For #worldmentalhealthday I thought I’d do a podcast. This has advice on how to dry plums, make apple butter, glean fruit & vegetables…and also a discussion of suicide. *shrugs* Here you go.
CW: Ableism, racism, Nazis, and centering of disabled voices.
Notice I gave a content warning for centering of disabled voices. I’m not doing this to be cheeky. Abled people think they not only have the right, but the obligation to center themselves in the disabled narrative. After all, disabled people are weak, feeble, befuddled and delusional; the disabled narrative is obviously too heavy for us to carry, too complex for us to understand. We’re no doubt extremely grateful that abled people can take over that burden for us.
After all, abled people are the experts in our narrative: they have a degree, or a disabled family member, or they’ve so angelically dedicated their lives to “helping us.”
When disabled people try to stand up and say, “Well, actually, you’ve got it wrong,” abled people get absolutely irate. They call us names, shout us down, then block us on Twitter and go around subtweeting about what problematic assholes we are for not getting the disabled narrative “right”.
Part of the problem here is that the disability narrative doesn’t get much press. Disabled people are trying really hard to get our seat at the table, but the table isn’t accessible. So those “experts” have so kindly decided they’ll be martyrs for our cause and sit in for us.
Consequently, even those who consider themselves on the forefront of the social justice movement don’t know what “neurodiversity” or “ableism” or “neurotypical privilege” are; they still insist on person-first language, and use phrases like “wheelchair-bound”, because they’re listening to the “experts” and not to disabled people themselves.
Another problem is the complexity of the disability narrative itself. “Disabled” is a wide swath of identity including both physical and mental disabilities. Most of us who consider ourselves disabled become a little lax in educating ourselves about disability. We think we know it all already, so when another disabled person says something we don’t understand, we tend to lash out.
Disabled people of all kinds are tired of this shit. I, personally, am completely done with it. So, I’ve given you your content warning. If you can’t handle disabled voices being centered without flipping out and being ableist, please go elsewhere on the internet where we can’t distress one another.
Thank you. Moving on.
Disabled people are the receptacle for a huge amount of bullshit. Abled people use us as crutches, scapegoats, and shields.
I’m not just talking about abled people on the right. The left is just as guilty.
Let’s start with how disabled people are used as crutches. The irony of this metaphor—an abled person using a disabled person as a crutch—is intentional. Yes, it’s is exactly that painful, awkward, and incapacitating.
So. If we’re thoughtful people, we know white people are to blame for electing Trump (and other leaders of his ilk around the white world). What most of us don’t realize is that we white folk used disabled people as a crutch to help get him elected.
Most disabled people wouldn’t vote for someone like Trump. After all, we know the violence behind the “personal responsibility” narrative. People have been trying to get us to pull ourselves up by our own bootstraps since the dawn of time, and all that’s happened is we’ve ended up on our asses in the dirt, with abled people shaking their heads and blaming us for not trying hard enough.
Disabled people know what will happen to us if Medicaid and other safety net programs get cut. A lot of us remember what it was like before those programs even existed in their current forms. And we know that, even if we can access those programs now, they provide the absolute minimum in benefit to us, leaving us in a position of perpetual instability.
Trump’s presidency is a literal death sentence for us. But our identity has been hijacked and used against us to elect him and prop him up.
Abled people see disabled people as burdens and fakers; victims and villains. Which part of this spectrum a specific disabled person will fall on depends a lot on factors like their race and how they’re disabled. For the most part, disabled people of color are more likely to be seen as villains: as dangerously crazy, or “fakers” who are working the system, while white people are infantilized and seen as helpless victims. But it is by no means that simple. All of us tend to be seen and portrayed as ALL of these things, even by a single individual, and all in the space of one sentence.
For instance, we’re spoken of as creatures created by cycles of poverty and abuse, brainwashed by victims’ complexes, who only need a chance to do “useful” and “productive” work so that we can get our “dignity” back. We’re not only brainless, childlike victims, but also conniving villains who are working the system, and only abled people can save us.
Trump claimed he was the only one who could create opportunities to get disabled people back to work. He’d bring back the jobs. He’d purge the “welfare” roles of all the lazy fakers who were draining the system. He’d put a new system in place and make us all reapply for aid, so those fabled disabled people who are really in need could get even better support. Plus, the military veterans who weren’t “strong enough to handle” the atrocities of war would have a new and improved V.A.
All of this rhetoric gets disabled people both going and coming. Not only are we fakers, but we’re weak. We’re not only burdens, but we have to bend over backward to prove to abled people that we’re worthy of being burdens, if we wish to get what we need to survive.
And this narrative helped elect Trump. Abled people thought they were helping us by buying into this bullshit narrative.
Abled people on the left also want to use us as a crutch to counter Trump’s agenda of dismantling Medicaid and Medicare and the safety net. I’m much more willing to be used as this type of crutch, but I really wish they’d give actual disabled people a seat at the table, instead of letting experts speak for us, and letting unethical reporters write both inspiration porn about disabled people “overcoming in spite of”, and sepia-toned tragedy pieces about how we get ourselves stuck in a cycle of welfare culture because of our infantile inability to see our way into a better—abled—way of life.
Now, let’s look at how disabled people are used as a scapegoat.
We’ve all noticed how, when someone commits an act of violence, they’re called a terrorist if they’re a person of color, or mentally ill if they’re white. All rational people know how this hurts people of color. Fewer people see how this hurts the neurodiverse.
Being neurodiverse or mentally ill has absolutely nothing to do with being violent. Say this again, because I’m almost positive you still don’t understand: violence and mental illness are completely unrelated things.
Committing an act of violence doesn’t mean you’re mentally ill.
Being mentally ill doesn’t mean you’ll commit an act of violence.
People who commit acts of violence are not statistically more likely to have a diagnosed mental illness. Mentally ill people are MORE likely to be hurt BY neurotypical people than the other way around.
Neurotypical people are the violent ones. Not us. Some of you reading this won’t believe me. Google is your friend. Do some research about the percentage of violent and other crimes perpetrated upon neurodiverse people as opposed to by them (and/or read some of the blog pieces I’ve wrote on this in the past), because I speak the truth.
So, calling white terrorists mentally ill is a cop out: it’s white people saying, “NOT ALL WHITE PEOPLE!” It’s white people thinking that people who commit those acts are somehow different from them. We white people can compartmentalize and “other” that hate and racism as “crazy”, so we don’t have to think about what ideas we ourselves might have that support and feed into the toxic mindset of a violent racist.
People on the left also call Trump “mentally ill”. He’s not. He’s just a dangerous asshole, and this isn’t the same thing at all. “I’m not trying to insult neurodiverse people,” is the answer I get when I speak up about this. “I’m just saying there’s legitimately something wrong with the dude.”
