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#americans with disabilities
magpiedminx · 4 months
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From Misa on Wheels
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quotesfrommyreading · 10 months
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When I’m out with Deaf friends, I put my hearing aid in my purse. It removes any ability to hear, but far more importantly, it removes the ambiguity that often haunts me.
In a restaurant, we point to the menu and gesture with the wait staff. The servers taking the order respond with gestures too. They pantomime “drinks?” and tell us they learned a bit of signs in kindergarten. Looking a little embarrassed, they sign “Rain, rain, go away, come again another day” in the middle of asking our salad dressing choice. We smile and gently redirect them to the menu. My friends are pros at this routine and ordering is easy ― delightful even. The contrast with how it feels to be out with my hearing husband is stunning.
Once my friends and I have ordered, we sign up a storm, talking about everything and shy about nothing. What would be the point? People are staring anyway. Our language is lavish, our faces alive. My friends discuss the food, but for me, the food is unimportant. I’m feasting on the smorgasbord of communication ― the luxury of chatting in a language that I not only understand 100% but that is a pleasure in and of itself. Taking nothing for granted, I bask in it all, and everything goes swimmingly.
Until I accidentally say the word “soup” out loud.
Pointing at the menu, I let the word slip out to the server. And our delightful meal goes straight downhill. Suddenly, the wait staff’s mouths start flapping; the beautiful, reaching, visual parts of their brains go dead, as if switched off.
“Whadda payu dictorom danu?” the server’s mouth seems to say. “Buddica taluca mariney?”
“No, I’m Deaf,” I say. A friend taps the server and, pointing to her coffee, pantomimes milking a cow. But the damage is done. The server has moved to stand next to me and, with laser-focus, looks only at me. Her pen at the ready, her mouth moves like a fish. With stunning speed, the beauty of the previous interactions ― the pantomiming, the pointing, the cooperative taking of our order ― has disappeared. “Duwanaa disser wida coffee anmik? Or widabeeaw fayuh-mow?”
Austin “Awti” Andrews (who’s a child of Deaf adults, often written as CODA) describes a similar situation.
“Everything was going so well,” he says. “The waiter was gesturing, it was terrific. And then I just said one word, and pow!! It’s like a bullet of stupidity shot straight into the waiter’s head,” he explains by signing a bullet in slow motion, zipping through the air and hitting the waiter’s forehead. Powwwww.
Hearing people might be shocked by this, but Deaf people laugh uproariously, cathartically.
“Damn! All I did was say one word!” I say to my friends. “But why do you do that?” they ask, looking at me with consternation and pity. “Why don’t you just turn your voice off, for once and for all?” they say.
Hearing people would probably think I’m the lucky one ― the success story ― because I can talk. But I agree with my friends.
  —  I'm Deaf And I Have 'Perfect' Speech. Here's Why It's Actually A Nightmare.
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lucyoccupy · 11 months
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Breaking the Silence: Speaking Out Against Disability Discrimination in the Legal System
Lawyers and the courts have a responsibility to comply with the ADA and ensure that people with disabilities are not denied access to justice.   Is #LinkedIn Woke now?  Third time they terminated my account coincidentally around the same time of aggressive and brutal lawfare. Shocking.  It’s #VirtuallyBookBurning, ramping for years.  Shame on them. Their actions also cut me off from prayer…
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Today, in “I’ll take any good news I can find”:
A production of Romeo and Juliet with Deaf actors signing their lines has been referred to as bilingual! Not just “accessible” or “diverse” but also BILINGUAL!
This makes me happy because the general idea of ASL (and other signed languages) is that they’re just a manual version of the spoken language. By that logic, Norwegian is just a higher-latitude version of German. Signed languages are languages of their own! With unique vocabulary, grammar, and dialects!
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esa-guide · 1 year
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Watch "Going through airport security with a Service Dog ✈️🦮" on YouTube
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happytxcowman · 1 month
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So the members of the discord at @bfpnola were explaining to me why BASL (Black American Sign Language) is a separate language than ASL (American Sign Language) because I was wondering if it was for a similar reason as AAVE (African American Vernacular English).
