by Alice Bolin
But Salander lends some of the melancholy of children’s literature, too. Pippi’s story, after all, is not only about how she brings excitement to a staid Swedish village, but the problem of her loneliness, as she seeks friendship and understanding in a world that wasn’t made for her.
I am charmed by Gabrielsson’s description of Pippi Longstocking, not only because it describes the near-superhero Salander so well, but because in spirit (though in not many practical details), it describes my dad, too. I always think of him as an impish mischief-maker, something of a manic pixie dream dad, whistling in public, sobbing at stories on NPR, flirting with babies, buying candy and stuffed animals, and generally pissing off uptight assholes. Once when he was walking with my brother, they saw a car with a “Who is John Galt?” bumper sticker, a reference to Ayn Rand’s Atlas Shrugged. He stuck a notecard on the windshield that said you are an idiot.
As I think about my dad and Pippi, it illuminates another common feature of the films, books, and TV that he likes: girls who kick butt. He was an early fan of Buffy the Vampire Slayer (though he believes it took a downturn after she graduated from high school) and is even more ardently committed to the cult teen detective show Veronica Mars, whose plucky heroine wields a Taser almost as well as Salander does. I first told him to watch Veronica Mars, and later, after he had breathlessly emailed me about Veronica and Logan and Dick Casablancas enough times, I regretted ever watching it. I used to think that he only had some embarrassing pervy attraction to girls who kick butt, and, I mean, he definitely does. But after he told me through tears that he “only wants Veronica to be happy,” I should have gotten the picture that he sees himself in them, too. I guess it is no surprise that he identifies with teenage girls, when there is an illustrious tradition of grown men expertly crafting young women’s entertainment, from boy bands of all eras to Sixteen Candles and Pretty in Pink to, indeed, Buffy and Veronica Mars.
“I definitely think he relates to those girls,” my mom told me. She reminded me of a scene at the end of the first Millennium series book, when Salander realizes she has fallen in love with Blomkvist and resolves to confess her feelings to him. When she finds him, he is on a date with another woman, and Salander is crushed. This is the most affecting part of the books for my dad, my mom told me. “He’ll just cry and cry about that part,” she said. All along I thought he saw himself as the valiant everyman Blomkvist, who comes to the aid of the sexy girl who kicks butt. I was wrong about that, and I shouldn’t make the mistake of thinking I have figured him out again. I told him that I thought he identified more with Blomkvist, but then it occurred to me that he maybe identified with Salander. “I don’t think I’m like any of them,” he told me stubbornly. “I just think the books have the ring of realism,” a description that in my opinion could not be more incorrect.
When I complained to my mom about my dad describing books that strain plausibility in every way as having “the ring of realism,” she explained to me how this is one of the phrases he uses indiscriminately to describe works that grab his imagination (the other is “the spark of greatness”) in the manner of, for instance, the cop show Hill Street Blues. This shorthand praise is another way for him to avoid analyzing his own whims. It’s also, maybe, a defensive posture to keep us from analyzing him.
This could be why I have delayed addressing what was supposed to be one of the points of this essay: whether my dad has autism and if it matters. The therapist he works with has suggested that he has Asperger’s syndrome, based on his difficulty reading conversational cues and other people’s moods; his short temper; his many intense enthusiasms; and his almost complete lack of social inhibition, which often leads to totally inappropriate behavior. When I asked him about it for this essay, it was the first time we had ever spoken about it. “Why are you asking me about that?” he said incredulously, and I explained that it made me think of him when Blomkvist privately guesses that Salander has Asperger’s because of her savant-like skills and social awkwardness. “Yes, that is one possible diagnosis,” he said about Salander. Of his own diagnosis, he would only say, oddly, that he didn’t remember it, comparing it to the apparent amnesia he developed in the 1990s when he had bursitis of the elbow. I pressed him, but he stood by his “no comment.” “I have zero memory of anyone ever saying I have Asperger’s,” he said. “I’d completely forgotten that and I hadn’t thought about it. I don’t have any thoughts or any opinions.”
