I Like Pink Stuff

I am trans, asexual, panromantic, autistic, and a writer. My preferred pronouns are she/her
~ Friday, February 15 ~
Permalink

awlmusic:

Katachi
Shugo Tokumaru

This is pretty great. 

I am re-reblogging because I wanted to say stuff earlier but was overwhelmed at the time.

This song is a Perfect Song for me.  It interacts with my autism and synesthesia perfectly and…  ~_~  nnng!

Everything from the harmonics to the rhythm to the singer’s voice…  <333

And the video is absolutely captivating. This video comes really close to encapsulating how I experience all music and I have never found anything that does that before.  So watch this and enjoy, because this is spectacular.

*goes to find everything ever done by Shugo Tokumaru* 

Tags: music synesthesia synesthetic actually autistic actuallyautistic autism new special interest? definitely a new special song
42 notes
reblogged via sistercrow
~ Sunday, December 16 ~
Permalink Tags: actuallyautistic autism stigma profiling abuse
23 notes
reblogged via sherlocksflataffect
~ Friday, December 14 ~
Permalink
Autistic Americans and individuals with other disabilities are no more likely to commit violent crime than non-disabled people. In fact, people with disabilities of all kinds, including autism, are vastly more likely to be the victims of violent crime than the perpetrators. Should the shooter in today’s shooting prove to in fact be diagnosed on the autism spectrum or with another disability, the millions of Americans with disabilities should be no more implicated in his actions than the non-disabled population is responsible for those of non-disabled shooters.
Tags: autism actuallyautistic gun violence
589 notes
reblogged via mommy-cuteella
~ Friday, November 30 ~
Permalink

jinglebellsnark:

sistercrow:

If anyone out there who is autistic and has the energy, could you check out this link, watch the video, and maybe give me some feedback as to your impressions of it?

To clarify, I only want feedback from people who are autistic themselves.  I don’t want to hear anything from family members of autistics or people who work with autistics or people who take care of autistics.  Allistics need not apply.  I sucks that I have to put this disclaimer here, but if I don’t then I am probably going to mostly get feedback from non-autistics and that isn’t really helpful to me right now.

Mainly, I am trying to wrap my head around this and the implications of the research as well as how it is being handled.  I have some issues with it personally and am mostly looking to see if any other autistics say the same things that I am feeling.  So if you do respond, feel free to mention anything at all about it, whether it is the research, the way the project is being presented, problematic language in the video or interview, etc.

Thanks!

Hmmm.

It seems pretty okay. As an Autistic person who actually plays World of Warcraft regularly, I really can see where Lissanna is coming from. World of Warcraft and before that Ragnarok Online filled my need for friends, in a way that was comfortable to me: Without face-to-face contact. 

World of Warcraft has also greatly helped my teamwork skills (in dungeons and raids, if you don’t work together, you can’t progress, simple as that), and my idea of work (I can now pick a goal for the day and accomplish it, whereas before I didn’t really understand the idea of step-by-step, it just wasn’t taught to me).

While there was some problematic language, I can chock that down mostly to the interviewer, and while I don’t like person-first language, that’s sadly the standard, so I can overlook that.

My main beef was the claim that “scientists and parents ask kids and adults with Autism what they need and about their experiences” which is wrong, wrong, wrong. We’re barely, if ever, considered important to the process of Autism research except, maybe, as guinea pigs. Nobody has EVER asked me about my needs, I was just placed into program after program of what my parents and teachers -thought- I needed, and was punished for objecting if it wasn’t what I needed.

Other than that, I’d say I actually want to meet Lissanna sometime, whether on the forums or in-game, and see what I can do to assist with her project. I do think she’s on the right track, but she needs neurodiversity advocates looking over her shoulder so she doesn’t step into Autism $peaks style dogma.

It’s sad, but I just cannot trust non-Autistics  when it comes to Autism research.

Okay.  Thank you!

I kinda had similar feelings about it.  Like, the research seems to be aimed at providing assistance to autistics who want to learn better facial recognition.  Some of it is problematic (“if we can make autistics look more normal than they will be more normal!”) and I couldn’t help but notice that she keeps slipping up and referring to autistics as “kids” even when she was just talking about their coworkers and classmates and whatnot.  Mostly, I was a bit frustrated that they kept talking about WoW as if it wasn’t something autistics actually played.  Like, before she came along, no autistic person had ever played a video game before?  *grumble grumble*  In a better world, she would have also been asking for autistics who play WoW to provide their insight and personal experiences with the game and how it has helped them.

