THE LITTLE MERMAID SERIES (1992-94)
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@toseesounds
THE LITTLE MERMAID SERIES (1992-94)
STOP CENSORING SUBTITLES/TRANSCRIPTS/CLOSED CAPTIONS
LET DEAF AND NEURODIVERGENT PEOPLE READ “FUCK”
I know this sounds jokey and funney but I am serious and it is ableist and infantilising and inaccessible so stop
Practicing some traditional art today 🌱
Hearing loss is like:
Having a hard time in group activities or conversations because you cannot always understand what people are saying.
(Feeling) left out in those “secret/mumbled” sentences that someone mouths or whispers. Meanwhile you’re too nervous or annoyed to ask them to repeat what they mumbled.
Needing to walk/sit/stand on the side of your good/best hearing side so you can understand what they’re saying with more ease.
Having a hard time understanding what people are saying if you can’t watch their lips as they’re talking.
Out of embarrassment you pretend to understand someone as they talk even though they have repeated what they have said multiple times.
The “smile and nod” gesture has become a daily habit and reflex in your life.
Locating most sounds are difficult unless you can visually see the source of noise.
Jumbling words together or stuttering over words, or having to re-say a word.
Knowing ASL and English language is complicated at times due to the complex barrier of ASL, and the natural language.
Only being told but not hearing yourself that the refrigerator makes noise, light switches click when turned on, and off, birds are loud, cups clank on a table when sat down, tires on a vehicle makes noise while driving.
Being called deaf when you’re actually hard of hearing. You can hear certain sounds and voices if heard from the right side and distance. It can sometimes be humiliating.
Deaf is complete loss of hearing.
Mute cannot speak but can can hear.
Hard of hearing is only a certain percentage of hearing loss.
Contrary to pollinate belief, hard of hearing people can be sensitive to sounds and may cause stress and anxiety.
You have constant ringing and humming noise in your ears and sound blockage frequently in between the ringing and humming.
For hard of hearing people, hearing aids can be annoying. Sometimes they can get in the way by making noises too loud, especially when being sensitive to noise. But when you don’t where the hearing aids, sounds are too low and not clear enough.
It’s difficult for hard of hearing people to understand people of different  nationalities and accents. It’s difficult enough to understand their natural language.
Closed caption is a best friend.
Watching a ghost hunting show is pointless unless the ghost jumps out and yells “hear I am, can you hear me now?”
Being home alone can be refreshing, anxious feeling. No one is there to interact with, and pretend to understand. But then the silence is worrisome because you cannot hear noises outside like others can in case of an emergency.
The people that get your attention without gestures instead of saying your name repeatedly before speaking are those you keep forever.
Reading facial expressions and body language become a lot easier when you cannot hear 100%. It’s great how the mind and body adapt.
You wonder how people can drive with loud music playing and talk to the other occupants in the car at the same time.
Driving with a window down, even in rain to hopefully hear the car honks or sirens while driving.
The awkward moment when someone is unaware of your hearing loss and they comment on the fact you’re watching their mouth.
Feeling emotionally drained after a social gathering due to the noisy environment and constant strain of comprehension.
Water activities and hearing loss do not mix well.
Being an introvert because it’s easier as a hard of hearing person.
As a kid, playing telephone was a game you always sat out during.
Text messaging is the greatest invention created.
Not being able to hear in the shower so you’re always waiting for someone to come in and murder you.
Speaking too low or soft for others to hear because you cannot hear how low your tone is, because in your head, you’re too loud.
Being able to sleep better as a hard of hearing person because sound doesn’t affect you as much as those that can hear.
Most people don’t like wind because of their hair or clothes. Hard of hearing people don’t like wind because it sounds like a vacuum inside their ears.
reasons bakugo is HOH
his quirk is LOUD explosions.
he’s always yelling/speaking loudly
he often leans in close when speaking to people
he cant hear ppls names so he calls them by nicknames
he says “HUH?!” and “WhAt?!” a lot
he gets very irritated when multiple people are speaking at once
pls add on!!!
Disabled people being killed off or cured in stories tells us very clearly that we are not wanted and it fucking hurts
Do you not want to be cured, though? Say, if you had the chance to live without your disability, would you not take it?
No I do not want to be cured of being disabled, many disabled people do not, I am not the problem to be fixed, society is.
Even for those who want to be cured, curing characters does nothing for them except remove representation
And even for disabilities that are solely or almost solely negative, like illnesses, curing a character that has a disease that cannot be cured in real life removes the representation to those people still living with the disease. I’d love to see representation of people with joint pain, and i’d fucking love a cure for my pain. But I wont get one. And curing a character when the people their representing can not be cured only serves to tell us “you can not be happy until you’re cured.” and we can’t be cured, ie we can’t be happy. Don’t even get me started on disabilities that aren’t bad like autism or deafness.
Curing characters does nothing for them except remove representation
If you add a bunch of extra shit and symbols or your own comments or unreadable fonts to YouTube video captions I’m mad at you right now specifically.
