20 Books of Summer, 19–20: Emily St. James and Abraham Verghese
Going out on a high! My last three books for the challenge (also including Beautiful Ruins) were particularly great, just the sort of absorbing and rewarding reading that I wish I could guarantee for all of my summer selections.
Woodworking by Emily St. James (2025)
Colloquially, “woodworking” is disappearing in plain sight; doing all you can to fade into the woodwork. Erica has only just admitted her identity to herself, and over the autumn of 2016 begins telling others she’s a woman – starting with her ex-wife Constance, who is now pregnant by her fiancé, John. To everyone else, Erica is still Mr. Skyberg, a 35-year-old English teacher at Mitchell High involved in local amateur dramatics. When Erica realizes that not only is there another trans woman in her small South Dakota town but that it’s one of her students, Abigail Hawkes, she lights up. Abigail may be half her age but is further along in her transition journey and has sassy confidence. But this foul-mouthed new mentor has problems of her own, starting with parents who refuse to refer to her by her chosen name. Abigail lives with her adult sister instead, and gains an unexpected surrogate family via her boyfriend Caleb, a Korean adoptee whose mother, Brooke Daniels, is directing Our Town. Brooke is surprisingly supportive given that she attends Isaiah Rose’s megachurch.

As Trump/Pence signs proliferate, a local election is heating up, too: Pastor Rose is running for State Congress on the Republican ticket, opposed by Helen Swee. Erica befriends Helen and becomes faculty advisor for the school’s Democrat club (which has all of two members: Abigail and her Leslie Knope-like friend Megan). The plot swings naturally between the personal and political, emphasizing how the personal business of 1% of the population has been made into a political football. Chapters alternate between Abigail in first person and Erica in third. The characters feel utterly real and the dialogue is as genuine as the narrative voices. The support group Erica and Abigail attend presents a range of trans experiences based on when one came of age. Some are still deep undercover. There’s a big reveal I couldn’t quite accept, though I can see its purpose. It’s particularly effective how St. James lets second- and third-person narration shade into first as characters accept their selves. Grey rectangles cover up deadnames all but once, making the point that even allies can get it wrong.
This was pure page-turning enjoyment with an important message to convey. It reminded me a lot of Under the Rainbow by Celia Laskey but also had the flavour of classic Tom Perrotta (Election). In the Author’s Note, St. James writes, “They say the single greatest determinant of whether someone will support and affirm trans people is if they know a trans person.” I feel lucky to count three trans people among my friends. It’s impossible to make detached pronouncements about bathrooms and slippery slopes if you care about people whose rights and very existence are being undermined. We should all be reading books by and about trans women. (New purchase from Bookshop.org) ![]()
The Covenant of Water by Abraham Verghese (2023)
All too often, I shy away from doorstoppers because they seem like too much of a time commitment. Why read 715 pages in one novel when I could read 3.5 of 200 pages each? Yet there’s something special about being lost in the middle of a great big book and trusting that wherever the story goes will be worthwhile. I let this review copy languish on the shelf for over TWO YEARS when I should have known that the author of the amazing Cutting for Stone couldn’t possibly let me down. Verghese’s second novel is very much in the same vein: a family saga that spans decades and in every generation focuses on medical issues. Verghese is a practicing doctor as well as a Stanford professor and you can tell he glories in the details of hand and brain surgeries, disability and rare diseases – and luckily, so do I.