But I guess the thing that was really bothering me was on the fundraiser page.  She keeps talking about facial recognition problems, then saying how autistics are unlikely to find jobs or make friends and how hard it is for us, and then seems to be making the case that the entire reason we have trouble in those areas is because of lack of facial recognition and social skills….  >.<  Completely ignoring the social stigmas surrounding autism and the fact that if employers had decent accommodations for people with disabilities, holding a job wouldn’t be quite so hard.  Or that if autistics weren’t treated as subhuman and there was a greater awareness in society about neurodivergence and whatnot, being singled out and mocked for being different might not happen as much and we would be better at making friends.

Mostly, I am just frustrated that whenever it comes to autism, the solution to making our lives better is always to change us to better fit into society, rather than trying to adjust society to be more inclusive of us as we are.

=/

Anyways, thanks for the feedback!  I’m still trying to formulate my thoughts on this and it really helps to have other people share their views =)

Tags: actuallyautistic actually autistic autism
2 notes
reblogged via shadow-word-death
Permalink Tags: actuallyautistic actually autistic autism
2 notes
~ Tuesday, November 27 ~
Permalink
  • Allistic: Autism is such a tragedy! My brother will never live a normal life!
  • Autistic: He might, he might not. Since he's 4, it's much too early to tell. And normal isn't a requirement for happy, anyways.
  • Allistic: YOU DON'T UNDERSTAND ANYTHING ABOUT AUTISM. HE CAN'T DO ANYTHING AND NEVER WILL.
  • Autistic: ....what?
Tags: autism actuallyautistic actually autistic chat wtf
96 notes
reblogged via goldenheartedrose
~ Tuesday, October 16 ~
Permalink

Stupid things NTs say #2

dumbthingsneurotypicalssay:

‘You’re not an autistic person, you’re a person with autism.

(Source: stupidthingsneurotypicalssay)

Tags: actuallyautistic autism
13 notes
reblogged via goldenheartedrose
~ Tuesday, October 9 ~
Permalink

[tw: transphobia, ableism, murder, suicide] Train Wrecks at the Intersections

magickal-halloween-cat:

girljanitor:

Comparing axes of oppression is often a terrible idea for many reasons. That is why I’m not attaching this to anyone else’s post; one of those reasons is that in those discussions, certain people’s voices get heard and other people’s voices are silenced, and I don’t want to do that to anyone, or have it done to me.

But when I came across this article by the mother of a trans man, the excruciating parallels of dehumanization from a parent with the overwhelmingly dominant narrative of “autism parents” in the media was horrifying, all-too-familiar, and triggering as fuck on a few levels for me.

To be clear: I’m a genderqueer (two-spirited; a specifically Native/Indigenous gender identity) person but I am still privileged over trans folks, especially trans women. I’ve been the target of quite a bit of abuse and awfulness specifically for not “conforming to gender”, especially as a child. But I cannot claim the trans experience because mine has been different in some important ways.

I’m also autistic as fuck.

When A.W. Paul, the author of the awful “parent of a trans person” story, says a sentence like,

Now the issue was knocking at my door.

about her own child, the dehumanization and easy willingness to reduce a human being to an issue reads all too much like an article published last year in the same section of the same damn publication, in which the author T. Fields-Meyer writes about his son with autism:

So what’s the parent of a living, breathing autism specimen to do with the constant barrage of speculation?

And when Paul says this about her trans child, I just about cried because it was all too familiar:

A transgender child brings a parent face to face with death. The daughter I had known and loved was gone; a stranger with facial hair and a deep voice had taken her place.

This narrative is practically verbatim the same exact dominant narrative in the media about autistic people. If you don’t believe me, have a gander at this guide to grieving over having an autistic child instead of the “normal” one you think the universe owed you, straight from Autism Speaks, a multimillion dollar organization dedicated to ruining autistic people’s lives:


Many parents must mourn some of the hopes and dreams they held for their child before they can move on. There will probably be many times when you feel extremely sad. With time, your sadness may give way to anger.

