ableism

bethsunshine:

themightyif:

frankensteinsmomster:

rubyvroom:

fileundermiscellany:

garurumvn:

mutisija:

studiousmedic:

mcride:

slaygnstonhughes:

gabrielleamaris:

the-prophet18:

universaldelusion:

cutecurvycoffeebrat:

Lol savage

I no longer believe in the human race.

This is the laziest shit ever

How lazy can humans get?

Have you never met white ppl?

yh but if you look outside your own personal reasons for using this, laziness, it actually looks a really great and practical way to put on your socks if you have a disability that hinders you from otherwise being able so without someone there to help you 

you do realise that there are people out there who literally have to travel door to door helping elderly people, disabled people and people with chronic illnesses to put on their socks? people are paid to help put on pressure socks to help with oedema? don’t you realise that if these people could have one of these tools, these caregivers could be doing something else and that this therefore is an incredible tool designed to cater for some of the most healthcare dependent people in our society? do you guys even realise there are other people living other lives?

i really wish i had this when my spine was broken and i had to wear a medical metal corset which made bending down impossible. i had to ask my mom to help me with socks and it was kinda humiliating.

My dad spends an hour in the morning getting dressed because he has no one to help him to get his socks on because his ankle is fused. If he had this it would literally save him an hour.

“Oh but people are so lazy!”

fuck off you ableist pieces of shit

Honestly I don’t even get how you could look at this and think “lazy”. This looks like more work for an otherwise able-bodied person than just putting their sock on the regular way. It’s pretty obvious this is meant for people who have trouble bending over, like come on.

You know how people go straight to “lazy” on this? Because we’re trained to think of most accessibility modifications as lazy. The disabled = lazy message is deeply embedded in our culture.

Does anyone know what this is called/where I could get it?
My mom has incesingly bad arthritis and the process of bending to put her socks on is getting harder for her. My dad could totally put the socks on it for her at night and then in the morning she could just slip them on.

It appears to be the Pratiflex PR001. They claim that the Pratiflex PR002 is more versatile, though. They’re Brazilian products, and my Portuguese is not so hot (nor is Google Translate’s). However, the website is here and you can apparently order them online for the equivalent of approximately US$20 (not including shipping, etc.) for the PR001 or US$34 for the PR002. 

The site says that they’re widely used in the States and Europe, but that they’re finally making them available in Brazil, so presumably you could find similar products from different companies elsewhere. A search for “sock applicator” turned up this Amazon.com category with several similar products, for example. From that page, this appears to be a good product, available for shipping in the U.S., for about $30.

So this is a teeny bit off topic, but there’s a group called the Tetra Society of North America, and if someone needs an assistive device and it isn’t commercially available yet, they have volunteers that are retired engineers and other design/handy types that will work together on solving a challenge you may have. They help make all kinds of things from adapted Wii remotes to specialized coffee pot handles to medical product adaptations. They are SO cool. This is their website: http://www.tetrasociety.org/ 

nouveauqueer:

thatscorpionbitch:

Like, 90% of infomercial style products were designed by/for disabled people, but you wouldn’t 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 it’s PRETTY FUCKIN HARD.) But now everyone just acts like they’re 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 go “Hey, who would a product like this benefit,” that would be really cool.

this makes so much sense and i apologise to anyone i may have hurt by not thinking it through before i made fun of infomercial products

katara:

seattl-ite:

katara:

I am sick of people thinking deodorant is optional

i’m sick of people thinking that they can judge others on a normal bodily function and that the only way they can be accepted is to wear something that is harmful/poisonous to your body. just because some men in the 1880’s decided bodily odor was no longer acceptable. 

bitch you stink 

In all seriousness there are millions of people out there who due to debilitating mental illnesses don’t have the same standards of hygiene as the average (there has been at least one ‘support and love these people!’ text post to that effect recently, which I suppose was most likely taken as seriously as most ‘support and love these people!’ text posts are.) Schizoaffective disorder, depression, even certain hideous types of OCD (yooooo) can lead to a person severely neglecting their personal hygiene. And then on top of that you’ve got millions of people who cannot afford deodorant, cannot afford to wash their clothes, are allergic to almost all of it etc etc. There’s no surefire way to judge a person’s circumstances.

atthefinishline:

People of Tumblr,
We (the d/Deaf/Hard of Hearing Community) in the UK desperately need your help.
With the riots going on in central London, everyone is having a say in it, but nobody is mentioning the disabled community who are going to be affected the most.

