the way people online talk about autism is getting really weird, like do they know that neurotypicals still have interests? that someone being passionate about a hobby doesn't mean they're autistic? you guys know that right
after 11 tabs, 2 video essays, 6 hours of chatting on discord, 4 meals, 7 zone-out sessions, 4 doodle pages, 2 illustrations, 10 hours of twitter scrolling, 3 hour naps, 1 DnD session, 7 hours of tumblr scrolling, 15 hours of switching between social medias, 5 youtube videos about my hyperfixation, 2 hours of wikipedia hopping, 4 mental breakdowns, 3 hours of make-up, 9 hours of outfit wearing, and 12 old youtube videos, I FINALLY finished my 5 minute homework! ^_^
hey autistic people who get overwhelmed by large groups or noise or conversation or etc etc etc you’re not evil for wanting to leave a family gathering. just so you know.
decided i’m gonna get this printed as a poster and just hang it above my bed so each morning i can wake up feeling like a victim of medical malpractice
Smtimes your house is haunted because there's a ghost sometimes your house is haunted because you miss grandma and your mom misses her even more sometimes your house is haunted because the subtext of how the last owners decorated rubs you wrong way sometimes your house is haunted because you've sublimated the fact that you didn't want to move in the first place and Sometimes your house is haunted because there's a carbon monoxide leak. Lots of options.
Not going to tag a very icky post that I found but it’s not hard to find. So, here’s your reminder that;
Self suspecting and self diagnosed autistic people are NOT taking resources from diagnosed people. You can’t get autism services without a diagnosis, you can’t go to any therapies really without a diagnosis and so on.
Autism accessories have a abundance supply. So yeah, get those ear defenders, get those sunglasses, get those stim toys.
You aren’t taking anything from diagnosed people.
Stop saying self diagnosed people are taking away from diagnosed people, because they’re not. They have their space in the community. The community is big enough for them.
saw a post the other day that said that psych survivors were overexaggerating and fearmongering for saying that people should be aware that having diagnoses on your record can be a danger + impede your life. and the more i think about it the more annoyed i am. because i think people need to know that there are exceptions to health privacy laws that can make having psych diagnoses and psych hospitalization history on your record risky depending on your circumstances. diagnoses follow you through your health interactions-you do not have to consent to have your information shared between providers. judicial proceedings are also an exception to the HIPAA privacy rule, so for things like custody battles, guardianship, getting orders of protection--the court can petition for medical records. there's so many other situations where even if they can't legally access your information without your authorization, people will require you to disclose diagnoses, records, previous hospitalizations and refuse to give you services/hire you/whatever unless you share that information with them. for example in many states anyone (a provider, a cop, friends and family) can disclose that you have certain psych diagnoses like bipolar to the DMV which then might require that you undergo drivers license review as frequently as every 3 months. my university is actively trying to kick me out right now because i had to disclose my medical record, psych diagnoses, and hospitalization history to them as a requirement to stay enrolled.
and i don't want to scare people or make people think that having a diagnosis on their records is automatically going to mean that it is weaponized against us. because i do know plenty of people who have never faced issues with their records. but i do expect that the community supports the people speaking out about the ways that we have been harmed by diagnoses creating barriers to accessing necessary parts of our life. instead of attacking us or saying that we're lying about things we are currently experiencing.
"Verbally, but not formally" = a professional told you that they think you have a particular mental illness, but nothing was formally written down, or no formal diagnosis was pursued.
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