cosmic-kemet:

anditwaspun:

tumblr was founded in 2007
facebook was founded in 2004
twitter was founded in 2006

All of these websites have been up for around 10 years, yet none of them have the option for closed captioning. Deaf/hard of hearing people’s enjoyment of media is hugely dependent on CC so make your websites accessible goddamnit.

Wow. Plz BOOST.

dearnonacepeople:

The way we speak is such an important part of activism and living in general. The ways we discuss oppression or ideas or identity impacts the way we think and act.

The creation of new pronouns, terms and identity words is not only permissible but imperative to changing larger issues.

queerkhmer:

All these things and people still use the model minority myth to silence Asian Americans by saying “we have it good”. 

bpdsei:

“not all cis people are transphobic” thats. a lie thats a complete lie hell even most trans people have some internalized transphobia that we try to beat down so idk where u cis folks are comin from saying ur not transphobic lol

im-significant:

churchrat:

the one piece of advice i would actually extend to people in recovery is this: the health benefits of brown rice over white rice or fruit over candy or whatever “good” and justifiable food over “bad” and “pointless” food are COMPLETELY MARGINAL compared to the health benefits of having the freedom to make the “wrong” choice. unconditional permission to eat is so much more valuable than eating the “right” foods.

#eating at all is a far bigger priority than eating ‘well’#(not saying that eating well isn’t a thing#just that when ‘well’ starts interfering with eating then it ceases to be well) (via songofsunset)

yeah all of this. When eating “well” interferes with eating at all then it ceases to be well. “unhealthy” food is healthier than no food at all. You are allowed to eat.

swifternet:

kali-ddong:

(Sorry if I make your dash ugly!)

“Are you wearing a mask?”
“When are you getting your face fixed?”

“Look at that girl! She looks so weird…”

These are the three most common reactions to my appearance.

My name is Kali, I am 18, I am a Korean-American, and I… look different.

I was born with a medical condition that (clearly) affects my face. Essentially my lymphatic system can’t properly circulate fluid so the excess fluid builds up in my face. It is difficult to remove because the tumor-like masses can interfere with my nervous and circulatory systems. Sure, I’ve had many, many surgeries done, but there is very little chance I will ever look “normal”.

They say to never judge a book by its cover. I always tried to live by that mantra. I went to a summer math program when I was 14 and was assigned a roommate. The moment I walked into the dorm room, she spoke to one of our counselors and requested a roommate change.

I never cried so hard in my life.

A book is more than its cover. I’m a Starbucks addict. I play three instruments. I write poetry.

And you wouldn’t know that by looking at my face.

A person in more than his or her face. I’ve struggled to fit in at college for this reason- that people still feel hesitant to talk to me because of my appearance. They say rude things behind my back. I had grown up with the same people from elementary school through high school, so people were used to me. I hoped people would learn to accept me in college, but I haven’t found that yet.

You can’t exactly tell Stanford students that they’re stupid, can you?

I guess the reason I’m posting this is to introduce myself, and to tell my story. I don’t want to be an inspiration. I’m not a hero. I’ve simply learned to accept myself.

Someday I hope others here do, too.

My name is Kali, I am 18, I am a Korean-American, and I… am more than my appearance.

Thank you for being so brave.

About Executive Dysfunction; for neurotypical people

geekhyena:

beowulfstits:

fuckyouephraimgoodweather:

beowulfstits:

Friends, family members and loved ones of learning disabled and mentally ill people need to have a working knowledge of what Executive Dysfunction is, and respect the fact that it is a prominent feature of that person’s psychology and life.

Executive Dysfunction is best known as a symptom of autism and ADHD, but it also features in depression, anxiety disorders schizophrenia, OCD (which by the way is also an anxiety disorder), personality disorders; etc, a whole myriad of mental illnesses and disabilities can result in executive dysfunction.

(fact: I have personally known people diagnosed with each ofthe above mentioned disabilities. let me tell yea having mental disabilities in aneurotypical world turns your life upside down and we often feel suffocatedand trapped by it with no way out)

Years ago when I was like 14 and had recently learned of my autism diagnosis, I watched a youtube interview between autistic people, and an autistic woman said something along these lines, “Sometimes, a lightbulb will burn out, but I cannot change it. I have the physical capability to change the lightbulb, and I want to change the lightbulb, and I know I need to do it, but because of my autism I just don’t do it. So the lightbulb remains unchanged for weeks. Sometimes people have to change the lightbulb for me.”

When she said that I related so much, because constantly throughout my whole life I have wanted and needed to do things with my wanting and needing being akin to my spurring an extremely stubborn horse who refuses to move. For the first time I learned that I wasn’t just “lazy”, I had a condition that prevented me from doing things as easily as other people can, but unfortunately it took me years since then to understand that.

