Trump and the Language of Mental Health around his Bigotry

A conversation that I wasn’t entirely enamored with occurred on Twitter recently regarding Donald Trump and mental health. This was between writers, journalists, and people with mental health needs (or people who fell into more than one of those categories) who agreed that Trump “doesn’t have the temperament to be President.” They disagreed about “whether [they] needed to frame temperament-issues in terms of mental health.” David Perry wrote about this – whether it was advisable to frame Trump’s behavior through a mental health framework. He presented varying arguments from multiple sides of the discussion. Some of the arguments included, several in response to each other:

  • argument 1: not talking about Trump’s mental health would increase stigma via silence on mental health
  • argument 2: “if he were dxed would… agree with you,” and that it was the armchair diagnosis speculation and use of “insane” as insulting that bothered them.
  • argument 3: temperament isn’t the result of mental illness
  • argument 4: mental illness is not a reason to be unfit for public office
  • argument 5: Trump isn’t right in the head and not even politicians are that self-centered
  • and it went on with other points, some that could be categorized under others.

I am quite inclined to agree with Finn of Expectedly that “Wrong does not mean crazy.” Finn wrote:

Trump’s disgusting plans are not the result of a mental illness; they’re the result of deep-set, unbridled bigotry that he’s exploiting to worm his way into the White House… The Republican Party as a whole deserves to be blasted… But this isn’t about mental illness; it’s about entrenched white supremacy, racism, misogyny, homophobia, transphobia, Christian supremacy and other prejudices.
People need to stop claiming that politicians – and their supporters – whose political views differ from theirs as a sign of a mental illness, as though people can’t hold different political beliefs without considering them rationally. This stereotype also comes with the insinuation that mental illness necessarily means the lack of agency required to arrive at a reasoned political decision, which is grossly untrue.

Discussing Trump’s mental health status is kind of getting into the territory where people will use it to say that people with mental health needs can’t be effective candidates for public office if they choose to run. People are also so eager to blame bigotry on mental health needs. It helps people, in my opinion, distance themselves from the thought that they could ever be bigoted about anything (when I don’t know one person who hasn’t screwed up in that regard at least once).

So, sure, being erratic and lying a lot could be a sign of mental health needs, but that doesn’t mean it’s the reason for things like Trump being a bigot. I’d like to make the point that people with mental health needs are people with many varying viewpoints on the world so if a person with mental health needs is a bigot, I would argue that the mental health needs are most often a coincidence. I know people with mental health needs who have done less than pleasant things – even, perhaps, said hurtful things about groups of people – in the middle of any sort of episode. I have had episodes where I’ve said less than stellar things, though I don’t think I’ve ever said bigoted things because of an episode – but I think it’s too easy to write Trump off as being a delusional, pathologically lying narcissist.

Finally, I really, really don’t think that talking about it in this context will lead to less stigma. In certain contexts? Remaining silent about mental health needs absolutely can increase stigma, can result in mental health needs being the bogeyman in the closet, a family’s dark secret, you get the drift – and I also advocate for the consent of the person in question. Even though Trump is a political figure and thus invites judgment, I feel like discussing it in this context invites severe judgment on people with mental health needs. It links bigotry to mental health needs because Trump is such a bigot that if people think Trump + mental health needs, they are going to start associating mental health needs with Trump-type bigotry.

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Everyone, particularly other people with mental health needs – and especially those with particularly stigmatized diagnoses like bipolar I/II/NOS, schizophrenia, or any mental health need involving psychosis, for instance – is welcome to weigh in on this. Read the comment policy before submitting a comment; I moderate comments. 

You call me expressive and miss the struggle it takes

Someone, back when I was in college, insisted I was expressive compared to an Autistic 10-year-old she knew: Yeah, but you’re different, you’re expressive. This post could go in a few different directions that I’d like to list because there were so many issues I (still) have with that statement:

  • that’s it’s okay to not be a wordsmith out loud or at all;
  • that comparing two people with an age difference of ten years – or comparing Autistic people to each other at all like that – isn’t useful;
  • that expressiveness doesn’t just come with words, so stop discounting people who don’t do them out loud well or at all;

and

  • my personal experience with the concept of expressiveness, movement, speech, and trying to go fast to keep up.

I chose the last one.

I may think in words, not pictures or concepts – but getting the worded thoughts to speech is another task entirely. Spontaneous conversation is hard. There’s this thing I do, which is simultaneously talk really fast, and not say half of what I wanted or meant to say. The speed at which conversations go doesn’t always give me the time to say the appropriate thing, so I spit out then closest thing in my head to what I mean. Sometimes it’s the wrong thing or makes no sense.

I don’t use spoken echolalia from pop culture and people around me so much as I use the same format for sentences over and over again, slipping in different words – or I stumble through words, speaking quickly but not always coherently.

I move in the same way I talk: scuffing and stumbling on stray objects. I can’t always find my body in space; I can’t always figure out object proximity because of visual processing and go crashing into it. I can’t cut food or tie shoelaces effectively, and learning how to do needlework was a short-lived venture. My feet drag the ground when I walk or I put my feet down with unnecessary force; there isn’t an in-between. Door frames are my enemy.

Or: I rock to other people’s rocking, flap to other people’s flapping, turn to look in the same direction as anyone I’m with – I’m echopraxic and copy movements. Or I don’t remember how to move at all. If I move, it’s fast, though – and it takes a lot of work.

I am tired of trying to move fast in conversations with non-autistic people (and sometimes other autistic folks). I am tired of the fast pace of movement I set for myself, lest I fall behind non-autistic standards. I am tired that the ways I communicate and move don’t seem to be enough for a lot of people.

