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Out There I Have to Smile

Illustration by Ashanti Fortson

Heather Lanier | Longreads | March 2021 | 16 minutes (4,473 words)

 
A few years ago on a gorgeous June day, I found myself in a windowless bathroom with forget-me-not wallpaper, my butt on a toilet, without any good reason to be there. It was a standard mothering move. Beyond the door, I could hear my two small kids laughing and eating cereal, so I stayed in this little space, smartphone in hand. In an hour, I was headed to a bowling alley with my kids, both of whom could now walk through a doorway on their own. And this was a brilliant new development, not just for the 2-year-old who’d learned to walk at the standard age, but for the 4-year-old, Fiona, who’d spent the past three and a half years in physical therapy striving toward this lofty goal. Forty-five percent of people with Wolf-Hirschhorn syndrome walk, said the report when I first got her diagnosis. Her ability to walk meant I no longer had to consider wheelchair or stroller accessibility. Her ability to walk independently meant she could navigate the tight turns around a bowling ball return without having to steer a clunky walker. So I was taking my kids bowling, as soon as I stopped pretend-peeing and reading on my phone.

I was reading a friend’s blog post about a recent appointment with her counselor. As soon as she mentioned her son, who has the same chromosomal syndrome as my daughter, she began to cry. 

The therapist asked, “Why do you always cry when you talk about him in here?” 

In here was the therapist’s office, maybe a subdued room with sage walls and elephant statuettes. Out there, my friend pushed her 4-year-old son in a wheelchair. 

My friend looked up at the ceiling a moment and thought. Why do I always cry when I talk about him in here? The answer hit her, and she sobbed. She managed this sentence, eked out between heaving breaths: “Because … out there … when I’m talking … about him … I have to smile.”

I put my hand over my mouth. The windowless bathroom. The forget-me-not wallpaper. I burst into tears. 

* * *

For bodies that don’t fit into a certain mold, for bodies we call disabled, out there can be a treacherous space. Out there has steps where you need a ramp. Out there has strobe lighting that could make you seize. Out there writes stories over your body (she’s sad, broken, wrong) when you just need toilet paper. 

For parents of kids with disabled bodies, out there can be exhausting. It maintains chipper myths about babies that your child breaks. What’s with that feeding tube? It tosses questions at your feet like it’s throwing you something between flowers and rotten fruit. Why’s she so small? What happened? What’s wrong? You answer with a smile, or you answer with fatigue, or you turn your head because none of your business

Out there is risky. Your son might sit in a classroom led by a teacher who doesn’t believe he can learn. Or your daughter might need medical care from a doctor who thinks she’s a tragedy. 

Out there is inconvenient. The doorway isn’t wide enough for your adaptive stroller. The wood chips of the town’s only playground are terrible for wheelchairs. The librarian concludes public story time with a craft that requires scissors, and you must now serve as your child’s occupational therapist, back hunched, palms sweaty, enabling the arduous work of cutting paper.

Out there is not exactly designed for your kind. 

* I use both person-first and identity-first language in this essay. As a nondisabled person, I don’t have a right to claim an identity for someone, so I err on the side of identity-first language until I know a person’s preference — and my daughter hasn’t indicated one. I also use identity-first language to stand with disability activists who argue that linguistic acrobatics to avoid the word “disabled” are a manifestation of our culture’s ableism. We do not say, for instance, “I am a person with femaleness.” #saytheword

As a white, straight, cisgender, non-disabled woman, I must imagine how this sentiment holds true for other bodies. My experience as a caregiver to a kid with disabilities* has put me in the closest relationship to this truth. Out there is not designed for many. 

Which is why in here spaces are so delightful. And it’s why, especially in early parenting, I often lingered in them for longer than I needed. Idling in the bathroom. Struggling to leave the house. In here applies little pressure. In here asks no questions. In here often lets you and your kin be as you are.

In preschool, my daughter Fiona walked stiltedly. Her gait was not the smooth coordination of typical preschoolers. She slapped her right foot down, and her left foot followed pigeon-toed, afterthought more than intention. She sometimes held her arms out, and because she was nonverbal, she said, “Ahh, ahh,” plowing toward whatever caught her eye. When we were out there, people sometimes looked at her because she was adorable and magnetic and thrilled by life. And sometimes people followed her with a calibrating gaze. I could tell that they weren’t admiring the cuteness of youth but instead trying to answer the question, What’s wrong? 

“You’re lucky,” a pediatrician said to me during a routine checkup. “At least you know what’s wrong. Some parents don’t even know that.” He looked up from my kid, his eyes sharp with intensity, and nodded. “You know what I mean?” But it wasn’t a question. 

Nothing is wrong with my girl, I wanted to say.

No, of course not, the doctor might have corrected. Inside he’d likely think, Yes, of course there’s something wrong, and then he’d recite the long list of diagnoses in her medical file: epilepsy, hypotonia, hydronephrosis, scoliosis, developmental delay….

Things her medical file has never listed: loves coloring, loves cheese, rocks a Converse sneaker, appreciates jalapeños, finds the beat, will increase speed tenfold for a turn at the swing.

Wrong can slide too quickly into another concept: tragic. There’s a prevalent Hollywood cliché (which bears no resemblance to real-life statistics) that disabled people wish to die. I didn’t need a child with Wolf-Hirschhorn syndrome to spot this cliché; I’d noticed it years before I had Fiona. Million Dollar Baby: a female boxer triumphs in fight after fight only to break her neck, end up quadriplegic, and ask her coach to help her kill herself; he obliges. Me Before You: a grumpy guy in a wheelchair is hell-bent on committing suicide, then falls in love with his caregiver who tries to show him that life is worth living. He kills himself anyway, because, well, you know, wheelchairs. The films are dramatic expressions of the old, ableist assertion that I’d rather die than live like that. 

What I didn’t realize until having Fiona is that if a person is intellectually disabled, a parent’s feelings often become a barometer for their kid’s worth. What my friend and I have known, without ever knowing we’ve known, is that our culture judges the worth of our kids by judging our contentment. I hadn’t named this until I sat in the bathroom and read my friend’s blog post on my phone, but along with all the obstacles to surmount or circumnavigate or abandon, out there obliges us to offer our cheer. Are we happy? If so, then maybe the lives of our children aren’t tragic. Out there I have to smile. 

* * *

In The Spirit Catches You and You Fall Down, Anne Fadiman tells the story of Hmong child Lia Lee, who has severe epilepsy. It’s a highly lauded book, and for good reason. But midway through, Lia suffers a massive seizure, nearly two hours long, and goes from a happy, hyperactive child to a  mostly unresponsive quadriplegic. “Vegetative state,” the doctors said, and I cringed, eager for Fadiman to take the phrase to task. Because Fadiman had thus far done a beautiful job revealing the cultural biases of both the Hmong family and their Western doctors, I figured she’d unveil the ableism inherent in ever likening a human to a carrot or a beet. I thought of Martin Pistorius, who spent 12 years in an unmoving body that doctors assumed was also “as good as not there, a vegetable,” but as he says years later in his TED talk, “I was aware of everything.” 

Fadiman fails here. She doubles down on the doctors’ sentiment, offering this description of patients in so-called “vegetative states”: “pasty-skinned carcasses with slack mouths, hair like straw, bodies that smelled of urine even after they were bathed.” Carcasses. The word cuts. It describes shells in which humans once lived. It should not be used to describe actual humans, still living. Fadiman agrees with the family when they think Lia’s soul is gone.

At this point in the story, Fadiman pivots to the mother, oh the mother, and how she adapts to her child’s altered life. Fadiman paints some beautiful portraits. The mother lovingly washes her daughter once or twice a day. The mother wears her daughter in a hand-embroidered cloth carrier. The mother feeds her daughter spoonful after spoonful of rice and then kisses her rice-covered face. “Sometimes I thought: this is not so terrible,” writes Fadiman. Mid-page, I thought Fadiman might lean toward valuing Lia’s new, altered life. Admittedly, she’d do so through the trope of Lia’s gifts to nondisabled people. Look at how much love she brings her family. But gift is certainly better than carcass. 

Instead, Fadiman pivots: “But whenever I began to be lulled by this relatively rosy picture, I was drawn up short by an explosion of rage from [the father] or, more frequently, by a sudden seepage of grief from [the mother].” The parents’ feelings tip the scales. Fadiman can’t see the value of Lia’s life if it brings not just love but suffering, if caring for Lia is not just a tender and physical act of love, but also a grief-stricken, arduous job.

Out there we all have to smile. 

* * *

Happiness is an encouraged performance in America whether you’re disabled or not. By analyzing photographs, Stanford psychology professor Jeanne Tsai found that U.S. leaders are over six times more likely to display “open, toothy smiles” than Chinese leaders. This same smile, what Tsai calls “the sign of American happiness,” also appears more frequently in American children’s stories and women’s magazines than in East Asian counterparts. “A lot of immigrants have talked to me about how exhausting it is being in the United States,” she told NPR reporter Maiken Scott of The Pulse, “because you have to smile all the time.” 

But the stakes of that performance are higher for disabled people and their caregivers. Princeton ethicist Peter Singer has kept his job even after arguing that parents of disabled babies should have the right to kill their kids. Because people with disabilities cause too much suffering, he says. 

The birth of a child is usually a happy event for the parents. …  It is different when the infant is born with a serious disability. Birth abnormalities … turn the normally joyful event of birth into a threat to the happiness of the parents and of any other children they may have.

Parents may, with good reason, regret that a disabled child was ever born. In those circumstances, the effect that the death of the child will have on its parents can be a reason for, rather than against, killing it.

Singer, whose book Practical Ethics is in its third edition, at one point suggests that his argument about murdering babies applies to disabilities that make a child’s life “so bleak” that it’s “not worth living.” (How would anyone determine a life “not worth living”? And who gets to decide such a thing?) But then he argues that hemophiliacs too could be justifiably killed in infancy because a woman will only have so many children, and the hemophiliac child might prevent her from having another, healthier baby. “It is … plausible to suppose that the prospects of a happy life are better for a normal child” than for a hemophiliac, he writes. 

I think of my college roommate, a gregarious extroverted gay man who competitively roller skated and also had hemophilia. While he blasted Latin pop through our kitchen and danced with joie de vivre and sang into a spatula, I, the “normal” non-hemophiliac person, brooded in my room to the tune of melancholy female artists like Tori Amos, while writing poems about romantic angst. Certainly, disability doesn’t determine happiness. 

What I didn’t realize until having Fiona is that if a person is intellectually disabled, a parent’s feelings often become a barometer for their kid’s worth.

But the bigger issue is this: Why should a person’s happiness — or lack thereof — be used in proving their right to live? And it’s not just Singer who delivers this message. Here’s disabled writer Nancy Mairs on the subject, from “On Being a Cripple”: “In our society, anyone who deviates from the norm had better find some way to compensate. Like fat people, who are expected to be jolly, cripples must bear their lot meekly and cheerfully. A grumpy cripple isn’t playing by the rules. Early on I vowed that, if I had to have MS, by God I was going to do it well. This is a class act, ladies and gentlemen. No tears, no recriminations, no faint-heartedness.” 

You’ll hear parents of kids with disabilities negotiate this pressure to be happy all the time when they describe their children. “He has Down syndrome, and he’s nonverbal,” a father will say, “but he’s happy!” Or a mother will say, “She has cerebral palsy, and she doesn’t walk, but she’s brought us so much joy!” We can’t fault the parents. They add this caveat of happiness because they know it carries necessary currency. 

