Can you do an age of onset poll for phobias?
Yep!
*this does not mean when you first realized that they are symptoms. But rather in retrospect when you looking back, with the context of the disorder, remember symptoms starting.
Can y'all please stop using words like "delusional", "psychotic", and "narcissistic" as insults. These are terms used to describe mental illness. Mental illness does not make people evil, stop acting like does.
Pyromania centered blogs
Pyrophilia list(wip)
Feel free to ask to be tagged or untagged, generally listing blogs we see most in pyro tags
Our own:
This one as well as @pyrocultureis and @bleu-flame
@burning-for-eternity
@cerviderous
@pyro-baby (last active 2023)
@wilczak
@abiggerbug
@ignis-and-pyromania (last active 2019)
@pyromaniad (last active 2021)
@always-an-angel-never-enough (has pyromania related posts, seen in pyro tags, warning in their bio for other content)
@pyromaniac-within-you (last active 2020)
@p-y-r-o-m-a-n-i-a-c (last posted 2019)
@pyromaniacs-and-flames (2019)
@pyromaniac9
General pyro safe blogs
@clusterrune
@edrecovery-space
@yandere-culture-is
@objectumluv
@fantasy-store
@vineyard-edits
@m4l4rky
Please feel free to suggest blogs to be added or other content we could make for the master list
Good morning to people who grew up and became pathological liars and now are attempting to stop Doing The Thing, you’re doing great
so here’s a quick lesson about having patience with kids.
I have a 6th grade student who isn’t really interested in doing her homework (big surprise). from my experience, kids who aren’t trying to do their homework usually fall into two general categories – “this is too easy and therefore boring” and “this is too hard and therefore i’m not even going to attempt”. it became clear by October that she fell into the latter group, but most of the staff chalked it up to “she doesn’t understand it”. I didn’t really believe it because she was a very smart, emotionally aware girl and it didn’t seem like she didn’t always want to try, just that she would rather do other things than struggle with her work.
yesterday, she got sent to my office, just so that she would have a space away from her friends to focus on her work, and she asked me to help her with two questions. I looked at them and they were fairly straightforward, simple questions about the results of using various amounts of force on an object. I did what I always do – I read the question out loud first, and then tried to help her use recall to figure it out. she did in a snap. I did the same with the second question, and before I even finished it, she went “OH!” and started writing her answer.
that’s when it hit me – she doesn’t have trouble with the material, she just has trouble reading and processing what she’s reading at the same time. big difference! I asked her and she confirmed that it was easier to hear a question and understand it than to read it and understand it. so I got her phone out, pulled up her voice recorder, and told her to try reading the question aloud and then playing it back to herself so she could process it and she looked like i had handed her the holy grail.
the moral of the story is that sometimes you have to set aside what you think is a problem with a kid and just watch for what’s easier for them. will she be able to do that during a test? maybe not, BUT now that she knows that the issue is processing reading and that she’s an auditory learner, she’s in a better position to ask for resources to help her work better in school.
so i’m off to the school counselor to let her know so she can possible get more tools for auditory learners.
I think I might be relapsing.
I don't even want to really say it because I'm afraid the second I say "I think I'm relapsing into compulsive lying," everyone is going to think everything I've ever posted is a lie and nothing I'll say will ever convince them otherwise. But I am. I am relapsing because of the situation at work and because I'm scared to go into work every single day and that's just making my mental state so much worse and now I'm compulsive lying again.
At least this time, unlike when I was younger, my lies are believable so I'm not getting caught when it happens. It might landslide back in that direction, it might not. I hope it won't. I'll try and talk to my therapist about it and see if we can figure out how to fix this.
This sucks. It could be worse, but still, it sucks.
(And no, before you ask, I'm not lying about the stuff I post online. Because online, I type out the lie but realize it before clicking post and I can just delete it. For me, compulsive lying is only really an issue in my real life. I can stop myself from lying online. And if I do lie, I can always delete the post fast. I'm not lying.)
Saw a post and it really got me thinking.
The post was talking about why don’t lower support needs, higher masking individuals even believe that higher support needs, low masking, “severely autistic” people, exist. And that got me really thinking. Because, I do think they know we exist. I just don’t think they want too.
