Tag Archives: abuse

Recommended Reading for 16 December, 2010

Talulah Mankiller at Life Under a Rock: Just the Facts, Ma’am (via Kiri) (post mentions domestic violence but doesn’t describe)

Even when I was very sick and had no idea what was wrong, I always had two versions of reality in my head: what I logically knew was actually probably going on, and what I emotionally understood was happening. The two rarely matched up, but that doesn’t mean that they weren’t both there. For years, various people made futile efforts to help me “grow up” and “learn to deal with things” by trying to get those two versions of reality to overlap as much as possible, but the fact of the matter is that they were never going to. Because those kind people, those lovely people, thought if I just understood that another, less emotionally volatile reality existed, then I would just magically walk right over there and everything would be fine.

Problem was, I’d been well aware of that reality the whole time. I just couldn’t reach it. Because, you know, MY BRAIN CHEMISTRY IS FUCKED.

Kiriamaya: “Why aren’t you angry?”

Because I’m fucking exhausted, that’s why. Depression means I don’t have much energy to begin with, and I have to use most of what I do have for school, work and social situations, which doesn’t leave much over to do activism or to be angry about shit. Oh, and I’m also trans, which means I have to constantly fight just to be seen as human (and usually fail). And I try to squeeze creative projects in amidst all this because that’s how I keep from killing myself.

Old Kentish Sign Language Put On the Worldwide Endangered List

A centuries-old sign language thought to have been spread throughout America by Kentish settlers is on the worldwide endangered list.

Evidence of the use of Old Kentish Sign Language dates back as far as the mid-1600s, but is now thought to be extinct thanks to the rise of British Sign Language in its place.

It is also thought to be one of the forerunners of American Sign Language, as a number of 17th century settlers on the island of Martha’s Vineyard near Massachusetts – the majority of whom knew how to sign – migrated from the Kentish Weald.

Disability Scoop: Violent Crime Odds Double for People With Disabilities

The findings come in a report released Thursday by the Department of Justice’s Bureau of Justice Statistics that looked at 730,000 nonfatal violent crimes during 2008 in which the victim had a disability. Overall, those with disabilities age 12 and older experienced crime at a rate of 40 cases out of 1,000. During the same period those without a disability were affected at a far lower rate of 21 per 1,000, the findings indicate.

ABC (Australian Broadcasting Corporation): Inside an isolated world

There are more than 300,000 Australians who are deafblind and an Access Economics report is predicting that with an ageing population that figure will top one million by 2050. The 7.30 Report’s Natasha Johnson spent a day with a woman who is deafblind to witness the many challenges she faces.

Recommended Reading for 15 December, 2010

Jody McIntyre: Student Protests, Part Three

From the corner of my eye, I spotted one of the policemen from the earlier incident. He recognised me immediately. Officer KF936 came charging towards me. Tipping the wheelchair to the side, he pushed me onto the concrete, before grabbing my arms and dragging me across the road. The crowd of 200 ran and surrounded him. I got back up and stood in front of the horses.

When I finally got home at 5am, exhausted but pleased at what can only be seen as a victory, I found that the picture of me being pulled from my wheelchair had been creating a bit of a storm online. But I am not the real victim. The real victims of yesterday are people like Alfie Meadows; a 20 year-old student who was rushed to hospital for emergency brain surgery after internal bleeding caused by police truncheons.

Abuses Reported at Mexico’s Institutions for the Disabled

MEXICO CITY — Ten years ago, a human rights group released a scathing, groundbreaking report on abusive, decrepit conditions in Mexican institutions for the mentally and physically disabled, moving the country to promise change and to take the lead in writing international agreements to protect the disabled.

But in a new report released Tuesday, the group, Disability Rights International, working with a Mexican human rights organization, said a yearlong investigation revealed “atrocious and abusive conditions” that included lobotomies performed without consent, children missing from orphanages, widespread filth and squalor, and a lack of medical care.

Making the Case for Irish Sign Language in Education

“As we say to parents at this stage, don’t think about your child at five . . . think about your child at 10, at 15 and at 25. Where is he or she going to be at 25? You know, part of a deaf community or a hearing community, but hopefully a mix of the two. And sign language is a critical aspect of that.”