Actually, I like the horse analogy. Imagine that you are a horserider, but your horse is entirely unwilling to move even if you want to move. You dig in your heels, you raise the reins, but the horse refuses to respond. Your wants and needs are the rider, and your executive functions (the parts of your mind responsible for getting things done) are the horse.

I think it’s incredibly dangerous for neurotypical loved ones to not understand, or be aware of, or respect executive dysfunction. Neurotypical can assume that we are just being lazy, careless, selfish or difficult, when in reality we want to do the thing but our brains prevent us from consistently and reliably doing the thing.

That misinterpretation can lead to toxic behavior and resentment on the part of the loved one, which will harm us emotionally and do us a lot of damage gradually over time.

That damage can take the form of internal self-criticism, complicating executive dysfunction even further and making it worse.

a note on ocd in particular tho is that like, a lot of things surround obsessions and compulsions and the rituals associated with it, so for the lightbulb example it might be ‘bugs may have touched the lightbulb. the lightbulb is therefore dirty. i need gloves. but im out of gloves. i need to go to the store. i need to find paper to open and close my house door so i dont come into contact with the dirty door handles. i need to remember my hand sanitizer. i need to buy the gloves. i need to sanitize my hands after paying the cashier. i need to open my house door with paper again. i need to wash off my keys. i need to grab a chair, but only move it with my feet, because someone i dont like sat or touched that chair, making it dirty.’ like. its a fuckload of steps to just change ONE fucking lightbulb and its why a lot of people with ocd, including myself, just..avoid cleaning shit up or doing things that need to be done. bc if we dont do it, it doesnt trigger the ritual process and its a fuckload less stress. its easier to sit in the dark than fuck with ocd rituals.

very Good addition

also I said this on the facebook post would you agree with it?

“but executive dysfunction I think can manifest differently depending on the disorder of the individual, for example, an OCD person might want to keep their room clean, but have the compulsion, “In order to clean my room I have to do XYZ, ABC, and FGH exactly right, and if I don’t do all of that correctly everything will be horrible forever” and because of the involved and anxiety-inducing nature of that process the room-cleaning seldom gets done.

Keeping in mind that I DON’T have OCD, I’m describing based on what friends with OCD has said. (If it isn’t clear, OCD isn’t always ‘I keep everything spotlessly clean and organized 24/7’; in fact the living space of an OCD person can be a total mess)”

And then you get into a spiral of ‘I want to do this but I don’t have XYZ/the spoons’ and then it builds up ans as it builds up you get more and more anxious and you put off doing it more……

gendermoony:

gendermoony:

every fictional character you love can be like you. They can have panic attacks and they can spend days in bed and they can go nonverbal and have executive functioning issues, I promise they can if you want that, and they’re still your fave. Everything you dislike about yourself and everything you dislike about your past can have happened to your favourite characters, nobody can tell you otherwise

Also I want to add that this post is super ultra mega for people who are autistic, psychotic, trans + basically everyone who gets bullshit for trying to find characters to relate to

catastrophicmisfit:

It’s not ‘becoming a trend ’ to identify yourself as transgender or agender or any other gender, what is happening is people are becoming more aware of different genders out there and finally becoming comfortable with themselves so don’t you dare try to take that away with ‘it’s just a trend’

withasmoothroundstone:

wheeliewifee:

princekilioferebor:

i guarantee there are a lot more neurodivergent ppl pretending to be neurotypical than the other way around 

YES. 1,000% fact.

Also there’s lots of neurodivergent people pretending to be different types of neurodivergent people.  And that is considered some kind of horrible pathology instead of a survival tactic.  I used that to survive situations where I would never have been able to pass for nondisabled, but where passing for various kinds of crazy or intellectually disabled, whether deliberately or accidentally, was necessary for survival reasons.  And I get treated as some kind of monster for having done that.  Whereas if I’d been able to go on feigning normality (which, if it can be said to have happened at all – which I have doubts about – would have lasted my 11th year (6th grade) and no more, not before, not since) that would have been praised.  There’s a double standard here:  Pretend to be other-type-of-neurodivergent and you must have some horrible disease that makes you pretend things for attention (um, no, it’s SURVIVAL, trust me).  Pretend to be neurotypical and you’re doing the world a wonderful favor.

Most autistic people I’ve met who were misdiagnosed or unofficially misidentified in various contexts as intellectually disabled or crazy, have at some point or another deliberately lived up to those expectations because it was the safest thing to do at the time.  (I actually ran a panel discussion on this for a conference once.  This is something that people admitted to doing whether they were considered “low functioning” or “high functioning” at the time they were doing it.   One guy said he even still used people’s expectations of him as incapable of understanding things, to get away with doing stuff he couldn’t otherwise do.  Which isn’t just a survival thing, it’s a person thing.)