No arguments here about that. There is legitimately something wrong with him. But that “something wrong” isn’t “mental illness” because despite what people think, neurodiversity isn’t “something wrong” to begin with. At all. Just please, stop. Neurodiverse people are not the trash barrel where you can throw all your goddamn issues. Instead, try dealing with them and admitting that “sane” people do very, very horrible and irrational things.
Disabled people are also used as a shield, which is sort of a hybrid of a crutch and a scapegoat.
I saw this a lot yesterday, during that Nazi march. White people said a lot of things like, “I understand that what they’re doing is wrong. But think of things from their perspective. Maybe they’ve suffered abuse. Maybe they’re mentally ill. Maybe they’ve had to struggle to pay the bills because their parents are disabled.” Etc.
Disability and mental illness are not shields that you can put up so that accusations of racism/bigotry will bounce off. It pisses me off that abled people try to blame neurodiverse people for being the perpetrators of all violence and racism, and then they also think they can shield white people from accusations of racism because of their supposed mental illness and disability. Abled people are exhausting.
Mental illness and racism have nothing to do with one another in the same way that mental illness and violence have nothing to do with one another. Mental illness and/or trauma will not lead someone to be a bigot. Those sick and dysfunctional ways of thinking are not neurodiversity. They’re just bigotry.
How abled people can be so fucking ableist and then accuse disabled people of being the root of all evil is just fucking aggravating.
I’m done with it. Please stop. For the love of GOD.
Elizabeth Roderick is an author and neurodiverse activist. She’s busy writing books, which abled people think is inspiring while simultaneously thinking that she’s a burden on society and should get a real job in order to get her dignity back. If you want to support her in her undignified and childish inspirational pseudo-work, you can find her on Amazon.
I’ve been thinking about ableism/bigotry in literary gatekeepers again. My last post on this stirred up wank. I’d appreciate it if y’all kept that to subtweets if you must, because I’m through making room for that ableism in my world.
I’ve been writing as always, and forging ahead in this career of mine. I’m working on my 17th full-length novel, and I’ve been pitching agents with an own voices YA—the (*counts*) twelfth novel I finished, about a bipolar girl navigating high school, first love, and institutionalization (sounds cool, right? It is 😊) .
Right now, I’m not making a lot of money off of book sales; most of it comes from the freelance editing/writing/consulting work I do. Deep in my heart, I know I’ve been concentrating my efforts in the wrong areas, and avoiding the work I really need to do. Because, no matter how much I enjoy editing and the other stuff, my goal is to make the bulk of my money off my own books.
In order to make money off of books, however, you have to do THE “M” WORD.
(I mean marketing, not some more interesting “m” word.)
I have five titles already published. I’m proud of those books, and people who read them like them. I’m utter crap at marketing, which is why I’ve been looking for an agent: for guidance and handholding in my marketing efforts, more than my publisher can give. But even with an agent, I’d have to do a lot of that work myself. So what am I waiting for? Why am I not doing it?
Marketing my books is no easy task, however. To start with, they don’t fall easily into a niche (especially my Other Place series). If you were to ask me who my audience is, I would probably say…people? Who like books?
More typical marketing efforts haven’t worked well for me. My romance and other genre fic author friends often try to take me under their wing and get me involved in Instafreebie giveaways, takeovers, anthologies…that stuff is hella fun, and I get great comments about my little romance short stories and such that I write, but it never translates into a major boost in sales. That’s because my full-length books are pretty much in the “other” genre.
Just like me, according to the neurotypical world.
Strangely enough, the only marketing method that gives me a sales bump is when I appear in-person to give talks about my writing and neurodiversity. I sell out of books at events like these, then get an e-book bump, as well. I think this might be because I’m a five-foot-tall, snub-nosed white lady who, as some officers at a recent CIT session I spoke at so aptly put it, doesn’t “look crazy”. I’m non-threatening. I may fidget a lot, but I’m told I’m an eloquent and compelling speaker. At any rate, people just seem a lot more prepared to listen to me in person than they do online.
So, I decided, it’s time for me to do That Thing That I Hate So Much: contact people. Specifically, to try to get book signings.
There’s an indy bookstore in Seattle that a lot of my friends told me to contact, because it was easiest for them to get to. It’s a place a lot like other bookstores I’ve done well at, so I wrote them a little email. I introduced myself as a neurodiverse own voices writer, and said I was looking for a signing to showcase my Other Place series, which is the story of a woman dealing with homelessness and addiction, and a schizophrenic man trying to make it in the art world.
I got a response back: “Thank you for contacting us. We don’t feel your books would be a good fit for our venue, because our clientele aren’t generally interested in romantic suspense.”
Readers, I should have left it at that. But, sometimes I’m so fatigued by ableist what-the-fuckery that I dissolve into a big bucket of can’t-even. I replied that the books aren’t at all romantic suspense (not adding that I fucking wish they were RS, because then I wouldn’t have to waste so much time talking to bitches like her, and could just do the Instafreebie and author takeover things that work well for RS authors). I tried to clarify what type of books they are…of course, I was just restating what I’d already made clear in the first email. And, of course, she didn’t reply.
I don’t know if literary gatekeepers (and others) even know how ableist they are. From the way they’ve said in the past that I’m “whining”, “bitter”, “delusional”, and that I “don’t know how publishing works” when I’ve spoken up about the ableism I encounter as a neurodiverse own voices writer, I’m hoping not. But, while I may not know marketing from the inside of my dog’s butt (I don’t know anything specific about the inside of my dog’s butt, for context), I do know ableism when I see it. I’m a goddamn expert on ableism. And gatekeepers: y’all are IT.
This events coordinator woman wanted to reject me, because of the visceral reaction people have when they hear someone is “mentally ill”, especially when that mental illness involves psychosis. She went looking for a reason to reject me. It wasn’t a reason that made sense, at all. I mean, the books aren’t by any logical yardstick romantic suspense, and also, how whacked-out do you think I am that I’d believe a bookstore could afford to alienate romance readers? You’re a BOOKSTORE. I don’t care how cultured you think you are: unless you’re a university store where students get their textbooks, romance of some sort is likely your bread and butter, or a good portion thereof. Additionally, even if the Other Place series was romantic suspense, it would be own voices romantic suspense with neurodiverse characters. That’s not “just” romantic suspense: that’s something that *should* be interesting to a more…(educated? Pretentious? I can’t find the right word here. They’re all inappropriate and/or more insulting than I want them to be)…readership.
I’ll get a signing eventually, but it doesn’t mean that this experience was okay.
So, gatekeepers: y’all are ableist (and prejudiced in other ways). I’m not whining. I’m not bitter. I’m just throwing the God’s-honest truth at you. It doesn’t matter that you already have a book with a neurodiverse character, or by an own voices author, on your list or on your shelves. We’re not a trophy that you can hold up to prove you’re not bigoted. We’re not that “one friend” you have that means you’re compassionate and progressive. We’re authors, writing great books, and you’re shutting us out with your (sometimes unconscious) prejudice.