I don’t think they want to know we exist. They know we exist, but keep us on the back burner. They live in ignorance bliss of us. I have what some people would think of as severe autism. Im nonverbal (although nonverbal later in life. But outside people don’t care about that. They see nonverbal as nonverbal), I’m intellectually disabled, need help in everyday life, etc. but I’m in the middle. I’m moderate support needs. To me, I’m not severely autistic. But to society, I am considered and seen as severely autistic because society doesn’t have the understanding of moderate autism yet. They don’t understand it. And I’ve seen more times than I can count that severe autism doesn’t exist. Not because they don’t believe in severe autism the label itself because it’s “harmful” but because they don’t believe that it’s just caused by autism. They often believe that’s it’s caused by comorbidities. Like ID, or cerebral palsy, or apraxia/dyspraxia, or mobility issues, or genetic conditions, and so on. Although none of this is bad.
They believe that autism itself can’t create severe autism. Which…isn’t true. Before, it was believed that severe autism was the only type of autism. That it was the only type that existed and if you weren’t severely autistic then you weren’t autistic. Then more research happened, then social media happened, and now..white, lower support needs, high masking, late diagnosed individuals are the majority of what’s being centered. And, that isn’t bad. We need awareness of all autism. But when one type of autism gets centered, it becomes a problem. It becomes the new norm. It becomes what everyone expects out of autism now. Which, isn’t true. Autism all of all types and traits exists. Autism of all support needs exists.
When people say severe autism doesn’t exist, they’re ignoring and saying that a BIG percentage of autistic people don’t exist. They’re saying that we aren’t real. That we aren’t on the internet, or in the communities they live in, or in their schools, or whatever. We’re everywhere. Severe autism is still a thing. It isn’t a misdiagnosis. It isn’t from comorbities, although if someone’s autism is more severe from comorbidities then that isn’t bad.
I think a lot of people need to be more aware of severe autism. And not just severe autism like me or my mutuals, or the people you see here on tumblr. But the ones with even MORE severe autism. The ones who live in group homes, residentials, institutions, and so on. The ones who aren’t on the internet. The ones who aren’t here blogging about their lives. We need to be aware of them too. We need to believe they exist, and believe that their autism is real.
Don’t erase severe or profound autism.
people who have meltdown because " small " thing go wrong - always bigger than people believe .
people who get angry and defensive when someone try bully and hurt - can not " just " ignore like everyone say .
people who feel actually violent when something upset - who need time and place to go hit things , so that not hurt people .
people who can not understand how stay calm and walk away - who instead get frustrate and say shut up go away .
and anyone else who relate to this - that can not control how react , not so easy like that .
there is benefits in have skill , but , not deserve to beat self up for not have skill . people should support if or when try learn , but also , should support even before learn , give outlets and patience .
some people will forever have less skill , because brain physically can not adapt and learn right . some people have episodes and crises where control impossible . still do not make bad person . still deserve support .
Hi, guys. So, just to warn you, I encountered an ABA "therapist" (child abuser) in the wild today so I'm saving a lot of posts that are very anti ABA and Autism Speaks. Don't know when I'll reblog them but all will be tagged as ableism, plus specific tags like "aba therapy" and "autism speaks"
[Plain text: That's not how telekinesis work]
(Disclaimer; I am not paraplegic, just a nerd)
Stop making Charles Xavier use his telekinesis to walk.
In order to do that, he would need to concentrate extremely hard and it would be very complicated. Keep in mind that he readily admitted that he's "no Marvel Girl," meaning that he's not a high-level telekinetic like Jean Grey, so he might not even be capable of the amount of control you're going for. If he is, it's not practical and there's no reason he would go for that other than the writer being ableist.
Guys, why go for ableism when there's already a far better thing Charles Xavier does? In canon, he uses his telekinesis when he needs to lift his wheelchair over stairs or other obstacles. In one instance where he did this, at a Hellfire Gala, it was him being petty because he's dealt with way to much to not enter the gala through the front door. At that point, he was being petty and that infinitely funnier than an ableist idea where he can magically move his legs even though there's literally no reason for him to do that.
Raven, he/him, 20, multiple disabled (see pinned for more details.) This is my disability advocacy blog
282 posts