#also 'I wish I couldn't mask then I'd be taken seriously'
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You don't want to be more ill or more visibly ill. You want it to be easier
#m/cc#mine#also 'I wish I couldn't mask then I'd be taken seriously'#the reason you mask is that people who can't mask *are treated worse*#masking is a traumatic experience in its own rite. it's awful covering up an essential part of you and having to learn who you actually are#but being unable to mask IS NOT A PRIVILEGE IN ANY WAY#the tags are a lot more venty than the actual post and the post itself is not meant to sound aggressive#but I'm just. STOP saying you want to be more visibly disabled or visibly divergent#you won't be magically accepted and unquestioned and accommodated for if your disability is visible#and I'd like you to think about: if not masking would lead to better treatment#why do people try to mask?#'because it was bullied into me.' so you were treated worse when you didn't mask?#people who can't mask didn't get a sign that said 'I can't help it' and become bullying exempt I promise you
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HEADCANON 004. IN ALL SERIOUSNESS...
... Sampo finds that nothing in life needs to be taken with the self-righteousness and pain that seems to characterize many of the people he has encountered.
He finds it excessive, how many times he had to hear someone angsting about their sad life story: many of these people are his customers, begging him for a discount for a price too high and taking in such a sad tone as they lament about their life and all that went wrong in it, that it'd melt the frostiest of hearts.
Not Sampo's.
Most of the time it's not because he's incapable of feeling empathy- but he refuses by principle, since it's clearly an attempt to swindle him. And he's the one that does the swindling- he won't miss to chip in their tearful monologue or their angry ramblings with that time, perhaps not so long ago, that they were crying misery from their pockets while simultaneously betting on the latest fighter in the Underground club, if he recalled correctly...? Doing this ends the tears, makes the anger and then the real bargaining come in, and saves Sampo from having to try and tape his eyelids open just so he doesn't fall asleep on them.
Sampo tends to be a whimsical being: he does things when he wants to, because he wants to, and expecially because it benefits him- he's enjoying himself, first and foremost. There's no shame in having to humiliate himself because, in the end, it gets him what he wants or needs- he considers himself the real winner. He doesn't lose face, not like the scorned party would like him to. it's a mean to an end, and the end grants him his wishes. He also finds funny how many justice acolytes and customers are seeking him out with such devoted anger to give him retribution for his actions- they clearly don't know how the business world works, and that everything has a price tag. They do seem to take things too seriously- take him, for an example. Even when scorned, his revenge is a funny, elaborated method to inflict pure emotional damage on the other person.
If we take his Path in consideration, the Nihility, I'd have to place him in the realm of the Masked God, the Dyonisiac Nihilism: these people tended to believe that the world was, one day, destined to end with nothing to come after it, and had embraced this truth with an optimistic spin to it. If the world was to end, then oneself should make the most out of it- there should be plenty of time to enjoy life, to fulfill their every desire and whim- and everyone who didn't abided to this much merrier view of life was stuck in the Apollinean Nihilism, trembling in fear for the end of the world while trying to live in denial of the truth.
The Dyonisiac Nihilism fits Sampo EXTREMELY well. He takes life lightly and makes the best out of it, acting on actions for a greater scope that will eventually benefit him and give him a great show that he put in motions behind the scenes. He's always seeking to keep himself entertained and well-off, and thinks that others that don't share this view are being weighted down by incredibly big burdens that they choose to place on their own shoulders. They're self-made martyrs, or have either been played in someone else's plans and couldn't figure out what was going on in time to wise up and avoid emotional scarring- and Sampo may feel kind of sorry for them for a few minutes.
I also really like that the paragon of Dyonisus / Aha. The Masked Fools are akin to slighty more mentally stable Bacchae for me. I grasp Greek mythology and stuff it in my mouth like a good sandwich and the filling is as many fucking comparisons to it as I can find.
#( OOC. ) ━ ANYWAY; moving onto another world...#( HEADCANONS. ) ━ an in-depth guide to THE CONMAN.#extremely important for me to put greek mythology EVERYWHERE
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Ligit because bpd and autism are so similar I can't tell which I have. I've been diagnosed with bpd but have been told I should get tested for autism. I'm fairly certain it's bod as most of my symptoms came after a really traumatic experience. If I am autistic then it's probably also with adhd or cptsd.
