#disability rights
Explore tagged Tumblr posts
Text
This reminds me of how some people keep fearmongering about rising rates of diagnoses of autism, adhd, etc. in student populations *as if it's a bad thing that these things are being diagnosed.* Just because there's a higher recognized occurrence of something happening (like transgender people diagnosed with ocd, autism, etc.) in a given circumstance doesn't mean that that circumstance causes that thing, anymore than there's anything more going on in modern diagnosis rates of autism, adhd, etc. beyond better and more widely implemented diagnostic tools.
On a related note, I'm tired of people acting as if people with diagnosed psychiatric, mental, or diagnostic disorders are unable to make appropriate decisions regarding their own bodily autonomy, up to and including gender transitioning. This is something that happens across the medical spectrum when it comes to psychiatric and developmental disorders, as if being neurodivergent means that you're unable to understand or do anything that is right for yourself, and I am *sick* of it.
something that should be taken with a grain of salt are the statistics talking about the high rates of mental illness + neurodivergence among trans people (ocd, bpd, adhd, autism, etc)
I see both sides of the political spectrum taking these studies at face value - conservatives say we're broken, and trans people try to come up with reasons why for example autism + gender dysphoria makes sense and why one of them feeds into another
at the end of the day you have to remember that we're the one category of people on this planet who are legally required to go see a psychiatrist in order to receive non-psychiatric medication and surgeries.
more trans people are in therapy by law than any other demographic of people, and as a result, this captures more comorbidities.
if I had to look at my own family & rates of mental illness?
mom, dad, 2 maternal aunts, maternal grandmother, paternal grandmother, sister, sibling, and me all have OCD.
7/9 of them are cishet, never been to therapy, never diagnosed. 2/9 are trans, required therapy for hormone treatment, and were diagnosed.
you don't have to do any math to just see that the resulting statistics end up intensely skewed.
and we can think back to how autism was virtually never diagnosed more than 50 years ago - ruling out any grandparents being included in statistics - and even my parents' generation (they're in their 60s now) wouldn't have been included either.
I don't think it's to anyone's benefit to accept these studies uncritically. a lot of these things are hereditary and far more prevalent in the overall population than people realize
#mental health#trans rights#disability rights#bodily autonomy#I was actually talking about this in my historical archaeology class today#Basically I feel that people who are zeroing in on supporting and backing up abortion rights have kind of the right idea#But they're being too narrow minded about it#POC and disabled people in the US have a long history of coercive sterilization#Sterilizing people under guardianship or care without their consent is still legal in 30-some-odd states#So I think they need to broaden their sights to focus on bodily autonomy regardless of ability gender or racial identity
9K notes
·
View notes
Text
Look, I get it, disability support is not as trendy as being an LGBTQ+ supporter or against racism, we might not have all that cool music and colourful parade floats, our flag has a lot of black. It’s not fashionable. No business puts the disabled flag in their logos on July.
Some of us make non-disabled people uncomfortable (to their own admission) because of how we exist in this world. Some of us slouch and drool, some of us have tics and spasms, some of us are missing limbs or parts of our faces. We might have bulky mobility aids and big and noisy equipment, some of us can’t avoid to attract attention, some of us are shaped in a “weird” way. We might walk and move too slowly or take a lot of time to express ourselves, to form thoughts and words. Some of us don’t speak. Many of us can’t fit in, can’t hide our disabilities and the way we look.
No, it’s not trendy or fashionable. I get it.
But the problem is that society has decided that there is only one standard to exist, to look, to be. The rest is abnormal, wrong, sick, broken…
It’s the mindset that needs to change. We should open up to all the different possibilities we could encounter, to the idea that what we are used to see is not necessarily the only right thing. Because there is no a “right” way to exist, to go through this World, to live, to look, to be. The more we open up to all of this, the more liberating it will feel. And it will be easier to accept the possibility of a future disability that might happen, to us and the people we love.
