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@phys-psy-disabled
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pedestrians don't seem to realize how exhausting using a wheelchair is, both manual and powered. i had to wheel around a hospital today with several ramps i had to go up and down multiple times, and even with my smoov i ended up with shoulder and chest pain and deep exhaustion.
people look at wheelchair users and think "well you're sitting down all the time that doesn't take effort" no actually it does. pushing a manual chair takes a lot of fucking effort, especially without a power assist. repetitive stress injuries are a huge problem manual chair users encounter all the time. going up hills and ramps is so deeply fatiguing.
this doesn't just apply to manual chair users btw. power chair usage can also be really exhausting, especially for people with complex seating needs. going over bumps and cracks can trigger many symptoms such as spasticity, pressure sores are common, even just sitting upright can be exhausting for many people.
basically don't assume using a wheelchair takes 0 effort, it really really does. getting to "sit down all the time" doesn't mean it's easy.
im gonna need you able bodied motherfuckers to stop comparing the extreme pain and exhaustion that comes with using a manual chair to being in a car for 8 hours. not even remotely the same thing.
Enlightening post! I must admit, I had not appreciated all these difficulties....this total level of difficulty. And then that very important addendum! I have been one of those people glad to stand and walk after too long being seated in a car—especially after surgery. But @smoov-criminal if that is not the closest approximation an able-bodied person might be familiar with, then what is?
I grant the proper answer may be "nothing at all", and even the framing of "scaled approximation" may be inappropriate. But that's one of the things I've got. That is part of how I relate to disability... through more discrete instances of my own debilitation and reliance on inadequate support structures (including sometimes structure in the literal, physical sense).
i wanna say i genuinely appreciate you asking politely. not everyone does that, so im happy to answer in detail.
for manual chairs the sitting part by itself might be somewhat similar to sitting in a car, though there are key differences, mainly the length of time being a relatively short car ride versus using a wheelchair up to 24/7. you also have to consider that wheelchair users are very very likely to have conditions that affect the ability to sit upright comfortably for an extended period of time. some people, such as those with SCIs, have poor trunk control (trunk sort of means abdomen) which means they may slump down in their seat (there are ways to mitigate this via the way ones chair is set up but i digress). people with hip problems can develop pain or dislocations due to the position ones hips must be in, as a few examples. for me personally i get bad soreness and fatigue in my legs from having them bent at that angle, i can only truly be comfortable with my legs fully elevated. and even with my $600+ cushion it starts to hurt after a while.
this is even more of an issue for power chair users, especially those with group 2 or 3 chairs. pressure sores like i mentioned are exceedindly common, especially for people who are very likely not be able to shift positioning independently, which is why things like tilt and recline exist, to take pressure off those spots (among other things like decompressioning the spine). someone who uses a massive bespoke powerchair may still experience extreme pain or other symptoms while sitting in their chair, and the only place they can actually be somewhat comfortable is in a special bed. its not relaxing to get to sit in a cushioned powerchair all day every day, because the people that need them often cant tolerate sitting for more than a short period of time.
and we havent even started talking about actually moving in a wheelchair. we cant talk about manual chair use without talking about repetitive stress injuries. your arms are not limbs that are designed for ambulation, they don't have nearly as much muscle as your legs and as such it is much harder to use your arms to get your body *and* often very heavy medical equipment around. is not an easy task even on completely smooth, flat, even ground, and given that the majority of ground that is traversed by the average person is neither smooth, flat, nor even, it's all that much more difficult. and again you have to consider that wheelchair users are disabled people who, more likely than not, have some sort of body systemic disorders that affect more than just the legs, which can make pushing all the more difficult. someone with me/cfs might push themselves into a pem flare. i have eds which is a large part of why i need my wheelchair, but it also affects my shoulders which means i get a *lot* of shoulder pain. ive got torn tendons in my shoulders and ive only been using my chair for 2 years and change, with a power assist. there are some people who desperately need a wheelchair but genuinely cant use their arms, shoulders to self propel without extreme pain, and powerchairs are prohibitively expensive, so lots of people just go without even though walking is extremely difficult.
and now we must talk about the difficulties of navigating the world around us *on top of* the difficulties of using mobility aids in the first place. imagine being completely barred from like half of the places you want to go to, and half the places you can actually go are like at least 4x as hard to navigate due to narrow aisles/paths, blocked aisles/paths, people that seem to lose all sense of spatial awareness when a wheelchair user enters their vicinity, cracks and bumps and other hazards, people leaving objects in the middle of the path, "accessible" entrances/parking spots being very out of the way, lack of automatic doors, lack of accessible (CLEAN) bathrooms, i could keep going.
