Disability Will Have You Thinking Shit Like “I’m Not Even That Disabled. I Can Manage As Long As

Disability will have you thinking shit like “I’m not even that disabled. I can manage as long as I limit myself to very specific careers, never go shopping for more than an hour or two at a time, keep my plans open so I can cancel and stay in if need be, and only go out a few nights per week at the most”

More Posts from Zodixyz and Others

1 year ago
The Consistent Dehumanization Language Used In Describing Palestinians In Western Media Is Unfathomable.
The Consistent Dehumanization Language Used In Describing Palestinians In Western Media Is Unfathomable.
The Consistent Dehumanization Language Used In Describing Palestinians In Western Media Is Unfathomable.
The Consistent Dehumanization Language Used In Describing Palestinians In Western Media Is Unfathomable.
The Consistent Dehumanization Language Used In Describing Palestinians In Western Media Is Unfathomable.
The Consistent Dehumanization Language Used In Describing Palestinians In Western Media Is Unfathomable.

The consistent dehumanization language used in describing Palestinians in western media is unfathomable. The consistent denial of seeing our children as children. For everybody seeing this, don't fall into this, seek out the truth and educate yourself because that's the best and only way we can help people in Palestine. We have to amplify their voices.

1 year ago

sometimes i start to slide back into the mindset of "what if I'm not really disabled and I'm just faking it" or "what if everything could be cured by just doing x, y, z" etc.

and then i remember that during lockdown in 2020 i spent 6 months — like every single minute of that six months — focused on taking care of my health and doing everything right

i slept 8+ hours, i drank lots of water, i got a decent amount of (non-straining) exercise, i went for walks and got fresh air, i ate balanced meals, etc. etc.

and my health got worse.

i did everything right, continuously, for months, and was still disabled. there is literally nothing i could have done to "fix it". i'm not faking it, i was alone (mostly) and trying to convince myself that everything was fine, and i was still in debilitating pain.

everything has been so much better with disability aids. having my cane has been life-changing. using sensory aids, life-changing! a non-disabled person wouldn't benefit this much from disability aids!!!

i think this is coming up again for me because I've become a relatively well-known person on campus for disability (and queer!) issues, and despite having all of my lived experience and the drive to deal with things, i still feel underqualified.

there are other people who are "more disabled", or have "been disabled" longer than me (since things were really only dealt with during lockdown after my experiment, it's only been like 3-4 years with a diagnosis). sometimes i feel like i'm taking away an opportunity from someone that would be more qualified to do things.

logically though, i'm not. most of these things i have either started myself, or other people have convinced me to get involved with because i seem "qualified" to talk about it. I've had four meetings this week about campus accessibility, people actively seek me out to ask questions, i do regularly deal with ableism and inaccessibility even if it's to a lesser extent than some other people — but the stuff i'm doing is to help everyone, not for personal gain. i'm not pretending to be disabled for selfish reasons. there are clear access barriers that directly affect me as well and i am doing everything in my power to take them down.

anyways you can't really fake being disabled, especially not to yourself. ;)

1 year ago

HOW AUTISM CAN INTERACT WITH A COMPLEX DISSOCIATIVE DISORDER

higher rates of introjection - this is something commonly spoken about in the online CDD community, meaning it is a shared experience even if there is little proper medical research on the topic. however, it has been observed that some autistic pwCDDs have more introject alters (specifically fictional introjects - sometimes called 'fictives') than their allistic counterparts. this may be due to hyperfixation on fictional media, or splitting alters sourced from special interests.

splitting due to overwhelm - meltdowns, shutdowns and other reactions to overstimulation in autistic people can lead to splitting new parts, as these situations can be highly stressful.

autistic traits differing per alter - since autism is a neurodevelopmental disability that affects the entire brain, every alter will have some variation of ASD. however, different alters may struggle with/experience different autistic traits! where one alter may struggle more with, say, language and communication skills, another alter may be more proficient in that area. however, the second alter may then struggle instead with a compulsive need for strict, unbroken routines. this is how the spectrum can present differently in different alters.