It’s not enough to just say “yes, disabled people deserve rights”. There should be an active step forward. Be uncomfortable. Get used to the idea of being around people who are not the “standard”. Be uncomfortable with the idea of a body and a mind that don’t work like you are used to.
#not sure if this post makes sense but it was on my mind since this morning#cripple punk#disability#cpunk#cripple#crip punk#crip revolution#disability justice#disability rights#chronic illness#disability pride#actually disabled#ableism#disabled blogger#spoonie
52 notes
·
View notes
Text
if you didn’t realize, ableism is actually bigotry and systemic ableism and inaccessibility are really oppression and it’s not something disabled people brought on ourselves by having bodies&minds that you think are inferior and therefore not worth fighting for. disabled people’s lives and wellbeing matter. we don’t have to earn our worthiness by doing “enough” to deserve a good life. nobody does.
#cripplepunk#neuropunk#actually disabled#disability rights#neurodivergent#chronically ill#madpunk#ableism#inaccessibility#actually autistic#ehlers danlos syndrome#higher support needs#autpunk#cpunk#disabled lives matter#tourettes#functional neurological disorder#mobility issues#physically disabled#my text
34 notes
·
View notes
Text
reminder that adhd medication isn't a luxury or preference, but a lifesaving medication. a 10 year long study in the usa showed that, when properly medicated, the rate of car crashes people with adhd get into goes down significantly--men's rate drops by 38%, and women's by 42%. the med shortage, denial of meds by doctors, rising prices, and the "war on drugs" has killed--with such a car dependent society, not driving frequently isn't an option, which means we need better healthcare and need it now.
https://shorturl.at/8VD8B
edit because i forgot to explain: short link is to an article by the washington post, it should be free to read
#adhd#disability#medication#mental health#war on drugs#adhd awareness#in the least shocking turn of events the government trying to imprison people fucks everyone over#ableism#disability rights#pls reblog to raise awareness#please check the most recent version I reblogged for dementia info!!!
29K notes
·
View notes
Text
oooooooooo I love fucking niche-est special interests
an interaction im very tired of in online autism spaces. aka when you don’t have a special interest / when your special interest isn’t [character] or [fandom]
#Ngl growing up mine was all just disability#service dog#americans with disabilities act#I memorized that shit#12 year old me was onto some shit bc we found dissociaDID and years later here we are#autism#special interest#disability#disability rights#The only friends I had in elementary school where the kids in special ed and a girl obsessed with Hamilton#Honestly I had the best conversations with them#I was just like#See? You people make sense#Why do “normal” kids act so fucking weird#And love screaming for some reason
28K notes
·
View notes
Text
10 children a day lose their limbs in Gaza. All hospitals in Gaza are basically barely functioning and the amputations are done in unsanitary conditions and without anesthesia
#yemen#jerusalem#tel aviv#current events#palestine#free palestine#gaza#free gaza#news on gaza#palestine news#news update#war news#war on gaza#children of gaza#disability#disabilities#disability rights#disability justice#genocide#gaza genocide
42K notes
·
View notes
Text
The nazis that you see in movies are as much a historical fantasy as vikings with horned helmets and samurai cutting people in half.
The nazis were not some vague evil that wanted to hurt people for the sake of hurting them. They had specific goals which furthered a far right agenda, and they wanted to do harm to very specific groups, (largely slavs, jews, Romani, queer people, communists/leftists, and disabled people.)
The nazis didn't use soldiers in creepy gas masks as their main imagery that they sold to the german people, they used blond haired blue eyed families. Nor did they stand up on podiums saying that would wage an endless and brutal war, they gave speeches about protecting white Christian society from degenerates just like how conservatives do today.
Nazis weren't atheists or pagans. They were deeply Christian and Christianity was part of their ideology just like it is for modern conservatives. They spoke at lengths about defending their Christian nation from godless leftism. The ones who hated the catholic church hated it for protestant reasons. Nazi occultism was fringe within the party and never expected to become mainstream, and those occultists were still Christian, none of them ever claimed to be Satanists or Asatru.