Fun fact. It's because of segregation. So when Sign Language in America was being taught. The schools were segregated, so they each dealt with deaf accommodations in their own way. White schools were taking a more integration approach so they highly frowned on the use of Sign and they were trying to get deaf kids to practice speaking.
However, Black schools were more opening to the use of Sign, so they had a lot longer to develop their Sign Language than White schools, as they were encouraging Sign at a time when white schools weren't.
Follow and support @bfpnola because they teach me so many things and it is so cool. 😁
-fae
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Physicians are using excuses to intentionally dissuade people with disabilities from their practices, researchers say in a new study exposing just how pervasive discrimination against this population is in health care.
In focus groups, doctors described making strategic choices to turn away individuals with disabilities. They reported telling patients with disabilities that they would require specialized care and that “I am not the doctor for you.” In other cases, physicians said they simply indicate that “I am not taking new patients” or “I do not take your insurance.”
The findings come from a study published this month in the journal Health Affairs. It is based on focus groups conducted in late 2018 by researchers at the Northwestern University Feinberg School of Medicine, the University of Massachusetts and Harvard Medical School with 22 primary care and specialist doctors who were selected from a national database.
Many of the participants described accommodating people with disabilities as burdensome and some used outdated language like “mentally retarded.” Doctors frequently indicated that individuals with disabilities account for a small number of patients, making it hard to justify having accessible equipment. They also had little knowledge of their obligations under the Americans with Disabilities Act, with one suggesting that the law works “against physicians.”
The latest study builds on findings published earlier this year from a survey of 714 doctors that was done by some of the same researchers. Just 56% of physicians who participated in the survey said they welcome people with disabilities at their practices and only 41% indicated that they could provide such patients with a similar quality of care to others. Meanwhile, more than a third of doctors queried said they had little or no knowledge of their legal obligations under the ADA.
“Taken together, the focus groups and survey responses provide a substantive and deeply concerning picture of physicians’ attitudes and behaviors relating to care for people with disabilities,” the study authors note.
The findings suggest that bias continues to greatly influence health care more than 30 years after passage of the ADA, which prohibits discrimination against people with disabilities, including in medical services.
Tara Lagu, a professor of hospital medicine and medical social sciences at Northwestern University and an author of the study, described the doctors’ attitudes toward the ADA in particular as “upsetting and disappointing.”
“Our body of work suggests that physician bias and discriminatory attitudes may contribute to the health disparities that people with disabilities experience,” Lagu said. “We need to address the attitudes and behavior that perpetuate the unequal access experienced by our most vulnerable patients.”
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benandstevesposts · 2 years
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https://t.co/RUeFT8TJqV
— Burnpits360 (@Burnpit360) July 31, 2022
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neuroticboyfriend · 5 months
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hey uh i don't think USamerican food (ex: all our candy, chips, fast food, etc.) is unhealthy because it's a nation filled with gross fat people ridden with diabetes... hear me out... maybe it's because this god forsaken country is effectively the birthplace of capitalism and they will put anything and everything in our food if it means we keep buying it. especially if we have no other options.
all the added salt and sugar is because they know people will keep going for it - they're also simple ingredients that are easy for them to procure (thanks to centuries of slave, and otherwise unethical, labor). all the harmful dyes is because they've been relentlessly marketing to us in such a way that they make out natural food to be dirty and inferior. all the "fat free!" food came about because of fatphobia... you do need fats in your diet, just in balance.
it's all because they (capitalist class) don't give a flying fuck about anyone if it means they can make money. of course we aren't nearly the only country where capitalism takes away peoples reasonable access to a balanced diet, and the USA does get slack on a lot of things for a lot of very good reasons. but... maybe that shouldn't fall on the oppressed people living here? especially not based on bigoted misconceptions? there are no conditions on not being a bigotted asshole to someone. not facing bigotry isn't supposed to be a privilege. and it doesn't have to be an acutely life-or-death bigotry to matter.
addendum: also whether a food is "unhealthy" is heavily subjective and reliant on the individuals health needs at the time. sometimes people really need that salty as fuck pack of potato chips... like a disabled person with electrolyte issues! or a poor person who hasn't had enough to eat!
tl;dr if you keep going on about how disgusting americans are because of our food, you're just fatphobic and ableist.