theres also the fact that human bodies receive a lot of information about their surroundings via proprioception, which gets very messed up when you're in a wheelchair. you no longer have access to the movements that your body does to understand the space its in, which makes navigating the world even more difficult because we don't have that sensory feedback. and for a population who is way more likely to deal with brain fog and other cognitive impairments you can see why this takes a lot of mental energy on top of physical.
there's even more that i could talk about but this post is already quite long. here's a link to a reblog my friend made that has some sources attached to it about repetitive stress injuries and other complications that might also be helpful.
as a conclusion, wheelchair usage requires a lot of effort, physical and mental. it is usually better than not being able to go anywhere at all, but not always. so keeping all of that in mind, try to share some extra kindness to the wheelchair users in your community.
thanks again for asking politely!
As a disabled person: a world with no modern tech, no modern medicine, no electricity, and no single-use plastics is a world that cannot keep a great many disabled people alive
Disabled people have always been a part of humanity, and we always will be
And if an imagined future doesn't involve keeping us alive, I want no part of it
By the numbers
Disability:
World Health Organization fact sheet
Key facts
An estimated 1.3 billion people experience significant disability. This represents 16% of the world’s population, or 1 in 6 of us. ...
Persons with disabilities have twice the risk of developing conditions such as depression, asthma, diabetes, stroke, obesity or poor oral health.
Persons with disabilities face many health inequities.
Persons with disabilities find inaccessible and unaffordable transportation 15 times more difficult than for those without disabilities.
Health inequities arise from unfair conditions faced by persons with disabilities, including stigma, discrimination, poverty, exclusion from education and employment, and barriers faced in the health system itself.
Overview
Disability is part of being human and is integral to the human experience. It results from the interaction between health conditions such as dementia, blindness or spinal cord injury, and a range of environmental and personal factors. An estimated 1.3 billion people – or 16% of the global population – experience a significant disability today. This number is growing because of an increase in noncommunicable diseases and people living longer. Persons with disabilities are a diverse group, and factors such as sex, age, gender identity, sexual orientation, religion, race, ethnicity and their economic situation affect their experiences in life and their health needs. Persons with disabilities die earlier, have poorer health, and experience more limitations in everyday functioning than others.
-via the World Health Organization, aka the WHO, March 7, 2023. Emphasis mine.
the thing is. knowing someone experiences hallucinations or trouble reading facial expressions or communication difficulties or any other symptom CAN help you to understand their behaviour and respond to it appropriately. but knowing someones diagnosis is never as helpful as it is to listen to them when they talk about how they can best be accommodated. and if “can you please speak slower” (for example) sounds like a ridiculous request from someone without a diagnosis and a reasonable one from someone with a diagnosis. well you’re the dick in that situation
One thing I really like about Beverly Engel's book It Wasn't Your Fault, which is about PTSD-induced toxic shame, is that quite a bit of it deals with people who haven't broken The Cycle of Abuse (TM) and have gone on to hurt others. That's a really underserved and vulnerable patient population, and statistically, it's also MASSIVE. I don't think I've read a single other self-help type book on PTSD and self-loathing that confronts the possibility that you're exactly as bad as you think you are.
I felt better that it so much as mentioned that children can react to abuse with ungovernable rage. Everybody likes the image of PTSD patients as internalizing everything and becoming doormats, which does happen, and often, but it's not the only narrative. Personally I've always hated my abusers and have always wanted everyone who so much as breathed wrong in my direction from ages 0 to 18 to burn eternally in hell. I *never* thought any of it was my fault and ever since I was a toddler I was willing to make it everybody else's problem, and it's really relieving to read a clinical perspective that acknowledges that abuse victims can act that way too.
It's wild to me that its such a neglected subset of abuse victims. Its really common. When I still lived with my parents and was still subjected to my father every fucking day I would lash out terribly at my mother, to the point when i went to visit them for years afterwards she was afraid I would lash out again. We've worked it out, I'm a much better person when I'm not regularly subjected to mental and emotional abuse, but like, its just so common.
I think it must be, at least partially, because, people hate the imperfect victim. Its easy for so many people to sympathize with someone who never lashed out. Less so for people to sympathize with people who are angry and lash out. Even though its a perfectly sensible reaction to being hurt over and over. I'm sure most people would like to think they would simply never.
