bodily 18
queer & disabled
we do not engage in discourse, we block freely, this is a catch all ramcoa focused blog, we are not educators
did aspd oc(p)d audhd dyslexic

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@illudsavants
bodily 18
queer & disabled
we do not engage in discourse, we block freely, this is a catch all ramcoa focused blog, we are not educators
did aspd oc(p)d audhd dyslexic
struggling with denial a lot lately
trying to convince ourselves we just watched too much horror media but. the horror media we consumed had nothing to do with the roots of our trauma
it just feels impossible no one noticed? we were 3. it went on for 3 years until we were moved. and we had a programmed reaction to having to leave.
but no one did notice. we were always shy. everyone assumed it was cause we were moved away from our mother. but the second we were gone from that place we stopped being so shy.
i feel insane. i loosely recognise this as programming too.
i want someone to tell me if we experienced it or not. i want a survivor to say yes or no to us. i know the answer to be yes. but i want it to be no. and i want the no answer to remove all of our symptoms.
im not even joking at this point. if someone came into our dms to decide whether we experienced it or not, we’d take it. just for the idea that just maybe it didnt happen. that we’re lying.
i hate that we can’t blame it on our psychosis either. in fact, our memories are clearer than ever now on antipsychotics.
i feel like im taking away from the survivor community simply by existing. i dont feel like i did go through it.
but theres no other word for it.
huge updates
no longer repressing the majority of traumas
communicating with other sidesystems
moloch is slowly recovering
struggling with the rest of IS outside of low rankers & moloch but progress is still incredible
- hands in dead animals (they were definitely real)
- drank lambs blood
- sacrifical lamb
- various csa
- flashing images brainwashing
i know we’re a bad person for it
but i cant help how fucking… Dysphoric? we get over it
how we cry and scream because we Weren’t what we wanted to be
i don’t want minority points
i just… this body hardly feels like ours
time to get high as shit to cope with this
plural love
didn't think this was possible honestly, was kinda wondering if you guys also had a similar experience. deep in my heart I feel loved though, scientifically I am intrigued.
I was showering, I had a pulsing headache, horrible and agonizing(nothing DID related, just hit it badly). I cried out for Scald because I wanted emotional comfort, he took my hand gently and said "here, I'll take half the pain" and weirdly it was like the pain dissociated from me, I felt it weaken to a tolerable state. Scald was in pain though, but even when I told him to stop he kept holding my hand. It was so strange that my pain just went from 100 to a 10, this is revolutionizing to me, plurality can ease physical pain
CDD (Complex Dissociative Disorder) Flag for ALL people with CDD.
Meaning of flag:
1. Trauma recovery, therapy, self-care and self-acceptance.
2. People with Complex DID/polyfragmentation or strong dissociation.
3. Diagnosed/medically recognized or undiagnosed/looking for a DID, OSDD, P-DID and UDD diagnosis.
4. medically recognized or self-recognized as system/plural.
5. "non-accepted" people with CDD. (Introject heavy, pro-endogenic, endogenic (like mixed origins, traumabased, etc.), etc.)
This flag was made by an undiagnosed CDD person, but medically recognized as a system.
"we support trauma survivors!" until the trauma survivor is an endo
"we support trauma survivors!" until the trauma survivor is traumaendo
"we support trauma survivors!" until the trauma survivor is an paratraumagen
"we support trauma survivors!" until the trauma survivor supports endos
"we support people with CDDs!" until the people who have CDDs support endos
"this is a safe space for those with CDDs!" until those with CDDs support endos
"we are anti-harassment!" until its an endo or pro endo
"endos are ableist towards CDD systems! protect CDDs!" until CDD systems support endos
"we're not ableist, endo are! we support systems!" until the system is proendo
"we are against fakeclaiming!" until an endo system breathes
"we provide resources for CDD systems!" until said CDD system supports endos
"we provide resources for traumagen systems!" until said traumagen system supports endos
"we would believe endos if they actually were backed by science!" until endos and pro endos provide sources
"we actually listen to science!" until the science doesn't support you side
"we provide sources!" except it's all just cherry picked sources that don't even prove them right
"we're good debaters!" until you actually have to do the debate
"we fight against stigmatization of disorders!" until someone with a stigmatized disorder supports endos
"we listen to CDD voices!" until that voice is pro endo
y'all like to claim to support CDDs, y'all claim to support trauma survivors, y'all claim to be proscience but you guys contradict yourself everyday.
when will you realize gatekeeping resources from pro endos gatekeeps resources from those with CDDs.
