If a community disability term, such as neurodivergence, contains diagnoses that in your experience are too different to be related, you can opt out of the term, but you do not get to disagree that the term still includes both for other people with those diagnoses.
I don't actually care what the coiner's intentions with a word were that much, beyond, "if even one person finds a wider or more inclusive definition meaningful, the definition expands to encompass their usage of it".
That's descriptivism, the idea that words only exist to be useful to us and that we shape their meaning to that end. It is the counterpart to prescriptivism, the idea that words have concrete, strict, static definitions and that we have to use the right words as accurately as possible and can't use words if they fit badly enough.
"Words have meanings" is a prescriptivist take, but so is "I don't feel neurodivergence includes xyz".
I mean this in a way less aggressive than it sounds, but quite simply, neurodivergence doesn't revolve around your experience of it.
I also find it symptomatic of the extreme cartesian dualist bias most people haven't actually examined that "physical disability" can include everything from neurogenic pain to irritable bowel disease to limb deformities to cardiac issues to asthma to paralysis to visual impairment and more, but neurodivergence and neurodisabilities are often limited to, if not the more palatable and less disordered forms, even just things that are primarily cognitive or emotional in nature.
To explain, cartesian dualism is the idea that there is a separate, nonphysical "mind" from the physical neurological structure of your brain and body - and that therefore essentially mental illness and neurodivergence are sicknesses and differences of an abstract consciousness that is little more than a different word for the idea of a "soul".
It's very disturbing to me that people think that, because we don't fully understand how bioelectrical and chemical processes or neurophysical structure inform the phenotypical presentation of disorders and neurodivergence with an array of cognitive-emotional symptoms, that we can simply just say "eh, it's not physical in the same way physical neurological symptoms are.
Okay, that's a mouthful, but basically, our entire consciousness - emotions, thoughts, the places in our physical bodies we feel our emotions (and store trauma), the physical symptoms of our mental illnesses, and so forth - they all are caused by one of essentially three categories of things.
Either the electrical signals passing between neurons in a certain order and direction, hormones and enzymes and proteins being chemically processed by receptors in brain and other bodily cells (which, it's important to note, mental illness and neurodivergence exist as a conversation between brain cells and other bodily cells), or the actual physical shape of the brain.
From what little we do understand, we know that electrical activity, chemical activity, and physical differences in the brain are responsible in some way for the psychological phenomena we study. We mostly just don't understand exactly HOW.
The similarities between primarily physical neurological conditions and primarily mental neurological conditions is that they are both a result of what is occurring in the neurological system (and to a lesser extent, in where the neurological system interfaces and communicates with other systems).
Migraines, nerve pain, epilepsy, bell's palsy, Parkinson's, tremors, stroke, lateral sclerosis - these are very different from things like bipolar, anxiety, OCD, NPD, AvPD, SzPD, PTSD, DID, autism, schizophrenia, ID, and so on, for many people.
It's why you can opt out of labels like neurodivergence for conditions you don't feel it fits.
But, crucially, you don't get to make that decision and universally define the word for others. The most inclusive definition of the word prevails, because there are people who do find that their experiences with things in each of those category are similar, or so closely related they can't be separated, or simply worth grouping together for the fact they occur in the same bodily system via the same or similar mechanisms.
For me, my chronic pain, my gut health issues, my MCAS, my autism, my anxiety, my PTSD, my DID, my chronic fatigue, my brain fog, my schizophrenia, my ADHD, my tremor, my dysautonomia, my balance issues and struggles with spacial awareness and lack of awareness of my physical body, the alexithymia that I've worked so hard to manage, my language and sensory processing disorders... it's all closely and heavily interrelated.
Some of it causes or worsens other parts (or in some cases is minimally suspected to, but I'm mainly focusing on the ones that inarguably directly cause the others here). My anxiety and PTSD trigger my gut issues. Inflammation from my MCAS triggers my chronic pain and brain fog and POTS and makes my anxiety, depression, and DID worse. My dyspraxia and sensory processing are worse when I'm brain foggy or in pain. Getting excited about special interests can make my tremor worse than anxiety can. This is kind of a weird one, but self-injury from BPD has caused nerve damage. Autism and ADHD cause a large portion of my chronic fatigue.
That's without even getting into where the symptom sets overlap.
Anxiety comes with tachycardia, shortness of breath, feelings of dread/doom, stomach upset, tremors, dysregulation of my sense of temperature, flushing, and more.
POTS comes with... tachycardia, shortness of breath, stomach upset, tremors, dysregulation of my sense of temperature, flushing, and more. And MCAS covers the "feelings of dread/doom", so when they are flaring up together...
Chronic pain is a symptom of depression and PTSD as well as fibromyalgia and nerve damage. Chronic fatigue is a symptom of just about every disability that exists.
Food sensitivities are as likely to be from neurodivergence as from eating disorders (which can be considered neurodivergent) as from GI issues. I see an allergist for my condition which is caused by dysregulation of gastrointestinal cells, which is suspected to potentially be related to trauma, which is also suspected as having a relationship with the dysautonomia present in my POTS, trauma for me which is as much a result of my neurodivergence and the casual ignorant and often nonmalicious ableism ingrained into every facet of society I faced as the abuse I went through. (And some of the abuse was a result of my disabilities, both primarily physical and primarily mental!)