Nazis were also not queer or disabled. They killed those groups, before they had a chance to kill almost anyone else actually. Despite the amount of disabled nazis or queer/queer coded nazis you'll see in movies and on TV, in reality they were very cishet and very able bodied. There was one high ranking nazi early on who was gay and the other nazis killed him for that. Saying the nazis were gay or disabled makes about as much sense as saying they were Jewish.
The nazis weren't mentally ill. As previously mentioned they hated disabled people, and this unquestionably included anyone neurodivergent. When the surviving nazi war criminals were given psychological tests after the war, they were shown to be some of the most neurotypical people out there.
The nazis weren't socialists. Full stop. They hated socialists. They got elected on hating socialists. They killed socialists. Hating all forms of lefitsm was a big part of their ideology, and especially a big part of how they sold themselves.
The nazis were not the supervillians you see on screen, not because they didn't do horrible things in real life, they most certainly did, but because they weren't that vague apolitical evil that exists for white American action heros to fight. They did horrible things because they had a right wing authoritarian political ideology, an ideology that is fundamentally the same as what most of the modern right wing believes.
#196#my thougts#leftist#leftism#jewish#jumblr#actually mentally ill#mental illness#neurodivergent#actually neurodivergent#world war 2#world war ii#history#queer#gay#queer history#pagan#athiest#athiesm#disability rights#communist#communism#socialist#socialism#anti conservative#anti christianity#christanity#christianity#mad pride#madpunk
30K notes
·
View notes
Text
Happy Disability Pride Month! 🩶💚❤️🤍💛💙🩶🌈 (x)
#disability pride month#disability pride#disability#disability rights#disabled community#disabled women#wlw#wlw history#sapphic#sapphic history#sapphics#lesbian#lesbian history#black history#lgbt#lgbt history#lgbtq#lgbtqia#lgbtqia+#history#herstory#photography#vintage photography#b&w#b&w photography#bw#bwphotography#debra st. john#1990s#source: pinterest
17K notes
·
View notes
Text
enough abo smut we need abo as a metaphor for the struggles those of us othered by society face in the healthcare field
"There are 6-9 genders in the omegaverse" wrong. There are 2 genders in the omegaverse. "Might be forced by biological imperative to fuck in a McDonald's" and "won't be forced by biological imperative to fuck in a McDonald's."
#am i talking about#women's healthcare#gender affirming care#medical debt#just general#disability rights#trick question the answer is all of the above#source: am all of the above#hiwaga thoughtvomits
3K notes
·
View notes
Text
Source video
Please reblog and share.
38K notes
·
View notes
Text
disability rights involves the right to do fuck all. the right to be a useless member of society and STILL be loved and cared for and have a fair standard of living. human beings are not defined by the capital we produce.
58K notes
·
View notes
Text
i wanna say fuck you to anyone who shame disabled, chronically ill & neurodivergent people, especially homebound folks, for "spending too much time on their phone/on the internet/etc." when it's the only (Somewhat) accessible way for them to experience the world. many people don't get to get out much even if they want to because of their disabilities. shaming someone for trying to connect with the world, make friends and engage with hobbies in ways that are accessible to them is beyond cruel and unnecessary
#cripple punk#cripplepunk#crip punk#cpunk#actually disabled#chronic pain#disability culture#fibromyalgia#disability rights#disability advocacy#physical disability#c punk#angry cripple#queer cripple#cfsme#chronic fatigue syndrome#chronic fatigue#arthritis#diabetes#neurodiverse#neurodiversity#neurodivergent#autism#autistic#adhd#actually autistic#hypermobile eds#hypermobilty syndrome#our writing
16K notes
·
View notes
Text
THIS THIS THIS
I haven’t talked about rtc in a hot sec because real life has absolutely kicked my ass as of late but this is such a correct opinion that I’m coming out of my flare up hidey hole to reblog this op u slayed so hard with this
hey RTC fandom, i wanted to talk about disability erasure in RTC, and how the fandom (and potential future productions) can do better than canon has done so far!
What is disability erasure?