Since our General Election, it has been announced that David Cameron and the Conservative government want to abolish a number of services that are completely essential and vital to us to be able to live.

What the hell is going on? What are you talking about?
Basically, in short:
The Department for Work and Pensions want to make getting DLA (Disability Living Allowance) / PIP (Personal Independent Payment, believe ti’s called this now) even more harder to be accepted, and many d/Deaf/HoH users will lose their payments, or will no longer be granted to receive it.
(I’m 22. I’m severely profound, and each time I’ve applied for this, I’m repeatedly denied entitlement because I’m ‘not deaf enough’!! The money I would have got from this would have went towards the funds to buying the kit that I need to support my every day life. At the moment, all the kit I need works out to about £1500. I can’t afford that with my current job that I work in.)

There is a scheme called Access to Work, which enables funds/grants to purchase equipment and interpreters. They’re wanting to scrap it completely. This is a complete NIGHTMARE for d/Deaf/HoH users. Why?
Some users speak only using BSL (British Sign Language), they need interpreters to communicate.
Some users need specialist equipment (loop systems/radio aids) to be able to work effectively in the work place.
Some users require advice, and don’t know who to turn to. Access to Work are meant to be there to help them out. (Though, in all honesty, many users have had a bad experience with them. I put an application in over a year ago, and it’s never been looked at… What does that say, ey?)

And… Lastly.. They want to privatise the NHS. Many of us d/Deaf/HoH users need the NHS to be able to get check ups on our hearing, for repair services, replacement services for our hearing aids/cochlear implants/bahas, and of course replacement mould impressions to stop our ears from hurting.
You used to be able to go into a walk in clinic and get all of these done within 20-30 minutes, but now you have to book an appointment (which most of the time they only offer you appointments 3-6 weeks ahead, not great in emergencies.) and even when you’re there, nothing gets done about it.
Yes, these services are free.. But they won’t be for long.
A friend of mine got a cochlear implant fitted for free, but decided after a couple of years they wished to get the other side done… Only for the NHS to turn around and say ‘You have to pay £33,000 to get the other side fitted.’ As a 20 year old University student, there is NO way they can afford that, to make a change to their lives.

I could go on forever with all the reasons why we are at greater risk, because we need these services to be available and free to us to be able to live.
Now that this government are still in power, our chances to get jobs, get money we’re rightfully entitled to to aid our everyday needs, get the right access and support through careers and medically are going to be taken away from us.
We need our voices to be heard. We may be the ‘silent’ community, but we have a loud voice.
Help us out. There’s petitions that need signing, and I’ve included a few links to back up the latest stories in the news about this.
Was hoping to plan a peaceful d/Deaf/HoH protest regarding this, but can’t do it on my own. If anyone wishes to help join me in London to get our voices heard, please do message me.

Sources:
Petition: Stop Changes to Access to Work

Access to Work cap criticised for being a “cap on the aspirations of deaf young people”


Whoever wins the election needs to stop the DWP bullying deaf employees


DWP releases document on cuts to disabled work access scheme hours after election result

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sailorstarengineer:

suasaa:

As a paraprofessional, I work with clients who can be extremely aggressive (biting, punching, charging, etc) and many suffer from PTSD, Austism, ODD etc. I do feel afraid in that moment but I am a TRAINED professional, emphasis on the TRAINED part. I don’t have a gun on me because I was taught to take down/restrain w/o one. How tf am I, a 5”2 woman working w/18-22 year old 6 foot plus men, able to take down aggressors w/o a problem but the mf police CAN’T?

Reminder to followers that police forces are often just as ableist as they are racist. In Anthony Hill’s case this was an unjust double whammy for him. Change needs to occur now.

