Category Archives: recommended reading

Recommended Reading for Wednesday, September 8, 2010

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

Today’s Recommended Reading is focusing on Service Animals!

Sharon @ After Gadget has been putting up videos of Service Animal Training. All the videos have transcripts at the source.

Level 2 Test Videos Part 1

Here’s our handling test. Test requires handling all paws, ears, and tail, without the dog fussing. On day one, I did it with him standing (because he was hyper), but that’s not typically how I do handling. I feel like he did pass it — he let my dad pick him up (twice!) so he could hold him to weigh him. I thought that was pretty good for someone he’s only met about three or four times. (For the record, Barnum weighed 64 pounds.)

Level 2 Tests Part 2

This is the first part of our L2 Crate test — the crate in my bedroom. The criterion for Level Two crate is that the dog enters the crate with no more than two cues, allows the door to be opened and shut, with no pawing or vocalizing. This is the crate we use the most. We had a false start, but I decided to consider it a fluke, because we use this behavior all the time.

Service Animal Discrimination: It’s more common than you think

Via Patient C’s: DC Cabs – No Rides for Service Animals, Change.Org has People with Service Dogs Can’t Catch a Cab in DC: (There’s an Action Item at the link)

ERC sent testers throughout the city in pairs: one blind person with a service dog and one person without. The people were “matched” according to race and age; the only difference was the dog. The person with the service dog was positioned so the cab would see them first, but a full 50 percent of the time, the driver ignored them in favor of picking up the person without the canine companion. Check out the video below — you can see several drivers pulling up the blind person, slowing down and then passing them by. In another 10 percent of the cases, the drivers added illegal surcharges for the dog.

Charles Crawford, an ERC member with a service dog, said being denied a cab is not only annoying, it’s “both hurtful and an insult to those of us who must rely upon the loving assistance of our dogs to travel independently.”

Speaker’s Corner: Shocker: DC Taxis Don’t Like To Pick Up Blind People With Guide Dogs

And one of the saddest parts of this entire thing is that the system in place for reporting problems with a taxi driver is to write down the taxi number and then call the taxi operator. Blind people can’t participate in such a system.

Brilliant Mind, Broken Body: Travel Fail

The driver said, “You didn’t mention the dog when you called dispatch. You have to mention the dog.” I told him that I didn’t have to, because legally they had to transport service dogs. He repeated himself. Then he said he wasn’t the cab who was sent for me; they would be along in a few minutes. He got into his cab and drove off.

I’m sure all of you out there in cyberland have seen through what he said. Of course he was the cab sent for me! I live on a little tiny residential street. Cabs are rare here, and I end up calling them more often than anyone else on the street, because I have the most need of outside transportation.

In the news:

More airports create areas for pets to take care of business (via The Disability Law & Policy e-Newsletter)

Dogs need to go, too. So airports are adding doggie restrooms.

Airports say “pet relief areas” enhance customer service. But they’re also being nudged by a federal rule that orders airlines to work with airports to install facilities for travelers who have service dogs.

Dogged by Lawsuit After Barring Service Animal From Office, Lawyer Settles for $50K

A Colorado Springs, Colo., lawyer who refused to allow a veterinarian and her service dog to enter his law office for a scheduled deposition in a civil action has agreed to pay $50,000 to settle a federal discrimination suit.

The Justice Department’s Civil Rights Division filed a complaint in the U.S. District Court for the District of Colorado last November against Patric LeHouillier of LeHouillier & Associates. The suit alleged LeHouillier violated the Americans with Disabilities Act when he refused to allow the woman and her dog — and the woman’s lawyer — to enter the LeHouillier law office in December 2006.

This is an older news article that Ginny Tea brought to my attention, but I think it is still relevant: Creature Comforts [7 pages long]

Jamie Hais, a spokeswoman for the D.O.J., said she couldn’t comment on why the department suggested the species restriction. But its proposal expressed concerns about public-health risks and said that when the original A.D.A. was written, without specifying species, “few anticipated” the variety of animals people would attempt to use.