But this can be exhausting. It turns happiness into a rhetorical strategy, and makes the faces of disabled people and their caregivers a walking argument that should never have to exist in the first place. 


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* * *

During Fiona’s second year, I started a blog called Star in Her Eye. I wrote it because my child’s eyes were bursting with divine luminescence, and yet an unsmiling pediatrician called her a “bad seed.” I wrote the blog because parents at playdates were talking about babyproofing their outlets, and I was talking about the interesting sculptures at the cardiac unit of the children’s hospital. I wrote it because my girl was coming up with ingenious ways to communicate despite her verbal limitations, and yet because she didn’t babble, an early interventionist declared her “at zero.” I was in a very different field of parenting than the baby books described, and I needed to find my people. I also needed to write about ableism — how I was encountering it, how I was exhuming it from myself. A deep and abiding ethics guided my decisions about what to write and how, but I always wore the weight of my words. Tell too much of a certain kind of a truth, and I could risk further deepening the pervasive story that kids like mine were the B word: burden. 

In December 2015, three years into the blog, the disability-themed online venue The Mighty published a satirical article called “Introducing: Meltdown Bingo.” In it, an autistic parent of an autistic child used a bingo card meme to make light of her son’s meltdowns. Readers were rightfully outraged, blasting the article for objectifying a kid’s suffering. (It was eventually taken down.) Critics also noted The Mighty’s slant toward publishing, as blogger Savannah Logsdon-Breakstone put it, “warrior mommy blogger content … focused on bemoaning how hard it is to parent a child with a disability. … This is a dangerous narrative.”  

The outrage fueled important conversations about disability representation (#CrippingTheMighty). But articles also popped up admonishing parents for writing about their kids at all. In an article published soon after, the advocacy website Ollibean suggested that parents should not write about their children if they aren’t able to offer consent, a principle that would eradicate the stories of certain intellectually disabled people, pushing them and their caregivers — disproportionately women — to the unwritten, invisible margins. During the years that I wrote the blog, Fiona could not offer me consent, and one of the things I often wrote about was our very efforts to help her communicate so she could loudly disagree with me. But that took time — many years with therapists and a speech device.

The challenges of parenting a disabled child — “the prejudice and ableism, fighting systems for an equal education, equal and accessible medical care, accessibility, insurance coverage for a new wheelchair or communication device,” the Ollibean article noted — are injustices built into a system that needs to change. This is 100% true. But the quote fell under the subheading, “It’s Not Your Disabled Child, It’s the System.” In other words, parenting a kid with disabilities isn’t ever hard because of the inherent difficulties of a disability. 

It was not hard, for instance, taking my infant daughter to a swallow study (to make sure she wasn’t dying from her own spit) and two kidney reflux exams (to make sure these vital organs weren’t at immediate risk of failure). It was not hard spending four years helping her learn to walk, or three years helping her tiny, fine-motor-limited fingers navigate a robust communication device so she could tell us what she wanted to eat. Likewise, it was not hard when my husband and I hovered over her body as she jerked in convulsions, her eyes pried open by erratic brain synapses, and it was not hard to check the clock while we did this. More than five minutes, and a seizure can cause brain damage. 

Of course it was hard. Or, it was not hard because hard is the word we use to describe cellophane-wrapped candy, while this is blade-sharp, a knife slicing through the gut. 

But if we can’t say it was hard, then how can we affect any change that would help people in power understand what kind of support we might need?

And yet, if I do say it was hard, then I am fueling, as Logsdon-Breakstone put it, “a dangerous narrative.” I’m risking the chance that people will see my kid, my glorious beautiful curly-haired feisty stubborn rascal of a kid, and think, That mom’s unhappy; that kid’s life is tragic

Tell too much of a certain kind of a truth, and I could risk further deepening the pervasive story that kids like mine were the B word: burden.

My facial expressions out there are territory over which ideologies are fighting. My emotions out there have rhetorical power. And I will use everything I have to argue that my kid’s life has equal value to anyone else’s.

So I’ve smiled. Especially in those early years, I smiled at the nurse who called my kid’s name in the waiting room. I smiled as she led us to a room for X-rays. How cute, she said to my 38-inch 5-year-old in purple hospital jammies. I smiled after I unfolded Fiona’s walker with a loud click at the library, eliciting stares, and I smiled while the teacher talked me through Fiona’s low report card scores. 

It wasn’t a conscious thing, the smiling, until I read my friend’s story while sitting in the forget-me-not-wallpapered bathroom. But when happiness becomes a rhetorical move, it’s a lot less fun than regular happiness. “The freedom to be happy,” writes Sara Ahmed in The Promise of Happiness, “restricts human freedom if you are not free to be not happy.”

* * *

In “Special Olympics and the Burden of Happiness,” Lawrence Downes of the New York Times argues that Special Olympics doesn’t give itself the freedom to be unhappy either. Downes describes the hours-long medal ceremony at the 2015 World Games as a “cascade of triumphant moments” and a “carefully thought-out strategy” where music swells and the crowd cheers as athletes receive their awards. According to Downes, the organization intentionally uses joy as a rhetorical strategy to advocate for the healthcare, education, and other rights of people with intellectual disabilities. The article acknowledges the global plight of people with intellectual disabilities, many of whom are denied an education, sequestered in institutions, and suffer abuse and neglect. If Special Olympics is trying for a revolution of sorts, “its revolution is televised, happily,” writes Downes, “on ESPN.”

But Downes subtly critiques the efficacy of this strategy, calling Special Olympics “an organization so good at making its athletes and the public happy, so bursting with good will and smiles, that nobody has to take it seriously. It has waged a nearly 50-year battle for inclusion and acceptance for people with intellectual disabilities, and people still think it’s a track meet.”

In March 2009, President Obama told Jay Leno of The Tonight Show about his recent bowling score of 129. “It was like Special Olympics or something,” he said with a laugh. Before the show even aired, he was on the phone, apologizing to chairman Timothy Shriver. According to Shriver, Obama invited the athletes to the White House to school him in the sport and “help him improve his score.” If the silence in news reports is any indication, the match never happened.

* * *

Our bowling match did happen. I eventually wiped my tears and left the in here space of the forget-me-not bathroom. I drove my kids to the bowling alley, parked the car in a blue-painted spot, and hung the handicapped placard on the rearview mirror. One by one, I hauled my kids out of their car seats. I held their hands as we crossed the parking lot. I opened the glass door for them, and in they walked. Right through the door.

When we got into the lobby, my heart sank: The lanes about 50 meters ahead were dark like a nightclub. Red and blue and yellow laser beams flashed across the floor, the ball returns, the scoreboards, and the seats. Pop music blasted from above.

From the shoe rental desk, my friend Kristy, Fiona’s godmother, came to us with a worried expression. “I’m sorry,” she shouted over the music. “They just turned them on.”

I exhaled. Kristy had called in advance to be sure, and the guy on the other end had said no, they didn’t do laser bowling during the day. 

I paused, standing near the entrance, trying to figure out what to do. “It’s not like she’s had seizures from strobe lights before,” I said, recalling the EEG where a technician flashed a light in Fiona’s face and measured her brain waves. “It’s just … it’s a risk.” Further inside, I watched the laser lights spin around, casting erratic, broken-up rainbows. New seizure triggers can emerge without warning in people with Wolf-Hirschhorn syndrome.

We rented our shoes and paid for a lane. The red and blue and yellow beams swirled around us. Miley Cyrus blared. “You wanna go first?” Kristy shouted two feet from my face. Any farther and I wouldn’t have heard her. Her teeth glowed white from the blacklight. I went after Fiona, who was toddling down the lane, ready to walk its length. The bottoms of her Converse sneakers glowed. 

The place was mostly vacant. Had anyone seen us in the dark, they would have seen two adults and two kids having a leisure afternoon. They would have seen the adults center a kiddie ramp at the top of the lane and help the kids push their balls down the ramp. They would have seen the balls make their slow-rolling treks toward the pins and knock a few down. Yay! the onlookers would have heard Kristy and me say as we clapped. The kids sometimes clapped too, and sometimes turned around unfazed, heading for another spot in the darkness.

These onlookers probably wouldn’t have seen my furrowed brow, or my eyes, straining in the dark, to assess whether my daughter was having myoclonic blinks or jerks. They wouldn’t have seen me silently curse this bowling lane for turning a fun outing into a shitty, stressful event. 

Neither would they have seen Fiona seize, because — thank God — she didn’t. And they probably would not have seen me smile much, either. But if I had smiled that day, it would have glowed bright as an incandescent bulb. 

* * *

In the summer of 2020, I published a memoir, Raising a Rare Girl. How could I write a book about Fiona that avoided the trap of the “my kid’s so happy” narrative? Because it turns out, my kid is happy — often exceedingly so. Fiona, now age 9, has way more joie de vivre than me. Though not yet a swimmer, she plows her body into ocean waves and screams with delight. She yawps for joy at the mention of Kit Kats. She is really, really stoked to go for walks around the block. She and my old college roommate would get along smashingly. And yet a story that emphasizes the “look, my kid is happy!” narrative would lodge her right into the very pressure Nancy Mairs identifies: “In our society, anyone who deviates from the norm had better find some way to compensate.” 

And how could I write a book that also avoided the “my kid is so hard” narrative? Because that’s true, too.

I tried to write a book that showed my daughter’s inherent value — and our culture’s denial of it — whether she was happy or not. I ended up writing a book about what it means to be human. “This belief in the virtue of the ‘happy’ and suffering-free life sterilizes and shrinks us,” I wrote toward the end, “minimizing what makes us most beautifully human: our tenderness, our vulnerability, the profundity of our capacity for heartache, the risks of which deliver us into immense joy.” What I tried to do was show, honestly, the joy and the grief, the hard and the beautiful, and say: It all belongs. 

* * *

You ask: Am I happy? I say, sometimes less than before. Because she wakes six times a night. Because regular trips to pediatric specialists are no strolls through the park. Because special educators sometimes see her as broken, in need of fixing. Because her needs often exceed my energy. Because every time I’ve hovered above her convulsing body at night, counting the minutes, I might have gained something like courage or “life experience,” but I also felt gashed  in a bodily place that I can’t find, I can’t name. 

Because loving someone has never been so hard.

You ask: Am I happy? And I say, sometimes ten times more than before. Because her fine, blondish-brown hair brushes my cheek when we snuggle. Because her sapphire blue eyes seek out mine every day. Because at age 5, after three years of speech therapy, she at last made a hard C sound. Come, she said, and I did. Because when she was 4 and I asked which hat she wanted to wear, this one or that, she pointed and said “gamma!” (meaning “that one”) with such high-pitched glee that it felt like I held not a red wool ski cap but a lifetime supply of joy. Because the stress of a swallow study, the labor of an orthopedist’s appointment, and the fear of EEG results make the good news of a clear airway, an unchanged scoliosis curve, and an unworrying set of brain waves all the more glorious. 

Because loving someone has never been so hard.   

What I ask is that my answer doesn’t matter in determining her worth.

* * *

Heather Lanier’s memoir, Raising a Rare Girl, was a New York Times Book Review Editor’s Choice. Her recent essays appear in The Atlantic, The Wall Street Journal, and Off Assignment. She is an assistant professor of creative writing at Rowan University. You can find her on Instagram at @heatherklanier

Editor: Cheri Lucas Rowlands

Illustrator: Ashanti Fortson

Fact-checker: Nora Belblidia

Binders Full of Men

Jennifer Berney | The Other Mothers: Two Women’s Journey to Find the Family That Was Always Theirs | Sourcebooks | February 2021 | 18 minutes (4,976 words)

 

Becoming Family,” Jennifer’s 2019 essay exploring traditional notions of heredity and paternity, is a nice companion to this piece.

