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I'm March. I'm multiply physically and psychiatrically disabled. not gonna list all my shit here. i use xe/they/fae/he/she pronouns. i'm queer. treat me like a decent person.

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@chthonic-pain
Welcome to this blog.
new pinned cause the last one was tmi
I'm March. I'm multiply physically and psychiatrically disabled. not gonna list all my shit here. i use xe/they/fae/he/she pronouns. i'm queer. treat me like a decent person.
Every time I express that I think it's shitty to say that genAI "hallucinates," people get weirdly pissy and combative with me.
But until real human beings who experience hallucinations are treated like human beings worthy of respect and dignity...I think perhaps it's shitty to keep associating hallucinations with being non-human, dangerous, and a liar.
It actually really fucking sucks that hallucinating is seen as monster-movie-scary, dangerous, inhuman, and worthy of scorn and/or mockery. It actually really fucking sucks that people who hallucinate or experience delusions can't get compassionate help or understanding, because everyone thinks it's an automatic sign of being dangerous, violent, and a liar. It's a massive problem that people look at hallucinations as "dangerous crazy person shit" that should be gotten rid of or locked away.
I find it crass, at best, to flippantly use the term "AI hallucinations" when real-life people get abused, imprisoned, and killed because they experience hallucinations.
But what do I know, I'm just a crazy person. ¯\_(ツ)_/¯
People in the notes keep proposing alternatives or asking me what they should say instead, and I really think y'all are overthinking it. You don't need to coin an entire new term. You can just say "AI generates misinformation." If you need it as a noun, "AI misinformation."
If you want to be provocative, "AI spits out garbled bullshit" works, too.
people dont get how exhausting it is to have so many different conditions. especially when theyre so heavily misunderstood and demonized in media. because even when people have heard of your conditions you still have to explain it to them & constantly correct them on shit the media gets wrong. & then you have to do it over again with the next condition. and the next. forever and ever until you die
I love informed consent, I love dignity of risk, I love the thought of having someone willing to tell me why the thing that I'm about to do is a bad idea, telling me in detail exactly what the consequences are, what's going to happen and why, and what's the worst that can happen, and then having no power to stop me when I decide to do it anyway because I'm an adult and I'm allowed to get my shit kicked in so fucking bad while doing something stupid if I so choose.
reminder to all disabled people that you’re allowed to tell people “i can’t do that” about stuff you can ‘technically’ do but which harms you or requires a period of recovery or preparatory rest etc. you don’t have to explain the complex nuances of your condition to anybody who demands it. i’ve found it’s honestly better to give the least amount of info about your symptoms unless you trust a person a lot. you hold the power over your health information. you choose whether or not to share the details of your condition with people who might not understand.
girl with ptsd voice: hey, so something really bad is gonna happen, right? you guys are picking up on that too, yeah? The other shoe is about to drop, I just know it.
Happy disability pride to people who are suicidal because of their conditions
Happy disability pride month to everyone with ptsd, happy disability pride month to everyone with complex ptsd, happy disability pride month to everyone who questions if their problems are big enough to count as a disability, happy disability pride month to anyone who questions if their problems count as a physical or mental disability, happy pride month to everyone who has a disability that causes people to stare, and to those whose disabilities are hidden, happy disability pride month to everyone who deals with any kind of disability physical or mental, you’re all badass and I want you to remember that this month okay
this disability pride month lets be kinder to folks with moral ocd . no more “if you really care about this minority , you’ll reblog this post” , “someone will die if you don’t reblog this” , etc etc , and all other kinds of guilt tripping reblog bait . at the VERY LEAST tag your reblog bait so we can filter it out and avoid unnecessary spirals . it’s 2026 , we need to move past using guilt to get engagement .
you are not immune to inventing an arbitrary set of rules that only you have to adhere to
daily affirmation i do NOT have a secret disgusting evil hidden within me that will some day make its way out
OCD Heritage Post
Quick shout out to the Down syndrome kid from my after-school program back when I was in grade school. Like yea he had the usual issues but he was a sweetheart and quite funny; and one day both his parents showed up at the same time to pick him up and I had the experience of meeting a family of genetically disabled people that had jobs and a home and a kid in school and it was a profoundly normalizing experience for me like I couldn’t take eugenicists seriously after that because like “no they totally can have whole entire meaningful lives with marriage and children and work and hobbies have you not met Dennis??” Anyway quick shout out to Dennis you were a real one
pedestrians don't seem to realize how exhausting using a wheelchair is, both manual and powered. i had to wheel around a hospital today with several ramps i had to go up and down multiple times, and even with my smoov i ended up with shoulder and chest pain and deep exhaustion.
people look at wheelchair users and think "well you're sitting down all the time that doesn't take effort" no actually it does. pushing a manual chair takes a lot of fucking effort, especially without a power assist. repetitive stress injuries are a huge problem manual chair users encounter all the time. going up hills and ramps is so deeply fatiguing.
this doesn't just apply to manual chair users btw. power chair usage can also be really exhausting, especially for people with complex seating needs. going over bumps and cracks can trigger many symptoms such as spasticity, pressure sores are common, even just sitting upright can be exhausting for many people.
basically don't assume using a wheelchair takes 0 effort, it really really does. getting to "sit down all the time" doesn't mean it's easy.
i wish there was more social existence you could participate in laying down. I wish there were cafes that were two little futon beds parallel to each other with a low table in between so you could eat and drink while lounging. I wish there were group activities like painting or glazing clay or theaters that were designed to have beds and bed-height tables instead of chairs. I wish there were beds alongside benches outside for anyone to use. I wish air mattresses or roll-out beds were as common as cheap shitty chairs at things like barbeques, beaches, and concerts. so much life would open up to me and be enjoyable if I could lay down instead of sitting or standing for prolonged periods and completely wearing myself down with pain.
can we get some rollator and walker appreciation 🗣️‼️ i see a lot of cane and crutch and wheelchair appreciation but where's the love for rollators and walkers ‼️‼️‼️
abelds have this funky ability where they hear disabled people say they "can't" do something and instead of hearing "can't" as in, cannot, they hear "i can if i push myself and i just don't wanna". which is really interesting!