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FAQ:
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I've seen lots of depictions of hearing aids and cochlear implants in writing and art, and very few of them actually match what that character would likely actually use. An especially common mistake is drawing hearing aids like they are wireless headphones, which is not how the vast majority of hearing aids look.
Here's a guide on hearing device types, uses, and how to better decide which one your character would have!
(Reminder that this is not medical advice, or perfectly tailored to every single situation. I am not an audiologist, just a Deaf person on tumblr.)
Hearing Aids:
[Plain Text: Hearing Aids]
There are many different types of hearing aids. Which type someone uses will depend on their hearing curve, the features they want, and the type of hearing loss.
1. Receiver in Canal.
Receiver in Canal (RIC) hearing aids are the newest type, and currently the most commonly prescribed. They have a small behind-the-ear component with directional microphones and processors, and are connected by a thin clear wire to an in-ear speaker, which is covered by a piece called the dome.
RIC are most commonly prescribed for: mild to moderate hearing loss (although they can be useful for some people with severe hearing loss), high-frequency hearing loss, noise-induced hearing loss, tinnitus, and auditory processing disorder. RIC are also available over the counter.
Benefits: small and discrete, fairly powerful, best integrated noise filtering systems, highest mapping customizability.
Drawbacks: sizing is not infinitely customizable, not good for more severe deafness, usually don't come in fun colors, difficult to use with low dexterity.
There are several different dome types, as I mentioned. Domes are soft silicone or plastic pieces fitted in diameter to the ear canal, but come in a few different shapes depending on the type of hearing loss. I'll talk about the most common ones, but there are a few other rarer custom types.
Open/Vented domes have slits cut in the silicone. They are the weakest at keeping sound trapped, but have the lowest occlusion effect (hearing your own voice loudly). They are good for mild to moderate hearing loss, but they can cause a lot of feedback, especially at higher frequencies, so they're most useful for high-frequency hearing losses. The amount of vents in the dome can be adjusted to reduce leakage.
Closed domes do not have slits or have very few slits. They keep more sound trapped, but have higher occlusion. They are good for moderate broad-spectrum and low-frequency hearing loss, since they allow less high-frequency noise to escape.
Power domes have no slits and often have multiple layers for maximum amplification. They have the highest occlusion effect, although people using power domes typically have hearing loss in the range of 60-80 dB, so occlusion is often necessary to hear one's own voice. Power domes can make the ear pressure feel unbalanced since there are no vents.
2. In the Ear / Completely in Canal.
In the Ear (ITE) and Completely in Canal (CIC) hearing aids are a less popular, but available, type. They feature a solid combined processor and speaker that sits in the ear canal. There is usually a small wire or clear plastic loop that fits along the curve of the outer ear both to keep it in place and to pull it out.
ITE/CIC are most commonly prescribed for: mild-moderate hearing loss when RIC is not preferred or available.
Benefits: no behind the ear component can be more comfortable, microphones in the ear have highest directionality, subtle.
Drawbacks: fewer features available, higher occlusion effect, can fall out more easily.
(There are some ITEs that have a behind-the-ear component for volume/power control and structural support, but the processor, microphones, and speakers are all in the canal piece.)
3. Behind the Ear.
Behind the Ear (BTE) are the most powerful type of hearing aid. The microphones, speaker, and processor are all present in the behind-ear component, which is larger than other types of hearing aids. This component is connected by a replaceable plastic tube to a mold, which is custom-fit to the user's ear and allows for maximum sound retention/amplification. Like domes, there are several types of molds.
BTE are most commonly prescribed for: severe to profound hearing loss, moderate or higher low-frequency hearing loss, children.
Benefits: sizing is fully customized, easy to use with lower dexterity, good for athletics (less likely to fall out), highest aesthetic customization, most powerful amplification.
Drawbacks: larger size, high occlusion, higher risk of ear infections, molds must be replaced as ear shape changes, tubes must be replaced regularly.
There are lots of different mold types. An ear mold is custom fit by creating a cast of the user's canal and ear shell. More or less of the "shell" of the ear can be covered by the mold. All molds have a vent hole to allow moisture to escape, but some molds have more holes cut into them to allow airflow or reduce occlusion. Some molds are hollow, while others are solid. (Molds can also come in lots of fun colors, including marbled or glittery, although insurance won't always cover these.)
