That’s why you call them impairments. (From Late Latin peiorare "make worse”.)
Why not? I have several traits I consider abnormal, and some I consider negative (i.e. unlike the merely abnormal ones, I wish to overcome them. And some cannot be overcome but are very normal - e.g. mortality.) - why should that characterization impair my effort or desire to survive and thrive? Or rather, why does it impair yours?
> There’s an approach out there called the “social model” of disability where impairment is regarded as a neutral (neither good nor bad) experience and the good or bad experience is how the impairment changes interaction with society.
If I may speculate, is this the answer? You want to be seen as good and desirable by society, so if any of the multiple meanings of a word used to describe you carry negative implications, that results in a reduction of your self-worth? Even when a word is merely objective description, used without moral baggage, its mere proximity to alternate meanings taints it?
A jerk is going to be a jerk regardless of the specific syllables used so why trip up well meaning people.
It was my impression the word latinx was generally mocked by people it's supposed to represent.
Latine:
- Lah-teen … rhymes white latrine
- Lat-ein-e … normal “lat”, Germanic pronunciation of “ein”, like the number one or Einstein, “e” pronounced either “ee” or “eh”
- Latin-e … latin-ee, rhymes with matinee,
- lat-tine … lah-tine as in the tines of a fork.
Or my favourite
- Latin-e … just “latin” but spelled with a silent “e”.
This is less than ideal… outside of using mispronunciation as a shibboleth, you normally want a group identifying word to be clearly identified and picked up by any possible group members regardless of if they have heard someone speak it. You want such words to be easily used by the people who identify with it, also crucially it’s self-adoption by the group that is being identified that matters… If no one you would call latine likes you calling them latine, or latinx, or Latino or Latina or Latin… you probably should just ask them what they want and call them that instead, that’s just my opinion from over in Australia where this particular identity/word fight appears to have mostly gone unnoticed against our own local issues.
https://en.wiktionary.org/wiki/latine#Pronunciation_3
Admittedly the question of how to pronounce a Spanish word in English is non-trivial and subsumes the question of how to pronounce Spanish and the question of how to pronounce English ... but apart from that no special case is required for the word "latine"!
It's not the "correct" term, and almost nobody I know of takes it seriously outside of really, really narrow little social media woke bubbles. If someone is a woman and of latin american origin, they will almost universally refer to themselves as latina and not care if others do. What idiotic nonsense to assume that something else is "correct" despite it going against the grain of a vast majority's word use.
I live in Latin America and have latin american family of all kinds. This aside from many friendships of both sexes and variable gender identifications too.
https://www.politico.com/f/?id=0000017d-81be-dee4-a5ff-efbe7...
I suffer from mental illness as well (a disability), and I certainly don’t consider myself normal. I’ve overcome my issues, and I’m perfectly happy talking about my experience at/in appropriate times/places. I just acknowledge that the average person within the realm of normal can’t relate to my experience.
Coincidentally, I get the most relatable feedback doing inspirational speaking at homeless shelters; there’s nothing about my life today that would indicate they consider me normal in their sphere. I’m all for learning to use the right language when talking to folks with disabilities, and your comment here seems insightful. I’m just not making the connection you’re trying to build.
Fundamentals: the social model essentially places the onus of accommodating disability on society as a whole rather than the disabled individual. A simple example is the difference between asking a person who cannot walk to climb stairs vs providing a ramp. The stairs represent the typical medical model (the disabled individual must adapt to how society works) and the ramp is the social model (society should adapt to how disabled people work).
It’s not so much about being normal as it is about _feeling_ normal. Viewing the world through the lens of the social model allows me to say, “this situation could be better” rather than “I could be better”. This is important became sometime the latter is impossible — there are features of my body that cannot be improved.
I’m pragmatic about this, BTW. I don’t think we should rebuild every aspect of society to accommodate the minutia of disability. I think it should be an aspirational value that we hold and act on when we can.
Does that help? I can talk about mental health in this context as well, it’s just a lot to put into a single post. :-)
Example: chronic pain messes with your ability to recall. These days I have more trouble recalling facts than I used to. This makes programming hard, as much as programming is about intuition and problem solving, it also depends on memorizing a lot of facts (what was that built-in function called again…?)
I started using Copilot a few months ago and, while I almost always reject Copilot’s suggestions, it’s been amazing for remembering names of things. For me it’s been much better than an IDE (for example) because it presents the things I have trouble remembering with some context code.
The good news is that after middle age, my immune systems seems to have mellowed, so now I actually can do normal things my condition precluded me from, like eating avocados or shrimps, for example.
I have mixed feelings about the things in this list. E.g. part of my disability experience involves my mental health and, when you’re talking about me, anyway, I don’t mind the term “mentally ill”.
On the other hand, it sort of irritates me when people who are well describe others as “crazy”.
Regarding your comment on disability being “abnormal and negative”, though, I have to disagree. I would not have survived the last few years if I had characterized my impairments as being abnormal and negative.
There’s an approach out there called the “social model” of disability where impairment is regarded as a neutral (neither good nor bad) experience and the good or bad experience is how the impairment changes interaction with society. It’s worth reading at least the introduction on the Wikipedia page, so I’ll link it.
Happy to answer any questions if you have ‘em!
https://en.m.wikipedia.org/wiki/Social_model_of_disability
Edit: To be clear, I’m just thinking about the list of words, not any sort of policy about what one can and can’t say. That’s a whole other can of worms!