A manila envelope from the country’s largest sperm bank arrived in my mailbox only three days after I had called to request it. I tucked it under my arm and looked around me before returning to my front porch, as if one of my neighbors might catch me—as if there were something forbidden inside. I sat on the step and ran my finger through the envelope seam to unstick the glue. California Cryobank, the catalog said at the top, in white letters on a royal blue background. My wife Kellie and I had already spent months trying to line up a community donor, but no one had come through with a yes. In contrast, this thing in my hands had come to me so easily. I had asked for it and, with the snap of a finger, there it was. Below the company’s name, there was a photograph. I’m not sure what I had expected—maybe a classic image of a baby growing in utero, maybe a mother looking into the eyes of her newborn child. But this photo featured two teenage boys wearing backpacks and smiling at the camera. They stood beneath a tree. It looked like an image I’d expect to see on a college brochure.

Kellie pulled into the driveway with her window rolled down. “Hey, lady,” she said and stepped out of her truck.

“Hey,” I said. My heart sped. I wanted to show her the catalog, but I didn’t want to overwhelm her. I tried to hide my grin.

Kellie sat down next to me. “What’s that?”

I handed it to her. “It’s from that sperm bank in California,” I said. “I called them.”

Kellie didn’t open it. She just held it in her lap.

I reached over and laid a finger on one of the faces on the cover. “Who is this supposed to be?” I asked her. “Are these the babies, all grown up?”

Kellie cocked her head and looked at me to make sure I was serious. “They’re the donors,” she said.

Shit. She was right. My excitement for the packet fizzled. These boys weren’t what I had in mind. Whoever designed the cover must have hoped to convey that these were young men at the peak of their health, but all it highlighted for me was that many of these donors were too young to be making decisions of permanent consequence. They looked like boys, not men. Staring at the picture made me think of factory farming, of dairy cows hooked to milking machines, of chickens dropping eggs in chutes. Were these boys ready to commit to a lifetime of knowing there were children out there that they had helped create? I suspected that most of them just wanted the money for textbooks or beer.

Kellie lifted herself from the step to go inside. I propped the catalog on my knees. Moisture from my skin condensed on the back cover. I flipped through the pages aimlessly, my hope dim.

* * *

My position on sperm—my insistence that a sperm bank was our best and easiest option—was in part based on an assumption I had held since childhood when I first learned of the existence of assisted reproduction. I assumed that the fertility industry wanted to help me, that sperm banks had been designed with lesbians in mind.

I understood that straight couples and single women used sperm banks too, but I had always figured that lesbian couples would make a large share of their clientele, that sperm banks would welcome us, and that our needs would be built into the design of their operation.

I was wrong about this. Sperm banks were not designed for lesbians.

California Cryobank, one of the first commercial sperm banks, opened in 1977 with a very specific purpose: to offer men a way to store their own sperm for future use. This meant that, for instance, a man undergoing treatment for cancer could store vials of semen before starting chemo and radiation, and in doing so could hang on to the option of fathering children someday. Sperm storage was originally envisioned as a niche market for men, available mainly as a safeguard against future infertility. Male sterility, the founders believed, had the potential to be psychologically “shattering”—devastating to a man’s ego.

Few were talking about male infertility as a widespread phenomenon. “Barren” was—and still is—a term applied only to women. Male infertility was seen as so profoundly emasculating that doctors barely mentioned it, even to each other. In the era predating the commercial sperm bank, if a couple had no luck conceiving a child, and if the microscope revealed that the husband’s lack of sperm was at fault, doctors simply recruited one of their male students or staff to donate fresh semen. Sometimes the doctor himself was the secret donor. The arrangement was casual. In many cases, there was no documentation or paperwork. No STD testing. No legal safeguards. No washing, freezing, or quarantining. Just sperm from a source that would always be anonymous to the couple that received it. The prevailing attitude was: Just fix the problem. The less said the better. This approach allowed the husband and wife to carry on as if they’d conceived the child unassisted. Many couples never spoke of the procedure again and never told their children.

It’s worth noting that both this hushed approach to donor insemination and the vision of preemptive sperm banking centered the male experience and ego. It took some time for established sperm banks to identify and fill what now seems like an obvious role: to provide a menu of options to straight couples in need of donor sperm. It took even longer for physicians to cede control and retire the practice of recruiting their own donors.

Commercial sperm banks adapted to help propagate more traditional families—to replace one man’s nonviable semen with another man’s viable semen, and in doing so, fulfill the promise of the normal: a husband, a wife, and children—the American nuclear family.

I assumed that the fertility industry wanted to help me, that sperm banks had been designed with lesbians in mind.

As I was coming of age as a lesbian and considering my future, it had never once occurred to me that the medical industry could legally withhold services from me or anyone else, that they could say yes to straight couples and no to queers, but in fact they did just that. Most sperm banks and fertility clinics turned away any woman who wasn’t conventionally married. Sperm banks weren’t made for lesbians.

It turns out lesbians didn’t need them. Instead, while sperm banks were growing, lesbians were developing networks to support each other. The idea that lesbians could become parents on their own terms was, at the time, revolutionary and connected to the larger feminist goal of giving women full control over their reproductive health. Lesbians and allies organized groups for queer women who wanted to become parents, either as partners or single mothers. They passed out instructions on how to perform inseminations with turkey basters, diaphragms, and needleless syringes. They found clever ways to source sperm.

One way completely avoided any doctor’s office. Several mothers of now-grown children have explained to me how it worked in Seattle in the 1980s.

If you were a lesbian who wanted to get pregnant by an anonymous donor, you needed to find yourself a go-between, a friend who would make things happen for you. The go-between would ask around and find a donor—often a gay man in the larger community. The donor could be a close friend, or a friend of a friend, or a colleague from work. The go-between would know him, but he would be anonymous to the recipient.

In these networks, there was paperwork involved: a survey that asked for basic medical and personal history, not unlike the donor files available to sperm bank clients. The go-between collected this and shared it with the recipients. She kept a separate file with personal information—the donor’s name, his social security number, the recipients he’d been paired with. In theory, this could be shared with the recipient family when the child turned sixteen, and the family could decide if they wanted to track down the donor and contact him. In practice, this exchange didn’t always happen quite like that. Through the course of the interviews I conducted, I heard anecdotes about forms being lost due to illness, death, and human error. However, community and memory are living things, and in some cases those who wanted to find their donors could do so by simply asking around.

Hopeful recipients charted their cycles with the same tools I used to chart mine: a basal thermometer, a chart, and a pen. When it was time to inseminate, the go-between was the emissary. She picked up the ejaculate (two women mentioned artichoke jars as the container of choice) and kept it warm as she transported it to the home of the woman who was trying to conceive. At that point the go-between helped, or bore witness, or got out of the way, but her role wasn’t just functional—it was spiritual. Her presence conveyed the blessing of the larger community.

Someone who was a go-between once would likely be a go-between multiple times. She would have a list of men who were ready and willing and who already knew the drill.

As I learned about these networks one generation later, I was amazed by their efficiency and by how many problems they solved. The network system outsourced the difficult legwork of finding a donor to the go-between, a person who, because she lacked direct personal investment, could more comfortably manage those negotiations. If Kellie and I had employed this approach, it would have spared us some pain. We had just spent two months waiting for an acquaintance to decide whether or not he’d be our donor, and he had ultimately ghosted us. If, say, our friend Dee had been our go-between, then the acquaintance could have delivered his no to Dee without feeling the pressure of our hopes. We wouldn’t have been hurt by his no, because we wouldn’t have even known about it. Instead, we would have simply sent our friend on a mission, and we would have heard back from her once she was successful.

What’s more, the network system preserved anonymity while allowing the would-be parents to rest easy knowing the sperm wasn’t coming from an unknown stranger but a community member who had ties to mutual friends. This system was free and spared recipients from having to medicalize the practice of babymaking.

They passed out instructions on how to perform inseminations with turkey basters, diaphragms, and needleless syringes.

Others have told me stories that capture another mode of conception that was common to lesbians in the ’80s: insemination via feminist health center. These centers—connected to the larger women’s health movement—were established and run by women who sought to empower their peers. This was the generation of feminists who got together in groups and learned how to view their cervixes using a speculum, a flashlight, and a mirror.

Olympia, where Kellie and I lived, had one of these centers, founded by a woman whose name is still legendary among locals: Pat Shively. Pat was a lesbian herself and a mother of three children from an early marriage. (It’s worth noting that heterosexual sex—often the byproduct of a youth spent in the closet—is the oldest form of conception available to lesbians.) When Pat opened the Women’s Health Clinic in 1981, she didn’t do so with the vision of helping fellow queers conceive but with the broader mission of serving diverse populations of women. Her clinic offered abortions, and she made herself available at any hour of the day or night to administer rape kits to women who had been sexually assaulted. I imagine that it must have been a small comfort to those women, in a moment where small comforts mattered, to be seen by someone who was capable of hearing and believing them, by someone who knew how to be tender and also how to fight.

Pat’s role as the local abortion provider made her vulnerable to death threats, and she took to carrying a Glock and wearing a bulletproof vest. In the photos I’ve seen of Pat, she has a small frame, short unkempt curls, and she is always actively holding something: a phone, a pen, a small child’s hand.

So, while Pat Shively may not have set out to make a clinic for the explicit purpose of helping lesbians conceive—while it may not have even been part of her original vision—it’s not hard to see how she wound up filling this niche.

Pat’s inseminations were in some ways similar to the informal inseminations that took place in doctors’ offices behind closed doors before the era of sperm banks. But Pat Shively didn’t have a range of male residents to recruit from. Instead, she looked for college-age men who didn’t smoke pot (studies showed that marijuana use interfered with sperm motility) and paid her donors $30 per specimen. By some accounts, she charged her clients $50 for the inseminations. By other accounts, she did it for free. Either way, it’s clear that she wasn’t getting rich on the practice.

In this arrangement, Pat acted as both medical professional and community member, a variation on the go-between. She taught her clients how to chart their ovulation and timed the inseminations accordingly. Since hers was a small-scale operation, her donor sperm was fresh, not frozen, and she often performed the insemination on the recipient’s sofa.

In both of these systems—network-facilitated insemination and women’s clinic insemination—family-making became a community act not limited to a bedroom or a clinic. Instead, they combined, to varying degrees, personal and clinical elements: the living room couch as the site of insemination, the needleless syringe as the conduit, the friend or partner as the inseminator, the documents that may someday be lost. Both methods centered the humanity of the recipient and allowed her to feel she was the agent rather than the patient.

And, in both of these scenarios, sperm was mainly a means to an end. Between the go-betweens and the recipients, between the clinician and her clients, there was sometimes discussion about what health issues they wanted to avoid or what aspects of someone’s ethnic or religious background they might prefer their donor mirror. Parents-to-be often sought donors who shared their religious or ethnic heritage. But in general no one had the leeway to insist on blue eyes, or a certain height, or an engineering degree, and it seems that no one obsessed over these details. The attitude that drove these systems was that DNA mattered a little, but not a lot. For the most part, women wanted to make a baby, and they wanted sperm from a donor who was reasonably healthy. That was all.

And, in both of these scenarios, sperm was mainly a means to an end.