I've had almost the opposite experience. Mind you finding dbt and cbt is hard where I live is hard. My counselor did her best to find a dbt course so she could do dbt with me. It was helpful but it just made me realize neurotypical people are EXTREMELY emotionally immature and led by their emotions ( at least the ones in my life) and that although bpd makes me run mostly based on my emotions I have to stop doing that. I have to be emotionally mature because if I'm not and I show my emotions in the same was neurotypicals do I'm "manipulative" and "attention seeking". When I do a good job of masking and keeping my emotions under control I "need help" and "need therepy" because despite me finishing dbt and learning everything I could from it I'm not allowed to be better because that means that I'm not the problem anymore. In dbt you learn to take accountability. Once you learn how to do that you realize how much neurotypicals don't.
The only people who have been understanding of my bpd have been health professionals. My counselor went out of her way to learn dbt so she could give me dbt. Then she also made sure I'd be able to go back to her in the future despite us using up all our available sessions. My family doctor helped me fill put paperwork so I could apply for disability as it was made very apparent I can't work without being a threat to myself. The doctor that diagnosed me told me about how the meds I was on (prozac) actually was making my depression worse because of my bpd and explained how there's not really any meds that can help with bpd. They expressed they were sorry that meds couldn't "fix" me like how I wanted. When I talked to someone else with bpd for the first time she shared in my wish of just being diagnosed with bipolar because that we could at least take meds for and they would help.
Whereas the people in my life have treated me like shit. When I was raped people didn't believe me (even after he distributed the video of it and I had to go to the police). I've been in 4 extremely abusive relationships by now and each one they manipulated me and gaslight me to the point I still question myself and my memory. When I express to someone how their actions effect me they say I'm manipulating them and gaslighting them when I'm holding them accountable and just want them to say sorry. My boundaries are crossed on a regular because I'm "just too sensitive". The few people who relate to some of my symptoms immediately go to thinking they have bpd then call me crazy when I suggest it's more likely autism as that fits their symptoms and manurisms more. When I ask to be driven to the hospital(the closest is half an hour away and I have no vehicle) because I think being in a ward would help me I'm attention seeking and when I attempt suicide(despite noone being there) it's manipulation (that was from my landlord btw).
Autism community is great though. Everyone there just treats me the same as them and are super understanding l.
Bpd is a bitch. I fuckin hope I have autism then maybe my symptoms would be taken seriously by my peers and not just health professionals
As a late diagnosed autist I will say one of the most damaging but transformative experiences I've ever had was being misdiagnosed with BPD.
Everyday my heart goes out to people with BPD.
The amount of stigma and silencing they face is astonishing and sickening.
I took DBT for years. Therapists use to turn me away because of my diagnosis.
I would be having full blown autistic meltdowns, crying for help literally - but because I was labeled as BPD ANY time I cried I was treated as manipulative and unstable.
As if the only reason I could be crying was if I was out to trick someone.
95% of the books out there with Borderline in the title are named shit like 'How to get away from a person with Borderline', 'How to stop walking on eggshells (with a person who has BPD)'
I was never allowed to feel true pain or panic or need.
That was 'attention seeking behavior', not me asking for help when a disability was literally inhibiting my ability to process emotions.
There were dozens of times where I had a full meltdown and was either threatened with institutionalization or told I was doing it for attention.
My failing relationships weren't due to a communication issue, or the inability to read social cues. No, because I was labeled borderline, my unstable relationships were my fault. Me beggong nuerotypicals to just be honest and blunt with what they meant was me pestering them for validation.
Borderline patients can't win.
And the funny thing is - I asked my therapist about autism. I told her I thought I was on the spectrum.
BPD is WILDLY misdiagnosed with those with autism and I had many clear signs.
Instead - she told me 'If you were autistic we wouldn't be able to have this conversation'. She made me go through a list of autistic traits made clearly for children, citing how I didn't fit each one.