“Caption editor’s note” NO
Stop it with your dumb “keikaku means plan” bullshit and just write what is said, that’s it
“Goat, standing on top of a barn, in response to the little girl: *screams*”
“*floodgates of his laughter finally open, laughing continues*”
JUST WRITE GOAT. JUST WRITE LAUGHS. This isn’t fuckin descriptive audio, it’s captions! Don’t write things that are visible! It’s not an essay with a 500 word minimum, it’s an accessibility tool! Don’t be a shit!
“I wRiTe LiKe ThIs To ExPrEsS a FuNnY vOiCe!”
NO. DON’T. It’s hard to fucking read! Say *distorted* or *sarcastic* if it’s actually significant to know! Don’t make shit harder than it is!
“(i agree uwu)”
Go to the FUCKING comments section if you have shit to say! It’s confusing to put it in the captions! You’re not fucking cute!
Bringing this back because apparently y’all didn’t pay attention the first time! Captions are an accessibility tool for those who are d/Deaf, hard of hearing, non-native speakers, or have audio processing problems, they are NOT a place for you to dick around and add commentary. It is not funny or cute; it makes it more difficult to understand what’s going on. Quite seriously fuck you if you know you’re doing this and continue to do it.
the Neurodivergent Childhood Experience™ is just [get treated differently by everyone and not really knowing why] [embrace being The Weird Kid] [hang out with a few other Weird Kids who are probably neurodivergent themselves and realize that they were the only people who treated you like a human being] [like things """"too much""""" and """""too obsessively"""""] [get shamed for showing symptoms of your disorder] [get called weird] [get ignored by "friends" for being weird] [try to be "normal" by observing the way neurotypicals act] [get called quiet and socially awkward] [get called weird] [become very distant and no longer able to form connections with people] [get called weird]
feel free to add on 😳
“The woman who was deaf began to tell us about this dream that she had about what heaven was going to be like. And she talked about how she met Jesus and how Jesus was everything that she thought that he would be. And then she said, ‘And his signing was amazing.’ Now her vision of heaven wasn’t that she should suddenly hear things, but that the barriers that stopped other people communicating in the way that she did were broken down. And she was able to communicate with Jesus in the way she’d always communicated with Jesus.”
- John Swinton in a 2015 Lecture
ADHD and autism often overlap so if I post something about my autism you relate to as someone w/ ADHD then always feel free to reblog it!
The actual medical term for this called comorbidity and there’s a ridiculously high overlap for autism/ADHD
“30% to 80% of individuals with ASD also meet criteria for ADHD, and 20% to 50% of individuals with ADHD also meet criteria for ASD” (Source )
Why is it that people get sad when I make Deaf/mental health/disability jokes like I'm Deaf/mentally ill/disabled and I'm telling the joke therefore you have permission to laugh. Them being sad makes me sad and I vote to make this not allowed.
This user is hard of hearing Decided to make this since I have recently discovered I have 80% hearing loss and need hearing aids soon
One Summer’s Day (Array Mbira) by xuan xuan
ok can we agree that the WORST feeling is when you’re just sitting around consciously procrastinating and you’re just overly aware that each second that passes is more time wasted and you like watch hours pass and you’re STILL procrastinating and you CANT STOP and your panicked brain is trapped inside a body that refuses to be productive and inside you’re screaming but outwardly you’re just eating chips
that’s not procrastination that’s executive disfunction
oh
Hey, I just want everyone to know that what the world is going through is a legitimate trauma. Full on. It fits the “official” definition and everything. This is a traumatic event.
That means that it’s normal and expected to find yourself using coping mechanisms that you thought you were done with, to find yourself numbed out, to be on the verge of constant panic attacks, to be acting impulsively and compulsively, to engage in very old patterns, to have wide swings of every behaviour especially regarding sleep, food, and sex.
The research shows that people in a traumatic situation who most often develop PTSD (which I would say we are all at risk of) or have their existing PTSD/C-PTSD intensified are folks who cannot or believe they cannot do anything about it the trauma event.
So, if you are able, look for a place in all of this where you can feel that you can do something. Harass a company not doing enough for its employees, sign a petition, check in on a neighbour, set alarms to remind yourself to eat (it’s on my own to do list for today), intentionally spend time every day doing straw breathing to shift your sympathetic nervous system response. You don’t have to become some social media hero, or spend all your time improving yourself. But if you can find something that makes you feel like you can do something for yourself that decreases the trauma load on you, it will greatly benefit you going forward.
If anyone has any questions about this, my asks are open, or you can message me. (I cannot do any online therapy, I am happy to share information about trauma itself and any tools that I know)
It is okay to reblog this.
- Registered Clinical Counsellor, with 10+ years specifically working with trauma
Y'all ever think of how Stanley Pines is canonically hard of hearing. He has a (I think it's only one) hearing aid, he mentions it and it's shown in the scene where he talks about how he's given up in season 1 episode 20.
You ever think about that
*acquires a new hyperfixation* great! this should keep me going for the next 2 months or 24 hours