[TW ableism] I Was One of the Scary Kids
The one tiny piece of light in this big stinking ableist mess is this article, and how much I can relate to it.
When I- and others who are autistic, have Mental Health Disabilities, or both — talk back with truth, we are denied. When we talk about how having xyz diagnosis doesn’t mean we will do stuff, when we point out that we aren’t mass murderers, we are shut down. When we talk about how yes, mental health reform is important but that it shouldn’t come out of stigma, coercion and false equivalence, we are told that we are calling other scary kids lost causes. When we point out that we don’t have enough information, we are dismissed. When we disclose, we are called too close to the issue. Even when our mothers join us.
In reality, only 5% — or 1 in 20 — of those in jail for violent offenses entered jail with a diagnosable condition. The other 95% did not present as diagnosable on entry. Most of those with diagnosable conditions are there on non-violent and drug offenses, including a number of which are a symptom of a lack of supports rather than their conditions themselves. Some estimates place the rate of Mental Illness at 50% of the inmate population, and yet only a very small percentage are there for violent crimes.
In reality, these impressions of us make us targets of crimes. People with “Serious Mental Illnesses” are more than twice as likely to be a victim of a violent crime. We are targeted for sexual assault, particularly if we are or are seen as women. We are likely to feel stuck in abusive relationships, or to have people use our diagnostic status as justification for abuse. And that is just the violent crimes — we are astronomically more likely to be victims of personal theft, and 4 times more likely to be victims of property theft.
<3 I’m glad it helps.
(also you seem really cool and like Thor and Loki and stuff going from your tumblr. Which I think is awesome. Yep.)
(Source: allies-person)
[“Autistic people are too violent to be allowed to play video games or watch the news.”
Great, now the pundits are trying to take away my Harvest Moon.]
So apparently the show The View had someone on saying basically the above, about how we’re too violent to be allowed to play video games or watch the news.
Now, I don’t know about you all, but one of my favorite game series is Harvest Moon. (Here comes the part where I go into full on sarcastic snark mode, FYI:) It’s an incredibly violent game in which the protagonist does truly horrific, despicable things like grow crops, raise livestock, fall in love and *gasp!* settle down to raise a family.
Despite the tenuous grasp on reality the “experts” are claiming I have, strangely enough I have yet to attempt to grow crops or raise livestock (orchids and bunnies really don’t count here), and as I am already married, I have not taken to going around giving cake and other gifts to the boys and girls I admire. Even stranger, I have not taken to anything with a sickle or hoe, be it plant, animal, or human, or attempted to milk the neighbor’s cat under the mistaken assumption that it’s a cow.
It’s almost like the “experts” don’t have the first fucking clue what they’re talking about.
Okay, snarky part done: It is exactly like the experts don’t have the first fucking clue what they’re talking about. I have some thoughts about this—a lot of thoughts, really—and I might even post them at some point. In the meantime, I just want to say: This is upsetting, and for a lot of us, this is very scary. If you need to vent your frustration and/or your fear, the “doors” of AH are always open to you and if you want something posted anonymously, just say so.
This is Dangerous
Those of you who keep up with ASAN already know about this. For everyone else, the Governor of Washington is challenging the protections the Olmstead Decision affords people with disabilities. This decade-old court case has moved people from institutions to their communities. Sign the petition. The appeal it addresses threatens the freedom and welfare of some disabled people. Consider contacting the Governor, especially if you are voter there.
"I Don't Know That Person's Program" a powerful article about abuse of DD people by Amanda
“DD people aren’t like regular people. When people do things to them that would be horrible if they happened to other people, there’s always a logical reason that justifies whatever is happening. Staff and case managers rarely if ever abuse power. All of their decisions have the best interests of clients at heart. So if something looks terrible, chances are that there’s a reasonable explanation behind it. I just don’t know what that explanation is. And I likely never will, so I’m not going to judge.”
(…)
And I know how people see us. As in, I know what we look like inside their minds. Sometimes we’re human — almost, anyway. Not quite. There’s something vitally important inside every real human. And to them, we either don’t have it, or are missing large chunks of it. So we go around in human bodies but there’s pieces missing in our minds and our souls. Even people who don’t believe in souls in any religious sense, still perceive something inside us as only partial.
