Category Archives: Creative nonfiction

On the radio in Columbus, OH

On the radio in Columbus, OH

I got to talk with Doug Dangler when I visited Columbus, Ohio, and he interviewed me for a great new series of video and audio interviews called “Writers Talk.” It was a wonderful experience, and very cool to see how my old employer the Center for the Study and Teaching of Writing is branching out! This is when it will be broadcast in Columbus:

Monday, November 8, 3:30 pm., WCRS radio, 98.3 & 102.1 FM.
Wednesday, November 10, 8:00 p.m. WCBE radio, 90.5 FM.

Lovely Review of Cover Me at Elevate Difference

Lovely Review of Cover Me at Elevate Difference

Published on Sept. 15, 2010, by T. Tamara Weinstein in Elevate Difference

“If you suspect that your experiences alone put the hell in healthcare, then Cover Me by Sonya Huber is the memoir for you. By the age of thirty-three, Huber had already endured eleven gaps in healthcare coverage, and had also been sent to collections for medical debt multiple times. She became an expert at scavenging for alternatives and at squeezing every drop of blood from the recalcitrant turnip that is the US healthcare system.

Cover Me is a moving portrait of how access to healthcare determines who is a “have” and who a “have not” and in Huber’s hands, the issues surrounding healthcare reform become clear and relatable. Improbably, given the toll the struggles exact, the author is also very funny, telling her stressful tale with an irrepressible sense of humor.

Huber began her adult employment journey as an idealistic labor activist and became a university professor. At one point, she held down three jobs at once, none of which offered healthcare benefits. The pressure to find affordable healthcare ballooned exponentially as Huber went from single working woman, to wedding a man who was also a healthcare “have not,” to becoming a mother.

But even as a single woman, the challenge of good health was daunting. Diagnosed with a disabling panic disorder, Huber was forced to scrounge for low cost medical clinics and sliding scale arrangements, at one point even bartering office cleaning services for therapy. She was often left to rely on two of the universe’s most unstable forces: luck and the kindness of others. At times, sympathetic doctors offered free pharmaceutical samples and dentists forgave their fees. But there were consequences, many of which could be filed under “you get what you pay for,” or more accurately, “you get what you are able to pay for.”

As a wife and mother, Huber’s determination grew even grittier. Schlepping her infant son through the frozen Ohio tundra to register for WIC and Medicaid benefits, and expertly working the phones to correct inevitable and near catastrophic bureaucratic errors, Huber became a master of resourcefulness and tenacity. Even during a rare stretch when Huber had coverage through an HMO, she found it to be Dungeons-and-Dragons-esque, requiring the right “passwords” to gain entry. (The passwords being properly worded referrals and appeals, and an intimate familiarity with the policy’s fine print.) If it’s true that insurance companies spew gobbledygook and denials to weed out folks who lack perseverance, they never counted on someone like Huber.

Huber’s Odyssean journey through the American healthcare system throws the institution’s inequities and ironies into stark relief. She describes working for a nonprofit whose mission is to provide low income workers with health insurance; however, in a stunning revelation of either outrageous hypocrisy or business-as-usual in fund-strapped nonprofits, that same organization was unwilling to provide Huber with healthcare coverage. Meanwhile, Huber’s boss, who had stellar insurance through her prominent surgeon husband, could brandish her benefits card and blithely obtain top care. Reading this, you will be tempted to hurl the book against the nearest wall, but you won’t because you’ll be too riveted to let go.

Huber’s story will resonate with anyone who has ever battled a medical bureaucracy. That is, with everybody in America. Her refusal to say “uncle” will inspire, and along the way, readers may even pick up invaluable tips on navigating the labyrinthine depths of both public and private healthcare. There is also a twist at the end that makes university bureaucracy even scarier than its medical counterpart.

One question nagged me throughout Cover Me: where is Huber’s husband? He seemed to hang back and let Huber take the front lines, a story known to too many wives and mothers. But that question aside, and because Huber is such a deliciously skilled writer, Cover Me is the best kind of memoir; it is engaging, enraging, tragic and funny. Fortunately, laughter as medicine is one thing the insurance companies have not yet managed to deny.”

Thomas Merton

Thomas Merton

I’m on a Thomas Merton kick this summer; I guess it’s the old Catholic in me combined with the yearning for contemplative Buddhist practice.
From Seven Storey Mountain:
“…the more you try to avoid suffering, the more you suffer, because smaller and more insignificant things begin to torture you, in proportion to your fear of being hurt. The one who does most to avoid suffering is, in the end, the one who suffers most: and his suffering comes to him from things so little and so trivial that one can say that it is no longer objective at all.” (82)
“All our salvation begins on the level of common and natural and ordinary things….And so it was with me. Books and ideas and poems and stories, pictures and music, buildings, cities, places, philosophies were to be the materials on which grace would work. But these things are themselves not enough. The more fundamental instinct of fear for my own preservation came in, in a minor sort of way, in this strange, half-imaginary sickness which nobody could diagnose completely.” (178)
“We have become marvelous at self-delusion; all the more so, because we have gone to such trouble to convince ourselves of our own absolute infallibility.” (205)
And on the tension between writing and being a monk: “By this time I should have been delivered of any problems about my true identity. I had already made my simple profession. And my vows should have divested me of the last shreds of any special identity. But then there was this shadow, this double, this writer who had followed me into the cloister. He is still on my track. He rides my shoulders, sometimes, like the old man of the sea. I cannot lose him. He still wears the name of Thomas Merton. Is it the name of an enemy? He is supposed to be dead. But he stands and meets me in the doorway of all my prayers, and follows me into church. He kneels with me behind the pillar, the Judas, and talks to me all the time in my ear. He is a business man. He is full of ideas. He breathes notions and new schemes. He generates books in the silence that ought to be sweet with the infinitely productive darkness of contemplation. And the worst of it is, he has my superiors on his side. They won’t kick him out. I can’t get rid of him…. “

