All posts by Ouyang Dan

About Ouyang Dan

is an extremely proggy-liberal, formerly single mommy, Native American, invisibly disabled, U.S. Navy Veteran, social justice activist and aspiring freelance writer currently living in South Korea on Uncle Sam's dime. She has a super human tolerance for caffeine and chocolate and believes she should use those powers for good. She said should. She is not a concise person, and sometimes comes on a little aggressively in comments. Sometimes her right arm still twitches when military brass walks past her, but she would rather be reading YA Lit or pwning n00bs. She can be found being cliche about music, overthinking pop culture, and grumbling about whatever else suits her fancy at her personal website, random babble.... She also writes about military issues for Change.org's Women's Rights blog. If you have something interesting to say email her at ouyangdan [at] disabledfeminists [dot] com. Lawyers in Italy looking to hold lottery winnings in her bank account may wait longer for reply.

Recommended Reading for 05 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.

Raising My Boychick: Vocally crazy: on privilege and the risks and benefits of being out

Openness, vocalness, outness are good for an invisible, marginalized group: we’re here, we’re [crazy], get used to it! It helps to replace highly distorted stereotypes with real faces, real lives, real persons. As more and more people in a group are out, more and more people not in that group know someone who is — and suddenly, they start caring. No longer is it just “those people” who have to worry about discrimination and hatred and violence and the loss of rights and dignity; it is someone you know, someone you might care about, someone you’re willing to stand up for. These are all very good, very important things.

But openness, vocalness, outness can be dangerous, even lethal, for an individual who is marginalized: when someone comes out as mad (or queer, or trans, or a rape or incest survivor, or any other oft-invisible oppressed way of being), they might risk losing their job, losing their children, losing their life. Outness cannot be dictated, imposed, or required. It must not be. It can only be chosen, based on an individual assessment of risk and worth, and the outcome of such calculations will change with each individual, and often with each situation.

Longwindania: PSA

One of my friends is working on a sexual education book for people with disabilities and their partners. Shanna’s very knowledgeable and passionate about responsible queer-positive, disability-friendly, kink-friendly sex education.

Disability on Dreamwidth: New licenses premises access law in Scotland

The Barred! amendment, passed by the Scottish Parliament as part of the Criminal Justice and Licensing Act, requires landlords to show how their premises can be accessed by disabled customers, when they apply for a license. The amendment is an important milestone in Capability Scotland’s Barred! campaign which aims to promote better access to pubs and clubs for disabled people.

Valley News: Temporary Custody

The unknown male subject found in the home? He was actually the 34-year-old African-American who owns the home and has lived there for four years.

And the part about taking him into temporary custody?

Hartford police neglected to say that in the process he was: blasted with pepper spray; struck with a nightstick; handcuffed, wrapped in a blanket and hauled — naked — out of his home, according to a neighbor and what the man says police later told him. When the neighbor tried to tell cops that the handcuffed man on the pavement was the homeowner — not a burglar — he said he was threatened with arrest for interfering in police business.

Moving Hands: Ashley Fiolek: a deaf motocross racer (Thanks to maxporter for the link!)

Today, I watched the final womens motocross race. I was about to fast-forward through it – I dislike motocross and I dislike racing, so it’s not a great combo. But then I noticed that someone was signing, so I hit “play.”

Turns out that the woman who was signing is named Ashley Fiolek. She is a deaf 19-year old who has won gold in the past. The segment that I’d seen was one of those special segments where they take a prominent athlete – usually somebody who is looking to repeat a previous victory – and interview her or him. In this case, they asked Ashley how she got involved in motocross and so forth. She communicates in ASL and uses an interpreter. (According to her bio on Wikipedia, she actually went to a deaf school as a child.)

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[@]disabledfeminists[.]com

Recommended Reading for 02 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.

