Transcribe Your Classes!
Please note that spots are filling up quickly for the Liberated Learning Youth Initiative starting this fall. The Youth Initiative provides students with disabilities access to a new Speech Recognition transcription system. During the project, students will be given special user accounts where they will be able to upload recorded lectures and receive speech recognition generated, multimedia transcripts.
Brief application forms are posted at Transcribe Your Class.
We encourage you to review the participation criteria on the website, share this message, and apply to participate. For further information, please contact:
Keith Bain, Project Director, Liberated Learning, Saint Mary’s University
Janice Stevens, Project Coordinator, Liberated Learning, Saint Mary’s University
Overarching Moderatrix Trigger Warning for Strong Language. And by “Strong Language” I mean that I swear a lot.
I pretty much knew that my life was going to get fucked up when my doctor had a Permanent Change of Station (PCS). I knew this, because according to the laws of karma to which I tend to adhere, shit was just going too perfectly for it to continue going my way.
Sometimes, gentle readers, I really just don’t like being right. Sometimes I do prefer to be wrong once in a while.
I would have liked to have been wrong when I had my appointment with Dr. Maybe. I have to see an Internal Medicine Specialist because they are the closest thing we have here to someone who can specialize in treating my condition. They are who I have to rely on to be my quarterback. When I called to make the appointment and explained that I knew that my regular doctor was PCS-ing and I would need to see whomever was replacing her, I was told that this doctor would have to do because he was not yet available. Fair enough. I made the appointment.
According to my pills (I have to count them) I would have just enough to make it that far. I can not run out. Let me repeat that. I CAN NOT RUN OUT. My quality of life bottoms out if I miss even one dose. I know this because sometimes I forget if I have taken my regular dosage or not, and I can’t take one “just in case” because “doubling up” would be worse than missing one. I know within a few hours if I have indeed missed that dose, because life begins to suck some major shit, and the fetal position begins to feel like too much effort.
I made the appointment.
Dr. Maybe greeted me. Told me within five minutes, and without really talking to me during that five minutes, or without really examining me, that I needed to lose weight and watch what I eat. Exercise and a diet change would help that, and that it would make the pain go away.
Just like that! The magical cure! The Bingo Card free space! Dr. Maybe has no idea what my diet at home is like (we make almost everything fresh, because we are very privileged to have a really great commissary and a local Korean market with fresh produce). He has no idea what my exercise routine is like, how much walking I have incorporated into my daily routine, how it makes me pass out from exhaustion at 1930 most nights and how it makes me weep with pain. How I try to swim once or twice a week, even though the Physical Medicine doctor and the Chinese Medicine specialist that I have consulted with both said I need to back off because it is causing more pain. Also, had he read my file, he would see that this condition began when I was active duty Navy, and in the best condition of my life, best shape of my life, and at the height of physical fitness, outperforming women two age brackets below me on Physical Readiness Tests just out of boot camp. It started when I was running seven miles a day on what I was told were just shin splints but were really stress fractures. It started when I had “Seeing Jesus” on a pain scale migraines that five days in the hospital couldn’t solve, but my commander insisted that I be out running again two days after surviving.
So, I’m gonna go with, no. The weight loss will not magically take the pain away, and my diet is just fine. What he can get me is a nice re-hashing of an old eating disorder battle, some nice body dismorphia, and a scorching case of shattered self-esteem. Not to mention no chance whatsoever that I will ever make an appointment with him again. Ever. Dr. Maybe is definitely a Dr. Won’t.
The pain was there before the weight. If diet and exercise is your answer, you are solving the wrong problem, doc. Fuck you very much.
I did receive a nice letter in the mail today from Medical. The Deputy Director of Clinical Services would like me to know that she has reviewed my file and decided, that for my own safety, she noticed that I have been receiving too many controlled substances from too many different providers over the last few months. As a result, I must now get all of my prescriptions written by Dr. Pre-Approved, and if she is not available (and since she is pregnant, as I found out, this might be a problem soon), I can petition to have Dr. Also Pre-Approved write them and have it approved on a case-by-case basis. These doctors are presumed to be not my primary care managers, and my PCM must get all of my scripts approved through one of them (in that order) before I can have any scripts. Ever.
