Tag Archives: australia

Recommended Reading for 24 December, 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?

The Broken of Britain: The GP’s Story by Dr Jest

So there you have it. Neither Pete nor Dud would have chosen to be where they are now, and neither has asked not to work when they were capable. Indeed both have rather struggled on when reason would have suggested they ought not. And I could name you a dozen others in a similar position. All present talk of making it more profitable to work than rely on benefit may sound very noble and high minded in the marbled halls of power, where hard graft means having a lot to read and a few late meetings to go to. It completely misses the enormous efforts made by the likes of Pete and Dud to keep going against the odds, and any move to impoverish them is little short of scandalous and should be relentlessly pointed out for the evil narrow minded bigotry it is.

Sarah at Cat in a Dog’s World: PWD and TSA

From information I’d heard from TSA administrators, I thought that the body scanners would reducethe need for physical pat-downs. Little did I know that TSA would use the new technology as an excuse to conduct more invasive pat-downs! It is obscene, especially when one considers that many people with disabilities don’t have any “choice” at all. If someone is unable to stand independently for ten seconds with their arms up, or if one wears any number of medical devices or prostheses…there is no “choice.” (And no, for many people, “don’t fly” is not a realistic choice.) There is, additionally, reason for concern about the radiation from the body scanners, particularly for cancer survivors and people who have a genetic predisposition to cancer. It is now pretty clear that body scanners, far from being a panacea, are making things worse. And people with disabilities are being affected disproportionately.

At Spilt Milk: Thanks for your help, doctor.

Make no mistake: I know that this only happened to me because I am fat. If I were a thin person and I walked through his door with the symptoms I described, he would have been forced to dig deeper. To ask me more questions, to hopefully come up with a wider range of options. Maybe run more tests.

United States: Megan Cottrell at ChicagoNow: Got a disability? You’ll see the difference in your paycheck

A lot of people might assume that if you have a disability, you might not make as much money as someone without a disability. But how much less? How hard is it for people with disabilities in Illinois to get by compared to their neighbors?

India: An unnamed special correspondent at The Hindu: Social barriers keep the disabled away from workforce:

Persons with disabilities are the last identity group to enter the workforce, not because their disability comes in the way of their functioning, but because of social and practical barriers that prevent them from joining work, a study on the ‘Employment Rights of Disabled Women in India’ carried out by the Society for Disability and Rehabilitation of the National Commission for Women (NCW) has said.

Guillermo Contreras at Chron.com: State sued over care for disabled Texans

The federal lawsuit, filed Monday in San Antonio, alleges the state isn’t providing some mentally and physically disabled Texans the opportunity to move into community-based settings, which advocates say are less restrictive and more rehabilitative than nursing homes.

Lastly, here’s a transcript of a story on Australia’s 7.30 Report program called Setting Sail:

Known as the ‘Everest of sailing’ the Sydney to Hobart race challenges the most seasoned of yachtsmen on what can be a treacherous ocean voyage.

Most of the focus is on the big maxi-yachts competing for line honours. But a unique crew of blind and deaf sailors is also commanding attention.

The charity organisation, Sailors With Disabilities, has been gifted a half-million dollar fast yacht, making them eligible for the first time in the prestigious Rolex Cup.

Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited. And have yourself a fabulous weekend.

Recommended Reading for 17 December, 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 States: Tampa’s ‘Sensitive Santa’ allows children with autism to get photographs, too by Shelley Rossetter at the St Petersburg Times:

The mall’s owner, Glimcher Realty Trust of Ohio, started Sensitive Santa in some malls nationwide two years ago and extended the idea to all its properties this year, said Kristy Genna, marketing director for WestShore Plaza.

Ireland: Deaf man can sit on jury, says judge by Eithne Donnellan at the Irish Times:

A HIGH Court Judge has ruled for the first time that a deaf person can sit on a jury in the Central Criminal Court.

Mr Justice Paul Carney yesterday ruled that profoundly deaf teacher Senan Dunne could sit on a trial jury with the aid of a sign language interpreter. He said objections to having a “13th person in the jury room” in the form of a sign language interpreter could be met by the signer taking an oath of confidentiality and the jury foreman ensuring that she or he was confined to translating what went on.

Just updating you on the situation in Sierra Leone (see RR for 3 December): In Sierra Leone, Disability Congress Writes President Koroma by Abdul Karim Fonti Kabia at the Awareness Times:

The NDC highlighted that persons with disabilities remain severely under-represented in political and decision-making positions; disabled hold only 0.01% of parliamentary seats, and; the current representation of disable persons in cabinet is at 0.0%.

Indonesia: City to Soon Issue Bylaw on Disabilities at BeritaJakarta.com

As form of its attention to the disabled, Jakarta capital city government plans to implement local regulations on building facilities and accessibility for the disabled, including the sanctions for the violators. At present, there are approximately 35 thousand disabled people in five administrative areas of Jakarta.