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batboyblog · 2 months
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Things Biden and the Democrats did, this week #7
Feb 23-March 1 2024
The White House announced $1.7 Billion in new commitments from local governments, health care systems, charities, business and non-profits as part of the White House Challenge to End Hunger and Build Healthy Communities. The Challenge was launched with 8 billion dollars in 2022 with the goal of ending hunger in America by 2030. The Challenge also seeks to drastically reduce diet-related diseases (like type 2 diabetes). As part of the new commitments 16 city pledged to make plans to end hunger by 2030, the largest insurance company in North Carolina made nutrition coaching and a healthy food delivery program a standard benefit for members, and since the challenge launched the USDA's Summer EBT program has allowed 37 states to feed children over the summer, its expected 21 million low income kids will use the program this summer.
The US House passed a bill on Nuclear energy representing the first update in US nuclear energy policy in decades, it expands the Nuclear Regulatory Commission and reduces reducing licensing fees. Nuclear power represents America's single largest source of clean energy, with almost half of carbon-free electricity coming from it. This bill will boost the industry and make it easier to build new plants
Vice President Harris announced key changes to the Child Care & Development Block Grant (CCDBG) program. The CCDBG supports the families of a million American children every month to help afford child care. The new changes include capping the co-pay families pay to no more than 7% of their income. Studies show that high income families pay 6-8% of their income in childcare while low income families pay 31%. The cap will reduce or eliminate fees for 100,000 families saving them an average of over $200 a month. The changes also strength payments to childcare providers insuring prompt payment.
The House passed a bill making changes to the Small Business Administration’s 8(a) program. The 8(a) is an intensive 9 year program that offers wide ranging training and support to small business owners who are socially and economically disadvantaged, predominantly native owned businesses. Under the current structure once a business reaches over 6.8 million in assets they're kicked off the program, even though the SBA counts anything under $10 million as a small business, many companies try to limit growth to stay on the program. The House also passed a bill to create an Office of Native American Affairs at the SBA, in order to support Native-owned small businesses.
The White House and HUD announced steps to boost the housing supply and lower costs plans include making permanent the Federal Financing Bank Risk Sharing program, the program has created 12,000 affordable housing units since 2021 with $2 billion and plans 38,000 additional units over ten years. As well as support for HUD's HOME program which has spent $4.35 billion since 2021 to build affordable rental homes and make home ownership a reality for Americans. For the first time an administration is making funds available specifically for investments in manufactured housing, $225 million. 20 million Americans live in manufactured housing, the largest form of unsubsidized affordable housing in the country, particularly the rural poor and people in tribal communities.
The Department of Energy announced $336 million in investments in rural and remote communities to lower energy costs and improve reliability. The projects represent communities in 20 states and across 30 Native tribes. 21% of Navajo Nation homes and 35% of Hopi Indian Tribe homes remain unelectrified, one of the projects hopes to bring that number to 0. Another project supports replacing a hydroelectric dam in Alaska replacing all the Chignik Bay Tribal Council's diesel power with clear hydro power. The DoE also announced $18 million for Transformative Energy projects lead by tribal or local governments and $25 million for Tribal clean energy projects, this comes on top of $75 million in Tribal clean energy projects in 2023
Transportation Secretary Pete Buttigieg put forward new rules to ensure airline passengers who use wheelchairs can travel safely and with dignity. Under the planned rules mishandling a wheelchair would be a violation of the ACAA, airlines would be required to immediately notify the passenger of their rights. Airlines would be required to repair or replace the wheelchair at the preferred vendor of the passenger's choice as well as provide a loaner wheelchair that fits the passenger's needs/requirements
The EPA launched a $3 Billion dollar program to help ports become zero-emission. This investment in green tech and zero-emission will help important transportation hubs fight climate change and replace some of the largest concentrations of diesel powered heavy equipment in America.
the EPA announced $1 Billion dollars to help clean up toxic Superfund sites. This is the last of $3.5 billion the Biden administration has invested in cleaning up toxic waste sites known as Superfund sites. This investment will help finish clean up at 85 sites across the country as well as start clean up at 25 new sites. Many Superfund sites are contained and then left not cleaned for years even decades. Thanks to the Biden-Harris team's investment the EPA has been able to do more clean up of Superfund sites in the last 2 years than the 5 years before it. More than 25% of America's black and hispanic population live with-in 5 miles of a Superfund site.