Now, it already takes me almost 30 days to make any appointment with a doctor I see regularly, and this new rule is basically forcing me to somehow fit another appointment into my schedule, balancing the 30-day schedule. I am only allowed two of my meds in 30-day allotments due to hospital policy even though TRICARE approves them for 90-days at a time. Fun. Scheduling is tight. The schedule doesn’t allow appointments to be booked more than 28 days out, and most providers are booked 30 days out already. I am already having to call daily to find out if I can even schedule appointments at all.
Also, over the last two years — repeat for fucking emphasis — TWO YEARS NOW the same doctor has treated me and written all of my scripts. I have not had any prescriptions written by any other doctor during the time I have been here in Korea with the exception of the time I sprained my ankle and was seen in the emergency room. Now, my doctor PCS-es and four days later this letter is drafted now that she is no longer here to advocate for me? Raise your hands if anyone else finds that odd or convenient.
I go immediately to the hospital’s Patient Advocate, who is supposed to liase between patients and medical staff. I explain all of the above about as calmly as I can and I am somewhere between barely controlled panic and simmering rage, with my partner filling in what he can. I ask to see what from what information they have based this claim. She asks me about two referrals I’ve had in the last two weeks, both made by my departing doctor (the referrals are all signed by her). Neither one of them gave me controlled substances, and I sought out their care to avoid increasing my narcotic usage specifically to avoid any impression of drug seeking, even though my use of controlled substances is very low, lower than even my departing doctor was recommending. I even try to ignore pain to avoid taking extra meds, which we know doesn’t work for chronic pain, but I live in a fairly scared state. The military deploys doctors often, and it is hard to make the switch easily for chronic pain patients. I have to walk a careful line. I wouldn’t even let the Physical Medicine doctor, who ordered my TENS unit (at my urging) and tried acupuncture, refill my pain meds because I didn’t want this exact thing to happen.
I demanded to speak with the Deputy Director who made this call. To confront her directly. I am told that she makes these calls to protect patients like myself from becoming addicts. I point out that first meeting with a patient and reviewing cases — speaking to humans — could avoid the harm such a thing as this situation is causing. Throwing a targeted policy at a person you don’t know could potentially harm a patient and is adverse to good patient care, and violates my rights as a patient. In my case, I was already doing, in theory, what is being asked of me. I simply want the chance to choose the doctor for myself and to have the doctor who treats me be the same doctor who prescribes my meds. Dr. Also Pre-Approved was the next doctor recommended to me, by my departing doctor, to try. He was the doctor briefed on my particular case. This should be my choice to make, irrespective of what list he falls on. Some arbitrary person who knows nothing about my case is not better suited to choose this than I am.
I demanded to have this letter removed from my file. While the PA insists that the language is ambiguous and doesn’t call me a drug seeker, I adamantly insist to her and point out all the ways that it in fact does, and explain why this will make my life more difficult. Why it places more burden on me. Why it creates more hours in the Second Shift for the Sick. How it has already created mistrust between patient and doctor for me, leaving me in severe amounts of “super legit” pain for hours while a Chief Corpsman (HMC) read through my record, one page at a time, to make sure I wasn’t seeking drugs before coming to the novel conclusion that I was a chronic pain patient in — wait for it — chronic fucking pain.
It is little things like this, little notes printed off by someone who has never met a patient, signed by someone too important to give a damn and too busy to be arsed to make time for people skills, that make life nigh impossible for PWD every day. We are not trusted with our own care. We are told how things are going to be, who is going to provide it, and how often it is going to happen. We are sideswiped with half-truth information, and always, ALWAYS thought the worst of.
We are vulnerable.
I guess this is why they have to crush us with these ableist policies.
They are, after all, for our own good, right?
Warning: Offsite links are not safe spaces. Articles and comments in the links may contain ableist, sexist, and other -ist language and ideas of varying intensity. Opinions expressed in the articles may not reflect the opinions held by the compiler of the post and links are provided as topics of interest and exploration only. I attempt to provide extra warnings for material like extreme violence/rape; however, your triggers/issues may vary, so please read with care.
Can you believe it already the end of September?
The Vibrating Square: Respect (Sent in by The Untoward Lady)
But it’s not about intent. It’s not even about the very real impact that such language has on people like me. It’s not even about the fact that what you said is hurtful.