RH Reality Check: Decriminalizing and the Global AIDS Epidemic

The International AIDS Conference’s theme of “Rights here, Right now” was clearly in evidence throughout the five days of the international meeting. An exuberant march through the streets of Vienna, a large human rights networking zone, multiple sessions on various aspects of human rights and numerous poster presentations addressed topics such as rights of sex workers and people with different sexual orientations, monitoring human rights violations, and combating stigma and discrimination. The subject receiving the highest level of attention, however, concerned the law: criminalization of behaviors and groups of people in the context of HIV/AIDS.

MÉDECINS SANS FRONTIÈRES (MSF): HIV/AIDS: The Stories and Trends Behind the Science

Despite the growing evidence that rapid scale up of HIV/AIDS treatment reduces unnecessary death, staves off disease, and reduces transmission of the virus, international donors are wavering and sending the message to scale back treatment plans.

European Disability Forum: From Spain to Belgium: The Disability Itergroup Explores the Job Yet to Be Done

29 July 2010 /// In the whilst of latest European warm wave, slightly before the European Parliament summer break, the Disability Intergroup held two meetings to sum up the achievements of the Spanish Presidency leaving office, and the challenges ahead for the incoming Belgian Presidency. Early July, a second meeting in Strasbourg focused on violence against women with disabilities. Ana Pelaez, one of the leaders of the European disability movement reminded the growing rate of violence against woman with disabilities in the EU.

Change.org’s Race In America Blog: Why Pop Culture Matters to Race Bloggers (Via Racialicious)

It may seem as if race bloggers are exceptionally preoccupied with blogging about pop culture. Indeed, whole sites are dedicated to debating the racial missteps associated with The Last Airbender, with a national boycott of the film underway in protest of the movie’s colorstruck casting. But, before you dismiss these efforts as unimportant, remember that the racial narratives in movies like The Last Airbender don’t just reflect contemporary racial attitudes — they also help define them. In short, challenging these pop culture icons is a key part of understanding — and changing — attitudes towards race in today’s America.

Pizza Diavola: ALERT: HHS Rule Banning Abortion Coverage in High Risk Pools

The Obama administration issued a rule yesterday that denied abortion insurance coverage for women in high-risk insurance pools (limited exceptions for rape, incest, and endangering the life of the woman). What exactly does this mean, aside from the steady eradication of a woman’s right to make decisions about her body, her future, and her reproductive choices herself? Well. The high-risk insurance pools are meant to provide health insurance to people who have been denied access to private health insurance due to pre-existing conditions. As a Planned Parenthood email puts it, these high-risk pools are for “some of the most medically vulnerable women in the country — those with pre-existing conditions such as breast and ovarian cancer, AIDS, diabetes, and other conditions that may make pregnancy extraordinarily dangerous.”

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[@]disabledfeminists[.]com

Recommended Reading for 30 July 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.

abstractions of chinchilla: HAND HOOKS. HOOKS FOR HANDS

Crazy Beautiful by Lauren Baratz-Logsted is the most giftedly bad book I have read in the past year and possibly ever, and if you fail to acknowledge its disastrous triumph, I will punch you in the speen.

rabble.ca: $10 million not enough to restore justice and dignity to Indigenous women in Canada

After 600 Aboriginal women and girls go missing or are found murdered in Canada, the federal government decides to throw-a-bone and give $10 million dollars. In March, the Canadian Minister of Justice budgeted $10 million over two years to address the issue of murdered and missing women in Canada, however, they have yet to figure out how to use the money.

The Neon Season: Never make friends with people who have more problems than you

I was talking (separately) to both sartorias and faithhopetricks about a peculiar YA and middle-grade genre which proliferated in the 70s, 80s, and to some extent 90s, which I think of as the “friendship is pointless” novel. This may overlap with the dog/horse/falcon/best friend/sibling/ALL the dogs die genre, but death is not essential in this genre, and many dead hamster/etc novels don’t belong to it.