“That’s simply not true,” says Frieden, who was an architect of the original A.D.A. While drafting the regulations, he said, Congressional staff members had long discussions about defining “service animal” and whether a trained pony could qualify. “There was general consensus that the issue revolved around the question of function, not form,” he says. “So, in fact, if that pony provided assistance to a person with a disability and enabled that person to pursue equal opportunity and nondiscrimination, then that pony could be regarded as a service animal.” They discussed the possibility of birds and snakes for psychiatric disorders, he said, but one of their biggest concerns was that the A.D.A. shouldn’t exclude service monkeys, which were already working with quadriplegics. Since then, however, monkeys have become the most contested assistance-animal species of all.

And, a video, courtesy of Speaker’s Corner (transcript follows):

Video opens with an image of a Golden Lab (?) in a service animal vest & harness. Text reads: “No Dogs Allowed: Discriminaition by Taxicans Against People Who Use Service Dogs”

A Report By: The Equal Rights Center (ERC), The WAshington Lawyer’s Committee for Civil Rights & Urban Affiars (WLC), Hogan Lovells US LLP.

Screen image changes to a person (who appears to be a white woman to me) with long blond hair standing on the sidewalk with a black dog.

Text: More than 25 million individuals in the United States report having vision loss; approxinmately 2.5 million of those are legally blind.

Federal Law requires taxicab drivers to allow service dogs in their vehicles, and prohibits them from charging a surchage, higher fare, or extra fee for transporting a service dog.

Despite these protections, people encounter discrimination on a daily basis.

Image changes to a dynamic one of a busy street. Cars whiz by a white-appearing person signalling for a taxi with a service animal. A taxi drives by and then stops for a person just 100 yards down the road.

Text: To view the report, visit www.equalrightscenter.org

Image changes to a still image of a person standing on the side of the road to signal a taxi – just beyond them is another person signaling a taxi with a dog at their feet – the dog appears to be wearing a service animal harness.

Text: The ERC conducted test in the District, each included two individuals, one with a service dog and one without, who stood on the same side of the block.

Image changes to a dynamic image of cars whizzing down a busy street with the two people in the above image standing just a few meters apart. A taxi slows down in front of the person with the service animal, then slowly drives up to the person without an animal, ignoring the person with the service animal entirely.

Image changes to a TAXI sign with a wheelchair symbol.

Text: In 60% of these cases, the tester with a service dog was subjected to at least one form of discriminatory treatment.

Image changes to a dynamic one of a busy street. Cars whiz by a person signalling for a taxi with a service animal. A taxi drives by and then stops for a person just 100 yards down the road. (This image is the same as the one described above.)

Image changes to a static image of a person who appears to me to be a white woman seated outside, holding a white cane.

Text: “These instances are both hurtful and an insult ot those of us who must rely upon the loving assistance of our dogs to travel independently” – ERC Member, Charles Crawford

Image changes to another service dog user signaling a taxi on the street. The taxi drives right by, but picks up another person without a service animal just a few car lengths away.

Image changes to a static image of someone holding a golden lab (?) dog.

Text: “Cabbies go whizzing by and I can’t see to know if they have somebody in their cab or if they don’t.” – ERC Member, Stan Berman

Image changes again to a taxi passing right by a person with a service animal signaling and poicking someone up just a few car lenghts away.

Image changes to a person with a service animal opening a taxi door.

Text: Help advance civil rights and learn more about what can be done to end discrimination against indivdiuals who use servive dogs.

Learn more and download the report at www.equalrightscenter.org

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Recommended Reading for September 7, 2010

Lisa Harney at Questioning Transphobia: QT and Posting and My Inability to be Consistent

Oh, and a lot of neurotypicals learn about ADHD symptoms, and they think “I lose my keys sometimes? I lose my train of thought! I miss deadlines!” And you know, it’s true. Everyone does these things occasionally. But the difference is that you do not do them every. single. day. This isn’t what your life is like, this is when you have a bad moment – you’re tired, overwhelmed, in a hurry, and bam, a thing happens. This is what life is like every day for ADHDers, and when we’re tired, overwhelmed, in a hurry, then it’s that much worse for us. So, I can understand if you relate to these symptoms? I’m sure most people do. But don’t generalize how you experience them (as not-symptoms, assuming you do not have some other condition that causes similar symptoms – or you’re not an undiagnosed ADHDer yourself) to how I experience them (as symptoms). For me, they are a daily impairment.