NPR is doing an investigative report called Home or Nursing Home

People ages 31 to 64 now make up the fastest-rising proportion of nursing home residents. One reason: As states face record budget gaps, the programs that help people live at home are being cut.

Muscular Dystrophy Org: Disabled children hit by Residential Education Transport cuts [This link has a moving image on the top that makes me dizzy to look at]

In a move condemned by the Muscular Dystrophy Campaign, when changes to mobility support claimed through the Disability Living Allowance come into force in October 2012, families with a disabled child in a residential school will immediately lose access to either adapted vehicles used to transport their children or the £49.85 a week allowance available to assist with the higher costs of accessible transport.

Howard Hyde Inquiry Ignores Ableism As Cause of Death

Note: This post discusses police violence against people with mental health conditions.

The results of the Hyde Inquiry were released on Wednesday.

Some things about the Hyde Inquiry, since I don’t think it’s been widely covered outside of Nova Scotia. I wrote this summary several months ago:

Howard Hyde had a diagnosis of schizophrenia. The treatments he was on were making him sick, so he stopped taking them. He became violent.

His wife called the mobile mental health team – a project in Halifax that will go to you rather than you needing to go to them. She then called 9-1-1.

Two days later, he was dead in police custody, having been tasered.

Various things went horribly wrong. Among them were -and continue to be – the police’s inability to deal with people who have schizophrenia, amongst other mental health related conditions.

What they should have done was taken him to the hospital. Which they did, for a bit, and then left, returning him to lock-up.

His wife had tried to contact them and make sure that he was okay, and that they were aware that he had schizophrenia.

“I really wanted him to be in the hospital and get the treatment he needed for psychosis,” she said.

He had been taken to hospital for assessment, and the hospital staff requested that he be returned to the hospital after his arraignment hearing. He was not.

Parts of the surveillance tape of the tasering itself are “missing”.

“Hyde began struggling when officers tried to cut the string from his shorts. Though images were not caught on tape, surveillance audio recorded sound of the scuffle. Edwards can be heard saying “Howard, sit down.” Fellow Const. Greg McCormack is then argued to have said “You’re going to be doing the f***ing dance next, Howard,” although his voice is muffled.

It was also revealed that more than 30 minutes of footage of Hyde in a cell waiting to be booked has gone missing.”

I’ve since learned that what was actually said to Howard as the police officers approached him with a knife:

A surveillance camera captured the moment when an officer told Hyde a utility knife would be used to remove a knot from the drawstring in Hyde’s shorts, saying: “I just have to cut off one of those balls there.”

Anyway, as I said, the results were back. After 11 months of looking into the death of a man who police were called to help, we’ve all been told that Howard’s murder was an “accident” and it had nothing to do with his mental health condition.

“The only useful approach is to understand that Mr. Hyde died because of physiological changes in his body brought on by an intense struggle involving restraint,” Derrick wrote. “He did not die because he was mentally ill.”

I suppose this is technically correct. Howard’s death was not because he was mentally ill, his death was because the police were ill-equipped to deal with someone having a mental health crisis. I don’t have statistics about the number of men having mental health crises that are murdered by police officers every year, but I do know that I can’t go a whole month without at least one report, and it’s an issue that the Chief Justice of the Supreme Court of Canada feels needs to be addressed.

I think it is naive to state that Howard wasn’t murdered because of his diagnosis. I think it ignores a frightening history of people with mental health conditions being murdered by police officers. I think it ignores that the criminal justice system is not equipped to effectively deal with people with mental health conditions. I think it ignores that there are limited resources available for people with mental health conditions and their families to get the help they need to cope with crisis situations.

I think it completely ignores the fact that Howard’s wife called the police for help, and two days later he was dead.

So yes, Howard Hyde isn’t dead because he had schizophrenia. He’s dead because ableism kills.

Recommended Reading for Thursday, December 8, 2010

I hate this time of year because I live in the Northern Hemisphere and it’s dark really early. At least we’ve been avoiding the snow-dumps I hear are all over central Canada, but it’s only a matter of time.

