The Americans With Disabilities Act (ADA) was just reformed so that disabled people canāt sue public businesses for discrimination because it would be discrimination against that business.
50% of all US murder victims by police officers are disabled
Bathrooms, entryways, seating, parking, and other public spaces are segregated for disabled people
Disabled children are required to go to segregated schools
Disabled people can’tā¦
Get married without losing their health insurance which is a death sentence
Have savings accounts
Have more than $2000 at any given time
Own or inherent property
Own jewelry worth more than $100 or other items worth more than $500 without reporting them to the government
It is legal for a parent to murder a disabled child if they consider that child an undue burden
This is an extremely short list of things you are leaving out of your social justice
[Image description – a series of tweets byĀ @EbThenĀ that say:
I shouldāve gone to bed before the Stephen Hawking news broke.
Seeing a headline describing him as having āovercomeā a ādebilitating diseaseā to āpublish books on the mysteries of the universeā is making me grumpy.
Stephen Hawking wasĀ an exceptionally privileged white English manĀ who had access to the necessary supportsĀ to successfully navigate a world that puts little importance on making itself accessible.Ā
I mean, he did pretty amazing stuff but it wasnāt amazing because he had ALS and used a wheelchair and AAC. Those are just things.
The amazing stuff Stephen Hawking did was amazing because he thought and said amazing things.
Stop being amazed that a few Disabled people do awesome world-changing stuff. Start wondering why more of us donāt.
Itās not because a wheelchair and AAC somehow get in the way of doing theoretical physics. Itās because a lot of us deal with ridiculously huge access barriers.
Also stop only valuing Disabled people who do awesome world-changing stuff. We donāt need to be supercrips to be worthwhile.
Disabled people are allowed to be normal schlubs and not be treated like that means weāre failures.
When you write a headline that implies ALS, a wheelchair and machine-facilitated speech are natural and expected barriers to being a successful scientist, youāre telling on yourself.
Those circumstances arenāt inevitable barriers to doing all sorts of science.
Whatās frustrating is that weāre talking about a Disabled person who had so much opportunity and access to excellent supports and tools and people still talk about that like itās tragedy.
And Iām thinking how many folks I know could benefit from those things.
Ableism is so fuck exhausting]
Hawking said as much and fought to keep the NHS fully funded in England and he spoke out against Trump trying to dismantle Obamacare.
He was keenly aware that his situation was a best-case scenario. The way the media makes him seem so tragic is frustrating, especially since he was anything but a tragic figure, by his own admission.
But thatās the thing, most abled people tend not to listen to our opinions about ourselves when they can live comfortably within their own false perceptions.
laws about minimum wage should apply to disabled people
laws about minimum wage should apply to incarcerated peopleĀ
everyone deserves a fair living wage for their labor
wait, they donāt???
Not even close. Disabled folks can be paid as little as $1 an hour in some cases at whats called āsubminimum wage.ā Prisoners are sometimes forced to work without pay at all.
Hi, I am an attorney in the disability field. Many disabled folks make well under $1 an hour in what are called āsheltered workshopsā. There are only three states right now that require people with disabilities to be paid at least minimum wage, and they are Alaska, New Hampshire, and Maryland. Goodwill is a major offender, but there are many, many others.
Hey guys, Iād like to talk about the #HR620 bill
I have trouble getting around in public. if thereās not enough space for me and my cane to get through then I canāt go there, and itās worse for people with wheelchairs because people do not consider the size of an average chair or motorized scooter (amongst other things. If you search youāll find wheelchair users discussing at length how this will effect them)
Weāre all already fighting nail and teeth to get accessible buttons, to get hand rails, to get any ramp at all, to get accessible public transportation. but forget going to the mall (at least to youthful stores), forget it if you live somewhere with historical buildings, forget restaurants with closed in dining rooms where you can barely fit even a body through.
And no one helps. People will stare at you while you struggle, watching like youāre a zoo creature. Iām lucky to have a fiancee who knew what she was getting into when she fell in love with me. knew there was a chance that she that sheād be doing all the physical work for me because 9 days out of 10 Iām in pain and thatās just how itās always been. Not everyone is this lucky. Some of us donāt have any way to get around and thats worsened by the fact that every time I go out in public I see these basic accessibilities being denied.