Contrast this approach with that of the typical sperm bank customer in our current climate. Today’s commercial sperm banks exclude potential donors not just for issues like low sperm count or heritable diseases, but also for height (donors that are five foot eleven and over are strongly preferred, and many banks won’t accept donors who are under five-nine) and weight. Gay men, who were so essential to the lesbian insemination networks of the 1980s, are to this day effectively banned from donating at all commercial sperm banks—a policy that is ostensibly to protect recipients from an increased risk of HIV, but makes little sense when one considers that all donors are tested and retested over a six month period while their sperm is quarantined and that there are no bans on other high-risk sexual behaviors. Straight men can engage in unprotected anal and vaginal sex with multiple female partners and still qualify as donors, while gay men—even those in long-term monogamous relationships—need not even apply.

Most banks actively recruit on college campuses and require their donors to prove that they have earned, or are in the process of earning, a degree from a four-year college, and some banks charge an extra premium for sperm from donors with an advanced or Ivy League degree.

Sociologist Amy Agigian points out that clients are the ones demanding this approach, citing a study where women “placed the highest value on the sperm donor’s education, ethnicity and height.” Agigian goes on to point out that any belief that a donor’s college education is somehow “transmissible through a man’s semen is further evidence of magical thinking about semen that abounds in our culture.”

To put it another way, sperm banks aren’t simply optimizing their samples for the potential child’s future health. They are optimizing to meet demands for children who will conform to societal norms around race and attractiveness. What’s more, they are selling a myth that an advanced degree confers heritable traits, that the Ivy League can be encoded into a child’s DNA.

Lesbians are now among the consumers driving these demands, and yet I can’t help but think back to the early days of lesbian low-tech inseminations and how, for the most part, they were driven not by eugenic ideologies but by personal connections. When it came to alternative insemination, lesbian recipients weren’t focused on making genius babies or maximizing genetics. They simply wanted families, reached out for community support, and received it.

I didn’t know any of this as I sat on my front porch, holding the Cryobank brochure. I didn’t know it, but for the first time, I sensed that Kellie wasn’t wrong—that buying sperm was complicated, that it was fraught with ethical dilemmas, and that the story behind the sperm we were getting was actually a story that mattered.

* * *

That night, as Kellie slept, I went online. When I Googled “sperm bank,” California Cryobank topped the list, and the rest of the first page was filled with companies that looked nearly identical to the brochure I’d already viewed. Their web pages featured chubby, smiling babies, welcomed by straight couples who looked more like J. Crew models than actual families.

I tried variations. “Sperm bank small” and “sperm bank gay friendly.” I didn’t get anywhere. With each search, the same corporations showed up. It was just before midnight when I finally added the word lesbian to my search and, bingo, the top result linked to a website that featured a woman, alone, holding a baby. She wore a hooded sweatshirt and a loose ponytail; she looked less like a J. Crew model and more like a person I might actually know in real life. Just above the picture was the tagline: “A trusted resource for women planning alternative families.”

Pacific Reproductive Services, it turned out, was a lesbian-centered cryobank founded by Sherron Mills in 1984. Mills, like Pat Shively in Olympia, had been helping lesbians get pregnant out of a community-run clinic. But as demand for inseminations grew, and as the AIDS crisis swelled, Mills wanted an actual donor insemination program that would meet FDA standards—no more fresh ejaculate on demand from a couple of handy donors.

The issue with mainstream sperm banks, as Sherron Mills saw it, wasn’t just that they refused to serve lesbians. Mills also believed that lesbians deserved medical care tailored to their specific needs. In a world where the medical model so often assumed heterosexuality, lesbians deserved a place where they could be at the center of the practice, not floating on the periphery.

Over twenty years later, I hadn’t known I would need this. I had expected, always, that so long as I lived in a progressive community, I’d be effortlessly folded into the larger system. But here I was, already longing for inclusion, seeking a place that had been designed with me in mind.

In a world where the medical model so often assumed heterosexuality, lesbians deserved a place where they could be at the center of the practice, not floating on the periphery.

As I clicked through the site, I learned that PRS was a comparably small operation and that, besides their alternative demographic, they distinguished themselves from larger commercial sperm banks by offering a catalog of what they called “willing to be known” donors.

“Willing to be known” didn’t mean what Kellie would have wanted it to mean. We couldn’t take these guys out for coffee and interview them about their life histories and their politics. We couldn’t even learn their names. But they did come with a promise—an unenforceable promise—that when our future child turned eighteen, they could access their donor’s name and contact information. It struck me as uncomfortable—a little scary even—that my child upon turning eighteen could make a call and add a stranger to our family. But in other ways it seemed preferable to a closed-door policy, our baby’s DNA a mystery that could never be unlocked. My personal stance on secrets was this: I only liked the ones that included me.

I didn’t know it at the time, but the “willing to be known” program was a variation on the Identity Release Program, which was developed and trademarked by the Sperm Bank of California in 1983. Today, in the era of DNA testing, all major sperm banks offer a similar open identity option, and many argue that it’s unethical to offer donors the anonymous option, since it is likely that any donor can now be tracked down, with or without their consent.

PRS was based in San Francisco where, coincidentally, I would be traveling soon. In just a few weeks, my mother would be attending a work conference there, and I planned to join her to visit a city I’d never seen before and eat good food, walk through neighborhoods, and shop for books.

Oh, and visit a sperm bank. Is that something people actually do? I wondered. I recognized the feeling of getting swept up in my own excitement and leaving my level head behind. I tried to talk myself down. There was no reason to make sperm the focus of the trip. Before this moment, I had been looking forward to San Francisco as a distraction from all of this. As I climbed into bed and spooned against Kellie, I could hear my own pulse where my ear pressed against the pillow. People typically ordered sperm online, I told myself, trying to settle my brain towards sleep. There was no real reason for an in-person visit. Certainly I shouldn’t let it become the focus of my trip. Maybe I wouldn’t even visit it while I was in town.

* * *

“I’m thinking of visiting a sperm bank while we’re here.” I said this within ten minutes of greeting my mother in the hotel lobby. Within an hour, we were searching for the address on a map. She wanted to come too. Her eagerness fed my own.

My mother, when traveling, resembled Big Bird; already tall, she seemed to gain another two inches and hover above any crowd we moved through, taking in the sights with a kind of transparent awe. Like Big Bird, my mother was trusting and curious, and would start conversations with anyone we came into contact with. By this, I don’t just mean that she made small talk with the hotel clerk or the cab driver, although she did. But I mean that she also sought chances to chat with the family standing outside the native plant exhibit and the couple seated at the neighboring table.

The sperm bank was less than two miles from the hotel where my mother and I stayed. Together, we walked through a neighborhood of restaurants and bookstores, and then took a left down a hill and descended into a district that was gray and industrial. I kept my eyes fixed on the numbers, and stopped when I spotted the address, 444 De Haro Street, outside a monstrous building built of concrete, glass, and steel. It was a Friday afternoon, and there was no one in sight, though the corridor was vast, with high ceilings and potted palm trees. I felt like an interloper in the corporate world, snooping around with my mother, looking for sperm. I was afraid that a roaming security guard might stop us and ask what we were doing.

But eventually I found it, up one flight of stairs and tucked around the corner. Inside Suite 222, the decor changed dramatically, from bank lobby to massage therapist’s office. The hall smelled of essential oils, of lavender and eucalyptus. A long-haired receptionist sat just beyond the entrance and greeted us. In an effort to keep my mom from talking first, I introduced us right away. “I called last week about visiting,” I explained. “I’ve been trying to settle on a sperm bank, and I just figured since I’m in town—”

“Of course,” she said, nodding. “You might want to spend some time in there,” she suggested, indicating a private room that featured houseplants, a round table, and two wicker chairs with floral-print cushions. “That’s where we keep the donor profiles.” She explained that there were two special binders that held childhood photographs of every willing-to-be-known donor. Each photograph had a number that corresponded to a profile in a separate binder. “Settle in, take as long as you want, and let me know if you have any questions.”

I reached for one of the photo binders first, and my mother took the other. They were wide three-ring binders stuffed with crisp sheets of plastic that shined beneath the light. Each page held two photos, one above the other. On blank sticker labels, someone had handwritten each donor’s number. Some of the photos featured newborn babies, red-faced and swaddled in blankets. Those weren’t so helpful. Others were school-issued photos from first or second grade. They had big smiles with missing teeth, or corduroy jackets, or Afros.

My mother and I sat side by side, studious. Each time one of us turned a page, there was the soft sound of plastic unsticking. Occasionally my mother would chuckle and tap my arm. I’d crane my neck to view her binder. Her choices were different than mine: boys with tidy hair, bow ties, and sparkling teeth. I liked the boys with the shaggy hair and awkward smiles.

What struck me about the binders was this: throughout my twenties I’d been paying attention to my feelings about individual children. Though I liked children in general, and though I was sure that I wanted to have my own, there were plenty of kids whom I could take or leave. They were the boys with buzz cuts and truck T-shirts who begged for toy guns at Target or the girls in faux-fur coats belting out pop songs I barely recognized. Certainly these children were adorable to someone, but they sparked nothing for me. There were plenty of adults I had no interest in or didn’t connect with. Why should kids be any different?

Then there were the kids I wanted to take home with me, the girl with long brown hair and freckles who leaned off the side of her father’s shopping cart. Or the boy with the wide eyes and gap between his teeth who drew pictures while waiting for his food to arrive in the restaurant. After recognizing one of these kids, I always told myself: my kid will be one of the loveable ones. As I looked through the binder of photographs, I had an instantaneous reaction to each one. Some of the photos didn’t interest me at all, but others tugged at my heart. It may have all been an illusion—a crooked bow tie or a Snoopy shirt may have signaled to me, erroneously, that this child felt like kin. The photographs in all likelihood could not predict how I would have felt about the donor as a grown man. But even if my intuitions were illusions, I appreciated them. The photos gave me a sense of control, a sense that I was choosing a person rather than a number.

I felt like an interloper in the corporate world, snooping around with my mother, looking for sperm.

My mother lost interest in the photographs eventually and let herself out of the room. As I pored over donor questionnaires that matched some of my favorite photos, I could hear her chatting with the receptionist, explaining that I had a partner, Kellie, who lived with me in Olympia. “You must get quite a few lesbian couples here,” she said. When she began offering the details of our lives, I hurried to join my mother at the desk.

As I approached, my mother put her arm around my waist. “I was telling her about your situation,” she said. I felt my cheeks grow hot.

The receptionist laid her hands on her desk, as if she had no other tasks to attend to. “Do you have any questions I can answer?” she asked me.

I had just one. I wondered where their donors came from. “Are they all in college?” I asked.

“We get some college students,” she said. “But, actually, we advertise on Craigslist. That’s how most of our donors come to us.”

I let out a laugh. I wasn’t quite sure what to do with this information, that the sperm at this clinic came from the place I associated with free couches and unwanted cats. It seemed that I could have chosen to be troubled by this. But, more than anything, I liked it. I liked the idea the donors were invited rather than recruited, that the call for them went out to the community at large.

“We get a better range of donors that way,” she explained. She was right—from the profiles I’d looked at, most of them listed actual professions rather than majors; I’d seen a doctor, a fireman, an electrical engineer.

That night, in the hotel room, my mother and I each sat on our own bed, each with a bedside lamp on, reading. As she read the book she brought, I spread open the folder that the receptionist had sent me home with. The files didn’t contain much information that was new to me. There was a FAQ page, a handout on how to chart your cycles, and some specifics on shipping and ordering, but I read every word carefully as if I were studying blueprints for a home I would soon build. 

This chapter has been adapted for publication on Longreads.