I am a care worker and we’re trained to restrain people who are hitting/kicking/strangling you, whilst causing as little pain as humanly possible. Seriously, they drill that into you on day one. You do whole classes practicing these moves in case you have to use them. Have I used them? Absolutely, and whilst afraid, and whilst things that could be used as weapons to badly hurt me were in the mix.

I would point and laugh at the pathetic human specimens who can’t deal with an aggressor without shooting them, if the whole thing wasn’t a horrible combination of racism, ableism and police brutality that’s about as far away from funny as you can get.

iamshadow21:

latkelyclintbarton:

adreadfulidea:

roachpatrol:

princess-neville:

The way that we learn about Helen Keller in school is an absolute outrage. We read “The Miracle Worker”- the miracle worker referring to her teacher; she’s not even the title character in her own story. The narrative about disabled people that we are comfortable with follows this format- “overcoming” disability. Disabled people as children.

Helen Keller as an adult, though? She was a radical socialist, a fierce disability advocate, and a suffragette. There’s no reason she should not be considered a feminist icon, btw, and the fact that she isn’t is pure ableism- while other white feminists of that time were blatent racists, she was speaking out against Woodrew Wilson because of his vehement racism. She supported woman’s suffrage and birth control. She was an anti-war speaker. She was an initial donor to the NAACP. She spoke out about the causes of blindness- often disease caused by poverty and poor working conditions. She was so brave and outspoken that the FBI had a file on her because of all the trouble she caused.

Yet when we talk about her, it’s either the boring, inspiration porn story of her as a child and her heroic teacher, or as the punchline of ableist, misogynistic jokes. It’s not just offensive, it’s downright disgusting.

the reason the story stops once hellen keller learns to talk is no one wanted to listen to what she had to say

how’s that for a fucking punchline

It’s not that I disagree that we should all be aware of what a badass Helen Keller became, because she had a long and amazing career as an activist and yes, a feminist hero. It’s that somehow when people talk about the ableism of the way Helen’s story is told they always seem to forget this: Anne Sullivan, her teacher, was blind. Seriously. From Wikipedia:

“When she was only five years old she contracted a bacterial eye disease known as trachoma, which created painful infections and over time made her nearly blind.[2] When she was eight, her mother passed away and her father abandoned the children two years later for fear he could not raise them on his own.[2] She and her younger brother, James (“Jimmie”), were sent to an overcrowded almshouse in Tewksbury, Massachusetts (today part of Tewksbury Hospital). He, who suffered a debilitating hip ailment, died three months into their stay. She remained at the Tewksbury house for four years after his death, where she had eye operations that offered some short-term relief for her eye pain but ultimately proved ineffective.[3]“

Eventually some operations did restore part of her eyesight, but by the end of her life she was entirely blind. Also:

“Due to Anne losing her sight at such a young age she had no skills in reading, writing, or sewing and the only work she could find was as a housemaid; however, this position was unsuccessful.[2] Another blind resident staying at the Tewksbury almshouse told her of schools for the blind. During an 1880 inspection of the almshouse, she convinced an inspector to allow her to leave and enroll in the Perkins School for the Blind in Boston, where she began her studies on October 7, 1880.[2] Although her rough manners made her first years at Perkins humiliating for her, she managed to connect with a few teachers and made progress with her learning.[2] While there, she befriended and learned the manual alphabet from Laura Bridgman, a graduate of Perkins and the first blind and deaf person to be educated there.”

So Anne Sullivan, disabled and born into serious poverty, learns the manual alphabet from a deaf and blind friend; passes that alphabet on to her deaf and blind student. This isn’t the story of an abled-bodied teacher swooping in to ‘save’ a disabled child; it’s a series of disabled women helping each other. Helen Keller’s story is the story not of one badass disabled woman, but of two. Anne and Helen were lifelong friends; Anne died holding Helen’s hand.

Also is there a book called “The Miracle Worker”? I thought that was the movie/movies based on “The Story of My Life” by Helen Keller. But I could be wrong. And I didn’t learn any of this in school in general but that’s neither here nor there.