Wider events play out in the background (wars, partition, the fall of the caste system), but the focus is always on one family in Kerala, starting in 1900 when a 12-year-old girl is brought to the Parambil estate for her arranged marriage to a 40-year-old widower. One day she will be Big Ammachi, the matriarch of a family with a mysterious Condition: In every generation, someone drowns. As a result, they all avoid water, even if it requires going hours out of their way. Her son Philipose longs to be a scholar, but is so hard of hearing that his formal education is cut short. He becomes a columnist in a local newspaper and marries Elsie, a spirited artist. Their daughter, Mariamma, trains as a doctor. In parallel, we follow the story of Digby Kilgour, a Glaswegian surgeon whose career takes him to India. Through Digby and Mariamma’s interactions with colleagues, we watch colonial incompetence and sexism play out. Addiction and suicide recur across the years. Destiny and choice lock horns. I enjoyed the window onto the small community of St. Thomas Christians and felt fond of all the characters, including Damodaran the elephant. It’s also really clever how Verghese makes the Condition a cross between a mystical curse and a diagnosable ailment. An intellectual soap opera that makes you think about storytelling, purpose and inheritance, this is extraordinary. ![]()
With thanks to Atlantic Books for the proof copy for review.

I read 10 of the books I selected in my initial planning post. I’m pleased that I picked off a couple of long-neglected review copies and several recent purchases. The rest were substituted at whim. There were two duds, but the overall quality was high, with 10 books I rated 4 stars or higher! Along with the above and Beautiful Ruins, Pet Sematary and Storm Pegs were overall highlights. I also managed to complete a row on the Bingo card, a fun add-on. And, bonus: I cleared 7 books from my shelves by reselling or giving them away after I read them.
April 3rd Releases by Emily Jungmin Yoon & Jean Hannah Edelstein
It’s not often that I manage to review books for their publication date rather than at the end of the month, but these two were so short and readable that I polished them off over the first few days of April. So, out today in the UK: a poetry collection about Asian American identity and environmental threat, and a memoir in miniature about how body parts once sexualized and then functionalized are missed once they’re gone.
Find Me as the Creature I Am by Emily Jungmin Yoon (2024)
The Korean American poet’s second full-length work is broadly about loss experienced or expected – but also about the love that keeps us going in dire times. The free verse links personal bereavement with larger-scale tragedies, including climate grief. “All my friends who loved trees are dead” tells of Yoon’s grandmother’s death, while “I leave Asia and become Asian” remembers the murders of eight Asian spa workers in Atlanta in 2021. Violence against women, and the way the Covid-19 pandemic spurred further anti-Asian racism, are additional topics in the early part of the book. For me, Part III’s environmental poems resonated the most. Yoon reflects on the ways in which we are, sometimes unwittingly, affecting the natural world, especially marine ecosystems: “there is no ‘eco-friendly’ way to swim with dolphins. / We do not have to touch everything we love,” she writes. “I look at the ocean like it’s goodbye. … I look at your face / like it’s goodbye.” This is a tricky one to assess; while I appreciated the themes, I did not find the style or language distinctive. The collection reminded me of a cross between Rupi Kaur and Jenny Xie.
Published in the USA by Knopf on October 22, 2024. With thanks to Atlantic Books for the free copy for review.
Breasts: A Relatively Brief Relationship by Jean Hannah Edelstein
From my Most Anticipated list. I loved Edelstein’s 2018 memoir This Really Isn’t About You, and I regularly read her Substack. This micro-memoir in three essays explores the different roles breasts have played in her life: “Sex” runs from the day she went shopping for her first bra as a teenager with her mother through to her early thirties living in London. Edelstein developed early and eventually wore size DD, which attracted much unwanted attention in social situations and workplaces alike. (And not just a slightly sleazy bar she worked in, but an office, too. Twice she was groped by colleagues; the second time she reported it. But: drunk, Christmas party, no witnesses; no consequences.) “It felt like a punishment, a consequence of my own behavior (being a woman, having a fun night out, doing these things while having large breasts),” she writes.
“Food” recounts how her perspective on her breasts changed when she had her two children via IVF – so they wouldn’t inherit Lynch syndrome from her – and initially struggled to breastfeed. “I wanted to experience the full utility of my breasts,” she explains, so, living in Brooklyn now, she consulted a lactation consultant known as “the breast whisperer.” Part 3 is “Cancer”: when Edelstein was 41, mammograms discovered Stage 0 cancer in one breast. “For so long I’d been subject to unwelcome opinions about the kind of person that I was because of the size of my breasts.” But now it was up to her. She chose a double mastectomy for balance, with simultaneous reconstruction by a plastic surgeon.