This is how it is already, with the Americans with Disabilities Act (ADA) in place, which holds the establishmentsā owners responsible for accessibility (or lack thereof) by fining them for not meeting the ADA standards.
Now, what #HR620 is going to do is strip these accessibilities even further, by putting the stress on the disabled rather than the inaccessible businesses. Essentially, a disabled person will have to contact the owner of an establishment with a written notice saying how in particular they broke the law, then thereās a lengthy waiting period before anything has to be done. This is going to be absolutely devastating to not only me but every single disabled person in the US.
Self advocacy is power, yes, but there is no way that theyāre going to listen if the only people speaking are disabled people. Please talk about this. Please share this message. Please tell your friends, your family, that if this bill passes the senate, disabled people will be set back miles.
And then, because the bill will be going through senate: call your senators and tell them how important it is that they donāt pass this. Tell them that the ADA has been important in assuring accessibility. Demand that they donāt allow #HR620, because disabled rights are human rights.
I mean, this is an obviously crazy-impractical half-assed undercooked sorta-half-idea that someone threw in there as anĀ āinnovationā that couldnāt possibly be enacted (for one thing, grocery chains will have a FIT), but letās focus on how cartoonishly evil this is:
Under the Trump proposal, which the Agriculture Department has dubbed āAmericaās Harvest Box,ā all households receiving more than $90 per month in benefits ā 81 percent of SNAP households overall ā would begin receiving about half their benefits in the form of government-purchased, nonperishable food items.
Those foods would include shelf-stable milk, juice, grains, cereals, pasta, peanut butter, beans and canned meat, fruits and vegetables, according to the USDA. The department estimates that it could supply these goods at about half the cost of retail, slashing the cost of SNAP while still feeding the hungry.
No fresh fruit or vegetables for you! No more actually choosing the food you eat, dietary requirements be damned! We hate poor families this much!
You really have to admire the mental gymnastics lefties like OP are capable of pulling off by arguing that literally giving poor people food is the exact same thing as making them starve to death. That type of impressive athletics is something youād only imagine seeing at the Olympics.
Hi!
Iām a disabled person whose family literally receives SNAP right now. Why we receive it or the circumstances under which we receive it is nobodyās business but ours: the social safety net is here for us because we fell on hard times. One of my disabilities? Celiac disease. And yes, that is an ADA disability.Ā
I cannot simply eat a box of food that someone gives me. Canned foods often use glutenated substances as preservatives, making them literally poison for me. I must very carefully choose my foods. A restricted diet is the only treatment for my life-threatening disease.Ā
So, yes, handing people like me a box of food absolutely is asking us to starve, because most canned meats, canned vegetables, and cereals are not edible by me, nor is it safe for those items to be eaten in a kitchen used to feed me; gluten adheres to porous surfaces such as Tupperware, plastic bowls, and non-stick cookware. That food cannot be eaten in my home without making me sick, so no one in my family can eat it either.
Now thatās leaving aside entirely the fact that I have a hard time, due to my disease, with absorbing nurtients from food, so I must carefully choose what I eat to maximize my nutritional absorption. Hint: canned foods have much lower nutritional value and would not meet my needs either.Ā
The article ā had you read it ā makes very clear that those proposing this hadnāt considered how to handle people with food allergies or celiac disease. So we could go with this massively-expensive, incredibly invasive, paternalistic, infantilizing and ineffective system that would leave someone like me not only hungry but sicker, making more use of the Medicaid that I currently receive because I am permanently disabled, and thus more expensiveā¦
⦠or we could keep it the way it is, not waste all that money setting up a ridiculously bad system that will make people sick, and trust poor families to know how best to feed themselves for their specific needs.Ā Ā
Oh, but wait! Thereās more! This plan would take money away from small mom-and-pop grocery stores and farms who currently accept EBT and supply a lot of the food stamp needs for rural working poor.Ā
It requires an awful lot of mental gymnastics to justify taking money away from small business owners and also giving poor people food less-nutritional food that a lot of us canāt even eat.Ā It takes absolutely none to sayĀ āgee, hereās your food money, you know better than we do what your individual needs are, sorry lifeās kicking you right now, hopefully things get better, I hope this system is here to help me if I need it.āĀ
But, you know, go off, I guess.
Except it is my business it is my business because you being on snap costs anyone who pays taxes money in the form of taxes. So yes it is my business and you shouldnāt be on it.