I don't think this is the whole reason, but, I think it plays into it.
Similarly, there’s a narrative of, you cannot experience grief over having fucked up. That if you are hurting because you caused harm, because you were the cause of harm, that you’re not allowed to grieve, because you “earned your sorrow. You deserve to bottle it up and to hurt for the bad things you have done,”
Which is punitive logic. It’s copthink. Which is bad.
important
In fact, you can actually give yourself trauma over fucking up too badly and doing, witnessing, or failing to prevent something evil that goes against your morals; for instance, if you steal your mother's life savings due to drug addiction, kill a civilian during a military operation (please do not join the military), or became abusive because you didn't have the tools and skills yet to handle BPD. In the field of psychology this is called "moral injury" or "perpetrator trauma."
there is a screen reader / magnification program that is the only one the low vision clinic knows of with these features and it is $650 Canadian Dollars behind specific approved vendors that require you to be geographically close to them and get government approval of a degree that I am only just now reaching after being visually impaired for going on seven years. I feel normal about this
if you can code a program that does any or all of the following:
Magnifies a display beyond standard options with keyboard / mouse movement inputs or voice commands,
Can read text on the screen,
Has different color filter options for text / background distinction,
Can change and magnify the cursor beyond standard amounts,
Works on Windows or more than just Windows,
Has a keyboard echo (says the character you've pressed on the keyboard out loud)
... there is a genuine, GENUINE need for you to code this and put it at a more accessible price point than $650 Canadian Dollars which I also just learned is a SUBSCRIPTION FEE AND NOT EVEN PERPETUAL. if you are reading this and able to code I am begging you. would genuinely change lives
It would kill half the 19-25 year olds online to realize "I can't help it I have trauma" is one of THE quintessential abuser excuses
Like there is a difference between "My trauma creates impulsive urges and has changed my instinctive reactions to be irrational, I need to relearn shit." vs "I'm traumatized so I Can't Help It and you're not allowed to expect better of me"
a lot of people assume psychosis hallucinations are super intense all-consuming horror movie shit like the memes about the hat man or always horrible debilitating things that make you dangerous to be around
but in my experience 95% of my hallucinations are getting spooked by very clearly hearing someone knocking on my door or calling my name from another room or hearing footsteps walking behind me which are "just" my brain recreating the horror of an abusive childhood
i *have* gotten the "bugs crawling all over me" hallucination once or twice though and yeah that one is exactly as terrible horrible as it sounds AUGH
(not trying to put you on blast specifically, you're just a good example to jump off of)
media and pop culture hypes up psychosis a lot as The Worst That Can Happen out of sanism, so even when you try and filter that cultural bias out you still assume it's based on something
when, no, psychosis is actually very simple: it's just hyperactive pattern matching. it's your brain's signal-to-noise ratio being off balance, it's seeing images in random static. it's not always this special uniquely big thing, it's in fact quite mundane a lot of the time.
no one is immune to psychosis, it's not purely the realm of the insane. anyone is one bad night of sleep or one bad case of food poisoning or one bad fever away from being just like me on my worst days.
and this, indeed, is why solidarity with the insane is so important: you, yes you too, are just one bad day from joining us, and no perceptions of being a "temporarily embarrassed sane person" will save you from the oppression of the psychiatric institution.
how manual wheelchair users move (explainer for non-users)
frequently when i’m out and about with someone walking, they can’t anticipate what path i will take and therefore they’re in my way pretty frequently. this is fine! i can politely ask them to step to the side. but it makes me think about how little non-wheelchair users understand the way wheelchair users move. as someone who used to walk everywhere, it was an adjustment period for me to figure out how to navigate the world in a chair. here are some things that didn’t occur to me so that you don’t cut off your friend right as they’re building momentum to go up a ramp 😆
for context, i use an active manual chair. the world is very different in a power chair. even among active manual chair users, there is a huge diversity in physicality and strategies for getting around. this is a general guide that i think will apply to most manual wheelchair users. i’m starting super basic and getting more complicated as i go.
———
1. manual wheelchairs are a momentum game. it is very easy to maintain speed and direction. but speeding up, slowing down, or turning, is hard. one thing this affects is if we’re on a wavy sidewalk or other twisty-turny walkway, that is a pain in the ass and i am taking as straight a path as i can.