Civil Rights Now!: Civil Rights Now! speech at Dec10 CLAS Forum on UN Convention on the Rights of Persons with Disabilities

As my lawyer friends say there’s no right without a remedy; because most BC voters with disabilities cannot afford a good lawyer their rights have very little meaning because they have no way to enforce them. And that’s why our governments, Health Authorities, businesses, School Boards, service providers and unions can do anything to you if you are a voter with a disability.

That’s why Civil Rights Now! believes BC voters with disabilities need:

  • Law which gives the equality provision of the Canadian Charter practical force and effect in their daily lives.
  • Law which gives them truly-portable, sufficiently-funded, consumer-driven Individualized Funding.
  • Law which gives them funding for test cases involving their civil rights.
  • Civil Rights Now! launched a campaign this year to persuade BC politicians to commit that whichever of them wins the next election they will enact such laws. By so doing they will fulfill the intent of the Convention and, more importantly, the equality provision of Canada’s Charter of Rights and Freedoms, many decades after it became the supreme law of our country.

Urocyon: Disability and UK fuel poverty

I felt pretty bad, because until I started reading about the extent of problems this winter, I hadn’t considered just how bad the situation is. (Bit of a shame this is another thing that it apparently takes larger numbers of middle-class people being affected to draw more news attention.) This is in spite of having dealt with parental disability-related poverty and substandard heating for years, in a colder-winter climate not moderated by the Gulf Stream. This isn’t the coldest month, but it’s supposed to be 10°F/-12°C tonight back home–not unusual. It honestly didn’t seem that cold to me, even though I was aware that last winter was the harshest in 30 years for the UK, and this one is looking to be if anything worse. (Climate change? No…) But, even though it isn’t very cold in absolute terms, if you’re not used to its getting, much less staying, below freezing very often? That’s a pretty big problem.

Then I started thinking about how disabled people just weren’t getting mentioned much.

Anna Racoon: The Orwellian Present – Never Mind the Future.

No, he can’t, he has no access to the Mental Heath Tribunal – Autism isn’t a mental illness. This action isn’t being taken under the Mental Health Act – it is being taken under the Mental Capacity Act. Under the MCA he only has access to a ‘Best Interests Assessor’ – who is appointed on a consultancy basis, and paid, by…..the Local Authority.

He can be deprived of his liberty for up to a year, which period can be renewed indefinitely, for the purpose of ‘assessing’ him – see above – being sent to Wales to ‘assess’ why he is unhappy at being locked up.

Sharon Brennan at Comment is Free: It’s now officially ‘unsustainable’ to support disabled people

Let’s be clear: this increased DLA caseload is not because of fraud. DLA has one of the lowest fraud rates of any benefits. In fact, government figures published by the House of Commons work and pensions committee suggest that benefit fraud for DLA, carer’s and attendance allowance among others has reduced since 2001 from 2.2% to 0.8% between 2008-2009 (the most recent year for which statistics are available).

Diary of an NHS Buff: The Government is implicated in creating negative attitudes to disabled

Clearly there is a negative perception of disabled people in the UK, which can undoubtedly be attributed in part to right-wing media representation of the disabled. The Daily Mail is notorious for this. A recent front page screamed, “75% of claimants are fit to work”, and carried on: “Tough new benefits test weed out the workshy”.

You expect this kind of thing from the Daily Mail. But what shocked me is that the 75% figure came from a press release from the Department of Work and Pensions. And the figure is wrong. So it amounts to blatant Government propaganda.

Recommended Reading for Wednesday, October 27

If you haven’t been following my tale of woe on my personal journal, I have a terrible ear infection and can’t hear out of either ear. But now I have antibiotics to treat the middle ear infection, so any day now I should be able to hear something. I hope. (Woe.)

Today’s Recommend Reading is not entirely about the budget cuts and slashing of disability-related funding, but a lot of it is. I really recommend following Where’s the Benefit? for more in-depth discussion of these cuts.

