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Book Club: So Many Ways to Sleep Badly

I guess this would be a good time to ‘fess up that I’ve never actually led a book club before. But I read a lot – that counts for something, right?

Anyway, today we’re discussing So Many Ways to Sleep Badly by Mattilda Bernstein Sycamore. I’ll start off by pointing out a few things I thought were interesting:

1. I felt like the most prevalent theme in the book was that of broken bodies. All through the story, Mattilda (the character, not the author – remember that this book is a novel and not a memoir, so we should start with the assumption that everything is fiction) complains of myriad aches, pains, illnesses, and injuries. If it isn’t the sinuses, it’s the hypoglycemia. If it isn’t the hypoglycemia, it’s the fibromyalgia. If it’s not fibromyalgia, it’s the jock itch or headaches or digestion problems or unexplained pain. As she deals with all these problems, the narrator makes it clear that views her body as a malfunctioning, high-maintenance machine – and that the incest she suffered as a child is a large part of that perception. On page 70, she writes, “My forearms are burning, why am I so fucking fragile? I’ll give you three choices: a. incest, b. incest, c. incest.” And on page 183: “I want to tell Rue that none of my pants fit either, but I can’t. I know it’s ridiculous, but it’s scarier than talking about incest, or maybe it is talking about incest – hiding and hating my body, poor helpless body.” What do you think is the connection here? Why are physical pain and sexual abuse so inextricably linked?

2. Although overall, I really liked the body theme, certain parts of it annoyed me – namely the narrator’s constant sarcastic tone when describing her ailments, and her reliance on alternative medicine like yoga, chi gung, acupuncture, and herbal remedies. The novel is fiercely critical of mainstream culture (more on that below), and yet the narrator steeps herself in trendy remedies that are contingent on class privilege, money, and a willingness to appropriate other cultures. What did you think of the narrator’s lack of self-awareness there?

3. Also on bodies: trying to sleep is another big theme in the novel. I don’t think Mattilda gets one good night’s sleep in the entire book. The title of the book points to this theme, so obviously it’s a big one – how do you think it ties in to all the other threads?

4. How about that narration style, huh? Michelle Tea says that Sycamore “makes stream-of-consciousness a lifestyle, a state-of-consciousness.” Did you feel like the style helped or hurt the story? It’s interesting how she uses events like the Iraq war to mark time, but it still feels like sections of the novel take place over a matter of weeks when, in fact, years are passing. Also, notice how Jeremy sort of fades out over the course of the second half? It’s very poignant when you realize that, after their rocky relationship and unstable friendship, he’s just not really present in her life anymore.

5. Politics – especially criticizing mainstream gay culture – play a huge part in Mattilda’s life and identity. On page 121, Sycamore describes “the worst Gay Shame meeting ever:” “People talking about not wanting to critique the community. I mean, we started Gay Shame to challenge the hypocrisy of gay spaces, and now people embrace the new hipster spot like it’s salvation. I’ve done my time getting smashed in terrible gay bars, but I’ve never thought that was community. Benjamin and Ralowe have been talking about leaving the group for awhile, but it’s the first time I think about it too.” In another part – sorry, I can’t find the page – she describes seeing gay and lesbian couples lining up outside city hall to get married, and describes it as the “most depressing thing ever.” I felt torn about this – on the one hand, genderqueer and trans communities have been thrown under the bus multiple times by gay and lesbian communities. On the other hand, at what point do you go from critiquing a community’s treatment of you to claiming that your way of life is superior to theirs? Did anyone else pick up a judgmental tone, or am I totally projecting? (And as a straight, cisgendered woman, do I even have a right to weigh in on this?)

6. I loved the dream sequences in the book. “Fish Tank” was by far my favorite chapter.

7. Here’s a line on page 113 that I loved: “The trick’s cute enough, I push him up on the kitchen counter, I’m grinding against him and he says let me ask you a question: are you gay? These people. Later, he says: what do you do for a living?”

