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Letters From Cancerland: Unplugged
By: April Nelson; Published: September 17, 2013 @ 1:23 pm | Comments Disabled
I once read an article in which the author described her habit of working herself into an illness requiring hospitalization about every two years. She did this routinely until a doctor finally pointed out to her that scheduling a vacation every so often would be a more cost-effective, healthier practice. The author, who had been eschewing vacations as a waste of time, became a convert.
I read that article decades ago. I read it back in the pre-computer, pre-cell phone, pre-tablet, pre-plugged in 24/7/365 era. Today, a similar article would have to start with the precept, “disconnect.” While I agreed with the author’s conclusion, I too have been guilty of not taking time for myself but instead pushing myself to the point of dropping.
Not this year. The first week of September, I took an unplugged, “health first” vacation. It was made possible by the generous loan of an ocean cottage by a very good friend and an unexpected opening in my husband's too tight schedule. A last-minute medical crisis of a family member managed to resolve to the point I felt I could leave town without worrying too much. So the first day of September, we were on the road to Cape Hatteras, North Carolina.
Living with myeloma, I never forget the reality of having a chronic, terminal cancer. Every time something new and different emerges (the latest being veins that spontaneously break), I flinch. I try to spend my days not dwelling on it, but the truth is that myeloma is never far from my mind.
But for the vacation, it was, at least much of the time. There is a timeless quality to the ocean, an eternal pattern in the waves. Sitting on the beach and watching them roll in, I could shove myeloma to the far corner of my mind.
To my surprise, my awareness of the cancer was strongest the first time we walked up over the dune and dropped down onto the shore. I stood for the longest time just watching the waves, closing my eyes to listen to the surf. Then I turned to my husband.
“I didn’t realize until just now how much I was afraid I would never see the ocean again,” I told him, my voice hoarse with emotion. I sensed a weight lifting from me as I took in the sounds, the smells, the sights. I stored them up greedily, hoarding them for when the surf is too faint and distant to sense.
Prior to our leaving on the trip, my husband asked me what I wanted to do while we were on vacation. My answer came quickly.
“Sit on the beach, listen to the waves, and do nothing.”
Okay, we did a little more than that. We toured Monticello en route to the ocean, and we ventured away from the cottage a few other times as well. And we did watch some old movies (old, old movies: “Giant” (1956) was the newest of the lot) on television. But a lot of the vacation was spent reading and resting and watching the waves.
The great naturalist Henry David Thoreau wrote, “[a] man may stand [at the shore] and put all America behind him.” He was writing of Cape Cod, which he walked the length of more than once in his lifetime. I was considerably farther south, but my sentiments were one with Thoreau’s.
On Cape Hatteras, I could stand facing the ocean and put all America, as well as all of my myeloma, behind me.
And I did.
April Nelson is a multiple myeloma patient and columnist at The Myeloma Beacon. You can view a list of her columns here [1].
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