Book tour planning

Book tour planning

I’m in the middle stages of what, I suppose, is officially called “planning a book tour.” What it feels like is that I email random people and lovely bookstore owners and say, “Hey, I wrote this thing that has some relevance but also some swearing. You don’t know me. Could I come and bother you and invite a bunch of people, all for the purpose of trying to sell my book?” Only, of course, it’s not just about selling a book. It’s about this darn thing that is so important to me that it almost brings tears to my eyes, and to the eyes of lots of other people: healthcare. The need of it. The lack of it. The agonizing fight to get something that now isn’t even a public option. The fact that the kingdom is lost every day for want of a nail, that people are dying and this problem could be solved. So that’s what the book Cover Me: A Health Insurance Memoir is about. It’s the mystery of healthcare and how we exist without it. I took years of my life and devoted a book to this obsession because I thought writing a book about it would help me figure it out. But none of us have figured it out. So there it is: a story of heartbreak, my own small story as one sliver of a national tragedy that we have resources to fix but that we refuse to. Kudos and beyond kudos to all the activists who have worked so hard on single payer work over the long haul, Physicians for a National Health Plan, and thousands of other groups. And there are still miles to go. So the book is about that, and about how much it sucks to try to put together a crazy quilt of coverage when all you’ve got to work with are scraps of our current smattered, over-privatized, pulverized, profiteered and pirated system. It shouldn’t even be called healthcare. It should be called health could-care-less, if it weren’t for all the dedicated health professionals working to provide healthcare in spite of the fiscal obstacles set up to penalize the poor. Holy smokes, I should stop there. I guess I still have some screed in me about this issue. Anyway, check out the developing book tour dates at Booktour.com and hit me up if it looks like a date would fit with your group and your schedule. I’m also totally into doing fundraisers and/or publicity and membership events for healthcare and single-payer organizations.

Immortal Life of Henrietta Lacks

Immortal Life of Henrietta Lacks

I just finished reading Rebecca Skloot’s “The Immortal Life of Henrietta Lacks,” an incredibly readable and riveting account of the personal and family story behind the cell line that has affected all of our lives via medical research, and which raises huge questions about medical ethics and consent. Kudos to Rebecca for all the massive cutting she must have had to do, as it was clear that she knew enough about her subject to be able to explain it clearly, which meant she probably had 300X the research that she had space for. Narrative science writing at its best, and I think I have not often seen a book like this with a folded and spindled and flipped structure. There’s a cool timeline that runs across the first page of each chapter to help orient the reader spatially, and I really liked that touch. It seemed to provide an extra graphic aid to the reader… and I am struck by this simple tool with how much more could be done in this regard, especially with complex stories that must be told in complex ways. I like the innovation of this hybrid visual element, and I found myself composing interview questions for Skloot as I read, mostly along the lines of her structural decisions, wanting to know how she kept the timelines straight as she wrote, all the configurations she must have tried, and what the conversation with her publisher was like regarding the structure. I wanted a whiteboard to graph it out as I read, as it seemed to invite that from someone really interested in structures of books.

A year passes

A year passes

Haha. I don’t know how a year passed since I wrote in this blog. Well, actually I do. So much happening, including the revision of a second and third book. The second is “Cover Me: A Health Insurance Memoir” from University of Nebraska Press, which I have to ship off next month. The third is a textbook, The ‘Backwards’ Research Guide for Writers, which will hopefully come out next year from Equinox. More to come. Now that it’s summer, all the updates. And vows of discipline for next year. :)

Floyd Skloot reading at Ashland University

Floyd Skloot reading at Ashland University

One of the major thrills of teaching at Ashland University’s new low-res MFA program for the past two weeks was hearing the closing reading and craft talk by Floyd Skloot, author of many books of poetry, four novels, and excellent works of nonfiction including the new “The Wink of the Zenith” and “In the Shadow of Memory” (from University of Nebraska Press).

This is the only talk on the craft of writing that’s brought me to tears. Skloot talked about the writing process for putting together his essay, “Kismet,” which dealt with the death of his brother. Twenty years ago, Skloot suffered a virus attack that resulted in brain lesions that damaged large sections of his memory and hindered his ability to process information. Despite this major obstacle he has continued a productive writing career. He spoke in this craft talk about the organic structure of the essay, a piece of seven sections that explore interlocking themes. One of his major points was the organic structure that resulted from the essay’s subject matter. He traced the evolution of the essay by guiding the audience through the insights and emotions that occurred after his brother’s death; since he had lost access to much of his childhood memories, he had to pay careful attention to any emotional triggers signaling a buried memory or association about his brother.

Although most of us don’t suffer brain damage, we confront the desire to overstructure our emotions, reactions, and memories, fitting them into a form that seems to us to make “sense.” Some of the most beautiful quotes shared by Skloot concerned his gratitude at having the process of writing nonfiction as a framework for reconstructing his sense of self:
“You get to say in the essay what you never say to others, what you never say to yourself.”
He also described writing as a “spiritual practice”: “You open yourself up and slow yourself down. Once you lose control and surrender to the material, you open the vents and other material can stream in. This requires a looser and more exploratory mode of working. It requires time and patience, a willingness to explore tangents, a willingness to be ruthless with the tangents.”