And then she told me that me identifying with the autism community was the BPD making me search for identity to be accepted - and that I wasn't autistic, just desperate to fit in somewhere.
I didn't get diagnosed for another ten years. For ten years I avoided the autism community - feeling as if I were just a broken person who wanted to steal from people who 'really needed it'.
Because of my providers - I began to doubt my identity MORE, not less.
Ten years of thinking I was borderline and being emotionally neglected and demonized by a system meant to help me.
To this day, I still don't trust neurotypicals. Not fully.
I know I'm not borderline now - but my heart aches for them. Not for the usual stuff. But for the stigma. And the asshole doctors. And the dismissiveness and threatening and the idea of institutionalization hanging over their head.
I love Borderline people. I always will. I'm not Borderline but if you are I love you and I'm sorry.
You're not a bad person. You're not a therapists worst nightmare, you are a human with valid feelings and fears.
Borderline people I'm sorry.
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(Sorry for sending so many asks dhdjd)
While we dont know yet if they will be plot relevant, something tells me that either Leo or Kii are gonna be the "Akechi" of the game, since it seems to mirror a lot the original game
Leo, well, his costume and persona looks so much like a power ranger/super hero, just like Princekechi. Maybe instead of a detective he is more of an actor working in some fetherman-like show.
Kii, we dont know a lot about him, but from his nickname (im pretty sure it means gold) and from the sticker he is dressed like some rich boy i feel like he will be a pain in the ass. Plus his persona has a lot of tree immaginery going on, thing that is usually connected with viking myths.
Also if someone can correct me: from what i know in asia, expecially China, freckles are a symbol of bad luck
(No worries!! I love getting asks, it's fun to have other people to talk to about this game and get ideas going!)
I think I might've pointed out something similar about Leo's superhero vibe reminding me of Crow back when we first saw him? That was months ago, so I might never actually have gotten it into a post, haha. But I absolutely agree! One of his datamined voice lines from the first beta mentions it being like a tokusatsu drama, so that's absolutely the vibe he's trying to go for, too. Admittedly, I do think he's more likely another Phantom Idol than a story character- I think he would've gotten as much focus as Soy in the trailer and promo info released, otherwise- but I suppose there's still hope for at least another few hours, haha!
If he is a Phantom Idol, I suspect he's not intended to parallel a P5 character, but he may still end up having similarities even if he isn't. I kind of got the vibe (again, from the teeny handful of voice lines we got in the first beta's data) that he might be a bit more outwardly nerdy/excitable than Akechi? Maybe "earnest" is the word I'm looking for? I'd totally believe that out of the mask/the real Leo at least has dreams of being an actor or something along those lines, especially in that kind of production.
For Kii, I think you're thinking of 金 (kin) for gold? Which doesn't necessarily mean it couldn't be tied to that, but as I'm sorta suspecting he'll also be a Phantom Idol (just with a story counterpart, like Tomoko), I'm similarly suspecting his Merope-given codename'll just be a shortening of, or joke on, his real name, much like all the confirmed Phantom Idols have been.
(For the record, my Japanese dictionary returns the following definitions for Kii (different words based on different kanji that "kii" could be written with): "odd; strange; queer; peculiar", "displeasure; offense; offence; disliking", "your will; your wishes; your request", "position of aircraft", and "Kii (former province located in present-day Wakayama and southern Mie prefectures)".)
I had originally only really noticed the top of his Persona was kinda like fire (kind of like Yosuke's Takehaya Susano-o in P4), but looking at it again, you are so right about the tree imagery going on! Maybe you're right about the viking thing, too (admittedly I've never gone too deep into Norse mythology, haha).
From his glasses + expression in the sticker (and disappearance of glasses in his All Out Attack cut-in), and how he seems more serious/cold as a Phantom Thief, my take on him had sort of been, up to this point, that he'd be more of a nerd that's perhaps trying very hard as a Thief/trying to look cool/trying to be taken seriously, or something along that line, and his real-world counterpart is the Mishima parallel (going by a guess from there that maybe Kii's a Phantom Idol, so it's like Kotomo). But I do agree that what we can see of his sock and shoe in the image does sort of have a "rich kid" vibe to it, haha. It could just be related to whatever his thief theme is?