Although anger is a natural part of the process, you may find that it’s directed at those closest to you – your child, your spouse, your friend or at the world in general. You may also feel resentment toward parents of typical children.

Then, when Fields-Meyer relates a comment from a *friend*:

Trying to make me feel better, she said, “When you have four children, you’re bound to have one who is a failure.”

It reads so much like every goddamn article from “autism parents”, the ones who utterly dominate just about every facet of media about autism. An excerpt from a  fairly typical article barfed out in an internet search:

Then I realized: it’s not just about Tom.  It’s about us: Tom’s parents.

In the long run, when our child is judged - and she will be judged - it’s us parents who are taking the brunt of the judgement, for better or for worse.

All too often, of course, no matter what we do as parents, our child with autism will always be judged as not quite good enough.

And a gem from the comments:

It’s raining here, I’m likely taking in fewer negative ions, or I’m tired, today I will say autism is my personal failure.

Essential characteristics of both narratives:

  • dehumanization of the child and reduction of the child to “an issue” that affects the parent more than the child.
  • The “this is all about ME” perspective.
  • Invocation of images of death; a “real” or “normal” child gone or disappeared and replaced by a stranger
  • constant concern over public opinion towards the parent for having a child that does not conform to expectations
  • speaking of the child as an embodiment of failure; either on the part of the parent or the child (notice A. W. Paul only gets jarred out of mourning when a “friend” implies a failure on her part as a parent, for fucks sakes)

That being said, it’s sad to note that either trans people or autistic people might be offended by comparison to the other group. Both are heavily stigmatized, and there is another effect of these specific narratives that manifests in the most horrible way possible:

Dominant social narratives of their inherent worthlessness leads to trans people being murdered constantly.

Dominant social narratives of their inherent worthlessness leads to autistic people being murdered constantly.

That is the effect of dehumanization. Of literally being viewed as less than human, other than human, not a person.

The psychological and physical ramifications of being treated and talked about this way by our own parents, by those who created us and are supposed to love us, are nigh unbearable, and are in fact unbearable for so many of us.

Because it IS unbearable.

It is UNBEARABLE.

Perhaps I’m stepping out of line with this comparison. I may be completely and utterly talking out of my ass on this. There are so many other overlapping issues that add to these oppressions, especially race. Being a person of color, and in particular being a Black person, adds so many attendant risks to just trying to exist…it boggles the mind.

Part of my perspective is shaped by having been a part of a LGBT community from 12 or 13 years of age, and understanding that transgender people are the most vulnerable among us, and that in many ways we must form a protective buffer around the most vulnerable of our brothers and sisters. Whether in the form of a couch to sleep on, a few bucks for food, a listening ear, or to fight tooth and nail against those who would do them harm.

My heart bleeds and screams and cries out for solidarity among those of us whose normal human variation leaves us without protection, betrayed by those who are supposed to love and cherish us, and to also point out that those of us who are both autistic and transgender (and genderqueer in various ways, and/or are people of color-especially Black people) are exponentially more vulnerable as these factors crowd and try to drown out our voices.

What I’m really trying to say is that I firmly believe that it is our moral, human duty to protect the things about humanity that are so worth protecting: those of us who are vulnerable. And so much of protecting those who are precious to us is about fighting; fighting tooth and nail for our right to exist, for our right to live without the constant barrage of dehumanization. I will fight every day to chew a hole in the world for myself and for those who can barely breathe in this world without being threatened with obliteration.

As an autistic nonbinary trans person, I thoroughly approve of this post.

Yeah, so, all of this right here.

The ways in which oppression is enacted on one group is often very similar to how it is enacted on other groups.  Different reasons, but often following the same paths and methods of execution. 

Tags: actuallyautistic autism trans parenting
124 notes
reblogged via nattys-other-blog
~ Wednesday, October 3 ~
Permalink

goldenheartedrose:

I have ceased being surprised at the offensive things allistics say in the name of “science”. Good Lord.