Disability erasure is, basically, finding ways to avoid acknowledging or depicting disability because of how it makes people uncomfortable. One example of this, and the most common thing that pops up in discussions of RTC, is taking a character that is canonically disabled or usually depicted as disabled, and depicting them without that disability.
When this happens in general, it is a problem because it deprives disabled people of a chance to see themselves represented in media. In theatre, it also often means that an abled actor gets a role that could have gone to a disabled actor - and this is already a problem even when the character is being depicted as disabled on-stage, due to ableism in the hiring/audition process.
We already have few enough disabled characters as it is - we don't need any less. Ricky is an important character to me and to many other disabled people. That's why I, like most of the fandom, do not support the 2022 script changes that made Ricky able-bodied and replaced his physical disability with a psychological trauma.
I won't discuss the script changes much here. Many other people, including Yannick himself, have already explained it better than I can. But suffice to say I think the new script is incredibly, inherently ableist.
But that's not the only example of disability erasure in RTC.
Disability erasure doesn't just mean taking a disabled character and making them completely abled. In fact, many people have correctly pointed out that Ricky still has a disability in the new scripts, because being unable to talk due to psychological trauma is a disability. And this is true, but it doesn't change the deliberate erasure of Ricky's physical disability.
Because all disabilities are different, it's possible to erase a character's disability even without making them fully abled. If a character has one disability, and you remove it to give them another - that's still erasure! Disability rep is not all interchangeable, and it does matter what disability or broadly what type of disability a character has.
I hope most of the fandom can understand that, for example, it would be a problem to make Noel bisexual. Even though bisexuality is still part of the queer community, it's erasure to do that for Noel - because he isn't just generic queer representation, he's specifically gay! And the same sort of principle applies to Ricky, because he isn't just generic disability representation - he is specifically a person with a degenerative disease, and a mobility aid user who cannot speak.
With the canon info that we have on Ricky's disability, based on the 2016 script, here are some examples of things that might not be making him fully abled but are still erasure:
Depicting Ricky not needing mobility aids, even if he can't talk
Depicting Ricky talking out loud, even if he still needs mobility aids
Depicting Ricky being a person who cannot speak & needs mobility aids, but having this be due to two unrelated disabilities that affect his speech & legs only (for example nonverbal autism & arthritis in his legs). Ricky canonically has a rare degenerative disease that affects both his speech and his mobility; it is very likely (all but stated outright in canon) that this is a neuromuscular disease which affects his whole body.
Removing the fact that Ricky has a degenerative disease specifically, and explaining his symptoms with a disability that will stay at the same severity throughout his life, when he canonically has a degenerative disease that he outright says will lead to an early death (even if this makes you sad to think about, which is 100% valid and understandable, it is not appropriate to erase outright)
But what about in the afterlife? What if Karnak allows Ricky to remove his disability or specific parts of it?
Pretty much every production of RTC involves Ricky, upon death, gaining some abilities that he didn't have in life. In most productions he discards his mobility aids, though there are some where he keeps them during most of the musical and only throws them aside for choreography, and some where he keeps them throughout choreography. To my knowledge every production of RTC also has him talking out loud after his death. This is all pretty easily explained by some sort of afterlife magic, or by Karnak actively choosing to remove (parts of) Ricky's disability.
And I'm sorry to say that it's still erasure.
I'm not saying this because I want to file RTC away as bad rep. I love RTC, and I love Ricky! I think Ricky is extremely valuable disability representation for so many reasons, and I also think there are some things that it could have done better.
I think having Ricky as an explicitly disabled character who becomes able-bodied due to magic later on is much, much better representation than simply writing his disability out of the canon entirely. It's a different level of erasure, because it still acknowledges him as a disabled character, and still acknowledges that as part of his backstory.
But using magic as a way to remove disability is lazy. It's a quick way to avoid having to depict a character as disabled for the entire length of a musical. And that means that the disabled fans who see ourselves in Ricky, don't get to see a character depicted as disabled or using mobility aids on-stage for the whole length of the musical.