I did a really quick search about freckles in China, and while I'm not sure if they're bad luck (again, quick search, maybe I missed something/didn't go deep enough) it seems like they do tend to be considered unattractive/ugly, which I believe was also the case even here in the US in the past. But that's a good angle to come at this from- personally I think the freckles are cute, but the developers probably had a different intention...
#seriously thanks for sending in asks! it's more fun for me this way#tbh the only time I probably *wouldn't* want a billion asks is if I have a billion things I'm trying to post already hehe#theories#leon#key#hoshihime98
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The test results that hot day in early August shouldn't have surprised me — all the symptoms were there. A few days earlier, fatigue had enveloped me like a weighted blanket. I chalked it up to my weekend of travel. Next, a headache clamped down on the back of my skull. Then my eyeballs started to ache. And soon enough, everything tasted like nothing.
As a reporter who's covered the coronavirus since the first confirmed U.S. case landed in Seattle, where I live, I should have known what was coming, but there was some part of me that couldn't quite believe it. I had a breakthrough case of COVID-19 — despite my two shots of the Pfizer vaccine, the second one in April.
I was just one more example of our country's tug and pull between fantasies of a post-COVID-19 summer and the realities of our still-raging pandemic, where even the vaccinated can get sick.
Not only was I sick, but I'd brought the virus home and exposed my 67-year-old father and extended family during my first trip back to the East Coast since the start of the pandemic. It was just the scenario I had tried to avoid for a year and a half. And it definitely was not the summer vacation I had anticipated.
Where did I get it? Who knows. Like so many Americans, I had loosened up with wearing masks and social distancing after getting fully vaccinated. We had flown across the country, seen friends, stayed at a hotel, eaten indoors and, yes, even went to a long-delayed wedding with other vaccinated people.
I ended up in quarantine at my father's house. Two rapid antigen tests (taken a day apart) came back negative, but I could tell I was starting to feel sick. After my second negative test, the nurse leveled with me. "Don't hang your hat on this," she said of the results. Sure enough, a few days later the results of a PCR test for the coronavirus (this one sent to a lab) confirmed what had become obvious by then.
It was a miserable five days. My legs and arms ached, my fever crept up to 103 and every few hours of sleep would leave my sheets drenched in sweat. I'd drop into bed exhausted after a quick trip down to the kitchen. To sum it up, I'd put my breakthrough case of COVID-19 right up there with my worst bouts of flu. Even after my fever cleared up, I spent the next few weeks feeling low.
Of course, I am very lucky. I didn't go up against the virus with a naive immune system, like millions of Americans did until vaccines were widely available. And, in much of the world, vaccines are still a distant promise.
"You probably would have gotten much sicker if you had not been vaccinated," Francesca Torriani, an infectious disease physician at the University of California, San Diego, explained to me recently.
As I shuffled around my room checking my fever, it was also reassuring to know that my chances of ending up in the hospital were slim, even with the delta variant. And now, about a month later, I've made a full recovery.
The reality is breakthrough cases are becoming more common. Here's what you should know about getting a breakthrough case — and what I wish I'd known when those first symptoms laid me low:
Is it time for a reality check about what the vaccines can — and can't do?
The vaccines aren't a force field that ward off all things COVID-19. They were given the greenlight because they greatly lower your chance of getting seriously ill or dying.
But it was easy for me — and I'm not the only one — to grab onto the idea that, after so many months of trying not to get COVID-19, that the vaccine was, more or less, the finish line. And that made getting sick from the virus unnerving.
After all, there were reassuring findings earlier this year that the vaccine was remarkably good at stopping any infection, even mild ones. This was a kind of bonus, we were told. And then in May the Centers for Disease Control and Prevention said go ahead and shed your mask if you're vaccinated.
"There was so much initial euphoria about how well these vaccines work," says Jeff Duchin, an infectious disease physician and the public health officer for Seattle and King County. "I think we — in the public health community, in the medical community — facilitated the impression that these vaccines are bulletproof."