Brilliant Mind Broken Body: After the Separation (Glad you are well again and home, Kali)
But I went through 2 1/2 days of my service dog not wanting to have anything to do with me, and that was their fault for separating us. I went through more pain at the hospital, I was alone, and I had to deal with days of my service dog ignoring me. If it weren’t for them, all I would have had to deal with last week was a nasty stomach virus.
Jessica says Continental offered her a couple of coupons to make good — one for 10 percent off of a flight and another for a free drink. She says she’ll need to give them to a friend because she’s given up on flying for the time being.
The perfect last day of a California summer drew a collection of advocates, supporters and community representatives to the Stockton Rural Cemetery. The gathering honored hundreds of people who had died anonymously while residing in the Stockton State Hospital, established in 1851 as the state’s first “asylum” and closed in 1996.
World-famous singer-songwriter and UN Messenger for Peace Stevie Wonder called on the international community to take action to enhance accessibility for all those with physical disabilities. Speaking at the opening of the annual meetings of World Intellectual Property Organization (WIPO) Assemblies on September 20, 2010, he challenged delegates to conclude an agreement on improved accessibility to copyright protected works by visually impaired persons (VIPs) within a year.
I hope all is well in your world on this fine Tuesday! Gentle reader, be cautioned: comments sections on mainstream media sites tend to not be safe and we here at FWD/Forward don’t necessarily endorse all the opinions in these pieces. Let’s jump right in, shall we?
Canada: Disabled-services flip-flop at Winnipeg Free Press:
The about-face came one day after an internal U of W memo was leaked to media and revealed a number of university programs to help disabled students were on the chopping block. The decision outraged students and raised eyebrows since it comes just weeks after the U of W launched a new disability degree program devoted to the “critical analysis of disability in society.”
USA: College Web Pages Are ‘Widely Inaccessible’ to People With Disabilities from the Chronicle of Higher Education:
The study found that more colleges are deploying basic accessibility features, like adding alternative text to images so a blind student can understand them with read-aloud software.
But those gains were offset by challenges from inaccessible emerging technologies. For example, a person with disabilities who can’t use a mouse will often be stymied by a Web site that requires users to hover their mouse over a page element to trigger a sub-menu.
Australia: Disabled drivers get no favours on private property from the Brisbane Times:
The Department of Transport, which issues disabled parking permits under its Disability Parking Permit Scheme, is powerless to protect drivers who park in shopping centres, with centre management charged with enforcing the scheme there.
India: Promote sign language, urges deaf association from expressbuzz.com:
More than 100 members of the Deaf Enabled Foundation, an NGO for the deaf, took out a rally on International Day of the Deaf, here on Sunday, from the Labour Statue to Light House.
And, also from India, framed in possibly the most patronising way possible, Movie made by deaf and dumb to premiere on Oct 9 from the Indian Express:
The movie Amir=Garib, to be premiered on October 9 in the Town Hall Auditorium, has all the essentials of a Bollywood flick, but one fundamental element — sound. The movie has been made by deaf and dumb people.
Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.
This edition, like the transportation edition earlier this month, was Anna’s idea!
Gentle reader, be cautioned: comments sections on mainstream media sites tend to not be safe and we here at FWD/Forward don’t necessarily endorse all the opinions in these pieces. Let’s jump right in, shall we?
Disability News Asia: Tata Motors buses for Commonwealth Games in India will be disabled-friendly:
Tata Motors will deliver disabled-friendly vehicles to the Delhi Government for the Commonwealth Games this year.
“We have an extra order to make 400 buses for the Delhi Transport Corporation to be used during the Games, of which some will be disabled-friendly,” Mr Ravi Pisharody, President, Commercial Vehicles, Tata Motors told Business Line.
flightmapping.com: EasyJet face French probe over disability policy:
France’s Transport Minister, Dominique Bussereau, has asked the French civil aviation authority, DGAC, to investigate allegations that easyJet would not allow disabled passengers to fly without a travel companion.
OC Transpo unveiled on Friday its new announcement system that will give riders both visual and audio alerts about upcoming stops.
The $12 million system will include an interior display showing the bus route number and each upcoming stop.