Get conscious of that shit, because y’all are assholes.
Elizabeth Roderick doesn’t think YOU are an asshole. You read her whole post. If you’d like to check out her books, she’d really appreciate it.
(CN: descriptions of ableism, ableist language, abuse, addiction, grunge culture, and a lot of navel gazing)
Well, this post is a long time coming. Those few people (if any) who read this blog without following me on social media have probably noticed something strange in my last few posts: I started identifying as autistic all of the sudden. I’m not in one of those bipolar states where I start thinking I’m an ancient, reincarnated deity, a really great painter, or someone who could make a good living as a televangelist. I really am autistic.
This diagnosis was a long time in coming. I’m not sure if I would have been better or worse off if diagnosed earlier. All I know, is I’ve suffered a great deal because of my neurodiversity, in ways I’m only now beginning to realize. Before, I blamed myself for the raw treatment I received. Ableism is a horrible thing, especially when internalized.
I was born in 1977, which is old enough to put me in the other army of the ageism battle than a lot of you. Autism wasn’t even a diagnosis until like 1984 or something, and it was well into the ‘90s before I’d ever heard of it.
When I was a kid, I spent a lot of time alone, nerding out on special interests: writing Lord of the Rings fanfic, cataloguing every species of plant that grew around my home, and trying to form telepathic bonds with my cats. I was so in my own head that I rarely had the “correct” reaction to social stimuli. I would often become overloaded in social situations and explode, or do strange things (like rubbing blankets on my face or licking someone’s silk shirt) to calm down. I didn’t care about wearing fashionable (or even presentable) clothing or brushing my hair. When my daily routine was interrupted, or if my environment were too noisy/frenetic, I’d have embarrassing meltdowns. I had very few friends, as you might imagine.
Anyway, if I’d been born in 2001, I would have been in all sorts of horrible programs and special ed classes. I dodged a bullet, I think (even though I was skipped a grade, which was a nasty idea because of my lack of mainstream social skills). Back when I was a kid, autistic people weren’t called autistic; they were “nerds” and “weirdos” (or worse, depending). We suffered horrid ableism—the same way we do now—but most of us were left more or less to our own devices. I didn’t have any formal brainwashing, but I was punished for my “bad behavior” and exiled for my social oddness. I hated myself for that behavior, but could never manage to control it.
I’ve spoken before about the physical/emotional/sexual abuse I suffered as a young teenager. Neurodiverse people are A LOT more likely to suffer abuse of all kinds, and I fell into that category. That was partly because of my lack of neurotypical social skills, and the scars ableism had put on me: I was a flashing target for abusers. I just wanted someone to pay attention to me, and figured I deserved whatever abuse I got, because I was such a disgusting, annoying loser who couldn’t act right.
I’ve discussed my other diagnoses ad nauseum, so I won’t go into it further here. At any rate, I was a psychological hot mess by the end of high school (not because I’m autistic or bipolar, but because of ABLEISM, to be clear). By the time I was in college, I was doing heroin to control the psychosis, depression, and anxiety.
I think a word about college here, because grandma Liz is in a sentimental mood.
I went to The Evergreen State College in Olympia, Washington, during the height of the grunge era (so yeah, Nirvana, Beck, Built to Spill, Sleater-Kinney and I all hung out in the same damp coffee shops, wiping our snuffy noses on each other’s alpaca wool hats). A lot of people have just recently heard about Evergreen, because of the protests there. That sort of thing is nothing new at Evergreen.
Evergreen was (probably still is) a great college for certain types of neurodiverse people, comparatively. No tests. No grades (just evaluations). And back then, you didn’t even have to declare a major. Also, you could do independent study courses, where you would propose an area of research to a professor, and if they approved it you could go on your merry way, researching dogs’ emotional responses to music in New Orleans as opposed to Austin, or whatever, and write a report at the end of the semester for your sixteen credits.
I thought I’d fit in great at Evergreen. I considered myself something of an intellectual and an artist (I’m a musician, and I wrote back then as well, though not as much as I do now). Additionally, I’d come out as bisexual in high school, and I knew they had a thriving LGBTQ (or just “gay” as we called it back then) community at Evergreen.
Unfortunately, I fit in even worse there than I had in my rural high school. I just couldn’t get social situations right, and boy were social situations complicated in college. That time, much like now, was one of radical exploration of culture and bias, and I always somehow ended up on the wrong side of those debates. Once, when looking for an apartment, I asked a friend who had a room for rent at her house. She told me I had to be a lesbian in order to rent there; bisexual wasn’t “gay enough”. When I pointed out she herself was currently dating a dude, though (which is what we called cishet males back in the days when we wore onions on our belts), she said she was a lesbian currently dating a dude, and she got mad at me for not understanding the difference.
I felt incredibly left behind by the entire social justice movement at the time, in fact. I was looked down upon for my abused woman syndrome; if I had any self-respect, I was told, I’d be able to rise above my abuse more than I had. Some guy friends of mine let me play in one of their bands once for a show; the women told them it was about time they had a woman in their band, but after they saw me play said I was too timid to be interesting. I probably made those girls think I hated them or something, because I couldn’t make eye contact or small talk, but still.
There were more social narratives in that environment than I’d had to deal with in high school, and I wasn’t good at social narratives to begin with. It was horrifying.
So I retreated. I completed my education by independent contract (living with Sandinistas in Nicaragua, and staring an organic farm business back home). I fell into my heroin addiction, and into another abusive relationship. I ended up in prison for the heroin eventually. I’ve gone on and on about those stories elsewhere in my blog.
I didn’t think of myself as neurodiverse. I just thought of myself as a failure, and too weak to do life correctly. Even when, a long time later, I began to recognize my neurodiversity, I continued to run on internalized ableism. I can’t help but think this is at least partially because I’d been alienated from the message of empowerment in college. The social justice movement is taking a long time to embrace neurodiversity.
I wanted to point this out only because this dynamic has not changed much in the SJW arena: there is SO MUCH ableism. People accept mental illness and neurodiversity (and the signs of abuse) as long as they follow the accepted narrative and fit into the box people are comfortable with. The whole thing about neurodiverse people is we don’t fit into that narrative the way neurotypical people expect, though.
We need to do better. I don’t want more young people to be driven away the way I was. If I had been embraced for what I was back then, my life might have gone very differently. We need to renounce ableism—even internalized ableism—and be a safe place for neurodiverse people of all kinds. We especially need to avoid ableism during call-outs (if you believe in call-out culture at all, as it currently exists). Pointing out homomisia etc. doesn’t mean much if you’re being incredibly ableist while doing it.
