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Shout out to fictives who feel uncomfortable and exposed by the fact that their sources exist as public media that anybody gets to see. The fact that anyone can just pull it up and see all of your history and traumas and mistakes, without your say or even knowledge. The fictives who don't even feel they're allowed to be upset about it because it's "just fiction" and therefore doesn't matter. Who feel like less than "real people" because of it.

We see you. You matter.

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“A pop can tab opener? Who needs that?”

It’s not for you.

“Why would anyone get a hairdryer holder, just use your hands to hold it.”

It’s not for you.

“Portable collapsible stools are proof of how lazy this generation is getting.”

It’s not for you.

“A chord assist of for a guitar? Why don’t people just user their fingers like everyone else?”

IT’S NOT FOR YOU.

Fun fact! Not everything is about or for you!

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The “I’m a fiction kin !!” Too “oh my god I’m a system” is real unfortunately

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ASL ALPHABET

the asl alphabet in the theme of our discord server mascot! therian/furry discord server !!

ftu with "cc_" at the start of the emoji name ^^

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btw chat lets stop saying shit like “REBLOG THIS OR YOURE A TERRIBLE PERSON” pls

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i’m gonna hold your hand with a glove on when i say this

when disabled/chronically ill people tell you they can’t do something, then that is not your cue to tell them that they can actually or that they’ll always find an excuse if they’re looking for one.

when a disabled/chronically ill person says they can’t do something, sometimes that doesn’t mean it’s outside the realm of possibility, sometimes it means if they (attempted to) do that, they will seriously hurt themselves.

when a disabled/chronically ill person says they can’t do something, sometimes it’s preventative care, and they refuse to do that thing to prevent a flare up from happening/their symptoms getting worse in the first place.

disabled/chronically ill people are not “looking for excuses”, they are giving you reasons why. something they don’t even have to do! so maybe just accept the reasons they give you.

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Sometimes it’s like my brain only works again when I hit my head.

It’s like a mechanism for my brain. It’s like I need it to function but I hate it because it causes pain and suffering.

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Reminder that schizo-spec and psychotic people who need full time care are an important part of this community. People living in psychiatric hospitals, people in prisons, people in care homes, people living with a care giver/family member, anyone who needs lifelong care is an important part of our community. Just because we can't always see them, or can't always hear their stories, doesn't mean we shouldn't stick up for them, support them, include them, and respect them.

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Autistic regression/loss of skills/change in skills and abilities in adulthood isn't as uncommon as people think.

It's simply not talked about, for a number of reasons:

People might be ashamed and only talk in private, or anonymously, especially older folks.

They may lose the skills to even communicate these challenges to others in a palatable or easy-to-make-viral way.

It gets blamed on something else, like other disability/mental illness, drugs/alcohol, workplace burnout etc, and isn't recognized as a feature of their autism.

Their internal experience could be more noticeable than the outward, so it isn't picked up on until there's consequences, or it never is.

They are undiagnosed or don't know they're autistic, so it's not recognized as a part of autism.

The skills lost or abilities regressed may be things the person doesn't care too much about or find valuable, so they don't make a big deal of it.

They don't have the platform to make this a known thing anyways, even if they are trying to get the word out.

Some people may not even notice they've lost skills or had a change in their abilities.

Many reasons.

It's important for the people who this may happen to, to know that they aren't making things up, that it's happened to others before, that they aren't some unicorn among unicorns.

Big changes or swings in skills and abilities and needs can, and do, happen to people, and it's a normal part of how their autism manifests, and they deserve to be met where they're at.

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target brand: pillowfort weighted stuffed animals part 2 !!

series 11: tan lion with light yellow cub, dark green alligator with baby light green alligator, blue elephant with baby light blue elephant, pink parrot with light pink chick

online exclusive: cream cat with grey kitten, light brown dog with cream puppy

series 12: blue dinosaur, pink dinosaur, yellow dinosaur, purple dinosaur

series 13: coming soon june 22nd; black and white cheetah/snow leopard

there you go!! thanks for reading :3 i love these silly guys !!

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Skill regression sucks.

I lose communication, community, hobbies, interests, routine

All because my brain isn't quite wired right

It sucks

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“if did not act less autistic, got abused so had no choice actually”

had no choice either except still could not act less autistic even if resulted in me being abused?

such a bad argument that dismisses higher level higher needs autistic people who also went through abuse

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New comfort toys is MLP Izzy doll with soft hair and fluttershy cake topper

Love play with Izzy’s hair :)

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Currently waiting for people to realise that yes, the autistic teens, kids, adults and elders who are always swarmed by aids, cannot speak, lash out, have limited speech, act “dumb”, run away into dangerous places (eg. Roads, pools ect.) when overwhelmed, are similar to the autistic stereotype or in general don’t act in a “civilised manner”

Have access to the internet

They are on tumblr

We are on tumblr

And we don’t appreciate being your punching bag, being excluded from conversations about accessibility, or used as a tool by high functioning autistics who want to say “oh look at me I’m not like the autistics who bite people or make weird sounds in public or need support, I’m just unique and have fun interests.”

We are real people and we are smarter then you think.

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friendly reminder that it’s not ok to mock how high tech AAC sounds

I Know it pronounces stuff weird sometimes and I Know it sounds robotic you don’t have to tell me. I know. some of us are hyper aware of it. stop pointing out shit we have no control over.

it’s mean to make fun of how somebody speaks verbally and it’s mean to mock somebody speaking with technology. don’t do it.

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shout out to clumsy people.

shout out to people with coordination issues.

shout out to people with dyspraxia.

shout out to people with apraxia.

shout out to people with muscle weakness.

shout out to people with paresis.

shout out to people with paralysis.

shout out to people with arthritis n/or joint deformities.

shout out to people with chronic pain whose pain makes it hard to control their movements.

shout out to people with chronic fatigue whose fatigue makes them hard to control their movements.

shout out to people with balance issues.

shout out to people with other conditions that make hard to control body n/or movements.

shout out to people who are undiagnosed n struggling with control movements.

it's not your fault. it's not your carelessness. you deserve support n accommodations. you shouldn't be judged or mocked. you deserve respect. your struggles deserve respect.