Leah Jane at The Quixotic Autistic: Travelling while Autistic:
I want to note something about travelling while autistic, especially across international borders. It is not easy. These days, flying is difficult enough for neurotypical travellers, but for those of us who are disabled, it takes on a whole new level of struggle, humiliation, and anxiety. My own experience is negligible, but others go through sheer terror in their effort to get from point A to point B.
Harriet Baskas at USA Today: Travelers with disabilities face obstacles at airports (really? really?):
[…]next month the Open Doors Organization (ODO) and the International Air Transport Association (IATA) will host a conference about universal access in airports. On the agenda: tools, technology and training to help both airports and airlines do a better job of serving travelers with disabilities.
Lastly, a quote from Mhairi McGhee of the Haringey Disability First Consortium:
In a city like London, if you can’t get about easily, safely and cheaply, then no matter how many hearing loops, braille leaflets or ramps there are, you do not have real access to services.
That’s from Disabled ‘can’t use’ half of all bus stops in the Hornsey and Crouch End Journal, or, should I say, the ‘Hornsey’ and Crouch ‘End’ Journal.
Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.
[Content Note: Not all of the links I have included in this piece have comments, but many of them do, and those comments are basically full of “Stupid disabled people wasting everyone’s time and energy by wanting the world to treat them like human beings” comments.]
If you’ve been following Canadian politics this week, you could very easily come away with the impression that the most significant – or perhaps even the only – thing going on with this week’s opening of the Federal Parliament was the Gun Registry Vote.
That there’s a federal court Charter challenge brought forth by Donna Jodhan arguing that blind Canadians are being discriminated against by the Federal Government for refusing to make their website content accessible to screen readers is not really getting a lot of attention. (Cripples these days! It’s like they don’t sell papers/make page views.)
A little bit of background information first. Canada has a Charter of Rights and Freedoms, which went into effect in 1982 and is the Thing against which laws and the like must be “tested” in order to be considered actually legal in Canada. To give some lovely controversial rulings, the reason Canada has no abortion law is because it was found to violate the Charter’s guarantee to security of the person (and no law has since been passed) and it was found that refusing to include “homosexuals” in protections against discrimination violated Section 15, or the right to Equal Protection Before the Law, even though sexual orientation wasn’t included in Section 15.
Section 15 is the important one here:
15. (1) Every individual is equal before and under the law and has the right to the equal protection and equal benefit of the law without discrimination and, in particular, without discrimination based on race, national or ethnic origin, colour, religion, sex, age or mental or physical disability.
(2) Subsection (1) does not preclude any law, program or activity that has as its object the amelioration of conditions of disadvantaged individuals or groups including those that are disadvantaged because of race, national or ethnic origin, colour, religion, sex, age or mental or physical disability.
Now, I Am Not A Lawyer, and it’s been about 10 years since I studied the Charter, so I’m going to leave that out there and not discuss my personal interpretations because they don’t matter. What matters is two things: 1) What the court says and 2) That the Federal Government is arguing that they shouldn’t have to be accessible to screen readers in court.
The latter is, of course, being read as Jodhan wasting tax payers money in a frivolous lawsuit, not the Federal Government for refusing to have accessible content.
From what I can tell, this is what’s going on: In 2004, Jodhan attempted to apply for government jobs online. However, the site wasn’t set up to allow screen-readers to access the site, so she was unable to do so. In 2006, she attempted to fill her Census out online, and again, the federal government website was not accessible to her screen reader.
On Tuesday [September 21], Jodhan will argue in federal court that her inability to apply for a position on the federal jobs website or complete the online version of the 2006 Census breached her equality rights under the Canadian Charter of Rights and Freedoms.
She will also argue that this violation and her ongoing inability to access the government’s online information and services constitute a breach against all blind and partially sighted Canadians, said Jodhan’s lawyer David Baker.
About 3 million Canadians have visual or other impairments that make it difficult to access the Internet.
The Federal Government is, in turn, is responding with “What, you think you should have a right to access the same information that everyone else can? Ha ha! Ha ha!”:
Internet access to government services and information is not a right guaranteed in law, the government says in its written submission to the court.
“Alternative channels available did allow (Jodhan) to access services and information independently, in a manner that respected her privacy and dignity,” it says.
With more than 120 government departments and agencies and more than 23 million web pages, “it is unlikely that the government’s web presence will ever be perfectly accessible to all,” it adds.