In this story, a young person meets a Person with a Problem: they are mentally ill, developmentally disabled, physically disabled, dying, very old, or being abused. The young person befriends them. Catastrophe ensues. The young person, sadder but wiser, learns the valuable lesson that you can’t ever help anyone, and people with problems are doomed.

helenair.com: Women-to-women PTSD: Post-traumatic support

“I asked them how many women from Vietnam they had treated, and he said I was the first,” said Evans, who now lives in Helena. “The first thing I saw, hanging on the wall, was a naked woman wearing only Harley chaps and a helmet. It was a place for the guys, very unwelcoming for women.”

So last August, Evans set out to establish a group specifically for military women, whether in active duty, the National Guard or the Reserve, where they could confide in one another and share their fears, their symptoms, their triumphs and their pain in a safe setting.

She knew the need existed for a women-specific program, since nationwide, 1.8 million women are military veterans, which includes almost 8,000 women in Montana. They make up 14 percent of those in active duty, and 15 percent in the Reserve and National Guard.

Serotek Blog: What is the Future of Screen Readers Anyway?

Serotek hopes wholeheartedly that in 2015 we can say the screen reader space has vanished. This change will be brought about through our efforts as a company, and through advocacy by consumers, to encourage universal accessibility in all mainstream products. When screen readers were invented in the early 1980’s they were essential tools to make an inaccessible digital world accessible. They were never meant to be a business, only a means to an end. They were developed by private companies aided by government funding to correct an inequity and make it possible for blind people to use digital tools to become economically viable again. They were for vocational rehab, helping us get off the dole and back to work as contributing members of society. Unfortunately this wonderful leg up soon became a barrier for blind people. Digital technology raced ahead but without universal accessibility built in. Screen readers lagged behind and rather than leveling the playing field, they tended to add extra cost and training while restricting access to the most advanced mainstream software features. Companies producing screen readers were more concerned with preserving the government funding cash cow than with helping the blind community achieve total equality. Fortunately that business model is finally disintegrating. We’ve been a part of the push to change the model from day one of our existence, but truthfully it didn’t really start to shift until mainstream companies like Apple embraced universal accessibility in their core product design.

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[@]disabledfeminists[.]com

Recommended Reading For 27 July 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.

Actress Marlee Matlain, a pale, middle-aged woman with medium blonde, hair past her shoulders, and who is hearing impaired uses sign language as she addresses guests marking the 20th anniversary of the Americans with Disabilities Act, the law designed to eliminate discrimination against people with disabilities and to make buildings more accessible by wheelchair, on the South Lawn of the White House, Monday July 26, 2010, in Washington. (AP Photo/J. Scott Applewhite)
Actress Marlee Matlain, a pale, middle-aged woman with medium blonde, hair past her shoulders, and who is hearing impaired uses sign language as she addresses guests marking the 20th anniversary of the Americans with Disabilities Act, the law designed to eliminate discrimination against people with disabilities and to make buildings more accessible by wheelchair, on the South Lawn of the White House, Monday July 26, 2010, in Washington. (AP Photo/J. Scott Applewhite)

Feminist Law Professors: CFP: Aging as a Feminist Concern, Jan. 21-22, 2011 Emory University School of Law

Aging is a feminist issue. The elderly, especially the oldest of the old, are disproportionately female. Among the elderly, women are more likely than their male peers to face a number of challenges, including poverty, disability and isolation. Yet, the legal academy, including feminist legal theorists, is only just beginning to pay attention to old age and its implications. This workshop will advance this agenda by bringing together a diverse group of scholars to explore the relationship between feminist theory, law and policy, and the concerns of the aging. We will focus on understanding how the relationship between age and gender can be theorized, as well as exploring how feminist legal theory can inform policy and law in the U.S. and abroad.

PR Newswire: As ADA Turns 20, Harris Interactive Survey Finds Lifestyle and Economic Gaps Still Remain Between Americans With and Without Disabilities

“We are privileged to live in a country that committed 20 years ago to equalizing rights and opportunities for people with disabilities,” said NOD President Carol Glazer. “The disability rights movement lags behind other civil rights movements and we have to catch up. There is a role for everyone. Governments need to remove disincentives for people with disabilities so they can start to work. Businesses need to realize the enormous contributions workers with disabilities can make. Schools need to prepare students with disabilities sooner for the world of work. And Hollywood should routinely feature more people with disabilities in their TV shows and movies.”