unpredictable social situations and the stress of social interaction can cause more switching - as social situations can be more stressful for autistics than our allistic counterparts, it should be noted that these can be triggers for rapid switching! we may rapid switch in order to find a part that is best suited to handle the situation, which can end in switching multiple times as a lot of autistic people struggle to cope in uncomfortable social situations, such as at school/work, during conflicts, or at events. (written with input from @kityenok; thank you!)

semi-verbality, verbal shutdown and abilities to communicate varying per alter - in autistics with variable ability to communicate, the proficiency at communication can vary between alters! in semi-verbal/semi-speaking pwCDDs, some alters may have a few more words than others, while others struggle more than the rest of the system. in autistics with frequent verbal shutdowns, there may be alters who rarely if ever experience speech loss, while there are others who are permanently in a state of verbal shutdown. the ability to communicate non-verbally (using body language, signing, or even using assistive technology and speech-to-text) can fluctuate, with certain alters being less effective at using these methods than others. (note: from what i have heard from non-verbal/non-speaking pwCDDs, all alters tend to lack mouth words. if this is inaccurate to your experience, feel free to share!)

of course, there are more ways that autism can influence and interact with alters in CDDs! if you would like to add to this list, feel free to do so. ^^

4 months ago

"ai is making it so everyone can make art" Everyone can make art dipshit it came free with your fucking humanity

1 year ago

In favor of our most recent post about people making "DID fakers" bingo, I made my own DID bingo card. Feel free to fill it out and see if you have a bingo

In Favor Of Our Most Recent Post About People Making "DID Fakers" Bingo, I Made My Own DID Bingo Card.

–John

Edit: OSDD systems or UDD systems can do this too. Basically just systems in general –John

1 year ago

one thing that I don’t see talked about often is headmates with different body types in the innerworld and how it can be difficult to adjust to the body

so here’s a shout out to:

alters that are plus sized within the innerworld but in a skinny body

alters that are skinny within the innerworld but in a plus sized body

alters with nonhuman features within the innerworld but in a human body

alters that are tall within the innerworld but in a short body

alters that are short within the innerworld but in a tall body

alters that have a different skin tone within the innerworld than the body

and anyone else I forgot!

I know that we aren’t actually how we see ourselves in the innerworld, though it can be a struggle to adjust to the body and come to terms with the fact that we are not how we perceive ourselves

(Endos and related, please do not interact)

-Arlene🪽🩵

1 year ago

My cats have this meow that means "please come with me to fix this" after which they'll lead me to the problem in question, usually a empty (or 'empty') food bowl or a closed door they want open. They look at the 'problem', they look back at me, clear message.

What fascinates me is how this illustrates what they percieve as being in the realm of my 'power.' I control the food, I control the door, sure, but my cats love to sit on the balcony in the sun, and it has happened plenty of times that on a rainy day they come get me, go to the balcony and show me... the rain. "Please fix this" they say. "Please get rid of the wet"

"Silly kitty," I say, "I can't control the rain." I then walk into the shower and turn on the rain.

1 year ago

One of the most validating things you can do as a system is try to act like one of your alters, you will very quickly realize you can’t, because it’s just not you. So whenever you need a validation boost, turn on a camera so you can look back on it, and then pick one of your alters and pretend to be them for a few minutes. It’ll look stiff and awkward and not quite right. Because it’s not them.

This tip has been from Apollo. Goodnight people’s

1 year ago

The kids on TikTok think that just because he was a classic country singer, Johnny Cash was conservative??? My babies he covered a Nine Inch Nails song in his seventies.

Classic country singers (the majority of which came from poor roots) were always talking about how much The Man sucked because they were taking money from poor rural folk. You’re gonna tell me that’s conservative?? Get outta here.

1 year ago

i love when people on here well be like “who DOESN’T want their blood to get sucked ? 🤨” well i hate to break it to you but the average person does not, in fact, want to have their blood get sucked. statistically there is a large amount of people who do not want this to occur. this is shocking and appalling, i know. the world is full of unsettling things

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zodixyz - zodixyz
zodixyz

Zero : They/Thema big ol' fruit with lots of love to give⭐️icon by @time-woods

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