It is. Port flush... uneventful. Blood work... normal. Examination... a quick once-over, with the doctor feeling my neck, armpits and groin for lumps, then a quick listen to my heartbeat and breathing, through the stethoscope.
Then, we get down to business. Dr. Lerner opens my file, reads through the radiologist’s report, and examines a miniature version of my CT scan pictures. Everything looks good, he tells me. There’s no change in the appearance of the scar tissue, what remains of the abdominal mass.
He’d like to see me in another three months – this time, after another PET scan as well as a CT scan. I ask him how long he thinks it will be before we can begin spacing these tests out, at longer intervals. He says he’d like to keep the three-month testing interval in place until at least two years have elapsed.
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Should that happen, he reminds me – should I discover a lump in the neck or armpit, for example, and a biopsy reveals it to be indolent lymphoma cells – the strategy could be simply to watch and wait for a while. Indolent lymphomas can be so slow-moving that “no action” is sometimes the best action. If an immediate response is called for, there would very likely be new treatments to choose from. The field of lymphoma treatment is changing so fast, Dr. Lerner points out, that even two years from now the treatment protocols could be completely different.
I ask him how long he’s planning to keep the implanted port in. As long as it’s not giving me any problem, he says, he’d like to leave it in “a while longer.”
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So, I’m in a two-year window. Every three months – once each season – I’ll submit to one sort of scan or another. I’ll of course be hoping the results continue to be as unexciting as they are today.
“Stable is good,” the nurse said to me, as she took my temperature and blood pressure, before the doctor came in. Indeed it is.
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