Thawing earth, tempered heart.

My neighbor and I kvetch about what the spring thaw reveals: dogshit and stove ashes running into pools of black ink. The mud is a housekeeper’s bane and a gardener’s promise. In the rain, we swap stories of illness and books and parenting. These days, I keep T. S. Eliot’s words in my pocket.

April is the cruellest month, breeding

Lilacs out of the dead land, mixing

Memory and desire, stirring

Dull roots with spring rain.

Inexorably (and grateful, so grateful to be here, writing), my days unfold towards that first-year mark of emerging from chemo, from the brutality of drugs that both scorched and healed my body. In rickety last summer, I started yoga classes, at first hardly able to climb the stairs to the third floor with its windows that overlook Main Street and the Village Diner and the blinking yellow light intersection. In this mindful class, those ER visits appear again, drift through my thinking, vanish. In my fifties, now, like anyone, I’ve lived through the gamut. The most fearful times of my life, I was often quiet, utterly focused, like the terrifying afternoon when my youngest baby had an allergic reaction and a stranger rushed us to the ER.

Enduring the chemo was like that, too, so many months of cowering beneath a rushing train, nearly always on some variation of the pain scale, intent on the single goal of survival. I longed for the everyday world. In this were small bright gifts. My daughter’s friend would sometimes raid my post office box and bring me books and letters and medical bills, news of the outside world, literary fodder.

Disease is a strict teacher, with lessons of endurance and patience, of non-negotiable acceptance. My world constricted so often, breathing through pain to survive a little more, a little longer. One afternoon in April, my daughters walked me outside the hospital. We sat on a bench beneath a profusely blossoming apple tree. Through the white-petaled flowers with their ruby hearts, the blue sky. We sat and talked. For ten minutes? Half an hour? What does it matter? The limitless spring sky, the infinite mystery.

April this year, not otherwise
   Than April of a year ago,
Is full of whispers, full of sighs,
   Of dazzling mud and dingy snow;
   Hepaticas that pleased you so
Are here again, and butterflies. ~ Edna St. Vincent Millay

Under the kitchen vinyl.

While the radio carries in terrible news, the carpenter tears off the vinyl on my kitchen floor. I run my hands over the worn maple boards that are revealed to the daylight again. In one corner, a rotten board where perhaps the sink leaked. The carpenter cut out those pieces, and I look down at the basement’s graveled floor. In another corner, there’s a blackened place where perhaps a woodstove once charred the flooring. He and I stand there, considering, wondering about who once lived in this house. I wonder about their patterns of heat and sustenance, these people who passed from this world, decades ago.

When the carpenter leaves, I vacuum, then sit on the cold floor while the cats sniff curiously. I rub my hands over these boards bruised from living and speculate that I can sand and polish this small space, quicken it again.

I began this project with a desire to take down a wall, open a room, and chase away the dismal memories of illness, to acknowledge that, indeed, this is the house where cancer devoured my body, tore at my flesh and mind. I survived. To continue surviving, I must revise my life, change my patterns of living.

I know a few of the names of the people who lived in this house on a village hillside. Now, barefoot on these cold hard-worn floorboards, I sense the mysterious stream of connection that runs between the dead and myself and those who will someday live here, when I have moved on myself, to other earthly or unearthly places. Who laid this floor I’ll never know, but I’ll put my hands and my muscle to it, lend my energy towards restorative beauty, towards the scantness I can do.

I am beginning to understand that healing is not about returning to what was, but about accepting the change and adapting to the brokenness. This is happening all around us, for people, for the land. People have done damage to the earth and to each other that can’t be undone. We can lament what was, but that won’t help us take care of what we still have. In fact, it might just hold us back. Nature herself keeps giving and never giving up. ~ Helen Whybrow. The Salt Stones

Making more tracks than necessary…

I’m standing on a dirt road, looking up at the blue sky unblemished by any smear of cloud as my friend wraps a scarf around her face, when a Subaru speeds over the crest. Jolted, I lurch to the roadside.

$750k in cancer treatments and I’m felled by wrong-place, wrong-time on an otherwise untraveled back road? Not this afternoon.

Bitter cold warnings jam the local news. In snow-drenched Vermont, February marks winter’s swing, where the daylight begins to rush back, the light tinged with warmth, suffused with this second-half-of-winter’s promise that seeds will stir again. In the meantime, I take off my mittens as we walk and talk about writing and people and the value of a precise query letter.

