Book Serendipity Strikes Again
Only two months since my last Book Serendipity entry, and already another 17 occurrences! I post these occasional reading coincidences on Twitter and/or Instagram. I call it serendipitous when two or more books that I’m reading at the same time or in quick succession have something pretty bizarre in common. Because I have so many books on the go at once – usually between 10 and 20 – I guess I’m more prone to such incidents. What’s the weirdest one you’ve had lately? (The following are in rough chronological order.)
- Characters with lupus in The Monsters of Templeton by Lauren Groff and Daisy Jones & The Six by Taylor Jenkins Reid [I also read about one who features in Lost and Wanted by Nell Freudenberger] PLUS I then read Wise Blood by Flannery O’Connor, who died of lupus
- Daisy’s declaration of “I am not a muse. I am the somebody. End of fucking story” in Daisy Jones & The Six by Taylor Jenkins Reid reminded me of Lee Miller’s attitude in The Age of Light by Whitney Scharer
- Mentions of old ladies’ habit of keeping tissues balled up in their sleeves in The Girls by Lori Lansens and Growing Pains by Mike Shooter
- (A sad one, this) The stillbirth of a child is an element in three memoirs I’ve read within a few months, Notes to Self by Emilie Pine, Threads by William Henry Searle, and The Chronology of Water by Lidia Yuknavitch
- A character’s parents both died in a car accident in The Monsters of Templeton by Lauren Groff and Saint Maybe by Anne Tyler
- Two books open on New Year’s Eve 2008 and comment on President Obama’s election: Ordinary People by Diana Evans and Rabbits for Food by Binnie Kirshenbaum
- Three novels in which both romantic partners are artists and find themselves (at least subconsciously) in competition: The Narrow Land by Christine Dwyer Hickey, The Age of Light by Whitney Scharer and Stanley and Elsie by Nicola Upson
- There’s a Czech father (or father figure) in The Florist’s Daughter by Patricia Hampl and The Girls by Lori Lansens
- I’d never heard of 4chan before, but then encountered it twice in quick succession, first in So You’ve Been Publicly Shamed by Jon Ronson and then in The Unauthorised Biography of Ezra Maas by Daniel James
- (Another sad one) Descriptions of the awful sound someone makes when they learn a partner or child has died in Hard Pushed by Leah Hazard and Jesus’ Son by Denis Johnson
- Alan Turing is a character in Murmur by Will Eaves and Machines Like You by Ian McEwan
- Antonie van Leeuwenhoek (a pioneer of microscopy) is mentioned in Machines Like You by Ian McEwan and The Making of You by Katharina Vestre
- A woman is described as smelling like hay in Memoirs of a Book Thief by Alessandro Tota and Pierre Van Hove and The Chronology of Water by Lidia Yuknavitch
- An inside look at the anti-abortion movement in Priestdaddy by Patricia Lockwood and Crazy for God by Frank Schaeffer
- The attempted adoption of a four-year-old boy who’s been in foster care is an element in The Ginger Child by Patrick Flanery and Machines Like You by Ian McEwan
- The loss of a difficult father who was an architect is an element in All the Lives We Ever Lived by Katharine Smyth and The Chronology of Water by Lidia Yuknavitch (and in last year’s Implosion by Elizabeth Garber)
- The improv mantra “Yes, and…” is mentioned in No Happy Endings: A Memoir by Nora McInerny by Sorry I’m Late, I Didn’t Want to Come: An Introvert’s Year of Living Dangerously by Jessica Pan
Dubiously Thematic Easter Reading
In 2015 and 2017 I came up with some appropriately theological reading recommendations for Easter. This year I’m going for a more tongue-in-cheek approach, as befits the unfortunate conjunction of Easter with April Fools’ Day.
Currently reading or reviewing:
The Egg and I by Betty MacDonald
I bought this on a whim from a local charity shop, based on the title, cover and blurb. I’m about one-third of the way through so far. MacDonald and her husband started a chicken farm in a mountainous area of the Pacific Northwest in the 1940s. Her account of her failure to become the perfect farm wife is rather hilarious. My only hesitation is about her terrible snobbishness towards rednecks and “Indians.”
