Aristotle and the Guide Dog

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Photo depicts guide dog Nira, a yellow labrador, sporting a new leather harness at Guiding Eyes for the Blind. She’s smiling. 


Sometimes I think about the world as the ancients did and imagine I can stand in a pond and observe all the chance things nature chooses to reveal. Blindness complicates this but only a little. The aim is to stay open. Watch less television. Live like Aristotle. And soon you find that life with a guide dog raises this art to a higher level–you enter the day on a dog’s terms, walk in Central Park before you are ready for new circumstances. You’re half awake and it’s very early and you find yourself in  conversation with a policeman who admires your dog. It’s also clear he admires you. You’re in the world despite all the obstacles. You’ve trained successfully to be in the world. The policeman doesn’t have to say this. It’s in his voice. He was just walking his beat and he came across a man and dog who together defy the odds. And you have given him something Aristotelian, a minor marvel at sunrise. And he has given you easy, mostly implicit admiration–the way Americans used to do this, the Gary Cooper way. It’s six am and you’ve already thought of philosophy and Lou Gehrig. This is guide dog life. I wouldn’t trade it for anything. 

 

  

Blade Runner

By Andrea Scarpino

“I didn’t grow up thinking I had a disability. I grew up thinking I had different shoes,” Oscar Pistorius said in last week’s lead-up to his 400-meter Olympic race. "I just see him as another athlete, another competitor. What's more important is I see him as another person,” said Kirani James, the runner who won the semifinal heat in which Pistorius came last, and the favorite to win the finals. Upon finishing, James embraced Pistorius; they traded numbers from their jerseys.

Pistorius, a Paralympics star, is now the Olympics’ first athlete who is a double-amputee, a man who runs on two carbon limbs. He has been followed by controversy, by international sports officials and armchair sports analysts insisting that his carbon legs give him an unfair advantage. He has fought hard to prove that isn’t the case—and his upright, bouncing exit from the race blocks—when athletes running on skin and bones can exit almost parallel to the ground, reducing wind resistance—should offer some visual proof to the studies that show he has no advantage.

But none of this is what most impresses me. What impresses me: this quote, again from the lead-up to last week’s race: “I’m not expecting to win.”

I’m not expecting to win. This from an athlete who is used to winning, to breaking records and winning gold medals against competitors like him, as well as competitors with one amputation, with no amputations. This from an athlete who likes to win. Pistorius wasn’t fighting to race against able-bodied athletes in the Olympics as a showpiece, the one “disabled athlete” with access to a world audience. He was fighting to race as a competitor—his competition understands that. He wants to win every time he leans into the starting blocks, every time a practice gets hard.

And this is what most impresses me: to know that you won’t win, that being born without fibulae is not insignificant—and to dedicate yourself to running faster than your own previous best. To still run as if you will win. What impresses me: to know that you might fall, that you might cross the finish line in embarrassment, or not at all—and to risk racing anyway. To know that detractors will tell all sorts of stories about your success or lack of success—and to shut them out entirely.

It’s one thing to have Michael Phelps-like confidence, prestige, privilege, to enter each race expecting to end victorious. It’s another to know at least part of the world sees you as a freak or cheater or worse. And to still compete. To still win the respect of your competitors.

Pistorius’ goal was to make the semifinal round in the Olympics. He did. And many of us rooting for him understand this as a gold-medal win in and of itself: an athlete with two carbon legs stealing the world’s attention. But what will stay with me long after the Olympics is Pistorius’ self-reflection—“I’m not expecting to win.” And the speed with which he ran anyway.

Invitation–Support the Anne Sullivan Macy Act and Improve Outcomes for Students with Vision LossInvitation–Support the Anne Sullivan Macy Act and Improve Outcomes for Students with Vision Loss

 

From our friends at AFB:

Dear Colleague:

Since its enactment more than 35 years ago, Public Law 94-142, now the Individuals with Disabilities Education Act (IDEA), has transformed educational opportunity for all children and youth with disabilities. However, the law does not adequately hold public agencies accountable for vital services and instruction such as braille, orientation and mobility, the provision of low vision devices, and a host of other essential services and instruction needed by students with vision loss to truly receive a free and appropriate public education worthy of their tremendous potential.

The Anne Sullivan Macy Act, comprehensive draft legislation endorsed by the American Council of the Blind (ACB), American Foundation for the Blind (AFB), Association for Education and Rehabilitation of the Blind and Visually Impaired (AER), Council of Schools for the Blind (COSB), Perkins School for the Blind, and VisionServe Alliance, would revolutionize America’s special education system for all students with vision loss, including students who may also have additional, and potentially even more significant, disabilities.