Australia: ‘Warringah Council is seeking feedback on design concepts for the Collaroy Disability Tourism Precinct,’ something you can read about in Disability precinct design feedback wanted at the Manly Daily. Also see Windfall for disabled, also by Brenton Cherry at the Manly Daily:

The vision is to create a holiday destination for people with disabilities and their carers as well as a specialist economic business hub for Collaroy.

It would be a place where not only access to the beach, including to the water using an amphibious wheelchair, is possible, but also restaurants, public transport, accommodation and entertainment facilities.

Here’s the page on the Warringah Council website. Collaroy is a beautiful place on Sydney’s Northern Beaches. I am so excited to hear about this proposal, and hope that more people will be able to enjoy that stunning beach!

Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited. And have yourself a fabulous weekend.

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 2 December, 2010

I am quite, quite as shocked as s.e. that it is December! 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?

There’s Respect, and Then There’s Respect by a rather strikingly beautiful, talented and intelligent woman by the name of Chally at the Don’t DIS My ABILITY blog:

I’ve been thinking about how “respect” for people with disabilities is often framed in negative and condescending terms. We’re only worthy of respect insofar as we play the inspirational martyr. We can be respected for struggling through what are supposedly inevitably hopeless, helpless lives. But we can’t be respected for fighting back against the systemic barriers keeping us down, or questioning our care.

Disabled want more by Fungi Kwaramba at The Zimbabwean:

The National Association for the Care of the Handicapped (NASCOH) said that 10 per cent of the country’s population live with disability. Even though there is a Disability Act the laws has not been enforced, and this has seen the continued exclusion of the disabled from mainstream activities.

UK: Spending cuts threaten disability arts festival by Helen Carter at The Guardian:

“DaDaFest is here to present the work of deaf and disabled artists, whose work is on a par with mainstream artists,” says the festival’s artistic director, Garry Robson. “Disabled and deaf people are not simply passive consumers of a tragic destiny but active participants in all areas of life, with a unique and valuable cultural perspective that we plan to share during the festival.”

Australia: Editorial: Shortfall in disability services at AdelaideNow:

While many services are stretched on days such as Christmas, it is hard to imagine an able-bodied person needing to book a taxi three months early to ensure they can enjoy lunch with family and friends. This shortage needs to be recognised.

Nearly half of Israel’s disabled forgo food, medicine, heat by Ruth Eglash at the Jerusalem Post:

According to a study by the National Commission for People with Disabilities, which was released on Monday ahead of the International Day of People with Disabilities to be marked worldwide on Friday, out of roughly 1.5 million Israelis who consider themselves disabled, 43 percent of those with severe disabilities and 29% with moderate disabilities went without food at some stage over the past year, while more than one-third of those with severe disabilities and 23% with moderate disabilities had to miss out on essential medication because they could not afford it.

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

Recommended Reading for 19 November, 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?

little light at Questioning Transphobia: clamavi ad te. Please note that the post discusses suicide, abuse, and murder of trans people. If you think you can handle it, though, it is powerful reading, as is everything little light writes.

When you have been told you are less than human–less than sacred–less than beautiful–your community has failed you. When you believe it, it is because your community has failed you. I do not intend to mince words. … You deserve better. Because you are not the problem. You are not broken. You are not worthless. You are not a problem and you are not a mistake.

Liz at Dis/Embody: Thoughts on World Usability Day:

Now, of course, usability is not the same as accessibility; it is focused on ease of general use, for a mass audience. And, usability doesn’t always incorporate a universal design perspective in which the needs of those who face the most challenges are centered, with the understanding that products designed for that group may also be more usable by others.

That said, usability and communication is an interesting theme, as it seems to implicitly tie back to media accessibility in particular.

Interviews conducted by Meena Bakhtash at the BBC: Voices: Disability and the Hajj to Mecca:

The annual Hajj pilgrimage – a religious duty that every adult Muslim is expected to do once in their lives – can be a tough challenge.

But the obstacles are infinitely greater for Muslims with disabilities, who choose to take the journey.

Melissa Jenkins at the Sydney Morning Herald: Disability package gets tick:

The Victorian government is taking the right approach by directing the majority of its disability package towards early intervention, advocacy groups and unions say.

Kirsty Whalley at This is Local London: Disabled girl from Norbury a “health and safety risk”, says school

A disabled 11-year-old girl has been rejected by an academy school because she poses a “health and safety risk” to other children.

That’s all for this time. Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.

Recommended Reading for 12 November, 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?

Sydney Morning Herald: Why I’m not in the queue for the disabled loo by Liz Ellis.

There was a debate over policy and procedure but ultimately it came down to human conscience, something that I am incredibly appreciative of. But should I really have to rely on human conscience overriding policy and procedure?

