Monthly Archives: February 2010

How Stigma Undermines Good Policies

There is sometimes significant pushback to talking about negative attitudes towards disabilities and PWDs. Those discussion are sometimes criticized for being too abstract, too removed from any practical effects on actual people. Sometimes people suggest that we focus instead on concrete policies and procedures that protect the rights of PWDs, so that tricky decisions aren’t left up to people who may act based on stigma.

As a policy wonk, though, I know that the best policy is only as good as its implementation. And if policy implementation and enforcement is in the hands of people with negative or uninformed attitudes towards PWDs, even amazing, sensitive, and nuanced policies will still lead to awful and horrific results.

For an easy example, imagine a company with a policy that required that  all newly hired employees be informed about their right to workplace accommodations for mental or physical disabilities.  The company works with disability rights groups to create a pamphlet outlining who is eligible for accommodations, what potential accommodations may be available, and the procedure for requesting accommodations and documenting a need for them. The disability rights groups make sure all the information is correct, that the pamphlet is available in alternative formats so it’s accessible, and that it emphasizes that accommodations are an employee’s right, rather than a bonus provided by the company. It is, in short, the perfect pamphlet.

Now imagine how much depends on the person who hands that pamphlet to the new employee. Take one scenario: the employee goes through a complete orientation and then is asked to wait in the lobby. When the employee asks why, the receptionist sighs “oh, it’s some stupid thing required by company policy. Just wait.” After 15 minutes, the designated human resources staffer comes out and thrusts the pamphlet at the employee, saying “Here, take this. It’s something I have to give you for policy. You have to sign here to show that I gave it to you.” When the employee asks what the pamphlet is about, the staffer replies “Oh something we have to do for disability, or whatever. Nobody is ever stupid enough to ask for any of these things, believe me.”

Compare that situation to one in which the employee sits with a single staffer to review all the new employee paperwork. At the end, the staffer says “There’s one more policy to review, and this one is especially important to our company. We place a high priority on accommodating employees with disabilities. Even if you don’t identify as someone with a disability, I want to review this with you so you can see how we ensure that employees with disabilities are equal players in our team. You might notice some employees with special equipment or who seem to have different schedules or other differences. This explains why we’ve provided these accommodations and why they’re not ‘special,’ but are important requirements for us to make sure that we accommodate and retain employees with disabilities.”

Exact same policy. Drastically different implementation that will certainly lead to drastically different effects on the individual employee in terms of willingness to identify as a PWD, request necessary accommodations, and their expectation of how the company will work with them on accommodation issues. I’d imagine that an employee in the first scenario might not ever request an accommodation for fear of being seen as a trouble-maker or someone trying to get “special rights,” or might have to go to a government agency or private attorney to actually enforce accommodation rights.

And those are the problems that can arise when attitudes and stigma complicate implementation of the actual policy as written – in both those examples, the new employee was actually given the pamphlet as part of the hiring process. What’s more troubling is when attitudes and assumptions lead to the policy not being implemented at all. There was a recent example of this with the United States Transportation Security Administration (TSA). As has been discussed extensively on this site and elsewhere, security theatre has resulted in implementation of all kinds of intrusive and extensive checks and searches of people flying commercial airlines. This is what happened last year in Philadelphia:

Ryan was taking his first flight, to Walt Disney World, for his fourth birthday. The boy is developmentally delayed, one of the effects of being born 16 weeks prematurely. His ankles are malformed and his legs have low muscle tone. In March he was just starting to walk.

Mid-morning on March 19, his parents wheeled his stroller to the TSA security point, a couple of hours before their Southwest Airlines flight was to depart. The boy’s father broke down the stroller and put it on the conveyor belt as [his mother] walked Ryan through the metal detector.

The alarm went off. The screener told them to take off the boy’s braces. The [parents] were dumbfounded. “I told them he can’t walk without them on his own,” [his father] said. “He said, ‘He’ll need to take them off.’ ” Ryan’s mother offered to walk him through the detector after they removed the braces, which are custom-made of metal and hardened plastic. No, the screener replied. The boy had to walk on his own.

The TSA policy is extremely clear about how to screen PWDs who use mobility aids such as braces:

  • Security Officers will need to see and touch your prosthetic device, cast or support brace as part of the screening process.
  • Security Officers will not ask nor require you to remove your prosthetic device, cast, or support brace.
  • During the screening process, please do not remove or offer to remove your prosthetic device.
  • The Security Officer will describe the explosive trace sampling procedure in advance to help you along with the process.
  • The explosive trace sampling process may require you to lift or raise some of your clothing in order to obtain the explosive trace sample. (Sampling areas can be accessed by you lifting your pant leg or shirtsleeve or by raising your skirt to knee-level.)