Tags: autism actuallyautistic
7 notes
reblogged via mommy-cuteella
~ Tuesday, October 2 ~
Permalink
bookworm24601:

sistercrow:

goldenheartedrose:

josephineanes:

This is a fucking joke. Genetics is NOT THE ONLY cause of autism, sorry to burst your bubble, angry uneducated annotator. “[the donations] go towards finding a cure, and there is no cure..” Yes, there is no cure, so money goes towards FINDING a fucking cure you ignorant asshole. You really think the money being donated is going to waste? You try finding the cure to a disability so complex that it has its own spectrum, it differs greatly from case to case, and there are multiple causes, known and unknown. 
An apology to your son for trying to reach out to the many who are unaware of autism and trying to find a cure? How about an apology from the FDA for thimerosal in vaccinations throughout the 90s. Bashing an organization designed for research in an area where it is STRONGLY needed is ignorance. This sickens me. 

Oh, look, curebie bullshit on my dash! Wonderful! 
It’s not like vaccinations have been proved time and time again to not have anything to do with autism.
Or like, you know, just being alive is linked to autism.

Wow.  Look at the ignorance going on here.
Yeah, autism is not caused by vaccinations.  A massive study found that vaccines did not cause autism (wait for it) YEARS BEFORE that conspiracy theory actually sprang into being.  That’s right, the study to see if vaccines caused developmental disorders was conducted BEFORE the controversy about their safety.
Also, FUCK OFF.  Many many many autistics don’t want to be “cured” as “curing” us would mean literally changing who we are.  Most of the autistics that do want to be cured (hint: even if they do, that is still their choice and not yours to make for them) want to be cured because they have internalized a lot of harmful messages and because they are treated like shit by society and like burdens by heir families.
A$ is a terrible organization that makes money by spreading fear and misinformation about autism and actively promotes the eradication of autistics.
On the up side, this is an amazing letter.  A++, parenting of autistic person done right.

Okay, everyone. CALM DOWN!!!!! Look, the truth is that no one, NOT EVEN THOSE WITH AUTISM OR WHO HAVE A FAMILY MEMBER WITH IT, understands autism. We (MEANING EVERYONE!!) have no idea if it’s a disease or not, if it’s psychological, or biological, what causes it, if there’s a cure, NADA!!! We DO know a few things that AREN’T true, such as the whole ‘vaccines cause it’ thing, just like we know that human beings have had autism for centuries; just like we’ve had people with cancer, or red hair, or brain deformities, or two eyes with different colors, or polio, etc. 
The only thing we know for sure is when someone has it. We know the signs and we figure out the best way for them to thrive in our society. But even then, since we don’t know what CAUSES it, finding out if someone actually HAS it, and ISN’T suffering from something else is a challenge. 
Bottom line: EVERYONE NEEDS TO STOP CRITICIZING OTHERS ON BEING IGNORANT ABOUT SOMETHING THAT NO ONE KNOWS ANYTHING ABOUT!!!
As for the whole ‘finding a cure’ thing: the way I see it, we should try to find a cure (IF one exists) so that way people who WANT it, can GET it. Besides, in order to find a cure, you have to find a cause, and I’m over a hundred percent positive that even those who DON’T want a cure, at LEAST want to know the PROVEN cause(s). 
As the sibling of a high-functioning autistic girl, and the neighbor of a low-functioning one, I’ve SEEN how stressful being a parent of a child with autism, OR just BEING a child with autism can be. It’s NOT POSSIBLE to interact with an autistic child the same way you interact with a child that does NOT have autism (Notice how I’m only mentioning CHILDREN because I’ve only ever been exposed to CHILDREN with autism). They don’t think the same way, and as such, you can’t TREAT them the same way. Because of that, some families don’t understand/can’t do that, so the children are seen as burdens and what not. It’s sad; I feel bad for the kid; but it sort of falls under the category of ‘not loving your child because he was born with a deformed hand’. You can’t fix the hand. You can TRY to fix the views of the parents, but at the end of the day, if a parent ever REALLY thought of their child as a burden, that kid is going to have to do something INCREDIBLE in order for the parents to change that view. And sometimes, not even THAT works. Regardless, YOU, as someone who DOESN’T view the child as a burden, CAN DO NOTHING ABOUT THAT. 
I agree, part of that DOES have to do with society. Society makes it difficult for autistic people to thrive. Society makes it difficult for EVERYONE to thrive, except for a small handful. Changing society is possible, but it’s incredibly difficult. Really, the only thing to do about that is to spread the word and advocate and what not. Or just do what me and my sibling do, which is to politely tell society to go fuck itself by walking around an outlet mall in mismatched clothes, singing Disney songs loudly and off-key, and laughing when people give us looks. 
I know nothing about Autism Speaks. Really. Except that it’s an organization that has something to do with autism. Therefore, I won’t bash it, or defend it. I just have a problem with people bashing stuff by using false information and those who go around pretending they know something they don’t.
And this, ladies and gentlemen, is why I DON’T participate in the debates my History class gets into about politics. 