The Globe and Mail: The sound (and sight and feel) of music for the deaf by Jill Mahoney.

Frank Russo helps make music for the deaf.

Working with a team of researchers, the Ryerson psychology professor invented a chair that allows deaf people to feel music through vibrations. He also works with both deaf and hearing musicians to compose music that focuses on vibrations and vision rather than sound.

The Los Angeles Times: Mentally ill prisoners get a second chance by Lee Romney.

Mental health courts are operating in 29 California counties, helping offenders and reducing crime in their communities.

As I mentioned a few days ago, I’m writing for the NSW Don’t DIS My ABILITY campaign at present. Here, have some tacky self-promotion!

…and I’m feeling good

This will be a bit of a shock if you’re invested in disabled bodies as broken and horrible and unlovable, so brace yourself.

I love mine.

Who Gets to Speak?

I’ve been thinking about this man ever since, and the way he read me as abled. But mostly I’ve been thinking about assumptions about the kinds of people who do disability advocacy. Namely, there’s a strong perception amongst the abled public that people with disabilities are unable to advocate for ourselves. Supposedly, our abled family and friends do it all for us.

That’s all for this time. Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.

Recommended Reading for Wednesday, November 10

I am apparently a month behind as I originally dated this for October. Oh self. If it were October, I wouldn’t be so far behind! Wishful thinking?

Captain Kitt at A Gentle Nerd of Leisure: Our Mental Health System? More Mental than Healthy! (Note this post also includes discussion of eating disorders, self harm, and sexual assault but mostly focuses on experiences within the Australian mental health system) (via vass)

Thing is, often those services are really hard to access! I’m great with search engines – thanks to a librarian Mother – so it’s easy for me to find where the services are. Actually getting help from them? Not so easy.

Laura Hershey at Spinal Cord Injury and Paralysis Community: Fairness for Attendants: Enacting Justice in an Unjust World

We can start by acknowledging the profound disconnect between the importance of the work and the compensation it offers. In understanding and analyzing this, we can call upon a radical understanding of how disability justice and worker justice intersect. Providing hands-on personal care has acquired over the years an aura of sentimentality. People are assumed to do such work out of pure compassion (which translates as pity), or because “it’s so rewarding” (rewarding in a vague, emotional, non-material sense). Within this framework, disabled people embody neediness, while support workers cheerfully fulfill our needs. Disabled people are passive objects of support workers’ active “caregiving.”

Elizabeth McClung at Screw Bronze: Aren’t You Proud?

We are, disabled and Able Bodied, all types of bigots, and one of the most supported forms of bigotry is how we encourage each other to give in to our fear of illness, and altered human function and form. Drool, and averting the eyes is ‘doing you a favor’ – haha. Yes, because having everyone glace, look away and then talk about you, because your being alive makes them uncomfortable is helping me? No, helping them. It is no different than spotting who the odd one is in grade school, and somehow, they end up with no friends. They are stared at. They are, as you will well know if you were one, asked, “Why do you keep coming?”, and the idea of invitation to a party, or even having anyone show up at one you host is laughable.

crabigail adams at if you don’t have anything nice to say, come sit here by me: i am disabled

of course, this is a fixed income. if i find one day that it’s not enough money to get by, i don’t have any options. i can’t apply for a better-paying job. i can’t further my education in hopes of a professional career & the attendant boost in income. this is it. & there are other caveats as well: if i ever decide to live outside the united states, i lose my disability money altogether. if i ever get legally married, the government will pull the extra money i get from the disabled adult child program & i’m back to just my $525 or so in disability money. i would have to rely on my partner to support me financially, which is a lot to ask of someone, & which is something that makes me very uncomfortable. i’m not sure what the rules are around having assets (ie, if i were to sign a mortgage, even if i wasn’t the sole person responsible for paying down the mortgage). i’m not sure how social service programs i may be eligible for if i were to have a child (ie, WIC) would impact my social security income.

Casekins at If My Hands Could Speak: Martha’s Vineyard – Utopian Society (Caseykins is not Deaf – I’m linking this because the history is very interesting.)

The prospects for deaf people on Martha’s Vineyard were completely different. Many of the former residents of the island were interviewed, and they paint an idyllic picture of what it was like to live in Martha’s Vineyard during this time. Because everyone had a deaf family member, everyone in the community knew sign language. Deaf people were farmers, store clerks, anything they wanted to be. Hearing people would sign to each other over the large expanses the island farms created, a deaf person could walk into a store and the clerk would always know sign. Deaf people were even elected to high political office, becoming mayors and council members for the island, a thing unheard of in the rest of the country. When telling stories about the community, the people who were being interviewed could only remember after much prompting if the people they were talking about were hearing or deaf.