Now, I understand that whenever you're making fanworks for a flawed piece of media (and every piece of media will have some flaws), there's a balance between being canon compliant and improving on canon. I don't think fans should be instantly labeled as ableist, or canceled, for writing canon compliant fic where Ricky's disability is erased in some way in the afterlife. I don't think it carries the same harm or weight - for one, it doesn't have the same reach as actual musical productions do, and on top of that, disabled people in the RTC fandom are already aware of the flawed parts of RTC's disability rep & we tend to be prepared for this when we go into the fandom.
I do think people should consider making Ricky disabled in the afterlife in fanworks. Many other parts of canon are changed in fanworks, so this one can be too!
And more importantly than that, I think more RTC productions (on the off chance anyone involved in a production of RTC is reading this post) should work to continue depicting Ricky as disabled on-stage throughout the whole musical. As I've said before, to my knowledge, there isn't an existing production of RTC that doesn't engage in some level of disability erasure, and that's something I'd like to see change one day.
But wait, if Ricky still couldn't speak out loud in the afterlife, wouldn't that mean cutting his song?
Actually, no!
I get this response a lot when I bring up the disability erasure inherent in Ricky consistently regaining his ability to talk upon death. I understand the concern - I think it would be awful if a production simply cut SABM in order to avoid depicting Ricky talking/singing out loud, and that doing so would also be a form of erasure in the sense that it would inevitably involve minimizing Ricky's character and removing parts of what made RTC such valuable disability rep in the first place (especially so if some of ricky's speaking lines, such as his post-SABM speech, are also cut with SABM).
But the fact is that you simply don't have to cut Ricky's song for this to work. There are real people who have performed in musicals without speaking/singing out loud, and still had major roles!
One way of doing this is with an interpreter. Ricky's actor would perform SABM in sign language, and another performer would sing the song as he signs it. It's important to note that when this is done, Ricky is still the main performer and still the focus of the song, and the interpreter is just that - an interpreter.
This method has been done in musical theatre before. One example is Joshua Castille, a Deaf actor, playing Quasimodo (an originally deaf character) in the 5th Avenue Theatre production of The Hunchback of Notre Dame. He performs in ASL, with singer E.J Cardona acting as the voice of Quasimodo. There are some clips online if you'd like to look it up!
There's another idea that I've thought of myself, though I don't know of any examples or if it'd been done. If Ricky was depicted using an AAC device on-stage, that would mean he talks using a synthesised (text-to-speech) voice. And we already have the technology to create singing with synthesised voices - it's called Vocaloid!
Of course, real world AAC devices generally can't sing, and programming a song into a vocaloid inherently takes a lot of time - you couldn't do it on the spot. But the whole premise of a musical is people singing on the spot when they wouldn't normally be able to! In RTC specifically it's explained as Karnak's doing, but pretty much every musical involves characters perfectly singing in contexts where they couldn't have possibly memorised/rehearsed the lyrics, harmonies or choreography in advance. I don't think it's that out-there to stretch this to Ricky singing using a vocaloid-like voice in a context where he couldn't have possibly programmed it into his device in advance.
I don't think these are the only ways it can be done, either - they're just some obvious examples. I just wanted to make it clear that it is possible to depict Ricky as a nonspeaking character throughout the musical, and this wouldn't have to involve cutting his song or removing his singing roles. I'd really like to see productions start to come up with creative ways of doing this!
Conclusion/TL;DR
Disability erasure is a problem in all existing RTC productions to varying degrees, and it's a problem in the fandom as well. Disability erasure isn't just taking a disabled character and making them fully abled - many cases of disability erasure in RTC involve Ricky still having a disability, but it's still erasure if aspects of the disability he canonically has are erased.
Contrary to popular belief, Ricky's inability to speak being erased in the afterlife is not just a necessary evil of the musical genre. Nonspeaking characters can be represented in musicals, and this wouldn't have to involve cutting his song!
Thanks for reading!
69 notes
·
View notes
Text
US people with disabilities in the supplemental security income (SSI) program can't have a penny over $2K in their bank account at any time in order to keep their benefits.