Frankly, if the Federal Government doesn’t think that their websites provide information in a timely fashion, and that access to that information isn’t something that they should prioritize, why are they bothering with them in the first place? And if they do think it’s important, why are they in essence arguing that “It’s important for most people, but not for the three million Canadians who won’t be able to access it?”
I support Donna Jodhan’s fight for equality of access to information for all Canadians. I hope you do, too. If so, I strongly encourage you to email your Member of Parliament and let them know. Perhaps if enough of us contact the government and let them know we value accessibility for Canadians with disabilities, they’ll start acting like we shouldn’t have to go to court just to get it.
This is the email I sent to my MP, who happens to be Megan Leslie, and cc:ed to the leader of the NDP. Please feel free to adapt it to send to your own MP. (This should give you their email address.)
I recently learned of Donna Jodhan’s Federal Court case, arguing that the Canadian Government must provide screen-reader accessible content on their websites, as reported in the Toronto Star (http://www.thestar.com/news/gta/article/863379–blind-woman-says-federal-websites-discriminate-against-the-visually-impaired) and the CBC (http://www.cbc.ca/technology/story/2010/09/18/to-blind-accessible-feds.html) In light both Section 15 of the Charter of Rights and Freedoms, and Canada’s recent signing of the Declaration of Rights of Disabled Persons, I’m appalled that the Federal Government would waste tax payers’ dollars in arguing that 3 million Canadians should not have the ability to access government services online or apply for government jobs online.
In this day and age, it’s ridiculous for the government to argue that access to the internet is not necessary. According to the Toronto Star, government lawyers are arguing “Internet access to government services and information is not a right guaranteed in law”. While I agree that this is technically true, in refusing to provide this access, the government is arguing that blind and visually impaired Canadians should have less access to government services and information than Canadians who are sighted.
Megan, every day it is clearer to me how many societal barriers are put in place that prevent people with disabilities in Canada from full participation. The time and energy the federal government is frivolously spending in defending their lack of web accessibility could be far better put to use in bringing the government’s websites up to the same standards as those in other countries, standards that are reasonable to expect in the 21st Century.
This is such an important issue, and I hope that the NDP will work to bring awareness of it to Canadians, and encourage the federal government to stop fighting against people with disabilities, but fighting for them.
cc: Jack Layton
Last week, Mathsnerd attempted to sign up for a new GoogleMail (know as Gmail elsewhere) account. I say attempted because this did not go well. At all.
Oh, wait, what’s that, Google? After trying more than three names, I have to go through CAPTCHA to prove I’m a real person? Okay, that’s kind of soon, but whatever. Gee, you sure scrunch those letters together and make them all wavy so that I have a real hard time figuring out what the hell you want me to enter…
Huh, okay, I’ve tried eight times, Google, and I can’t seem to read it well enough that you’re satisfied that I’m a real person. And while you offer a “read-aloud” accessibility option for the CAPTCHA down below for submitting the form (which, incidentally, doesn’t work in Chrome, yeah, you know, YOUR BROWSER!), for the CAPTCHA to keep trying different handles you conveniently don’t offer any alternate options.
Captcha is a sort of Challenge that a user must pass when a program thinks that the user might be a spambot instead of a person. Wikipedia’s article looks useful if you want to learn more about it. It’s certainly not the only Challenge software out there, but it is one that is widely used, especially by Google-related products, such as their web-based email and their blogging software, Blogger. In fact, Google likes Captcha so much they bought the company in 2009, making Google responsible for implementing their accessibility policy.
Some Captchas, including the ones used by Google, have an audio option. I’ve occasionally tried to use the audio Captchas, which are a series of numbers read outloud with a large amount of background noise, designed, I assume, to keep an automated system from being able to distinguish the Challenge. I’m an experienced audio typist, so while I found this irritating, I could cut through it. Earlier this year, Blind Bargains did a study and found that 73% of blind users were unable to succeed at the Captcha Challenge – and blind users, according to Google and Captcha, are exactly who the audio function is designed for. [1. Thank you to Codeman38 for bringing this study to my attention.]
Google has an Accessibility Feedback Form. In order to use it, you must have a Google Account. Depending on any number of factors, your attempt to get a Google Account to discuss their accessibility problem with Captcha could require you to pass a Captcha Challenge in order to prove you are an actual person.