NPR: RI Rep. Langevin Presides over House for 1st Time

Langevin said his temporary turn wielding the gavel marks an important step for people with disabilities and he hopes it inspires others.

“What a powerful symbol of inclusion and opportunity for anyone who wants to serve in the United States Congress,” he said in a telephone interview with The Associated Press on Monday. Congress has become increasingly accessible in the past decade for people with disabilities, he added.

Post-gazette.com: Pennsylvania getting up to speed on assisted living care

Now that it’s an official designation, the door is open for the state’s 1,400 personal care homes to apply for assisted-living status, which carries higher standards in terms of larger living space, private bathrooms, kitchen appliances, resident independence and other aspects.

No facility is required to change to meet the requirements of the new category — and it’s impractical for most older and smaller homes to do so — but if they don’t, the door is closed to them to market themselves as “assisted living.” They also will be shut out of new government funding that is supposed to cover facilities’ cost of caring for a limited number of low-income, assisted-living residents sometime in 2011.

“If indeed the state starts funding assisted-living services, it will of course encourage more providers to get into it,” said Ron Barth, president of PANPHA, a state trade group of nonprofit long-term care operators.

NPR: How the Disabilities Act Has Influenced Architecture

[Audio at the link with transcript]

Prof. PONCE DE LEON: So I have a private practice, and we designed a library for Rhode Island School of Design about now six years ago. And in the project, we designed with universal design principles.

So for example, when we designed the cubicles for the library, no two cubicles are actually the same. We used software that allows you to design for variation as a way of creating a whole range of cubicles that had different sizes, differing height tables, different height seating, different widths, so that we could accommodate many different body types in a very subtle way.

SIEGEL: So depending on one’s individual needs, one’s individual size, or for example if one used a wheelchair, you could find a space that would work for you in that.

Prof. PONCE DE LEON: Exactly. You’re actually acknowledging that we all have different degrees of abilities. So at RISD, since you have a student body that is there for four or five years at a time, there was a great possibility that a student may find actually their favorite spot, maybe because their legs are longer than the average or maybe because their height is a little shorter. And it enabled us to embed different ranges of abilities within the design of the space.

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[@]disabledfeminists[.]com

Quick Press: Action For Access

Passed along to me via email is this downloadable and printable survey, Action for Access.

You go to the website, and follow the instructions for download. The survey can be taken to locations on the map, then matched up (to my understanding) with the online version, to rate local businesses and establishments in the UK on their accessibility.

There are instructions for following up on the information you provide.

If anyone is interested, or has tried this survey and followed up on it, I would be interested to know how successful they found it (or even how accessible they found the survey itself).

Recommended Reading for 26 July 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.

i<tag>: Interactive Technology and Games Conference

(Conference Information at the link)

Miami Herald: National Guard and Reserve Suicide rates climbing

Explanations are hard to come by. The suicides could have nothing – or everything – to do with the victims’ military service.

“It is the separation from our families, it is the lack of a support structure in our personal lives sometimes, financial challenges, relationships – we know that,” Navy Adm. Mike Mullen, the chairman of the Joint Chiefs of Staff, said during a recent talk about the suicide problem to troops in South Korea.

Switchin’ to glide: “J’y étais” “I was there” Histoires de femmes en zones de conflit. Stories of Women in Conflict Zones.

[Trigger Warning]

(Transcript at the link, and link to French/English bi-lingual video)

Those interviewed have been displaced by mass violence, ranging from the Holocaust to the Rwandan and Cambodian genocides, to political violence in Haiti, Latin America and South Asia. The project hopes that the act of listening intently to how these survivors speak of their memories, may bring us to an understanding of what these experiences mean to them and how they can be retold. Recording their process of remembering and telling will also help us better understand the impact of mass violence and displacement on those who have sought refuge in Montreal and the ways in which their sense of home and community has been affected.