Disabled People Protest Against The Cuts That Will Kill

Data from Family Resources Survey and the National Equalities Panel found that:
· 75% of disabled women and 70% of disabled men are already at the bottom end of Britain’s income distribution scale living in poverty.
· A tenth of disabled woman have incomes below £31 per week and a tenth of disabled men have incomes below £59 per week including earned income and benefits.
· Under the coalition government’s economy drive disabled people are set to lose at least £140 per month through direct cuts to disability benefits (initially devised to pay the extra costs of being disabled) alone.
· The Tories have threatened to remove our DLA saying that the number of claimants must be reduced by one-fifth.

rich at arbitrary constant: Osborne: Welfare cheats are “like burglars”

I’ll start by reminding people that most disability benefits are not work- or sickness-related. For example, Disability Living Allowance (DLA) helps with the additional costs of disability, primarily related to personal care. It is for people under 65, though you can continue to be in receipt of DLA over the age of 65 if you have it before you are 65. (Attendance Allowance is the equivalent for people over 65. Both are non-means tested.)

And rather than pejorative statements that play to Osborne’s prejudices, let’s introduce some facts.

CripChick’s Blog: thoughts on national coming out day

today is national coming out day. as i think about what this means for me as someone who is so out, yet so so closeted, friends and i are on a conference call going over notes from a recent summit where self advocates with developmental disabilities worked to create policy recommendations on community living. (sadly this is needed because too many providers use gov’t dollars set aside for community living to do things that are really hurtful to disabled people).

we asked people to talk about what group homes and other residential facilities for disabled people often look like. this is what the notes reflected.

Kali at Brilliant Mind, Broken Body: Disability services – hit or miss

Now, one of the interesting things I have to point out here when talking about how my law school handles my disability is that my law school is semi-autonomous from the greater university. It creates an…interesting…situation for disability accomodations. Not bad entirely; it’s had pros and cons for me. The way getting accomodations works for me is like this: I bring my doctor’s letter to the law school’s disability coordinator, who we’ll call W. The disability coordinator faxes the letter over to the university’s disability resources center. ( I officially have a file there and a counselor, but I’ve only really interacted with her over one issue.) The disability resources center sends back its evaluation of what accomodations I’m to be accorded. W and the law school student resources secretary then arrange for the accommodations.

Corina Becker at No Stereotypes Here: Adults Count Autism Survey

Not long ago, I heard about a survey being done by the Redpath Centre on the needs of Autistic Adults. Looking at the website, I see that the purpose of the survey is to gather materials in order to advocate for better services. Curious and always willing to help out, I emailed them, and received this reply.

In the news:

UK: The Guardian: Disabled people among the hardest hit by spending review: Osborne limits employment support allowance to one year. “After one year, people with assets, savings or partners who work will no longer receive benefits. Single people with no assets may be able to qualify for a means-tested safety net, but everyone else will have to manage on their husband or wife’s salary – no matter how low it may be – or dip into any private savings they may have.”

UK: The Guardian: A whirlwind of hatred against the disabled: Just how far are we, as a society, prepared to let violent crime against the disabled spiral upwards? [Trigger Warning for discussions of violence against disabled people, including sexualised violence] “The statistics should shame us all. Nine out of 10 people with learning difficulties have suffered bullying or harassment.”

Recommended Reading for Wednesday, October 20, 2010

Good Day, all. It’s been a stressful week at Chez Anna (I’m putting this together at 5 a.m. my time) so forgive me for oversights, please.

Kali at Brilliant Mind, Broken Body: I am not your metaphor

This is something that has bothered me for a long time, and actually led to one of the very few spats between the boyfriend and I (quickly mended, once we both cooled off a bit). I really hate the use of disability-based metaphors. Hate them, hate them, hate them. I believe that they’re part of what makes disability such a fearful, distorted, tragic cloud to people who are able-bodied.

It’s all well and good to say they’re bad, but I think it makes more sense if I actually go through some of the more common disability metaphors so you can see what I mean

DeafMom:Embracing My Deaf Self

My life took an interesting turn at that point. Once the grief subsided and I dried the tears, I entered a new world filled with deaf and hard of hearing people. It wasn’t easy– because I had spent the previous 19 years of my life hiding my hearing aid and feeling quite uncomfortable with anything that reminded me that I was “different.” It took awhile for me to learn American Sign Language and get to the point that I embraced a deaf identity. Once I did, there was an amazing transformation in my life: Yes, I am deaf and gosh-darn-it, that’s perfectly ok.

shiva at Biodiverse Resistance: When Will We Be Paid For The Work We’ve Done?