-sincerely, a tulpa trauma survivor
please do not let online system spaces convince you that you need to label and have every single thing in your system figured out. that’s an extremely unrealistic goal and you’re not any sort of faker for not knowing every single thing.
just be.
What are some things other psychotics do to differentiate between hallucination and reality? And what are ways some of you hold off symptoms? Looking to get a nice thread for people to help each other going here, this stuff isn't posted about enough.
Ways we prevent symptoms/stop them from progressing:
Make background noise to prevent auditory hallucinations. Most of ours start by hearing something that we can't identify the cause of in the background, and our brain starts the spiral from there. So we listen to music all the time and sleep with a fan on every single night, even in the winter. We just point it away from us if we don't want it making us cold.
Blame the cat (or other pets). Any weird movement, scratching, crunching or thumping? That's just Jerry, don't worry about it. He's a silly cat that does cat things even while we're sleeping. Any noise can be blamed on pets or the wind, which stops the paranoia from setting in and making everything bad.
We also tell ourselves that if there was an actual issue like an intruder or monster, the cat would hiss or scream, and the dog would be barking or making noise. This can be applied to many pets.
Stay busy. Focus on something--art, video games, tv shows and films, craft, gardening, anything that keeps you thinking. Don't let the anxiety get to you, just stay focused on your regular life.
Laugh at it. You're hallucinating a monster in your peripheral vision? Name it Fred and tell him to pay rent. You hear weird noises? Tell them to come back with a warrant. For us, treating symptoms like they're jokes or not serious makes us less anxious and therefore makes it easier to get back to a point where we're okay.
Having a friend or a pet near you can help. We feel safer and less alone when we see another living thing near us that's safe. We don't feel as much like we're trapped in another dimension that way.
How we differentiate between reality and unreality:
Touch it. This one only works for things you're not scared of, and if you don't have tactile hallucinations. It's not foolproof! But when we're seeing things like bugs and stuff, reaching out to touch them causes them to fade away so we know they're fake.
Ask friends and other trusted people if they "heard that" or "saw anything". If they're psychosis friendly, feel free to explain and be specific. If not, be vague and keep it to simple things like "hey did you hear anything? I couldn't tell what it was", if that will be safe enough. Having people to ground you can be great.
Look at how others around you are acting. Are they running or interacting with the thing in question in any way? Do they seem to look at it or no? If no one is noticing, it's less likely to be real.
These won't work for everyone and some of these might be harmful to others, but they're helpful to us. You know best what will help you!
Please feel free to add your own! We need more discussion around psychosis that isn't "scary evil person disorder and how to deal with people who have it".
We have hallucinations from trauma. We get them for pretty much every sense, and sometimes can differentiate because of sensory disabilities.
How we prevent/halt symptoms:
We keep it very quiet whenever possible, or wear headphones with known media playing. We can’t hear well, and background noise tends to bring auditory hallucinations.
Putting together memories. The faucets come with yelling and screaming because our perps would try to get us out of the bathroom when we locked ourselves in.
Flashlights. Some of our visual hallucinations run when we look, and we can deal with them being in the room if they’re not being a nuisance.
Closing doors. We had a friend who saw people in doorways, and we see eyes and hands in the cracks. Can’t occupy a space that doesn’t exist.
Wearing long clothes. We know we can’t feel hands on bare skin if we don’t have bare skin available.