*sigh*
Hey look, a person who doesn&#8217;t have autism telling people who DO have autism how we ought to be reacting to stuff, when they SAY RIGHT THERE THAT THEY KNOW ABSOLUTELY NOTHING ABOUT THE THING WE ARE UPSET ABOUT.
Also, if you want to make friends and charm people with autism, please don&#8217;t do so by comparing us to fatal diseases and inconsequential physical features.  Autism is a huge part of who we are and how we see the world.  Autism is not a disease.  As shocking as this will be to you, we KNOW THAT AUTISM IS NOT A DISEASE. Just going off of the definition of diseases.  Just because we don&#8217;t know the exact cause (the bulk of the evidence points towards it being genetic you ignorant fuck), doesn&#8217;t mean we don&#8217;t know what it is or what it does.  It is a developmental disorder.  Its effects are well documented and we know a lot about it.  Just because you don&#8217;t doesn&#8217;t mean that nobody does.  And even still, WHEN AUTISTIC PEOPLE TALK ABOUT WHAT AUTISM IS AND HOW IT WORKS, YOU SHOULD VALUE OUR OPINIONS AND LIVED EXPERIENCE AS DIRECT EVIDENCE.   At the same time, autism is a very real disability, so comparing it to the colour of your hair is really dismissive and condescending.
And here is the thing:  we are actually pretty good at determining if people have it.  We are getting better all the time. 
But wait, you don&#8217;t know anything and just wanted to jump in and tell us to calm down.
So let me educate you.
Autism Speaks wants to find a way of prenatally testing for autism.  Why?  So if a parent is pregnant with an autistic fetus, they will be able to abort the fetus.  And while the choice to abort for any reason is a personal one in the hands of the pregnant person, this form of selective abortion is common with pretty much ever neuroatypicality out there that can be tested for.  Go look up the rates of abortion of fetuses confirmed to have down-syndrome since prenatal testing for it was developed.  It is staggering.  As a result, the rates of people who have down-syndrome has dropped dramatically.
Secondly, if a cure is developed, I GUARANTEE that it will not be optional and up to the person with autism if the are a child (probably not even if they are adult either).  Go look up the rate of cochlear implants in deaf infants.  CI&#8217;s were originally intended only for those over the age of 18 who could consent.  Almost immediately, however, parents of deaf infants began pushing to be allowed to have them installed in infants.  I won&#8217;t get into the controversy surrounding CI&#8217;s as I am not deaf, but you can find plenty of deaf people on Tumblr who have spoken their minds about the subject.
So, lets review:  You are not autistic and are admittedly entirely ignorant of A$ and why autistic people don&#8217;t like the organization but still felt compelled to make your opinion on the subject heard over ours.
A$ is a terrible organization that seeks to find testing for autism so that it can be determined prenatally.  A similar thing happened with down-syndrome and resulted in a sever drop in the rates of people born with it.  When society chooses a set of characteristics about people that make them less worthy of being born and actively seek to reduce their numbers in the population that is known as eugenics.  I should not have to tell you why eugenics is terrible.
If a cure were found, it would involve directly changing who a person is in order to bring them in line with what society wants.  This cure would almost certainly, very quickly, become something that the person being &#8220;cured&#8221; would have no choice about.  This means that A$ and similar organizations are essentially seeking a way to eliminate all autistics.
When you actively seek to eliminate all members of a people group based on who they are, that is called a genocide.
And finally, you are a silencing jerk who would rather we all play nice than actually listen to what autistic people have to say about autism and the major organizations that specialize in autism that are most visible publicly.
If you want to be a good alley and help, DO SOME FUCKING RESEARCH BEFORE YOU OPEN YOUR MOUTH.

bookworm24601:

sistercrow:

goldenheartedrose:

josephineanes:

This is a fucking joke. Genetics is NOT THE ONLY cause of autism, sorry to burst your bubble, angry uneducated annotator. “[the donations] go towards finding a cure, and there is no cure..” Yes, there is no cure, so money goes towards FINDING a fucking cure you ignorant asshole. You really think the money being donated is going to waste? You try finding the cure to a disability so complex that it has its own spectrum, it differs greatly from case to case, and there are multiple causes, known and unknown. 

