#anti fakeclaim

[tommyssupercoolblog]

"i know they're faking DID/OSDD because their alters are cringe!!!!" This may come as a shock to you, but sometimes, people's coping mechanisms, are cringe.

so when their brain introjects or creates someone, it's also cringe.

[interrobang-sys]

Every part of queer is accepted here

However, ableism won't be tolerated here

Nor will arguing

If you wanna argue take it somewhere else

I will be busy enjoying my m-spec lesbian greyromantic bive headcanons and my objectum boyfriend and all of the other lesser known queers

Transid, truscum, radqueers, fakeclaimers, radfemmes, terfs, and other pieces of shit dni

If you're anti-objectum, please leave. There are so many forms of objectum. I love my plushies, a platonic amount, and love my Rammie plush as queer platonic. If it doesn't harm the person, leave them be. This isn't to say I condone everything that objectum has been classified under (aka its broad term, paraphillia, which includes things like necrophillia, which I do not condone under any circumstances) but this is to say I do not judge.

[rayssyscourse]

I'm not doing much tonight and feel like (civilly) talking syscourse, anyone got questions or thoughts (or half-formed ramblings? those are my favorites; my notes app is full of them /lh)

[chronicsymptomsyndrome]

Can we please for the love of god stop telling teenagers they’re too young to have aches and pains. Can we please stop being dismissive about these things. Fakeclaiming is disgusting period, but it is exponentially harmful to youth. Just because you didn’t start hurting until your 20s or 30s or 40s doesn’t mean every teenager complaining of chronic pain must be lying. I learned the hard way that if kids are invalidated enough about this, they will just learn to accept constant pain as a fact of life. And then they will need surgery they can’t afford in ten years bc it turns out constant pain is NOT a fact of life. At any age.

p.s. same goes for mental health

[thefruitybasket]

“You can’t be a system!! You and ___ both do this!!!”

We still share a brain.

“You and ____ LOVEEE this!!”

We still share a brain.

“You and ____ talk very similarly!!!”

We still share a brain.

[cozmo-system]

fuck. you.

yeah let’s just ignore real qualified therapists telling trauma victims they can cope without harm via fiction. everyone listen to some random dipshit on pinterest because the TOTALLY know more than anyone with years of education and experience

[zeros-sys]

it's killing me that systems think they are faking or lying because they haven't had other alters front in a while, headspace has been silent, your communication is down, and overall just "feeling like a singlet"

because number 1, cdds have more symptoms than just alters, number 2 it's a covert disorder, and number 3, you are an alter!

no one experiences the same level of their symptoms for any of their disorders every day.

if my avoidance to food due to arfid is more noticeable some days, why is it different for having alters in osddid?

cdds are covert disorders. they will try and hide your symptoms because it's the whole point of their existence. don't blame yourself for a survival mechanism your brain created to protect you!

and I see so many people forget this, especially hosts, but you're an alter! if someone else doesn't front, that doesn't suddenly make you a singlet because you are still part of a system

you can make mistakes or be wrong, but don't fakeclaim or feed yourself misinformation in order to realise that!

[talkingattumble]

Hi guys! Here’s some advice from a cane user on how to spot a fake cane user/disability faker!

YOU CANT

You can not spot a “fake disabled” cane user. You can not know if someone’s “really disabled”, much less by just looking at them. Here are some common misconceptions.

“Cane users always need their canes. If they walk without it or put it away when it’s inconvenient, they’re faking”: WRONG! Many cane users are what we call “ambulatory” cane users. This means they don’t always need their canes to walk. I’m an ambulatory cane user, and I experience really horrible leg pain on the daily. However, I don’t always use my cane, and when I don’t need to walk or stand a lot in a certain place I don’t use it. And when I do use it, I may lift it off the ground or carry it in places that are sandy, gravelly, or otherwise hinder my cane.