In this case, the attitude of the individual employees staffing the TSA checkpoint in the airport clearly trumped the policy. The parents of the PWD had no choice to comply or not be allowed onto their plane. When they complained to the TSA supervisor on site, they were told to “calm down and enjoy [their] vacation.” There are a lot of negative attitudes and assumptions being displayed here: PWD are probably faking and don’t really need their mobility aids; the dignity of PWDs isn’t important and can be overridden for “security concerns,” and enforcing the rights of PWDs is just making an unreasonable fuss.

That’s why it’s important to fight against stigma. Because it matters.

“Saying conjoined twins are disabled is insulting!”: Evelyn Evelyn, redux

[Cross-posted to Hoyden About Town]

Something that has really struck me about the conversations around Evelyn Evelyn is the reaction that “Conjoined twins don’t have a disability! To say they do is insulting!”

Not all commenters make the link between the two statements – some stop at the first – so I’ll take these two separately.

A little background: Evelyn Evelyn is Amanda Palmer and Jason Webley’s new ‘art project’, presented as fact but understood as fiction, in which they “discover” poor struggling musically-gifted conjoined twin orphan women, save them from their child porn and circus-exploitation past, and help them – in a long drawn-out process, due to the women’s traumatic fallout and difficulty relating – produce their first record. Palmer and Webley dress up as the twins to perform on stage, co-operating to play accordion, ukelele, and sing. They can barely restrain their sniggers while they interview about this oh-so-hilarious and edgy topic. More in the Further Reading.

“Conjoined twins don’t have a disability!”

So, a note on normalcy. The idea that some people would shout in defence “But conjoined twins don’t have a disability!” took me by surprise. I wonder how these people are defining “disability” in their heads, if they’ve ever thought about the subject – do they picture a hunched figure, withdrawn, unable to work, self-care or socialise? Do they picture someone undergoing huge medical procedures, someone with prostheses or other visible aids? What is the image in their heads?

Because disability can be all of these things, and none of these things. Disability isn’t a checklist, or a fixed point. Disability – and normalcy – are socially constructed. Disability is the interaction between a characteristic or a group of characteristics often called “impairments”, and a world that recognises people with these characteristics as abnormal.

Disability is considered a tragedy, a fate to be avoided at all costs. Disabled people are those that society defines as “abnormal”. Disabled bodies are the ones that don’t fit in typical boxes. Disabled people are people that the physical and social environment doesn’t accommodate. Disabled people are considered defective, deformed, faulty, frightening, feeble, freakish, dangerous, fascinating. Disabled people are stigmatised, laughed at, looked down upon, marginalised, Othered. Disabled people are medicalised. Disabled people are defined in terms of how currently-nondisabled people view them.

Disabled bodies are those that are subject to the able-bodied stare.

It is obvious with the most cursory of glances that in our society, conjoined twins are disabled. Society does not accommodate them. They are medicalised from fetushood. They are spectacle. Their operations are videoed and broadcast across the world. They are displayed, tested, stared at, discussed, and mocked, purely because of the shape and layout of their bodies. They are the subject of comedy fiction and “inspiring” tragedy nonfiction.

How can people simultaneously look at this project as funny and edgy and worth paying money to stare at, while considering conjoined twins to be “not disabled”? Why are their bodies so hilarious, then? Why is it so funny when Palmer and Webley cripdrag-up in that modified dress? Why do they snigger and smirk as they talk about “the twins” and their tragic tale? They do this – you do this – because you do see these bodies as Other. Fascinating, bizarre, freakish. Fodder.

People with disabilities resist these definitions, resist being marginalised, Othered, stared at, compulsorily medicalised. (Just as we try to resist, where possible, being beaten, abused, raped, exploited, exhibited, forcibly sterilised.) We laugh at ourselves plenty. We reclaim terms like “crip” and “gimp” and “crazy”. This does not grant able-bodied people free rein to mock us, to play schoolyard imitative games, to use child porn survivors as a little bit of “colour” for their projects.

There is a lot more to be said on the social construction of normalcy. I strongly recommend Lennard Davis’ Enforcing Normalcy . For more reading, check out this booklist at Hoyden About Town, our booklist here at Disabled Feminists, and our blogroll.