K__ at Feminists With FSD: Book review — The Camera My Mother Gave Me [trigger warning for sexual assault]

The negative reviews usually contain some variation of gross-out due to TMI or frustration with Kaysen’s lack of progress in treating her pain medically. It’s TMI and gross because vaginas and vulvas are generally considered vulgar and gross – at least outside of feminist circles – sometimes even within feminist circles, because don’t talk about vaginas too much or else you reduce yourself to a big walking vagina – and thus it’s a shock to read such frank language and descriptions about the vagina.

Tammy Worth for the Los Angeles Times: Mental health parity act may affect your medical benefits

Other provisions of the bill require out-of-network coverage for mental health services, parity of coverage of medical and mental health medications, and if someone is denied coverage of a mental health service that is deemed medically unnecessary by the insurer, patients have the right to find out why.

Andrew Palma for the Golden Gate [X]press (San Francisco State University student newspaper): University loses scholar, activist

Longmore is arguably most well known for his 1988 protest outside the Social Security Administration’s Los Angeles office. He burned his book about George Washington, written word by word with a pen in his mouth and a keyboard, to protest policies that penalized disabled writers for counting royalties from their work as earned income.

Adrian Morrow for the Globe and Mail: Efforts to battle chronic pain found lacking

Some 80 per cent of people around the world who suffer from chronic pain can’t get the treatment they need and governments must step up their efforts to tackle the issue, says Michael Cousins, an Australian anesthetist and the driving force behind the first International Pain Summit [. . .] Earlier this year, he had a hand in drafting a national pain management strategy for Australia – the first in the world – and the summit, which takes place in Montreal on Friday, will draw up guidelines to help other countries follow suit.

Recommended Reading for 06 September 2010

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.

Galt Museum Blog: Making a Difference (Thanks to Penny from Disability Studies at Temple U. for the link!)

As I called her earlier this week to book a class, she related the following story to me.
For years, Blanche has told students about her limited vision and says that if they see her out and about in the community, they should come up to her and say oki (Blackfoot for “hi) and introduce themselves because she won’t be able to see them. In August this year Blanche was at Wal-Mart shopping with her son and grandson. As she was sitting there, a young girl walked past her, stopped and then walked towards her with her hand-outstretched. When she got in front of Blanche she said “oki” and then “oki, Museum Lady.” She was with her young brother and turned to him and said “this lady works at the Galt Museum. You and me and Mom and Dad should go and visit her there one day.”

Public News Service: Disability Activists: Dump the Pity

For 60 years, Jerry Lewis has hosted the Muscular Dystrophy Association annual Labor Day telethon. And for about 20 years, one of “Jerry’s Kids” has been at odds with him over the way the money is raised.

Mike Ervin appeared on the telethon when he was six years old. Now he’s a writer and disability rights activist who speaks out against the telethon because he claims it promotes stereotypes of people with disabilities as objects of pity.

Deafinitely Girly: Things my ears do instead of hear!

Isn’t it amazing how my ears are so utterly useless at their originally intended purpose, and instead able to tell me when someone loves or hates me, and when danger is nearby?

Did they miss the memo about actually having to hear, too?

Pipecleaner Dreams: Special Exposure Wednesdays

Well, for many reasons, Ronnie does not like DeafTalk at all. But, yet another interesting turn of events happened at the doctor’s office. Ronnie was on a standard size exam table. The DeafTalk machine was positioned in front of him. Only problem – the interpreter could only see Ronnie’s knees.

VictorVille Daily Press: Change in ADA regulations concerns local service-animal owners

That will all change next spring when service rats, cats, birds and some others will be disallowed under ADA amendments recently signed by U.S. Attorney General Eric Holder. The new rules will allow canines to continue to be used as seeing eye dogs and to alert seizures, but dogs will not be allowed to be used as service animals for emotional support. In recent years, dogs have helped bring normalcy to children with autism, soldiers returning from war with post traumatic stress disorder and more.