There are too many types of molds and considerations to really get into exact types here, but if you look up behind the ear hearing aids there are tons of references online. [One type of mold I've seen a lot in real life but that I can't find the name of online are sort of square-shaped solid (often colored) plastic with lots of holes in them. They remind me of a waffle.] In general, the more severe the hearing loss, the less "air space" there's going to be in the mold.
4. Bone Conduction.
Bone Conduction hearing aids (BCHA) are probably the closest-looking in real life to those headphone ones, although many of the over-the-counter devices calling themselves BCHAs that look like headphones are in fact just bone conduction headphones. Prescribed BCHAs are often two individual rectangular devices, attached via stickers or a headband. There are a few that go behind the ear, although no component of the aid is in the canal.
BCHAs are bone conduction rather than air conduction, which means they get the sound to the cochlea by vibrating the skull bones rather than sending sound through the middle ear. BCHAs are often temporary aids (see BAHA in the CI section of this post).
BCHA are most commonly prescribed for: severe conductive or mixed hearing loss, microtia/atresia, and young children.
Benefits: more powerful and safer long-term for conductive hearing loss, typically no in-ear or over-ear component.
Drawbacks: require an external component (stickers or headband) to stay attached.
5. Airpods / Actually just headphones
Did you know, Airpods were recently approved by the FDA as over-the-counter hearing devices? The noise filtering technology makes smart wireless headphones a possible alternative for mild hearing loss, auditory processing disorder, tinnitus, or anyone who can't get prescription hearing aids. These are not a long-term solution, nor are they used by audiologists, but for people who just need a bit of a boost, having their headphones in all the time might be their way of navigating the world.
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All hearing aid types have their benefits and drawbacks, and no aid will ever be perfect for someone. Even the best hearing aids available can't make someone become Hearing. Some people who are severely to profoundly deaf report hearing aids giving them around 60-80% of what a hearing person can hear, and this number improves with decreasing severity of hearing loss. Still, nearly all d/Deaf/hoh people struggle to some degree with auditory processing. They may use hearing aids to give them general awareness of background noise (eg fire alarms), or for a boost while lip-reading, even if they don't help in understanding noise more generally. Hearing aids can also die or malfunction, removing the benefits they provide.
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Cochlear Implants:
[Plain Text: Cochlear Implants]
Cochlear Implants, or CI, are surgically implanted devices that stimulate the cochlea.
More on CI in one second, because I promised a return to BAHAs, which are a type of surgically implanted hearing aids. They get to go in this section because they are implants.
BAHA stands for bone anchored hearing aid (as opposed to BCHA, which stands for bone conduction). BAHA are the long-term alternative to BCHAs. A titanium plate is anchored to the skull, and an external hearing aid component attaches to the plate and vibrates it.
BAHA are most commonly prescribed for: severe to profound conductive hearing loss, microtia/atresia. (One of the major use cases for BAHA is Treacher-Collins Syndrome, which often causes bilateral microtia. Since the hearing loss is purely conductive, and traditional hearing aids do not typically fit people with microtia even without atresia, BCHA/BAHA are the best aids.)
Back to CIs. Unlike BAHAs, cochlear implants are implanted into the cochlea to directly stimulate the auditory nerve. They bypass the outer, middle, and inner ear systems, so they are useful for any type of hearing loss.
In order to qualify for a CI, one needs profound hearing loss across all or most frequencies, and the presence of both the cochlea and the auditory nerve (CI won't work without those structures). Someone can qualify for a CI in one ear but not the other; even if someone is qualified to receive implants in both ears, they're expensive and the surgery has risks, so many bilaterally deaf people have only one implant.
In the United States, CIs are approved starting at 9 months old, but not any younger. (This is a problem for auditory development--although CI are often billed as a "cure" or "complete treatment" to deafness, the reality is that even bilateral CI users who received speech and auditory therapy from the moment their devices were programmed still lag behind hearing peers in auditory development, because they are deaf. But that's part of a larger conversation regarding deaf development and audism.)