Now that means, get a job, make money and take care of yourself so you arenāt on this program is fine with me.
And before you get offended at me even suggesting such a thing, is this not what you want? To be independent and self sustaining?
Oh but itās hard. Still doesnāt change my position. Work is hard difficult and at times dangerous but if we want this world of ours to keep spinning it must be done.
So donāt sit there and tell anyone itās not my or anyoneās business that you use this system that costs people money, because it is. And your job as a being with the ability to reason, is to self improve. So improve yourself and gain your independence.
My being on SNAP costs you less than a hundredth of a penny a year. So you may have exactly a hundredth of a pennyās worth of concern about my circumstances.Ā
That said, I have a job. I own a business, as a matter of fact. Youād know that if you took so much as a cursory look at the header of my Tumblr.Ā
Let me rock your fucking world: most people who receive SNAP have at least one job. Most of us (like me) have two or more.Ā
Let me rock your fucking world again: I could be eligible for disability, but I choose not to seek it for as long as possible, if ever. I am permanently, multiply disabled, which you would know if you had actually read everything that I wrote. I am literally doing everything within my power to be as independent as possible for as long as possible.Ā
I work hard. I work as hard as my body will allow me, and sometimes more than, causing myself to become sick, to require hospital admission, because I seek again the kind of independence that I used to have before a tumor was taken out of my spine, permanently scarring my spinal cord, and setting off a chain reaction that left me at the mercy of a body that would no longer obey me. I went from having a hefty 401K, a job in the finance industry, and significant savings to starting a business that Iād be able to run around the restrictions of my body because I can no longer work a traditional 9-5 job. I physically cannot do it. I continued to work my finance job for 4 years after my tumor was removed, as my health has slowly deteriorated, until my job was eliminated. I will never be able to work a 9-5 job again, because I will not have FMLA protection for my unpredictable flare-ups. That is not my opinion: that is the assessment of four different doctors. See also: I could seek disability and probably get it, but choose not to do so for as long as I can.Ā
Let me rock your fucking world yet again: I have paid more in to the system than I have ever gotten out of it. You havenāt paid a fucking penny to me, because I paid in to the system for my entire working life, from before I was even an adult.Ā
But even if none of that were true, even if Iād never been able to work a day in my life, even if I never had worked a day in my life, even if I didnāt work my fucking ass off as much as my body will let me, even if I werenāt constantly turning out new products for my business, new writing for my patrons, making as much money as I can, you still donāt get to have a fucking opinion about why Iām on SNAP, you know why?
Because the right to food is recognized in the 1948 Universal Declaration of Human Rights (Article 25) as part of the right to an adequate standard of living, and is enshrined in the 1966 International Covenant on Economic, Social and Cultural Rights (Article 11).
Food is a basic human right, as recognized internationally, and understood by everyone who isnāt a solipsistic jackass.Ā
I know itās really scary to think that you, too, might suddenly be unable to adequately provide for yourself, and acting out of that fear makes you insist that everyone who needs help must simply not be working hard enough, because the alternative is that our economic system is broken and that, G-d forbid, you might suddenly, through no fault of your own, be at the mercy of the same system that you purport works for everyone. You might not be able to provide for yourself if you got sick, or if something went wrong, and thatās scary. I get that.Ā
But Iām under no obligation to pat your bottom and reassure you that youāre right, golly gosh, if I worked harder I wouldnāt need any help, and so your deeper fears that you might find yourself in my shoes just arenāt true, because youāre totally in control of your situation with all your hard work, and an uncaring universe would never do you dirty the way itās done me.Ā
So fuck off, bro. And leave everyone else who needs a little help alone.Ā
People will really go out of their way to blame poor people for being poor and disabled people for being disabled.
Itās honestly heartbreaking that so many people feel that way about SNAP. Like. They donāt care for their fellow man enough to feed them when theyāre hungry. Hungry kids? Also not worth helping, apparently, as like 75% of SNAP recipients have kids in the household.
Iām infuriated that this seems to be a common sentiment. How selfish and cruel do you have to be to tell someone who is less fortunate than you that they arenāt working hard enough to deserve to eat? All because you pay a few dollars in taxes per year? Iām just. So disappointed that so many people are that selfish.