It's hard to keep dialing up and down your risk calculations. So if you'd hoped to avoid getting sick at all, even slightly, it may be time for a "reset," Duchin says. This isn't to be alarmist but to clear away expectations that COVID-19 is out of your life, and keep up your vigilance about common-sense precautions.
With more people vaccinated, the total number of breakthrough infections will rise, and that's not unexpected, he says. "I don't think our goal should be to achieve zero risk, because that's unrealistic."
How high are my chances of getting a breakthrough case these days?
It used to be quite rare, but the rise of delta has changed the odds.
"It's a totally different ballgame with this delta phase," says Dr. Eric Topol, a professor of molecular medicine at the Scripps Research Translational Institute in La Jolla, Calif. "I think the chance of having a symptomatic infection has gone up substantially."
But he adds, "Quantifying that in the U.S. is very challenging" because our "data is so shoddy."
The vaccinated still have a considerably lower chance of getting infected than those who aren't protected that way. Look at data collected from Los Angeles County over the summer as the delta variant started to surge in Southern California: Unvaccinated people were five times more likely to test positive than those who were vaccinated.
Recent research has tried to pin down how well the vaccines are working against preventing any breakthrough cases during the delta surge, but much of that comes from other countries and estimates vary significantly.
In the U.S., a study published recently in The New England Journal of Medicine concluded that vaccine effectiveness "against any symptomatic disease is considerably lower against the delta variant," dropping from over 90% earlier in the year before delta was the predominant strain to only about 65% in July. Research on breakthrough infections over the summer in New York found the vaccines were still overall about 80% effective against any infection. Each study has its limits.
It's hard to disentangle what's most responsible for the rise in breakthrough infections this summer — whether it's the delta variant itself, waning immunity in some people or that much of the U.S. dropped public health precautions such as masking.
"We don't have good evidence of what's the cause, but we do know all of these things coming together are associated with more breakthroughs," says Rachael Piltch-Loeb, a public health researcher at the Harvard T.H. Chan School of Public Health.
How careful do I need to be if I want to avoid a breakthrough?
Looking back, I wish I'd taken some more precautions.
And my advice is different now when friends and family tell me they want to avoid having a breakthrough case such as mine: Don't leave it all up to the vaccine. Wear masks, stay away from big gatherings with unvaccinated people, cut down on travel, at least until things calm down.
The U.S. is averaging more than 130,000 coronavirus infections a day (about twice what it was when I fell sick), hospitals are being crushed and the White House has proposed booster shots. Scientists are still making sense of what's happening with breakthrough cases.
What's clear is that in many parts of the U.S., we're all more likely to run into the virus than we were in the spring. "Your risk is going to be different if you are in a place that's very highly vaccinated, with very low level of community spread," says Preeti Malani, an infectious disease specialist at the University of Michigan. "The piece that's important is what's happening in your community."
Even with delta, the goal is not to go back to a lockdown mindset though, Malani says. "My hope is that people who are fully vaccinated should really feel like this risk is manageable."
She says, "Feel good about spending time with your friends or having a small dinner party, but make sure everyone is vaccinated."
What does a "mild" case of COVID-19 feel like?
In my case, it was worse than expected, but in the parlance of public health, it was "mild," meaning I didn't end up in the hospital or require oxygen.
This mild category is essentially a catchall, says Dr. Robert Wachter, who chairs the Department of Medicine at the University of California, San Francisco. "Mild" can be "a day of feeling crummy to being completely laid up in bed for a week, all of your bones hurt and your brain isn't working well."
"So even if we call them mild cases, as you've seen, sometimes these are ones you really don't want to have if you can avoid it," he says.
There's not great data on the details of these mild breakthrough infections, but so far it appears that "you do way better than those who are not vaccinated," says Dr. Sarang Yoon, an occupational medicine specialist at the University of Utah Rocky Mountain Center for Occupational Environmental Health who was part of a nationwide CDC study on breakthrough infections. "In general, in terms of symptom duration, it's much shorter."