Through the practice of oral history, Life Stories intends to create cultural and historical materials for Montreal’s diverse communities, to foster collaboration and partnership between them, to develop interdisciplinary pedagogical tools and to make a significant, original contribution to the preservation of historical memory in Canada, by raising questions about the long-term repercussions of crimes against humanity.”

Scottish Disability Sport: Paralympic Pathway Experience

As an extra bonus for the young people, Paralympian Simon Jackson, plus tandem pilot Olympian Craig MacLean, GB Wheelchair Rugby Player Michael Kerr and Scotland CP Football captain Jonathan Paterson attended the event. They also participated in a Q & A session. This offered the youngsters  an opportunity to engage with the established performance athletes and receive tips about their personal involvement in disability sport. Fraser Penman, a pupil from Uddingston Grammar School, was delighted with his opportunity to speak to a Paralympic champion. “It was great to talk to Simon,” said 15-year-old Penman. “He gave me the address to his website because I was interested in maybe trying to get involved with judo.”

Change.org’s Women’s Rights: It’s Not Just Bullying, It’s Slut Shaming: The Case of Phoebe Prince

If South Hadley and other Massachusetts schools are really serious about instituting anti-bullying programs, they need to look further than research on teenage psychology. They need to look at a culture that sexualizes women at an extremely young age and then castigates them for their sexuality, and that consistently engages in the victim-blaming of girls and women.

A high-schooler interviewed for Bazelon’s story said it best: “The girls found out she’d been with the boys, and true to high-school girls, they got mad at the girl instead of the boyfriend.” This isn’t just “normal” behavior for high school girls. It is something taught by our media and our society, and something that has been largely ignored in the case of Phoebe Prince.

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[@]disabledfeminists[.]com

Recommended Reading for 23 July 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.

Cube: Modern Warfare 2: Gaming with a Disability, Junkyard talking with Ian (MW2 Gameplay/Commentary)

I was able to get an opportunity to talk with Ian who is paralyzed from the middle of the chest down. Not letting his situation dismay him from playing video games he has been able to adapt and come up with a solution to overcome his disability.

Sustainable Diet: Common Ground Organic Farm & Veteran Cooperative

[donation solicitation at the end of article]

The model-of-care has been successfully demonstrated with over 60 Marines, veterans and military families at the current program called Operation Recovery.  The model-of-care is now positioned to expand and serve hundreds of active duty, veterans and their families through a financially sustainable program called, The Common Ground Organic Farm and Veteran Cooperative. Mr. Bornt has a lease-option and an opportunity to purchase the ideal property for the expansion – a 70-acre farm with existing residences and infrastructure within 40 miles of downtown San Diego and 28 miles from Camp Pendleton.

The potential of the veteran farm cooperative has generated collaborative interest from Camp Pendleton Marine Corps command and Chaplains, Balboa Hospital ASYMCA, Alliant University, Palomar Collage, the VA PTSD clinic and many other local and national veteran service agencies. The farm will provide a safe, familiar decompression zone, immediate veteran employment, veteran short-term housing, and peer-to-peer treatment training and veteran micro-enterprise development.

Wheelchair Diffusion Blog: Marine Veteran Invents Powered Beach Wheelchair

Blaker states that he was inspired and motivated by his Marine buddies, some of whom suffered injuries that made mobility difficult.

“I worked on cobras and hueys the avionics systems, so that’s where I got all my understanding of electronics and what not,” explained Blaker.

Blaker served six-years as a Marine, and was stationed all over the world, and after finishing his service, he now spends his time building wheelchairs that work on the beach. He was inspired to extend the freedoms non-handicapped people enjoy to those who still want to experience the beach.

Rhivolution (Dreamwidth): Practicing my dropkick skills: OCD

So I saw the book Saving Sammy at the public library, and after picking it up and skimming the inside cover, I sort of couldn’t bear to read it, mostly because the subtitle is ‘Curing the Boy Who Caught OCD’.