* * *

Jennifer Berney writes to explore the human state of longing. Her essays have appeared in Tin House, The Offing, Brevity, The New York Times, The Washington Post, and many other publications. You can find her on Twitter at @JennBerney.

Editor: Cheri Lucas Rowlands

‘Plant-Based Eating Is Probably One of the Blackest Things I Could Do’

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“Plant-based eating has a long, radical history in Black American culture, preserved by institutions and individuals who have understood the power of food and nutrition in the fight against oppression,” writes Amirah Mercer in “A Homecoming.” The piece, published at Eater, explores Mercer’s path to veganism and the plant-based diets of the Black diaspora. While Mercer’s journey to a plant-centered diet initially brought up feelings of loss — “my veganism initially seemed like a rebuke of the rituals I had always known” — Mercer finds immense power in what she learns. Exploring veganism isn’t actually straying from her roots, and the shift is a way — as singer Prince once expressed — to liberate oneself and the world from injustice. “As a Black woman in America,” Mercer writes, “my veganism is, in fact, a homecoming.”

Just as I began to plateau on plants, my grandmother gave me a copy of Bryant Terry’s 2014 cookbook, Afro-Vegan. Seeing the words “Afro” and “Vegan” together on the book’s cover disrupted everything the mainstream had ever shown me about veganism. Terry, who is the chef in residence at San Francisco’s Museum of the African Diaspora, uses the foodways of our ancestors as a historical guide for plant-based eating, combining classic Southern, Caribbean, and African dishes into a uniquely Black vegan cuisine: There were recipes for stewed tomatoes and black-eyed peas, grits with slow-cooked collard greens, and a mango-habanero hot sauce. I felt overwhelming power in the sudden and profound realization that I didn’t have to stray from my roots in order to explore my veganism.

Food is political, and that is especially true for Black Americans. A lack of access to healthy food is a problem that disproportionately affects Black and Latino communities — a condition that the U.S. Department of Agriculture formally describes as a “food desert,” though the food justice activist Karen Washington prefers the more apt term “food apartheid” — which are defined in large part by the nearly century-long legacy of redlining.

Decades of U.S. agricultural policies that overwhelmingly favor meat, dairy, and corn have caused many Americans to load up on a diet rich in fatty, processed, and refined foods, but the ill effects of the standard American diet (appropriately also called the SAD diet) are heightened for racial and ethnic minorities. Systemic racism within the dietetics industry has kept Black dietitians out of the field — their number has fallen by nearly 20 percent over the last two decades — while the resulting Eurocentric view of diet and nutrition has severely constrained its approach to non-Western cuisines and cultures. Not only is there a lack of knowledge about the nutritional foundation of many traditional diets, but people from non-Western cultures are pushed toward Westernized views of health and wellness even though, for instance, people of color are generally less able to process dairy products.

Both health care and food policies are greatly affected by who is voted into office. Unfortunately, African Americans have historically been and continue to be victims of voter suppression, which takes away our ability to advocate for health care policies that nourish our families. And so for many in the Black vegan community, plant-based eating can be an act of protest against this disenfranchisement.

Even as Africans in America adapted to their new environment, they retained their Indigenous knowledge of plant-based nutrition. Those forced into slavery on smaller, poorer farms, or in areas where the plantation economy was not dominant, such as New Orleans and the Gulf, kept their own gardens, a practice described by Twitty in The Cooking Gene as “little landscapes of resistance: Resistance against a culture of dehumanizing poverty and want, resistance against the erasure of African culture practices.” In Hog and Hominy, Opie quotes a Scottish-born visitor to North Carolina who remarked that Black people were “the only people that seem[ed] to pay any attention to the various uses that wild vegetables may be put to.”

Chattel slavery, the influence of European foodways, and the interests of a capitalist economy disrupted the plant-centered African diet. That disruption was never repaired, as the government failed to deliver on its promise of “40 acres and a mule” after the Civil War, despite the 1865 special field order to reallocate 400,000 acres of Confederate land to the Black farmers who had tilled it for 250 years. Andrew Johnson — Abraham Lincoln’s successor and a sympathizer with the South — overturned the order and returned the land to the plantation owners. Denied the right to land ownership, African Americans who stayed in the South after the Civil War had little control over the food they grew to feed their families. (Of the Black farmers who have managed to acquire their own land between then and now, some 98 percent have had it taken from them.)

Read the story

The Geography Closest In

Photo by Mats Silvan/Getty Images. Edit by Cheri Lucas Rowlands.

Miranda Ward | Adrift | Weidenfeld & Nicolson | January 2021 | 15 minutes (4,339 words)

The bald conclusiveness of a positive pregnancy test draws a clear line between yes/no, this/that, knowing/not-­knowing. For a moment at least it clarifies everything, or distils it, into a single and irrefutable piece of knowledge. This certainty, when it comes to the body, is rare (later a doctor will tell me: if everything in medicine were as reliable as a pregnancy test, my job would be a lot easier), so I hold on to that piece of knowledge, which is proof of my own productivity, for as long as I can.

But doubt, worry, have a way of threading their way through even the solidest conviction. Threat is everywhere: a light fever, an undercooked egg. Indeed the more I read the more I realise how fragile a pregnancy is, how it isn’t as simple as a positive test and a baby nine months later, which is something I suppose I always knew in the abstract but never had any real frame of reference for before. I was aware that some of my friends and acquaintances, for example, had had miscarriages, but I had not until now really understood what it meant, in both practical and emotional terms, to have to hold an awareness of this terrible possibility always alongside a hope, a longing, for it not to happen to you. Most of what I know about pregnancy, in fact, comes from fiction, from books, films, TV: the way certain signifiers – wooziness, weakness, nausea – are used to suggest a pregnancy before it is confirmed; the way, once it is confirmed, a woman must somehow both alter her behaviour drastically and hardly at all, vomiting copiously into a bin at work seconds before giving a presentation just as if nothing is amiss, but studiously avoiding, suddenly, a whole litany of food and drink; most of all the way a baby is almost always the inevitable result of a pregnancy. The plain fact of it – that at least one in four pregnancies end in miscarriage, perhaps more, since sometimes a woman might miscarry before she even knows she’s pregnant – had somehow eluded me, or else I had somehow failed to think of it in tangible terms.

What does that statistic actually mean, practically speaking? It means that nothing is a given. It means that there are people – a lot of people – for whom the result of a pregnancy is not a baby. It means that even the purest elation is often shaded, especially in the early weeks, when miscarriage is most likely, with fear.

I develop a set of superstitions for protection; certain shirts for luck, certain routes home from the library or the grocery store, certain songs skipped or repeated. An aping at control. And for a while everything is normal, in the sense that nothing is normal, in the sense that I feel slightly ill, weary, a little as if I am not myself. My overriding emotion is happiness, but there is also a part of me that feels as if I have become separated somehow from my body, as if it is acting of its own accord, and the thinking part of me is just along for the ride. There are psychological adjustments to make – I have to play the phrase I’m pregnant over and over to myself to believe it; I have to think about what is good for me not in terms of my body only, but also in terms of the invisible body-­to­-be inside me. There are physical symptoms, too, though they are mild (another thing I didn’t realise: that while some pregnant women are indeed debilitated by illness or weariness, not everyone is). I am never actually sick, though I am dogged by a whisper of nausea that asserts itself at odd times and leads me to keep a pack of digest­ives on my bedside table. I can feel a largeness, a tenderness, to my breasts, and although I know it’s far too early for the pregnancy itself to show I feel fuller somehow, heavier than I was before I knew, as if the knowledge itself has some weight or substance to it.

This is not an unpleasant feeling – because it is a novelty, and because the pregnancy is so unequivocally desired – but it is hard to escape a sense of uneasiness, too. I find myself tracing familiar routes around Oxford, where I’ve lived for years, ever since I moved to the UK after university; I know the roads well, and yet I feel every encounter between feet and pavement to be different now, because I am differently bodied. What I have is a sense, visceral and unignor­able, that my body no longer belongs wholly to me – and in a way it doesn’t. As I walk I feel not exactly a ‘we’, but a blooming plurality, an ‘I and…’, perhaps, the assertion of a possibility taking physical form. Where once I occupied my mind during walks with long, elaborate daydreams, there now seems to be no room for anything other than the immediacy of experience and the planning and execution of the tasks of my own daily life. I take to listening to radio shows and podcasts, tuning out my external surroundings and internal circumstances, focusing on the minute details of, say, a true crime story, losing myself in the voice of the presenter.

* * *

Geographers write about the inseparability of the body from our experience of place: we sense places, are bodily present in them, see them, hear them, smell them, move within them. How else do we know a favourite room or city or mountain trail? The body, as Tim Edensor writes, is the means through which we experience and feel the world.

To which he adds: bodies are not only written upon but also write their own feelings upon a space in a process of continual remaking.

What I am struck by in the delicate earliest weeks of pregnancy is that I am being both made and unmade; rewritten. The pregnancy is largely unspoken of: we have told our doctor, and our parents, which perhaps lends it a weight in the world that it wouldn’t yet have had we not told anyone, but day to day I move through the hours without anyone but us knowing, because the pregnancy is still invisible. When I stand in front of the mirror I see nothing different, but nothing the same, either. When I go to the swimming pool, as I do most mornings, an almost religious habit, the place of it has shifted, though the change is microscopic, under the surface. On a quiet morning I watch the play of sunlight on the bottom of the pool and I am in a foreign country. In the changing room, pulling off my wet suit after a shower, I am self­-conscious for the first time – can they tell? But I want them to tell, even though there’s no way they possibly could, even though when I think of it I have the sense not so much of the world tilting on its axis but of the axis itself having drifted elsewhere. I smile knowingly at a visibly pregnant woman undressing and she looks away, uncomprehending or embarrassed or both. I am the foreign country, or else I have lost the map of this place. Walking home, along the same roads I have always taken, the green of the trees fading into yellow, I feel somehow both lonely and plural.

* * *

And then.

One morning, a few weeks after that first definitive, positive test, I wake up and feel my old self again – that is to say, not ill, not weary, not plural or novel – and that evening I experience some mild pain, a quick gush of blood which soon slows to an ambiguous but ominous trickle, and a sense of doom. I am not sure what the appropriate reaction is: denial? Despair? I cannot summon the energy to cook or even to eat dinner; although it is still early I retire to bed, lying on top of the duvet, curled into a question mark. Alexander lies down next to me, his body settling around mine. He tells me the things I both want and don’t want to hear: that it’s OK, that we don’t know for sure that anything’s wrong yet, that he loves me. He’s meant to be playing football in twenty minutes. Do you want me to stay? he says. I’ll stay with you. No, I say vehemently, as if this is in fact an uncharitable suggestion, you should go, you should play, what can you do at this point, what can I do? Nothing. Even after he’s pulled his socks over his shinpads, laced up his boots, he hesitates at the door: are you sure you don’t want me to stay? I don’t want you to stay, I say emphatically. If I were being honest – with him, with myself – I’d say exactly the opposite: stay, please. Instead I lie back and stare at the wall for an hour until he gets home and we go to sleep.

The next morning I call my GP, who arranges an emergency scan for me at the hospital. The soonest the scan can be done is in two days, so in the interim period I carry on as usual: I go to meetings, answer emails, run errands. It’s not as hard to do this as I would have imagined it would be, and after all, what choice do I have? But it’s also indicative of the ongoingness that will characterise much of the next two months.

I cannot summon the energy to cook or even to eat dinner; although it is still early I retire to bed, lying on top of the duvet, curled into a question mark.