Third Try
Tumblr has been eating my posts. This originally included a response to Scarborough’s comments. I will not rewrite that. Others have rebutted it. Not for the first time, I was late because of the car. The response to Autism Speaks is also unimportant. They will not change because I ask. I still have something to say: in the wake of commentary on national television to the effect that we are ticking time bombs, I saw autistics defend our place in society in an unacceptable way.
”We are not mentally ill” is no defense. Yes, I saw that written outright. Saying we are not like those people is visting the palpable sense of awareness shoved on us moments before on someone else. It short-sighted, unethical, and cruel. It is two oppressed groups, in some opinions, two subgroups of one oppressed group, allowing themselves to be pitted against each other. Scapegoating one group of people, saying we are worthy because we are not them, is as inhumane when we do it as when anyone else does. Bigotry is bad from any source.
Tell this radio station to STOP advertising the Judge Rotenberg Center!
The station is WKTU Lake Success, which broadcasts from Long Island to the New York City metro area.
The Judge Rotenberg Center is a center in Massachusetts that uses what they call “aversive therapy,” (HUGE TRIGGER WARNING ON LINK) which the United Nations has condemned as torture.
Contact information of the station:
Phone number: 1-212-377-7900
Toll-free (U.S.) phone number: 1-800-245-1035
Official website (has a “shoutout” box on the left sidebar): http://www.ktu.com/
Unofficial website (has a wall to write on): http://streema.com/radios/WKTUI couldn’t find any email addresses, but if anyone can find email contact information for WKTU Lake Success, please add that information.
UN finally does something about JRC
TW on the link for electric shock torture, institutions, abuse of kids with disabilities
It’s about time.
Hope they finally manage to get it shut down
Important Anouncement:
Autistics, allies, disability advocates, and disability activists, State Representative Sanchez of Massachusetts has expressed approval of the Judge Rotenberg Center. He has brushed off attempts to question his support of the torture of children on American soil. We are invading his Facebook page tonight. Please participate. People with our labels are suffering on his watch. Innocent kids are shocked until their skin burns. He thinks this is a good idea. Show up. Be civil. Do not make threats. Post your own sentiments or links. Post late at night into the early morning hours. We want him to wake up to this. We want people to see it before his staff can take it down. Please signal boost this message. I hope to see you there.
Petition: Tell AMC, Regal Cinemas, and other major movie companies to incorporate captions into all movie showings!
Here’s the petition I said I would start to try to get movie theaters to respect the needs of folks with hearing deficits. Captions are necessary for many people who have hearing loss to understand what is going on in films. There’s no reason why there can’t be captions to help them out. I’m going for 100,000 here, and I think that if everyone who reads my tumblr promotes the petition to at least one person, we can make that goal. Please help me make that happen!
This is funny because most movie theaters have at least one theater that has captions running backwards at the back of the theater, allowing the hearing impaired to use a mirror to read the captions without impedeng the experience of other moviegoers
make sure that what you’re petitioning for doesn’t already exist. otherwise you’re going to look like an asshole.
Wow… that sounds like an unnecessarily horrible way to watch a movie.
why the hell would you want to be lookking at a mirror when you’re supposed to be watching a movie
I used to work at an AMC and I can vouch for this. Basically, people who were hearing impaired had to wear these stupid glasses on their face that reflected the backwards captions from the back of the theatre. I wore one once out of curiosity and it was nothing but a fucking headache. Literally.
It’s possible to run close-captioned movies without completely stripping away the dignity and convenience of those with disabilities. As for ”impending the experience of the other movie-goers”…? That’s a load of horseshit.
OH NO I CAN’T DEAL WITH WORDS ON A SCREEN
Operas have been doing superscript where they just shoot a projector with the translation on a smaller screen directly above the stage so people can understand the lyrics. It’s not all that hard.
Supertitles at operas are my favorite things. <3
Mirrored subtitles would be enormously more distracting then correct direction ones. I’ll start spending mental energy to read them (I mean really mirroring text does not obscure it that much) and, you know, end up super distracted.