2. wheelchair users also have to pay attention to the slope and condition of the pavement, so our path somewhere will be different than yours, even if we’re taking the same route to the same place. for example, i usually have to go down slopes straight, not diagonally, to avoid tipping over sideways. one area this affects is crosswalks. many intersections have one curb cut for both roads you could cross, which means i will go down curb cuts to a crosswalk as if i am aiming for the middle of the intersection.
your path in orange, mine in blue. to you it seems indirect, but to me it’s the path of least resistance.
i also will be building speed in the second half of the crosswalk. this is a much easier way to tackle a ramp. if i approach with momentum, i won’t have to drag myself up the slope once i get to it.
3. building momentum and maintaining it is only half of the job. the other half is stopping. manual wheelchairs cannot stop on a dime if they’re moving with any kind of speed. if i tried to stop immediately when going downhill, i would fly out of the chair. so don’t walk right into the path of a wheelchair in motion and then stop! i will have to turn to the side very quickly and hope i don’t tip. i can’t tell you how often parents pushing strollers will stop their stroller directly in my path and then get offended when i am alarmed and turn sharply to avoid hitting their child. from their perspective, i was being careless and going “too fast.” in reality, normal walking speed takes a few feet to slow down from and stop.
4. in terms of slope. see this street in san francisco?
i can’t go down this street, it’s way too steep. i would give myself friction burns on my palms trying to control my speed. if i was in a situation where there was no avoiding this street, like in an emergency, i would be breaking my straight-slope rule and zig-zagging in the middle of the road.
this would require several zig-zags back and forth, more than the four that i drew. i also could not go up this road other than with this method. up or down, i risk tipping over sideways if i’m not careful.
4. in a similar vein, consider terrain. slopes with grass or carpet take huge amounts of energy to get up. this grassy hill isn’t insurmountable, but it would take me like thirty minutes to get up there. honestly i would probably go backwards, because it’s easier to pull yourself up a slope than push yourself.
other types of terrain can be completely immobilizing, though. this decorative gravel pathway is beautiful, and inaccessible to me. my casters (front wheels) simply will not go through that.
5. in terms of walkways and obstacles. if there’s a deep gap in the pavement lined up the way i’m going, and it’s, say, an inch wide, that is an obstacle for me. my casters are one inch wide, and my back wheels are an inch and a half. i’ll get stuck in it like a train on a track.
i have to straddle this, even if it means being too close to the middle of the sidewalk and preventing us from walking side by side.
similarly, if a crack is greater than an inch high, i’m gonna wheelie over it. at two inches, i have to. a wheelie may require a change in speed, either faster or slower depending on the person.
i have 4 inch casters, so a lip as little as 2 inches will stop me in my tracks. a lip as little as one inch, hit with any speed, can knock my casters out of square. casters can get knocked out of alignment pretty easily depending on the chair. i’d rather not have to pull out an allen wrench and a level, so i’m gonna wheelie.
this happened when i hit about a 1.5” lip on a pavement crack when i was going downhill at maybe 3mph.
6. putting it all together. see how diagonal this crack is?
this is another situation where i have to go straight relative to the slope. because that crack is wide, it will probably also require a wheelie. if i tried to approach that straight relative to the sidewalk, my left caster would get up the slope, i’d wheelie, then my right caster would land in the crack. i have to go this way.
(also lol at the trash can blocking the curb cut)
these are just a few things to keep in mind when walking about with a wheelchair user! ofc the best strategy always is just to listen when someone asks you to move out of their way 😆 but i think being able to anticipate movement a little better will help it seem less random. feel free to ask any questions!
"I am not a vessel for your good intent" goes hard as a line from a disabled perspective. Abled people care so much more about being their idea of a good ally than they do actually being a good ally. They shove their good intent right down your throat and then act surprised when you tell them they're suffocating you.
[ID: An image of a sign with a blue background and with a graphic of a stick figure in a wheelchair at the beginning, resembling disabled parking space signs. The text below the stick figure reads "I am not a vessel for your good intent." /ID]
For disability pride, think I want to focus on this one thing that been bothering me
Been very frustrated lately by lack of phone call accessibility as someone who lacks speech but needs a lot of resources to stay healthy.
With rise of AI, it's only getting worse and worse.
More places changing their systems to incorporate AI answering machines.
Thing is...
Whenever I hear most people ranting about this change, it's usually about how annoying it is from an abled-person perspective or environmental or ethical impact.