I would have imagined, too, that a miscarriage was a definite thing – yes/no, this/that, knowing/not­-knowing – a neatly shaped happening with a beginning, a middle, a definitive end, each closely following the other. Women say, ‘I had a miscar­riage’, and until now I have always heard their experience as being something contained, even while brutally uncontrollable: all those stories of blood-­drenched bathroom floors, of unimag­inable agony, of horror and shock, of sadness and then resolution (often in the form of a baby arriving a year or two on, as if some consolation must always be offered): what I understand now, of course, is that these stories are told retrospectively, packaged in the way that all stories, to some extent, must be. But when I phone the doctor I’m unsure, grammatically speaking, how to phrase my concern: do I say to him that I have had a miscarriage, that I’m having one, that I’m worried I might have one in the future? The idea of the miscarriage in progress perplexes the part of me that imagined that this is a thing that can only happen privately, violently, suddenly, because it is a thing that is happening without much noise at all, and meanwhile here I am transcribing an interview, here I am meeting with a freelance client, wearing a new skirt I bought yesterday from the charity shop, here I am buying groceries and planning dinner, with nothing but a question mark inside me.

Alexander and I take a taxi to the hospital for the scan; it’s early morning and the driver is playing loud Pakistani pop, which is somehow soothing, and drowns out my own thoughts. In the waiting room Alexander scrolls restlessly through his phone. A little plastic radio on a cabinet in the corner of the room is pumping out cheerful tunes punctuated by cheerful radio host banter. I take my book from my handbag and lay it on my knees, open at my marked place. Knausgaard, A Death in the Family. In his younger-­self narrative, the author’s father has just died, while in his current­-self narrative, his partner is heavily pregnant, lumbering around, practically bursting with new life. But I cannot read on. I become fixated on a single paragraph, a description of a piece of artwork, which strikes me as incomprehensible. I read it over and over again until my name is called.

The scan reveals an embryo with no heartbeat. I lie on the bed, naked from the waist down, a blue plastic sheet draped over my legs. Alexander holds my hand while the ultrasound technician swirls a wand around inside me, talking us through the image of my uterus on the screen. It is illegible to me – darkness, light, hazy shapes – but to her the meaning is crystal clear. I’m so sorry it’s not the news you were hoping for, she says. She gives me a wad of tissue to wipe myself with before leaving the room to let me get dressed. She leads us back to the waiting room, which is fuller now, no one making eye contact, the radio still humming; a doctor will see you soon, she says, to talk to you about what happens next. ‘Soon’ is an ambiguous word, and time becomes difficult to perceive; we are there for what feels like both an eternity and an instant. I take my book out again, stare again at that same page; Alexander unlocks his phone, moves his finger across the screen in a kind of robotic motion.

What I am struck by in the delicate earliest weeks of pregnancy is that I am being both made and unmade; rewritten.

Sometimes these things resolve naturally, the doctor says when we are finally called in to see her; sometimes intervention becomes necessary, or desirable. She schedules me for another scan the following week, so we can monitor whether there’s been any change: in other words, whether the products of conception, as the embryo is now known, have been partially or even wholly expelled. After the scan, she says, we can decide how to proceed; you don’t need to make any decisions now. Good, I think, though I’m a little hazy on exactly what kind of decision I might be called upon to make; she has described the various forms of intervention but I can’t quite situate them in relation to my own body, my own products of conception.

She is very young, the doctor, soft-­spoken, apologetic. She says to call if anything changes before my next appointment, if I have any concerns. She gives me a business card, circles a phone number that’s operational 24/7. To minimise the risk of infection, she adds, seemingly as an afterthought, you shouldn’t take baths or swim.

No swimming. Of course. But I am thrown by the thought of this: the removal of the most obvious physical coping mechanism I have for dealing with what is essentially an entirely uncontrollable physical situation. I realise I’ve said this out loud without really meaning to. A silence falls, either respectful or uncomfortable.

I’m a swimmer too, the doctor says suddenly, as I’m standing to leave, abandoning, briefly, her professional distance. I’d hate not to be able to do it.

After the appointment we walk to a Starbucks near the hospital. It’s dark and anonymous inside, and smells of sweet pastries and wee. I order a latte, two shots, why not, and we sit at a counter at the window, watching buses trundle by. It’s mid­-morning and the place is full of new mothers and their prams, though occasionally someone in scrubs or a suit hurries in and then out again. Alexander texts his boss to say he won’t be coming in to work today. Not just the day but the month, the year, stretches out before us, suddenly open. What will we do with it? What can we do? The coffee is too hot, tasteless, the milk burned, but I suck it down in a rush, turning the inside of my mouth furry. Before all this, the test, the pregnancy, the ungrowing embryo, we were planning a wedding; we had set the date, hired a venue, made arrangements with the registrar. We should have cancelled everything – my due date was too close to the wedding date – but we never did; too superstitious, or preoccupied, or both. Now, of course, I say, devastated, amused, we won’t need to change the date. We can simply pick up where we left off. I feel myself begin to rewrite the map again, to slip in and out of familiarity with myself and my surroundings. There’s a simplicity to it all, underneath the ambiguity, the anguish, that makes me almost giddy: for what is this but a reversion to my natural state, a return to old routines?

A thought – terrible, comforting – hits me square in the face then, that there’s relief to be felt. The awful thing, the dreaded thing, has happened, and I need no longer fear it. I hate myself for feeling this but can’t let go of it, either, because I think it’s a way forward, a way out, a small tremble of light.

* * *

The second scan is no more or less enlightening than the first: there is still an embryo, there is still no heartbeat. No change, in other words: an unwanted stillness.

The doctor gives me a leaflet, which outlines in clinical language the three ways of managing a miscarriage when preg­nancy tissue remains in the womb: expectant, medical, surgical. The first is the wait-­and-­see approach, taken on the assumption that the tissue will pass naturally out of the womb with time. The second involves taking a course of medication to stimulate the passing of the tissue out of the womb: a potentially painful, lengthy, and often messy process, not always entirely effective, sometimes necessitating the third approach anyhow, which involves surgical removal of the tissue.

I still don’t know how to decide what to do, so I put it off: if nothing’s happened in a few weeks I’ll opt for some kind of intervention. I want above all to trust my body to do whatever needs doing, but already it’s betrayed me once, so what do I know?

Still no swimming, obviously, the doctor says sadly. Other­wise, proceed as normal.

As normal. Nothing is normal, I start to think – but then again, in a kind of terrible way, everything is normal again, isn’t it?

* * *

The present­-tenseness of the event, the miscarriage, which is not so much an event as a continual unfolding of uncharted territory, a vast grey area, makes it virtually impossible to talk about in any way that makes sense of what is actually happening. I don’t know what to tell people because the language I have is not elastic enough to encompass something which is past, present and future all at once. So I do what the doctor suggests: I proceed more or less as normal, going to meetings, going to the supermarket, scrolling mindlessly through Twitter, doing the laundry, eating, sleeping, working. I let myself lose track of time. At one point, in a notebook, next to a to-­do list, I write: The calendar is a kind of enemy, reminding me of the facts of things, the time it is actively taking to go through this process of miscarriage. I take to walking – long, slow strolls at the very edge of dusk, through parks and quiet suburban neighbourhoods that smell of woodsmoke and exhaust fumes. I feel my muscles going slack, and an irrational fear grows daily: what will my body become while I can’t swim?

My fear is really a form of vanity. I know that with each day or week that passes without a swim my body will start to look subtly different. I’ll lose, am losing, the public indicators of my fitness – the muscle, the shape of my arms and legs, the things that say to other people that I’m disciplined, that my body is under control. And I don’t want them to see what I know: that nothing is under control, that this body is not working properly, that athletically, reproductively, it is not doing at all what it’s supposed to do.

Mostly, though, if we’re honest, it’s the changes in our bodies that are in control of us, not the other way round.

Words come to me on my walks, as they used to on my swims. Some of them are obvious. Why is this happening to me? I think selfishly, inevitably, as I climb the hill to the park on a soft bed of wet leaves, fresh-­fallen after a night of howling wind. But other things, too, drifting like the smoke and the fumes. Disobedience. Betrayal. Softening, slackening, slowing. Undisciplined. Back at home, in my notebook, I write: I guess I feel disconnected from a part of myself. Not that I’m not still the same person or can’t be again, but that for a while I and some other part of me are not quite coinciding. I’m talking about the swimming, not the miscarriage, or at least ostensibly I am. I have a deep sense of geographical dissonance, like a dream of a familiar place in which the location of everything is slightly wrong, so that you round the corner and suddenly come upon a street that should be miles away, or discover that all along there has been an extra room in your house.

One Sunday afternoon, sitting in a booth at my local pub, I see a woman I used to see most weekday mornings at the pool; she always wore a bright pink cap, a navy swimsuit. She’s about my age, sitting with a friend, eating lunch. Perhaps it’s her local too, I think, for the first time realising, stupid as it sounds, that these people I’ve been brushing up against at the pool are people with lives outside that context, just like me.

Occasionally I log on to Facebook and check the page for the triathlon club I belong to. I look through the list of times from a recent 400-­metre time trial, spotting familiar names, noting the improvements, and wonder how much I, too, could have improved by now. For a moment I’m gripped by something which feels a little like jealousy but isn’t quite – desire, perhaps, something almost carnal. But then the desire, or whatever it is, fades: I’m here now, and maybe, if I can admit it to myself, I’m actually a little relieved that I’m not sweating away in a pool, that I don’t have to worry about how fast or smoothly I can cut through the water, how hungry I’ll be later, how tired.

* * *

The poles of the earth have wandered, the journalist John McPhee once wrote: even that which seems most permanent and solid is, in its own way, shifting. It’s true literally – think for example of the tectonic plates, the movement of the continents, which still, on average, drift a few centimetres a year apart, about the rate at which our fingernails grow, as the geographer Doreen Massey frames it, a reminder that the body is never in stasis either. In other words the whole world is a continual work in progress; the present is not some kind of achieved terminus, Massey writes. To underline this idea, she describes the slow movement of what she calls the ‘migrant rocks’ that came, over the course of millions of years, to form Skiddaw in the Lake District. Solid and eternal as it seems, she says, the mountain is not timeless. Like she and her sister, staying in a hotel in Keswick, it’s just passing through. It was once elsewhere. It will be elsewhere again someday.

It’s easy to lose your footing here, to feel that nothing is solid, but I’ve always found something comforting about this idea that place is essentially unfixed. The rigidity of permanence would be too much to bear, surely: who wants to be stuck in the same place forever? Who can know and love anywhere and not see that a point on a map is one thing, a living, breathing place quite another?

It’s a concept that scales well – if the world is a work in progress, then so too is a city or a street or a swimming pool. So too is the body, which is, after all, as the poet Adrienne Rich puts it, the geography closest in; it’s the first place, the place we must make peace with – subject, like all places, to the pressures of time, of external rhythms and events, changing from moment to moment, year to year, getting older, bigger, smaller, more or less capable of performing certain tasks, more or less like it was at the beginning.

There’s a simplicity to it all, underneath the ambiguity, the anguish, that makes me almost giddy: for what is this but a reversion to my natural state, a return to old routines?

