Some Disability Flags Based Off Of The Stripes From The Original (@capricorn-0mnikorn) Flag! These Are

i feel like tumblr has kind of changed the meaning of the word "echolalia" into something that can be more precisely described with "vocal stimming." people on here use echolalia to mean "repeating a word or phrase over and over because it feels good" which fits the definition of vocal stimming. that's the established term for doing that; echolalia usually means something else.

the classic meaning of echolalia isn't repeating a word that sounds good, but is actually a conversational pattern where one person repeats the last thing that got said. for example, someone might say to me, "i'll bring you the rest of the articles tomorrow" and i'll reply back "articles tomorrow." it could also be just repeating yourself after you've finished talking, like i'll say a sentence, think i'm done, then catch myself repeating the last few words of the sentence.

i also do this in ASL, so it isn't just about the mouth-feel of the words. also the words don't necessarily have to be particularly pleasing or stand out in any way. when i do it, i'm not even really trying to communicate anything, it's just how i process language. that's different from vocal stimming, which is when a word is so pleasing to say that you say it over and over again.

the reason i care about this distinction is that echolalia is a majorly stigmatized feature of autism (though it also occurs in other neurodevelopmental conditions that affect language). it's often seen as a sign that an autistic person is "low functioning" or as something to be trained out through ABA. i've never met another autistic adult with echolalia, and when i do it, it confuses the hell out of whoever i'm talking to unless they know about it as an autistic thing. i just hope that other autistic people with echolalia know that they aren't the only one who does this, and it isn't anything to be ashamed of

Simone Biles saying “Mental health is more important than sports” on the biggest platform she could have possibly done it from is why she’s incredible, actually

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i feel like a fake bipolarian bc it feels like my episodes DO match that cartoony "mood shifts in a couple of seconds" instead of gradually shifting over the course of weeks. it feels like i have no stability i'm either depressed or hypomanic.

It's completely normal to question your diagnosis--I did for many many months following mine. The most important piece of advice i can give you is to speak to your doctor if you feel like you've been misdiagnosed. I can't diagnose you, all I can do is tell you my personal experience.

in my experience, though, there could be explanations for how you feel while still being a "real" bipolarian!

"my episodes DO match that cartoony "mood shifts in a couple of seconds" instead of gradually shifting over the course of weeks."

this is called emotional lability. one explanation is, actually, hypomania. it's not a symptom spoken about frequently, but hypomania can cause intense and frequent mood swings, including intense sadness that mimics the hopelessness we see in depression. it is one of the reasons hypomanic people are often misdiagnosed with bpd. 

another explanation is mixed episodes, not just feeling both at the same time, but switching from one to the other over the course of days or within a day. I think there's a misconception that mixed episodes aren't very common. talking to other bipolar people, i think they are pretty common, and this will lead me into this next point,

"it feels like i have no stability i'm either depressed or hypomanic."

this is normal in bipolar disorder! These are called sub-syndromal symptoms. between episodes, some bipolarians experience symptoms regardless of not being in a full-blown episode, and it can feel like you're never really stable.

That being said, if you experience frequent mixed states and sub-syndromal symptoms, two traits common in atypical bipolar disorder, its completely possible to feel the way you feel!

Again, I cannot tell if you are Really bipolar through an ask on the internet, and if you feel that you have been misdiagnosed, please speak with your doctor! They will know more than a blogger on tumblr dot com. But as far as I Know, these are normal bipolarian experiences. 

I hope this helps, I hope you figure it out soon, and I hope you’re well! <3 

Hi! I’ve been diagnosed with BP2 just today, I will start with the meds tomorrow and I am looking for friendly blogs to follow.

I am new to everything and don't even know what I need but your blog looks nice 🙊 also, what is your propic? Is it a pride flag? Does BP have one?

Looking for advices as someone completely new on the matter! 🙈

welcome to the community! im glad you found my blog helpful and if theres ever anything i can do to help just let me know! As for your questions:

some friendly blogs to follow

@lumberjackloving // @bipolstar // @bxpolar // @bipolarbotany // @bipolarpng // @basicbipolarbitch // @actuallybipolar2 // @hypomania-dreams // @bipolarblueberries // @bipolarbuttercup // @lamiictal // @bipolar2andbpd // @bipolarmoss // @bipolar-type-2-confessions //

and @compassionatereminders, @positiveautistic, and @recoverystuff aren’t bipolar specific but they are my favorite reovery/positivity blogs!

that should get you started!

My profile pic

My profile pic is indeed the flag that I made for Bipolar Disorder! It’s a redesign of a slightly more popular flag which can be found here.

Some Advice

Comply with your meds! If you have a problem, speak to your psychiatrist, don’t just go off of them yourself, it can be dangerous.

Set a regular sleep schedule. sleeping too much or too little can induce or worsen depression or hypomania so going to bed and waking up the same time every day is a good idea.