Which are important valid reasons to be upset. I share those sentiments too.
But feel like disability is once again forgotten about within important discussion about change.
AI creates terrible language accessibility issues.
In fact, that's why it so annoying to deal with it.
In the past, if a place didn't have a call center or desk person to answer calls, they use extentions.
That meant you had to press a few numbers to get the right person.
Now with AI, you're expected to have a full conversation with a robot.
Tell them why you're calling, who you need to speak to, verify your info so the humans don't have to later, etc.
These bots can be bad at understanding what able-people are saying, so imagine how they handle these disabled callers:
People who use AAC (speech aids/devices)
People who slur, stutter, have "strange" voice or pronunciation
People with rapid or disorganized speech
People who use poor grammar & who don't speak full words or sentences
People who mix up similar common words
People with "deaf accent"
(i don't know if there is a different preferred term for this. Im sorry if I sound offensive. Please Lmk)
People with non-communicative speech such as vocal tics, echolalia, or babbling
Anyone who uses speech or language in a way that needs a human mind to interpret
Anyone whose voice sounds notably different
Ability to understand what AI is saying can be harder too:
d/Deaf people and other hearing differences
Auditory processing disorder
Receptive language disorder
Developmental disability, especially intellectual and learning disabilities
(AI can't help people who need things explained a certain way. AI unreliable and fails to adapt a lot.)
Anyone who frequently can't make out sounds and/or speech
Anyone who frequently has trouble with meanings in conversation
The problems I often face with AI answering machines (and that I'm sure many other disabled people have faced as well):
AI slightly mishearing me/my device
AI mishearing so badly that it basically makes up a fake conversation
AI not hearing me/my device at all
AI registering tics and stims as answers
AI "explaining" an instruction by repeating the same instruction again word-for-word
AI directing me to the wrong person without trying to confirm what I said
AI sometimes just... hanging up on me right after I speak my first answer...
These are the machines being put in front of
hospitals
doctors offices
mental health centers
pharmacies
transportation and in-home care
health insurance member services
medical supply companies
government resource agencies
non-profit organizations
advocacy groups
justice centers & other legal resources
customer service lines
many other places disabled people often need to access from home
It's another example of some of the most vulnerable being pushed away from the things we need, and we're also being forgotten in these discussions about things that can affect us a lot
Next time someone is ranting about AI job interviewers, please also remember:
the AI pharmacy assistants that make it impossible for someone with a speech disorder to sort out their meds
the AI scheduler that won't allow a D/deaf person to access the right extension of the clinic to set up an appointment
the AI agent that confuses an intellectually disabled person into anger and tears
the AI answerer that hangs up on a mentally ill person seeking help in crisis because they aren't speaking coherently enough
Human beings need to be at the forefront of human resources and issues for disabled people especially. Please remember us. Please fight.
Happy disability pride ♡
sources say there are muscles in the back of my neck. and they want to kill me
it’s called the trapezius and you can stretch it!
do these three daily or even every other day and your neck pain will lessen within a week and disappear in a month
If you actually wanted to criticize something about Solarpunk
Okay, as I am currently Solarpunk posting, let me talk about the topic that in regards to Solarpunk actually is worth critiquing. If you actually - you know - do interact with the community and the stories.
Because here is the thing: Solarpunk as a genre generally tends to be actually quite good about most of the base infrastructure. Most writers in the genre do actually think about how energy is produced and how the associated supply lines work. They think about how food infrastructure works. And how people get around. And how the internet works. They also do seem to have some thoughts at least about how waste management works - though admittedly that is often a bit less thought out other than "renewable materials" and "recycling". Not perfect in that area, but... at least some thought is there.
No, the big issue is health - and disability care.
Look, I am a disabled person myself. I cannot walk long distances on my own. I struggle with stairs. And I need to take 12 different medications. 9 of them daily, the other three in weekly or biweekly intervals. I need to see specialist doctors at least once a month - usually more often. And frankly: I still actually am still more abled than a lot of other people. I can still work. I can still travel with fairly little preparation. I can still do fun stuff without needing to overthink it. And while I do need my medication: I will survive if I am without any single one of them for a week. All of them for a week gone would be an issue. But some of my medications are at times hard to get due to international supply chains and... that is fine. I can live through that.
But others can not.
And this is an issue that a lot of Solarpunk stories just do not consider.