At any rate, it was a long, long time before I was able to love myself for who I am.
I won’t go into the long process of accepting my bipolar and PTSD, which came first; I’ve written about that elsewhere on my blog. But my acceptance of those parts of myself led me to the neurodiverse community. There, I finally found others who believed as I was coming to believe: that having a brain that worked differently was something to be proud of, rather than ashamed.
Of course, most people in the neurodiverse community don’t really believe psychosis or bipolar are things to be proud of, and things that don’t need curing. They aren’t…but that’s another subject I’ve gone on and on about in other posts.
Finding the neurodiverse community taught me a lot about autism, something I was researching anyway at the time, since I was having real marriage difficulties. My last husband was undiagnosed autistic—I’m sure of this now. I used to think it was his autism that was causing our marital difficulties, but as I learned more about it, I realized that autism wasn’t the problem at all. It was his abusive, toxic masculinity that was causing our marital difficulties.
As I learned and interacted more with people in the autistic community, though, I found myself identifying with them a lot. People talked about needing to fidget and stim, their social difficulties, their emotional overloads… that was me in spades. Eventually, I took an online diagnostic test, which was pretty definitively in the “most likely autistic” category. So, I took another, with the same result.
It’s taking me a while to get used to the new label, but not as long as I thought it would, since it fits me so well. I haven’t yet decided whether I’ll get formal testing. It could open up new counseling opportunities, but I’m not sure how effective those would be anyway. The only real reason I’d get formal testing is to avoid the reactions of doctors and neurotypical people when I tell them I’m self-diagnosed. I’m so used to ableism at this point, unfortunately, that this consideration doesn’t hold much water with me, though.
Self-diagnosis is valid; a lot of us would bang our heads on the wall trying to get a diagnosis otherwise. It would have been cool if a doctor had spotted I was autistic earlier, so that I could have perhaps gotten more appropriate psychological care. But doctors don’t know much about autism. They say things like, “You’re just smart/shy/introverted/anxious,” or, “You’re not autistic! An autistic person wouldn’t be able to sit here talking with me like this! An autistic person wouldn’t have a job!” Or, “Sure, you might be autistic, but we’re all ‘on the spectrum’.”
Ableism abounds. Neurodiverse people are scalp-deep in it all the time, so we kind of have to get on with things despite it. Diagnosing ourselves is just one aspect of that.
If you’re interested in taking the test yourself, here’s one…I’m not finding the first one I took, for some reason. That one was cool because it had a graph of where in the “spectrum” you were with regard to your social life, romantic life, and intellectual life. If someone has the link to one like that, I’d appreciate it.
If you’re interested, I got a 37 on the Psych Central test that I linked to above 😊
It’s time to write another blog piece about neurotypical privilege! And yes, I think about this stuff all the time, unfortunately. (I have to.) So I have new insight on almost a daily basis.
A lot of people don’t know what neurotypical privilege means; even a lot of neurodiverse people don’t seem to know what it means. But my life is a study of it, so I’m in a unique position to describe what it is and how it affects neurodiverse people.
I am a neurodivergent person. What that means is my brain works differently than most people’s. Yes, I know—everyone’s brain is unique. However, mine is unique enough that I have a good deal of difficulty functioning in society on many levels.
I am bipolar, autistic, and have PTSD. I have a lot of trouble communicating with people sometimes, and I’ve had trouble maintaining steady employment and housing. My neurodivergence has put me in prison (for self-medicating), and has brought me into conflict various times with the police (for nonviolent behavior, to be clear). I have difficulty maintaining relationships of all kinds, as well, and not because I’m a jerk—this is one thing I’ve never been accused of by anyone who knows me—but because I’m flighty, have trust issues, and I often misinterpret what others say and am misinterpreted in turn.
Even though my neurodivergence has caused this level of disruption in my life, I still have some measure of neurotypical privilege. NT privilege is, like most other types of privilege, a spectrum…and I won’t even get into the interplay with other types of privilege, because that gets too complex. I’ll leave that discussion to others.
As some of you know, I’m waking up today alone for the first time in weeks. The man better known to y’all as Boy—my partner—went back to California yesterday. Hopefully he’ll be back soon.
Boy is schizophrenic, and he has even less NT privilege than I do. It affects every aspect of his life at all times, and is completely disabling. This isn’t, however, because he’s not capable, intelligent, or fully functional, because he is. He’s one of the most amazing people I’ve ever met. He may function in a different way and on a different schedule, but he’s completely able to take care of himself. He has a rich and full life.
The immense majority of Boy’s problems come from other people’s ableism—their mistreatment of him based on their apparent need for him to function like everyone else.
People interpret neurodiversity—and/or what is called “mental illness”—as dangerous. When they see someone acting in a way that’s different than the norm, they get angry and afraid. But statistically, neurodiverse people are much more likely to be hurt by neurotypical people than the other way around. Both Boy and I are prime examples of this. I’ve been taken advantage of and worse during psychotic breaks. Boy has been beaten into a coma, and has been wrongfully arrested and involuntarily committed on various occasions. On none of these occasions were either of us armed or posing any actual threat to anyone. We were just being who we were born to be.
The stories of many of these incidents are peppered throughout my blog and my Tinkerbell anecdotes, if you’re incredulous or interested in the specifics.
Boy and I—especially Boy—are often kicked out of public places (libraries, parks) and private businesses for doing nothing else besides cheerfully being neurodiverse. Restaurants suddenly have no tables available when we show up. We’re followed around stores because we’re suspected of shoplifting (we aren’t). So many laws and rules are targeted at people like us: vagrancy and loitering laws, involuntary commitment laws, forced sterilization laws, the right to refuse service, and “no shirt no shoes”, for example.
Neurodiverse people aren’t hurting anyone by loitering/muttering to themselves/”babbling” (word salad isn’t actually a thing, people—we make perfect sense if you know us). The vast majority of our behavior is completely benign, and even when we’re in the midst of a psychotic break we’re really unlikely to be violent. We may have trouble following instructions (you would too, if you were in our state of mind), but we’re just scared and confused. If we’re treated with respect and compassion, the situation is likely to be resolved quite peacefully and to the benefit of all.
But instead, we’re treated brutally—hurt, killed, imprisoned, kicked out. People think we deserve it. That we’re doing something wrong.
We’re not doing anything wrong. We don’t deserve it.
Neurotypical privilege is the ability to get through life without being hurt/killed/imprisoned/oppressed/harassed, etc., simply for having a brain that works differently than the norm.
I’m sure I’m missing some points and/or conveying stuff in a way that confuses some people. I’m happy to discuss and clarify, and welcome being called out on anything I’ve gotten wrong. But anyone who wants to argue the very existence of NT privilege, or say they have a schizophrenic cousin and so they know better than I do…please just don’t.