Sometimes we’re in control of that change, or we think we are. Exercise in particular gives us the illusion of power over our own physical futures. Take your recommended thirty minutes of activity a day and stave off all kinds of bodily evil. Lose a bit of weight, add a bit of muscle, establish a routine, live forever, or longer, anyway. The geographer John Bale wrote of exercise as a literal form of recreation: through time, repeated action, the body is re-­created so that it works better. It incorporates knowledge, becomes stronger, fitter. Progress. Maybe next week, or the week after, I’ll be faster than I was last week. All it takes is discipline, resolve, another few thousand metres racked up. Most of all denial: of the body that wants, of the possibility of vulnerability or limitation. A few years ago, I remember, I became obsessed with watching Olympic swimming races; I trawled YouTube, read interviews with the athletes, fascinated by all their talk of sacrifice and discipline. And isn’t this why I watched in the first place? To see what happens when we write certain kinds of want out of our body, and one singular, possessive, demanding want into it: to be the best, the fastest, the one standing on the highest platform of the podium?

Mostly, though, if we’re honest, it’s the changes in our bodies that are in control of us, not the other way round. The fact of the matter is that not that long ago, my body was capable of run­ning 13.1 miles, of swimming 3,000 metres without complaint; not that long ago, my body was actually hosting another body, or the beginnings of one.

And now everything is different, and everything will be different again someday, and different again, and different again.

This excerpt has been lightly adapted for publication on Longreads.

* * *

Miranda Ward is a freelance writer, editor, and lecturer. Her memoir Adrift: Fieldnotes from Almost-Motherhood is published by Weidenfeld & Nicolson in the UK. She grew up on a cattle ranch in California and now lives in Oxford.

Editor: Cheri Lucas Rowlands

Shelved: Yoko Ono

(Photo by Gijsbert Hanekroot/Redferns — Getty Images)

Tom Maxwell | Longreads | January 2021 | 9 minutes (2,485 words)

Much is known about John Lennon’s self-described “Lost Weekend” — an 18-month separation from his wife Yoko Ono from the summer of 1973 to early 1975 — in which the former Beatle made records, produced records, drank, and took drugs to excess, and got kicked out of The Troubadour and various Los Angeles studios. Much less is known about how Ono spent her time back in New York.

In 1974, Ono recorded A Story at The Record Plant in New York. More than just another solo album, A Story was to be Ono’s first musical effort independent of her husband. Lennon produced or otherwise participated in all four of her previous recordings. Because of this, and the circumstances surrounding its creation, A Story is a statement of independence, a kind of personal manifesto. As a direct result of the couple’s reconciliation the following year, A Story was shelved at Ono’s direction. Most of its songs would resurface in later releases, sometimes in an entirely different emotional, as well as musical, context.

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I Will Always Love You: A Dolly Parton Reading List

Dolly Parton attends the 61st Annual GRAMMY Awards at the Staples Center on February 10, 2019, in Los Angeles. (Photo by Axelle/Bauer-Griffin/FilmMagic via Getty Images)

Central Florida doesn’t do glamour. I know because I was born and raised in Lakeland, Florida, the birthplace of Publix supermarkets and where Ernest Hemingway’s first wife, Hadley Richardson, died in a nursing home. Growing up, my sister Abby and I had a never-named game where we’d see a figure skater, Vanna White, anyone, wearing a pretty dress on television, and then we’d passionately bicker over who got to have the rhinestoned, beaded, or sequined costume. We knew what glamour looked like, and we wanted it. By the time I’d graduated high school, I knew glamour in real life. I’d seen it in person three times.

My high school band competed in an annual competition up in Gatlinburg, Tennessee. Each year, when the music part of the trip was over, we’d go to Dolly Parton’s dinner theater show one night, and spend a day at her theme park, Dollywood. And inside Dollywood, inside Chasing Rainbows, a museum dedicated to telling Dolly’s life story, was my pilgrimage: a collection of Dolly’s rhinestoned, beaded, and sequined costumes, more beautiful and breathtaking than anything I’d ever bickered over in the never-named game of my childhood.

Two years after high school, I moved to New York City and dug my heels into culture shock. Five years in, I got into a Dolly Parton-themed holiday party put on by a fancy New York PR firm. I glided through the night among the well-dressed and well-heeled. I sipped moonshine and peach iced tea with a party-themed name like it was mother’s milk. I danced to Kylie Minogue performing Dolly covers. And I held my head up high all night because I’d long already seen the installation in the front room, a sparkling display of Dolly’s costumes on loan from Dollywood.

I won’t say Dolly Parton changed my life. I’ve only just read her 1994 memoir “Dolly: My Life and Other Unfinished Business,” loaned it to three people, gave it as a wedding present, and have the first and only edition in paperback and hardcover. I recently got the first Christmas album Dolly recorded with Kenny Rogers, “Once Upon A Christmas.” I’m pretty proud of that. I don’t own any Dolly T-shirts or anything like that (maybe I should), I just think she’s a gift to humanity — a living, breathing embodiment of dreams. Maybe you agree, maybe you don’t. Dolly would say, “It’s hard to be a diamond in a rhinestone world.” Maybe she’s not for you, even though she’s for everyone. But, hey, don’t take my word for it.

1. “Outta That Holler” (Sarah Smarsh, Slate, October 2020)

In this excerpt from her 2020 book, “She Come By It Natural: Dolly Parton and the Women Who Lived Her Songs,” journalist Sarah Smarsh describes Parton’s brand of implicit feminism. By harnessing the value of economic agency and sexual power to overcome the poverty that defined her childhood — born the fourth of 12 children, “wearing dresses made of feed sacks” and “dyeing her lips with iodine from the family medicine cabinet for lack of lipstick” — Parton has shaped the person she is today.

She reminds her audiences that, no matter where they came from, everyone can identify with being shamed one way or another, and no one deserves it. Never be ashamed of your home, your family, yourself, your religion, she says, and adoring crowds applaud. One need look no further than her immense LGBTQ following to know that Parton’s transformation from a slut-shamed, talented teenage bumpkin to entertainment superstar contains a universal struggle that has less to do with being Appalachian than with being human. If her presence and the appreciation it instills in people could be whittled to a phrase, it’s “be what you are.”

2. “The Grit and Glory of Dolly Parton” (Emily Lordi, T: The New York Times Style Magazine, November 2020)

The person and brand that is Dolly Parton did not just happen overnight. Emily Lordi provides an overview of Parton’s decades-long career, illustrating how it’s been furthered not by reinvention, but through the reintroduction of Parton and her music, all while Parton herself engages with the times. Lordi first interviewed Parton over the phone, then in person after providing a negative COVID-19 test.

People want her gifts, her glow, her time; and Parton, who, as she says, “loves everybody and wants everybody to love me,” is often happy to oblige. She can’t sit still anyway — and early on in the pandemic, she decided to keep working, as long as her team could do so safely. Last May, she released “When Life Is Good Again,” a song of reassurance that justifies the journalist Melinda Newman’s claim, in Billboard, that, during the coronavirus crisis, Parton seems to have appointed herself America’s “comforter in chief”: “When everything is on the mend, / I’ll even drink with my old friends, / Sing and play my mandolin … And it’s gonna be good again.”

3. “Dolly Parton Steers Her Empire Through the Pandemic — and Keeps It Growing” (Melinda Newman, Billboard, August 2020)

The daughter of an industrious sharecropper father and a musically inclined mother, Parton is a savvy businesswoman whose earliest and latest decisions in the music industry are only the core of her empire. As Melinda Newman writes, “Her legendary body of music is just the start of what makes her Dolly. …”

She sounds surprisingly giddy as she talks about the next chapter of her career as if it’s her first. “I’m touched and honored that I’m still around and that I’m able to still be important in the business,” she says. “I honestly feel like I’m just getting started. I know that sounds crazy but I really feel like I might have a big music career, record career. Who knows?”

4. “Dolly Parton on How to Be More Like Dolly Parton” (Anna Moeslein, Glamour, November 2019)

In an interview with Parton, Anna Moeslein and Parton review “Heartstrings,” a Netflix series in which each episode is based on a different Parton song. They also discuss emotions and Parton’s position on what people can do to bring “a little Dolly in their own lives,” as well as fashion and beauty.

Well, I think it’s always important for us to be allowed to be who we are, all that we are, and appreciate that. And I know being a woman in this world…I’ve always been proud that I was born a woman, and I’ve joked that if I wasn’t, I would have been a drag queen. That’s my favorite line, but it’s probably true. I love being able to express myself, and I want to be seen and appreciated for who I am. So I’ve always appreciated and loved people for who they are. Because we don’t need to all be the same.

5. “Is Dolly Parton the Voice of America?” (Rachel Riederer, The New Republic, December 2020)

Citing Jad Abumrad’s Radiolab podcast (“Dolly Parton’s America”), Parton’s Netflix series, shoutouts from Nicki Minaj and Drake, and even a history course at the University of Tennessee, Rachel Riederer discusses the latest Dolly Parton renaissance. And, given the political landscape of the U.S., Riederer wonders if there’s a place for Parton’s enduring position to sidestep politics — which Abumrad refers to as “Dollitics.”

You cannot talk about sharecropping without talking about politics, and to say more would not be her style. She was not shy about her desire to sell books or to present her life as a fairy tale, and you sell a fairy tale by focusing on the romance and adventures of the rising princess, not the conditions that made her a scullery maid.

6. “Springtime for the Confederacy” (Aisha Harris, Slate, August 2017)

When I mentioned Dolly’s “dinner theater show” above, I was intentionally vague. Despite my setup, I know Dolly is human. And humans are complicated. Dolly’s dinner show seems complicated, too, but really, it’s not. The show, known until 2018 as “Dolly Parton’s Dixie Stampede,” is performed before an arena split into the “North” versus the “South,” where the audience, feasting on a four-course dinner eaten without cutlery, cheers on white-washed narratives of colonization, then the Antebellum South, then a performance competition between the North and the South. As a high schooler attending the show, I sat and watched from the North side, not fully grasping how problematic the programming was. I suppose I could do what Parton did in the Billboard article above: plead “innocent ignorance.” As an adult, I know better.

The last time I saw the show was in 2006. Aisha Harris reviewed the show in 2017, after watching it the same week as Unite the Right, a white supremacist rally, descended on Charlottesville, Virginia. At the rally, a neo-Nazi intentionally drove into a crowd of counter-protesters, killing an innocent woman, Heather Heyer, and injuring others. (The president notably remarked in the aftermath that there “were very fine people, on both sides.”) Harris recorded the experience of the dinner show from start to finish, without holding back.

While the show makes zero mention of slavery, that’s not to say there were no references to the Civil War. The war was alluded to both in the overarching North-versus-South conceit and through details both subtle (the gray and blue color schemes on each side) and blatant: The racing piglets were named after Abraham Lincoln, Ulysses S. Grant, Robert E. Lee, and Scarlett O’Hara. Dolly says that the show is about bringing back “those good old times,” referring to her childhood, but of course she wasn’t around during the days of Grant and Lee.

Harris wrote a follow-up to this piece after the show responded to her initial review, and again in April 2018, when the show dropped “Dixie” from its name.

7. “Living with Dolly Parton” (Jessica Wilkerson, Longreads, October 2018)

Jessica Wilkerson, who grew up in East Tennessee, where Dollywood is located, confronts the worldviews of her upbringing with those acquired as an adult after moving away from home for graduate school in New York. Weighing the socioeconomic implications of Dollywood’s hiring practices and confronting “Dolly Parton’s blinding, dazzling whiteness,” Wilkerson strikes a reluctant balance, compartmentalizing more than one version of Dolly Parton.