There are several horrible things here. First, the uncritical use of the term “trainable”, dating from the workhouse-era classification of intellectually impaired people into those who could be “trained” to do “useful” work (often with “training” methods that basically amounted to torture) and those who could not (particularly disturbing coming from a “special education” teacher!). Second, the assumption that her “functioning level” (a heavily loaded and problematic term in itself) will never change throughout her lifetime, and that, despite Brown demonstrably being in reality an adult, her “functioning level” is that of a child, meaning that Masaki buys into the “eternal child” stereotype of learning-disabled people – historically and still used to deny them adult sexualities, adult roles within families, and all the basic rights, freedoms and responsibilities that anyone else is assumed to gain automatically on reaching chronological adulthood – which is perhaps even more disturbing as an attitude held by a teacher whose pupils she considers herself “mentor and so much more” to. Thirdly, the glib “wouldn’t it be nice” comment, which is more patronising “inspirational” crap, making disabled people into ciphers of innocence rather than real, flawed and complex people.

MarfMom: A Call for Posts

A Call for Birth Stories From Women With Disabilities

Whether you knew about your diagnosis ahead of time or not, whether you had a vaginal birth or a c-section, I want to hear your story. Positive birth stories are awesome, but if yours wasn’t what you hoped please feel free to submit it too because I want to keep this blog real and the reality of having a disability is that sometimes our deliveries are complicated. I’m going to leave the term disability open-ended, but I’m basically looking for high-risk pregnancies (or what would have been if you’d known your diagnosis). You don’t need to have a connective tissue disorder.

Anne at Where’s the Benefit: The Damaging Effect of how People Perceive disability benefits

If you are one of society’s more vulnerable members, you will have to fight for everything and wade through reams and reams of red tape. That is the experience that many of us have. And people who become eligible for disability benefits and try to claim them are often completely shocked. Some do not have the energy, emotional strength and/or intellectual capacity to go through all of the form-filling and bureaucracy involved in applying and apppealing.

But so long as the myth persists that it’s simple and easy to apply for disability benefits, people will believe that anyone who says it’s not is making a fuss over nothing, or sticking up for so-called scroungers – and when people become eligible for these benefits and try to apply, they will continue to be absolutely gobsmacked when they find out how difficult it is.

In The News

Canada: The National Post: Bygone Braille. “Advocates blame funding shortages, not enough qualified teachers, and decisions by administrators to deny Braille instruction to children with low vision because of an emphasis on encouraging these students to read print. Educators say this assessment couldn’t be further from the truth and argue that today’s diagnostic tools have honed the art of identifying those who truly require Braille instruction and those who don’t.”

Australia: Australia Misses the Plane on Accessible Tourism. “Based on general population statistics of age acquired disabilities the total expenditure of this group in the travel sector is likely to exceed 22% in ten years time. Not only is this relevant to Australia’s domestic tourism market but the majority of Australia’s inbound tourism is sourced from countries with similar age demographics.”

UK Learning Disability Coalition protests in Birmingham at Government cuts. “The campaigners from Birmingham, many of whom use social care support, held up “Cuts Incident” boards displaying the frontline services which they fear will be affected by the Government’s Budget and Comprehensive Spending Review and subsequent cuts that will be made by local councils.”

Recommended Reading for 18 October 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.

The first two links were sent in by Penny at Disability Studies from Temple U! Thanks Penny!

Knitting Clio: Ableism and NARAL Pro-Choice America

via NARAL Pro-Choice America, which is running a pro-choice slogan campaign.  Here are the choices:





I voted for the first one — why?  Because using “insanity” to discredit opponents trivializes persons with mental illness — a group that already experiences social marginalization and oppression.

Media dis&dat: South Carolina woman with Down syndrome volunteers as teacher’s aide in special ed classroom (Extra Special Trigger Warning for description of exploitative labor practices passed off as Very Special Favors done by abled folk)

“She had been working at a fast-food place, but they were really taking advantage of the fact that she was disabled,” Masaki said. “So, I offered her a ‘job’ here.”