Elizabeth Roderick is an author and neurodivergent activist. You can find her (and her neurodiverse characters) on Amazon.
I’m going to give myself a little break this lovely Sunday morning and do another blog post about living in my tiny house, and how I’m working toward my goal of subsistence farming, and independent living as a neurodivergent person.
It’s been closing in on a year since I last posted about this. Yikes! Time gets away from me when I’m so busy.
A lot has happened since my last tiny-house post. My mom had a triple bypass in February, for one. It’s really brought home the fact that all of the hardship that led me back to the family farm in the first place was well worth it, because this is where I belong. I was able to help my mom out and be there for her during her recovery, and it’s brought us closer together as a family.
It was a beautiful fall, and an early (and pretty hard) winter. The first hard frost came early in October, and since our last one had been on June 15 (! – really, super late for this
area), we didn’t get enough tomatoes to can or freeze. I fried up quite a few green ones, though. Just thinking about the fried green tomato po boys and bahn mi (on homemade rolls) I ate is making me hungry right now. So good with veggie bacon and sprouts; or tofu, thin-sliced cabbage, Korean-style turnip pickles, and sriracha mayo.
I tried ripening some of the green tomatoes indoors, but without much success. I’ll hopefully get more ripe ones this year, but there are always some green ones left over when it freezes. I may sauce some of them this year, because green tomato puree/sauce is a great addition to soups, enchilada sauces, salsas, etc.
I did string a lot of peppers, can a lot of peaches, make jam galore, and Kid and I had
plenty of dried plums, pears, and cherries to gorge ourselves on during the cold winter months and fight off ye olde scurvy. I also gleaned many pounds of chestnuts from a neighboring orchard (gleaning happens after harvest, so is not stealing. It’s produce that otherwise would have been left to rot.) I wrapped those up in tinfoil and roasted them in my potbelly woodstove, quickly learning that you have to score them beforehand or they’ll explode, sometimes right in your face, the shrapnel burning your eyeballs and curling your eyebrows. For those uninitiated, chestnuts are a little difficult to peel sometimes, but they’re SO good—really meaty and savory. I like roasting them in the oven with potatoes and root vegetables, and as a yummy addition to mashed potatoes and gravy. I’m going to experiment more next winter with grinding them into a paste to use in crusts, breads, and desserts. (Making a cookbook of all our recipes is something Kid and I are working on, but we have so much else going on, that it may take a while.)
This year is off to a great start. I’ve been working on expanding the farm business. We opened a little nursery (selling vegetable, herb, and flower starts we grew in our greenhouses). We were able to make costs (pay for the seeds and soil) plus a few hundred dollars on top of that, and we still had ample plants left over to fill our own gardens. I call that a success.
We’ll also be selling fresh fruit, vegetables, and herbs—I’m already selling snap peas, turnips, basil, and cilantro. I have plans to start a worm farm soon, to save money on soil next year and increase our profit margin, while increasing the quantity of plants we grow.
I also hope to have enough extra eggs to sell soon, and maybe fresh chicken. The “fresh chicken” thing probably needs explanation…I used to be a vegetarian, but since my financial situation changed and I moved back to the farm, I’ve had to take a more practical approach.
This all started when (fucking asshole) neighbor dogs came in and killed a bunch of our chickens last winter. I’m so poor, that it just didn’t make good economic and moral sense to throw away good protein, so I butchered the poor things. It wasn’t too bad, though it was definitely an olfactory experience, and one that brought me into touch with my place in the food chain; as I labored at cutting out all the bad meaty/organy bits while leaving the good ones, I imagined hundreds of generations before me, working so hard just to feed themselves and their families, at peace with the fact that we are able to live
because other organisms die. There’s a sort of meditation to it.
So, anyway, still on the subject of chicken death, last year we had about thirteen chicks hatched on the farm by our own broody hens. Nine of those (eek) were roosters. They were wreaking havoc: fighting each other, brutally gang raping the hens, and traumatizing my parents’ border collie, who is autistic (this isn’t some ableist joke, nor am I comparing my dog to people to be clear—I’m serious, and I’m autistic so I have insight). She’s very noise-sensitive. Whenever the roosters would get into a kerfuffle, she’d pace and whine and be really upset. When a certain rooster crowed, it really set her off: she’d spin circles and snap at that rooster. I really felt for her, because she couldn’t walk away from the situation and it was really triggering for her.
So, before I moved back, my dad would give the roosters away to a guy down at the feed store who would slaughter them himself. I figured, if we know they’re going to be killed anyway, we should just own that fact and butcher them ourselves. My family reluctantly agreed, so we had a good old-fashioned butchering day in the spring. We rounded those cocks all up, my dad killed them and I processed them. I thought it was going to be horrible, but it wasn’t so bad because it was just family work, for a good purpose. We talked with each other so the togetherness could decrease the sting of mortality, and I just thought about those poor, gang-raped hens (it was really awful) and the poor dog, and it was a lot easier.
(Incidentally, if you’re a vegan who wants to harass me about this, I am quite literally doing what I need to survive. I’m neurodiverse, and disabled, and farming is the way I’ve come up with to make a life for myself and Kid. I’m happy to discuss the ethics of all this with you, but please don’t police my choices.)
I increased our chicken flock by twelve this spring by buying chicks (ten americaunas, and two silkies because I couldn’t help myself), and so far we’ve had seven chicks born on the farm. As I said, we lost some of our flock to (stupid fucking) neighbor dogs, so we’re currently standing at about 30-ish birds altogether. We eat all the eggs now ourselves, but hopefully I’ll have some extra to sell by fall.
We also got two hives of bees!! This is really exciting. I love watching them. The hives are already big enough that we had to add the second brood boxes, and hopefully we’ll be able to put on the honey supers by the end of summer. If all goes well, we’ll have honey next summer.
