It’s the masterpost that no one actually asked for, but I really wanted to make. I’ve found a lot of resources, but they were never in one place. So instead of searching all over the place all the time, I decided to make this.
This also includes resources for schizoaffective disorder, which I’ve never seen a masterpost for! I didn’t include things like “Dealing with a bipolar loved one”, but I might make a separate post for friends/family.
Basic information:
About Bipolar Disorder (DBSA)
Bipolar Disorder (NIMH), Bipolar Disorder (Mayo Clinic)
Overview of Bipolar Disorder (pdf)
Bipolar I (WebMD)
Bipolar II (WebMD)
Cyclothymia (Mayo Clinic), Cyclothymia (WebMD)
What is rapid cycling? (DBSA)
Schizoaffective Disorder (NAMI), Schizoaffective Disorder (Mayo Clinic)
Diagnosing bipolar disorder NOS (verywell)
The secret life of manic depression (pdf)
BPD vs BD (post by homojabi)
Mania and hypomania:
Mania symptoms (psych central)
What is mania and hypomania? (WebMD)
What is a manic episode? (healthy place)
Coping with mania (healthline)
Dealing with this manic episode (living manic depressive)
Behavioral strategies for preventing mania (pdf)
Cognitive strategies for preventing mania (pdf)
How to prevent a hypomanic episode (pdf)
Hypersexuality information post (OP deleted, so it’s on bipolarnet)
Depressive episodes:
Depression in bipolar disorder (black dog institute)
Everything you’ve ever wanted to know about bipolar depression (bphope)
Cognitive strategies for preventing and managing depression (pdf)
Behavioral strategies for preventing and managing depression (pdf)
Depression laundry tips (depressionresource)
Mixed episodes:
Mixed episode symptoms (psych central)
How to treat mixed mood episodes (bipolar burble)
Bipolar episodes with mixed features (WebMD)
Schizoaffective disorder:
Living with schizoaffective disorder (psych central)
Living with schizoaffective disorder (brain blogger)
What is schizoaffective disorder?, self care, + treatments and support (mind.org)
Psychosis:
Talking to friends about psychosis ( @therapidcyclist )
Surviving halloween with psychosis ( @mentalhealthwarrior )
How to deal with paranoia when you’re alone ( post by skailu )
How to handle hallucinations (post by schizotiger)
Treatment and medication info:
crazymeds (mood stabilizers, anti-psychotics)
Bipolar medication guide (help guide)
Bipolar disorder - What medication is available? (mind.org)
Bipolar disorder - treatment (nhs)
What to do if your parents refuse to let you have access to mental healthcare (posted by abusedkidproblems)
Self care / executive dysfunction:
Dysfunctional’s guide to functioning ( therapidcyclist )
Grounding kits ( @depressionresource )
What to do when showering is too hard (depressionresource)
lowspoonsgourmet and no-more-ramen
articles on college and bipolar disorder (ibpf)
Fact sheet on recognizing and preventing future episodes
Bipolar self care post (unfortunately OP’s theme is nearly impossible to read, so it’s on bipolarnet)
Apps:
Bipol-app, Booster Buddy, Daily Feats, Daylio, Emoods, iMood journal, Mango Health MediSafe, MoodPanda, Pacifica
note: I’ve tried to make sure all of these apps are free!
This ended up being really long already, but feel free to add to this. If your post was featured here and you want me to remove it, let me know! Please let me know if any links are broken.
you are so valid!!
your traits/symptoms are valid!!
your experiences are valid!!
self-dx is valid!!
executive dysfunction is valid!!
nonmedicated ppl are valid!!
medicated ppl are valid!!
autistic + ADHD ppl are valid!!
stimming is valid!!
hyperfixations are valid!!
comorbidities are valid!!
all ADHDers are valid and your efforts don’t go unseen!! keep up the great work funky neurodivergent ppl!!!
I found this table describing two different ways bipolar disorder can present, classic and atypical. It’s interesting because while we talk more about the classic presentation, the atypical presentation is actually more common (it was discovered second, hence the name)
The most interesting thing to me personally is while many with bipolar disorder will fully recover between episodes, many won’t–they will experience subsyndromal symptoms. which is why i, and possibly many of you too, find myself in a sort of depression lite™️ even when im not in a full-on episode.
Here’s a video that goes over the chart and explains the difference between the two and a little bit of the history behind their discovery.
I haven’t seen anyone talk about this on tumblr, so I thought I’d bring it up. It‘s not diagnostic material, but psychologists do use these terms when deciding what medication will (probably) best treat your specific case, with the classic presentation responding better to lithium and atypical responding better to anticonvulsants and atypical antipsychotics
isn’t that neat?
for my fellow psychotics who struggle with thinking someone is in their house, a method I’ve found that really works are these guys:
i put them on my front door and anytime it opens they ring. that way if i think someone has broken in or i see someone who isn’t there i can think back to if the bells have rung, and if they haven’t i can assure myself it’s not real. obviously it’s not fool proof, like if you are prone to auditory hallucinations, but it has really helped me calm down in time to avoid major psychotic breaks. it’s a real lifesaver
nonpsychotics encouraged to rb
I think people need to get better at saying “maybe, maybe not” or “do I really need an answer?” when faced with uncertainty. this is something that gets taught to people with OCD, but I think the masses would benefit
“what kind of attraction am I feeling?” would it be the end of the world if that question didn’t have an answer?
“am I allowed to identify as x when I’m not sure if it applies to me?” maybe! who cares!
literally. you can apply the “fuck around and find out” method to anything
continuously feeling the need to hunt for answers is going to eat you up inside. take it from me. your life gets so much easier when you let yourself be unsure
the idea that meds/therapy can’t fix problems caused by situational/societal issues can coexist with the idea that meds and therapy can be very helpful for many people and shouldn’t be demonized or presented as useless for risk of scaring people away that might really benefit
listen to me. thoughts do not have moral weight. a thought will never hurt anyone. the actions you take because of a thought can hurt yourself or other people, but the thought itself is powerless and there is no such thing as thought crime.
"but i have thoughts about being violent towards people! towards children! surely that makes me dangerous!" are you being violent? for real? with your actions? if not, then you are not actually hurting anyone
"but i have thoughts that are offensive and hurtful! they're bigoted, or they're horribly rude, or they're invalidating to others! i'm a horrible person." and what are you doing with those thoughts, exactly? are you taking bigoted actions, or saying those rude things, or taking steps to actually invalidate people? no? well then. no one is getting hurt. and in the meantime, if it really bothers you, doing things like helping unlearn your biases (both against minorities and just, like, against furries and theatre kids and shit) might help some of those thoughts go away, but sometimes you just get shitty thoughts.
"but i have horrific thoughts about sex!" are you hurting people. are you forcing people to do things they don't consent to. or are you just playing the upsetting possibility in your mind over and over again, and acting like that's even remotely the same thing?
thought. crime. is. not. real. OCD. is. hell. (and anything else that may cause intrusive thoughts.) but it does not define you. your thoughts will always, always come secondary to your actions. you're gonna be fine.
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
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?
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