I really don’t blame him for having no thoughts or opinions. No one even raised the possibility that he was on the autism spectrum until he was sixty-eight, and charging someone that age with a condition we often associate with childhood is complicated by a lifetime of ambiguities and examples to the contrary. As he approached his eighth decade, the methods he had learned to navigate the world were just his personality, as they are, I assume, for everyone. He was also unwittingly encountering a fateful tendency in my family to monumentalize the eccentricities of its members, to talk and laugh about them among ourselves and with strangers—write about them, even—until the picture shifts into focus, and those eccentricities reveal themselves as dysfunction.
And no matter his age, I’ve come to see autism spectrum diagnosis as an alienating thicket, where there is no textbook case. At his therapist’s suggestion, he read David Finch’s memoir The Journal of Best Practices, the story of Finch being diagnosed with Asperger’s as an adult and using this new self-knowledge to become a better husband. Despite what would seem to be obvious commonalities between Finch and my dad, he found no applicable lessons in his story, and he thought the book made Finch look, frankly, like a jerk. Finch and his wife, Kristen, were on an episode of This American Life in 2012, where Kristen, a speech therapist who worked with disabled kids, says that she and her coworkers would always joke that their husbands were autistic. The stereotypes in that joke are uncomfortable for me in both directions. Joking about men’s emotional stuntedness seems at best inaccurate, at worst self-reinforcing, and joking about autistic people as socially retarded and robotic almost certainly increases their ostracization. But it also collapses the almost endless variation among people with autism spectrum disorders: my dad didn’t recognize Finch’s compulsions, which isn’t to say he has none of his own.
I found myself combing through websites about the autism spectrum, many of which are compiled by civilians who have the disorder themselves, who I think are also trying to come to terms with the many ways one can have autism. One particular website called Inside Perspectives of Asperger Syndrome and the Neurodiversity Spectrum describes possible autism spectrum symptoms across an exhaustive list of categories, including work, sex, eating, sleep, phone problems, “spacing out,” and even allergies and drug sensitivities. The primary sources on every page are testimonials from web users who identify as having autism and related conditions, like Asperger’s and ADHD, describing their own experiences. Many of these don’t describe my dad at all, while others do with eerie accuracy. During the conversation we had about his possibly being autistic, this description was dinging in my head: “Some have problems with reciprocity & timing and either talk on and on without letting anyone else get a word in edgewise, constantly interrupt others without realising that it’s disrespectful to do so, or say nothing at all unless asked a direct question.” There is of course also the claim that many with autism “are able to hyper-focus intently on the same thing for hours, days, sometimes weeks on end, and keep up a special interest for years”—see Sjöwall, Wahlöö, Larsson, et al.
One of the most helpful things I read on Inside Perspectives is this eloquent description from one of the site’s users of the problem with seeing autism as a disorder:
If you have one neurodiverse trait you are more likely to have additional neurodiverse traits. I am not sure why this is. The more of these traits you have, the more difficult it is to function . . . If you can’t function in society because you have too many of these traits and/or they are too intense then it becomes a disabili
ty. And when it becomes a disability then they have to put a label on it. . . . The ‘clump traits together and give them a name’ strategy is fundementally [sic] flawed . . . Labeling falsely claims you have one thing, not a group of things which may be better treated individually.
But viewing the autism spectrum as a matrix of possible traits evokes all the problems of mental health diagnosis, because, to put it simply, everyone has traits. The American Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders (DSM) does not seek to describe what a healthy person looks like: psychological “normalcy” is judged only by an absence of any of the dysfunctions it addresses. Considering the gargantuan length of the DSM, there are nearly as many ways to be crazy as there are to be alive. But despite the DSM’s attempt at exhaustiveness, it remains very difficult to wrangle a human being’s habits, thoughts, desires, quirks, and pain under the heading of a single diagnosis of mental illness. This is underlined by the manual’s primary use, which is not therapeutic, but clerical: a diagnosis of a disorder with a DSM classification is often the requirement for an insurance company to authorize treatment.