I increased my vegetable garden by 300%, tilling up a bunch more bottom land by my cabin. I’m growing lots of different stuff, including popcorn (I eat SO MUCH popcorn) and soybeans. I’ll sell some of it, but I’m digging a root cellar to store more of my vegetables and squash
. It got down below zero last winter, and was in the teens a lot, plus we had several feet of snow that stayed all winter, so the veggies didn’t keep in the ground at all. I was left having to go to the food bank and purchase food. I’m doing pretty well digging the hole. I’m hindered somewhat by the desire of my dog, my cat, and myself to lie in the cool dirt (which is unproductive in the traditional sense), but more by some physical problems: I’m getting a deep ache under the shoulder blade,
and numb/tingling fingers, with an inability to grasp or lift things with that hand. It makes it hard to dig/hoe, and I have to sometimes rest for days on end (from strenuous arm-using physical labor, anyway) and drink my herbal painkilling tea. If ONLY I had a strong, sexy BOY who loved digging holes and eating fresh vegetables, and who could help me out…but I guess some people are just buttholes and don’t want to move up here, and I guess I’m not helping my cause by talking about how decrepit I am. I’ll get my hole dug by myself anyway. I don’t
need any strong, sexy boys. *flounces*
As an aside, the weird thing is, if I were getting paid to dig someone else’s hole (not a euphemism), I would have quit and gotten worker’s comp for the injury, and would be in physical therapy and maybe having surgery. That would undoubtedly be the healthy thing to do, but I like digging holes if they’re my holes; I have to do it because no one else will do it for me; and I’m afraid of getting treatment because they’ll say, “stop digging darned holes, dammit” which is advice I will not heed in any event, at least not in the summer. So, I’ll soldier on and see what happens with my arm; if I need to get it looked at, I’ll do it this winter when I’m idler (as long as I get my wood all cut beforehand…and as long as Trump’s Deathcare bill hasn’t been put into effect yet CALL YOUR REPS, U.S.-IANS!)
All this farm work takes at a minimum three hours a day, often a lot more. It’s obviously not paying the bills yet (which, thankfully, are minor, because I own my car, have no debt, use barely any electricity (and we’re going solar!), have well water, etc. My only bills are my phone and my car insurance). I supplement this income with freelance editing, freelance writing, and a startup called Authordock that I’ve become involved in. It’s a website that helps writers with their publishing goals: I critique pitches, queries and first pages; give advice; direct clients to opportunities like pitch competitions; and provide resources by composing advice articles and making how-to videos…it’s a really cool project. The result of this is that, now that I’m, as people say, “lazy and unemployed”, I’m actually working 90-hour weeks, and yet making half a pittance. This is another way that disabled people end up making super-subminimum wage: the work we’re able to do isn’t something society values very much, so is underpaid.
I also have, you know, some books published (I’ve had several come out this year, and I have a short story in the next edition of a bestselling anthology, which comes out in a few days). That does bring in a little money, but I have very little time left for marketing, so not much at all. So, I’ll do that thing where I tell you I’m super poor and disabled (not that you should pity me—I love what I’m doing, I just make very little money at it). I don’t have a tip jar, so if you like hearing about my tiny-home and farming adventures, you should consider buying one of my books. People say they’re really good! And they’re ownvoices books, with neurodiverse and queer characters. They’re my way of trying to share my strange world with others. If you buy them, consider giving me a review, and/or recommending them to others who are into that sort of books.
Think of buying ownvoices books like donating to a charity, except you’re not paying for marketing and executive salaries: you’re making a contribution toward someone’s independent, sustainable living and/or affirmation as an important member of society. In my case, you’re not only affirming my worth, you’re keeping me off the streets or out of an institution, making sure Kid has a stable and happy mom (and new socks when she needs them, which is too often), PLUS you get great books. This is such a win/win/win, y’all!
I’m trying to get an agent to help with the book marketing thing. My publisher is great, but their marketing apparatus isn’t really the best for my kind of books. If I had an agent directing and supporting me in my marketing efforts, I think I’d do a lot better. I have a handful of fulls out with agents right now, of my thirteenth novel—an ownvoices YA contemporary romance/magical realism about a young woman with bipolar psychosis trying to navigate high school, first love, the foster system and the mental health system. Wish me luck!
I have lots of other plans for my life—selling hand-woven baskets, and other crafts made with natural and upcycled materials, for instance, as well as the cookbook and some other things. Plus, I have a short story on contract for another anthology coming out in September, and I’m working hard on writing my seventeenth full-length novel. Another tiny house is also in the works, to give us more kitchen space and Kid her own bedroom. But I think I’ve rambled enough for this post, so I’ll talk about all that later.
Thank you for reading!
I’m going to write another bitchy blog post, because I’m organizing my thoughts. I invite all people to read, and comment if you want, but this is really a conversation that needs to happen within the neurodiverse community, without paying a lot of attention outside input.
I love the term neurodiversity (or neurodivergence*). When I first heard it, a light came on in my mind. I finally had a word for something I’d felt my whole life: that “mentally ill” isn’t the right word for who I am, because I’m not ill. This is just my personality, and you can’t (nor should you want to) cure me of it. (Yes, I want/need some symptoms treated, but that’s a different discussion.)
The problem is, the term “neurodiverse” is a catch-all term for A LOT of different sorts of people. This is one of those “duh” statements, but I think we need to meditate on it. I hear a lot of people say “I’m neurodiverse, too,” (or, worse yet, “my aunt is neurodiverse”) as a precursor to statements indicating they think they understand what life is like for ALL neurodiverse people.
I don’t want to stop using the term “neruodiverse”. I lurves it, and don’t want to complicate the language by having more and more terms, or just labeling ourselves with our diagnoses. “Neurodiverse” expresses an idea about all of us, that we’re not ill and are okay the way we are, and thus is a good catch-all term.
But we all need to check ourselves when we start thinking we understand what it’s like for all people under the neurodiverse umbrella. There’s a huge spectrum not only of different diagnoses under that umbrella, but also of levels of marginalization. Some of us struggle daily with the problems our neurodiversity causes us. It’s affects everything we do, and every conversation we have with others. Other people’s neurodiversity has only a minor effect on their lives.
If you have minor clinical depression, for instance, you’re neurodiverse in my opinion (unless you choose to not identify that way, of course). Depression is something I experience, and is super shitty. It can make you miss work, sabotage relationships, hurt yourself. But, in the case of minor depression, most people won’t know you have it unless you tell them.
On the other end of the spectrum is my partner, Phoenix. He has schizophrenia and can’t even walk silently into a room without people reacting to his neurodiversity: his strangeness radiates from him like a glow—a beautiful glow, in my opinion, but not in the opinions of most others. He’s one of the very best, coolest, smartest, kindest people I’ve ever met, but most folks will never know that because their reactions to him are almost uniformly negative. They avoid him, or have a (misguided) “protective” anger reaction (for instance, they call the cops on him for yelling and pacing in his yard. They beat the shit out of him for talking to himself, because they think he’s “talking shit” about them). At best, they pity him and don’t take anything he says seriously.
You can imagine the effect this sort of marginalization could have on a person. Phoenix is positive and confident, but he’s told me on various occasions that before I came along, he thought he’d be alone for his whole life.
I, for the sake of you knowing my viewpoint, fall somewhere in between that. I struggle daily with my bipolar and PTSD on an internal level, and it’s been a defining force of my entire life path. It’s destroyed more than one relationship, and caused me to seek out abusive and toxic ones. It’s landed me in prison. It’s made it extremely hard for me to maintain employment for more than a few years at a time, and has cost me many promotions because of latent bias (and no, I’m not being paranoid. I have direct evidence). The list goes on. But in my daily interactions, at least at times I’m not in crisis, people generally just think I’m a little bit eccentric or “off”. It certainly colors their reactions toward me, but they might not even guess at first blush that I’m neurodiverse. Plus, I have the advantage of not being one of those people that comes off as creepy. At least it doesn’t seem like it, usually, based on how I’m treated (I mean, I’m not creepy, right? Tell me if I am). So my neurodiversity doesn’t isolate me in that way (though it will cause me to self-isolate at times).