An apology to your son for trying to reach out to the many who are unaware of autism and trying to find a cure? How about an apology from the FDA for thimerosal in vaccinations throughout the 90s. Bashing an organization designed for research in an area where it is STRONGLY needed is ignorance. This sickens me. 

Oh, look, curebie bullshit on my dash! Wonderful! 

It’s not like vaccinations have been proved time and time again to not have anything to do with autism.

Or like, you know, just being alive is linked to autism.

Wow.  Look at the ignorance going on here.

Yeah, autism is not caused by vaccinations.  A massive study found that vaccines did not cause autism (wait for it) YEARS BEFORE that conspiracy theory actually sprang into being.  That’s right, the study to see if vaccines caused developmental disorders was conducted BEFORE the controversy about their safety.

Also, FUCK OFF.  Many many many autistics don’t want to be “cured” as “curing” us would mean literally changing who we are.  Most of the autistics that do want to be cured (hint: even if they do, that is still their choice and not yours to make for them) want to be cured because they have internalized a lot of harmful messages and because they are treated like shit by society and like burdens by heir families.

A$ is a terrible organization that makes money by spreading fear and misinformation about autism and actively promotes the eradication of autistics.

On the up side, this is an amazing letter.  A++, parenting of autistic person done right.

Okay, everyone. CALM DOWN!!!!! Look, the truth is that no one, NOT EVEN THOSE WITH AUTISM OR WHO HAVE A FAMILY MEMBER WITH IT, understands autism. We (MEANING EVERYONE!!) have no idea if it’s a disease or not, if it’s psychological, or biological, what causes it, if there’s a cure, NADA!!! We DO know a few things that AREN’T true, such as the whole ‘vaccines cause it’ thing, just like we know that human beings have had autism for centuries; just like we’ve had people with cancer, or red hair, or brain deformities, or two eyes with different colors, or polio, etc. 

The only thing we know for sure is when someone has it. We know the signs and we figure out the best way for them to thrive in our society. But even then, since we don’t know what CAUSES it, finding out if someone actually HAS it, and ISN’T suffering from something else is a challenge. 

Bottom line: EVERYONE NEEDS TO STOP CRITICIZING OTHERS ON BEING IGNORANT ABOUT SOMETHING THAT NO ONE KNOWS ANYTHING ABOUT!!!

As for the whole ‘finding a cure’ thing: the way I see it, we should try to find a cure (IF one exists) so that way people who WANT it, can GET it. Besides, in order to find a cure, you have to find a cause, and I’m over a hundred percent positive that even those who DON’T want a cure, at LEAST want to know the PROVEN cause(s). 

As the sibling of a high-functioning autistic girl, and the neighbor of a low-functioning one, I’ve SEEN how stressful being a parent of a child with autism, OR just BEING a child with autism can be. It’s NOT POSSIBLE to interact with an autistic child the same way you interact with a child that does NOT have autism (Notice how I’m only mentioning CHILDREN because I’ve only ever been exposed to CHILDREN with autism). They don’t think the same way, and as such, you can’t TREAT them the same way. Because of that, some families don’t understand/can’t do that, so the children are seen as burdens and what not. It’s sad; I feel bad for the kid; but it sort of falls under the category of ‘not loving your child because he was born with a deformed hand’. You can’t fix the hand. You can TRY to fix the views of the parents, but at the end of the day, if a parent ever REALLY thought of their child as a burden, that kid is going to have to do something INCREDIBLE in order for the parents to change that view. And sometimes, not even THAT works. Regardless, YOU, as someone who DOESN’T view the child as a burden, CAN DO NOTHING ABOUT THAT. 

I agree, part of that DOES have to do with society. Society makes it difficult for autistic people to thrive. Society makes it difficult for EVERYONE to thrive, except for a small handful. Changing society is possible, but it’s incredibly difficult. Really, the only thing to do about that is to spread the word and advocate and what not. Or just do what me and my sibling do, which is to politely tell society to go fuck itself by walking around an outlet mall in mismatched clothes, singing Disney songs loudly and off-key, and laughing when people give us looks. 