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.

Recommended Reading for 3 September, 2010: Transportation Edition

This edition 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?

United States Department of Transportation: AirTran Fined for Violating Rules Protecting Air Travelers with Disabilities.

Of the $500,000 penalty, up to $60,000 may be used to establish a council to help the carrier comply with federal disability rules and hire a manager for disability accommodations. Up to $140,000 may be used to develop and employ an automated wheelchair tracking system at AirTran’s major hub airports within one year that will generate real-time reports of the carrier’s wheelchair assistance performance.

Canada: CBC News: Brain-injured man mistreated on bus: family. (Yes, slightly strange headline.)

After a conversation with the driver of a bus he boarded in Lower Sackville, N.S., on Saturday, Wilcox said he was ordered to the back.

He said the driver then apologized to other passengers, telling them she usually kicks drunks off the bus. When Wilcox tried to explain he was not drunk, no one wanted to listen, he said.

New York City, USA: Transportation Access: Transit Advocates Announce Lawsuit Against MTA.

The lawsuit charges that the service reductions violate the Americans with Disabilities Act (ADA) and state law by denying people with disabilities the right to accessible transportation. The plaintiffs are seeking a permanent injunction requiring the MTA to immediately restore lost service to buses, subways and Access-A-Ride.

United Kingdom: From The Guardian’s Letters section: Travel cuts will leave disabled and older people stranded.

Transport for All is extremely concerned about how these cuts will affect older and disabled Londoners. The threatened cuts of over 7,400 hours of ticket office staffing every week across the London network will have a disastrous impact on the freedom and independence of disabled and older Londoners.

Ashley’s Mom at Pipecleaner Dreams: Suggestions.

Yes, I know, I have written many times in the past about the issues surrounding bus transportation in my school district. Well this post is not going to dwell totally on the negative. Bus services were, for the most part, excellent this summer. They did however start to fall apart this last week of school. And, I have a few suggestions so that doesn’t happen in the future.

Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.

Recommended Reading for 02 September 2010

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.

Sorry for the late post, folks! Pesky little Typhoon and all!

ITWeb: 1up for gamers with disabilities

It’s hard to say if there is any disability that limits someone from gaming, according to Coe. “With so many innovative peripherals such as over-sized buttons, muscle twitch sensors, and thoughtful customisation, I think we can modify anything for anyone.”

The Living Artist: Accessibility FAIL: Ross Park Mall

17th in line, 90 minutes to go until opening. Feeling my back starting to twinge, I sat down on the floor. A minute or two later, mall security guards came over and told me I had to stand. Even when we explained that I had a back injury and couldn’t stand for very long, they cited “safety issues” and said again, I had to stand. Since I didn’t feel like getting into an argument (and possibly getting all three of us kicked out), Aiden and I left.

Think Progress: Alan Simpson Says Veterans Who Are Agent Orange Victims Are ‘Not Helping Us Save The Country’

The system that automatically awards disability benefits to some veterans because of concerns about Agent Orange seems contrary to efforts to control federal spending, the Republican co-chairman of President Barack Obama’s deficit commission said Tuesday.

Former Wyoming Sen. Alan Simpson’s comments came a day after The Associated Press reported that diabetes has become the most frequently compensated ailment among Vietnam veterans, even though decades of research has failed to find more than a possible link between the defoliant Agent Orange and diabetes.

“The irony (is) that the veterans who saved this country are now, in a way, not helping us to save the country in this fiscal mess,” said Simpson, an Army veteran who was once chairman of the Senate Veterans’ Affairs Committee.

Rolling Around In My Head: The Battle

Three days ago we went to our local grocery, which had just opened after going through a several month closure due to renovations, and I noticed something slightly odd and yet wildly infuriating. They have 7 or 8 checkout aisles, one of which is designated as a wheelchair lane. It’s a lovely lane for me especially when I am in my power wheelchair. I’m wide, it’s wider, the lane is widest – a lovely fit wouldn’t you say. It’s so much better than what they had before. So, anyways, back to being annoyed – which through a mammoth act of will I manage NOT to be all the time. They had all the aisles open, that’s ALL of them, except the wide wheelchair aisle.