A representative passage: “Gathering eggs would be like one continual Easter morning if the hens would just be obliging and get off the nests. Co-operation, however, is not a chickenly characteristic and so at egg-gathering time every nest was overflowing with hen, feet planted, and a shoot-if-you-must-this-old-grey-head look in her eye.”
The Sheep Stell by Janet White
I’m reviewing this reissued memoir for the TLS. It’s a delightful story of finding contentment in the countryside, whether on her own or with family. White, now in her eighties, has been a shepherd for six decades in the British Isles and in New Zealand. While there’s some darker material here about being stalked by a spurned suitor, the tone is mostly lighthearted. I’d recommend it to anyone who’s enjoyed books by Gerald Durrell, James Herriot and Doreen Tovey.
Representative passages: “Shepherding is a strange mixture of tremendous physical work alternating with periods of calm, quiet indolence.” & “A dare, a dream and a challenge. I could have hunted the whole world over and never in a lifetime found anywhere so right: warm, high, pastoral and severed by the sea.”
The Trouble with Goats and Sheep by Joanna Cannon
Mrs. Creasy disappears one Monday in June 1976, and ten-year-old Grace Bennett and her friend Tilly are determined to figure out what happened. I have a weakness for precocious child detectives (from Harriet the Spy to Flavia de Luce), so I enjoyed Grace’s first-person sections, but it always feels like cheating to me when an author realizes they can’t reveal everything from a child’s perspective so add in third-person narration and flashbacks. These fill in the various neighbors’ sad stories and tell of a rather shocking act of vigilante justice they together undertook nine years ago.
Sheep are a metaphor here for herd behavior and a sense of belonging, but also for good versus evil. Grace and Tilly become obsessed with a Bible passage the vicar reads about Jesus separating the sheep from the goats. But how can he, or they, know who’s truly righteous? As Grace says, “I think that’s the trouble, it’s not always that easy to tell the difference.” It’s a simplistic message about acknowledging the complexity of other lives and situations rather than being judgmental, and matches the undemanding prose.
Reminiscent of Rachel Joyce, but not as good.
Vita Nova by Louise Glück
My first collection from the prolific Pulitzer winner. Some of the poems are built around self-interrogation, with a question and answer format; several reflect on the myth of Orpheus and Eurydice. The first and last poems are both entitled “Vita Nova,” while another in the middle is called “The New Life.” I enjoyed the language of spring in the first “Vita Nova” and in “The Nest,” but I was unconvinced by much of what Glück writes about love and self-knowledge, some of it very clichéd indeed, e.g. “I found the years of the climb upward / difficult, filled with anxiety” (from “Descent to the Valley”) and “My life took me many places, / many of them very dark” (from “The Mystery”).
Best lines about spring:
“The spring of the year; young men buying tickets for the ferryboats. / Laughter, because the air is full of apple blossoms.” (from “Vita Nova”)
“Spring / descended. Or should one say / rose? … yellow-green of forsythia, the Commons / planted with new grass— // the new / protected always” (from “Ellsworth Avenue”)
Plucked off the shelf for their dubious thematic significance!
To Rise Again at a Decent Hour by Joshua Ferris
Animal, Vegetable, Miracle by Barbara Kingsolver
Wise Blood by Flannery O’Connor
So You’ve Been Publicly Shamed by Jon Ronson
The Resurrection of Joan Ashby by Cherise Wolas
Happy Easter to all those who mark it, and have a good week. I have a few review-based posts scheduled for while we’re in Wigtown, a trip I hope to report on next Monday, when I will also attempt to catch up on blogs and comments.
A Journey through Chronic Pain: Heal Me by Julia Buckley
Julia Buckley can pinpoint the very moment when her battle with chronic pain began: it was a Tuesday morning in May 2012, and she was reaching across her desk for a cold cup of coffee. Although she had some underlying health issues, the “fire ants” down her arm and “carving knife” in her armpit? These were new. From there it just got worse: neck and back pain, swollen legs, and agonizing periods. Heal Me is a record of four years of chronic pain and the search for something, anything to take the pain away. “I couldn’t say no – that was a forbidden word on my journey. You never know who’s going to be your saviour.”