There is no separating it for me. They are not different enough to deny myself a label that acknowledges that and never will be. Neurodivergence and neurodisability (a term I coined) as well are as much for people like me as people who have fully discrete separate symptoms.
I even find the separation of disabilities into "physical" and "psychological" to be a bit of a misdirection. Psychological disabilities are physical. They manifest through physical symptoms. Even emotional symptoms are experienced by the body on a physical level, though a lot of us neurodivergent folks struggle with awareness of that (I know I did and often still do).
Anxiety is often a rapid heart rate and sweating and shortness of breath. Depression is pain and appetite suppression and often low blood pressure. Sadness can be chest pain and throat tightness. Excitement often has near identical physical manifestations as anxiety. Happiness is usually felt throughout the whole body. Sensations of different temperatures, breathing, pulse, and gut functions are most primarily associated with emotion.
"Trust your gut" even means "trust your intuition", meaning your subconscious mental sense of safety vs danger, for this reason.
"My heart plummeted."
"My heart was in my throat."
"My stomach was roiling with nerves."
"I felt a cold sweat on my neck."
"I knew in my gut I could trust her."
These are how people describe emotions.
Even where the symptoms are either not identifiably physical or not experienced as physical in the consciousness (such as thought patterns), they are caused by physical processes in an actual physical organ. Their cause is the same at a fundamental level as a primarily physical symptom such as pain - while they may occur in different locations in the neurological system, or may be triggered by different sets of chemicals, at a basic level they are both physically occurring in the same bodily system.
Even separating out the brain as an organ from the rest of the body has actively limited scientific progress. It's only as modern science has actually been analyzing it in concert with the other bodily systems that it is responsible for both controlling and processing feedback from that large advancements in our understanding of neurology have been made.
The organ responsible for telling every other organ what to do and understanding what happens in every other organ cannot be compartmentalized and analyzed on its own. At least, not if we want any actual useful data.
I often wonder, for people who do have discrete symptom sets, is there a reason other than simply "it doesn't make sense to group it with my other neurodivergence" for saying they "disagree" with the definitions of neurodivergence and neurodisability that they are allowed not to use for themselves?
Is it possibly that neuroableism is so rampant in our society and even in disabled spaces that they simply haven't examined their own internalized biases and bigotry and they don't take neurodisabilities, including their own, as seriously as disabilities they consider more physical?
Is the idea that they have been as physical as their other disabilities all along scary or threatening because it means that in shoving them off into the realm of "mental" disability they've been pushing themselves past their limits to "overcome" something that is just as painful, just as harmful, and just as concretely, profoundly disabling as their other disabilities? That they were just as unable to do the things their disability prevented them from doing and hurting themselves just as much by trying to and then blaming themselves on top of it for the ways they "fell short" due to said disability?
This is not meant as an attack. I sometimes have the people who say this stuff unintentionally stumble on trauma triggers, but I don't dislike them. I wish I was more capable of having these conversations without really essentially running and hiding. I try to use this blog for that because I'm able to ignore it more easily than my main blog when I'm in a heightened state, and because it's more of a controlled environment where these conversations are intended to take place.
These are questions I'm asking specifically from analyzing past attitudes of mine. I didn't necessarily share them publicly, but there was a time where I felt similarly. I'm not asking out of some concern-trolling, either. I acknowledge that what I talked about is only one possible explanation for that belief, and if that is the case, I'd simply encourage the people for whom it's true to be patient with themselves and let themselves be disabled, whatever that means for them.
I don't even think it's necessarily a super harmful belief, although I think it crosses a line when the belief goes from "that's not how I use neurodivergent for myself" to "I don't think it's useful for neurodivergence to be defined that way in general". I think it's one we should all interrogate, sure. Providing a possible explanation is my way of trying to open up a conversation about that. Eliminating a possibility as wrong still gets us closer to a more accurate understanding, even at an individual level.
I think put quite simply though, if that is the case, I don't feel condescending and patronizing pity. I'm angry on all of our behalf that we live in a society that so deeply ingrains those ideas into us in order to uphold the oppression of all disabled people, and especially to sow disunity between us to disrupt our efforts at organization and liberation. I'm angry that we've been taught to hurt ourselves in this way. I'm furious that we've been convinced that this is the right way of understanding and dealing with disability.
So, to loop back around and neatly tie this post off with my original point: I would like to motivate people to examine WHY they label certain diagnoses as neurodivergent/neurodisabilities and others as not. I would encourage them to remember that an umbrella label including diagnoses of theirs that they don't want to use that label for doesn't make the definition wrong. I'd remind them that they are absolutely welcome to use a more restrictive definition individually without challenging the general definition, because words can mean multiple things.
And I'd say that the most important thing is just to remember when discussing this is that other people may consider a shared diagnosis to be neurodivergent where you don't, and that "disagreeing" with them is fundamentally "disagreeing" with their identity and how they experience it, which however well-intentioned is still bigotry. It doesn't make you a bad person, but it is a harmful action and the right thing to do is whatever needs to be done to not continue to harm others. Whether it's as simple as just stopping or as complex as analyzing the entire lens through which you view neurodivergence, the important thing is respecting that neurodivergent identity means different things for different people.
And after all, at least in English, 95 percent of the 3000 most frequently used words have multiple meanings, as do 100 percent of the top 1000 most used words. Words like go and set have upwards of 300-400 definitions! Rather than treating definitions like a math problem, right or wrong, let's treat them as interpretive, and facilitate communication by asking people which they mean.
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