even though you didn’t have that problem last time. I will reinforce to the nursing staff that they are offered as requested, although the pain pills only every eight hours.” This is very reassuring.
I love Dr. Adi Gridon. I especially love his creed: My goal is to make you live, not
not to keep you from dying.
---Florence
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