Accessibility in Solarpunk Worlds
So, here is one of the core issues: when most people hear "accessibility" they first and foremost think of wheelchairs, hard of hearing people, and blind people. And that is of course only a small fraction of people who are actually disabled.
We are on tumblr, so chances are y'all have been told about this just a bit. You likely know that people in a wheelchair usually can walk to some degree but might struggle with balance, or exhaustion, or other issues. Some people might be in a wheelchair on some days, and not on others.
You might also know that people with autism and ADHD and other neuro differences might just need environments that are not as bright, not as loud, and so on.
But chances are that other than this... you do not know much. And it is not your fault. It really is not. Because this is just not taught. And currently a lot of people kinda try their best to fully "other" the disabled people. So you do not think of disabled people as people who are largely "functioning" as society expects them to.
But yeah. Disability can have a lot of faces, and even the same disability can look completely different in different people.
You know. Not everyone likes to use wheelchairs. Not everyone who has lost a limb wants to use prothesis. Not everyone who is hard of hearing finds hearing aids useful. Not everyone with ADHD profits from medications.
And then there is the other big issue: cars.
Because a lot of Solarpunk conversation rightly criticize cars and the car centric infrastructure we have. But the issue is if we do not have car accessible infrastructure it also means that ambulances cannot access a lot of areas. And... those are kinda important.
And of course there also is just the additional bit that while I absolutely think that we should finally get away from car centric infrastructure. But some people will just need cars of some form. Because for one reason or another public transport, bikes and the like will not be working for them. And this is an issue that a lot of people engaging in Solarpunk just do not want to admit.
Petrochemicals and Medication
And then we have that one big issue. And that is petrochemicals.
Right now a lot stuff in our society is in some way or form tied to petrochemicals. So to oil. We take the oil out of the earth for fuel, but as we only use some part of it for the fuels, some part for plastic, and some parts for... other stuff.
And some of this other stuff is medications.
A lot of medications on the market right now go back to some chemicals that originates with the petrochemical industries. And some of those chemicals we right now cannot produce without earth oil being involved at some point.
No, this is not all medications of course. There is a bunch of stuff that is largely done without petrochemicals involved. Stuff that might be produced by fungi, bacteria, or - we have to remember that - genemanipulated animals. But even those medications currently at times still need some solvents or other materials either to work, or to be stabilized for longer than a few days.
And of course a lot of other things related to medicine are super dependent on Petrochemicals. Syringes are made of plastic. A bunch of other stuff is as well. And while for those maybe we might at some point be able to recycle that stuff into a good quality - but right now we are actually not able to do that.
A lot of people who disagree with anarchism or Solarpunk keep saying that the issue is somehow related to people no longer caring for disabled or sick people. But generally, I do not think it is a problem. Humans always have been taken care of one another. Medical jobs tend to be generally the kind of job people like doing - or would like doing if they were not constantly overworked and underpaid.
But one issue we need to keep in mind is... that we still will need to pump oil for the time being. Because otherwise people will die due to no longer being able to access life saving medication.
The Invisibility of Disabilities
One of the core issues with all of this is - of course - that disabilities tend to be treated like invisible within even progressive circles. Everyone is kind of aware that disability exists, but people who are not themselves affected often will just straight up ignore anything that goes past wheelchairs, blind and hard of hearing people.
Often enough, even among leftist people, there is also the narrative about "We will just heal everyone for good", not realizing that a) this is very unlikely, and b) that this is actually eugenicist ideology.
In Solarpunk people tend to actually think about most other infrastructure. Food, information, energy, water. That tends to be taken care of. But medical infrastructure? Infrastructure for emergencies? That is often the kind people do not think about enough.
And again: yes. It is highly likely that if we had a world in which we were not working ourselves to death, where we are not constantly stressed, where our basic needs are being taken care of, and where we have community, a lot of acquired disabilities would be more rare. We know that people who have community and less work stress will be much, much less likely to develop cancer or heart disease.
But there are still disabilities that will be there from birth. There will still be disabilities in old age. People will still have accidents. And people will still suffer infectious diseases. And yes, some people will still have cancer and stuff.
So, ideally any Solarpunk story should account for that. And for how they are supposed to get care, and medication, and pretty much anything else needed to survive.
(Art in this blog once more from Solarpunk Seed Library.)
unfortunately for me feeling sleepy isn’t a full time job but my body sure tries
except, of course, when it’s time to actually fall asleep. then i have energy enough to fight god