Bee Movie (2007) dir. Simon J. Smith & Steve Hickner X-Men: First Class (2011) dir. Matthew Vaughn
Alisa U Zemlji Chuda
"I'm Dorothy Gale from Kansas"
PUT YOUR BEARD IN MY MOUTH

if i look back, i am lost

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Sade Olutola
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❣ Chile in a Photography ❣
$LAYYYTER

tannertan36
Misplaced Lens Cap

ellievsbear

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ojovivo
NASA

pixel skylines

Kiana Khansmith
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Monterey Bay Aquarium
seen from Tunisia

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@melliilla
Bee Movie (2007) dir. Simon J. Smith & Steve Hickner X-Men: First Class (2011) dir. Matthew Vaughn
him saying this is extra funny when you consider the fact that at no point during that film do maurice and clive kiss with tongue so there was no real reason for them to be doing this
hey I'm sorry I stopped in the middle of that sentence my brain decided to flush its cache and I totally forgot what this conversation was
wait
yea that's funny
It took Oscar Wilde like 65K words to say this exact thing.
i’m normal about everything ever
they are best friends
The Boy and the Heron (2023)
Florence Welch performing in Glasgow, 2023.
STOP THINKING THERE IS A DEADLINE. THERE IS NO DEADLINE. TAKE A DEEP BREATH AND TAKE YOUR TIME.
A Winged Hussar’s Zischägge, Poland, ca. 18th century, housed at the Wawel Royal Castle State Art Collection.
I was gunna put this in the tags but it’s a lot. When i first started going through the process of getting a diagnosis, i was labelled with ODD. I immediately took issue with this, it seemed like an unfair diagnosis based entirely on the session the psychiatrist had with my parents (which mostly consisted of “my child is being really difficult on purpose”), and Hoo Boy when i tell you ODD immediately strips you of your ability to call out anyone on anything, that would be an understatement. I couldn’t even disagree or bring up my concerns about the validity of MY OWN DIAGNOSIS without it being labelled as oppositional defiance. Whenever i displayed any negative emotion the “treatments” did so much more harm than good. When you label someone as ‘defiant’ (ugh), when that word is put on their medical record, that person is never allowed to complain about anything again. Knowing that POC are disproportionately affected with this diagnosis makes me feel sick, i can only imagine what’s being swept under the rug as someone just being “defiant to authority”, not even just in the medical field but as justification for police brutality and mass incarceration. When i say medical racism kills people, this is what i mean.
this is so fucking important. reblog.
I was labeled ODD as a child, and lemme tell you.
When I was eleven, I was put on a med I reacted negatively to. I don’t remember its name, but if I ever see the pill again I will KNOW. Within a week of beginning it, I told the school nurse I didn’t want to take it; I didn’t know the word “apoplectic” at the time, but that’s how it made me feel. It wasn’t irritation, it wasn’t anger, it wasn’t even rage—it surpassed all those things. The slightest issue left me literally blind from the level of anger I felt (yes, “seeing red” is a real thing). Someone bumped my desk at school ON ACCIDENT and my pencil hit the floor, and I nearly stabbed the offender with it. I was so furious, all the time, it was hard to think. I was becoming afraid of myself.
The nurse called my psychiatrist, who told him I had ODD and would naturally refuse to take my medication—even though by this point I’d been on multiple meds for many years, and I was objecting only to the single medication, it was clearly a sign of ODD and trying to manipulate my environment. I hadn’t been on the med for the full month it took to get up to a maintenance dose, so I couldn’t possibly be having bad side effects.
I had to take the medication.
The next day I hid under my desk and refused to come out. I was seeing things that weren’t there.
I begged not to take the meds. Again I was told I’d have to.
I was now on day nine of the medication and the special ed teacher literally had to physically move me into the nurse’s office.
I looked at him and said “tell Dr. X that if I have to take that pill today, he can explain to my mom why I cut my throat tonight.”