CIs have a small disc that magnetically attaches to the skull near the implant site. That disc transmits the sound through the bone, which is then transmitted to the auditory nerve. Usually, the disc is connected to a wire, which runs to a behind-the-ear processor piece. CIs have a couple different types, just like hearing aids. I'll run through them pretty quickly.
1. "Button" CI.
These are fairly new. They only have the magnetic disc; all the processors and microphones are inside it. They're less visible, but less powerful.
2. Behind the ear microphone.
The BTE component contains the microphones and processors. There is a hook to keep it in place on the ear, but no part of the CI goes into the ear canal. These have similar directional power to BTE hearing aids.
3. In-ear microphone.
The processors are on a behind-the-ear component, but they receive signal from a microphone positioned at the opening of the ear canal. These give the best directional sound filtering, since they receive the auditory input from the same place as a hearing person, often with the benefits of the shape of the outer ear.
4. Mixed type CI + hearing aid.
These are also very new! Previous CI techniques, and many surgeons today, destroy residual hearing, so when the CI processor is disconnected, the user receives no auditory input, even if they had some before getting a CI. However, some new techniques can preserve residual hearing, and the cochlear implant can be combined with a hearing aid. This device looks like a BTE hearing aid with either a mold or power dome, but also connected by a wire to the magnetic disc of a CI.
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What type of CI a person has depends on the technology when they were implanted, what sound quality they want, or what they can afford.
The sound from CIs don't match how hearing people hear things. CI have way fewer neural connections than the cochlea has. Bilateral CI is often more effective for oralism than unilateral, but even then, CIs do not replicate natural hearing.
A CI can be implanted at any age, although it's most "effective" in infancy or adults with new-onset hearing loss, rather than people who have grown up d/Deaf. Getting a CI in adulthood is a very personal choice and can have a lot of meaning for a Deaf person.
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Gene Therapy:
[Plain Text: Gene Therapy]
This post has gone on long enough, and this isn't a hearing assistive device, but it is something to consider in a sci-fi or post-modern setting, and something we (the Deaf community) have to deal with right now.
There are currently new therapies (around 3 years in trial) that target OTOF mutations that cause severe to profound congenital deafness. OTOF mutations cause the loss of a protein that turns cilia movement in the cochlea into neural signals. The gene therapy introduces the gene that codes for this protein into the inner ear.
A small study on around 20 children, teens, and young adults with profound hearing loss (>100 dB) saw hearing curves change to 56 dB +/- 30 dB. I couldn't get the raw data because I couldn't access the study, but that means the average participant is still moderately hard of hearing and still needs hearing aids and accommodations. Depending on the metrics for calculating that error, there was likely at least one participant who remained severely to profoundly deaf after the gene therapy, and no participants became medically hearing.
We still have no data on if this gene therapy lasts forever or what kind of side effects it has. It also only works for a specific class of OTOF mutations, which account for many cases of congenital genetic deafness, but not all. Every single study on the gene therapy is produced by one company. This technology has not yet been peer-reviewed or tested for long enough. Nevertheless, hearing people are treating this as a cure, that the Deaf community doesn't want.
If a deaf person wants access to a technology like this, that is again their choice. Forcing this onto infants and children without autonomy or the ability to make an informed decision is horrible. The push to "cure" deafness goes hand-in-hand with the destruction of Deaf culture. It is eugenics. If you're going to include gene therapy or some other magical "fix" to deafness in your story, think about that.
Wanted to submit her for Black Girl Magic May but probably finished it late due to timezone variations akdndh. Anyways, I wanted to share my oc ciça :) this is my best drawing i have of her yet and im quite proud
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Overview of some topics when it comes to drawing characters who are burn survivors.
DISCLAIMER. Please keep in mind that this is an introductory overview for drawing some burn scars and has a lot of generalizations in it, so not every “X is Z” statement will be true for Actual People. I'm calling this introductory because I hope to get people to actually do their own research before drawing disabled & visibly different characters, rather than just making stuff up. Think of it as a starting point and take it with a grain of salt (especially if you have a very different art style from mine).
Talking about research and learning... don't make your burn survivor characters evil. Burn survivors are normal people and don't deserve to be constantly portrayed in such a way.