Caught. OCD. Cure.

Now, for those of you not aware, a few years back, the US National Institute of Health concluded that in some children with sudden onset OCD and/or Tourette syndrome (henceforth TS), the conditions appeared after the children had had a strep infection, and that this could possibly be causal. Your bog standard OCD and TS are, apparently, slow onset in pre-pubertal cases, and these cases came on rapidly, like a switch was thrown. This proposed condition is called PANDAS, an acronym for something I’m too spoon-less to write out here involving strep and pediatrics and psychiatric disorders and stuff.

Teach Me Tonight: CFP: Fat Studies Edited Anthology

CFP for fat studies edited anthology

Julia McCrossin and I were approached at the PCA/ACA Conference by a publisher and asked to put together a fat studies anthology. The result is the call for papers listed below. Please feel free to distribute far and wide with our thanks.

If you have any questions, please feel free to email either Julia or me. Our addresses are listed below. Huge thanks, and I look forward to hearing from many of you! 🙂

~Lesleigh Owen

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[@]disabledfeminists[.]com

Recommended Reading for 22 July 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.

Repeating Islands: Call for Submissions:

Simone A. James Alexander and Dorsía Smith Silva are seeking submissions for an edited collection on Caribbean Mothering (to be published in Fall 2012).

This anthology will examine the diverse and complex experiences of motherhood and mothering from a broad, interdisciplinary perspective. The organizers welcome submissions that explore major cultural, political, historical, and economic factors that influence the lives of Caribbean mothers, such as migration and transnationalism. Also encouraged are writings that represent the relationships between Caribbean mothers and their children; perspectives of single Caribbean mothers; relationships of extended motherhood in Caribbean communities; and colonial, post-colonial, and modern representations of Caribbean motherhood from literary, historical, biological, sociological, political, socioeconomic, ethnic, and media perspectives. This incorporation of a variety of disciplines and methodologies will give insight to the issues on mothering within the Caribbean context and provide a space that recognizes the significance of Caribbean mothering. The aim of this volume is to foster work on mothering that integrates the disciplines of feminist ideologies, literary criticism, and cultural analysis as well as represent the diversity of the Caribbean islands and the Caribbean Diaspora.

WIRED: Danger Room: Obama Loves This Freaky PTSD Treatmen; The Pentagon, Not So Much

Concerns over risks, especially that the injection can trigger seizures, hit a key artery or puncture the lung, are valid, Lipov admits. Still, they’re rare: A 1992 study evaluating 45,000 SGB cases found adverse effects in 20 patients. And Lipov has come up with a distinct method, which he calls the “Chicago Block,” that targets the C6 vertebra rather than the traditional C7. Because C6 is farther from important arteries and the lungs, it’s less likely to be implicated in problems during an SGB procedure.

“Realistically, 1 in 100,000 people might have serious complications,” he admits. “Say we treat 300,000 veterans — that’s three people. Compare that to the military’s suicide rate.”

Online Journal: Don’t you know there’s a war going on?

For an American military already stretched to the cracking point, the human cost spreads beyond the immediate casualties of the battlefield. June was the worth month ever recorded for US Army suicides, the service reported last Thursday, with soldiers killing themselves at the rate of one per day, 32 confirmed or suspected in all. Twenty-two of them had been in combat; 10 had been deployed two to four times. What’s more, by the spring of 2009, according to The Washington Post, “The percentage of the Army’s most severely wounded troops who were suffering from PTSD [post traumatic stress disorder] or traumatic brain injury had climbed to about 50 percent, from 38 percent a year earlier.”

The one bit of good news: “Senior commanders have reached a turning point,” the Post reported on Sunday. “After nine years of war in Afghanistan and Iraq, they are beginning to recognize age-old legacies of the battlefield — once known as shellshock or battle fatigue — as combat wounds, not signs of weakness. [Army Vice Chief of Staff] Gen. Peter Chiarelli . . . has been especially outspoken. ‘PTSD is not a figment of someone’s imagination,’ Chiarelli lectured an auditorium of skeptical sergeants last fall. ‘It is a cruel physiological thing.’”