Yoon's study, published in June with data collected before the delta surge, offers some reassurance: The presence of fever was cut in half, and the days spent in bed reduced by 60% among people with breakthrough infections, compared with unvaccinated people who got sick. "These are meaningful decreases," says Matt Thiese, an epidemiologist and colleague of Yoon's who worked on the study. "It can be the difference between having a fever for almost nine days and having a fever for just under three days."
A recent study from the U.K. also shows that if you're sick because of a breakthrough case, it's generally not as bad, and people have fewer symptoms. In fact, the top five symptoms for people with a breakthrough infection were headache, sneezing, runny nose, sore throat and loss of smell. Notably absent: fever and persistent cough, which are in the top five for unvaccinated people, according to the data compiled by the U.K. researchers.
If I get a breakthrough infection, how sick could I get?
Even with delta, the chance of getting a case of COVID-19 that's bad enough to send you to the hospital is still rare.
If you're vaccinated, the risk of being hospitalized is 10 times lower than if you weren't vaccinated, according to the latest data from the CDC. Those who get severely and critically ill with a breakthrough case tend to be older — in one study done before delta, the median age was 80 — with underlying medical conditions such as cardiovascular disease.
When I was sick, one thing was in the back of my mind as I monitored my symptoms: Would I have problems catching my breath?
Thankfully, when you get exposed, the vaccine has already set you up with antibodies, a first line of defense, that will neutralize parts of the virus that attach to the mucosal surfaces of your upper respiratory tract, says Torriani at UC San Diego.
"That initial moment when our body is attacked by the virus, that can lead to some disease," she says. It's a bit of a race. The virus may cause you to get a cold, but, in most people, your immune system will "get its act together and thwart that infection from going down into your lungs," Wachter says.
That later stage of COVID-19 also seems to trigger the immune system to get "overly exuberant" and attack your own body, causing severe respiratory problems such as shortness of breath and destructive inflammation. "So if you can prevent that sort of second stage from happening," Wachter says, "you can prevent a lot of the severe illness from COVID." Other parts of your immune system, such as T-cells, are also ready to kick into action if you get sick.
If you're concerned, you can keep an eye on your oxygen levels with a pulse oximeter. That's much more important than your temperature or symptoms, he says.
Can I spread it to others, and do I need to isolate?
Unfortunately, you still have COVID-19 and need to act like it.
Even though my first two tests were negative, I started wearing a mask at my house and keeping my distance from my vaccinated family members. I'm glad I did: No one else got sick.
The delta variant is more than two times as contagious as the original strain of the virus and can build up quickly in your upper respiratory tract, as was shown in a cluster of breakthrough infections linked to Provincetown, Mass., over the summer.
"Even in fully vaccinated, asymptomatic individuals, they can have enough virus to transmit it," says Robert Darnell, a physician scientist at the Rockefeller University. "Delta is very good at replicating, attaching and inserting itself into cells."
The science isn't settled about just how likely vaccinated people are to spread the virus, and it does appear that the amount of virus in the nose decreases faster in people who are vaccinated.
Even so, wearing masks and staying isolated from others if you test positive or have symptoms is absolutely critical, Darnell says. He also advises getting tested if you are exposed to someone who has COVID-19, even if you've been vaccinated, "because you could very well get infected or ill, and you want to protect those around you, including all the children who aren't vaccinated."
Could I get long COVID-19 after a breakthrough infection?
The chance I might go on to develop long COVID-19 was front and center in my mind when I had a breakthrough case.
While there's not a lot of data yet, research does show that breakthrough infections can lead to the kind of persistent symptoms that characterize long COVID-19, including brain fog, fatigue and headaches. "Hopefully that number is low. Hopefully it doesn't last as long and it's not as severe, but it's just too early to know these things," Topol says.
Recent research from the U.K. suggests that vaccinated people are about 50% less likely to develop long COVID-19 than those who are unvaccinated. The underlying cause of long COVID-19 is still not yet known, so it complicates the picture for researchers even more, but this early evidence offers some reassurance.
"There may be some symptoms like fatigue [that linger], but studies appear to show that vaccination might also decrease the chances of getting long COVID symptoms," Torriani says.
This is not true for everyone, and it's a compelling reason to avoid getting infected altogether, Wachter says. "Some of those mild cases will go on to be long COVID, so you have to factor that in," he says.