New York Times: Study Says Brain Trauma Can Mimic A.L.S.

A peer-reviewed paper to be published Wednesday in a leading journal of neuropathology, however, suggests that the demise of athletes like Gehrig and soldiers given a diagnosis of amyotrophic lateral sclerosis, commonly known as Lou Gehrig’s disease, might have been catalyzed by injuries only now becoming understood: concussions and other brain trauma.

Although the paper does not discuss Gehrig specifically, its authors in interviews acknowledged the clear implication: Lou Gehrig might not have had Lou Gehrig’s disease.

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.

Recommended Reading for August 31, 2010

Pamela Paul for the New York Times: Can Preschoolers be Depressed?

In the winter of 2009, when Kiran was 5, his parents were told that he had preschool depression, sometimes referred to as “early-onset depression.” He was entered into a research study at the Early Emotional Development Program at Washington University Medical School in St. Louis, which tracks the diagnosis of preschool depression and the treatment of children like Kiran. “It was painful,” Elizabeth says, “but also a relief to have professionals confirm that, yes, he has had a depressive episode. It’s real.”

Mary Crawford for the APA Monitor: Parenting with a disability: The last frontier

Social psychologist and bioethicist Asch says that a lack of familiarity may be one reason for professionals’ biases toward people with disabilities. “Very few professionals know people with disabilities as peers,” says Asch, who teaches at Wellesley College in Wellesley, Mass. “Their only contact with people with disabilities is in a crisis situation, where the professional is [called on for help]. So the notion among some professionals is that people with disabilities always need help and can never give help or nurturance to another human being or provide a child with security or protection.”

Naomi Jacobs for the Guardian‘s Comment is Free: Disabled people do have sex lives. Get over it.

This is not a story about “taxpayers’ money” – most disabled people who have local authority-funded care plans are only allowed to spend these on basic services such as help with washing and dressing. What it is really about is moral outrage over an isolated case, which is also a smokescreen for much more disturbing attitudes towards disabled people’s lives.

CBC News: Down Syndrome group slams Emmys

“With race, sexual orientation and disability, you are talking people’s core identity — things that are unchangeable,” she said. “What do we get out of making fun of things that people cannot change, other than degrading them and making them feel they are not part of society.”

Amber Dance for the Los Angeles Times: In the Works: Microneedle patches could take the sting out of shots

The Band-Aid-like patches, coated with microscopic needles, generally don’t hurt. Moreover, they may actually work better at delivering vaccines and some medications, according to recent research.

Recommended Reading for 30 August 2010

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.

Venus Speaks: Despair

Now, I don’t have a good history with the social security office. The two times I visited one, I was brushed off. I don’t know if they took one look at a mostly able-bodied young girl and said, hey, she must be trying to trick us, but it sure as hell felt like it – they told me that I needed to apply online, entirely online, and that they were so far booked into the future that there was just no point in scheduling. As in they refused to schedule me.

And lo, as I am filling out the disability report tonight, not only do I lose the internet and all my progress, but I just happen to notice before it goes down that you can’t apply for SSI online, you can only fill out the adult disability report, print off a few forms, and schedule an interview. You know, that interview that my local office couldn’t afford to give me.

Those Emergency Blues: The Title is About the Power

Titles, in short, are about establishing status and power. Why else worry about them? They are utterly irrelevant to actual patient care and one’s ability to do the job. Insisting on their use can create an atmosphere of professional intimidation that suppresses the free exchange of information. Health care professionals expressing power over patients is definitely not a good way to create therapeutic relationships. Implicitly saying (or believing) the title makes you a better person or supplies you with definitive or superior knowledge about patient care is dangerous as well as destructive to collaborative relationships with other health care professionals. In the end, it results in bad care of our patients, and of each other.

Pipecleaner Dreams: A Modicum of Sense

Well, at least the Academy of Arts and Sciences haven’t completely lost their minds. I was appalled when I first heard that the TV show, Family Guy, got an Emmy nod for their song, ‘Down Syndrome Girl.’