“To say that conjoined twins have a disability is insulting!”

This one’s quicker and easier to debunk. No, it’s not insulting. It’s as simple as that. It’s not an insult because being disabled is not an inferior state. Saying that someone is disabled is no more insulting than saying “Lauredhel’s a woman” or “Barack Obama is black”.

Being disabled just is.

~~~

Further reading on the Evelyn Evelyn conversation:

Annaham’s post here at FWD, Evelyn Evelyn: Ableism Ableism?

Amanda Palmer’s blog: The Whole Story Behind “Evelyn Evelyn” [WARNING: invented story about child sexual abuse and exploitation; the other links discuss this also]

Amanda Palmer’s blog: Evelyn Evelyn Drama Drama

Jason Webley: Blog #1 – Evelyn

Amanda Palmer’s twitter, in which she remarks “setting aside 846 emails and removing the disabled feminists from her mental periphery, @amandapalmer sat down to plan her next record.”, and follows up “pain is inevitable. suffering is optional.”

SPIN magazine: Meet Amanda Palmer Proteges Evelyn Evelyn

Sady at Tiger Beatdown: AMANDA PALMER WANTS TO SHOCK YOU. Just Don’t Get Upset About It, ‘Kay?

TVTropes: Rape Is The New Dead Parents

The linkspam roundups: First, Second, Third (and possibly more as time goes on)

Recommended Reading for February 17th

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. I attempt to provide extra warnings for material like extreme violence/rape; however, your triggers/issues may vary, so please read with care.

four people in uniforms and helmets on hockey sleds

new jersey newsroom: Sled Warriors: Children with disabilities teach disabled veterans how to play hockey

Here’s a twist. Imagine a child teaching an adult? Well, it’s being done right here in the Albany area where the kids’ Sled Warriors ice hockey team is holding a teaching clinic for adults.

The twist, you see, is this: the adults are disabled war veterans. Their teachers are youngsters who are athletic, strong-willed, courageous and determined – and physically challenged. It’s all part of the Stride Adaptive Sports program, a fairly new therapeutic recreation-related service for individuals with disabilities that spans many Northeastern states, including New Jersey.

hkfreeman at The Living Artist: Ableist Activism

It is a great irony that as I have become more aware of and invested in the need for social justice activism, I am less able than ever to participate in it. […]

In short, I am irked that right when I am most willing to Do Something, I am drowned in ableist pleas to Do Something that I cannot do. I am doing what I can – my art, blogging, participating in discussions when and where my spoons permit – but in the face of those endless pleas for phone calls, personal appearances, and donations, my best attempts are framed as pathetic excuses for avoiding “real” activism.

Times of Malta: Gozo churches urged to provide easier access for persons with disabilities

The National Commission, Persons with Disability, said today that complaints about lack of accessibility increased by 76 per cent last year compared to previous years. […] Mr Camilleri attributed the increase in complaints to the fact that people with disability were becoming more aware of their rights.

An area of concern, he said, was that despite the commission vetting building development plans submitted to Mepa, several new buildings still did not provide for access for persons with disability, meaning that the buildings were not built according to the approved plans.

BoingBoing: TSA forces travelling policeman to remove his disabled four-year-old son’s leg-braces

Philadelphia TSA screeners forced the developmentally delayed, four-year-old son of a Camden, PA police officer to remove his leg-braces and wobble through a checkpoint, despite the fact that their procedure calls for such a case to be handled through a swabbing in a private room. When the police officer complained, the supervising TSA screener turned around and walked away. […]

The screener told them to take off the boy’s braces.

The Thomases were dumbfounded. “I told them he can’t walk without them on his own,” Bob Thomas said. “He said, ‘He’ll need to take them off.’ ”

Ryan’s mother offered to walk him through the detector after they removed the braces, which are custom-made of metal and hardened plastic. No, the screener replied. The boy had to walk on his own.

Media Access Australia: Promoting captions at a young age benefits Deaf and hearing impaired students

Introducing captions at an early age has benefits beyond the individual child, as it impacts on changing attitudes and practice for all concerned. […]

The article looks at how using captions in a family setting from a young age promotes positive attitudes towards captions. Ensuring that all content viewed in the family home and at school is captioned helps normalise a child’s experience. Griswold also encourages the hearing impaired child to take ownership and become the ‘technology expert’ for switching captions on.

The Guardian: Anti-terror body scanners may be illegal, ministers warned

Ministers should act immediately to ensure that the use of full-body scanners at British airports is lawful, the ­Equalities and Human Rights Commission has warned.