Although this is a likable book, the retelling is quite flat; better that than mawkish, certainly, but none of the experiences feel particularly unique. It’s more a generic rundown of what it’s like to be female – which, yes, varies to an extent but not that much if we’re talking about the male gaze. There wasn’t the same spark or wit that I found in Edelstein’s first book. Perhaps in the context of a longer memoir, I would have appreciated these essays more.
With thanks to Phoenix for the free copy for review.
January’s Nonfiction Releases: Clarke, Heminsley and Lalkhen
Three new books with medical themes (no surprise there), including the first Covid wave in the UK; fertility and body issues in a new queer family; and pain management strategies.
Breathtaking: Inside the NHS in a Time of Pandemic by Rachel Clarke
Clarke is a palliative care doctor based in Oxfordshire. She runs the Katharine House hospice but during the coronavirus pandemic has also been on active duty in the Oxford University Hospitals system. If you’re on social media you have likely come across some of her postings as she has been equally vocal in her praise of the NHS and her criticism of Boris Johnson’s faltering policies, which are often of the too little, too late variety. So I was eager to read her insider’s account of hospital treatment of the first wave of Covid in the UK, especially because her previous book, Dear Life, was one of my top two nonfiction releases of last year.
The focus is on the first four full months of 2020, and the book originated in Clarke’s insomniac diaries and notes made when, even after manically busy shifts, she couldn’t rest her thoughts. Her pilot husband was flying to China even as increasingly alarming reports started coming in from Wuhan. She weaves in the latest news from China and Italy as well as what she hears from colleagues and disease experts in London. But the priority is given to stories: of the first doctor to die in China; of a Yorkshire ICU nurse’s father, who comes down with Covid and is on a ventilator in an Oxford hospital; and of her patients there and in the hospice. She is touched that so many are making great sacrifices, such as by deciding not to visit loved ones at the end of their lives so as not to risk spreading infection.
A shortage of PPE remained a major issue, though Dominic Pimenta (whose Duty of Care was my first COVID-19 book) pulled through for her with an emergency shipment for the hospice – without which it would have had to close. Clarke marvels at the NHS’s ability to create an extra 33,000 beds within a month, but knows that this comes at a cost of other services, including cancer care, being stripped back or cancelled, meaning that many are not receiving the necessary treatment or are pushing inescapable problems further down the road.

From January 26, 2021
A comparison with Gavin Francis’s Intensive Care, published earlier in the month, is inevitable. Both doctors bounce between headlines and everyday stories, government advice and the situation on the ground. Both had their own Covid scare – Clarke didn’t meet the criteria to be tested so simply went back to work two weeks later, when she felt well enough – and had connections to regions that foreshadowed what would soon happen in the UK. Both give a sense of the scope of the crisis and both lament that, just when patients need compassion most, full PPE leads to their doctors feeling more detached from them than ever.
However, within the same page count, Francis manages to convey more of the science behind the virus and its transmission, and helpfully explores the range of effects Covid is having for different groups. He also brings the story more up to the minute with a look back from November, whereas Clarke ends in April and follows up with an epilogue set in August. A book has to end somewhere, yes, but with this crisis ongoing, the later and more relevant its contents can be, the better. And in any book that involves a lot of death, mawkishness is a risk; Clarke so carefully avoided this in Dear Life, but sometimes succumbs here, with an insistence on how the pandemic has brought out the best in people (clapping and rainbows and all that). Her writing is as strong as ever, but I would have appreciated a sharper, more sombre look at the situation a few months later. Perhaps there will be a sequel.

From January 6, 2021
With thanks to Little, Brown UK for the free copy for review.