Also I mean like any sort of thing that requires glasses is not going to work for someone who, you know, already needs glasses for other things.
this still needs lots of signatures, please sign/pass it around if you can.
2012: The Year of Living Fatly « Fat Heffalump (via sailorbaby)
“offensively, obnoxiously fat”
YES
(via grrlyman)
Problems With the LA Times Autism Series, Part 2
Alan Zarembo points out an important issue for families dealing with autism in his second article: not all have the resources to make navigating systems and acquiring and directing services someone’s full time job. Racial and class inequity is rampant. Children whose parents are under financial stress, work long hours, do not speak English, experience prejudice for other characteristics, or are not adept at handling bureaucrats are seldom treated fairly by social welfare systems. What Zarembo fails to acknowledge is the reason: when there are not enough resources to go around, people in a position to be assertive and threaten lawsuits will get them. “Waging a small war with gatekeepers” for services is necessary because Zarembo’s assertions in the previous article that autism diagnoses are commonly used to snatch additional education money for children who do not need it are false. Programs that help autistic children get the most out of their educations are often underfunded. One interviewed mother told the reporter she sought services from the state and was turned away. Children whose parents are not in a position to fight slip through the cracks.
Most autistic people in this article are fairly young or not known to be communicative in verbal, signed, typed, or written words, but it is disconcerting that the story is doughnut-shaped thus far. It encircles its central characters without ever touching them, highlighting the absence of their perspectives.
Neurodivergent Sexuality(!!!)
As per its header, this blog is dedicated to celebrating and exploring “sex, (a/)sexuality, and consent among people with mental illnesses and/or developmental disabilities.” Populations like ours face sky-high rates of sexual violence coupled with bigoted misconceptions about what our sexualities, sexual behavior, desire, and consent are “allowed” to look like. Different stereotypes apply to differing sorts of neurodivergence, but the final message is clear: the sexualities of developmentally disabled and/or mentally ill people are supposed to be anyone’s but our own.
In this climate, Neurodivergent Sexuality seeks to be a place where mentally ill/developmentally disabled people have to option of speaking openly about our own relationships to sex and hearing what other people have to say. Anyone is welcome to follow, but in the spirit of the blog, we’re only seeking submissions from people who identify as having at least one developmental disability or mental illness (full submission guidelines here). When you send in your submission, you have the option to “tag” it with various iterations of your clinical labels. This helps other users search our site, but it also means that your post might wind up in many other people’s tracked tags. This is great for visibility (and “reclaiming the autism tag” if that’s your thing), but whether or not you want to tag is entirely up to you.
“Neurodivergent Sexuality” has four mods and contributors: Devyn,Theskinofourteeth, Emily, and Kavitiya.
We are so, so excited, you guys.
What hate can look like
You know it’s bad when something you read on Tumblr gives you nightmares and you wake up furious, with tears all over your cheeks from crying in your sleep.
In this dream I’d been running for public office in a world not that different from this one. I was running because of the inequalities that, just as in the real world, ensured that disabled people were impoverished and dying at higher rates with the whole world saying that nobody hates disabled people, it’s just the natural order of things and disabled people who object are a bunch of whiners who want something for nothing.
There’s a lot of cultural customs in the dream world that weren’t the same as the real life USA so I’m not going to focus on those except when they highlight some real point.
I’d been going to go to some kind of event for candidates but I found my way being blocked at every turn.
They put me through what had been going to be a lengthy physical exam, but stopped at the first part. The measurements taken of my legs showed some incredibly subtle physical sign of the reason I almost needed a leg brace and did need physical therapy in infancy (in real life too). They said this was an immediate disqualification from even running for office.
I tried to tell them it wasn’t ethical on any level to put an arbitrary physical standard on who could run for office. I was outraged that they’d patronized me by letting me think I could ever run, when they knew the physical criteria were such that a full time powerchair user could never hope to run even if they hadn’t found the much subtler leg deformity.
They told me that the criteria weren’t unfair in any way, certainly not oppressive. Nobody hated disabled people after all. They were just acknowledging certain truths about the world. We would never be able to do what nondisabled people could do. That meant if we held office we put everyone at risk. And that wasn’t fair to everyone else. Those of us who objected only wanted special rights, we were already equal after all.