The med was discontinued, but only because my nurse took me seriously but without panic, called my mother, and asked her to call my shrink, and had me do my classwork in his waiting room while we waited for the return phone call. He intervened because he realized he’d only ever heard me object to a med once before, and it was because I was physically ill and afraid to eat (which the medication required) lest I throw up in class. On that occasion he offered me some crackers and had me stay in the office for twenty minutes to see how my stomach did, and when the crackers stayed down he gave me a few more and my medication, which I took without complaint as soon as I knew I could take it safely. Clearly if I was suddenly begging not to take a medication, something was wrong.
Without that nurse, I might be dead today, because of “oppositional defiant disorder.”
I want you to reread all of this post before my addition, and then I want you to reread my list of side effects, and then I want you to think about how many “Black person goes crazy out of nowhere, kills someone, tox report was clean, cops baffled” stories you’ve seen. I can think of at least three.
Lemme say, I'm one of a few black kids I know (especially AFAB) that got diagnosed with ADHD in the 90. Like Early 90s.
And it was a Fucking Stars Aligned MIRACLE.
Because in order for me to be diagnosed or even had it thought to be the following had to happen:
My mother worked at a daycare before I was born.
It's predominantly black but there are other races there (yes this is Important. Please also keep this in mind that this is Early in research about ADHD and ADD at the TIME).
A lady (black) recently got her son diagnosed. My mother was talking to her because she didn't know, the information wasn't wildly available. She had to learn by word of mouth what went on how to find these people.
The programs for it were available but weren't Affordable for my mother.
I had primarily White Doctors (yes this is important)
My first two doctors were actually *good* doctors. I had my diagnoses and was put on Ritalin * (sp) then.
I had a teacher in Kindergarten that didn't know what ADHD was(White teacher). She actually was a good teacher that decided to research what information was available at the time and Took an Active interest in how to teach me and the other kids in the class.
The Previous teacher (White) in Pre-K didn't do any of this. She didn't bother to actually teach. My mother recounts that this lady for real just said "I don't know. Blackmantagirl just got the devil in her."
That is to say: She thought I was being disobedient on purpose and as a result I was 100 percent usually sent to the office for a paddling (it was legal and it was a Private Christian school. SO...).
*skip Some Years and at least Three terrible teachers*
I got another doctor (white) that I was transferred to. What a lot of people fail to realize is a lot of medications that they do NOT recommend for kids now is usually because they've already tested it on kids before and it was BAD News, Jim.
So, the new white Doctor was a dismissive type of ass. The type that threatens kids because he wanted to flex his power over them. (I have literally been threatened by him. He told me he'd tell my mother to cut whatever hobby I liked then if I wasn't responsive to whatever the fuck he wanted to talk about)
At this point, I'm pretty sure he's writing up that I'm manipulative and possibly had ODD.
I was prescribed medications that they really tell you not to give kids these days unless like you absolutely last resort had to because of the side-effects.
There's one medication they gave me that sounds a LOT like Prismatic's but I don't know the name. I know what it is if I see it ever again.
But this medication definitely caused me to Hallucinate. (or rather believe I was infested with fleas) It was bad enough that my grandmother, who's a nurse, basically said Enough Of that and just chunked the meds out. All of them.
(one other one had a side effect of repressing your appetite that we didn't know about. And so I had been taking it before Lunch. It SUCKED that we didn't know about it.)
Anyway, the point of this is also:
Even when Black Kids are rightly diagnosed, we're still going to get shit from people who either think we're faking, or don't care to actually do any work about it. Instead, they'll punish us MORE. Or throw us in the SpEd classes to get rid of us in the general classes if they don't want to do any of the work.
Because that's ALSO what happened to me the following year after the Bad Year.
I actually could read quite well and could do normal course work, but they decided due to the former and my medical history that I should be in this class. (I could see it if they wanted me in there for things like Math, because it's my weakest subject and I have trouble understanding anything but.. I digress).