So those are some things that I noticed. Thoughts?


6 thoughts on Book Club: So Many Ways to Sleep Badly

  1. I haven’t read the book yet, I have about twelve other books I have to read for a course, but this one is going on the reading list. I’m really interested in the themes about sleep and the “broken down” body.

  2. i also haven’t gotten to the book, but i wanted to try and talk about one thing.

    you mentioned the apparent relaionship between incest and physical pain.

    i was raped at 5 by a family friend, and then for years by my step-father. i was diagnosed with Acute Intermitent Porphyria when i was nine, fibronalgia and rhumetory arthritis at 15. and the second two, the diagnoses INCLUDED th fact that i had been sexually abused. the rhumetologist who diagnosed me didn’t actually believe in fibromalgia, he thought that it was an expression of the mental ills that happen when one has been sexually abused.
    which, by the way, is total bullshit, evidenced by the fact that some pain meds work and others don’t (if no pain meds work i could see it being mental. if all worked, i could see it being mental at treatable by placebo effect…)

    even worse, way too many doctors also think that fibro is a mental illness – not necissarily a result of abuse, but that showing the symptoms of fibro, the pain and sleep issues and everything, means that there is nothing physically wrong with the person, they are just unsane (not necissarily INsane, just not as sane as everyone else). the fact that so many people with fibro develop depression (chronic pain causes chronic depression, that is just a FACT) makes the whole thing worse. doctors refuse to treat fibromalguia, and instead try to treat what they assume the problem to be. so i get spoken down to, told that its all in my head, ignored, neglected, mistreated and misdiagnosed… this perception problem on the part of doctors has almost killed me once, and led me to have to use a cane and/or a walker for over a year, becase NO ONE WOULD BELIEVE THERE WAS AN ISSUE. i had a neurologist say to me “yes, you have areas of pin-point nerve death, but the reason you are in so much pain is because you are fat”.
    turn out i had displasia of the hip and needed a couple of surgeries to fix it. and it could have been fixed – easier and with less complications – WHEN I WAS 9, HAD ANYONE EVER BOTHERED TO LISTEN TO ME!!!!!

    so… yes, it seems that a lot of people who were sexually abused develop fibro. but i know a far larger number of people with fibro who WEREN’T abused and who DON’T have mental health issues (except that all invariably develop depression from the pain). it appears, to me, to be a false correlation. and one that causes a LOT of harm. but one thing that may be true… most people who suffer chronic illness as children/teens think that they are suffering because they deserve to be punished. this was how it was with me (and lots of others i know). so when i was abused by my step father, i didn’t say anything, i thought i deserved it. people who are abusers are really good at finding people who will blame themselves for the abuse, and that may explain the high correlation that appears to be present. if that makes sense.

  3. Julie, thanks so much for choosing So Many Ways to Sleep Badly for the book club!!! Both the first book club for feministe and your first book club — I’m honored…

    And I like what you picked up about the theme of broken bodies, and especially the contradictions/potential lack of self-awareness the narrator faces in trying to heal her own body…

    Denelian, so true about the way fibromyalgia is dismissed and mistreated, compounding the effects of the mistreatments that may cause the overwhelmed in the first place…

  4. If a particular ritual or herb relieves a medical symptom, I don’t understand how it can be “appropriated.” If it creates a real effect, it’s not just cultural property or belief. If it’s just a superstition, it’s just a superstition, so it’s not doing anyone any good regardless of where they grew up. I feel the same way about practicing a religion – if God X really exists and really works in people’s lives, who’s to say that people of cultures where the religion is not widely accepted need to go to heck (or whatever happens to nonbelievers) and stop appropriating other cultures?

  5. Mattilda – Welcome!! I’m honored that you stopped by!

    Denelian – thank you for sharing your experiences. That sheds a lot of light on the character. And I’m so sorry that you’ve had to deal with so many close-minded and abusive people.

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