Having exhausted the conventional therapies available privately and via the NHS, most of which focus on cognitive behavioral therapy and coping strategies, Buckley quit work and registered as disabled. Ultimately she had to acknowledge that forces beyond the physiological might be at work. Despite her skepticism, she began to seek out alternative practitioners in her worldwide quest for a cure. Potential saviors included a guru in Vienna, traditional healers in Bali and South Africa, a witch doctor in Haiti, an herbalist in China, and a miracle worker in Brazil. She went everywhere from Colorado Springs (for medical marijuana) to Lourdes (to be baptized in the famous grotto). You know she was truly desperate when you read about her bathing in the blood and viscera of a sacrificial chicken.
Now the travel editor of the Independent and Evening Standard, Buckley captures all these destinations and encounters in vivid detail, taking readers along on her rollercoaster ride of new treatment ideas and periodically dashed hopes. She is especially incisive in her accounting of doctors’ interactions with her. All too often she felt like a statistic or a diagnosis instead of a person, and sensed that her (usually male) doctors dismissed her as a stereotypically hysterical woman. Fat shaming came into the equation, too. Brief bursts of compassion, wherever they came from, made all the difference.
I was morbidly fascinated with this story, which is so bizarre and eventful that it reads like a great novel. I’ll be cheering it on in next year’s Wellcome Book Prize race.
Heal Me: In Search of a Cure is published today, January 25th, by Weidenfeld & Nicolson. My thanks to the publisher for a free copy for review.
Julia graciously agreed to take part in a Q&A over e-mail. We talked about invisible disabilities, the gendered treatment of pain, and whether she believes in miracles.
“I spent a day at the Paralympic stadium with tens of thousands cheering on equality, but when it was time to go home, nobody wanted to give me a seat on the Central Line. I was, I swiftly realised, the wrong kind of disabled.”
Yours was largely an invisible disability. How can the general public be made more aware of these?
I feel like things are very, very gradually moving forward – speaking as a journalist, I know that stories about invisible disabilities do very well, and I think as we all try to be more “on” things and “woke” awareness is growing. But people are still cynical – Heathrow and Gatwick now have invisible disability lanyards for travellers and someone I was interviewing about it said “How do I know the person isn’t inventing it?” I think the media has a huge part to play in raising awareness, as do things like books (cough cough). And when trains have signs saying things like “be aware that not all disabilities are visible” on their priority seats, I think that’s a step forward. Openness helps, too, if people are comfortable about it – I’m a huge believer in oversharing.
“I wondered whether it was a peculiarly female trait to blame oneself when a treatment fails.”
You make a strong case for the treatment of chronic pain being gendered, and your chapter epigraphs, many from women writers who were chronic pain or mental health patients, back this up. There’s even a name for this phenomenon: Yentl Syndrome. Can you tell us a little more about that? What did you do to push back against it?
Yentl Syndrome is the studied phenomenon that male doctors are un/consciously sexist in their dealings with female patients – with regards to pain, they’re twice as likely to ascribe female pain to psychological reasons and half as likely to give them adequate painkillers. In the US, women have to cycle through 12 doctors, on average, before they find the one to treat their pain adequately. There are equally shocking stats if you look at race and class, too.
I did absolutely nothing to push back against it when I was being treated, to be honest, because I didn’t recognise what was going on, had never heard of Yentl Syndrome and thought it was my problem, not theirs. It was really only when I met Thabiso, my sangoma in South Africa, that I felt the scales lift from my eyes about what had been going on. I make up for it now, though – I recently explained to a GP what it was, and suggested he be tested for it (long story, but we were on the phone and he was being incredibly patronising and not letting me speak). He hung up on me.
“In my head I added, I don’t care what they do to me, as long as it helps the pain.”
Meatloaf sang, “I would do anything for love, but I won’t do that.” Can you think of anything you wouldn’t have done in the search for a cure?