Everyone who cares about the scope and quality of special education for students with vision loss is invited to join in the national effort to work for the legislation’s prompt enactment and/or incorporation into IDEA. While the process for congressional review and reauthorization of IDEA promises to be a long one, advocates should begin now to educate federal policy makers about the critical need for the array of improvements that the Anne Sullivan Macy Act embodies.

You can find the full text of the draft legislation and a petition to sign at:

http://www.AFB.org/MacyAct

An array of supporting explanatory materials can also be found at a joint AFB and Perkins School website at:

http://www.ECCAdvocacy.org

If your school, association, agency, parent network, service organization, or other group can join the growing roster of organizations endorsing the Anne Sullivan Macy Act, we’d love to hear from you! Send an email confirming such endorsement to:

MRichert@afb.net

Named for Helen Kellerís beloved teacher, the Anne Sullivan Macy Act would strengthen the Individuals with Disabilities Education Act (IDEA) and improve results for the more than 100,000 children and youth with vision loss, including those who also have additional disabilities. Key provisions of the legislation include:

∑Ensure that every student with vision loss is properly identified regardless of formal disability category or classification so that all students with vision loss, including those with additional disabilities, are counted and properly served.

∑Expand knowledge about the scope and quality of special education and related services provided to students with vision loss through refined data collection that tracks all students with vision loss, regardless of formal disability category or classification.

∑Expect states to conduct strategic planning (and commit such planning to writing) to guarantee that all students with vision loss within each state receive all specialized instruction and services needed by students with vision loss provided by properly trained personnel.

∑Clarify that proper evaluation of students with vision loss includes evaluation for studentsí needs for instruction in communication and productivity (including braille instruction, and assistive technology proficiency inclusive of low vision devices where appropriate); self-sufficiency and interaction (including orientation and mobility, self-determination, sensory efficiency, socialization, recreation and fitness, and independent living skills); and age appropriate career education. Such instruction and services constitute the Expanded Core Curriculum, the body of services which teachers of students with visual impairments and related professionals are expertly trained to provide.

∑Ramp up U.S. Department of Education responsibilities to monitor and report on statesí compliance with their obligations with respect to instruction and services specifically provided to students with vision loss.

∑Assist parents and educators of students with vision loss through regular and up-to-date written policy guidance from the U.S. Department of Education.

∑Establish a national collaborative organizational resource, the Anne Sullivan Macy Center on Vision Loss and Educational Excellence, to proliferate evidence-based practices in the education of students with vision loss, to keep special educators current with the latest instructional methods, and to supplement state and local educational agency provision of the instruction and services constituting the Expanded Core Curriculum.

 

Confessions of a Man on Fire

When doctors don’t know what you have–you know, “the thing” that bends you low, makes you sweat, causes you to entertain prayer, forces you to jump up and down like a mechanical toy from the 19th century, they call it an “idiopathic” condition. 

 

Now of course there are different kinds of not knowing when it comes to the body. There’s not knowing and there’s not knowing. I hope this clears things up. 

 

I have one of the commonest idiopathic ailments and you might have it too: I fucking itch all over. We’re not talking a minor league, Sunday school itch–the kind Huck Finn had when they told him not to scratch in church–that ain’t idiopathic my friend. We know why Huck was itchy. In fact studies have shown that ministers, preachers, priests, rabbis, zen masters, imams, and school teachers can cause itching by doing nothing more than moving their eyes. There’s a scientific term for this. Preachers who make you itch just by looking at you are known as ohptho-idio-paths, which is an elevated way of saying you break out in hives because they really don’t fucking like you.  

 

There. I’ve dropped two “f bombs” in three paragraphs. But this reflects how serious idiopathic itching is. The doctor doesn’t know why you itch. You just boil all over with purgatorial pins and needles, with no part of your body unaffected. 

 

You might be allergic to wine. Maybe food. Maybe air pollution. Agribusiness. Laundry detergent. But you live without those things as an experiment, sequentially, sober, starving, hiding in the cellar, stinking so badly the dog won’t come near you and nothing changes. You itch like an electrified sponge. 

 

In my case the thing that most helps is an over the counter generic drug called loratadine–an antihistamine that’s commercially marketed as Claritin. When I take it the itching is vastly reduced. I stop tearing at my skin. I even get some sleep. 