Or, if you flip that coin, I am tired of the way people dismiss the struggle to move fast and the struggle to sound like I know what I’m talking about and call me expressive. 

I want to learn to stop going so fast. I want to learn that it’s okay for me to take long pauses, stimming idly as I let the words form and coalesce into sentences.

I don’t want to hear that I’m expressive.

I want to learn that it’s okay to never be able coordinate my movements when I turn toward a door frame, resulting in the inevitable collision. I want to learn that I can focus on my movements, unapologetically Autistic in the ways my hands move, slowing to let myself tap invisible pianos and move my hands back and forth to the music.

I want people to learn to value diversity in communication and movement. I want people to make the effort to understand me, as I make the effort to understand them.  I want people to learn that the ways I speak and move are, now and always, acceptable and valid.

I Fear for My Fellow Autistic People: On Media Misrepresentation

Recently, a piece appeared in a major news outlet. The main premise of the article described a mother’s fear that her autistic teenage son will kill her, her other son’s wish that his brother would die, and the lack of respite services where she lives. It was a very personal piece. This article more than irks me; it plays into very dangerous stereotypes. It plays into the idea that autistic people are inherently dangerous, that we are burdens. And dangerous stereotypes in the media, whether in fiction or opinion pieces or livetweeting an autistic person’s meltdowns have real life consequences.  

First, let’s talk about autism and violence.

Autistic people have many dangerous stereotypes about violence, particularly mass shootings (the idea that we are likely to be perpetrators) surrounding us; the mass shooting one is false. However, when individually aggressive, we usually have an outside stressor. When I was in school before college, it was people touching me; the overwhelming sensory overload; the frustration of not being able to put words to all my feelings; and the constant wear and tear of terrifying social interactions and bullying. I was flailing hands, panic attacks and tears, bolting down the hall, and slapping anyone who touched me. Fortunately for me, I was not considered intimidating and dangerous for a variety of reasons, just in need of more support. 

But continual aggression is usually a sign that something is very stressful. This is a checklist that can help identify those sources. Tumblr user Lysikan, a non-speaking autistic person, has created a set of posts that can help reduce meltdowns – one of the primary times an autistic person can become aggressive while overloaded and panicked.

Next, let’s talk about her other son’s hatred and death wish for his brother, and media narratives surrounding autism, disability, and our murders.

And also what I fear almost more than anything, the murder of another autistic or disabled person by their caregivers or family members. Let’s talk about filicide. Let’s talk about how the same story occurs over and over again. A disabled person is murdered by a caregiver or family member. The media picks up the story. Sometimes they report on it as a mercy killing. They almost always talk about the burden of caring for a disabled person. The victim is a throwaway in their own story. Many people have already explained this in countless blog posts. It should be beating a dead horse, but it’s really not. Many people act on their wishes. I have heard of far less, if any, killings of caregivers by autistic people than killings of autistic people by caregivers. This is why I fear the death of autistic people at the hands of caregivers and family members far, far more.  

Finally, let’s talk about responsible journalism, disabled people’s right to privacy – and real life consequences.

I will absolutely agree that there is a need for more respite services. I will absolutely agree that more services need to happen! But there are frankly better ways to deal with this than publicly posting in a major news outlet the intimate details of an autistic person’s personal life. There are better ways to deal with this than to promote dangerous stigma. There are private actions that could be taken that would protect the autistic person’s confidentiality and not promote stigma.

One is to actively work to reduce the autistic person’s meltdowns using the strategies linked above. Another, if this resource is accessible, is to see a professional about your feelings of stress or anxiety. And – these kinds of stories are not isolated. They are patterns; “autism parents” routinely post in and on public spaces and blogs intimate details of their child’s life and how miserable their child makes them.

This is extremely dangerous for autistic people.  First, it effectively outs them to the world, and could make it impossible for them to do things without people realizing it and judging. Second, it directly leads to real life consequences. Elizabeth Bartmess notes in “Autistic Representation and Real Life Consequences” that

This is shown in several similar ways in fiction and in real life. Autistic people are represented as burdens on others, particularly their families, when they embarrass neurotypical siblings or have greater support needs. This is more common for characters written to “low-functioning” stereotypes…. In real life, we are presented as burdens as well… This has consequences. At the extreme end, media or other parents justify parents murdering autistic children. Abuse is common, by friends, people on the street, caregivers, and others such as paid service providers, foster care providers, and transportation providers. In general, people with developmental disabilities have drastically higher rates of abuse; abusers may target autistic individuals…

The Pacific Alliance on Disability Self Advocacy (PADSA) resource guide on media misrepresentation states, “Even when people don’t directly cite these stories, they seep into culture. People form their opinions and take their actions based on prejudices.”

Both the autistic teenager’s mother and this major news outlet had a responsibility to autistic people to report in a way that does not increase stigma and cause more consequences for autistic people. They chose the stigmatizing, stereotyped, and dangerous way of talking about autism. I am afraid of these stories and will continue to speak out against them. I am not afraid for myself, but for all my autistic brethren living in dangerous situations. I think of all the people that may make harmful or fatal choices because of this irresponsible news story and fear for all my autistic and disabled brethren.

Additional Resources

On Disabled People’s Right to Privacy (Especially Those With Caregivers) and Media Misrepresentations

On Responsible Reporting and How to Respond to Media Narratives of Disabled People

For Parents on Autism Acceptance, Meltdowns, and Aggression

On Filicide

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