Actually, let me highlight that: In order to tell Google about their problems with accessibility, you need to be able to pass through the inaccessible Challenge.
Those of you who already have Gmail or GoogleMail accounts, you can contact Google to raise your concerns at their Accessibility Feedback Form. The Feedback form has a lot of fields to fill out. I just filled out the one that I felt was most applicable, and it went through without requiring me to put in any more information.
Here is a template you can use. Please feel free to use, edit, or adapt this for your own purposes.:
I was very distressed to learn that Blind users and users with other disabilities were having difficulties in signing up for Gmail accounts through the Captcha challenge. One user has detailed her experiences here: http://accessibility-fail.dreamwidth.org/33494.html , and as well, Blind Bargains reports 73% of their users had difficulties with using the audio version of Captcha: http://www.blindbargains.com/bargains.php?m=5383
I know that Google wants to be a more accessible service for users around the world. I hope that the accessibility people at Google will have the opportunity to look into these complaints and work with various people with disabilities in order to solve these problems.
Thank you for your time.
This is an issue that cuts to the heart of the problems with inaccessible web content. Obviously there are thousands – maybe millions – of blind or otherwise visually impaired users of the internet, but in this increasingly-flashy internet age, where not only information but job applications are going increasingly online, web accessibility is a huge barrier to people’s participation in society. Google, as we all know, is a huge multi-national company with the ability to make an incredible difference by working with users with disabilities in order to make the web more accessible to us. By contacting Google, you will be adding your voice to the chorus asking for greater web accessibility.
Gentle reader, be cautioned: comments sections on mainstream media sites tend to not be safe and we here at FWD/Forward don’t necessarily endorse all the opinions in these pieces. Let’s jump right in, shall we?
From BBC’s Ouch, by Charlie Swinbourne, Deaf country life v deaf city life:
I’m soon to become a Dad for the second time, so we’ve started thinking about the long term, and where we want our children to grow up. With houses on the pricey side for anything bigger than a shed in our area of West London, we’re currently wondering whether we’d be better off bringing up a family outside the city. […] The capital is full of opportunities for deaf people, with weekly deaf pub meets, regular events, accessible cinema and theatre performances, and numerous deaf centres and sports clubs.
Badgermama presents Kids and wheelchair manners:
Please stop yelling at your kids just because they’re 20 feet away from a wheelchair! Nothing bad is going to happen. It really pisses me off when someone grabs their kid, yanks them “out of the way” and yells at them, just because I’m in the same grocery aisle or on the same sidewalk. Usually, the kids are nowhere near me. All these people are doing is teaching their children that people in wheelchairs are scary and weird.
Some good news from ysobel of i hear the voices when I’m dreaming in *sags in relief*:
So, there’s been this whole saga with trying to get a ramp to the front entrance of our church, made vastly overcomplicated by the fact that the church is a designated historical site blah blah blah. […] The church appealed to the city council, who had it on the agenda for tonight, after several postponements on their part.
Leah at Cromulent Words writes You Can’t See My Pain:
You don’t see me not talking about disability in class because I’m fraid of being silenced again. You see someone who doesn’t care about the assignment.
At random babble…, our own OYD writes Medical Autonomy Chronicles: The Virgin Pap Smear (do be warned, it’s graphic):
For all the talk of how having sex outside of marriage or whatever message had been pounded on me for however long, and how it would leave me hollow and leave me feeling worthless and damaged, and for all the ways I had been told that casual sex would leave me reeling and feeling depressed and with a hole of missing self-esteem, nothing I did in my consensual sex life has ever compared to the way that pelvic exam and pap smear felt to me, a fourteen year old girl. A person rising on the crest of womanhood, not yet there but ready to fly, and having had myself violated before I took my first steps.
Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.
Jesse the K hopes you can take a disabled feminist to tea this month. Her previous guest post was 20 Years and a Day for the Americans with Disabilities Act.
These guidelines come out of my experience working on WisCon, a 1000-person annual convention in a recently remodeled hotel.
There are many elements to making your event wheelchair-accessible. While U.S. law requires minimal wheelchair access, never rely on a venue’s general assertion of “oh yes, we’re accessible.” Those little wheelchair stickers? Anyone can buy them and post them at will, even at the bottom of a flight of steps.
