some of y’all will be like “yeah i support autistic people” and then go bully the weird kid at school
I don't want to detract from a post so I'll give my rant here.
Have you ever seen that post about where Rogue is asking if mutants could really be cured and Storm said no, because there was nothing wrong with them? And people were calling Storm's ability one to "make clouds" and really taking the situation at face value? Storm was right.
First off, Storm's ability isn't just "make clouds." Her ability is omega-level- for the record, that's the second most powerful level. It means her powers do not have an upper limit. Storm is an incredibly powerful mutant and she had to learn to control herself from a very, very young age. Because Storm's ability is far more dangerous than Rogue's could ever be.
To start, when Storm caused weather to happen somewhere, she was basically taking that weather away from somewhere else. If she were to use her power to summon rain and end a drought in one place, she would be taking that rain from someplace else and could cause a far deadlier drought without realizing. Ororo was told this at a young age. There is absolutely no safety in her "making clouds." She has to be extremely careful what she does or she could cause a catastrophe.
Additionally, the level of power Storm has is literally world-ending. If she wanted to, she could wipe out continents, even the world. If she lost control of her powers, she could kill hundreds, thousands, millions, billions. Ororo was a child when she manifested. In some canons, she was a child when she learned exactly how powerful she was. But, child or teen, she still had to adjust to exactly how dangerous she was. She had to look back and see how many times she could have ended everything. Such difficult lessons for a child to learn, but she learned them.
Storm's control is legendary. She had to learn to keep her emotions completely and utterly in check as they react hard when she's upset. To keep omega-level mutations under control as perfectly as she does is one thing. It's infinitely more impressive that she has as much control as she does when her powers are triggered by her emotions. Storm's ability to exist without being a constant threat to everyone around her is the product of years, maybe decades, of hard training to keep herself in check.
Storm does not just make clouds. She absolutely knows what Rogue is going through. But Storm is also old enough to see the full picture.
Number one, Rogue has only recently come into her abilities. Control very much could be possible for her. She's new to all of this.
Number two, there is no evidence that the cure is safe. Given the amount of genocide that goes on against mutants, the older ones were probably worried it was yet another attempt at wiping them out. Even if it wasn't, what if it hadn't been properly researched? What if medical trials hadn't been done properly? Had they bothered to look into what a "cure" would do to someone with a physical mutation like Wolverine's? There's so much unknown and the adults all know it. They don't know enough to know if this is dangerous.
And number three, the cure was dangerous. As Magneto says, how long before parents had the right to force this cure on their children, employers on their employees? How long would it have been before the cure became mandatory? They could not trust humans with a cure because humans were demonstrating a long history of wanting all mutants gone. Hell, humans literally weaponized the cure, shooting people with darts and forcibly injecting them with it, in the same movie! How long would it have been for them to go mask-off eugenics and genocide? They couldn't even make it the full movie without proving Magneto right, that this cure was going to be used to hurt them.
No matter what, the cure was a bad thing. Storm had the wisdom to know that. Rogue didn't.
This isn't comparing autism to depression in the "wanting a cure" debate, this is two high-support-needs autistics debating the autism cure thing. One desperately wants to not be autistic, the other understands that the cure is potentially unsafe and has some extremely dangerous implications. Maybe, one day, Rogue could be cured if she wanted to be. But that cure existing then, when people hated mutants, was only going to end in eugenics and genocide and could only be a bad thing. Regardless of the good uses of it, it would be used to turn all of them human.
Storm knew what she was talking about. Stop acting like she didn't.
Does anyone here have any experience with Intermittent Explosive Disorder, or know anyone who does? 😕
had an interaction a few days ago that i’m still thinking about. I was talking to two students about the Day of Silence protest coming up that friday, and both of them seemed interested but needed more information. Both of these students were disabled with relatively high support needs for communication, processing, and learning. At least one was intellectually disabled.
I explained the basic premise of Day of Silence, and one of the students asked me to repeat myself, explain again. I did this several times, and she was engaged with me, even if she wasn’t processing yet she clearly wanted to know more and was interested in what i was saying. Her para-educator then came over and said it wasn’t worth trying to explain anything to her because she wouldn’t understand.
The para-educator’s intentions were good, she wanted to save me time and believed i may not have known this student was disabled. But to say that, in front of the student, as though she couldn’t hear the comment, is rude at best and downright hostile at worst. Furthermore, to be in a position in which you are the one in charge of helping this person navigate the world, and to believe they only deserve information that you think they can digest, is such an awful way to view someone you are supposed to help. This student was asking me questions, she was listening, and honestly - who cares if in the end she didn’t understand? just because we don’t end up understanding something doesn’t mean we can’t engage with it.