At one point one of them somehow towed my powerchair away when I was outside of it. Forcing me to use a crappy manual one that hurt even to sit down in, and get pushed by someone. I was trying to get to an event for candidates I’d been told I shouldn’t even try to go to because of steps at the door. I went in my manual chair anyway. The “steps” were really a single step so tiny practically all chair users could get over it.
With friends I stormed into the building and began a loud protest of everything that happened. I was ostensibly welcomed. They acted like the protest was cute, something a child might think up. They told me how inspiring I was even after I’d said “fuck inspiration, we demand equality”.
One woman saw an exaggerated (compared to real life) bit of evidence of how sloppy and uncouth I was: A shirt I once wore plastered with oatmeal. In real life what happens is smaller but similar. The woman led the group in explaining to me why this shirt proved I was childish and incapable of ever functioning in adulthood let alone in office. I was humiliated and crying but everyone acted as if it was all totally within their rights to do this. Every objection I had was instantly shot down as irrational and childlike. Because rational mature people always excluded us, and this was inherent in the very definition of work.
The dream only got weirder and more fucked up from there. At every level possible in this dream, I was being oppressed at every turn by people who swore they couldn’t be oppressing me because they didn’t hate me.
Here’s the thing:
Hate isn’t a special extra strong kind of anger.
Hate is — among other things — the desire that someone else not exist. It’s not any less hateful when it comes with a smile, a pat on the head, a sugary voice. Hate isn’t an emotion, it’s an action and a state of being.
When people say lives like mine are not worth living, that’s hate.
When people create arbitrary standards to shut people like me out, that’s hate.
When a society bends over backwards to meet the needs of some people, while calling the needs of other people special, unnecessary to meet… the kind of thing that’s just optional, something to if anything be dealt with on a personal level, never a societal one (because that would take effort and change), that’s hate.
When most people get acres to play around in and disabled people get one square foot each. And where nondisabled people get to step into our square foot when they want. But our every millimeter out of line is met by all hell breaking loose because we are just too damn demanding — that’s hate.
When I go to the emergency room and they don’t want to treat me because they have real people they want to treat. People who have some chance of quality of life, you know. People who don’t look like they (in the words of an actual guy at the ER, about me) “have the cognitive functioning of an infant”. That’s hate.
When actual murderers of people like me get all the sympathy because they were already sentenced to live with us? That’s hate.
And so much, much more.
It doesn’t matter if hate looks like anger or like pity or like apathy or like sweetness and light. It’s still hate. It still says, forcefully enough that we die all the time, “don’t exist, you’re not worth what we are”.
And I don’t have the time to waste on people who refuse to acknowledge that any of this is real. I have a life to protect — to protect at all times because very few other people are willing to protect what they see as a costly and fruitless life. But damn it I’m still here and I’m going to stay here as long as I can no matter how many people can’t see the forces trying to erase me. And I’m not talking metaphoric erasing here. I’m talking forces that don’t want me or anyone remotely like me to exist. If you can’t perceive them and insist they’re not there — you’re working for them.
It doesn’t matter if hate looks like anger or like pity or like apathy or like sweetness and light. It’s still hate. It still says, forcefully enough that we die all the time, “don’t exist, you’re not worth what we are”.
And I don’t have the time to waste on people who refuse to acknowledge that any of this is real. I have a life to protect — to protect at all times because very few other people are willing to protect what they see as a costly and fruitless life. But damn it I’m still here and I’m going to stay here as long as I can no matter how many people can’t see the forces trying to erase me. And I’m not talking metaphoric erasing here. I’m talking forces that don’t want me or anyone remotely like me to exist. If you can’t perceive them and insist they’re not there — you’re working for them.
TSA to launch disability hotline
Interesting news. I’m skeptical for how much this will really accomplish, but it is something.
I strongly support Senator Schumer’s call for passenger advocates at airports, and will be looking into what people (especially PWD) can do to advocate for this.
I wonder how well-versed these disability hotline people are with regards to “mental” disabilities (for lack of a better word). The article mentions invasive searches of people who wear medical devices, which is certainly important, but so is the mistreatment of people who act weird, “crazy,” etc.