Some Body to Love: A Family Story by Alexandra Heminsley
From Heminsley’s previous book, Leap In, I knew about her getting married and undergoing IVF. It was also a book about outdoor swimming; I appreciated her words on acquiring a new skill as an adult and overcoming body issues. This memoir continues the story: in 2017, after a gruelling journey through infertility treatment, Heminsley finally got the baby she wanted. But not before a couple more heart-wrenching moments: the lab made an error and notified her that she shared no DNA with this last embryo, and while heavily pregnant she was assaulted by a drunk man on a train. Both incidents left her feeling a loss of agency. “Why was I consistently being deemed the least reliable witness of my own reality?” she asks.
As they adjusted to new life with a baby, Heminsley started to notice that she wasn’t connecting with her husband, D, like she used to. She felt emotionally unsupported and, in fact, jealous of D’s relationship with their son, L. And while they’d never been the most conventional couple, D’s changes of appearance and wardrobe seemed like a sign of something bigger. Indeed, when L was six months old, D told Heminsley, “this body doesn’t represent who I am” and announced a decision to begin transitioning.
As D moved towards having a body that fit their identity, Heminsley, too, needed to get back in touch with her body. After books like Running Like a Girl, she was considered an exercise guru, but she didn’t see herself in the new obsession with Instagram-ready images of fitness perfection. This is not, then, primarily a memoir of queer family-making, because D’s transitioning was not Heminsley’s story to tell and mostly occurs in the background. Instead she focuses on what she does know and can control: her relationship to her own body.
However, this entails what can feel like irrelevant flashbacks to her teenage years of undergoing rehab at a military clinic in Germany for hypermobility, trips to Trinidad and Italy, and the genesis of her two sporting memoirs. Much as I applaud the sensitivity to trans and body issues, the book ends up feeling scattered. Still, the writing is so candid and the narrative so eventful that you’ll race through this even if you don’t normally pick up nonfiction. (For a bit more information, see my short write-up of the virtual book launch.)
With thanks to Chatto & Windus for the free copy for review.
Pain: The Science of the Feeling Brain by Abdul-Ghaaliq Lalkhen
Originally from South Africa, Dr Lalkhen is an anaesthesiology and pain specialist based in Manchester. In a nutshell, his approach is “biopsychosocial,” meaning that he seeks to understand pain not just as a physical phenomenon resulting from acute injury or damage but as an ongoing process that is affected by emotional and psychological factors. Particularly in the context of chronic syndromes, he acknowledges that pain can continue even when its immediate cause has been repaired. Mental preparation can come into the equation: if a patient assumes they’ll wake up from surgery healed, they may be alarmed if pain persists. Lalkhen talks about managing patient expectations, perhaps with something as simple as the promise, “we’ll aim to get your pain down to a 4 after surgery.” In part, he blames Western society’s Cartesian philosophy for treating mind and body as separate rather than a system.
There are genetic and psychological reasons people might be predisposed to chronic pain. Pain itself can then change the brain chemistry, making the body more alert to pain signals. People can choose one of three paths, Lalkhen observes: “You can spend your time agitating about the alarm going off, you can try to ignore it (but the ignoring of it actually takes up more energy), or the final alternative is to learn to live with this deeply unpleasant situation.” Those who opt for pharmacological solutions can become addicted to opiates, which are less effective over time. Non-drug-related therapies involve the desensitization of nerves, the injection of anaesthetics or steroids, or the implanting of spinal cord stimulators. But all of these strategies have their limitations, and can diminish in efficacy. The patients he sees in his pain clinics may be disappointed that, rather than offering a panacea, he wants to wean them off their current pain relief and help them develop a new way of thinking about pain.
I felt I learned a lot from reading this. Lalkhen is careful to state that he is only referring to non-cancer pain (cancer pain in terminal patients will take all the morphine you can throw at it). Like many physicians, he worries about the modern epidemic of overtreatment and our obsession with wellness. I especially enjoyed the discussion of the understanding of pain and its treatment from the ancient world onward, and in particular the history of opiates. The prose is not literary, but this is an accessible and informational read if the subject matter draws you.