The commission’s head, Trevor Phillips, told the transport secretary, Lord Adonis, ­serious concerns existed about invasion of privacy and there was an apparent lack of safeguards to ensure scanners were operated fairly and without discrimination.

L.A.Times: What makes Sammy run wild [meloukhia’s comment: “…the article gets better. Oh my stars, does it.”]

Obsessed with success, they find themselves in frenzies when the industry’s harsh reality clashes with their desires. Now, their condition has a name: Hollywood NOS. […]

Dr. Todd Zorick, a psychiatrist and professor at UCLA’s Semel Institute, calls the condition “Hollywood Not Otherwise Specified,” or Hollywood NOS. The unofficial term is a wry reference to the “NOS” designation in the Diagnostic and Statistical Manual of Mental Disorders, the bible of psychiatric ailments, which refers to a condition that impairs a patient but doesn’t fit with any specified, recognized disorder. Hollywood NOS describes a negative pattern of behavior for the sole purpose of achieving validation. The patients usually display a combination of symptoms: impulsiveness, anxiety, poor self-esteem and some personality disorder traits.

A program on disability rights in Australia

A couple of days ago, Australian investigative journalism television program Four Corners aired a story called Breaking Point. It covers some of recent Australian disability rights history, personal stories from many individuals and families, discussion of a proposed national disability support scheme, differences between the UK and Australian systems, all sorts of things. It’s rather long at the better part of an hour, but you may find it worth just dipping in, if only a little, particularly if you’re not familiar with disability rights in Australia.

From the program website:

The system of assistance for people with a disability in Australia is broken. Carers know it, charitable organisations know it and so do the governments. Now the federal government says something must be done. It’s holding an Inquiry, with the intention of creating a new and fairer system. It’s even considering a national disability insurance scheme. But will the system be reformed in time to save the families now at breaking point?

Here’s a transcript of the program.

You can access the program itself here as well as extended interviews, further reading and news highlights here.

Do check it out!

Quoted: Rosemarie Garland-Thomson on staring

The first element in the staring process is for the staree to develop a keen sense of being scrutinized. This anticipation and preparedness arms the staree with the proper relational tools to manage expected staring encounters with great effectiveness. The second element in this process is to decide how to oversee the dynamics of the stare itself when it inevitably comes one’s way. If one looks directly at starers, it will only confuse or embarrass them. The staree must assess the precise attitude of the starer, measuring intentions and attitudes so as to respond in the most effective way. Facilitating your starers’ maintenance of face means relieving them of anxiety, understanding their motivations, and working with them to overcome their limited understanding of human variation and their social awkwardness at facing it. The third element is literally manipulating the eyes of the starer. One evaluates when to turn away, stare back, or further extend the stare. Sometimes it is best to allow the staring to go on in order for the starer to get a good look. Another procedure is to use eye contact and body language to terminate the stare as soon as possible, although this risks being interpreted as hostile. Another option is to redirect the stare. For example, some starees report using their own eyes to guide the starer’s immobilized eyes away from the part of their body that has captured the gaze, subtly rescuing the hapless viewer from the embarrassment of the stuck stare and restoring the ritual of casual face-to-face encounters. Finally, the staree can and often must enlist conversation to direct the staring process. Staring has an inherent narrative component that the staree must always address in some way.

Rosemarie Garland-Thomson on page 180 of “Ways of Staring” Journal of Visual Culture 5.2 (2006): 173-192.

I so like this redirecting of power in the staring relationship. Do go read the whole article if you can. Also, some of you might be interested in a video I posted on Feministe recently in which Garland-Thomson (a feminist disability scholar!) talks about her work around staring.

Recommended Reading for February 16th

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. I attempt to provide extra warnings for material like extreme violence/rape; however, your triggers/issues may vary, so please read with care.

frida writes: Valentine’s Day: Sex and Disability 2 [warning: discusses sexual abuse]

Here’s what I want: a movement from a culture of abuse and denial of our rights to sexual autonomy.

The Age: Bible bashing the homeless, Abbott style [This man wants to be our P.M. Seriously. ~L]

I was in Canberra last week and had the opportunity to ask Opposition Leader Tony Abbott whether a government under his direction would continue with the Rudd government’s goal of halving homelessness by 2020. His answer was no.