But the aftermath of Dollywood left me low-spirited. I was nestled into a cozy room in the log house my dad built on top of a ridge, where we lived. From the peak of that ridge, I could stand and see the Smoky Mountains, where Dolly Parton grew up and where she built a simulacrum of her mountain childhood. Hers felt more real than mine. I was sad, but jealous, too. I lived in the real world of Appalachia. A world of layaway stores and packaged foods, bleary-eyed workers and stressed-out mothers. I longed for the simulation.

Alison Fishburn is an American writer living in Paris, Ontario.

What Happened to Cruise Ship Workers Once the Passengers Were Gone?

Photo of the Carnival Breeze by Andy Newman/Carnival Cruise Lines via Getty Images

CW: suicide

Last year’s investigations into the COVID-19 outbreaks on cruise ships at the start of the pandemic, including Princess Cruises’ Diamond Princess and Holland America’s MS Zaandam, revealed horrific vacations gone wrong for passengers from around the world. But what happened to the tens of thousands of crew members who remained trapped on ships even after all the guests had disembarked and found their way home?

At Bloomberg Businessweek, Austin Carr tells the devastating stories of cruise line employees found dead — in apparent suicides — aboard Carnival and Royal Caribbean ships, including Jozsef Szaller, a shore excursion manager from Hungary on the Carnival Breeze, and Mariah Jocson, a waitress from the Philippines on Royal Caribbean’s Harmony of the Seas.

Interviews with affected crew members and their families suggest that despite assurances from cruise operators that crew were well cared for, their mental health was at times an afterthought. An October 2019 study on the mental well-being of crew, commissioned by a group affiliated with the International Transport Workers’ Federation, the big maritime trade union, found that even before the pandemic about a fifth of mariners surveyed said they had suicidal thoughts. High levels of depression stem from the jobs’ long contract lengths and stressful demands.

On April 29, an electrical engineer from Poland on Royal Caribbean’s Jewel of the Seas disappeared while the ship was anchored in the Saronic Gulf, south of Athens. Ship security cameras captured him leaping into the water that morning, according to Greek authorities. Two weeks later, on May 10, Evgenia Pankrushyna, a waitress from Ukraine, died after jumping overboard from Carnival’s Regal Princess near Rotterdam. Around this time a Chinese contractor was found dead on Royal Caribbean’s Mariner of the Seas. A crew member aboard the ship says many believed it was another suicide, though the company said he’d died of natural causes. Next was a Filipino cook, Kennex Bundaon, who was found dead in his cabin on Carnival’s AIDAblu. Four days later, another worker from the Philippines died in an apparent suicide on Virgin Voyages’ Scarlet Lady.

The details of the deaths of Szaller and Jocson are still not clear, even to their families, who are “desperate for closure.” In Szaller’s case, Carnival has refused to discuss the specific circumstances of his death with his parents, while the father of Jocson, the Royal Caribbean employee, says that his daughter had never shown signs of depression and kept telling him that she wanted to go home. He just wants to know the truth about her death.

It wasn’t just the claustrophobic environment that was distressing. Workers say cruise companies constantly changed repatriation schedules, offering only vague guidance on when or how they’d return home. Without customers on board, Carnival moved many contractors off duty, meaning they could sort of enjoy the amenities of the ocean liners. But that also meant their salaries were eventually cut off—a scary situation for those supporting families on land. The weeks dragged on with limited entertainment options. Internet access was complimentary on some boats, but it could be painfully slow or strong enough only for social media and texting.

Vilmos says communications with Carnival broke down soon after. As the Szallers tried to organize the retrieval of their son’s body, including figuring out which jurisdiction would have to declare him legally deceased, they began to see the cruise company as having had a role in their son’s death. Its labyrinthine corporate structure—a web of international entities designed to lower Carnival’s tax liability—compounded their grief.

Even now, the Szallers have been unable to have Jozsef declared legally deceased. Vilmos says the coroner’s report should move things forward, but it’s been frustrating enough coordinating with U.K. authorities on behalf of his son, a Hungarian citizen. And that’s not even half the headache. As Vilmos frames it, how do you officially process a death that occurred in international waters, on a ship registered in Panama, that’s owned by a company operating in the U.S.?

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Ten Outstanding Short Stories to Read in 2021

Author Kelly Link (Photo by Awakening/Getty Images)

The #longreads hashtag on Twitter is filled with great story recommendations from people around the world. Pravesh Bhardwaj is a longtime contributor — throughout the year he posts his favorite short stories, and then in January we’re lucky enough to get a list of his favorites to enjoy in the year ahead.

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Longreads Best of 2020: Investigative Reporting

All Best of Longreads illustrations by Kjell Reigstad.

All through December, we’re featuring Longreads’ Best of 2020. This year, our team picked and featured hundreds of in-depth investigations published across the web. Here are our top picks.

If you like these, you can sign up to receive our weekly email every Friday.

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The Last Patrol (Nathaniel Penn, The California Sunday Magazine)

In July 2012, U.S. Army First Lieutenant Clint Lorance gave an order that killed two Afghan civilians on a motorcycle near an operating base outside of Kandahar, in a volatile region in Afghanistan. Lorance was convicted of murder. The narrative weaved by Sean Hannity and others at Fox News framed Lorance as a war hero; he was pardoned by Donald Trump in November 2019 and served six years of a 20-year sentence. The former Army officer, who had been advised to take interviews only from conservative media outlets, agreed to talk with Nathaniel Penn, and the result is an incredibly riveting and comprehensive piece on his case.

Arriving on the dirt road that led into the village, the patrol discovered two of the three Afghan men lying beside a ditch. They were dead. Their companion had run away. Near them, the motorcycle leaned on its kickstand.

It wasn’t at all the scene Lorance had imagined. “If I would have been up there,” he told me, “and would have known that they were stopped and off their motorcycle, I would never in a million years have said, ‘Fire at them.’ I would want to go talk to them and get intel out of them. I’d be like, ‘Who are you? Where are you from?’ I would want to know everything about them.”

A woman and two children stood near the bodies, weeping.

Holy shit, Lorance thought. Did we just kill good people?

The way to find out was to do a Battle Damage Assessment. Skelton was the intelligence specialist who carried the SEEK. But Lorance wanted Skelton to follow him into the village to carry out the mission and get the biometric enrollments. The engagement with the motorcycle had been necessary and unfortunate, but it wasn’t important. He ordered two of his men to conduct the Battle Damage Assessment while he proceeded into the village. They had the necessary training, even if they didn’t have the SEEK. They knelt by the bodies.

Captain Swanson, who had been alerted to the situation, was radioing Lorance from headquarters. What was happening? he asked. Were the dead men combatants or civilians? Had Lorance done the Battle Damage Assessment?

No, Lieutenant Lorance replied, they hadn’t been able to do the Battle Damage Assessment. The villagers had taken away the bodies.

As he spoke, he knew he had just made a critical mistake. He should have said that his men would get to the Battle Damage Assessment eventually, that they didn’t have time to do that shit right now. Because when you speak over the radio, “you might as well be putting your hand on the Bible,” as one member of the platoon told me.

In the years to come, Lorance’s decision not to use the SEEK device for the Battle Damage Assessment would prove to be crucial and polarizing. It would contribute both to his imprisonment and his pardon.

The weeping woman was screaming now. Lorance told himself that her tears didn’t necessarily mean he’d done anything wrong. The men whose bodies she was crying over could be insurgents. That shocked him — the idea that the Taliban had families, too. It had never occurred to him before.

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‘Hue’s Hue’: Katy Kelleher’s Column on Color

(Photo by Óscar J.Barroso/Europa Press via Getty Images) (Photo by Europa Press News/Europa Press via Getty Images)

We’re huge fans of Katy Kelleher’s writing on color. She recently wrote a spot-on piece for Vogue about Pantone’s odd “color of the year” choices. (Spoiler: a drab gray, paired with a pale yellow.)

Over at the Paris Review, she does in-depth profiles of color as part of a column named — get this — “Hue’s Hue.” We’ve shared a few of these nerdy delights as editor’s picks in the past; we especially loved recent ruminations on periwinkle, russet, and verdigris. The entire series is worth your time.

Periwinkle goes by many names. You might know her by one of her more fabulous monikers, like sorcerer’s violet or fairy’s paintbrush. In Italy, she is called fiore di morte (flower of death), because it was common to lay wreaths of the evergreen on the graves of dead children. The flower is sometimes associated with marriage (and may have been the “something blue” in the traditional wedding rhyme), sometimes associated with sex work (because of its supposed aphrodisiac properties) and also with executions. I grew up calling her vinca, a pretty little two-syllable name, taken from her proper Latin binomial, Vinca minor. My mother cultivated periwinkle in our forested Massachusetts backyard, encouraging the hardy green vines to trail over the boulders and under the ferns. I would have been delighted to know even a fraction of vinca lore back then, but I knew nothing except she was poison. I could eat the royal-purple dog violets, but I was not to pick the vinca. Vinca was poison and poison meant death.

Mary Stuart was six days old when she became the Queen of Scotland. Her precious body was guarded from that moment onward, moved like a pawn on a chessboard from one castle to another. Maybe the people would have loved her if she hadn’t been spirited away to be raised in France in 1548, but perhaps they wouldn’t have. Maybe Mary was doomed to always be loathed for her femaleness and her Catholicism. By the time she returned to the newly Protestant Scotland at age eighteen, she had spent over a decade in the French court, developing a taste for elaborate gowns and flashy jewels. She was tall and graceful, beautiful according to some accounts, but this didn’t endear her to the common people. While Mary was strutting around in fine lace and velvet and elaborate lockets, her people were told that God wanted them in chaste, sober clothes. Embroidery was deemed “unseemly” as were “light and variant hues in clothing, as red, blue, yellow and such like, which declare the lightness of mind.” Instead, the Scots were told to wear simple fabrics in “grave colour,” such as “black, russet, sad grey, or sad brown.”

This depressing list comes from a summary of the 1575 General Assembly of the Kirk, recorded in the Domestic Annals of Scotland. Although the upper classes continued to wear silks and velvets and pretty bright dresses, most people wore their sad rags. It was more practical, to be dressed in dark gray and black and brown. Life for the lower classes was hard. The clothing reflected this fact.

And yet, thrown in with those drab colors was russet. In this context, russet was both a general chromatic descriptor and a specific type of rough spun cloth, colored with a mixture of woad (a member of the cabbage family that was used to make a blue-gray dye) and madder (a similarly yellow-flowered herb whose roots could be turned into a pinkish-brown dye). Russet wasn’t a bright color, but it was at least more cheerful than “sad grey,” it had a bit more life than black. While Mary, Queen of Scots reportedly wore vivid scarlet under her black mourning clothes, her people dressed like dead leaves and gray stones. At their most vibrant, they could wear the color of rust, of dirty root vegetables, of aging fox fur.

Verdigris is the ur-turquoise. The name comes an Old French term, vert-de-Grèce (“green of Greece”). It is also sometimes known as “copper green” or “earth green,” since the pigment was commonly made from ground-up malachite or oxidized copper deposits. Certainly, verdigris owes a great debt to copper (symbol: Cu), as do the gemstones turquoise (chemical composition: CuAl6(PO4)4(OH)8·4H2O) and malachite (chemical composition: Cu2CO3(OH)2). In America, we’re more likely to call these green-blue shades turquoise (from the Old French for Turkish, or “from-Turkey”) or Tiffany Blue (coined in 1845 with the publication of the Tiffany’s Blue Book catalogue and trademarked in 1998) than we are to invoke old-timey verdigris. Yet I prefer the odd old name, with its vivid consonants and slithery tail. The word sounds unstable, fittingly fluid for such a liquid hue.

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