Wrap ourselves in sheets. We feel buggy when we can’t see our skin, so we sleep covered, with our hands and head under a pillow.
With bugs, we poke them with our cane. If they’re bitey, we crush them or cup them and leave the stuff outside for a few hours.
Naming them. All spiders are named Greg, real or not. We have a giant rot monster called Twinkletoes for its shiny hooves.
Identifying a source. If we taste blood, we might bite our lip. Once the real taste fades, so does the hallucination.
Grounding tastes. We have Sourpatch gum and lemon drops for grounding, but the flavor is so strong they obscure our sense of smell.
Breathing through our mouth. Some olfactory hallucinations are really bad and resistant to external changes. Can’t smell if you don’t use your nose.
Go out. We live alone, and being with people distracts from the hallucinations and delusions we usually experience there. They usually reset with some time away.
Getting used to it. We only share hallucinations with passive influence/blending, so we leave notes just in case. There are body parts in the cabinets? Cool, move, I need the beans.
How we differentiate symptoms from external reality:
Getting closer to noise. We should hear the sound better the closer we get, but hallucinations don’t do that for us.
Turning off background sounds. Some hallucinations go away, others stay at the volume and clarity they were.
Putting on our glasses or changing distance from visual hallucinations. They stay at the blurriness they were rendered in or disappear.
Blowing on little things. We feel some of the things we see, so we look for movement. Things that might bring tactile hallucinations run if the touch isn’t skin.
When we had a dog, we trained him to run after things if we looked at it and gasped. If he didn’t go, it wasn’t there.
Take a picture. Especially when we’re reading, we take photos to more clearly see the object. If it’s obscured or has something in front of it, we don’t see it on camera.
Snap. We fall into the belief that the place we’re in isn’t real or we’re not physically here if our hearing fades too much, so we snap close to our ear to hear something.
Safety plans. We have a set of responses when the voices fall into repeated phrases, an allowance for how much we’re allowed to hurt or neglect the body, people who can remind us that what we were taught isn’t true or isn’t here now.
Not all of our hallucinations are plain bad, but they do tend to tie into flashbacks. Many of our tactile hallucinations don’t go away until they’ve run their course, and all but our auditory hallucinations are pretty stubborn. We mostly get on by learning to tolerate them, and they become less prevalent by working on memories.
We rarely admit to having hallucinations because people will discredit our trauma as delusions. All of our symptoms tie back to memory time, so removing that worsens our reality testing. We wish people would stop using phrases like “schizo” and “psychotic” to describe others who’ve hurt them. We feel isolated from other systems because of our psychosis.
Having friends with similar symptoms has been huge for our feeling safe interacting with outside people. Having a therapist who understands unreality is necessary for our healing. Some of our hallucinations will probably stay after we heal, and that’s okay. We are not bad or wrong for our symptoms.
feeling better as a non-emotional part is in front.
i just wanna die before i can become a leech to them
i dont want to be like my mother or my uncle
i dont want to do that to them
but im so fucking broken
im sad and lonely and tired
i hate being a bother
hate knowing ill be living with my grandparents because i cant live anywhere else
and then theyll die
and ill have nowhere
i want to kill myself.
i don’t want to keep struggling.
if i can get the car keys i’ll be fine. just turn on the car and bam. take a nap. it’ll be over.
it’s better them finding me like that than hanging or in a pool of vomit.
im so tired. i dont want to live. i dont know why people wont let me die.
i love them. i do. so much.
i just cant. its so hard. i know im selfish. i know theyll hate me for it. but if im dead it doesn’t matter.
is it a temporary solution if my entire life looks like shit? i just wanna be free.
i dont care that we were raped and tortured. whatever. we’re free now.
i care that we’re basically useless now. that we can’t do anything. that we’re just depressed and lazy.
All of the Prehistoric Pride guys in one collective post to celebrate pride month. Choose your fighter and have an awesome time :D
More suggestions are always welcome, I sadly was not able to cover everyone, but I will do more of these in the future!
I am going to add more and more to the collection as I get them done :D