they/it || I post art sometimes! tagged under #my art Original posts describes, reblogs might not be. Tagging is inconsistent, but if you want something tagged send me an ask! background id: a minecraft "failed to connect to server" error message that reads: "Failed to connect to server/ This server has been destroyed by evil xisuma". /end id profile picture id: a digital drawing of my sona, a human with their face covered by their hair and a mask. the mask has a cartoon smiling face drawn over the top of it. They wear cat paw gloves. /end id <\p>
When my family first moved to the UK, we faced a similar risk to our wellbeing & safety as many are facing now, albeit for different reasons. in light of everything happening in Ireland & the tensions increasing in Glasgow, and the perennial England, here’s a list of actionable things to do for people who may be targeted & anti racist allies.
MY HOME IS ON THE LIST/LIKELY TO BE TARGETED, WHAT CAN I DO?
* it may bring you peace of mind to have a go-bag ready, just in case. A go-bag is a bag with everything in it that you need to get out a volatile situation quickly. Any bag that can be secured (buttoned or zipped) will do. In your go-bag, you should include;
- any shelf-stable medication (tablets, inhalers etc.) if you are on medication that needs to be refrigerated, leave it in the fridge until you have to leave
- Sanitary items; toothbrush, toothpaste, sanitary pads & tampons, deodorant. If you have very young children with you, you may also want to take your nappy bag.
* If you have to leave, a go-bag is a convenient way to ensure you have everything of importance with you.
* If you are being supported by an asylum seekers or refugee charity, or are a member of a gurdwara/temple, mosque, synagogue or church, reach out to your religious leaders. They may be able to provide direct support, or put you in contact with organisations or other congregants who can help. If you are friendly with your neighbours, it may be worth contacting them too.
* IN THE EVENT THAT “PROTESTORS” DO COME TO YOUR HOUSE, CALL 999 IMMEDIATELY, AND FOLLOW ANY INSTRUCTIONS THEY GIVE YOU. MOVE AWAY FROM ANY WINDOWS. DO NOT OPEN YOUR DOOR UNLESS INSTRUCTED TO DO SO BY EMERGENCY SERVICES.
I’M AN INTERNATIONAL STUDENT/CARE WORKER/NHS WORKER, WHAT SHOULD I DO?
* Contact your student welfare office/NHS Trust/agency for advice, support and referral to organisations that may be able to provide assistance
* if you live in or commute through an area that is likely to be targeted, contact your lecturers and your faculty to find out whether remote study is possible; if you work in care or as part of the NHS, find out if it is possible to change shifts.
* If it would provide peace of mind, prepare a go-bag as listed above
* Reach out to your the uni society or student’s organisation for international students or students of specific ethnic origin; they may be able to provide you with direction to resources and peer support. If your university has a Marxist or Socialist society, reach out to them for mutual aid with a travel buddy etc., for getting to and from your place of study/work
* If you are a member of a gurdwara/temple, mosque, synagogue or church, reach out to your religious leaders. They may be able to provide direct support, or put you in contact with organisations or other congregants who can help.
* If you are friendly with your neighbours, it may be worth contacting them too for assistance with travel to & from work.
* Report any racism or racialised violence you are subjected to. NHS staff have a right to refuse to treat patients who harass, abuse, threaten or insult them; if a patient is racist to you, where possible, ask another member of staff to take over their care.
PERSONAL SAFETY:
* do not leave your home unless strictly necessary. If it is necessary to leave, don’t do it alone.
* use NextDoor, WhatsApp, social media and word of mouth to avoid commuting through “protestor” road blocks, areas of active conflict etc.,
* When travelling, use Share My Location or Life360, and keep at least two people aware of your expected time of arrival at your destination with instructions to contact the police if you do not let them know you’ve made it safely
* do not directly confront any individuals involved, or allow them to bait you into becoming confrontational
* only record if it is safe. Do not record individuals directly/from up close
* Do not directly intervene. If you see violence occurring, contact emergency services and if safe to do so, record what’s happening.
ALLYSHIP & HOW TO HELP:
* if you have neighbours, friends, coworkers or acquaintances form targeted communities, reach out to them. Ask them what you can do to help them feel safe.