Try tracking your mood with an app like Daylio or Bearable, that way you can see patterns and swings at a glance

Just like winter can cause depression in people without bipolar, spring can bring hypomania in those with bipolar. Just a heads up since spring is right around the corner

Blue light, the kind of light phones and computers give off, can cause your brain to stop making melatonin, the sleep chemical. That can cause or worsen hypomania during spring time so consider using an app or program designed to block the blue light from around 6pm until you go to bed during springtime.

your symptoms might not look exactly like other people’s symptoms and that is absolutely okay. bipolar presents in different ways for everyone. dont worry about faking or ‘doing it wrong’

make some friends in the community! this community has made me feel a lot better about my diagnosis. its a very welcoming and friendly group of people! Welcome, and congrats on a diagnosis <3

I find myself explaining to people a lot recently why using "bipolar" "narcissistic" "psychopath" etc is an issue, because it can be hard to articulate in the moment, so here it is all together:

The terminology that is related to certain conditions, disorders, and neurotypes being appropriated by others to be used in commonplace situations necessarily creates problems for those whose conditions these terms are supposed to belong to and help. It stigmatises certain behaviours, makes them the butt of the joke, or underplays how debilitating they can be.

For someone who has to live with bipolar disorder, people using "bipolar" or "mania" loosely suggests that the actual bipolar people are overreacting, or else that their condition is a joke when in fact this condition not only hinders them in an ableist world, but also brings violence and discrimination against them because of the condition.

Such also is the case for personality disorders and complex disorders like schizophrenia. Using "psychotic" as an insult or a modifier erases the fact that it's a condition which most aversely affects the psychotic person, it stigmatises them as dangerous when in fact psychotic people are the ones more likely to receive violence than inflict it statistically and historically.

Saying psychopath when you mean a serial killer and sociopath when you mean someone who is cruel is also wrong in that same vein because these are ((now redundant)) subtypes of anti social personality disorder, which does not make people more likely to cause harm or to be "evil" or abusive, but rather causes issues in their own lives due to a lack of empathy, which must also not be confused with a lack of compassion.

Narcissistic personality disorder similarly is a cluster of self esteem issues, identity crisis, and a fragmented sense of self that shows itself in certain behaviours. Borderline personality disorder also is similarly stigmatised, when in fact people with this disorder are far more likely to be victims of abuse. Terms like "narcissistic abuse" or "borderline abuse" suggest that these people abused you because of their disorder, which is not at all true, and any idea of abuse can already be encompassed simply by calling it "abuse" plain and simple rather than stigmatizing a bunch of people in the process of this.

All of these disorders, though not curable, still are treatable in that people are trying to get help and adjust to life despite their symptoms. This only becomes possible as long as these symptoms and terminologies are not stigmatized any further by an ableist society. The terms used to describe these disorders are meant to HELP the people with those disorders. Not to become an excuse to treat these people worse and make them feel unwelcome.

prescribe me adderall or i will start cooking meth in my fucking bathroom you fucking psychiatrist

please dont use spoon theory terms unless you have physical disabilities / chronic pain/illness. the woman who came up with it used it as a metaphor for what it’s like to live with lupus, and as far as I know it’s not applicable to people who do not have physical disabilities or chronic pain/illness. if you do then carry on but otherwise please don’t.

shit, sorry, didn't know. that's my bad, i'll edit or delete my last stuff that used it. sorry!!

I'm in a support group for queer adults with disabilities (before I joined i didn't even know there *were* groups for that overlap, it's amazing and I love it) and we had our digital meeting on Monday. I shared your most recent flag update, where you had moved the new version to the public domain. Especially since we were talking about the ADA and its anniversary, it was very fitting. Everyone really liked it! Several people commented about the symbolism, in particular. So, just letting you know of some responses from outside tumblr. Thank you for putting it out there!

Thank you!

(Confession: At the time you first sent me this ask, the new version of the flag was not yet in the Public Domain. But it is, now! 🏴🎇🏴)

Shamelessly plugging the new version, again – especially since I want it to eclipse the old one:

To the extent possible under law, Ann Magill has waived all copyright and related or neighboring rights to Visually Safe Disability Pride Flag. This work is published from: United States.

And for those who want detailed ‘specs’:

The ratio of overall breadth to overall length is 3 to 4. The ratio of the flag’s overall length to the width of each stripe is 10 to 1 (So the ratio of the overall length to the width of the combined stripes is 2 to 1).

The Hexadecimal codes for each of the colors are:

The Field: #585858

The Red: #CF7280

The Yellow: #EEDF77

The White: #E9E9E9

The Blue: #7AC1E0

The Green: #3AAF7D

Now, as to the symbolism: in the original flag, the zigzags were meant to represent “navigating around barriers.” But instead, they were the barrier – so they were removed.

So let me put the story of the new symbolism into words – here and now– and thereby bring it into being:

The Black, as it was from the beginning, represents rage and mourning for those who’ve suffered violence and abuse because of their disabilities.

The five colors, in order from left to right, represent bodily disability, neurodivergent disabilities, invisible and/or undiagnosed disabilities (always in the center, because any disability can be invisible at any time), mental illness/emotional disabilities, and sensory disabilities.

The colored band starts at the top of the hoist, which is a starting place of honor, and ends at the fly, which represents moving outward into the world.

Walls and locked doors (behind which Disabled People have been hidden for too long) are right angles, and square. And so the colored band is a diagonal that cuts across those right angles, in defiance.

The five stripes are parallel, to represent our solidarity.

There! How’s that?