 

So why then did I spend last night “not taking it” and playing a game of mind over matter?  Why did I lie on my bed of fire and send brain messages to every part of my straining body?

 

 The answer?  It’s the Lutheran Olympics. It’s a Scandinavian thing. 

 

Brain to feet: “C’mon guys, can’t we all just get along?”

 

Feet to brain: “Captain, the engine room’s on fire and the door’s locked!”

 

Brain to hands: “Now just stop that! Grow up!”

 

Hands to brain:  “Help! The tarantulas have escaped! They’re in our mittens!”

 

Other parts of the body have requested anonymity. 

 

Please don’t try this. We are, as they say in TV land, trained professionals. 

 

 

 

 

 

 

Grace Under Pressure: Goodbye to the Dog Who Saved My Life

 

 

I was traveling in Chicago when Connie called to say that Corky had had a seizure. She’d stumbled in our kitchen and had became disoriented. The message was “not to worry” as a local vet said she was not suffering from something serious. Corky, at 13 was still for all intents in great health, and happy to be at home with Connie who worked at her computer. Corky and Connie had a special bond. I believe it was Corky who led me to Connie in the first place. Corky, my street guardian and matchmaker. My fairy tale dog. 

 

When I came home from the conference Corky looked fine. She even brought me a shoe, one of her happy domestic eccentricities. Always one shoe. Always pleased with herself. 

 

Outside winter was turning to spring. It was that funny season when the snow has gone but the world is not yet green. I’ve always thought of this as the moment when winter’s ghosts are preparing to leave the earth. I believe there’s more to the Ides of March than we customarily admit. As green comes to the branches the dead are rising. 

 

A week later Corky had another seizure, this time in the evening. She was disoriented, walking sideways, her eyes half registering us. We rushed her to a 24 hour veterinary clinic where a kindly young vet examined her and concluded that whatever had happened was minor. Corky looked better, more alert, even wagged her tale. We took her home. 

 

Later that night she had a massive attack. She emptied her bowels and fell to the floor. My beloved was dying. 

 

In the morning we took her to our regular vet but she wasn’t in. An assistant told us to leave her and come back. 

 

We found a breakfast place and drank coffee and began to plunge seriously into worry. Corky was such a remarkable girl, so loyal, so deeply loving, it was next to impossible to imagine life without her. Could she be made better? Oh please! We ate our melancholy breakfasts, Connie and I, while pursuing hope.  

 

When we went back Corky was lying on a blanket with an I.V. attached to her foreleg. she was panting heavily. We were told that it was a brain tumor and there was nothing they could do. It was time to say goodbye. My stepson Ross stood behind me, radiating both love and strength. 

 

“Courage,” said Hemingway, “is grace under pressure.” I have never felt especially courageous. But it occurred to me that Corky had spent her life protecting me. More than once she had taken evasive action that had saved my life. She was always looking out for me, concerned and yes, spiritually affirming. My dog. My special angel. I knew that I had to force back my tears. I lay down on the floor beside her, held her, and sang to her our special walking song. And she died in my arms. 

 

 

Disability Politics In A Time Of Capitalist Crisis: Could History Repeat Itself?

(New Politics)
August 3, 2012

DUNEDIN, NEW ZEALAND– [Excerpt provided by Inclusion Daily Express] A recent article in the British Observer by Ian Birrell discussed an ominous development that has historical connotations. “The demonization of the disabled is a sign of the times” outlined how more and more British disabled people are being increasingly subjected to bullying and hate crime.

This rising incidence of disability harassment has followed austerity-driven measures by the British Conservative-Liberal Democrat Coalition Government to cut disability benefit payments. In tandem with these moves, the right-wing tabloid press has engaged in a vicious anti-disability campaign targeting so-called disability benefit fraudsters or as they colloquially label them “scroungers.”

Birrell’s article set out to measure the impact that this sustained campaign has had on the life of one man, Peter Greener. Greener lives with multiple sclerosis, in the English city of Hebburn. He was the subject of a recent campaign of torment and abuse by his neighbor involving, among other things, name-calling and object throwing. The neighbor’s campaign climaxed in his anonymously calling a benefit fraud hotline in an attempt to discredit Greener but the neighbor’s actions backfired when welfare officials found that he was not a fraudster. Subsequently, Greener’s torment ended when the neighbor was arrested and jailed for his hate crime.