Consider supporting me on ko-fi if you find this to be helpful.
Edit: How are people seeing this post where I specifically talk about burn survivors being normal, real people, and still tag this as "TW body horror"? Not a single one of these drawings or pictures is a fresh injury. All of them are healed. How the hell would you feel if someone tagged a photo of you as "trigger warning: gore"?
Disabled people are not your fucking body horror. Grow up.
Alright, because clearly some people need it, let's talk about writing blind characters (again).
So. You want to write a blind character for your story or AU, but you yourself are sighted and don't know any blind people irl. The media is not your best outlet for finding good or accurate portrayals of blind people, and you're a little stumped on doing your own research. Maybe I can help fill in a few gaps?
(Note: I AM a blind person but I am only one blind person with one blind experience. There will be others with different backgrounds, different acuity levels, different overall conditions, different points in their lives of when they lost their vision, all of these things that will color how their blindness impacts their lives. Please when doing any research into representing a minority group ALWAYS seek out multiple experiences to gain a better, fuller understanding. I will be offering a viewpoint as someone who was born blind (ocular albinism), uses a cane, grew up relying on old school screenreading and magnification tools (and mainly just uses magnification now), reads and writes Grade 1 Braille (but has begun Grade 2), and has participated in many blind programs and communities since I was a young teenager. There is no "correct" way to be a blind person, there are just "different" ways, and they are all equally true and valid.)
First things first, canes:
Give your blind characters a cane!!! Most blind people are very interested in being self-sufficient and independent, and one of the best ways for us to achieve this is the freedom to navigate our own surroundings. Your cane is your best tool for this!
A lot of blind folks will also want a guide animal and that does take place of a cane, but also there will be a lot of instances where you will not be using your guide animal! They will take breaks!! They will need to sleep or rest!! They will not be suitable for every outing or excursion! Blind folks, even with guide animals, will still own a cane for these instances.
(There is also an instance where a blind person will want to use sighted guide. It's most comfortable doing this with people you are familiar with, but it works in a pinch with strangers too who are willing. However, a lot of folks don't know how sighted guide works. So to explain, essentially all it entails is the blind person will hold onto the space just above your elbow, and will walk about half a step in pace behind you. You do not need to do anything with your arm besides leave it relaxed (do not fold it up), and give out some verbal cues of changes in direction, warnings of upcoming steps up or down, or pauses for other passerbys or traffic. Reading out signs or keeping the blind person informed of what street you're on might also be helpful, but ask the individual what it is they desire from the sighted guide. Sometimes we don't need much, just someone to keep us from running into things if the sun is in our eyes.)
(Relatedly though do not do not DO NOT grab a blind person without their consent. DO NOT grab them, move them around, or any other nonsense like this. Do not TOUCH THEM without asking first, and if they say no, that means FUCKING NO.)
Now, how do canes work?
Most blind folks will use a white cane that is about to the height of reaching your chin standing up straight, so that when you extend it outwards it will reach far enough ahead of you to anticipate things at a distance (and you can also just as easily pull your cane in a little more to better reach things closer up).
Canes are most commonly made of metal or fiberglass, and these days a lot of them are folding canes (easy for stowing away while in transit on a car or bus or when seated anywhere).
The grip is soft with a cord hanging from its top that is used to loop around and hold in place the cane when folded, and when you are holding your cane outward in use your pointer finger will extend downward for best control over your tool.
The tip is made of hard plastic that can be slipped on and off because it will need to be regularly replaced as frequent use will wear it down, and these tips can come in a number of shapes, but the most popular you will see are a marshmallow tip (large and, well, shaped like a marshmallow), or a pencil tip (long and thin, this tip is my preference). People might switch out which tip they use depending on the terrain as well.
When in use, you hold your cane extended outward in front of you, and while you want the tip on the ground to be angled centered to your body, you are going to want the grip resting somewhere off to the side around your hip or just above (this way if you encounter a crack or something else in front of you that your cane will snag on, you will not wind up stabbing yourself in the gut with the grip. That shit hurts, avoid at all costs).