Well, I refused a spiritual surgery from John of God – I would have had the medical clamp up my nose or happily been cut into, but I was phobic about having my eyeball scraped – I had visions of Un Chien Andalou. So I had said repeatedly I was up for the other stuff but wouldn’t do the eye-scraping, and was told that probably meant I’d get the eye-scraping so I should go for the “invisible” surgery instead. But I can’t think of anything else I wouldn’t have done. The whole point, for me, was that if I didn’t throw myself into something completely, if I didn’t get better I’d never know if that was the treatment not working or my fault. Equally, my life was worthless to me – I knew I would probably be dead if I didn’t find an answer, so I didn’t have anything to lose.
Having said that, I know I would have had major difficulties slaughtering a goat if I’d gone back to Thabiso – I’m not sure if I could even have asked anyone else to do that for me.
Looking back, do you see your life in terms of a clear before and after? Are you the same person as you were before you went through this chronic pain experience?
There’s definitely a clear before and after in terms of how I think of my life – before the accident and after it. The date is in my head and I measure everything in my life around that, whether that’s a work event, a holiday, anything else – it’s always XX months/years before or after the accident. I don’t have the same thing with the day I got better because I try not to think about what happened and why, so I still calculate everything around the accident even though I should probably try and move my life to revolve around that happier day.
Largely I’m the same person. I still have the same interests and the same job, so I haven’t changed in that way. But I’d say I’m more focused – I lost so much of my life that I’m trying to make up for it now. So I don’t watch TV, I don’t go out to anything I’m not really interested in, I didn’t go to the work Christmas party because I could think of better things to do than stand around sober shouting over music … so I’m more ruthless about how I spend my time.
I also think invisible illness – or people’s reaction to it – hardens you. You have to grow a shell, otherwise you wouldn’t get through it. So I’m probably more brusque. I’m also really fucking angry about how I was treated and how I see other people – especially other women – being treated and I know that low-level anger shows through a lot. But as I said to a friend (male, obviously) recently, when he read my book and was upset at my anger: once you start noticing what’s going on, when you see people’s lives ruined because of pain, when in extreme cases you see women dying because of their gender, how can you not be angry? I think we should all be more angry. Maybe we could get more done.
You got a book contract before you’d completed all the travel. At that point you didn’t know what the conclusion of your quest would be: a cure, or acceptance of chronic pain as your new normal. Given that uncertainty, how did you go about shaping this narrative?
For the proposal for the book I did a country-by-country, treatment-by-treatment chapter plan (it was wildly ambitious, but pain and finances put the dampeners on it) and suggested the last chapter would be at a meditation retreat in Dorset, learning acceptance. I put in some waggish comment like “assuming I don’t get cured first hahaha”, but secretly I knew there was no way I could write the book if I wasn’t cured, partly on a very literal level – I physically wouldn’t be able to do it – but more because I didn’t see how I would ever be able to accept it. I actually postponed the deadline twice for the same reasons, and when I realised deadline 3 was looming and I wasn’t better and I was going to have to suck it up and write it I was distraught. I genuinely thought that putting all that I had been through onto the page and having to admit that I had failed – and failed my fellow pain people I was doing it for – would kill me. So I don’t know what I would have done if it had come to the crunch; luckily I got my pot of white chrysanthemums and didn’t have to see what happened.
You are leery of words like “miracle” and “cure,” so what terms might you use to describe what ended your pain after four years?
Something happened, and it happened in Brazil. But I would never tell anyone to hop on a plane to Brazil. What happened to me happened after four years of soul-searching and introspection as well as all those treatments. If I’d gone to Brazil first, I don’t know what would have happened.
Who do you see being among the audience for your book?
I’d love people who need it to read it and take what they need from it, but I’d also love doctors to read it – as an insight into patient psychology if nothing else – and I’d love it to be seen as a continuation of the whole #MeToo debate. That sounds holier than thou, and obviously it’d be great for people to read it as a Jon-Ronson-meets-Elizabeth-Gilbert-style romp because I’d feel like I’d succeeded from a writing point of view, but to be honest the only reason I wanted to write it in the first place was to show what’s happening to people in pain, and once I got better, the only thing that mattered to me was getting it into the hands of people who need it. I know how much I needed something like this.