Birrell though goes into detail as to how Greener’s case is not an isolated one, particularly during the current crisis of capitalism that is the European Sovereign Debt crisis. He outlines how the reported level of disability harassment has increased in Britain, the result of an implicit campaign by both the UK right and its media allies to discredit all disabled welfare claimants.

I would argue that this represents a renewed campaign to label disabled people as a “burden” to society, a view that is gaining renewed currency as governments throughout Europe and the world seek to slash social expenditure in this time of crisis. I am aware as a New Zealander of the detrimental impact of economic and social reforms, particularly on disabled people, in my own country.

Entire article:
Disability politics in a time of capitalist crisis: could history repeat itself?

http://newpol.org/print/node/638
Related:
The demonisation of the disabled is a chilling sign of the times (The Guardian)

http://tinyurl.com/ide0803121b
Benefit cheats stories ‘colour attitudes to disabled people’ (BBC News)
http://www.bbc.co.uk/news/education-19048294
Disabled people need positive images not ‘benefit scroungers’ label says charity (Xperedon)
http://www.xperedon.com/news_1549
What the opposition writes:
Paradoxical policies help in driving up federal debt (Journal Gazette)

http://tinyurl.com/ide0803121d

Shame on Netflix

Netflix Seeks Permission To Appeal Order To Comply With ADA
(National Law Journal)
August 2, 2012

BOSTON, MASSACHUSETTS– [Excerpt provided by Inclusion Daily Express] Netflix Inc. asked a federal judge in Massachusetts for permission to appeal his ruling that the Americans with Disabilities Act of 1990 requires the company to provide closed-captioning text for its web-only streaming video.

Netflix filed a motion on July 27 asking U.S. District Judge Michael Ponsor to amend his June 19 order denying Netflix’s motion for judgment on the pleadings and to certify an appeal to the U.S. Court of Appeals for the First Circuit.

Ponsor, a senior judge in Springfield, Mass., issued the order in National Association of the Deaf v. Netflix Inc. The organization, along with a number of additional advocacy groups, sued Netflix in June 2011 over its lack of closed-captioned text.

In its motion, Netflix called Ponsor’s order “the broadest-ever extension of the ADA’s scope, thereby opening the door to amorphous and seemingly limitless regulation of the Internet in a way Congress did not envision and no other court has accepted.”

The company added that Ponsor’s ruling, the first applying the ADA to streaming technology, conflicted with the Twenty-First Century Communications and Video Accessibility Act of 2010. That law established a regulatory scheme for closed-captioning on streaming video content.

Entire article:
Netflix seeks permission to appeal order to comply with ADA

http://tinyurl.com/ide0802122

Micro Memoir: Dinner in the Valley of Kings

Here is the story, writ small: it’s nothing you would recognize anyway, the egyptologist who works in the basement of a Scandinavian library and hasn’t been to a tomb for a decade, but still he sees five centuries on a remembered wall. He could live, you understand, with infinite cosmological mistakes. He was an excellent dinner companion.

Chicken Sh*t

By Angel Lemke

Just a couple weeks ago, I wrote this, in my (overdue) seminar paper for my course in Ethics After Postmodernism: “[I]t is really discomfort that motivates ethical action. Rorty argues that ‘it is best to think of moral progress as a matter of increasing sensitivity, increasing responsiveness to the needs of a larger and larger variety of people and things’ (429, Rorty’s emphasis); we should understand ‘sensitivity’ here to mean not just a vague awareness of the other, but of an actual felt sense that the other is if not a part, at least of extreme importance to our relational selves such that in cases of injustice ‘a failure to intervene would make us uncomfortable with ourselves’ (430, Rorty’s emphasis). In this conceptualization, comfort becomes not a capitulation—for example, remaining in the closet at family gatherings in order to make one’s homophobic grandmother comfortable—but an ever-receding horizon at which we continually aim. In this conceptualization, no single person or group’s comfort takes greater priority; or, as the Buddhist tradition has it, ‘No one is healed until everyone is healed’. . .We might ask, in our example, first, that our homophobic grandmother simply acknowledge our same-sex partner’s existence, rather than expecting her immediate transformation. Discomfort becomes a tool that serves a pedagogical purpose in our ongoing journey toward true collective comfort rather than merely being an unpleasant feeling that we would all like to avoid.” I’m not sure that passage says anything new to those of you who are involved, one way or another, in anti-oppression work. I’d venture that it’s a bedrock principle of the movement, finding discomfort a productive site for growth and self-reflection. But right now, it seems strangely prescient. I cite my paper because I’m about to make some people uncomfortable. And I want to make sure they know: it’s not for nothing. It’s because I think we can all be better than we are. Rather, I should say that I’m about to refuse to make some people I love feel comfortable. When the latest Chick-fil-a flap started popping up in my Facebook feed, my initial reaction was, “Um, this is news?” I briefly considered posting or linking to posts that listed Chick-fil-a alongside the myriad other organizations with leadership who spout hate (The Salvation Army, for instance) or who try to put on gay friendly faces while still funneling money to anti-gay politicians and initiatives (Target). But by the time the Jim Henson Company posts started, I felt pretty much like a commenter on a friend’s post who wrote:

“I've been avoiding chik-fil-a for years because of the homophobia, and when I've mentioned that I wouldn't buy from them or some of the two dozen other openly gay-bashing companies out there, thatI see fit to abstain from, I got scoffed at. But lo and behold, when a muppet makes a stand, we all jump into that bandwagon. And don't get me wrong, I approve and I'm not trying to be all hip about it, but chik-fil-a is hardly the only corporation that has been openly endorsing anti-gay movements and since we all have google, why does it take a talking frog to get people to notice something?” In short, my attitude was “Over it,” followed by an eye roll and some muttering about how they probably use factory farm chickens, too, and how no one does their homework about where their money really goes, and the more things change, and other jaded leftist mutterings, etc, etc. A general resignation to the apathy of the masses. But then a strange thing started happening. People who have for years presented themselves to me as straight allies—not terribly active ones, but people who don’t oppose same sex marriage and have more than one “gay friend” and are generally good people—started acting very strangely. They weren’t acting apathetic at all. They seemed to care about this issue. . .or at least they cared about it enough to want to make it go away, to make it seem as though it shouldn’t have been an issue in the first place. First, a straight male friend interrupted our text conversation to ask if we could still be friends if he had dinner at Chick-fil-a. I thought was a bad joke, and did what I do when bad jokes fall flat; I didn’t respond. When he checked in at Chick-fil-a later on foursquare, I started thinking about the position such a text put me in if it were—as it appeared—in earnest. The way the question was posed, my options were either say, “Sure, I’m cool with you knowingly providing profits to folks who think I’m an abomination” or “No, I’m another one of those angry lesbians who’s all ‘sensitive’ and ‘political’ and ‘making a ‘big deal’ out of things.’” You know, some days you just don’t feel like fighting the good fight. Even when you TOTALLY are a sensitive, angry political lesbian. Since there was no good answer in the multiple choices, I left the question blank, in hopes that the questioner would independently recognize the design flaw in the exam. And someone at HuffPo did a better job of addressing the “making a big deal out of things” response better than I could, anyway. (http://www.huffingtonpost.com/conor-gaughan/chick-fil-a-homophobia_b_1711566.html?utm_hp_ref=fb&src=sp&comm_ref=false) Then this popped up in my Facebook feed: “Being conservative doesn’t mean I can’t love everyone. . .Straight, gay, AND chick-fil-a :).” I’ve spent a long time puzzling over what that one means. The best I can come up with is that it’s an argument that fast food patronage is apolitical. I’ve never been to a Chick-fil-a. I had to look up how to spell it today when I sat down to write. I’ve lived in Ohio all my life, and by the time they started to penetrate this market, I already knew about the heinous politics, and I was making a general effort to eliminate fast food from my diet, for both political and health reasons, so I just never went. What I am beginning to gather, however, is that they make one hell of a chicken sandwich. I mean, it must be the best chicken sandwich some folks have had in their entire lives. It must be a life-changing, willing-to-risk-life-and-limb-for-a-taste-of-that-fine-fine-chickeny-goodness kind of sandwich. Why else would so many people who are avowedly not-homophobic be trying so hard to justify their continued patronage? Though I loathe most of the national dialogue on gay marriage on all sides (there’s more than two), and will rattle on in snarky-leftist-Michael-Warner-and-Dean-Spade-quoting glee about how marriage is the wrong goal, I can’t deny that there has been much change since I came out, only a decade and a half ago, and that I fully expect to see gay marriage legalized, for better AND worse, in my lifetime. And what I think is going on in my Facebook feed and among my more casual straight allies is the gradual realization that it is going to require more from them than “liking” the I Support Gay Marriage in Ohio page. That it is going to require more than having some gay friends. They might have to have uncomfortable conversations with their family members. Or their church communities. Or their co-workers. They might have to give up their chicken. This is where the rubber meets the road, folks. Put up or shut up time. This is when being an ally gets uncomfortable, when you have to give up some of your privilege. I think you’re starting to realize that, and I think some of you want us queers to say it’s okay to chicken out. I’m here to say that it’s not. A couple years ago, Sarah Schulman’s Ties that Bind: Familial Homophobia and Its Consequences was a devastating read for me, not because it told me anything I didn’t already know, but because it was so angry, because it galvanized my anger, and because it made it clear to me that I could not go on making straight folk feel comfortable about their heterosexism. It’s pretty plain in Schulman’s account: “Are homophobic family members evil? Well, not if you be