We step aside for intermittent vehicles, a silver pickup, a friend’s Prius, a Corolla with split exhaust. A year ago, I’d been sprung from a stay at Dartmouth-Hitchcock and returned to my cancer-and-chemo habits that shifted from bed to couch to what felt like a Herculean effort to open my notebook at the kitchen table and scrawl a few lines, my shaky pencil a balloonist’s line that tethered me to the world. What I didn’t know then was that the hard things I’d endured in my life, some of my making, some not so (sobriety, a divorce, selling a house and lighting out for new territory with my daughters, writing and selling books, the pandemic, the constant wear of subpar home economics), was training for the next 10 weeks. In what is now a blur of that back-and-forth from home to Dartmouth, at one point my oncologist’s eyes widened just the slightest; I wondered if my life was tapering to its end. Was my body about to be driven under?

But not last winter. Not this sunny afternoon, either. What rich luck to walk on a Vermont ridgeline road, the snowy mountains in the distance, finches in a roadside maple. To work, to share a plate of roasted salty Brussels sprouts with a friend, bake a chocolate cake for my daughter’s birthday.

I will never escape this cancer, whether I live a year more or thirty. Its fearsome and awesome power churns through my heart. How it revealed unequivocally to me the brutality and dearness of this world.

Meanwhile, as I cherish these days, these hours and minutes, the country where I live hemorrhages, the last moment of a man’s life pounding through the chaos, his words to a stranger, “Are you okay?” illuminating suppurating wounds. All the things, sadness and delight and such sorrow, the radiant sunlight. Each of us, moving along our paths: separate, together.

Be like the fox
who makes more tracks than necessary,
some in the wrong direction.
Practice resurrection.
― Wendell Berry

No Restitution.

As a child, I went rarely to a physician: once for strep throat, secondly when I was eighteen for a required physical to enroll in college. I had a smallpox vaccine in sunny Santa Fe, surely one of the last in this country as my younger brother skipped this one. My mother brought her three kids to elementary school clinics for DPT and polio vaccines in gloomy Manchester, New Hampshire. We were healthy kids, and my mother, an RN, believed firmly in keeping healthy kids out of the medical system.

As a 21st century cancer patient and now survivor, I inhabit a different world. Through the Dartmouth-Hitchcock portal, I message my oncologist (my oncologist? this pairing of words still makes me cringe), who kindly replies. My recent bloodwork results are “unrevealing.” I’m reading Geraldine Brooks’ Caleb’s Crossing, a gift from a friend, set in the 1600s, and I study that “unrevealing” word, pondering its roots. I have a slightly-above-average vocabulary, and yet this disease has shoved me against so many words I’d never encountered. For instance, salpingectomy: removal of a fallopian tube.

Among much else, I’ve observed how my oncologist (again, that wincing) uses language: use words precisely for what is known and what is not known. The precision of oncologist and surgery saved my life; yet, I was never given the illusion that all is known. For now, on this cold morning, crossover between a full moon already waning and the rising sun barely quickening the horizon, I’m well. Which arrows to the heart of the human condition. The nascent day stretches long, an infinity of possibilities.

“There is no restitution for people like us, no return to days when our bodies were unscathed, our innocence intact. Recovery isn’t a gentle self-care spree that restores you to a pre-illness state. Though the word may suggest otherwise, recovery is not about salvaging the old at all. It’s about accepting that you must forsake a familiar self forever, in favor of one that is being newly born. It is an act of brute, terrifying discovery.”
― Suleika Jaouad (in all her awesomeness….)

Trainwreck.

On the year anniversary of beginning chemotherapy, childishly I crab at my siblings. It’s a small thing—a bad internet connection, a request to make a phone call that might have taken 10 minutes—and I’m angry as all get-out, fury galloping in my blood. The common lingo is that chemo equals nausea, like a bad flu. That is not true, or was not true for me. Enduring chemo was like lying between two burning rails while a train sped over me. I held myself still as could be to survive that months-and-months-long train (how could something be so large?) rattling over me. Sure, there’s a few moments where the train slows, and you think maybe I’ll survive this, but steaming metal rushes right over your face, your mortality far closer than spitting distance. While the rest of the world is immersed in meetings or drinking wine in Spain or skiing, there you cringe, the pain so intense in your bone marrow that morphine means nothing.