Sanguinity: To Kill a Mockingbird, Huck Finn, High School Curriculums, and Canon

One huge tension coming up is the ought/is problem. Yes, I think you could probably do a great lesson plan that includes [To Kill A Mockingbird] if you teach TKAM from a historiographical perspective (as one might do when studying sketchy roadside historical markers): who wrote it? when? why? why did they write it this way? what else was going on then? who did it become popular with? why? And so on. I’d also pair it with Mildred Taylor’s Roll of Thunder, Hear My Cry to open up a discussion of other ways a similar story could be told, and differing opinions about how similar characters or situations would play out. (I cannot find the comment now, but someone pointed out that TKAM casts Tom Robinson as a minor, almost throw-away character in the story of Tom Robinson being on trial for his life!) I like Bingo’s suggestions of how to demonstrate that the issues of racism in TKAM are not ancient history, nor confined to the South. I’d also incorporate many of Larissa’s ideas about teaching Huck Finn, if I could find parallel resources to do it with TKAM (or leverage the Huck Finn resources to work with TKAM). Additionally, because TKAM and Huck Finn are both canon, I think you can have an excellent discussion of the phenomenon of canon, how canon got to be canon, what doesn’t appear in canon, how does canon shape and/or reflect society, etc. Most importantly, I would try to pull all this off so that the discussions are worthwhile for students of color — I wouldn’t want this to become the Great Race Learning Experience for the white kids, while the black kids are sitting there having to process/deflect/cope with the racism in the novel(s) but not getting anything out of it to make their stress worthwhile.

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[@]disabledfeminists[.]com

From Sea to Shining Sea: Bad Ass Disabled Vets Refocus Their Military Training

Military personnel learn to apply their earliest military training to many parts of their lives. From the first moments of boot camp our lives are broken down and that training is ingrained into our very being. We take that training with us long after the uniform hangs unworn in the closet and the neckerchiefs lie in the drawers. Even today, I can write a business email in all acronyms, because it is still the most formal and proper way I know. One time we “tossed racks” because Kid couldn’t find something and insisted it wasn’t in her room. I can fit many t-shirts in a drawer or suitcase, thanks to a certain Chief, who, incidentally was not my division chief, but who seemed to think the sun shone from my arse nonetheless.

For some, it helps to pull us through the unexpected twists that life hands us. I am sure I am not the only person who will endure more pain than is required before complaining because I believe it is expected.

For Marc Esposito, a 26 year-old Air Force Sergeant and member of a special tactics squadron until his humvee hit a roadside bomb, his training helped him focus trough the year of rehab at two separate medical facilities, including the Walter Reed Medical Center, where he re-learned how to walk.

Now he is using that focus — that training — to ride with Sea to Shining Sea, to raise awareness for the Special Operations Warrior Foundation for wounded veterans, and in his own words,”[T]o hopefully show any kind of disabled American you are still capable of doing amazing things […] and hopefully change the perception of what it means to be an athlete.”

Sea to Shining Sea is a group of 17 cyclists, most of them disabled veterans, who started the journey of some 4,000 miles from San Francisco on 22 May, by dipping their wheels in the Pacific Ocean, and plan to end it by dipping their wheels in the Atlantic in Virginia Beach on 24 July. They have averaged about 50 miles a day.

Some people don’t understand that the training doesn’t leave you. It isn’t something you take off, and in some cases, this is a very good thing. The drive it takes to recover, the intensity it takes to stare illness and injury head on, the nerve it takes to accept that your career may be forever ended or changed … all of that comes from the part of you that is broken down and rebuilt ahead of time. All those weeks, months, years ago when you step off the bus and dress to that line for the first time. They rebuild you up, and it becomes a life skill that you use to accept, use, and build upon.

