Content Note: COVID-19
for Nina, Q, and Fenrir
Content Note: COVID-19
for Nina, Q, and Fenrir
Content notice: (reclaimed and unreclaimed) anti-LGBTQ+ and ableist slurs, mentions of anti-LGBTQ+ and ableist violence, discussions of anti-LGBTQ+ prejudice and ableism.
Content Notice: HIV/AIDS, COVID-19, mentions of drugs and alcohol
Another thing inspired by the current pandemic. One of my professors (a historian, naturally) is encouraging us all to write and record our feelings on this. As if I need encouragement!
Anyway, this one is in response to watching the documentary We Were Here and recognizing a lot of the locations mentioned in it. Two people can exist in the same place but in completely different worlds if they live at different times. This is about worlds of plague, worlds of health, worlds of turmoil, worlds of peace.
(And public transit. It’s also about public transit.)
Content Notice: (internalized) ableism and anti-LGBTQ+ bigotry, suicide/self-harm, cure/shiny Aspie autism politics, drug use, smoking, drinking, COVID-19, sex/relationships, (reclaimed and unreclaimed) slurs.
I wrote a thing. I haven’t written here in almost a year but I needed to write this, right now. There’s a lot of discourse from disabled people who were homebound/socially isolated before COVID-19 stay-at-home orders around abled people complaining about being stuck at home. I have thoughts. I have a lot of thoughts about this. Being at home, with my family, is not good in a lot of ways for me. I’m safe and secure, don’t worry, but I miss a lot of the things I had. But a lot of the things other people had and complain about missing are things I never had.
I hope you like it.
EDIT at 2119 hours on 11 April 2020: About an hour after posting this, I learned that Mel Baggs, whose work I cited in this post, died today. I am heartbroken. Mel was an unyielding, blunt, incredibly advocate for people with intellectual and developmental disabilities. Hir video In My Language was the first piece of by-and-for autistic people media I ever consumed. I owe so much to Mel’s advocacy. We all do. Rest in power, Mel. We will carry your work forward.
Content Notice: discussion of bodies, genitals, surgery; anti-transgender and anti-intersex bigotry; biologic essentialism
April 25th is Save Student Newsrooms day. In the words of the movement’s own website, Save Student newsrooms is “[a] campaign to educate people about the challenges facing student-run newsrooms,” especially challenges around funding and editorial independence.
The first time I heard about Save Student Newsrooms, it was in a spoken announcement from one of the managing editors of the paper I work at, urging all of us to write an editorial about it. I did not hear the announcement correctly. I heard that it was a movement around “safe student newsrooms” and, in my infinite wisdom and auditory processing issues, almost wrote an editorial about it. I didn’t end up writing the editorial because I learned that it was “Save Student Newsrooms,” but I kept thinking about the issue.
It’s the end of April again. This is that editorial.
Content notice: person-first language, dehumanization, ableism, medical discrimination, academic discrimination
Content warning: functioning labels, discussion of person-first/identity-first language.
Content notice: institutionalization, deprival of rights, psychiatric violence, sexual harassment/assault, medical malpractice, involuntary treatment, guardianship, functioning labels, and a description of lobotomy.
you can’t tell
just from reading my posts
that i decided to stop speaking
there are circuits in my brain
stitched on a backpiece of linen mounted on steel frame
and two circuits here are important:
the one that makes language in my brain
the one that makes my mouth move
these are different but
both are needed to make my spoken words
i watched a friend recite his ASL poetry
hands flapping in rhythmic motion
in the middle of a blocked-off, art fair street in san jose
i sat with him and listened to his voice on his talker,
which he posted recently that anthem will pay for part of
(hopefully medi-cal will pay for the rest),
and wondered if i could ever be like that.
there’s a divide where someone forgot to make the stitches,
a divide where my mouth flaps endlessly
caught up in sounds that nobody else understands
where i know what i want to say
but i can’t say it
where i feel the words inside of me
but my mouth won’t make them
there are endless metaphors i could use –
if my goal was to make non-autistics more comfortable –
and that i won’t use because this isn’t about making anyone comfortable
i use the limited words i have
on the people i know don’t understand
everyone else gets the robot
(can i call myself a cyborg now?)
everyone else can still listen
i make rules
don’t look over my shoulder
don’t try to guess what i’m gonna say
i’m 20 years old
treat me like an adult
(not the one from the art fair in san jose)
told me a story about an autistic man who,
when given a letter board for the first time at 20,
spelled out F-U-C-K Y-O-U.
that’s what you get for not presuming competence
for making an adult watch PBS Kids
just because they can’t talk.
“can you talk? say something!”
yeah, how about,
go fuck yourself!
i went to a party and said hello to everyone on my phone,
and most people didn’t blink.
one guy kept asking,
“what’s wrong? are you sick?”
and i kept telling him,
it’s a long story.
because where do you start,
when a lifetime of meltdowns and overloads and social hell,
when a lifetime of sensory seeking,
when a lifetime of useless knowledge & special interests,
when a lifetime of being autistic
(on top of all the other illnesses and trauma)
begins to make sense?
and then slowly,
you begin to realize that it’s not you,
it’s the rest of the world,
and it’s not your fault for needing help,
and it’s not your fault for being different,
and it’s not your fault for being autistic.
there are no rules here
only people refusing to understand
and when there are no rules
there is only room to grow.
I wrote this from the iPad I bought specifically to use as an AAC/text-to-speech device. The exact app I use is called Speech Assistant and is available for Android and iOS for $10. It’s a great customizable app for someone who is able to type and use text phrases without pictures.
I wanted to write about being non/semi-speaking because it isn’t apparent from the way I write that I don’t speak. This is true of many people who use AAC. It’s often also a complaint in autistic circles in general: that non-autistic people don’t think we’re autistic because we look too “normal” from the way we type or write online. (The difference between online communication and in-person communication is massive, to say the least.)
I still can speak but I choose not to. It’s so draining to have to speak and if I have to choose between speaking and ending the day too tired to do much of anything and not speaking and ending the day with energy to enjoy myself, I’d rather have energy. I like communicating. People are nice to be around (some people; some of the time). But speaking is hard.
And, finally, I learned a lot about AAC and being autistic as a participant in the Autism Campus Inclusion program sponsored by the Autistic Self-Advocacy Network. I spent a week in DC with about 20 other autistic people and I was so impressed by how quickly we bonded as a group (especially since autistic people, by nature, are not very social). This poem is for everyone at ACI 2018 – you know who you are.