So, what I’m saying is, someone with minor depression can’t know what it’s like for people like me, or people like Phoenix. And I can’t know what it’s like for someone with Autism, or schizoaffective disorder, etc. But I can probably identify with what other neurodiverse people go through better than most neurotypical people can, and I will endeavor to listen and be accepting—to be a “safe space” for other neurodiverse people to express their feelings and experiences. I will never say neurodiverse people are “doing it for attention” or any of those other horrible, marginalizing things neurotypical (or self-hating neurodiverse) people say.
The reason we label ourselves as neurodiverse is to try to seek out people who understand what it’s like for us, and will listen and accept us for who we are. Thus, it’s very, very important to be careful of behaviors in the community that can cause us to marginalize and isolate our peers even more. We need to be there for one another. Let us remember to listen and be good allies, as well as good peers.
* I don’t like that this term as much, for the silly reason that I don’t like the novel Divergent. We all have our quirks.
I’ve been inspired by the women who ran from NYC to DC to raise money for Planned Parenthood. I’ve had an idea, and I want to put out feelers to see what kind of support this idea would have, because it will be a difficult thing to do and I need to know it would have an effect before I set out to do it.
I would like to walk from here (Yakima, WA) to our state capital (Olympia, WA), a distance of around 180 miles. I would be living homeless, in order to raise awareness and money about the plight of the homeless and neurodiverse. I wouldn’t be accepting money directly for these causes – I would ask for pledges to charities like NAMI.
I’d like to know who would be willing to donate, and who would help me by amplifying my social media presence with regard to this. I would love to hear your thoughts, and would love it even more if you’d retweet, reblog, or share this post to see if any of your friends might be interested in supporting me one way or another on this journey.
If I got enough awareness, my next trip would be to DC.
And yes, I’d be living homeless, as authentically as possible, but I’d make it as safe as I could in ways I will brainstorm with you and discuss later.
Who’s with me?
It’s been a long time since I ranted at y’all. I can’t say I’ve been saving up things to rant about, because I’ve trained myself to let stuff go so that it doesn’t dissolve my brain in caustic acid. But this rant needs to happen.
This is going to be the most brutal window into what it’s like for me to live with mental illness that I’ve ever given you. I’ve decided that my entire recovery depends on me being emotionally honest with myself and others, and on not playing the victim by putting up with other people’s shit. My feelings are important, and it shouldn’t be okay to hurt me just because I act “crazy” sometimes.
If your life is too pretty, you might want to stop reading, because you probably won’t understand any of this.
Neurodiverse people put up with discrimination, both subtle and otherwise, constantly. So much, in fact, that a lot of us don’t even realize that it’s happening, and we end up being the ones to apologize when we’re the ones suffering from prejudice.
Neurodiversity comes in a lot of forms and levels, from nearly constant, full-blown psychosis to mild, periodic depression. There’s also autism, which I won’t speak to here because I’m no expert, though I have observed that autistic people suffer a lot of the same types of discrimination that “mentally ill” people do.
There is really only one all-encompassing way to describe all forms of neurodiversity. It’s an inability, at some level, to correctly play society’s game. I know most neurotypical people feel this applies to them, but they’re fundamentally misunderstanding what I mean. “Not being able to play society’s game” doesn’t mean you’re sometimes weird or awkward or say the wrong thing…as far as I can tell, that stuff is a big part of society’s game. Neurodiversity means that you act in ways that make you fundamentally incompatible with social norms, in ways that affect your ability to get along with others and be “functional”. This isn’t voluntary; it’s just the way we are.
I’ll clarify here that, while it can affect your ability to get along with people, neurodiversity is not a synonym for “asshole”. Yes, some neurodiverse people are assholes, or they act like assholes sometimes (like everyone else), but not all assholes are mentally ill. I’m really damn tired of people saying Trump is mentally ill, for instance. That’s an insult to mentally- ill people. Trump is just a self-involved, inconsiderate, manipulative, unintelligent fuckhead. NOT. THE SAME. THING. It seems like assholes do pretty damn well in society a lot of the time. By getting elected president of the U.S., for example.
Hardly anyone would say that they hate neurodiverse people. It’s just like hardly anyone would say they’re racist, but it doesn’t stop them from doing/saying racist things. With neurodiversity, others don’t really understand what it is or what it looks like, so they end up punishing and demeaning us, even on an institutional level, for behavior we can’t easily control, or can’t control at all. They’re discriminating against us for being who we are.
I can understand why that is, though. Sometimes, neurodiverse behavior isn’t pretty. Neurotypical behavior isn’t pretty sometimes, either, but the neurodiverse have the disadvantage of having more overblown reactions to “triggers” (and I shouldn’t put quotes around this word, because it’s the correct use of a word that is used incorrectly so often) than neurotypical people do, and also of not usually being able to wait until they’re behind closed doors to have those reactions. So, we’re often the ones that get called the asshole for having an episode, when others either don’t know the context (didn’t see what led up to us acting that way), or don’t even understand what set us off.
Unfortunately, in the case of those who know us well, these triggers become a really good way to intentionally or subliminally manipulate and abuse us. They say or do something they know will set us off, and then point to us and say, “See? She’s the bad one.”
Neurodiverse people can be hard for others to love. We get rejected and isolated, some of us on a daily basis, sometimes in just about every interaction. This contributes to the progression of our illness, and becomes sort of a feedback loop. What neurotypical people don’t realize is that y’all are just the same as us. We’re no more threatening, toxic, or hard to deal with than you are, on average, though there are jerkwipes on both sides of the line. We’re just different. We express our emotions differently, because our emotions can take us over more powerfully than they do neurotypical people, but that doesn’t mean we’re dangerous. It just means y’all have to give us a minute, and we’ll be back with you shortly.
And, when we come back, it will probably with an apology—though we rarely get one in return from you guys, because you rarely see what it was you did that was insulting/abusive/discriminatory, while we’re trained from birth to think that we’re in the wrong, because we don’t fit social norms.
In order to be a true ally of the neurodiverse community, you have to understand the above, and accept it, instead of chiding us or being derisive about our behavior. Accepting us goes far beyond language policing or treating us like children who need coddled and taken care of, and then ignored when we’re having a fit. We’re adults— valid, wonderful human beings just like you guys—and should be treated as such. Doesn’t mean you have to like what we do, but it’d be nice if you’d understand and forgive us, and take a look at yourself, as well.
