I’ve Realized How Little I Care About The Whole “transid” Thing Because I’ll Go To Their Blog

Common things in DID that no one likes to talk about

- switches that feel like you’re turning into someone else rather than them taking control (non-possessive switching)

- being unable to recognize amnesia until something requires you to remember something you forgot

- staying in the front for weeks at a time

- being unable to communicate with alters internally (this is so common why does everyone act like this is weird?)

- feeling like you don’t have any problems because you feel disconnected from them

- constant denial

- rapid identity, label, and appearance changes

- comorbidities, particularly personality disorders, anxiety disorders, and the schizophrenia spectrum

- autism (there is science pointing towards autistic people being more susceptible to trauma)

- disliking your system

- wanting final fusion

I'm on your side, even when it's not what I want.

You deserve Joy.

( A Rumination by BAANDIT buddie edit in dedication to the times Buck stepped into it with Eddie. )

One of the main problems around people with personality disorders (particularly cluster B), psychotic disorders, OSDD/DID/other CDDs or other stigmatised mental conditions is, well... Everything we do gets put back onto our disorder. Every fault, every misstep, every mistake is used as proof to say that the stigma of us all being horrible people is right.

We can say "not everyone with x disorder harms people, and in fact we're more likely to BE harmed and abused than we are to hurt others" as much as we like--and of course, that's a true statement. But the moment someone with a stigmatised mental illness does something wrong, it's "of course you'd do xyz, you're a narcissist" or "checks out with the psychosis".

Someone with ASPD could cut someone off for any valid reason, but anyone else could spin it into "yeah, that's sociopaths for you". Someone with psychosis could wrongfully accuse someone of something and without being given a chance to apologise, suddenly it's "this is why we don't trust delusional people like you" and you're discredited from here on out. Someone with DID could genuinely forget that their alter had an argument with someone and be trying to sort it out, but no one wants to hear that something was forgotten in the amnesia, so and all they get is "see, people with DID just blame everything on their alters".

People with stigmatised disorders are just like anyone else. They're not evil or uniquely capable of harm, but that also means they're not incapable of making mistakes. Everyone is entitled to their own limits but I think people need to be more aware that disabled people can make genuine mistakes and one slip up or argument doesn't mean that pwNPD is secretly manipulating you. Sometimes people are manipulative and you need to be able to tell the difference--just like neurotypicals, disabled people can be abusive. But blaming mistakes or even genuine malice on someone's disorder does nothing but harm a marginalised group of people. If you wouldn't say "of course you would, you're neurotypical" to someone abusing someone else or if that wouldn't make sense to you, why would you do it to disabled people?

let me get this straight. he plays the piano, he has a tragic backstory, he is doomed by the narrative, AND the mechanics call him their princess? is charles leclerc real or is he a fanfic character

I shouldn't make a conclusion on if I have a serious life altering disorder by myself without a professional opinion, therefore I can't and don't know for sure if some of the people I call head mates within the system are actually alters or if they're just the side affect of my living situation and an overactive imagination with a side of diagnosed ADHD. I will not overthink this and ponder if I'm even a system at all and that I'm just appropriating a disorder that I do not have. although I have always stated that I suspect that I have it and have never definitively stated that I have said disorder because I am not a professional so even if I've done a year and a half worth of research and have been provided many bonafide articles, I am still unsure until I go to a professional about this. And no I will not overthink that some professionals are essentially toddlers with a clip board and a piece of paper at times, even if I'm only saying that because of my experience with doctors and multiple professionals. Especially ones that had extremely terrible bedside manners.

I have endured trauma, and I have had blocked memories. I have experienced the symptoms of DID. I have an online journal of most of the symptoms that I and the others can remember that we have experienced. I am fine and I will not overthink my validity as a possible system based around what strangers say on the internet.

/slowly going insane.

-Viv

i am simply an Alive Bobby Nash Truther until the bitter end. they can have a live feed of the inside of that man’s coffin as his body decomposes in the corner of every single episode from here on out and i will continue to believe that he will rise from the grave and continue to live his best most chaotic life with his hot wife and his cringefail bisexual son assigned to him by the HR department at the LAFD and his beloved dear paramedic friends who come to him for life advice and his son in law/narrative parallel with extreme catholic guilt and a nobel prize for pioneering new batshit ways to repress emotions and discovering previously unknown stages of grief. it is what he deserves

Shout out to the ten year old who just got diagnosed. Shout out to the housebound fourteen year old. Shout out to the eighteen year old who can’t go to the university they wanted. Shout out to the twenty two year old who can’t get a job. Shout out to the twenty six year old with a caretaker. Shout out to the thirty year old who can’t buy their own house.

Shout out to young disabled people. We exist.

I love talking to kids about disability bc

1. they often just Get It, and

2. they have 0 concept of disability as a tragedy or something pitiable.

I've watched kids get into an argument with a teacher bc they thought wheelchairs were cool. I told a kid that I can't stand for too long sometimes and they replied, "That's okay, I can't do cartwheels sometimes, but I just do other stuff then. You can sit down with me if you want". Today a girl asked me what the headphones on a classmate's desk were for and I told her that headphones are important for some kids because noises bother them, and she said she wished she had headphones at home, because her baby brothers make a lot of noise and it makes it hard to think. The idea that different people could use tools at different times is intuitive and simple and when accessibility aids are explained neutrally, kids don't see them as bad or unfortunate, they're just things that are useful.

Even mental disability!! In Kindergarten the other day one of the kids asked me why his table partner got stickers when nobody else did. I started off by saying, "Well, when you do your work well, it feels good, right? That's your brain giving you a reward," and the kid just right away went, "Oh, and the stickers are like his reward?" YES! You are 5 and have a better grasp on ADHD than most adults! Kids blow me away every day.