With thanks to Atlantic Books for the free copy for review.

If you need to like a protagonist, expect frustration. Some of George’s behaviour is downright maddening, as when he obsessively plays his old Gameboy while his mother and Jenny pack up his childhood room. Tracing his relationships with his mother, his sister Cressida, and Jenny is rewarding. Sometimes they confront him over his shortcomings; other times they enable him. The novel is very funny, but it’s a biting, ironic humour, and there’s plenty of pathos as well. There are a few particular gut-punches, one relating to George’s father and others surrounding nice things he tries to do that backfire horribly. I thought of George as a rejoinder to all those ‘So-and-So Is Not Okay at All’ type of books featuring a face-planting woman on the cover. Greathead’s portrait is incisive but also loving. And yes, there is that hint of George, c’est moi recognition. His failings are all too common: the mildest of first-world tragedies but still enough to knock your confidence and make you question your purpose. For me this had something of the old-school charm of Jennifer Egan and Jonathan Safran Foer novels I read in the Naughties. I’ll seek out the author’s debut, Laura & Emma.
The family’s lies and secrets – also involving a Christmas run-in with Bruce’s shell-shocked brother decades ago – lead to everything coming to a head in a snowstorm. (As best I can tell, the 1995 setting was important mostly so there wouldn’t be cell phones during this crisis.) As with The Book of George, the episodic nature of the narrative means that particular moments are memorable but the whole maybe less so, and the interactions between characters stand out more than the people themselves. I’ll Come to You, named after a throwaway line in the text, is poorly served by both its cover and title, which give no sense of the contents. However, it’s a sweet, offbeat portrait of genuine, if generic, Americans; I was most reminded of J. Ryan Stradal’s work. Although I DNFed Kauffman’s The Gunners some years back, I’d be interested in trying her again with Chorus, which sounds like another linked story collection.
Mills and Shaw consider the same fundamental issues: bi erasure, with bisexuality the least understood and most easily overlooked element of LGBT and many passing as straight if in heterosexual marriages; and the stereotype of bis as hypersexual or promiscuous. Mills is keen to stress that bisexuals have very different trajectories and phases. Like Wilde, they might have a heterosexual era of happy marriage and parenthood followed by a homosexual spree. Or they might have simultaneous lovers of multiple genders. Some might never even act on strong same-sex desires. (Late last year I encountered a similar unity-in-diversity approach in Daniel Tamet’s Nine Minds, a group biography about autistic people.)
I’ve also read Watts’
Daniel Clowes is a respected American graphic novelist best known for Ghost World, which was adapted into a 2001 film starring Scarlett Johansson. I’m not sure what I was expecting of Monica. Perhaps something closer to a quiet life story like
Ince is not just a speaker at the bookshops but, invariably, a customer – as well as at just about every charity shop in a town. Even when he knows he’ll be carrying his purchases home in his luggage on the train, he can’t resist a browse. And while his shopping basket would look wildly different to mine (his go-to sections are science and philosophy, the occult, 1960s pop and alternative culture; alongside a wide but utterly unpredictable range of classic and contemporary fiction and antiquarian finds), I sensed a kindred spirit in so many lines:
I read this over a chilled-out coffee at the Globe bar in Hay-on-Wye (how perfect, then, to come across the lines “I know the secret of life / Is to read good books”). Weatherhead mostly charts the rhythms of everyday existence in pandemic-era New York City, especially through a haiku sequence (“The blind cat asleep / On my lap—and coffee / Just out of reach” – a situation familiar to any cat owner). His style is matter-of-fact and casually funny, juxtaposing random observations about hipster-ish experiences. From “Things the Photoshop Instructor Said and Did”: “Someone gasped when he increased the contrast / I feel like everyone here is named Taylor.”