I know nothing about Autism Speaks. Really. Except that it’s an organization that has something to do with autism. Therefore, I won’t bash it, or defend it. I just have a problem with people bashing stuff by using false information and those who go around pretending they know something they don’t.

And this, ladies and gentlemen, is why I DON’T participate in the debates my History class gets into about politics. 

*sigh*

Hey look, a person who doesn’t have autism telling people who DO have autism how we ought to be reacting to stuff, when they SAY RIGHT THERE THAT THEY KNOW ABSOLUTELY NOTHING ABOUT THE THING WE ARE UPSET ABOUT.

Also, if you want to make friends and charm people with autism, please don’t do so by comparing us to fatal diseases and inconsequential physical features.  Autism is a huge part of who we are and how we see the world.  Autism is not a disease.  As shocking as this will be to you, we KNOW THAT AUTISM IS NOT A DISEASE. Just going off of the definition of diseases.  Just because we don’t know the exact cause (the bulk of the evidence points towards it being genetic you ignorant fuck), doesn’t mean we don’t know what it is or what it does.  It is a developmental disorder.  Its effects are well documented and we know a lot about it.  Just because you don’t doesn’t mean that nobody does.  And even still, WHEN AUTISTIC PEOPLE TALK ABOUT WHAT AUTISM IS AND HOW IT WORKS, YOU SHOULD VALUE OUR OPINIONS AND LIVED EXPERIENCE AS DIRECT EVIDENCE.   At the same time, autism is a very real disability, so comparing it to the colour of your hair is really dismissive and condescending.

And here is the thing:  we are actually pretty good at determining if people have it.  We are getting better all the time. 

But wait, you don’t know anything and just wanted to jump in and tell us to calm down.

So let me educate you.

Autism Speaks wants to find a way of prenatally testing for autism.  Why?  So if a parent is pregnant with an autistic fetus, they will be able to abort the fetus.  And while the choice to abort for any reason is a personal one in the hands of the pregnant person, this form of selective abortion is common with pretty much ever neuroatypicality out there that can be tested for.  Go look up the rates of abortion of fetuses confirmed to have down-syndrome since prenatal testing for it was developed.  It is staggering.  As a result, the rates of people who have down-syndrome has dropped dramatically.

Secondly, if a cure is developed, I GUARANTEE that it will not be optional and up to the person with autism if the are a child (probably not even if they are adult either).  Go look up the rate of cochlear implants in deaf infants.  CI’s were originally intended only for those over the age of 18 who could consent.  Almost immediately, however, parents of deaf infants began pushing to be allowed to have them installed in infants.  I won’t get into the controversy surrounding CI’s as I am not deaf, but you can find plenty of deaf people on Tumblr who have spoken their minds about the subject.

So, lets review:  You are not autistic and are admittedly entirely ignorant of A$ and why autistic people don’t like the organization but still felt compelled to make your opinion on the subject heard over ours.

A$ is a terrible organization that seeks to find testing for autism so that it can be determined prenatally.  A similar thing happened with down-syndrome and resulted in a sever drop in the rates of people born with it.  When society chooses a set of characteristics about people that make them less worthy of being born and actively seek to reduce their numbers in the population that is known as eugenics.  I should not have to tell you why eugenics is terrible.

If a cure were found, it would involve directly changing who a person is in order to bring them in line with what society wants.  This cure would almost certainly, very quickly, become something that the person being “cured” would have no choice about.  This means that A$ and similar organizations are essentially seeking a way to eliminate all autistics.

When you actively seek to eliminate all members of a people group based on who they are, that is called a genocide.

And finally, you are a silencing jerk who would rather we all play nice than actually listen to what autistic people have to say about autism and the major organizations that specialize in autism that are most visible publicly.

If you want to be a good alley and help, DO SOME FUCKING RESEARCH BEFORE YOU OPEN YOUR MOUTH.

Tags: I can't I don't jasbfdlbfkjbsdjfblbfjkvkH smbjl allism allism speaks cure allism now autism actually autistic actuallyautistic autism speaks assholes ignorance ableism
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