In the first round, I had a common and horrific reaction to one of the drugs, rituximab, which stole my breath and shook my bones so hard the bed rattled. The room filled with people in scrubs. I did not know one person’s name. They kept talking to me, and I could not understand a single word. I was under that train, remember, the wheels hammering on tracks.

I never considered myself a warrior battling cancer. But my body was a war zone between two matched enemies: would the chemo quell the lymphoma, or would all of us go down together? A year later, in remission, I’m suffused with gratitude for my life, for so many people who got the train off me. And yet, a year later, there are days I’m still turning the pieces of my life over and over, wondering WTF? Like anyone, jab a shovel into the soil of my life, and the layers appear infinite. Twenty-two years ago, I left my crying four-year-old (“I want to come!”) behind and drove to the airport with my brother in my sister’s time of need. I had left in such a rush that I’d forgotten my driver’s license. It was not long after 9/11, and I had to cry to get on the plane without ID, but I finangled it. Coming home, we hit a snowstorm. My friend and her four-year-old drove over the White Mountains in a white-out to bring me home. At the crest of Franconia Notch, she pulled over. I got out to clean snow from the windshield and lights. No one else was on the road. Snow billowed through a freezing wind. I looked through the window at her son in his carseat between us. I had bought him a little toy, a hexagon of blue fluid with a yellow fish, and he was turning it around and around in his hand, so the fish would swim. It seemed like we were the last three souls on the planet. Such a long and treacherous way home to my little daughter and her twiggy braids. But my friend drove carefully in her red pickup. That story shook out into all’s-well, something that needs no bow-tie of a moral. Simply, all were saved. Our lives went on.

So many pieces of a life. On this Thanksgiving morning, how grateful I am to remain yet here, disease-and-treatment battered, broken by fate and my own rough actions. The terrain of the living.

… And last, I’m honored to have been nominated for a Pushcart Prize (a secret dream of mine) by Under the Sun for my essay “Weeds.”

Crazy-Making.

Yesterday, my oldest and I made that drive again down I-91 that flanks that Connecticut River. My knitting in my lap, I counted exits, St. Johnsbury first exit, then the second, the third that heads east to New Hampshire’s White Mountains, the fourth Barnet, which I took when I stayed at Karmê Chöling. We talked about fall colors and a meatball recipe and family, of course, all the way down to exit 13, the Norwich and Hanover exit, where we stopped for coffee and scones, as if a good luck charm. Coffee and sweets, not a dash to ER. We watched the time, careful not to be late for what I hoped would be a mere routine check-in.

All summer this day has hovered in my mind — what will this day reveal? — but this past week this coming journey was as near to me as something I held in my hand as I went about my days, doing what needs to be done. The day before, talking with friends, the fear of this day erupts and I hear myself on the verge of screeching, nearly crying. All summer, I’ve relished my good life, learning to walk again and eat again, to read on my back porch in that hand-me-down butterfly chair. To marvel that I am not in pain. That I might sleep and reasonably expect I might wake in the morning exactly as I want, in the pre-dawn darkness drink milky coffee and write. That I will witness the unexpected autumn buds on a yellow rose bush open, these final velvety blossoms of the season.

At Dartmouth, we wait again in 3K, in the cancer center. I am no longer one of the pallid-gray-faced chemo patients, hobbling, enduring. How desperately I never want to return here. My oncologist gently reminds me that he’d assured me I’d pull through this winter, even as I was admitted again and again and again, a dozen times. Add to that, more ER visits.

Later, a friend asks about the scan’s sign-off, but the only rules that matter are what the hidden mysteries of my blood and flesh reveal. The markers are that the lymphoma has not returned. I know that the reaper’s scythe heads towards me as that inarguable blade poises over each of us. But not this day for me. Not yet.

Driving home, people crowd the interstate bridges with RESIST signs. As our car sails beneath the metal and steel, we wave. I’d told the oncologist that my wellness plan was four-fold: eat real food, walk, do my work, and try not to go crazy.

He said, This is crazy-making. Just do your best.

There is only one heart in my body, have mercy
on me…

Thank You for letting me live for a little as one of the
sane; thank You for letting me know what this is
like. Thank You for letting me look at your frightening
blue sky without fear, and your terrible world without
terror, and your loveless psychotic and hopelessly
lost
with this love

~ Franz Wright