Brown’s unpaid job is to be a teacher’s aide in Masaki’s classroom. While the position is voluntary, Brown works like the two full-time paid teacher’s aides, Rita Evans and Wendy Usary. The paid aides help Masaki with the classroom teaching everything from potty training to table manners to play time to desk work.

Brown helps control the children and helps keep the classroom running the three days a week she’s there.

The following post, which made me so angry I really cried because I hate the world sometimes, was sent in by reader Blake:

NYTimes.com: Mentally Ill US Citizen Wrongly Deported (TW, because the title doesn’t even begin to cover how awful this is!)

A mentally disabled U.S. citizen who spoke no Spanish was deported to Mexico with little but a prison jumpsuit after immigration agents manipulated him into signing documents allowing his removal, a lawsuit filed Wednesday alleges. His lawyers say the agents ignored records showing his Social Security number, while prison officials wouldn’t tell concerned relatives what happened.

Health Behavior News Service: Kids With Chronic Illness, Disability More Apt to Be Bullied

The study showed that students who reported having a disability or chronic illness — no matter where they lived — were more likely to be experience bullying from peers than those who did not. For instance, in France, 41 percent of boys with a disability or chronic illness reported undergoing bullying compared with 32 percent of boys without. Gender, however, was not a factor — boys and girls were victims equally often.

In addition, when students with a disability or chronic illness were restricted from participating in school activities, they had a 30 percent additional risk of being bullied.

Garland Grey at Tiger Beatdown: The Problem with Policing Someone Else’s Mental Health

Marginalized people are particularly susceptible to having their emotions pathologized, partly because their experiences aren’t typical. When young queers are experiencing depression related to the stigma of their sexuality, people like Tony Perkins swoop in to point the blame at their sexuality, and not the stigma that they themselves are perpetrating. Women, queers, the disabled, people of color, political dissidents, atheists; all of these groups have a history of being labeled “insane” to control them.

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 14 October 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.

Crazy Mermaid’s Blog: Mental Illness Medication Side Effects

One of the biggest reasons for noncompliance is the side effects of the drugs. Especially for those with more severe cases, the side effects of strong doses of medication can cause horrific side effects. So horrific, in fact, that the patient makes the conscious decision to stop taking the medication to avoid those side effects. Living with the mental illness becomes more appealing than living without it.

Diary of a Goldfish (Thanks, Deborah, for sending this in!): Coming Home Undefeated

But it also helps that I am choosing to live with them now, because it is a sensible and practical thing which I actually want to do, not because I don’t have any other options. And it helps a very great deal, that this situation is not permanent. I think it would be a lot harder without plans for the future.

Deaf Echo: It Gets Better. It Really Does. (Thanks, codeman38, for the link!)

A few hours later, I received an email from some guy named Terrence, who told me he had just finished captioning the clip. I guess I’m a little slow these days, because I made no connection between Terrence and Terry.

That’s right. Terry, Dan Savage’s husband, took time out of his day to transcribe their video clip, figure out the program, and upload the captions so that gay deaf kids could have access.

Because. It. Is. Just. That. Important.

Penelope Friday: Read About Cost to the Poorest  of the Newest Welfare Reforms (Thanks, Rosemary, for the link!)

And explain patiently to me that if a family is earning £44000 then they don’t need child benefit. Even if it is the father who earns the money, and the  mother who may depend on the child benefit to have any money of her own (which yes, is often the case, even these days). When women have been able to use their years of claiming child benefit to count for contributions to National Insurance, and now will presumably lose that benefit alongside the present money.

Disability Scoop: SNL Offers Apologies For Disability Cracks

After repeatedly mocking New York Gov. David Paterson for being blind, “Saturday Night Live” used the governor’s appearance on the show’s season premiere Saturday to make amends.

During the show’s “Weekend Update” segment, the real Paterson made an appearance to take some jabs at Fred Armisen’s impression of him and set the record straight.

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 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.

Brilliant Mind, Broken Body: Emergency Fail (Thanks for the link, Kali!)

The ER supervisor said I had the option of going elsewhere.  Bullshit.  When you’ve been brought in by ambulance because you’re barely able to stand with tons of assistance, you don’t have the option of going somewhere else.  Especially when somewhere else is on the far side of the city.

