According to the responses to the 2021 American Community Survey available on the US Census Bureau website, approximately 13% of Americans self reported some form of disability. Initially, I thought that this was a high value simply because there's so little perception of it in media, unless that media is specifically designed to show people with disabilities. But then I looked a bit deeper into it. Nearly 50%(it was like 48 point something) of those who reported a disability reported an ambulatory disability. Given this figure, I wonder if the percentage is underreported. A lot of mental health and disability has only been accepted in mainstream media in recent years. There are also questions I have like:Do correctible vision deficiencies count as disabilities? I would argue yes. I wear glasses. It's not something I think about a lot, but without my glasses, I would be hard-pressed to function normally within society. They are an accommodation. Yet in a group of 25-30 people(the class i was in when i was thinking about it), I easily counted at least 5 who wore glasses. Obviously, that's not a large enough sample size to make any kind of assumption off of, but I think I could probably find similar numbers if i looked in other places. Part of me doubts that I was marked as having a vision difficulty despite having and wearing glasses. And it's made me think and wonder if 13% wasn't that large of a number after all. I mean, it's a massive population. It's 42 million people, but I wonder if the number is even larger than that. What do you think?
So, I think it's complex. I'm not saying you are wrong in your investigation, but due to the personal nature of disability, it makes me wonder, too. I think the answer will be just as complex, is what I am saying.
Simultaneously, disability is very common, but the idea of being "unable" to live or be productive makes it so that disability becomes a taboo. It leads you to believe that disability is uncommon, or only exists in the "extremes". I do think that contributes to the perception people have of their disabilities, especially in being in denial about their disabilities disabling them.
I think you can generally say that certain things, like eye vision, can be disabilities, as long as we also recognize that it exists on a spectrum. I also have eye glasses, but if you ask me what I'm disabled by, I probably wouldn't bring that up unless it is relevant, in the narrow ways it is for me personally. I think that's part of why the ambulatory statistic is high. There are many situations where your disability doesn't really... disable you, but you're still disabled because there are aspects of your life you either cannot do, or you need help in order to do.
Thirteen percent is a large number, but when you consider the vast array of disabilities, the number of veterans and elderly, and (like you said) the number of people likely either in denial about their disability or the people for whom education doesn't include disability, the number could very well be thirteen or higher.
It's interesting that ableism is so ubiquitous, yet so many of us are disabled (with or without our knowledge).
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long rambling personal about chronic pain under the cut
on thursday's pt session they were having me work with someone different cause my usual was taking time off. he asked if anywhere hurt more during an exercise and i said my knees and he got all serious and had me do a thumb hypermobility stretch and asked if eds runs in my family, if i experience any other joint pain and for how long. i told him 'uh idk' and 'yes all over' and 'as long as i can remember but it's gotten really bad in recent years and i also have nerve pain' and then we just kinda looked at each other. and then he was like '...alright keep going with the exercise, i'm thinking' and at the end when he said goodbye he seemed like sad or guilty and opened the door for me and i didn't realize why at the time because the session had been harder than any of the others but not like insane but OH MY FUCKING GOD has my pain been bad this weekend. it's times like these that i'm glad i live with my family.
and also. i researched eds in more depth and. it's fucking uncanny. how the hell did this not come up when i was researching before because it is like exact and touches on some symptoms i hadn't even considered to be related to my pain. if it's not heds it's probably hsd i guess?? which is
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sighs, y'know I don't talk about it much on here, but I do wish fandom was....better. I wish it was better! I wish that there was an air of community again, where people aren't bullied, or compared to one another, where there's no sense of competition because everyone's gettin' attention. I wish artists (fanartists, writers, graphics and gifmakers and fanvidders and everything and everyone in between) were more appreciated. I wish people didn't have to use the block button so liberally. I wish fandom experiences were more positive, end of, because I am so....so tired of hearing absolute horror stories of how people I know have been treated in fandom, or hearing stuff in my periphery. I wish fandom was a celebration of love again, something that lasts for a good long while. I wish it could be a positive experience for people, instead of something awful that turns them away from stories that mean so much to them, because of the grief and bitterness and anxiety that fandom drowned it in.
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I got sad because I realised that it’s been 5 years this September since I was diagnosed with my first mental illness, and now, 5 years later, I’ve been diagnosed with 10. Because I was 14 at the time, so much of my identity is wrapped up in one disorder or another, which I think is unavoidable if your teenage years are spent in excruciating psychic pain which you were lucky enough to have diagnostic labels for.
The problem is I don’t know how to disentangle it and form my own identity now. For better or for worse, almost every action I take can be explained by a disorder.
However, I’m going to start making a distinction to myself. I think the lines are blurrier than I want to accept. Something might be partway caused by a disorder but also part of me, and it doesn’t have to be solely one or the other. My disorders are a part of my personality and they affect the way I think and act, but they’re not the only part of my personality. My kindness and thoughtfulness and resilience may be influenced by my disorders but they are mine to claim and mine to have, regardless.
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can you do a meme/prompt list about chronic illness, pain, or even terminal illness? i know it's a potentially triggering & heavy subject but it's something that i'm dealing with and i find it really, really, really cathartic to write those sort of subjects out. if you're uncomfortable with that sort of thing, i totally get it & understand! i figured i should just ask <3
hi my love!! i want to start off by saying that i'm absolutely good to go to take on the chronic illness/pain angle, but i would like to take my time with it and do some research so that i can at least try and make it respectful and accurate, you know? but i'm not leaving you with nothing! an absolutely FANTASTIC meme maker, @rpmemes-galore made a list of prompts for that purpose, and i'm going to pop them under the readmore for you to use. again, i'm not saying no!! i'm just saying that i'd feel much happier giving ye a list of memes that i'm knowledgeable of and able to say "yes, this seems accurate to me, i researched it through many reputable sources and perspectives" you know?
thank you for the request, and for the space to decline it! i completely understand the catharsis in writing out these subjects, and that's why we're here, so we can have that experience in a safe zone. i'm truly so sorry that you're dealing with such a heavy situation, and i hope that these prompts, and the prompts i'll eventually post, will offer you the catharsis you're searching for.
i wish you all the best, and all the love i can give.
blue.
LINK TO CHRONIC PAIN PROMPTS.
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