Depending on your specific needs, the terrain, and other factors such as lighting, crowds, or space available, there are a few different ways you'll actually use the cane. You can either have it running straight in front of you, tapping to the sides of you at 10 o'clock and 2 o'clock, or shorelining (where you keep a regular tap at your center and then at whatever edge your are walking by, whether it be the edge of the sidewalk or a wall, etc). When at rest, your cane should be pulled to stand up straight and held close so that it does not become a tripping hazard for others.
Your cane is an extension of your arm, it is a part of you. Treat it kindly, and if you see a blind person with their cane, do not touch it!!!! Even when folded up, leave that cane alone!!!!!
While not all blind people will want to use a cane, especially those with higher visual acuity, it is HEAVILY ENCOURAGED that all at least own one just in case they ever find they need it. Your blind character SHOULD own a cane and know how to use it. The likelihood of your blind character being one of the few who do not use one/do not find a need for one is so unlikely that at this point if you choose to go that route it's uh. It's just kind of insulting, that us needing such a tool is seen as so unnecessary, by sighted people no less. Give your blind character a cane.
What about Braille?
Braille is a tactile way of reading and writing, and it is very useful for a lot of blind people! There are a couple of different ways to write Braille: with either a slate and stylus, or with a Brailler.
Slate and Stylus:
This (older, but still useful) method is simpler in that it is much less cumbersome than a Brailler, but it does take a bit of brainpower as it requires essentially writing upside-down. How it works is your slate is sort of like a long metal sleeve that opens for you to slide a piece of paper in between the two sides of the slate. On the slate itself is the shape of a Braille cell (two columns of three rows of dots), and with your stylus you poke holes into that cell to make up whatever shape constructs your letter/word/number/punctuation. Most slates will have several cells along a line, and several lines to work with so that you do not have to move your slate around the page too often.
Brailler:
A Brailler takes the job of the slate and stylus and makes it a bit more streamlined, but it is more cumbersome to transport as a Brailler is not too different from the size and shape of a typewriter (don't worry, it IS smaller, at least, and has much fewer keys). You roll your paper in and clamp it down just like on a typewriter, and you have six main keys that make up the six dots within a Braille cell. When typing, you will press down whichever of those six keys at a single time that makes up whatever letter/word/number/punctuation you are trying to write, and then move on to the next (there are also keys for entering down, a spacebar, and one other that, I will admit, I have never once used so I do not know what it does lol. I think it is some kind of backspace for if you miss something? Backspacing is very difficult to do in Braille, for obvious reasons, so there are more limited scenarios in which backspacing is going to be beneficial).
Braille, being what it is (a tactile form of written language that requires the reader to run their fingers over the words repeatedly, allowing for erosion of those shapes overtime) necessitates using paper of a thicker size and shape than normal 8.5x11 printer paper. And even with the use of contractions (you begin learning these in Grade 2 Braille, and it is A LOT) Braille takes up a lot of space to write, so Braille books themselves are often very large and weighty.
This often means that a lot of blind people will prefer audiobooks over Braille books, as that is simply more practical in this day and age, but Braille is still an incredibly important resource that we should not be quick to overlook. We can read and write our own Braille, and this freedom of accessibility should not be taken for granted. Though a lot of blind people who still have residual vision might not be taught Braille growing up (I myself was not put in Braille classes outside of the few things here and there that my vision teacher taught me — it was not until my teenage years of spending more time around other blind people that I started self-teaching), I think this is a massive disservice to the community, that EVERYONE (sighted people included) could benefit from learning Braille.
What else do blind people use to help them in their daily lives?
Your mileage may vary on what you as an individual might need, but I will try to break down a few other helpful bits of information that you might find useful in writing blind characters!
Magnifiers:
(Side note: Not every blind person is totally blind. In fact, most blind people do have some level of residual vision. This might only be some small perception of light and shadows, but sometimes it is a usable amount of vision. There is some relativity in what is considered "legal blindness" depending on where you live, but if you find yourself with vision even at its most corrected with glasses or contacts to still have an acuity that falls below a certain point (for example, in the US this point is 20/200), you would probably benefit from considering yourself blind and seeking out resources to help!!!)