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Okay actually making this bullet points because I have a lot of feelings about it and don't want to be misunderstood. More TL;DR version here
"I wish I was visibly disabled/had X disability instead because my invisible disability isn't taken seriously"
Visible disabilities ALSO aren't taken seriously! No, you would not automatically be taken more seriously, get better care, or have your needs more respected if you were in a wheelchair. Or had cancer. Or couldn't mask. Or had a limb difference. People will still think you're lazy or lying or incompetent
"If I was more severe I'd get the support I need"
Healthcare neglect and lack of resources also affect people who are more severe, even in cases where it's obvious someone needs assistance. Severe people also cannot afford their treatment, cannot travel to places they need to go, do not qualify for charities or disability, experience shortages of medical necessities, are rejected by bad doctors, and cannot access resources they need, just like "less severe" folks. Not to mention severe folks may also be at the mercy of carers, group homes, legal guardians, etc. Severe people get rejected by charities, clinics, and more BECAUSE they're severe - I've had doctors reject me more than once for being too complex. No referrals out, no better qualified specialist, just rejected with a "good luck." The same way that less severe people are rejected for not being "bad enough" to access the service. Resources open up to you at a certain level of severity; resources ALSO close
"If I was more severe, I would have gotten early intervention"
That's not necessarily true. Would you have been diagnosed with the chronic condition you have, or would you have been labeled as a liar or exaggerating, or told you'd grow out of it? And some people are very obviously not abled as kids and still do not get help, whether because parents veto it or because the resources just plain don't exist there
If you did get early intervention, was it accurate and helpful? Would you be diagnosed correctly and given helpful treatment? Would you have been put in programs that severely dehumanized you and caused harm? Would you have to endure the stigma of being visibly different, instead of the stigma of being invisibly different? You would have had a name for what was wrong with you, but it also would become a slur and an easy way to exclude you. You'd still be told you're using it as an excuse, you'd still be bullied and feel broken. You'd still have trauma from growing up disabled
"I wish I'd never been able to mask"
I want you to really, genuinely ask yourself then: why did you mask? Was it beaten or bullied into you? Would there have been consequences for being obviously different? Now consider that there are people who endured the same thing and couldn't mask. They still got abused and traumatized in the same way and kept being abused and got all the negative consequences that come from being inescapably different. People didn't see them continue to be weird and go "oh man I think this kid can't help it, we should stop bullying them"
Masking is traumatic for many, many people! But not being ABLE to mask is not better or easier in any way
"Visibly disabled people and people with common conditions are less acceptable targets for discrimination/have more accommodations"
No. They just aren't. People with disabilities are discriminated against, period. And people are still fully willing to mock visibly disabled people
People in wheelchairs still can't access buildings, get told to drop out of school, and are told their needs are too complex or told they just shouldn't exist in public spaces. Blind people are still told there's no good accommodation for them or that their accommodations are unfair. Having a common or visible disability doesn't change these things. Invisibly disabled people have to fight for their accommodations at their job because they don't "look disabled" and jobs don't want to accommodate them. Visibly disabled people often don't get the job in general - because jobs don't want to accommodate them. The problem is not whether your disability is visible, it's that jobs don't want to accommodate for disability
"People treat me like I'm fully abled and then get upset when I can't handle it"
Visibly/severely disabled people also deal with assumptions. We're assumed to be bitter (or perpetually cheerful), incompetent and helpless, lazy, weak, or any other number of stereotypes, and people get angry when you don't fit that. We face violence for not being appropriately grateful to abled people, get denied jobs because it's assumed we can't do them (and are assumed to be a charity hire if we DO get them), get approached at random to ask why we haven't killed ourselves yet, and all sorts of mistreatment because our disability is obvious. Disabled people who are unable to work aren't treated kindly by anyone, still have to struggle to get by, and often struggle with getting on disability no matter their severity. The struggles are different, but not easier
In short: visible and invisible disabilities have unique traumas and struggles, but being more obviously disabled is not easier than having a hidden disability. Please stop saying you wish you were visibly or more severely disabled
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