I really don't think a lot of abled and low support needs disabled people realize how many of us rely on the kindness of others to stay alive. Imagine if your entire survival and existence was pinned to being likeable enough.
Friendly (or unfriendly if you're against this) reminder that this blog is supportive of ALL disorders. This blog does not think ANY disorder inherently makes someone a bad person, and is against any disorder being demonized. This blog wholeheartedly believes that a bad person having a disorder, yes, even if things that are also symptoms of their disorder are part of what caused harm, does not make the disorder a "bad" or "evil" disorder or excuse ableism and demonization directed towards the disorder.
Yes this includes personality disorders
Including npd and aspd
Yes this includes all psychotic disorders & disorders that cause psychotic symptoms
Yes this includes paraphilic disorders. All of them.
Yes this includes disorders that cause, or are even characterized by, attention seeking
Yes this includes disorders that directly have lying as a common symptom
Yes this includes dissociative disorders
Yes this includes any disorder with "gross" symptoms
Yes this includes physical disorders too
Yes this includes disorders that can cause loss of control of any kind- control of speech, control of body movement, etc.
Yes tis includes disorders that make someone "look scary"
This goes for literally any fucking disorder. There are not exceptions.
It's so weird to me when people are like 'but that will cost the government money!' So what? They're the government, they're supposed to be spending money. What, you want them to take your tax dollars and then do nothing with it? Lock it all up in a big government vault and just look at it? Why are you so scared of giving a third grader lunch or a homeless person a house.
Why is it so hard for people to be empathic towards others? Like not even just strangers cause, sure you’re gonna meet a dick every now and then, but like family?
My sibling could not understand the fact that I cannot sleep in a “normal” schedule. I literally cannot fall asleep at night if I am not exhausted from staying up way too long. If I try to go to sleep before midnight, I won’t fell asleep and just roll around in bed and get anxious for not sleeping in the correct time and then be awake even a longer time. I have cried so many nights cause I was stressed about sleep.
I was certain that people could understand that all of us are different people and that sleeping schedules do not always fall in the correct way, but no. They were adamant that I just haven’t tried enough and that I could fix my sleep by just going to be earlier, but like no? Wouldn’t one think that if I have had these issues since I was born that I have tried to fix it? I haven’t been twiddling my thumbs about this. Being undiagnosed ADHD is already bad enough, not getting sleep is even worse.
I pulled out so many different researches and different medical diagnosis, but no. Nothing. They have never had issues with sleep, so ig it just doesn’t exist ¯\_(ツ)_/¯
It’s also so much fun to explain that cause of ADHD there is stuff that I just cannot do. I just cannot make myself do them and there is no way to go around it. There is a mental block that keeps me not doing stuff. I just don’t get it why can’t people understand that sometimes people just can’t. There is no way to push forward and sometimes there is just stuff that cannot be done. Thank god for the meds helping a little bit with the mental block and all. I’m just so tired of needing to explain myself every time that there is a conversation.
"If tampons should be free, then so should my diabetes meds."
Yes? Yes they should be? Your life-saving medication that you need in order to live for a condition you were born with should be given to you at no cost?
"That's not autism, they need help"
"That's not an autistic thing, that's wrong and they need therapy"
"That's not because of autism, they shouldn't be let out of the house"
Often, it IS autism. Often, it IS because of autism.
But a lot of those symptoms/behaviours tend to be labelled as "bad autism" or "scary autism". Due to that, it becomes a taboo topic to talk about in public spaces, in online spaces.
There has been a lot of backlash in online autism spaces when these very common and real behaviours of autism are talked about, and it needs to stop.
Just because you don't relate to it, or don't want to be associated to these behaviours doesn't mean it's not real for autistics to experience due to their autism.
It is so important for the "bad" symptoms, the "scary" symptoms to be talked about in autistic spaces. People need to be educated about the whole spectrum and how it presents, not just the "quirky" side of autism.
When you refuse to acknowledge these as autism things, you are actively hurting a part of the community that needs the most understanding and support.
you might have been on this earth for _____ amount of time as a disabled person but you will never know yourself better than a middle age person trying to cure your disabilities
Drag King Portraits, London, Paris & NYC, (1995-1996), The Drag King Book, Del LaGrace Volcano
when disabled people talk about fakeclaiming, i think most people on here think we’re talking about rude anons, or some stranger on the bus saying you don’t really need that cane. But we’re also talking about like. The social security administration. Doctors who are in charge of treating us; who deny care because they think we’re faking. Family members who withdraw material support because we aren’t improving when they think we should, and refuse to look for alternative caregivers. And this kills people. Disabled people die without benefits that would keep us housed and fed, without necessary medical treatments, without our care support systems. Fakeclaiming isn’t just rude. It’s deadly
Just to talk and enjoy my stuff. I have two side blogs ;) Read my pinned post ! Humans are fascinating
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