I can recommend the ‘62 version of “The Miracle Worker” with Anne Bancroft and Patty Duke. It’s blatant about Sullivan’s impoverished background and eye problems – her rage on Helen’s behalf isn’t abstract at all, it’s very, very personal. And that’s the most amazing thing about this movie: Anne and Helen are the angriest people on earth. I have no idea if that was erased from the remakes but in the original they are both allowed to have a ton of anger about what has been done to them and what they have been denied.

Anyway, I’ve rambled enough. Here’s a picture of Helen Keller meeting Charlie Chaplin:

image

omfg I am so mad right now because not only did the kids biography of Helen Keller I read when I was younger erase all her activism, but it very explicitly completely erased anything about Anne being blind herself.

There were scenes of her WATCHING Helen from across the room or yard, and it was all very “oh my, I just MUST save this poor little disabled girl, no other deaf blind person has EVER BEEN EDUCATED and basically it was awful and shitty.

I think everyone should read Helen and Teacher. It’s an absolute brick of a book, hundreds of pages, but it is wonderful. It’s about their whole lives, right up to Helen’s death in old age. It talks about Helen’s feminism, socialism, and campaigning for everything from equal rights to sexual health. Helen Keller was not a syrupy, greeting card girl who existed to make able people feel warm and fuzzy, she was a tireless academic, political activist and writer. She was making noise about the issues she cared about from the moment her partnership with Annie Sullivan began, and she never stopped.

seasidehare:

disabledtalk:

(TW: Ableism, Medical Abuse, Neglect, ED (Weight), Ableist Language)

 

Three years ago, a 6-year-old Seattle girl called Ashley, who had severe disabilities, was, at her parents’ request, given a medical treatment called “growth attenuation” to prevent her growing. She had her uterus removed, had surgery on her breasts so they would not develop and was given hormone treatment. She is now known by the nickname her parents gave her — Pillow Angel.

The case of Ashley hit the media in January after publication of an article in a medical journal about her treatment. It reappeared in the news recently because of the admission by Children’s Hospital and Regional Medical Center that the procedures its doctors had performed to stop Ashley from growing and reaching sexual maturity violated state law. In Canada (as in Australia), a child can be sterilized only with the consent of a court.

At the time of the initial publicity about growth attenuation, Ashley’s parents wrote on their blog: “In our opinion only parents of special needs children are in a position to fully relate to this topic. Unless you are living the experience, you are speculating and you have no clue what it is like to be the bedridden child or their caregivers.”

I did live the experience. I lived it not as a parent or caregiver but as a bed-ridden growth-attenuated child. My life story is the reverse of Ashley’s.

Read More

Important.

(Inspired by this and the various responses to it.)

Things Ricky Gervais has done:

-Called a disabled woman a ‘freak’ (and more) to her face

-Written many, many jokes and shows where the punchline is ‘disabled people are fucking hilarious’ (seriously, it’s basically his thing)

-Enthusiastically used the word ‘mong’ on Twitter as an insult; would not stop

-Been generally an arrogant, cruel, ableist douchefuck

Things Ricky Gervais has not done:

-Contributed anything at all to actual science

the end.

PSA for the Able-Bodied

iamateenagefeminist:

My mother uses a scooter to get around, she has multiple sclerosis (MS) and cannot walk. She also has very limited hand coordination and fine motor skills. She needs a lot of help to do basic things.

My mother cannot use the bathroom in a normal sized stall.
My mother needs space on each side of our van to get into her scooter.
My mother needs to use an elevator to get between floors.

When an able-bodied person uses the handicap stall, parks in the handicap spot, or uses the elevator reserved for handicapped people they are lowering my mother’s quality of life.

Those services are there so people like my mom can enjoy the same quality of life that you and I enjoy. They are not there for able-bodied people to use. Please stop using them.

I can’t tell you the amount of times we have skipped on a restaurant because able-bodied people were taking up the handicapped parking spots, or the number of times my mother has been unable to use the bathroom because able-bodied people are taking the stall she needs (and for many who are not able-bodied, having to use the bathroom means having to go right that second).

It is ableist to use resources for handicapped people when you are able bodied.

My mother too has many stories like this. :(

The worst ones are when non-disabled people park in the disabled spaces. (Often happens in Milton Keynes for some reason). I’ve come so close to kicking cars before.