* If you live in an area likely to be targeted, reach out to any vulnerable people you know. If safe and possible, offer to let them shelter with you in the event they need to leave home
* If you see any incitement to violence online screenshot it; it may prove useful in the event of individual “protesters” being prosecuted
* If you see any specific areas being discussed as targets, alert anyone you know at risk in the area
* Reach out to local refugee & asylum seekers’ organisations, to organisations supporting foreign national care & healthcare workers, and to churches, mosques, gurdwaras; they may be looking for short term assistance in helping to provide for vulnerable members of their community
CHARITABLE ORGANISATIONS FOR ASSISTANCE & TO SUPPORT:
* NASC Ireland; refugee & asylum seeker charity
* Doras.org; migrant, stateless persons, refugee and asylum seeker rights advocates
* Jesuit Refugee Service; religious refugee & asylum seekers charity
* Irish Refugee Council; supporting stateless displaced persons & refugees in NI & ROI
* International Student’s House (IE & UK WIDE): provides hardship funding and help to international students
* PathFinder (UK WIDE); supports international students
* Care International (GLOBAL); global carer’s charity
* Choose Love (IE & UK WIDE); charitable organisation supporting refugees and asylum seekers
* Praxis UK (UK WIDE); supporting refugees & asylum seekers
* The Runnymede Trust (IE & UK WIDE); antiracism education charity
* Migrant’s Rights Network (IE & UK WIDE); advocacy and support for migrants and refugees
* ShareTheMeal (GLOBAL); providing meals for refugees and those fleeing conflict globally
* Amnesty (IRELAND, UK & WORLDWIDE); human rights NGO
* UNHCR & UN Refugee Council (GLOBAL); UN refugee bodies supporting those seeking asylum, fleeing conflict & internally/internationally displaced worldwide
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i am not a psychiatrist but i do find it really weird how autism checklists are so often focused on "outward" signs of autism rather than what is going on internally. i don't know how to explain it but "do you make eye contact with other people" feels like a much less relevant question than "how does it feel when you have to make eye contact with other people?"
while i'm here, the other one that always pisses me off is "do you interpret idioms literally, for example 'bull in a china shop'?"
well, no, obviously. i know what "bull in a china shop" means because that is a popular phrase with a clearly defined meaning. and if i hadn't heard it before, then i would still not interpret it literally, because it has the cadence of an idiom and i would probably be able to work out from context what it meant. what is the point of this question
third and final complaint: "are you good at noticing subtext?"
i feel like the problem with this question is best illustrated by a conversation i had with a friend a while back, where i said something like, "i feel very safe with you because you don't do subtle hints and you are always very straight-up with me about what you are thinking and feeling."
and he laid a hand on my shoulder and was like, look dude i'm gonna be straight up here. i am subtle with you constantly and you simply do not notice <3
[Image description: tags which say #i will say that the external-focused diagnostics is a problem with every single psychiatric criteria #like. read through the DSM and it's just 'in what ways is this person a Problem for other people' and its so fucking insidious]
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.
I've seen some good points in the notes that not everyone who needs hearing aids has the appropriate aids, and not every d/Deaf person uses hearing aids or CI at all. Those are both excellent points! This guide was more meant to describe what an appropriate hearing aid should look like, mostly so people have a reference to not draw hearing aids like they're headphones or give characters the completely wrong type of aid.
But yes, when considering what type of hearing assistive device your character would have, here's an incomplete list of things to think about regarding if they have the "proper" type of aid:
Can they/their family afford the aids? Hearing aids are expensive and not always covered by insurance; cochlear implants are even more expensive because they are surgical *and* the device itself requires updates. There are also costs for speech therapy.
How long ago were their aids last updated? Once they're an adult and their ear size stops changing, the same aid can fit forever, even if the features no longer work for their hearing loss. They may have an aid that's not powerful enough for their current needs.
For CI: bilateral vs unilateral implantation. If they're unilaterally deaf (or only one ear qualifies), they'll only have one processor. While audiology recommends two CIs for the best sound quality, many people who are bilaterally deaf only have one implant.
Do they use their aids? Many Deaf people may not use hearing aids or CI because they don't want to hear, or they don't think it benefits them. (Relatedly, do they have scars from CI/BAHA implantation, even if they don't connect the processors?)
Are they in a setting where they would be given a modern hearing aid? This post did not cover historical types of hearing aids, though I might do that in the future. If you have a sci-fi setting, maybe hearing aids look different--perhaps the processors have gotten even smaller and more powerful. (Domes and molds will probably look fairly similar though!) A historical or fantasy setting may not have hearing assistive devices at all.
irritating as fuck when people get mad at Black people existing in premodern historical fiction/fantasy media. like first of all, you're racist. and second of all, you are acting as though Black people didn't exist in premodern Europe which is simply false. especially when we're talking about the Mediterranean, like what the fuck do you people think is along the southern half of the Mediterranean Ocean?? everyone's on boats, there are GOING to be interactions with Black people in Northern Africa, and there are GOING to be Black people in Mediterranean Europe. stop being stupid. your imagined homogeneous white European past is not historical reality, get over it you massive losers
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The Tube Post has been updated for 2026! Endless thanks to @andstuffsketches for the amazing art (!!!), @rowenabean for checking this over for me (all remaining mistakes are my own), @kelpforestdwellers for extra tips, and @appleyblam for an editing pass. Thank you all!