I’m going to give an example of what subtle discrimination looks like, and then an example of what pure acceptance looks like.
I’m not doing this to call anyone out. This is a true attempt to educate, because educating people about this sort of stuff is part and parcel of my survival in this society—I don’t have a chance in hell of ever being “normal”, so my only hope is to try to get people to accept me (and hopefully others) on our own terms. Besides, in the following examples, I’m calling myself out more than anyone, because I was also in the wrong.
Even though my shrink tells me my PTSD is more symptomatic lately (I was recently assaulted), I don’t always realize that I’m freaking out. Believe me, I’m working on it. I’m the only one who can control my behavior. I have a harder time with it than neurotypical people do, but I will get stable again, because I’m a pretty tough lady.
The only way I’m going to get better is by being emotionally honest with myself. Similarly, the only way neurotypical people are going to be good allies of the neurodiverse community is to be honest with themselves, and aware of their own behavior toward us.
So, my PTSD is from abuse. As a young teenager, I was physically/emotionally/sexually abused for a long period of time. This abuse has colored the progression of my entire life. It was a huge cause of the end of my last marriage, because when my husband said something insulting, I would have an overblown reaction, which would cause him to become more insulting, and so on.
I’m in a fairly unstable state now, so whenever someone says something that I perceive to be abusive or insulting, I freak out. Maybe not as much as when I’m unmedicated, but still.
There was a large amount of wank on my personal Facebook page, and a local group page, a couple of days ago because of a couple dogs that killed some of my chickens. I won’t go into the whole story; if you want it, I didn’t delete or alter the thread. It’s on my FB feed.
Long story short, this one dude ended up telling me I’m naïve, and that the dogs should have killed my chickens because they had as much right to eat as I did. Garden variety asshole, right? Except I actually need those eggs to eat since I’m living on a tight budget since my divorce, not to mention the chickens were my pets. The guy knew that. So this statement felt a lot like things my ex used to say to me about me being immature and worthless. I got really agitated, and I reacted without really thinking. I told him, “If you think you have every bit a right to eat as a dog does, kill yourself and make yourself into dog food for rescue dogs.”
This was a horrible word choice, but in my mind at the time, I was turning the tables and re-stating what he’d just said to me. I realized later that it was a poor word choice, but at least it got the guy to shut the fuck up, so I thought it was no big deal. Except it’s the internet, where everything is a big deal.
Another lady came back days later, and read only my statement. She admitted she didn’t read the context, or anything he’d said. All she saw was me freaking out. So, I was the one that got all the blame. “I know you care about people with mental illness, so I just wanted you to be aware that what you said is wrong.”
I apologized for what I’d said, but I also pointed out the irony to her. She didn’t call the other guy out for being abusive and demeaning. Be aware, I said, that my reaction is what mental illness—a PTSD trigger—looks like. That’s what true “awareness” of mental illness is.
She never responded. This is typical. We get rejected as not worth listening to, as hysterical, as an asshole. Rejection is another trigger for me, like it is for a lot of us. Instead of going off on that lady, I figured it would be healthier to go off on a blog piece, in the faint hope of educating someone.
Now, let me call myself out even more by showing you what true acceptance of mental illness looks like. I’ll give a trigger warning, though I don’t think trigger warnings are healthy when we’re dealing with real-life events. We can only heal by facing our triggers. But, anyhow, this is a pretty graphic description of physical violence and verbal…I won’t call it abuse in this case. But in another context it would be.
If you are my mom/dad, I suggest you stop reading now.
A certain friend of mine and I were having ourselves a fun white trash evening recently. Long story short, he was goofing around and called me a “dirty whore”.
I knew he was goofing around, but this brought me to a standstill. “Don’t call me that.”
He, though, didn’t see what the big deal was: he was just joking, and I knew it. So, he called me a dirty whore again.
I reacted before I knew what was happening. It was like watching myself from the outside. I punched him. Not hard, but in the exact same place he’d been punched another time, which had broken his tooth and ultimately put him in a coma for three days.
So, he (who is neurodiverse, also) had the same reaction. He punched me in the eye. Again, not hard, but it was enough to bring me to my senses.
We were both blasted off into PTSD land. He was alternating between threatening to call the cops if I didn’t give him money, and gently examining my eye and saying, “Oh, my God Liz, are you okay?” Then yelling at me for making him hit a girl. I for my part, was sobbing and apologizing my ass off and begging him to not leave or call the cops. See? Good ol’ white trash fun all around.
We calmed down eventually and talked. “Someone called you a dirty whore before, right?” he said, and I nodded. “I’m sorry, I didn’t know,” he said.
“I’m sorry I punched you, especially right where that other guy did.”
And we spoke no more of it. Neither of us needed an explanation. Neither of us judged or even pitied the other. We understood one another. To us, it wasn’t that big a deal. Just a couple people overreacting like the freaks we are. Neither of us had so much as a bruise, to be clear.
That’s what it takes to accept people like us. Most of you won’t be able to do that, because our behavior is so easy to point at and say, “wrong”. Most of you, having read this, will be horrified, and will unfriend me/never talk to me again, because you don’t want to be associated with toxic people like me. But your behavior is just as wrong sometimes, it just takes longer to explain why because the abuse is emotional, and/or you do it behind closed doors so it’s harder to call you out on it.
So, if you want to be our allies, be patient with us, listen, and try to understand. It will require putting up with some bullshit, yes. But it will be worth it. We’re wonderful people, and you’ll also find a lot of us more willing to put up with YOUR bullshit than most, because we know what it’s like to do things we’re not proud of, and be rejected.
As some of you know, I recently finished drafting my SIXTEENTH manuscript!
I would like to celebrate this milestone, along with the upcoming release of LOVE AND WAR, the third installment in THE OTHER PLACE SERIES, which is set to drop on March 7, 2017.
I would like to send you all cake and champagne and kisses, but the logistics of that are difficult. Instead, I’m going to have a contest. I’m going to pick SIXTEEN WINNERS. Fourteen of those winners will get a free Kindle copy of one of my books – their choice. The second place winner will get a free signed paperback of one of my books – again, their choice. The grand prize winner will get a signed paperback, AND A $50 AMAZON GIFT CARD.
Yes. I did say $50. And I meant it.
The rules are simple. If you are already signed up for my newsletter, you are entered. If you’re not signed up yet, SIGN UP HERE to enter. You’ll also get a free anthology for signing up!
If you want an EXTRA ENTRY, refer someone else to sign up for my newsletter, and either comment on this entry , send me a DM on Twitter or Facebook, or shoot me an email to tell me who you referred.
Winners will be picked randomly on MARCH 7, 2017 – which is the release date for LOVE AND WAR.
Thank you for your support!