Haven’t heard it? Well, here is a sampling of the lyrics:

And though her pretty face may seem a special person’s wettest dream. […]

You must impress that ultra-boomin’, all consumin’, poorly-groomin’, Down Syndrome girl. […]

ABC News: Too Special for the Special Olympics (via Patricia E. Bauer, thanks to Nightengale for the link!)

The problem arose when Jenny’s school district entered an agreement with the Special Olympics, promising to abide by the organization’s rules. That meant no court time for Jenny, though the organization won’t say whether it’s because of the oxyen, or Simba, or both. [sic]

Ablegamers: Bungie Punishes You For Quitting Early

The fear is that disabled gamers who need to quit in the middle will be labeled as rage quitters. Certain people’s disabilities can hit at a moments notice, forcing them to quit out of a game. While according to the statement Bungie is only punishing those who habitually quit, it doesn’t discuss how they gauge that. Is that a certain percentage of total games? Frequency? What?

What has gone so wrong that it has come to this? Has Bungie exhausted all other options before walking down this path? Not really.

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.

Recommended Reading for 27 August, 2010

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?

United Kingdom: ESA: It Doesn’t Add Up by lilwatchergirl at Through Myself and Back Again.

No wonder there’s so much anxiety around the ESA medical assessments. Anxiety that won’t help those who already have long-term illnesses, or mental health problems, or acute life-threatening conditions – or who are already living in fear and poverty as a result of the War on Welfare Claimants.

When Persistence Pays Off by Emma/Writer In A Wheelchair at Disability Voices.

I’d love to think that they’ve done this just because of my complaints but I’m not naive enough to do so – and I know I’m not the only person whose had those problems. But it’s a definite example of why complaining, campaigning and advocacy are so important. And what happens when your persistent – because it really can pay off.

Statistics on Accessible Tourism – a Continuing Issue by Ivor Ambrose, guest posting at Access Tourism NZ.

One of the most Frequently Asked Questions posed by business owners and tourist agencies is: “How many disabled tourists are there”? And then there is the more probing question: “So, if it is not just about disabled people, how many people actually need better access, and what kind of things do they need?”.

Canada: Ottawa makes voting easier for disabled from CBC News.

The new voting machine, called a Voter Assist Terminal, has a high-contrast touch screen with a zoom function to enlarge type size. It also has tactile buttons with Braille on them; a sip/puff device for people with limited mobility; a rocker paddle; and an audio function that enables voters to hear the choice of candidates through headphones.

A New Financial Access Frontier: Persons With Disabilities by Elisabeth Rhyne at The Huffington Post.

According to Harvard Law professor Michael Stein, 650 million people around the world, nearly 10 percent of humanity, have a disability, and over 80 percent of these people live in developing countries. Yet, in research studies, fewer than 1 percent of the clients of microfinance institutions, dedicated to serving the world’s financially excluded people, were found to be persons with disabilities.

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Recommended Reading for 26 August 2010

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.

Westborough News: Marines shoot calendar for male breast cancer research

They are the few. The proud part has been a bit more of a struggle.

“Most guys don’t want to reach out, don’t want to tell anyone they’ve got a woman’s disease,” Pete Devereaux said yesterday as he talked with fellow male Marines who’ve been diagnosed with breast cancer.

INCITE! Blog: Reflections from Detroit: Reflections On An Opening: Disability Justice and Creating Collective Access in Detroit

We would not just think about disability as separate from class, age, race, queerness, family, children, gender, citizenship, violence, but we would understand it as intimately connected.  We would think, not just about “conference and workshop time,” but we would also think about social time and what social spaces were accessible and how we would make sure no one was isolated or left out.  Because in our movements much of the relationship building, socializing and bonding is done in very inaccessible ways in very inaccessible places—we know this all too well.

New York Times: When Battlefield Humor Backfires (Extra Trigger Warning)

And so the doctor’s determination not to lose a contest of wills undermines the opportunity to have successful discussions about treatment. The patient instantly senses that the doctor distrusts and dislikes him, and this, coupled with the patient’s lack of respect toward authority figures, leads to a rapidly deteriorating situation, often ending in a discharge against medical advice — much to the team’s relief.