Intellectually disabled individuals and disabled individuals in general are not infants, they’re not incapable of learning or connecting with others. Yes, they may need extra help, and yes, some topics may be too complex for them to tackle, but let the individual decide that for themselves.
TLDR: The person who was supposed to be helping an intellectually disabled student navigate the world decided for that student what they could understand. In doing so, she projected her beliefs about the students abilities and overshadowed the student’s ability to define her own boundaries. Intellectually disabled people deserve the autonomy to decide for themselves what they want to engage with at a given time, not told they are too dumb to understand.
Communicating about problems is hard for me.
I don't know why. If I'm having a problem like I'm sick or I'm having a migraine or I can't do something, I can't just tell people that verbally. It gets harder to make my thoughts come out of my mouth. I stutter and I pause and I use a lot of filler words and even then, usually I can't actually say what's wrong. If I can manage to say it, I can't... like, if I tell my manager that I can't do a specific task right now and she pushes back and says there's no one else to do it or that if I can't do it she'll send me home, I can't stick up for myself. The second I meet a tiny bit of resistance, I always fold. I always try and force myself to stick it through. Even if it's an issue where I really, really need to go home, I can't communicate that with my words.
Writing out what I need to say is better. I can write out my thoughts and feelings way easier and better than I can speak them. So I write down what I want to say. I explain the issue, and I explain why said issue is causing a problem and why I need some intervention here. But even then, actually communicating with that is hard. Because it's hard to just hand my manager a note. It feels weird. Like, socially, it feels like I thing I absolutely should not be doing. But say I manage to give her the note. Now I need to explain why I am handing her this note and we're back to the first problem. And if she chooses to push back, I still can't help but fold.
I don't know what it is. But it's hard to deal with
Have you ever been writing a disabled character and wished there was just one great source on as many pieces of adaptive technology, medical equipment, accessibility devices, and whatever else have you as possible? Have you ever spent hours scouring the internet trying to find a source with everything your disabled character might need?
Well, have I got a site for you.
Rehabmart is an online store with a catalogue of thousands of rehabilitation, medical, and accessibility devices, ranging from simple things like canes to major medical equipment like cardiac catheterization items, all listed with what the items are, what they do, and even how they help certain symptoms or non-specific conditions. All of this is sorted neatly into several dozen simple categories on this page here. The information provided on the site may not answer your every question, but it's a fantastic starting point for the largest range of items I've ever seen from one source.
Consider checking it out.
(Disclaimer, I am endorsing this site as a writing aid, not as a place to buy medical equipment online. Please only buy equipment from sources you can trust to be safe.)
To my knowledge, my hair started turning grey when I was ten. But, from what I remember, I was super surprised to find a grey strand so it might have started sooner than that. My hair has also steadily been getting greyer since then.
When I talk about visible autism on my blog, I’m usually not talking about those who are clocked as quirky and weird. Although that’s completely valid, I’m not talking about them. I’m talking about those of us who are VISIBLY autistic. Those of us who are clocked as those autistics. Who are clocked immediately as having something wrong with them. Those of us who are named as slurs. Who are yelled at. Who are attacked. Who are glared at, pointed at, stared at, pitied. Those of us who are automatically assumed to be with caregivers. Those of us you see talked about in medical journals and on the news as “inspiration” when we graduate or get invited to prom.
This is us. This is who we’re marked as. This is who we are seen as. We are seen as less than, as animals, as objects, as “inspirations”. When we accomplish something it’s usually not seen as our accomplishments but as the accomplishments of our caregivers and support staff.
I get so mad when someone comes onto my blog, MY blog. Me. A visibly autistic, nonverbal person, and doesn’t even look at my tags or pinned post and says “Omg me too, I’m seen as quirky and awkward, I’m visibly autistic 🥰” and like…go you but I’m not talking about you. I’m not talking about “low masking”. Im talking about LOW masking. No masking or very very low masking. Those of us who are immediately seen as autistic.
And it’s frustrating. It’s frustrating when people come into my blog and say this because, you DON’T get it. You just don’t. You don’t get what my life is like, what my experiences are. What it’s like to be LOW masking or no masking. You don’t get that. And yet you try and squeeze yourself in. And that hurts. It hurts to have people who won’t ever understand this squeeze themselves in. Stop doing this.
hi! i just started this blog as a safe space for compulsive/defensive liars to vent, and find community and support. you deserve to be supported in your recovery! this will mostly be a place to vent, so please submit asks or posts of your experiences that you need to get off your chest. i will also be posting/reblogging some recovery/positivity stuff as well.
Raven, he/him, 20, multiple disabled (see pinned for more details.) This is my disability advocacy blog
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