You know this economy. That amount is completely unlivable & makes it hard for people with disability to save for the future or have a safety net for emergencies.
A new bill would raise the max to $10K (or $20K for married couples). It would make a world of difference.
Show support by contacting your reps.
Edit: Had the word petition on the mind, mistakenly called it that.
37K notes
·
View notes
Text
I really need non-disabled folks to understand that assistance for disabled people cannot be the same for every disabled person out there!!! Why it is so difficult to grasp this concept??
So, I went to book airport assistance with the company I’m travelling with for a holiday trip, and I explicitly said that I ONLY NEED ASSISTANCE TO GET ON AND OFF THE PLANE AND THAT I DON’T NEED A WHEELCHAIR!
What they tell me? That the only assistant option they can provide is the wheelchair option.
Why?? Like, why?? I’m literally asking you to do half the job. Why would you do more when I don’t need it and why would you waste a wheelchair when I don’t need it?? I don’t want to be pushed in a wheelchair by someone I don’t know, it makes me really uncomfortable. And besides, I can walk, so why??
But you know what the usual problem is? That assistance for disabled people isn’t centred around the comfortability of disabled people, it’s still centered around the comfortability of non-disabled people, so they can spend less money, less energy and less thought.
One standard applied to anyone, who cares, right?
And if you complain you’re just an annoying, whiny, selfish cripple who wants everything. You should be grateful that you even have assistance.
NO!! Assistance and accessibility ARE NOT A PRIVILEGE. THEY ARE HUMAN RIGHTS! And you do not bargain on human rights! You do not discount human rights! You are not grateful for human rights!
And another issue here is that the decision-making processes are only made by non-disabled people who don’t listen to what disabled people need.
Please, listen to us disabled people. We know what we need. We know our bodies. We know what makes us comfortable and what not.
But we can’t be the only ones here yelling at the wind. We need allies. We need people to understand that this is not a dignified treatment. This is not how you give people equal opportunities.
#cripple punk#disability#cpunk#cripple#crip punk#crip revolution#disability justice#disability rights#chronic illness#disability pride#disabled revolution#assistance#airport assistance#actually disabled#human rights#accessibility#ableism
20 notes
·
View notes
Text
i want to take the time to talk about a series of disabilities that no one takes seriously or even recognizes as a disability, which is food intolerances, and allergies. if a person can get sick if they eat the wrong foods, they are disabled, as this illness will make them unable to function all because they ate the wrong food. it's not okay to guilt someone for seeking foods that won't injure them.
in 2022, i began to lose my ability to digest land meats (pork, chicken, cow, etc.), animal milks, and eggs. it started slowly but quickly progressed to every type of land meat. i am only able to digest seafood, plants, nuts, seeds safely without becoming horribly sick. i tried to buy cow's milk because it is cheaper recently and became so ill it was genuinely traumatic. i have never been that sick in my life before. i cannot safely ingest cow's milk, the cheaper option, because it will injure me for several days or even weeks at a time. this happens to me with all land meats as well.
i cannot eat eggs. i cannot fried rice that has egg, i cannot eat most sauces like mayo or ranch dressing because of their high egg content. i cannot eat anything dressed in mayo as a sauce. anything that is baked or brushed or washed with egg is a risk. my digestive system really hates eggs in particular and they are inescapable.
people who can't digest or process lactose, gluten, meats, seafood, eggs, nuts, seeds, beans, fiber, certain fats, proteins or sugars don't have their needs considered very often, nor taken seriously, especially when that person is poor. people with digestive issues need to be able to eat foods that don't hurt us- it's not our faults that alternative milks, breads, pizzas, snacks, sauces, dips, spreads, meats and more are significantly more expensive. we still need to be able to eat foods that don't harm us regardless of how much money we make.
#disability#physical disability#disabled#invisible disability#disability rights#digestive disorders#digestive health#food allergies#food intolerance#lactose intolerance#our writing#about us
7K notes
·
View notes