I’m closing comments on this one because I’m hip-deep in alligators (do people still say that?) and I always feel bad when people’s comments sit on Recommended Reading posts for days until someone can look at them.

The 2010 Don’t DIS My ABILITY Campaign Has Kicked Off!

People. People. I cannot even tell you how excited I am. In November-December in New South Wales, the awesome-est state in Australia1, we have a little something called the Don’t DIS My ABILITY campaign. There are loads of events run around the state leading up to the International Day of People with a Disability.

My personal favourite bit is the campaign magazine, Made You Look. You may remember that Lauredhel wrote about playground accessibility for disabled parents for the magazine last year. This year, Ouyang Dan and I both contributed pieces. OYD’s is on ableist language and is called “Think before you speak,” mine are “Type (re)Cast,” about popular culture representations of PWD, and “Seen and not heard,” on my experiences of being young and disabled. If you’re in NSW, you can pick up a hardcopy at your local library, all over Sydney and at loads of regional newsagencies (full list of places you can obtain the mag here). If you are elsewhere, you can download a copy, in one go or in sections, if that’s easier.

But that’s not all! Check out the Don’t DIS blog. I’m going to be writing there over the next month about such topics as who gets to speak about disability advocacy, narratives of disabled laziness, where conversations about disability tend to stop, body image while disabled and what respecting disabled people means. You yourself can participate: check out this post about blogging for the campaign here.

It’s going to be a fabulous month, readers.

  1. My esteemed co-blogger Lauredhel might disagree with me there.

Recommended Reading for 1 November, 2010

Welcome to November. 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?

Queen Emily at Questioning Transphobia: attacking the already vulnerable:

In the UK, people with disabilities have been among the hardest hit by the recent Thatcher 2.0 ConDem cuts of the Osborne Review. The employment support allowance (ESA) which was previously able to be claimed until the person finds a job has now been set with a limit of one year. I’m sure that’ll be of great comfort to people, cos disabilities also expire after year amiright?

It’s election time in the United States. Melissa Mitchell at Service Dogs: A Way of Life: Cast your vote November 2.

I ask you, my loyal readers how can we as a community expect our current rights to continue to be protected, our equity as members of society to be validated, or our issues to be seen as important when we are not seen as a community that votes?

Also, Leah at Cromulent Words: Voting and Privilege:

And what do you need to do after you’ve recognised your privilege of voting access? You can either use your privilege to uplift the people you oppress or you can ignore it and continue to harm (directly or indirectly) the most vulnerable people in our country.

New South Wales, Australia: ABC News: Thousands rally for disability services funds

The State Government committed funding for disability services five years ago under the Stronger Together program, but money for the next five years has not been included in the forward estimates of the next budget.

Times of India: Sleep disturbances ups work disability:

A new study, conducted by the Finnish Institute of Occupational Health in collaboration with the universities of Turku and London, has revealed that sleep disturbances increase the risk of work disability and may slow the return to work process.

That’s all for this time. Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.

Recommended Reading for 22 October, 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?

At Astrid’s Journal, Multiplicity Myths:

I wrote this collection of myths a few years ago, intending to create a multiplicity page on my website. That never got to be, but I still like this list. I have edited some parts where appropriate.

At Tunisia Online News, Tunisian-Italian project to benefit blind people in Gafsa:

A project as part of a Tunisian-Italian partnership to promote the status and integration of the disabled in society, will soon lead to the building of a house for visually impaired and blind people in Oum Larayes in the governorate of Gafsa (South western Tunisia).

From the Los Angeles Times in the United States, Georgia settles suit on confinement of disabled people:

In a settlement that will serve as a model for enforcing the rights of the disabled, the Justice Department reached an agreement with Georgia to move many patients with mental illnesses and developmental disabilities out of the state’s notoriously dangerous psychiatric hospitals and into the community.

From 3News.co.nz, NZ offer world first service for deaf:

Until today, [15 October] New Zealanders who are hearing impaired and deaf have had to use a fax machine to make contact with 1 -1 -1.

[…]

At midday a system was switched on which allows the seven thousand members of the hearing impaired and deaf community to text for help.

From Pro Bono Australia, Judge Caps Court Costs on Disability Case -PIAC:

A decision in the Federal Court is expected to have national ramifications for public interest litigants according to the Public Interest Advocacy Centre, PIAC.

[…]

The Public Interest Advocacy Centre was acting on behalf of Julia Haraksin, who tried to book a seat on a Murrays coach from Sydney to Canberra.

Bizarrely enough, I’ve taken a Murrays bus from Sydney to Canberra myself and was just thinking about their lack of accessibility yesterday! Here’s hoping Julia Haraksin wins the case.

That’s all for this time. Send your links to recreading[@]disabledfeminists[.]com. Let us know if/how you want to be credited.