In justifying his stance, Abbott quoted from the Gospel of Matthew: ”The poor will always be with us,” he said, and referred to the fact there is little a government can do for people who choose to be homeless.

WA Today: Fine print hides risk of genetic test offer

Insurer NIB has begun offering its customers cut-price personalised genetic tests – which could expose them to higher premiums or even leave them unable to get life insurance or insurance payouts.

But the company says it has no ulterior motive and only wants to help its members manage their health. […]

Under the official “Genetic Testing Policy” of the Investment and Financial Services Association of Australia, life insurance companies can demand that a prospective customer hand over the results of any genetic test they have had done.

Vindy.com: Police trained to deal with disabilities

Township law enforcement is becoming more attuned to interacting with residents with a physical or mental disability.[…] “The major thing that can happen is the officer doesn’t realize the disability right away,” he said. “The officer will react on what he perceives is happening instead of what is actually happening.” […]

[Patrolman Tom Collins] said one thing officers should realize is that, like someone who raises his or her voice when worked up, a deaf person’s hand signals become more exaggerated. “Officers shouldn’t take that as a sign of aggression,” he said. […]

Kloss said no matter the severity of the disorder, those with autism usually have a set way of doing things. He said officers need to be aware of what could force an autistic person out of his or her comfort zone.

The Canadian Press: HEALTHBEAT: Drugs tested to improve learning in Fragile X syndrome, may give autism hints

Now a handful of drug makers are working to develop the first treatment for Fragile X, spurred by brain research that is making specialists rethink how they approach developmental disorders. “We are moving into a new age of reversing intellectual disabilities,” predicts Dr. Randi Hagerman, who directs the MIND Institute at the University of California, Davis, a study site. […] The experimental drugs have an unwieldy name – mGluR5 antagonists.

Media dis&dat: California law will clarify information about administering insulin to school-age students with diabetes

“This law will effectively address the dangerous situations currently faced daily by California’s school children with diabetes,” said Dwight Holing, Secretary?Treasurer Elect of the American Diabetes Association. “If passed, this legislation will clarify existing law and help children with diabetes in California public schools to get the care they need and are entitled to under federal and state laws.”

“Depriving these children and their parents of an effective solution to this critical health issue is a civil rights problem that can best be solved by the legislators of this state,” said James Wood of Reed Smith, LLP, pro bono counsel for the American Diabetes Association.

New York Times: Study Suggests More Veterans May Be Helped by Talking About Killing

Mental health experts said the new study confirmed findings from research on Vietnam veterans and did not break much new ground. But they said it underscored that treating stress disorder among veterans is often very different from treating it in people who, say, have been raped or have been in car accidents.

“People don’t understand the moral ambiguity of combat and why it is so hard to get over it,” said Rachel Yehuda, a professor of psychiatry at Mount Sinai School of Medicine in New York. “What makes combat veterans ill is not always about being a victim, but, in some instances, feeling very much both a perpetrator and a victim at the same time.”

Recommended Reading for February 15th

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. I attempt to provide extra warnings for material like extreme violence/rape; however, your triggers/issues may vary, so please read with care.

Rick Hansen with the olympic torch

Rick Hansen carries the Olympic torch. [image source]

Assiya at For a Fairer Today: Olympic ceremonies win

Every day, I am reminded that people with disabilities are considered lesser by society. Which is why, when Rick Hansen rolled in tonight bringing the torch, I smiled so wide my face hurt.

Haddayr: Plucky Cripples Don’t Let Lack of Bingo Card Stop Them [I recommend reading the tongue-in-cheek comments on this one!]:

I asked for help and you delivered! Here’s the final disability bingo card for reporters! Folks seemed like they wanted one for Stuff People Say To You, so I might tackle that one next.

ballastexistenz: Aspificating snobbery over the DSM all over again

And some of us might rightly find it insulting to be referred to as the ones that others had to be oh-so-tragically “lumped in with” (you know, “crazy”, “low functioning”, “retarded”, “autistic”, or other categories that people seem to do their darndest to distance themselves from). Like we have disability cooties or something from the way some people behave, and like having the medical people put us in the same category as our “betters” is such a terrible threat (and like it changes anything about who any of us really are). […]

Anyway as much as this is a rant against snobbery it is also a call to remember what is important. Look to that beautiful shifting central set of attributes that make us alike and different. Stop using the periphery to divide us.