I gained the most insight from the wonderful autistic writer and rhetorician Melanie Yergeau, who discusses the problem of diagnosis on her blog autistext.com. As she writes, “For many, diagnosis is validating and/or leads to self-understanding. Diagnosis can explain a lot.” But a disease model of autism, where there are degrees of severity and some have it “worse” than others, effaces the individual value of autistic people. Yergeau writes powerfully for the model of disability that relies on disabled people’s rights to advocate for their own needs:
Whether your disabled child screams in the grocery checkout line or testifies in front of Congress, he is self-advocating. Whether your disabled child throws peas in your face or writes a snarky blog post or falls asleep during board game nights or says NO in all capital letters, she’s self-advocating. And none of these things is less noble or gutsy than the other.
All people have needs that flow from their humanity, not from a predetermined list of problems that we call disability. Diagnosis and the vocabulary that it trades in should be tools to help people understand themselves and ask for what they need. It follows, then, that if the language of disability doesn’t help someone advocate for himself or herself, he or she should be free to reject it.
For my dad, navigating the “neurodiverse traits” that make functioning more difficult individually—like helping him to remember not to make too much noise around the house, to reflect more on his emotions, not to give in so quickly to frustration—is most helpful, and it doesn’t require him to align all the vagaries of his personality with a diagnostic label. The autism designation isn’t helpful for him. The autism spectrum is one more place I’ve looked for my dad, with only partial success. My mom told me that, library cataloger that she is, one of her greatest interests is in creating typologies, finding categories and seeing where things fit. But she has never been that good at categorizing the people close to her, not suspecting that there was anything in my dad’s weirdness that might be explained by someone else’s weirdness. “I tend to be accepting of the way that people are,” she told me helplessly, which might be another way of saying that love is blind.
Larsson died of a heart attack shortly after delivering the manuscript for The Girl Who Kicked the Hornet’s Nest, never living to see his novels published, much less the worldwide sensation they would become. Per Wahlöö died after he and Sjöwall finished the tenth Martin Beck novel, blessedly missing most of the social degradation he had warned against. These deaths are both eerie in the same way: socially conscious writers not living to know how right they were. Sjöwall cheerily admits now that “the project” was a failure. “Everything we feared happened, faster,” she told The Guardian in 2009. “People think of themselves not as human beings but consumers. The market rules, and it was not that obvious in the 1960s, but you could see it coming.” What would have been harder for them to see coming was the murder of the Swedish prime minister Olof Palme in 1986, eleven years after they wrote about a fictional Swedish prime minister being assassinated in The Terrorists.
The most remarkable thing about reading the Millennium series now, in the spring of 2017, is their overwhelming, prophetic resonance with the scandals of the 2016 election and the Trump administration, as they involve neofascists, computer hackers, sexual misconduct scandals, Russian spies, government corruption, evil billionaires, and journalistic integrity. It makes me wish Larsson had lived to comment on it, although I assume the current era would immediately make him wish he were dead.
Many people have noted the marketing brilliance of changing the title of Larsson’s Men Who Hate Women for the English translation, shifting the focus from creepy men to always more salable “girls.” Men Who Hate Women could be another alternate title for my book, and I have chosen, maybe hypocritically, to sell it on girls instead. In the end, the careers of Larsson and Sjöwall and Wahlöö turn out to be Dead Man stories, where men leave their wives and collaborators to deal with their absence for decades. This female survival is probably the truer story and, I think Larsson, Sjöwall, and Wahlöö would agree, a better one, but it doesn’t have the same addictive glamour that comes with a Dead Girl. In Roseanna, one of Beck’s colleagues mentions a movie that the suspect they’re trailing goes to see. “It has a wonderful ending,” he says. “Everyone dies except the girl.”