I was place in a class where people who actually needed it were at a very slower pace and school level than me. (and even then, the schools 100 percent failed one student who couldn't read at his grade level. He was reading at a first grade level. He was in seventh grade.)
And a large part of this is because there aren't enough POC (particularly at that time Black Doctors) in the field. Because it deeply matters when you get a doctor that is very familiar with your culture and the way your people work.
It prevents a lot of abuse and misdiagnoses. (that was literally my issues with a lot of places is because until I was in a predominately black school, I was treated pretty awful by teachers and principals that didn't Understand the Culture and didn't WANT to)
I didn't get a black doctor until my mid teens. When I've figured out how to manage shit my damn self with coping mechanics (but I definitely should've had an actual Doctor to Help. Actual people that could've given me better tools.).
He actually understood and thought I was misdiagnosed. But the main point is he treated me like a person.
He wasn't combative.
He was interested in what I had to say. He didn't dismiss me. He understood what my issues were and was able to explain them to my mother in a way that didn't give me protective mode. (that White doctor further up that was an ass literally upset my mother that I ended up hating him for it. )
My Kindergarten Teacher was also a Good Person and Good teacher. She put in the work. She tried to understand even if we were culturally different, she didn't send me to the principal's office every time I fucked up as a kid. She tried to make sense of it and tried hard to keep me in class. (I went from literally an F to an A, is what I'm saying.)
Both that doctor and that Teacher Saw humanity in me as a kid and I'm forever grateful for them in particular. (and also a few others but mainly them.)
Like if more black and other KOCs had these types of people, that ODD wouldn't even be a thing (even for white kids because I think the entire thing is just BULLSHIT excuse to be an asshole to people. Full stop. ).
Incidentally, if you want a great example of why we need to destigmatize mental health treatment, I read Manta’s comment and shot her a PM. We’re about the same age, so it stands to reason we may have been prescribed the same medication.
I NOW KNOW THE NAME OF THE MEDICATION THAT MADE ME WILLING TO KILL MYSELF JUST TO GET AWAY FROM IT. She told me what she was on, I looked up a photo, and damned near dropped my phone. In just a few hours I can call my current (very good) psychiatrist and have this name put on my file so it is never prescribed to me ever again, even by accident.
The atmosphere Tumblr has fostered, in which it is safe and acceptable to say “same hat?”, has made me quantifiably safer today. We need to work together to make it like this everywhere.
So one thing that isnt highlighted in Blackmantagirl's story is why we need affirmative action. That is how we get more black doctors, but we also need more doctors who grew up dirt poor, and ones that came from a variety of different backgrounds.
Understanding the culture, having someone that really HEARS what you are saying, having someone who wont dismiss your fears and will validate your experiences is direly important to you, but it also is important to medicine.
Both of my parents are doctors and when I was little they were both great doctors. But when my parents got divorced that was the start of my mother becoming not such a great doctor.
My dad has the same sort of autism that I do where the societal pressures to not make friends with people outside your comfort zone... well all people are a bit uncomfortable so why would someone of a different race or significantly poorer make any difference?! And on the other side of things my mother had lunch with Trump's sister in 2022. My mother used to listen to people, get the situation that was their life and see how their poor health fit into that. Now, she just talks about her stats and her tricks to limit time with patients.
My Dad on the other hand, retired from normal medicine and goes to a clinic and sits with people and gets a summary of the last 10 years of their life and puts the pieces together for them with a diagnosis. Medicine as a whole has been shifting my mother's way my whole life... and my parents used to both complain about that. Now my dad who has a variety of friends complains SO bitterly against the way medicine is going, and my mother who retreated into her comfort zone is helping spur on medicine over the lemming cliffs and diving over with it.
This too shall pass but like holy fuck
Edgar Allan Poe, from a letter to Mrs. Maria Clemm, July 1849