But yes, magnifiers. Whether they be glass ones you hold, or digital software on your various devices, magnifiers can be useful for both looking at things up close, and even perceiving things far away! A magnifier with built-in lights for reading, a screen magnifier with various contrast options for browsing your computer, a stand magnifier you can jury rig with a shoelace to tie around your good eye for hands-free Lookin (shoutout to 13yo Awpie on this one lol), bioptics for watching live theatre or films or even reading a menu at a coffeeshop (designed as tools to help people with low vision drive, these binocular lenses mounted onto normal glasses lenses have countless uses beyond their original intent), or, yes, even your standard everyday binoculars if you wanna sight-see beyond your usual scope. Most blind people with some amount of residual vision will have an arsenal of preferred magnification tools to choose from, so you should put a fair amount of consideration into what your character might most enjoy!
Screenreaders:
Used by both blind folks with total vision loss and blind folks with some residual vision, screenreaders have been around probably a lot longer than you think, and are indispensable tools that almost every blind person has at least some experience with, even if they do not prefer to use it in their daily lives. Most magnification software comes with its own built-in screenreader, but there are plenty that have existed on their own without being part of a magnification software (shoutout JAWS), but even devices and operating systems now are being designed with screenreaders built in-house too. The quality does vary from program to program, and people who use these regularly are going to Have Opinions on what they prefer, but if your character has low enough vision that using magnifiers would be more tricky than helpful, then they are GOING to make a lot of use out of screenreaders. I recommend attempting to use the screenreader on your phone sometime, just to see what it's like. It's actually a lot of fun!
Large print, tactile tools, color-coding, etc.:
There are a lot of ways in which blind folks will help themselves navigate the world without/with limited sight. Whether it be large print/Braille labels put on all of their household appliances, everything in their bedroom or office organized by color/in specific orders/marked with something tactile (puff paint was a popular go-to when I was a kid), or otherwise, blind folks will make their spaces heavily curated to their needs, and if we've been doing it for a long time (years or even our whole lives) we're going to be very good at it. Don't move a blind person's things in their space around without their explicit consent — everything has a place and we for the most part are going to be very used to keeping together a carefully constructed mental map of our surroundings, DO NOT INTERRUPT THAT.
And on the subject of mental maps...
Orientation and Mobility!!!
Not every blind person has gone through some degree of O&M training, but if you grew up blind and had access to resources in education to accommodate your disability, you are probably familiar with this class. What this entails is essentially being taught the tools and tricks for navigating out in the world independently, and if you've already spent years of your life needing to do this, you likely already have learned plenty of things on your own without the instruction.
But what the instruction does often cover is using your cane, identifying landmarks around you (whether by sound, smell, keeping mental track of how many right and left turns you make from a specific location you can remember), how to navigate crossing streets, keeping track of what other pedestrians are doing to assist in your own understanding of the flow of traffic, and how to orient yourself in a situation when you find yourself lost.
Not every blind person is going to have the best memory or mental map, but it is something we do have to more heavily rely on than sighted people, so the likelihood of your blind character being pretty adept in navigating familiar stomping grounds or adjusting quickly to new terrain after going over it once or twice with assistance is, all things considered, going to be pretty high.
And while we're talking about what blind people are and are not likely good at...
Heightened senses???
Blind folks, and I cannot stress this enough, do NOT. HAVE. SUPER. SENSES. Our hearing is AVERAGE. Our taste buds are AVERAGE. Our sense of smell and touch is AVERAGE. What MIGHT be above average is the amount we rely on these things, and thus our proficiency in utilizing them is going to be HIGHER THAN PEOPLE WHO DO NOT. But even still blind people are not immune to comorbidity of disabilities. Sometimes blind people are Deaf as well!!!
Do not write your blind characters with super hearing. Do not write your blind characters with supernatural abilities to tell who a person is by smell across an entire fucking room (unless that person is particularly known for being...odorous (in a good or bad way!!!). Do not write your character able to feel a piece of cloth and know exactly what its weave and fiber is unless they HAVE REASON to be so familiar with textiles. DO NOT WRITE YOUR BLIND CHARACTERS TO MAGICALLY HAVE VISION (METAPHORICAL OR LITERAL) UNDER CERTAIN CONDITIONS WHEN THEY OTHERWISE DO NOT. Commit to your character Being Blind, or do not bother at all.