If you would like to download the zine for your own use, you can find it for free on itch.io.
huge fan of when characters love each other and are closely bonded in an explicitly nonromantic way. however ☝️ i am very much not a huge fan of what happens when characters like this are introduced to fandom
if you're having trouble sleeping the best you can do is put a bright object close to your face and look at it for at least 30 minutes. if that doesn't work you can close your eyes but make sure to think really hard about a bunch of bullshit
one thing i am quite grateful to Brian David Gilbert for is the phrase "If you needed ME to tell you that... I'm glad I told you that."
it has been etched into my brain for the past six years, fundamentally altering how i consider knowledge gaps held by others, as well as myself. people usually need to be told stuff before they can know it! that's how knowing stuff works! this is an extreme example played for laughs but it's a legitimately helpful philosophy!!
it's always ethical to kidnap an outdoor cat and make them an indoor cat. shithead owner will just assume a car or coyote got them. outdoor cats are bad for the environment, local wildlife and themselves. the only one that benefits from an outdoor cat is the lazy piece of shit owner that doesn't want to actually look after their cat. give that outdoor cat a better life, a longer life.
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[ID: Four stills from Wallace and Gromit: A Matter of Loaf and Death (2008), a Claymation film. In the first frame, Wallace- a cartoony, bald white man, is sitting at a table and gesturing outwards with his hands while the subtitles read, “And I’m not a fruit cake, am I, lad?”
The next frame shows Gromit, a cartoony dog, who is stirring a cup of tea with a pinky extended, looking away from Wallace with his eyes wide and brow lifted like he is a little taken aback. The third frame shows him squinting at Wallace in polite disagreement or perhaps in a sarcastic placating manner.
The fourth is a slightly wider shot showing them both, and some other items on the table in front of them. Gromit is reaching over to give Wallace a sympathetic, if slightly condescending, pat on the shoulder, while Wallace looks down sadly into his own cup of tea. / end ID]
I don’t think there’s anything inherently wrong with relating to characters, “they’re literally me” etc but if that’s the only way you engage with stories you’re kinda missing the whole point of Characters being vehicles through which we can see perspectives outside of our own. and also you’re going to get upset when the Character acts in a way that is not Personally Relatable to You
doubly for shipping. at risk if biting the hand that feeds me, a well written fictional relationship should ideally be more than a didactic template for how to have a nice relationship
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this makes me so happy as a fat hairy guy who likes skirts and dresses i never get to see guys like me in dresses it’s always skinny twinks this makes me so happy 🥺🥺
med people are so annoying "This family's 8 year old child who was about to go through a major surgery and kept crying that she was hungry so they pitied her and gave her food, she then had a heart attack in the surgery. They're so stupid 😒" girl they didn't know that could happen or why it happens. it takes so little time to explain to them that will happen instead of telling them "no food" with no explanation 10 times
"Before surgery, your body’s reflexes that protect your airway are relaxed by anesthesia. If there’s food or liquid in your stomach, it will near certainly come back up and go into your lungs, which can cause choking, a severe lung / heart infection or even a heart attack. That’s called aspiration, and it is life-threatening. It's hard, but it's only a single day to prevent near certain death. Not eating or drinking beforehand massively lowers the risk and helps prevent these life threatening situations under anesthesia." <- TIP: patients have brains which allows them to receive information just like you
I have four kids. I’ve had one or another of them need some kind of surgical procedure that requires anesthesia four or five times over the past 15 years.
This Tumblr post is the first time someone has explained to me *why* I couldn’t feed them before those instances.
I’m not stupid. I understood that just fine. Hell, my kids would have understood that just fine. But no one bothered to tell us.
i did know this before having kids (i have six). we have a kid that's needed multiple procedures requiring anesthesia. and every single time, i am asked multiple times if i'm sure he was not given any food or water after a certain point.
every single time i have had to say, "i understand that if he had food or water, he could aspirate it into his lungs under anesthesia. i am not lying to you." THEN someone would make a little note and i would stop being repeatedly asked.
not a single time was that risk explained to me. the only reason it came up was because i already knew. i still don't understand why it isn't standard pre-op counseling or pre-op check information, when me as a parent acknowledging the actual risk also put THE MEDICAL STAFF at ease because i conveyed that i had informed understanding as reason to not lie about giving my kid food.
"maybe some people will get nervous and refuse surgery" okay so they need more counseling about risks and anxiety, not less information in a way that actually does endanger their child or themselves!