And it allows you to meet any task head on, using whatever you have left.

Sometimes all you have left is enough and you have no other desire but to give it.

Because that is all we know.

We know to take what we have left, and give something back.

Sea to Shining Sea is nothing short of Bad Ass, and I am not doing them justice, because I have struggled over days to write this post. I have wept a little at what these people have done with what they have kept and done. I am so proud of them, and so humbled to know that they, through their hardest, darkest times, have pulled through because of a common link and have spun it around to something positive, and to something healing, and are finding a way to use it to raise a positive message for disabled veterans everywhere.

Thank you to s.e. smith for the link, because ou is always looking out for me.

Recommended Reading for 19 July 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.

Hope Is Real: Fibromyalgia Is Not Caused By Men

I remember the invite said that the speaker thinks women have fibromyalgia, because of the stress of men not providing enough for women. This statement offends me to the core and it is just another example of patriarchial bullshit. It is not that I do not think we need each other, we do. People need people in order to survive, but I do not believe that there is one group of people who needs to care for womyn more than another. There are all kinds of communities of people who care for each other. What I take the most offense is it is the language of domination. It is not men who need to take care of womyn, but rather it is people that need to take care of people. I am not interested in someone solely taking care of me, but in being in a relationship where people take care of each other. I am interested in reciprocity

CTV News: Counsellors cite Afghan war for military domestic abuse [trigger warning for descriptions of violence]

“Our anecdotal evidence is that there is an increase in the amount of domestic violence, and in the amount of children who are seeing violence in the home.”

Many military members are now shouldering the residual stress of two, three or four tours in Afghanistan or more, Lubimiv said.

“When a soldier returns home, many have talked about feeling like strangers, not knowing where they fit. And it takes time to close that particular gap. And if there are, on top of that, mental health issues — or if there is already an issue of conflict or discontent in the couple’s relationship — then all of that gets magnified by the new experiences that they each have faced.”

Most troops will work through their issues on their own and gradually reintegrate, Lubimiv said. “But many don’t respond in that way, need additional help or haven’t been identified.”

Wisconsin State Journal: Vets cheer change on PTSD claim

The rule change will have its greatest effect on Iraq and Afghanistan veterans because so many non-combat personnel encounter roadside bombs, and because there are few places not in danger of mortar attacks or suicide bombs.

Even Wisconsin National Guard troops performing administrative jobs in Baghdad’s Green Zone were within range of mortar rounds that insurgents occasionally lobbed in blindly, said Bob Evans, the state Guard’s director of psychological health.

Most of the 3,200 members of the state Guard who had duties as prison guards or support personnel in Iraq last year underwent stress that could lead to PTSD, Evans said.

“I’ve seen people who weren’t even close to the battlefield who came down with PTSD and anxiety disorders,” Evans said.

Anishinaabekwe: We Are a Generation of Healers

We are a generation of healers because we can choose to turn the intergenerational trauma to intergenerational healing. We can start with ourselves and our families. I have been really blessed to have a family that is open and committed to healing. I know many people who have had to completely cut themselves off from their family and do healing on their own. In my healing work I have been able to reflect the inner work I have done on my family. In turn, each individual in my family can reflect the healing that they have done onto each other. I have worked in the Native community and will continue to do so. I can reflect and send the healing I have experienced in myself and in my family into the community. Healing happens in a circle.

Deeply Problematic: Wendy Garland dies after abuse and neglect from family

The death of Wendy Garland is horrific. Her abuse went unnoticed, unchecked because of ableism: societal devaluation of people with disabilities and misplaced trust in abled family members. Garland’s death is a direct result of abuse on the part of her caregivers, the people in her life that some want to canonize and position as her selfless saviors. Parents, partners, siblings and other folks taking care of persons with disabilities can be wonderful, but they are not necessarily helpful: they can hinder, they can neglect, they can abuse, they can hurt, they can kill.

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[@]disabledfeminists[.]com