Bonus: Sweden cleared the final major barrier to become NATO's 32nd member. The Swedish Foreign Minster is expected to fly to Washington to deposit the articles of accession at the US State Department. NATO membership for Sweden and its neighbor Finland (joined last year) has been a major foreign policy goal of President Biden in the face of Russian aggressive against Ukraine. Former President Trump has repeatedly attacked NATO and declared he wants to leave the 75 year old Alliance, even going so far as to tell Russia to "do whatever the hell they want" with European NATO allies
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switchcase · 4 months
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We really need to stop this increase in people making assumptions about disabled peoples' access to care and their finances. Yes, especially if you are also disabled and saying this.
You don't know them. You cannot Decide that they must be wealthy or privileged or have never had poor medical experiences for having mobility aids or having had certain medical procedures or currently being treated or having diagnoses.
You just sound ignorant when you say stuff like "you clearly don't know what not having access to medical care is like" and prattling off a bunch of first world medical experiences to someone that not only has experienced every single one of those things already but grew up in the global south. Sorry you had those experiences but it doesn't mean you can tell other people what their experiences are or must be.
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decolonize-the-left · 1 month
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"I was learning more and more about what discrimination was, and equally important, I was learning that I needed to become my own advocate. I was entering college, Long Island University, and I had always wanted to be a teacher, and sol minored in education and I took all the appropriate courses, and then when it was time for me to go for my license, I had to take a written exam, an oral exam and a medical exam. At that time, all three of those exams were given in completely inaccessible buildings, so I had friends who carried me up and down the steps for these exams, not in a motorized wheelchair in a manual wheelchair.
But I passed my oral exam. I passed my written exam.
My medical exam was something completely different. One of the first questions the doctor asked me was, could I please show her how I went to the bathroom. I was 22 years old and you know when you go for any kind of an interview, you think about all the kinds of questions that people could ask you?
That was not one of them."
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pinkeoni · 10 months
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So I’m gonna say something crazy… but have you ever considered that maybe, just maybe… and hear me out… the core four group in the show about “outcasts and wierdos” ISN’T supposed to have a straight-white-able-bodied-all-american male that people from that group can easily project on to? That maybe the straight-white-male audience might have to contend with the fact that they find relatability in characters who are black, disabled, or gay? That MAYBE there isn’t supposed to be this pov character that easily fits into these conventions that they’ve been so used to seeing in popular media but that’s also kind of the point?
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cashthecomposer · 1 year
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Just so other Americans know, service dogs do *not* need to be wearing gear that says "service animal", nor do they need papers, nor training from any specific entity.
All they need is training to do at least *one* task that serves to aid an individual with their disability. That's it. This training can come from anyone, anywhere, you can even train them yourself, that right is specifically noted by the ADA.
They must be well behaved and 100% under control, and potty trained. If they are at all disruptive to others in either regard, they can be asked to leave, and you must comply, though you can come back without the animal. A fear of dogs or allergy to dogs is not a valid reason for someone to turn you away. Patrons must be accommodated, both those with the dogs, and those with the related issues. You may not be isolated or otherwise treated differently from other patrons.
People working can ask only two questions to confirm that the dog is a service animal:
(1) is the dog a service animal required because of a disability, and
(2) what work or task has the dog been trained to perform.
That's it. If you refuse to answer, you will be asked to leave, and you must comply. These two questions are the only questions that you *must* answer, any others are not allowed: they cannot ask about the person’s disability, require medical documentation, require a special identification card or training documentation for the dog, or ask that the dog demonstrate its ability to perform the work or task.
You will still be charged for any damages caused by the animal.
Hope that clears up the many misunderstandings I see. I have a service dog, and I'm happy to answer any other questions anybody might have about how this whole thing works.
Thanks for reading, here's a sleepy dog tax as a reward for making it this far.
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disableddyke · 1 year
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“why don’t you just go see a doctor” i go see doctors and they perform $10,000 worth of basic tests that i’ve had done hundreds of times and already know will come back normal and then when they inevitably do, they tell me they don’t know what’s wrong with me and send me home with zero answers, the same problems and a medical bill i can’t afford. don’t tell me i just need to see a doctor.
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