Someoneās reasons for needing assistance are their own. If the Health and Human Services department deemed that someone is eligible for benefits, thatās the end of it. No one deserves to invade on a personās privacy. SNAP recipients are actual human beings who DESERVE RESPECT.
Some people can lift 200 pounds. But if they carried it everywhere they went for an entire day without ever putting it down, theyād severely tear their muscles and cause permanent damage to their body.
Some people can enter a 140° car in the summer to get something out of the car. But if they stayed in the car, theyād die from the heat.
Some people can hold their breath underwater for 30 seconds. But if they tried to go scuba diving without the necessary gear, theyād drown.
Clearly, someone doing something for a short period of time does not automatically mean that they can do it indefinitely with no problem.
So why do people assume that if someone can walk for a few seconds, they donāt need a wheelchair?
Clearly, someone doing something for a short period of time does not automatically mean that they can do it indefinitely with no problem.
Also, think about this in terms of mental health as well.
You can have a good day, and pass for normal, just not all the time.
I donāt understand why people assume thereās this sense of entitlement when someone with depression or chronic illness complains about being bored. Itās not like weāre sitting there with endless resources in front of us, turning our nose up at all the options we have and whining about everything being tooĀ boring. Itās not just boredom – itās lack of stimulation and enrichment.Ā
When you have a condition that severely restricts your ability to do things, you get⦠understimulated, socially deprived, restless⦠and that translates to boredom. I wish more people understood that when I say Iām bored what Iām really saying is, Iāve barely been able to leave the house for five days and I feel like staring at the walls or scrolling through my phone for another eight hours is going to make me lose my mind.Ā
This is absolutely true. Itās calledĀ āoccupational deprivationā which is fancy OT words forĀ ānot being able to do almost anythingā basically. Thereās a whole academic literature about how bad it is for people to be occupationally deprived and how it screws you up psychologically.
Iām actually in the beginning stages of writing an article about occupational deprivation in bedridden people. Itā²s basically a case study of me – Iāve been bedridden for decades – but Iād love to hear from other bedridden spoonies if youād like your thoughts included. Message me!
Like, 90% of infomercial style products were designed by/for disabled people, but you wouldnāt know that, because there is no viable market for them. THey have to be marketted and sold to abled people just so that any money can be made of off them and so the people who actually need them will have access.
I think snuggies are the one example almost everyone knows. They were invented for wheelchair users (Do you have any idea how hard it is to get a coat on and off of someone in a wheelchair? Cause itās PRETTY FUCKIN HARD.) But now everyone just acts like theyāre some ~quirky, white people thing~ and not A PRODUCT DESIGNED TO MAKE PEOPLES DAY TO DAY LIVES 10000X EASIER.
But if at any point you were to take your head out of your own ass and goĀ āHey, who would a product like this benefit,ā that would be really cool.
This makes informational make so much sense now.
Like⦠of course thereās no reason for that guy to knock over that bowl of chips. However, the person it was actually designed for has constant hand tremors that would make this pretty rad, but since we donāt want to show that in a commercial, hereās an able bodied guy who canāt remember how gravity works.
Shit. Those commercials suddenly get a lot less funny when you realize itās pretty much just people ineptly trying to mimic disability.
Or like the thing for the eggs? Like, oh, it cracks eggs perfectly, you only need one hand?
IT WAS DESIGNED FOR PEOPLE WHO ONLY HAVE THE USE OF ONE HAND.
Or the juice bottle pourer? For people whoāre TOO LAZY TO POUR THEIR OWN JUICE? Or FOR PEOPLE WHO HAVE DIFFICULTY BEARING WEIGHT IN THE HANDS.
Itās amazing how with just a few words by a few people, my whole perspective on something can shift entirely.Ā
I feel so ignorant for never having realized this before.
Most people I know who own infomercial products are elderly, disabled and poor.Ā
thank you – best public service announcement I have seen in a really long time
[Brooke Winters tweeted: āAs a disabled person I donāt want to be told I can do anything if I put my mind to it. I want to know that what I can do is good enough.ā]
Oh my.
This. So much. This.
And if I may be so bold as to add:
As a disabled person I donāt want āSupportā if youāre only willing to support me in āovercomingā my disability, or in trying to be ānormal.ā
I want to know I have your support in being happy, and living a joy-full life. Even if that life looks weird to you.