There’s an entire shelf of 2-in (5,08 cm) thick books on this topic; so consider this the Twitter version. Links to helpful resources appear on June Isaacson Kaile’s site.
David Hingsburger is a long-time disability rights activist who’s begun using a wheelchair in the last few years. His essay “12 Steps? Me, I’d Rather Sit” captures the frustration of a last-minute change from an inaccessible venue to one that worked for him:
…These things are difficult because while I appreciate everyone’s understanding, I didn’t want it. While I was thankful for the extra effort made to find a room immediately, I didn’t want it. What I wanted was simple. Accessibility.
Accessibility doesn’t just mean I get easily into a building. Accessibility means anonymity. It reduces the need for compassion, understanding, special consideration, to Nil. It allows me to slip in unnoticed and set up quietly. This doesn’t mean it masks my disability, it just makes it mean something very different.…
Verify & report
Do an on-site survey with someone who’s truly familiar with the needs of wheelchair and scooter users. (Not all wheelchair users automatically have this knowledge, just as not all walking people know everything about sidewalk construction. Some non-wheelchair users also have these skills.)
Check for level paths to every area. A single, unramped step is as significant a blockade as two flights of stairs. Wheelchairs need at the very least 36″ (1 m) for corridors and 60″ (1,5 m) to turn around.
Describe any non-conforming areas in your publicity and program: forewarned is forearmed, and it demonstrates that you’ve actually checked the place out. Don’t use the term “wheelchair-friendly,” which has no defined meaning. Do reference any standards the venue meets: “ADA compliant” in WisCon’s case.
Make sure that stages are ramped as well. (Our venue can only ramp one stage at a time. This requires members to self-ID at reg, and program coordination to place ensure the ramped stage and the wheelchair using panelists are in the same room. I know from experience it’s easy to blow this one.)
Wheelchair Parking aka Blue Zones
Providing designated wheelchair parking in all seating areas permits wheelchair users the same freedom to come and go as those using the seats. Well-meaning non-disabled people will often say, “oh, but of course I’ll move a chair out of the way if you just ask.” And from their viewpoint, that’s a one-to-one personal issue. But from perspective of us wheelchair users, it’s a one-to-many problem, since we must ask for seating rearrangement every where we go.
While leaving empty spaces seems like a solution, chairs inevitably migrate further apart, filling them in. The inexpensive and highly effective alternative are “blue zones,” 36 in (1 m) squares outlined with 1in (2,54 mm) blue painters’ tape. It’s bright, stays down on carpet and comes up easily.
If you know how many wheelchair users are in attendance, be sure you make that many blue zones at the big get-togethers. (Otherwise, 1 for every 100 is a rough guideline.) Always have at least one blue zone, especially in the smallest program rooms (where crowding is most an issue). When you have room for two, put one up front and one in the back. The former is great for the wheelchair user who may also have hearing or vision impairment; the latter works well for those of us who get claustrophobic and need to be able to leave right away.
Today’s Recommended Reading focuses on how to make event-sites more accessible to people with disabilities, and experiences people with disabilities have had with accessibility at events and in their communities.
Accessibility Discussions: How To
This list is no where near comprehensive (I went a hunting for a few specific ones I know I’ve read and couldn’t find), so please feel free to leave more links in the comments!
Are you looking for ways to outreach to more people? Are you trying to get people involved? Are you trying to keep them involved? How a document reads and looks affects whether people can understand the information being shared. This is a checklist for document accessibility. It also includes some tips to think about when making programs or services accessible to all people.
Glenda Watson Hyatt at Do It Myself: A Checklist for Planning an Accessible Event
Whether planning a meeting, workshop or multi-day conference, your goal, no doubt, is to assist all participants, including those with disabilities, to feel welcomed and able to fully participate in the event
This checklist is intended as a starting point in planning an accessible event, which likely requires more than ramps and wheelchair washrooms. The key is to consider every aspect of the event and what barriers a person with a disability – whether it be physical, mobility, hearing, sight, or cognitive – might face, and how you can eliminate or minimize those barriers to ensure all participants feel welcomed.
Access Fandom Wiki is a tool to help make Science Fiction conventions and conferences more accessible to people with disabilities. Within you will find specific instructions and resources for carrying out these aims.