NPR: Administration To Appeal Ruling in Stem-Cell Case

The Justice Department said an appeal is expected this week of the federal judge’s preliminary injunction that disrupted an entire field of science.

Judge Royce Lamberth on Monday threw the research community into disarray when he said a federal law invalidated Obama administration guidelines on human-stem-cell research. He concluded that two researchers challenging the Obama stem-cell policy stood a good chance of success as the case moved ahead in the courts.

The judge said any scientific projects using human embryos required their destruction, which flouts a longstanding federal law.

Something More Than Sides: Dear Doctor: Actually, I *Am* Sick

Let’s completely ignore the actual health concerns in exchange for shaming a young girl. Classy. And let’s not forget the fact that, were I suffering from an eating disorder, this is not the way to broach the subject. I left that appointment feeling shamed and humiliated, and with no answers.

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.

Recommended Reading for Wednesday, August 25, 2010

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.

Disability Bitch: Disability Bitch gets a bit of hot action:

The reports have led certain commentators to describe sex with disabled people as “one of the last taboos”. Amazing. Simply by having sex and being physically abnormal, I am engaged in some debauched endeavour, of which most people dare not speak. Such a thrill!

But, readers, shall we talk about it? I think we should. I did a little journalistic investigation of my own and discovered that this story did not simply land in the tabloids from nowhere. It was, shall we say, inspired, by a report in Community Care magazine, the industry journal for social workers. Community Care had published an article on the question of whether Individual Budgets for disabled people should be used to pay for sexual services. It was seemingly initiated by a debate between social workers on their own internet forum, a debate which ended up being quoted widely in the national press.

Laura Hershey: Remembering Two More Heroes

Barb was a T1 paraplegic who also had multiple sclerosis. In the 1980s, she worked in the independent living movement in Missouri and Oklahoma. Then she decided she wanted to start a business designing and selling advocacy posters and other products and service. She encountered opposition when she asked help from Kansas Vocational Rehabilitation. They tried to use the rules to limit her choices; she taught herself the rules and beat them at their own game. Based on that experience, Barb wrote a consumer manual aptly titled “How to Kick Ass and Win.”

Keri: not funny (interesting discussion in the comments as well)

Okay, so I know that the community I’m ranting about is kind of made for people who are obsessive and/or compulsive about lists and correct data and having everything Just Right. That means there are going to be jokes and comments about OCD, since a lot of what appeals to people of this community might come across as OCD-type things to people who don’t give a shit.

But, seriously, folks? It’s getting old and Very Unfunny. The first time I saw the “CDO is like OCD, but better: it’s alphabetical, like it should be” “joke”, I thought it was [stupid], but made sense for people who don’t really know about OCD except for media depictions. But people keep using that joke. And it is not funny. It’s not funny the same way the “dog = god” dyslexia “joke” isn’t funny. It trivializes a very real disorder and creates misunderstandings of what it really is.

Dave Hinsburger: The People Who Are The “R” Word (Dave does a lot of posts and discussions and goes into classrooms to give talks about “the R word”. I really recommend reading his posts about it, and perhaps pulling them out the next time someone insists that no one calls actual people r#tarded anymore.)

No matter what the fearless defenders of freedom of speech say, there is a huge difference between a word to describe something that slows fire and someone who learns differently. There’s a huge difference between a thing and a person – but, no, maybe not. After reading their diatribes regarding their freedom to spit out hurtful words, they may, really, not see people with disabilities as fully human with a human heart capable human hurt.

Haddayr: ‘Drive-by’ ADA Lawsuits?!??

Who cares if you “turn business owners against the ADA?” I don’t want them to feel warm and fuzzy. I want them to OBEY THE LAW. Businesses will not do right by people unless they fear lawsuits. They have no motivation other than money. As a matter of fact, the ADA has no enforcement arm and they depend on people filing private lawsuits to get places to comply.

In The News:

US:
Disability Scoop: Despite Reforms, Problems With Restraint And Seclusion Persist [Trigger Warning for discussion of abuse of students with disabilities] “According to state records, teachers in at least three Iowa school districts have violated the rules, which limit the types of restraint allowed and circumstances in which they can be used.”

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