Capildeo is a nonbinary Trinidadian Scottish poet and the current University of York writer in residence. Their fourth collection is richly studded with imagery of the natural world, especially birds and trees. “In Praise of Birds” makes a gorgeous start:
The virus is highly transmissible and deadly, and later found to mostly affect children. In the following 13 stories (most about Asian Americans in California, plus a few set in Japan), the plague is a fact of life but has also prompted a new relationship to death – a major thread running through is the funerary rites that have arisen, everything from elegy hotels to “resomation.” In the stand-out story, the George Saunders-esque “City of Laughter,” Skip works at a euthanasia theme park whose roller coasters render ill children unconscious before stopping their hearts. He’s proud of his work, but can’t approach it objectively after he becomes emotionally involved with Dorrie and her son Fitch, who arrives in a bubble.
This is just the sort of wide-ranging popular science book that draws me in. Like
I was delighted to be sent a preview pamphlet containing the author’s note and title essay of How to Read Now by Elaine Castillo, coming from Atlantic in August. This guide to cultural criticism – how to read anything, not just a book – is alive to the biased undertones of everyday life. “Anyone who is perfectly comfortable with keeping the world just as it is now and reading it the way they’ve always read it … cannot be trusted”. Castillo writes that it is not the job of people of colour to enlighten white people (especially not through “the gooey heart-porn of the ethnographic” – war, genocide, tragedy, etc.); “if our stories primarily serve to educate, console and productively scold a comfortable white readership, then those stories will have failed their readers”. This is bold, provocative stuff. I’m sure to learn a lot.
After a fall landed her in hospital with a cracked skull, Abbs couldn’t wait to roam again and vowed all her future holidays would be walking ones. What time she had for pleasure reading while raising children was devoted to travel books; looking at her stacks, she realized they were all by men. Her challenge to self was to find the women and recreate their journeys. I was drawn to this because I’d enjoyed
“My mother and I have symptoms of illness without any known cause,” Hattrick writes. When they showed signs of the ME/CFS their mother had suffered from since 1995, it was assumed there was imitation going on – that a “shared hysterical language” was fuelling their continued infirmity. It didn’t help that both looked well, so could pass as normal despite debilitating fatigue. Into their own family’s story, Hattrick weaves the lives and writings of chronically ill women such as Elizabeth Barrett Browning (see my review of Fiona Sampson’s biography,
I loved Powles’s bite-size food memoir,
Music.Football.Fatherhood, a British equivalent of Mumsnet, brings dads together in conversation. These 20 essays by ordinary fathers run the gamut of parenting experiences: postnatal depression, divorce, single parenthood, a child with autism, and much more. We’re used to childbirth being talked about by women, but rarely by their partners, especially things like miscarriage, stillbirth and trauma. I’ve already written on
Santhouse is a consultant psychiatrist at London’s Guy’s and Maudsley hospitals. This book was an interesting follow-up to Ill Feelings (above) in that the author draws an important distinction between illness as a subjective experience and disease as an objective medical reality. Like Abdul-Ghaaliq Lalkhen does in
Rewilding is a big buzz word in current nature and environmental writing. Few could be said to have played as major a role in the UK’s successful species reintroduction projects as Roy Dennis, who has been involved with the RSPB and other key organizations since the late 1950s. He trained as a warden at two of the country’s most famous bird observatories, Lundy Island and Fair Isle. Most of his later work was to focus on birds: white-tailed eagles, red kites, and ospreys. Some of these projects extended into continental Europe. He also writes about the special challenges posed by mammal reintroductions; beavers get a chapter of their own. Every initiative is described in exhaustive detail, full of names and dates, whereas I would have been okay with an overview. This feels like more of an insider’s history rather than a layman’s introduction. I have popped it on my husband’s bedside table in hopes that, with his degree in wildlife conservation, he’ll be more interested in the nitty-gritty.