SexAbility: Decision Made (Warning: Some images and content NSFW) Thanks to K for the link!

So I’ve finally decided to shut down SexAbility. I know folks have said before, “keep it up, it’s a good reference. But honestly? It’s more trouble then it’s worth. And truth is…

Crozier Center for Women: Jon Stewart’s Rally to Restor Sanity (Thanks to Monica for the link)

The implicit message behind the “Rally to Restore Sanity” is that individuals influencing America’s current political climate are “insane.” Crazy. Wacko. It’s Stewart pointing at a picture of Beck and circling an index finger around his ear. And it pisses me off.

Australian Broadcasting Company: Mentally ill “falling through the cracks”

“The number of consumers who’ve come to us and found that they just can’t get on, they can’t communicate with the agencies and they’re left often in great poverty, in great mental concern,” [Mr. Asher] said.

McClellan: Woman’s disability not evident to judge

Attorney Jeffrey Swaney was at the Social Security office representing another client when Marcella’s case was called.

“I was sitting in the waiting room when they called her. I knew it was an appeal, and I remember thinking, ‘How could this woman have been denied?’ You could see she was profoundly disabled,” he said.

Later that afternoon, Swaney got a phone call from Lisa. She had seen his ad in the Yellow Pages about Social Security disability claims.

“She said her aunt had just had an appeal and had been denied and she started describing it, and I said, ‘I was sitting right behind you.'”

So Swaney took the case. He said the problem was a lack of medical documentation.

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 September 21, 2010

Natasha Tracy at Breaking Bipolar: Stop Minimizing Mental Illness: Worst Things To Say

I feel, sometimes, that I am at war with the mentally-well world. This isn’t to say that many of them aren’t lovely or that I have a desire to harm anyone, but I do feel embroiled. And it’s mostly because the well population just doesn’t understand what it is to be unwell. They demonstrate this heartily by repeatedly saying the worst things possible to a person with a mental illness.

The Guardian: Letters: Living on benefits is in no way ‘a lifestyle choice’

It is quite possible for a person from a very rich and privileged background to genuinely care about the plight of the poor, and to do something constructive to improve it (Osborne to cut £4bn more from benefits, 10 September). It is much harder for such a person to have any real comprehension of what it feels like to live in poverty, with little or no prospect of escape, no matter how hard they work.

Michael J. Berens at the Seattle Times: Hundreds of adult homes conceal abuse, neglect [strong trigger warning for content related to abuse]

In fact, a Seattle Times investigation has found, such cover-ups by adult family homes are not unusual. The Times found that over the past five years, at least 357 of the adult family homes in this state have concealed cases of abuse or neglect of their residents. Many of those cases involved serious injury or death. In dozens of these cases, untrained or unlicensed caregivers mishandled residents’ medications, sometimes giving them fatal overdoses. In other cases, residents became ill after being denied basic care and hygiene.

Ally at Every Crooked Step Forward: Courage…And Other Things I Don’t Have

That I am a person with a disability who identifies as asexual is not a forgone conclusion. That I belong to both groups is incidental, and that both groups have been mistakenly thought, by people who are not part of that group, to denote a lack of maturation or inability to understand one’s social or physical development, does not mean I am, in fact, immature, or that I do not know my own body. The fact that I am asexual is not proof about the presence, or lack of a sexual desire in a person with a disability, or zir understanding of zir sexuality, or zir ability to express that desire, if indeed it does exist. The fact that I have a disability is, similarly, not proof that all, or even most, people who identify as asexual suffer from some kind of physical, mental, or chemical deficiency.

Blackamazon at Having Read the Fine Print…….: We’re supposed to be impressed

However

I get less and less likely to feel solidarity with it when THAT phenomena where in your experimentation , goals for what inclusion looks like , and execution are serious matters and the stuff you got it from , the places it came from aren’t even notable .

As well as EVEN less likely to believe it’s just experimentation or poking and prodding when certain aspects of those personae like your race,class, sexuality are seemingly

a) ignored

or

b) only poked in ways that continually exhibit you as a edgy for a member of privileged class or consistent appropriator or chosen vessel.

It’s not my job to tell you haw to do it but if you wish to explore why is THAT section so often missed .