“Cane users walk abnormally without their canes, someone who walks normally without their cane is faking”: WRONG! Many ambulatory cane users can walk in a way that seems “normal”. This doesn’t mean they’re not in pain, or not “really disabled”. This just means that their condition doesn’t cause a noticeable difference in walking, and likely manifests in a different way.

“Cane users always need their cane, someone who doesn’t use their cane at home is faking”: WRONG! Cane users may not use their canes at home, because at home they may be able to do things like sit down wherever and whenever, regain more spoons, and use other mobility aids. Additionally, some ambulatory cane users only need or use their canes when they are doing something physically taxing, like going on a hike or standing in a long line.

“My cane user friend told me this person looks like they’re faking, so it must be true”: WRONG! Being a cane user doesn’t immediately make you an expert on all different conditions and experiences. Your friend does not know the random cane user walking down the street, they are going off looks and stereotypes. Disabled people are not immune to being ableist.

“They enjoy their cane too much/they’re too happy/they decorate their cane, so they can’t actually be in enough pain to need a cane” WRONG! We’re people like everyone else, and we experience positive emotions too, even if we go through a lot of pain. To me, customizing my cane is like getting a tattoo or putting streaks in my hair, it’s a way of self expression. And we deserve to be able to talk openly about our full experience, which include the parts we’re neutral or happy about.

“They’re one of those cringey teenagers who name themselves arson and like dsmp, so they’re probably faking” WRONG! Do I even have to explain why saying someone isn’t disabled because of their name and interests is messed up and also stupid? Or did you already know that and just wanted to make fun of a disabled teenager?

“They’re too young to be using a cane, so they must be faking” WRONG! there are lots of disabilities or injuries that can cause young people to need a mobility aid. For example, I use a cane for my fibromyalgia.

“They only use it in private places, and never in places where people recognize them, so they must be faking” WRONG! In a world where anyone can just randomly take out their phone, take a picture of a cane user, and post them online to be made fun of, it can be stressful to use a cane in public areas. Also, they may not want people to ask questions, or they may feel embarrassed about it.

“I saw them switch hands, so they must be faking” WRONG! There are different reasons a cane used might do this, but I’m going to use my experience as an example. My fibromyalgia is not consistent. Sometimes one leg hurts more then the other. But as I said, fibromyalgia is inconsistent, and sometimes my other leg will start to hurt more or need more support, which is when I switch hands. And when both my legs hurt equally, I may switch my hand if it’s getting too sore.

“They told me they feel like they’re faking when they use their cane, doesn’t that mean they don’t really need it?” WRONG! Imposter syndrome is strong in a lot of disabled people, especially when for a lot of our lives we were told by doctors that we were fine and just being dramatic. Anxiety is also comorbid with a lot of physically disabilities, which only strengthens this. To add to this, something that I’ve felt and seen other disabled people talk about it, when their disability aid lessens the pain, they start thinking “well I’m not in that much pain so I don’t really need it” even though the reason they’re not in that much pain is because of the aid. I know it seems dumb, but imposter syndrome can be that strong and affects disabled people a lot.

“They don’t have a diagnosis, so they must be faking” WRONG! First of all, diagnoses are expensive. On their own they’re often already expensive, but counting the tons of tests you have to take to confirm the diagnosis? Absolutely ludicrous. Some may also choose not to get a diagnosis, so that they don’t have to deal with the prejudice and setbacks of being diagnosed. Also, some people use a cane for injuries, and for stress or fatigue related pains.

These are only a few of the things I commonly hear from fakeclaimers, and I wanted to just put out a reminder that fakeclaiming hurts the disabled community much, much more than it does ableists. Next time you see someone with a cane switch hands, or someone with a wheelchair stand up, or someone with crutches put them down, before you immediately call them out to a friend, take a picture, or write a post: does your fakeclaim rely on stereotypes? Are your reasons things that apply to ambulatory aid users?

If so, just stop. Be mindful. Please.