Feminists with Female Sexual Dysfunction: FSD news from the NVA and the DSM

Then, via Helen @ Questioning Transphobia, we also now have access to a draft of the DSM-V (Diagnostic and Statistical Manual of Mental Disorders.) The final version of the DSM-V is currently slated for release sometime in 2013. So be sure to check out that draft, too!

Why is this important? There’s a couple of different reasons; for one thing gender identity disorders and sexual dysfunctions are listed in the DSM, (yes even sexual dysfunctions caused by medical/health issues,) which is a powerful force behind having disorders recognized, researched, diagnosed, and treated. The manual is not without a fair share of controversy, however, particularly from a feminist perspective.

There are also some new sexual health diagnoses up for consideration, including hypersexual disorder (but not Restless Genital Syndrome? Is that up for consideration, and if not, why?) sexual coerison disorder, sexual disinterest disorder in women and men (related to hypoactive sexual desire disorder,) and, notably, Genito-Pelvic Pain/Penetration Disorder. This would include vaginismus & dyspareunia not due to a medical condition. (Pain due to a medical condition would still be under code 625.x – vulvodynia falls under this category.)

Astrid at Astrid’s Journal: Temper Dysregulation Disorder with Dysphoria: The Missing Link or a Can of Worms?

There is a new childhood mental disorder being proposed for DSM-V: temper dysregulation disorder with dysphoria (TDD). When I first read its criteria, my thoughts were: “Finally, it’s about time people are acknowledging not all children’s irritability is bad behavior.” Quite honestly, if this disorder had been around in DSM-IV in 1994, I would’ve been a surefire candidate for a diagnosis, except for the fact that autism should be ruled out first – but then again, I’m not sure autism would’ve been the first thing a shrink thought of when seeing me if TDD had been on the books.

The Pursuit of Harpyness: Ms. M on Living With Chronic Illness, a Guest Post

Those of us who live with invisible illnesses live in two worlds – the one where we “pass” if we are having a good day, and the world we retreat into when our symptoms flare. We may drop out of sight for a day or two or three, but people are so busy they may not notice we’ve been gone.

Other People’s Worlds: Temple Grandin talks the HBO movie

This is a transcript of Temple Grandin’s first interview with the Autism Women’s Network after the premiere of HBO Films’s biopic Temple Grandin. She also talks about augmentative communication and education. […]

Temple Grandin: Mick Jackson picked out Claire Danes. The reason why he picked her out was he’d seen her do a reenactment of the Andrew Wyeth painting “Christina’s World,” which is a painting of a lady that’s crippled. Claire Danes dragged herself across the street in New York like she was Christina, and then Mick decided that she’d be the one. Then, of course, Claire Danes, she became me. She didn’t just act me and learn the lines—she became me.

Pop Culture: The Good Wife & Disability

About two or three weeks ago, I finally got around to noting the existence of the show The Good Wife. And then I watched every episode I could, as quickly as I could, because wow is this show good.

It’s one part legal drama, one part family drama, and one part mysterious conspiracy theory drama. The Wikipedia summary is pretty good: “The storyline focuses on Julianna Margulies as Alicia Florrick, the wife of Peter Florrick (Chris Noth). Her husband has been jailed following a very public sex and corruption scandal. She returns to her old job as a litigator to rebuild her reputation and provide for her two children.”

Except the whole article somehow manages to skip over how feminist the show is. In the early episodes, Alicia has a male coworker who is pretty damn sexist to her, including talking down to her, ignoring what she says entirely, and acting like her being both older and a parent makes her not very smart. Later episodes have her pointing out how she keeps getting shunted aside to “hand hold” clients, which she admits is important but is curtailing her career. And these things are shown as being bad, not as being acceptable because, you know, woman.

The show is filled with interesting relationships between women as well. We’ve got Alicia’s relationship with both her investigator, Kalinda, and one of the managing partners, Diane. Both relationships are complicated by professional needs and the fact that they’re still working in a sexist office environment. Diane is involved in EMILY’s List, and there’s an implication that her “pet project” is looked down on by her male colleagues.

At home, Alicia’s mother-in-law has come in to help care for the kids while she’s working and Peter’s in jail, and their relationship is also complicated, with concerns about parenting and their different views of Peter’s prison sentence.

I just love this show. Love it.

But I’m not just talking about it here because it’s awesome. It also managed to (mostly) side-step some disability fail that I was expecting.

The rest of this is full of spoilers for Season 1, Episode 4, “Fixed”.
Continue reading Pop Culture: The Good Wife & Disability