Larsson died at fifty, after years of working too much, eating too much junk food, drinking too much coffee, and smoking too many cigarettes. There has been extended drama involving his partner of thirty years, Gabrielsson, who, since they never legally married and Larsson left no will, is not entitled to any of his posthumous millions. His death was ironic and unjust, having happened at altogether the wrong time. I can’t help but think about my dad when I read about Larsson’s heart attack: how Larsson’s colleagues found him in a chair, breathing heavily and in a cold sweat, and even then he did not want to admit he was sick. My dad was probably in congestive heart failure for weeks before my brother and his boyfriend found him hunched over in a parking lot, gasping for air. I burst into terrified tears when I saw him on a gurney in the emergency room, looking so gray and puny. “It makes me cry, too,” he said and sobbed.
Insofar as this is a Dead Girl story with a happy ending, you know that my dad got better. His cardiac emergency became another episode in his life, another story underscored, appropriately, by reading. In the hospital after his angioplasty, he had a paradoxical reaction to a sedative that launched him into an hour-long panic attack. Every sixty seconds, he would jump out of bed and run around his hospital room, endangering his fresh stitches. At one point my mom, her nerves completely shot, picked up The Girl Who Kicked the Hornet’s Nest and began to read from Salander’s trial. This was the only thing that soothed my dad, and she read to him until he fell asleep.
Part 2
Lost in Los Angeles
There There
When I turned twenty-five, I lived in Los Angeles. That is, I was in Los Angeles, and I was, ostensibly, alive.
I don’t know what else you call it when you come to Los Angeles but then your job prospects fall through and you have to survive on your wits and your friends’ couches and your birthday money.
I had never even been to California before I decided to move there. As I drove down from the Sierra Nevada foothills on Highway 20 (“The 20”?) toward my aunt and uncle’s house in the northern Sacramento Valley, I found myself exclaiming out loud to no one, “Look, a palm tree!” Because I grew up in Idaho, my entire frame of reference for California was as a place people left to retire in the Northwest, and as vaguely fancy. I still have difficulty shaking that last idea. When I discovered I didn’t get cell phone service in my aunt and uncle’s house, I could only think, outraged, “In California?”
My more recent frame of reference for California comes from books, which tend to paint it as a sun-drenched and c
ontradictory collection of tropes revolving clumsily around a nonexistent center. Joan Didion has devoted at least a portion of each of her four essay collections to trying to understand California, and she spends all of her 2004 book Where I Was From parsing the state’s contradictions. “This book represents an exploration into my own confusions about the place . . .” she writes early in Where I Was From, “misapprehensions and misunderstandings so much a part of who I became that I can still to this day confront them only obliquely.” These misunderstandings are mostly related to the way that California’s imagination of itself—as native, independent, and wild—is at odds with what has from the beginning been its essential character: it is immigrant, corporate, and overdeveloped. As Didion writes, “A good deal about California does not, on its own preferred terms, add up,” or, as she quotes from W. B. Yeats in the epigraph to her first essay collection, Slouching Towards Bethlehem, “The center cannot hold.”
Or as my cousin Tony told me in a dark comedy club in Santa Monica, “There is no there there.” This might be Gertrude Stein’s most Gertrude Steiny quote, but it is not that sphinxlike when taken in context. She was describing how she felt when revisiting her childhood home in Oakland: the loss one can feel for a place when its fundamental character has been so changed that, while it isn’t gone, it is not exactly there either.
But Stein’s koan works just as well when describing the literal and existential decentralization one experiences in Los Angeles. I missed three-quarters of the show that night, including Tony’s set, because I couldn’t find the club. I wandered dumbfounded around Santa Monica’s prefab “promenade,” two sterile streets of luxury storefronts and chain restaurants, passing the same stores again and again, until I realized that I had actually been circling around the club—it was tucked in an alley, the entrance to which could be found, I was told later, because it is “near the Hooters.”