And on this note, if you want to supply your blind character with some magical ability that allows them to bypass some pretty average blind person needs like using a cane/sighted guide/guide animal, reading Braille (or otherwise utilizing magnification or audio tools), or taking the time to put in the effort to learn how to navigate, organize, plan ahead, or customize their space to be accessible to them to their specific needs, If Your Blind Character Can Essentially Pass For Sighted Except When Being Blind Will Look Cool, you need to rewrite your character. Full stop.
What else are bad stereotypes, inaccuracies, or otherwise offensive mischaracterizations that should be avoided when writing blind characters?
We do not, have never, WILL never, want to touch your face. Cut that shit out right now.
Barring very specific conditions, a lot of blind people do not have white/cloudy eyes. For a lot of us our eyes look not too different from how a sighted person's eyes will look. But please please PLEASE actually research what condition your blind character has that caused their blindness so you can accurately portray what that would look like (for example, my albinism doesn't really effect the color of my eyes beyond they do SOMETIMES look red under certain lighting due to how easily light passes through to reflect off the blood vessels in the back, but this is under specific conditions and is not ALWAYS. Also people with albinism often have nystagmus, a condition that causes the eyes to constantly shake in a specific direction (mine shake from side to side). Knowing these details will allow you to most accurately describe/draw your character's features).
Also barring specific conditions/light sensitivities/personal self-consciousness in how the eyes might look (again, depending on very specific conditions), blind people typically do not walk around in sunglasses outside of any same reason a sighted person would have them on. A blind person with total vision loss will, quite frankly, probably not a give a fuck about ever paying for a pair of sunglasses that they do not need. It is so uncommon for blind people to needlessly rock a pair of sunglasses that at this point it's just a weird trope that y'all need to slow the fuck down on. We have pretty eyes that we will want to show off too!!!
Characterizing blind people as not having opinions on looks and appearances or even being above racism/colorism (????) is uh. Not true. Just not true. There is a degree to which blind people will not care about theirs or others appearances, especially to the point of really small details that a blind person might not even be remotely aware of if it does not come up in regular conversation (your clothes being wrinkled in a certain way being very easy to miss on a social level vs. something like, fatphobia), but we are just as capable of bigotry and prejudice. We do not have to see a person to have biases about them, and we are not immune to sucking in this way.
Characterizing blind people as being "wiser" or more open-minded about others and the world around them, having an "inner vision" of beauty or some shit... also Big Fucking No. Being disabled does not make you a more patient and understanding person. It does not make you smarter or more kind-hearted. It does not make you gentle. Cease this. We are all Just Some Guy like any other non-disabled person.
This is a lot of information, but I really do hope more people take the time to get to know what real blind people in real life are like. I hope that more sighted people take the time to care about viewing blind people as people, and not an interesting commodity to put in their stories for angst or spice or whatever the fuck. I hope that sighted people start pointing out ableism and bigotry in their communities so that we are not always left to do it ourselves, where other sighted people are less likely to listen to us, anyways. I hope that more people think about inclusion of blind folks in their spaces, of accounting for translating visual mediums into something we can engage with too, of acknowledging that we are just as likely to exist on the web and irl as sighted people are. I hope that including us is seen as less of a burden, less as something to complain about, less as something that sighted people feel the need to get our sympathy over when we simply ask to be given just as much of a chance to participate as anyone else.
I hope that you see us, and you treat us as one of your own. Not as something other. We are far more alike than we are different. So wise up and start acting like it.
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OP turned reblogs off but as someone with a crazy wicked scar that's been called "body horror" a few times, I really wanted this on my blog
in fact I think all of these are beautiful, cool, neat, or just neutral. nothing negative about any of it. also goes for implants, I've known people with implants of all kinds be made fun of, but that shit isn't ugly or gross either, it's just neutral and or positive
Hello Mrs. CBC! I hope you had a good ask break! (Or at least a semi-restful one lol)
With artfight coming up in a month, I’m looking for new people to follow, and I wanted to see if it was ok if I asked Black artfighters to promote themselves below. I’m super excited for this upcoming event and looking forward to finding new artists I love :D