[mxmorbidmidnight]

Can the “disability allies” who know nothing about disabilities stop fake claiming disabled people. You’re not a hero and you’re not going to get a pat on the back. All you’re doing is making it so disabled people do not receive the support and care they need.

For the last fucking time. It’s better to let a few fakes run around than jeopardise the health and wellbeing of entire communities. If someone is spreading misinformation or harm, that should be dealt with. That is when you take action. Most definitely not when you look at someone and you think they “don’t look disabled”. You cannot determine a persons medical conditions based on vibes and a single video of them. Come down from heaven arsehole you’re not Jesus Christ himself.

[thehealingsystem]

if you ever wonder why I don't interact with the traumagenic community as a traumagenic system this is why

[delphientropy]

based on recent events

[pluralhottakes]

sometimes pro endos and anti endos should just. chill. interact. don't limit yourself to only interacting with people with morals that are 100% the same as yours. everyone's all "no one is perfect" until the imperfection is that they don't agree with you on something. like no actually flaws aren't just skills people aren't good at, they're also moral things

tl;dr just chatting with people who disagree with you is ok and not everything is about syscourse

.

[chronicsymptomsyndrome]

Nobody is “too young” to be cynical or jaded or hate their life. There is no appropriate age for that. If someone is experiencing that at any age, their mental health is at risk. Doesn’t matter how young they are, or how easy their life seems. Just because existential dread didn’t hit you until later in life, doesn’t mean everyone else gets to be so lucky.

“You think life sucks now? Just wait until you’re grown” okay grandpa what if they don’t make it to adulthood? What if it gets worse until they only see one way out and they take it? Stop being dismissive. Stop forcing your problems onto young people and start taking them seriously about things. Period.

(Inspired by this post)

[thefruitybasket]

Calling people a “sysmed” when being a system is a MEDICAL thing is crazy..

This blog is NOT endo safe!

* Post made by Davis !

[yrfemmehusband]

Debunking popular fake claiming points when it comes to tics and tourettes:

"I saw an older video where they didn't tic once!"

1. A trait of tourette's is waxing and waning tics. This means the diagnostic criteria takes into account that some people will go days to months without ticcing, or without ticcing severely.

2. Many of my tics are nearly microscopic. How do you know they weren't? Did you have a full body view of them? How do you know they weren't wiggling their toes nonstop, or maybe those couple of sniffs you wrote off were tics.

"their family/friends came forward and confirmed they're faking!"

1. My little brothers literally forgot I had tourettes. It can also be completely missed in childhood, many women and other people who were AFAB go undiagnosed until adulthood. Sweet Anita? She wasn't diagnosed until 27.

2. Family isn't always a reliable source and many people are estranged from family members, if you aren't very close with a person and their family, don't take their family's word at face value. De

"sometimes they tic a lot, and sometimes you don't see it at all for hours/days/weeks!"

See point one about tics waxing and waning. You are literally describing a symptom.

"Every time someone brings up tics around them they start ticcing!"

This is literally how tics work. If you are reminded of them you will have them. Especially if someone brings up a specific tic.

"you can see they put thought and effort into their tics, tourette's doesn't work like that!"

Clearly, you don't know how it works if you're saying something like this. No one knows how it works or feels unless you have it. Sometimes it looks like I put effort or thought into a tic when it was entirely involuntary. Sometimes, I do put thought into a tic. There's a part of tourette's called a Premonitory urge and it's the feeling you get before you tic. If you wanna get the feeling to go away, sometimes it's better to force out a tic.

It's not helpful to anyone to claim someone is faking, EVEN IF THEY ARE. We will NEVER have any way of knowing if some random online is faking tourettes and honestly the tourettes community has bigger things to worry about, and so should you.

[urfavoritesecretadmirer]

People when a child with a childhood trauma disorder is a child: 😭😭😨😨😨😭😭😭😨💀💀😨😭😭😭😨☹️☹️😨😭😭😨