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Artfight
FAQ:
Q: Can I repost your drawing?
A: No, but thanks for asking.
Q: Can I edit your drawing?
A: No wtf. ?
Q: Will you make a tutorial about drawing [injury]?
A: No, I have roughly zero (0) experience drawing injuries.
Q: Will you make a tutorial about drawing scars?
A: I was considering it at some point but the burns one took years off my life. So also no, sorry.
Q: Have you made a tutorial about [blank]?
A: I've done:
Blindness
Burn scars
Cleft lips
Down syndrome
Facial paralysis
:)
Q: Will you make one for [insert other disability]?
A: IDK. If you saw me draw a character with that disability before, chances are the answer is "possibly". Just please be aware they take a lot of time to make. But you can drop a suggestion in the ask box if you want.
Q: [character writing question]?
A: Please send it to @cripplecharacters instead. I'm here just to draw blorbos from my brain.
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Tutorial for drawing characters with cleft lip! Sorry that it's mostly unilateral-centric but it makes up the vast majority of resources and photos. Still tried to get tips for drawing bilateral clefts in though.
Keep in mind that this is an introductory drawing tutorial and has some generalizations in it, so not every “X is Z” statement will be true for Actual People 👍
If you draw any characters using this feel free to tag me!
Consider supporting me on ko-fi if you find this to be helpful.
I don't know who I'm saying this for, but when one is drawing characters with cleft lip and/or palate, it is important to recognise that clefts go through bone as well as soft tissue. The reason why I'm saying this is because a lot of people just draw a normal face and then draw a line through the lip and put a gap between two teeth.
Because people with clefts have missing bone, the topology of the face is completely different to a regularly formed person's. This still applies to repaired clefts, to what extent depends on the original severity of the cleft and the success of the surgeries + orthodontics.
(I am going to use the word "cleft" by itself several times for the sake of brevity, please know I am referring to maxillofacial clefts every time. Clefts can occur outside of the maxilla, where they are known as craniofacial clefts, I will not be covering those right now.)
I find diagrams like this to be misleading, as they present the cleft like a thin "cut" in an otherwise fully formed head.
This is a more accurate visualisation of the condition, a cleft is more like a "gap" or "chasm". Tissue, both soft and hard, that would've been present in this gap is missing completely. That's skin, bone, muscle, teeth, and everything else.
People with clefts will often have a bone taken from usually the hip to be added to the upper jaw, to substitute for the absent material. People with clefts are also often missing adult teeth. Cleft repairs take a very long time, and that's under accessible healthcare of relatively high quality. The missing bone in the upper jaw causes most with maxillofacial clefts to have underbites, because the upper jaw is too short. Underbite correction is often the very last major surgery to be carried out. It is often done in the early twenties, because bones have stopped growing in length by that point in most people's lives. It is important to pay attention to the age of your character with a cleft. I don't expect you to have planned out an entire medical history, but the structure of a face with a maxillofacial cleft changes dramatically throughout early life. I think the underbite is the biggest thing I want to see more in people's cleft characters; remember the underbite caused by a cleft is due to a short upper jaw and NOT a long lower jaw.
For unilateral clefts, the nostril on the side of the cleft is smaller than the other, unless the cleft stops a while before reaching the nose. The cleft-side nostril also often has compromised breathing ability, causing many with clefts to rely on breathing through the mouth instead. People who are still going through treatment can have a fistula connecting the inside of the mouth and the nasal cavity. This fistula causes trouble with eating and drinking, as material passes into the nose and food can clog the fistula up. On the bright side, it can allow for the very cool party trick of being able to drink through the nose or eject fluids through the nose from the mouth. The deformed shape of the mouth affects pronunciation as well, since the jaws don't align as they should, people with clefts have to "cheat" to perform certain sounds. The voice also often sounds nasally because of increased airflow into the nose.
Even though the clefts are maxillofacial, effects can extend to the ears. People with clefts often get frequent ear infections especially as children, some have a flattened ear canal on the side of the cleft, and some have impaired hearing and may require hearing aids.
So I kind of forgot what the point of this was, but I just often see clefts treated by artists without them as a superficial detail that you can plaster onto a character's face with no structural changes. It is important to consider the underlying bone structure and how that affects the facial surface, and if the character is undergoing repairs how far along they are.
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Height: 136.8 cm / 4'5.9" (high elf average: 178.2 cm / 5' 10.2")
Personality: Aloof, detached, eerily calm, quiet, cryptic. No ambition or interest in power or politics; content as is.
Personal Resonance (magic): "Celestial Cartographer," sees fractured glimpses of past or future aligned with current night sky; visions arrive unbidden.
Status: Department of Vertebral Column (DVC, Sovereign Territory), known as "The Meridian."
Diagnosis Summary:
Congenital growth hormone deficiency (GHD), also known as pituitary dwarfism, a form of proportional dwarfism (where, unlike disproprtionate dwarfism types like achondroplasia , little people with proportionate dwarfism’s body proportions follow that of average height person, but smaller / shorter).
Epilepsy.
Level 1 autism, non-masking. Visible presentation: aloof, disinterest in social interaction, special interest in astronomy and magical astronomy.
Extra Considerations:
Department of Vertebral Column (DVC) - highest executive structure of the Sovereign Territory, answering directly to The Professor. Mephistophe/The Professor's inner circle. Consists of five members (currently).
As member of DVC, oversees The Observatory (name TBD), important structures for observing stars as original source of magic, critical in magical astronomical and celestial archeological fields as well as wider implications for magic use as a whole.
Quilted cape depicts an accurate star map of the current night sky. Updates live. Stars made of seed beads; lines stitched by thread.
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(Design notes: technically night sky & constellation in world different from our world, but that involves inventing things, so used irl sky. helpful reference: https://www.skymaponline.net/)
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[please do not tag as “inspo” “to reference” (for own character designs) or similar!]
Is there any actual basis in reality for people with no vision keeping their eyes closed all the time? No one I know ever seems to do it although I've known folks who don't use the lights in their house and similar things. Obviously the media recurrence is probably just pigeonholing coming from visual shorthand
Hey!
Some people who are fully blind from birth do in fact keep their eyes closed. Basically, you require muscles to keep your eyes open, and if you don't use them then they atrophy (like every other muscle). IIRC, Tommy Edison has talked about this on his youtube channel since it applies to him personally.
But for people who went blind later in life or were born with usable vision you don't really see that. Keeping your eyes open is just a habit that's borderline impossible to drop, even if you can't see anything [anymore]. There are some exceptions where people might no longer be physically able to open their eyelids anymore, like with nerve damage, or if they had both of their eyes removed and their eyelids atrophied over time, or they have some comorbid condition that affects their eyelids, but that's just rare.
Either way it's a more realistic shorthand than the dreaded blindfold that doesn't have any basis in reality. Still overused in media though.
Hi, I have a POV character with a spinal cord injury and I was wondering if it’s ok to mention medical supplies like catheters/night bags if it’s part of their routine. I won’t detail their voiding habits or provide medical exposition / actual toileting scenes, but instead just reference them buying catheters/other supplies or a sentence mentioning they disconnect the night bag if it’s a scene where they’re waking up. Is this reasonable or would it be better if it isn’t mentioned at all?
Hi!
Please mention medical supplies! Most people don't even know what these are or why they're necessary! You're right that you don't need graphics of "how people with SCIs pee" but having a cath or a bag is just a part of your character's life. Plus, it always makes us super happy to see our medical devices and supplies represented in media! :) [smile face]
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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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