The title is the word for winter in the Northern Sámi language. Galloway, a journalist, traded in New York City for Arctic Norway after a) a DNA test told her that she had Sámi blood and b) she met and fell for Áilu, a reindeer herder, at a wedding. She enrolled in an intensive language learning course at university level and got used to some major cultural changes: animals were co-workers here rather than pets (like the two cats she brought with her); communal meals and drawn-out goodbyes were not the done thing; and shamans were still active (one helped them find a key she lost). Footwear neatly sums up the difference. The Prada heels she brought “just in case” ended up serving as hammers; instead, she helped Áilu’s mother make reindeer skins into boots. Two factors undermined my enjoyment: Alternating chapters about her unhappy upbringing in Indiana don’t add much of interest, and, after her relationship with Áilu ends, the book feels aimless. However, I appreciated her words about DNA not defining you, and family being what you make it.
Native American poet Sharmagne Leland St.-John’s fifth collection is a nostalgic and bittersweet look at people and places from one’s past. There are multiple elegies for public figures – everyone from Janis Joplin to Virginia Woolf – as well as for some who aren’t household names but have important stories that should be commemorated, like Hector Pieterson, a 12-year-old boy killed during the Soweto Uprising for protesting enforced teaching of Afrikaans in South Africa in 1976. Many of the elegies are presented as songs. Personal sources of sadness, such as a stillbirth, disagreements with a daughter, and ageing, weigh as heavily as tragic world events.
Coming in at under 260 pages, this isn’t your standard comprehensive biography. Sampson instead describes it as a “portrait,” one that takes up the structure of EBB’s nine-book epic poem, Aurora Leigh, and is concerned with themes of identity and the framing of stories. Elizabeth, as she is cosily called throughout the book, wrote poems that lend themselves to autobiographical interpretation – “her body of work creates a kind of looking glass in which, dimly, we make out the person who wrote it,” Sampson asserts.
Ante remembers the years when her mother was absent but promised to send for the rest of the family soon: “You said all I needed to do was to sleep and before I knew it, / you’d be back. But I woke to the rice that needed rinsing, / my siblings’ school uniforms that needed ironing.” The medical profession as a family legacy and noble calling is a strong element of these poems, especially in “Invisible Women,” an ode to the “goddesses of caring and tending” who walk the halls of any hospital. Hard work is a matter of survival, and family – whether physically present or not – bolsters weary souls. A series of short, untitled poems are presented as tape recordings made for her mother.
In “Happily Ever After,” Lyssa works in the gift shop of a Titanic replica and is cast as an extra in a pop star’s music video. Mythical sea monsters are contrasted with the real dangers of her life, like cancer and racism. “Anything Could Disappear” was a favourite of mine, though it begins with that unlikely scenario of a single woman acquiring a baby as if by magic. What starts off as a burden becomes a bond she can’t bear to let go. A family is determined to clear the name of their falsely imprisoned ancestor in “Alcatraz.” In “Richard of York Gave Battle in Vain” (a mnemonic for the colours of the rainbow), photojournalist Rena is wary about attending the wedding of a friend she met when their plane was detained in Africa some years ago. The only wedding she’s been in is her sister’s, which ended badly.
The obsession began when he was eight years old and someone brought him a dead swift fledgling for his taxidermy hobby. Ever since, he’s dated the summer by their arrival. “It is always summer for them,” though, as his opening line has it. This monograph is structured chronologically. Much like Tim Dee does in
As I’ve found with a number of Little Toller releases now (On Silbury Hill,
Whitney’s father, Ron Davis, is a Stanford geneticist whose research has contributed to the Human Genome Project. He has devoted himself to studying ME/CFS, which affects 20 million people worldwide yet receives little research funding; he calls it “the last major disease we know nothing about.” Testing his son’s blood, he found a problem with the citric acid cycle that produces ATP, essential fuel for the body’s cells – proof that there was a physiological reason for Whitney’s condition. Frustratingly, though, a Stanford colleague who examined Whitney prescribed a psychological intervention. This is in line with the current standard of care for ME/CFS: a graded exercise regime (nigh on impossible for someone who can’t get out of bed) and cognitive behavioural therapy.