July 29, 2024
The sun blazed down on the hospital parking lot. It was nearly full, I had to park a half-dozen rows out. Sweating, I walked inside and inhaled the cool indoor air. I checked in for my 22nd CT (computed tomography) scan in five years.
This one was supposed to be decisive, the first scan since I started an oral chemo drug four months ago. I now wear sunglasses everywhere to protect my red, irritated eyes, and can’t taste vegetables or fruit.
The reception area was crowded. I got in line, the receptionist gave me a digital disc, the kind you get at restaurants that blinks to let you know your table is ready. I took a seat. In ten minutes the device glowed red.
A clerk gave me a paper bracelet, I signed a form. She led me to the outpatient waiting area. A half-dozen patients stared at their cell phones. I completed another form. A nurse called my name.
“How are you this morning?” she asked. We walked to a tiny exam room.
“Which arm?” she asked. I showed her both. She poked at a vein in my right arm. “This is good.” She pushed the vein, it moved under the skin. “Uh-oh, it rolls. We’ll go with the left.” In a few seconds she had inserted the IV link. I felt nothing, she was that good.
“Back in here,” she beckoned. I followed her, as I had followed others for the dozen CTs I’ve had in that cramped chamber. I’d met a lot of nurses at the hospital, but didn’t recognize her.
“Looks busy,” I said.
“We’re always busy,” she said with a smile. “Day and night, 24/7.”
I emptied my pockets and slid onto the bench fitted to the CT device, which is a giant donut. She covered me with a blanket.
“Have you had a CT?” she asked.
“I’ve had around 20,” I said. “Here and in Virginia. We moved here three years ago.”
“Oh? Where in Virginia? I used to live in Centreville. We moved here 17 years ago when my husband got a job at GE. I’d never go back to Virginia.”
“We lived in Woodbridge.”
“Whenever we visit I’m amazed at the traffic. It’s awful.”
She hooked my link to the tube through which a saline solution and a dye flow to enable the CT device to illuminate your organs. I stretched my arms above my head. She started the dye flow, I felt the warming sensation as it ran through my veins.
“All set.” She disappeared into the control room. The bench slid me into the donut for a test run. The nurse revved it up, it hummed. “Hold your breath,” a computerized tone commanded. I puckered as it scanned me. Half a minute later it said, “Breathe.” I exhaled and gasped.

It was the same drill as the last time, and all the times before that. Two passes through the donut and I was done.
“The radiologist will look at the scan and send it to your doctor with his report,” the nurse said. “You can read it on ‘MyChart’ probably later today.”
I stuffed my wallet, phone, and keys in my pocket.
“Drink plenty of water to get the dye out of your system. Have a great day,” she called. She already was moving on to the next patient.
The visit had taken under an hour. The routine now is much faster than just a few years ago, when patients had to drink two quarts of metallic-tasting liquid and wait an hour until it “painted” their organs. The pre-scan fasting is down to two hours from six.
The CT is easy, once the patient is on the bench and prepped it’s over in a few minutes. It creates a ghostly black-and-white image of your insides. PET scans and MRIs are harder and take longer, although in most cases are more precise. If the doc orders a PET the patient knows they’re on track for the next step, a biopsy.
The scan report was posted on the “My Chart” site that evening. It showed some reduction, a few centimeters, in the liver and pleura tumors. After six years of cancer: biopsies, surgeries, chemo, two months of radiation, a year of immunotherapy, and all those scans, some good news. Helped along by prayers of hundreds of people, many I know, many I don’t know.
Two days later Sandy and I showed up at the Cancer Institute, where the oncologist and I first met nearly four years ago. The phlebotomist drew three vials of blood for his inspection. We walked to his office. He extended his hand and grinned, “How are you feeling? Scan looks good.”
I mentioned the tired, bloodshot eyes. He nodded and turned to a computer monitor and pulled up the scan image. “The drug is working,” he said. “That’s big, because it’s experimental. Labs are great. Creatine is a bit high.”
I knew the drug is intended for cancers that I don’t have. No drug exists specifically for thymic carcinoma. I’m an experiment, the doc’s only patient with this problem.
Sandy brought up the low blood sugar, the loss of taste, the optometrist’s prescriptions.
The doc said, “Lay off the drug for two weeks, see if that makes a difference. If you’re still doing well I’ll reduce the dosage. We know the drug is working. So I’ll see you in two weeks.”
“Lay off the drug”: I wondered. Health care almost always amounts to more drugs, more tests, more side effects. Let’s try going the other way. Then too, some of us are blessed, gifted in ways we do not earn. Some other Power is in charge.
The pills are in a drawer, two unopened vials next to the four empty ones. The two weeks will fly by. This guy knows his cancer. I’m a test case. We all have our tests. We soldier on.