When you are planning a meeting or event, you want to make sure that everyone can participate, including people with disabilities. By planning ahead, you can build accessibility into every aspect of the meeting.
The two main areas you need to consider when planning an accessible meeting or event are:
- physical access to the meeting space
- access to the meeting contents and proceedings.
Here are some general things to keep in mind.
Disability Access @ Stanford – Planning an Accessible Event (One of the things I like about this one is the “questions you should be able to answer” section, because I’m amazed at how many people cannot tell me where their barrier-free entrance is, even when they have one.)
Q: How do I get from [point A] to [point B]?
Familiarize yourself with stair-free pathways in the vicinity of the event (e.g., parking lot to main entrance) and to notable locations…
Q: Where is the nearest wheelchair accessible bathroom?
Know ahead of time where the accessible bathroom is, and how to get to it from your event location.
Accessibility Discussions: Experiences Of
alias_sqbr: Using a Mobility Scooter at WorldCon
Walking is easy on the brain and hard on the legs. Using the scooter is the reverse, the level of concentration required is somewhere between walking and driving, and by the time I got back to the hotel after my first excursion I needed a mental break and did the rest of my (much less taxing) exploration on foot. It got easier with practice, and was also much less taxing indoors in a familiar space without the worry of cars etc. The convention centre was perfect, lots of big empty flat carpeted areas. I got up now and then when it was more convenient but still ended up doing MUCH less walking than normal and as a result was much less tired and in pain than I would otherwise have been, and got to enjoy a lot more of the con as well as being able to go out to dinner etc. One issue was that all that sitting gave me a sore bum/lower back/legs, and I became quite uncomfortable on the plane trip back. I’ve been doing a lot of half lying with my legs out since getting home and am fine now. My brain is also less fatigued, once I got used to the scooter the general lack of fatigue made me more mentally awake than I usually am at the end of a con.
“But I thought everywhere was accessible now.”
How I loathe that sentence. It usually follows my asking “so why did you hire somewhere inaccessible for your event? Because now I can’t come.”
For example, I’ve just spent the last 3 days at a film festival/conference tied to my course… I arrived on Thursday, picked up my ticket and was told by cinema staff “it’s in screen 2, which is not accessible.”
And, of course, the “but I thought…” line swiftly followed from the director of the event who’d hired the venue.
Ira Socol at SpeEd ChangeTo be fully human
I move through a lot of schools, and through a lot of public spaces, and everywhere I go I see people who are made to be less than fully human. The high school kids who can not read sitting in classrooms during “silent reading” time. The girl in the wheelchair set off to the side of the middle school choir because everyone else is on risers. The poor reader at the bank or hospital faced with piles of incomprehensible paperwork. The man or woman denied the ability to go out to eat because of too few or badly placed “handicapped” parking places. The child who struggles with writing who is denied the right to communicate in his classroom. The university students forced to spend large amounts of money and time to “prove themselves” “disabled.”
Codeman38 at Normal is Overrated: Of Privilege and Auditory Processing
The Normal Auditory Processing Privilege Checklist
- I can watch first-run movies in any theater and still understand a majority of the dialogue without having to attend a specially scheduled screening with subtitles.
- I can understand messages broadcast over PA systems without a lot of difficulty.
- Lectures are just as easy for me to comprehend without visual feedback such as PowerPoint as they are with visual feedback.
Heather Farley at Oh Wheely… Blogging Against Disablism Day
These people have no idea of the impact they have on my sense of worth. And they don’t care. That shrug of ‘it’s not my problem, it’s yours’ means that I am excluded from that part of life. I’m apparently not worth their effort. On the flip side I have to say that for every person who shrugs there are another five people offering help, opening doors, and keeping my faith in humanity alive. Unfortunately it’s the ‘shruggers’ who stick in my psyche.
For every little battle I fight there are ten more that I have to let pass by. There just aren’t enough hours in the day to argue the toss every time. And every time I do I become less important in my eyes, less worthy of my effort, less deserving of theirs.
If you’re on Delicious, feel free to tag entries ‘disfem’ or ‘disfeminists,’ or ‘for:feminists’ to bring them to our attention! Link recommendations can also be emailed to recreading at disabledfeminists dot com. Please note if you would like to be credited, and under what name/site.