lieve that evil does not have a human face. Yes, the people who won’t take responsibility for their dying gay son, won’t invite their lesbian sister to their wedding, won’t allow their gay cousin to hold their child, won’t praise their gay co-worker, won’t send their gay son a birthday card, vote for anti-gay politicians, give money to a homophobic church, love films that diminish gay people—those people may have all kinds of great attributes. You may love them. They may have taken you fishing when you were six or made you a quilt for Christmas or had a great sense of humor or looked just like you. That is what evil looks like. Evil knows great old songs, can be weak and vulnerable, can love you, can feed the hungry, can pick out a book because they were thinking of you. Evil can have Alzheimer’s. Familial homophobia is deeply human, as all evil is the product of human imagination.” Devastating. So many people in my life become evil in this light. Some of you become evil in this light. But, mercifully, there is also this: “[A]ll people have the option to judge and act ethically. That there are individuals in all situations who do take responsibility proves the availability of moral behavior as a possibility for the others. There were always white people who opposed slavery, always German Christians who opposed Fascism. There are always Jews who oppose the Israeli occupation, always Americans who oppose the war with Iraq, always men who work for abortion rights. There were always capitalists who opposed the persecution of American Communists and Russian Communists who opposed the persecution of the Jews.” So there is hope. But what she doesn’t stress is that it will be HARD, that having the courage of your convictions always is. You don’t get to be an ally and funnel money to a hate-monger. The two don’t mix. You have to choose. I don’t care how uncomfortable that makes you. (For how uncomfortable it makes ME, see the link above.) I am here to tell you that you have to choose. In talking about my plans to write this with a friend earlier, I planned to throw down the gauntlet by announcing my plans to live a conviction that I’ve had for some time but have been failing at because it requires giving up some conveniences and some privileges, because it will require more work than I’ve been willing to put it in. The kind of conviction that I can talk about on Facebook, and then forget about when I go about my daily life. I’ll write of it another time, because I think it is crucial to make such choices public, to offer other ways of being in the world, to make clear what our values are, but in reaching this point in my angry lesbian screed, the particulars of the conviction that I needed to be called to live at this moment in my life seem less important than reminder that you who seem so eager to be let off the hook for yours have given me that it’s ALWAYS going to be hard. That waiting until it’s easier is a cop out; is unjust. That discomfort we feel? We can try to make it go away, hide in being apolitical, drug ourselves on carbonated sugar water, or the very real suspicion that one person’s act won’t make a difference; we ask those who are being discriminated against to tell us its okay. Or, we can be better. You choose.

Reddit-Powered Show Gets Zach Anner Rolling Again

(Mashable)
July 31, 2012

NEW YORK, NEW YORK– [Excerpt provided by Inclusion Daily Express] In 2010, Zach Anner submitted an audition tape to Oprah’s “Your OWN Show” contest. When the Internet got wind of it, the web couldn’t stop laughing. The wheelchair-bound comic charmed the online communities of Reddit and 4chan with self-deprecating humor that poked fun at his own affliction — cerebral palsy.

More than nine million votes later (despite an alleged voting rig, which Redditors debunked), the Internet convinced one of the biggest cultural influencers in cable television, and arguably America.

The show, Rollin’ With Zach Anner, was a travelogue for the disabled. Four episodes later, it was canceled due to poor ratings.

Despite a short-lived cable career, Anner is asking his web audience to give the travel show a second chance, and he has help from Reddit co-founder Alexis Ohanian.

The new web series Riding Shotgun With Zach Anner lets Reddit users decide where Anner will travel. He will shoot in eight cities over the course of six weeks.

Entire article:
Reddit-Powered Show Gets Disabled Comedian Rolling Again

http://mashable.com/2012/07/18/zach-anner-show-reddit/