---------- Forwarded message ----------
From: Shilpaa Anand <[email protected]>
Date: Thu, 19 Jan 2017 10:46:05 +0530
Subject: {Disability Studies India} FW: Non-Politics of Disability
To: "[email protected]"
<[email protected]>

Hello All,
Some of you may have already seen this NY Times piece but I'm sharing it
anyway because it resonates so much with the Indian context as well.
Happy reading!

---------- Forwarded message ----------
From: John Lee Clark <[email protected]>
Date: 19 January 2017 at 09:00
Subject: [DS-HUM] FW: Non-Politics of Disability
To: [email protected]


The Opinion Pages

The Non-Politics of Disability

Jay Ruckelshaus

https://www.nytimes.com/2017/01/18/opinion/denouncing-
trump-wont-help-disability-rights.html

The morning after Donald J. Trump’s election victory I posted a status
update on Facebook that drew praise from both my liberal and conservative
social media friends, and revealed something I’d thought impossible — a
limit to his stalwart supporters’ loyalty. The post wasn’t exactly neutral;
I lamented what Mr. Trump’s election means to me, a wheelchair user, and
recalled the boorish example he set in mocking Serge Kovaleski, the Times
reporter, who has a congenital joint disorder.

My partisan posture was clear, but still, the post elicited warm messages
of encouragement from even strident Trump supporters. One response was
revealing: A friend claimed that the president-elect would do wonders for
the country, even as she wholeheartedly denounced him on this issue. (For
the record, Kovaleski does not consider himself to be disabled.)

That a statement on disability garnered sympathy from across the political
spectrum was unsurprising, at least to me. I’ve grown used to my wheelchair
trumping (forgive me) other political and moral concerns. Rarely, if ever,
do people contest my claims that we must do more for those with
disabilities: Greater access? Better employment training? More flexible
school curriculums?

“Of course!” they invariably respond. “Who could argue with that?”

Disability rights enjoy a seemingly ironclad moral consensus, an ostensible
unanimity that is striking given America’s entrenched polarization and the
antagonism surrounding other identity movements.
Many are wary of L.G.B.T. rights or the Black Lives Matter movement, but it
seems beyond the pale — almost cruel — to oppose disability rights. Nobody
wants to be anti-disability.

Initially, this harmony would seem helpful. Free from partisan discord,
advancements for the approximately 57 million Americans with disabilities
should be easier to achieve, borne aloft by the wings of certain progress.
Why, then, do rampant unemployment and educational disparities endure, and
why does success remain the exception?

I think part of the reason is the insulation of our pro-disabled political
consensus. Its logic is rooted not in any deep belief in the equal worth of
citizens with disabilities, but rather in a general aversion to disability.
This is related to the charity impulse that has always surrounded
disability — and has constrained liberation efforts by assuming that
inequities are unfortunate but natural realities to be mitigated through
compassion, rather than politically structured injustices. There is also a
profound lack of disabled people in the public sphere, meaning any
substantive discussion that does occur is extremely rare.

I suspect many people I talk to about disability maintain an implicit hope
that, if they nod as vigorously as possible, the issue will simply go away.
In this way, support for disability rights is similar to the act of
expressing perfunctory thanks to military veterans. It temporarily absolves
us of the responsibility to address the heart of the matter.

Moreover, the apparent moral consensus may be mostly superficial. In trying
to enact accessibility, disability advocates encounter increasing
resistance as the effort and costs involved in proposals come closer to
being realized. (Consider the neighborhood store that decides it’s just too
costly to install a ramp, or the community lecture that excludes deaf
attendees by refusing to hire a sign-language interpreter.)

Instead of facilitating change, false unity actually restrains change.
It stifles the more substantive conversations true progress requires.
And our inability to speak honestly — and contentiously — about disability
shows how the politics of disability is in this sense non-political. We are
the worse for it.

In addition to greater participation in the public sphere, true progress
for citizens with disabilities will require a willingness to confront the
issues head-on, even when — especially when — citizens disagree on
competing solutions. We must politicize disability — not in the cable-news,
grandstanding kind of way, but in the term’s more formal sense.

The work of the Belgian political theorist Chantal Mouffe can help
illuminate what’s at stake. Mouffe begins with the premise that human
relations are inherently antagonistic: Political change always requires
controversial transfers in power or prestige, and it is an illusion to
imagine politics without confrontation. Per this “agonistic” conception of
democracy, a healthy political order is one that prefers vigorous,
good-faith argumentation to complacent consensus.

Until we publicly recognize real disagreements surrounding disability and
accessibility, Mouffe would insist, we are doomed to a vacuous, empty
debate that is neither political nor productive.

Recall the Kovaleski incident. I’m not suggesting that the abhorrence of
Mr. Trump’s actions is open to legitimate questioning. But in their
forcefully reassuring comments and messages, my friends prevented any
serious discussion of disability at the level where reasonable disagreement
does exist. Where will the money come from to fund disability employment
schemes? How do we even define “disability”?
Despite — and, I would argue, partly because of — the broad condemnation of
Mr. Trump for his insensitivity, there was no substantive public discussion
of such issues.

You may be thinking, haven’t we had enough politics lately? Maybe it’s a
blessing that disability isn’t as political as it might be; it avoids the
drama and messiness that now seem to define our common life.

Avoiding politics might be possible if disability were an exclusively
private affair. But it is fundamentally a public concern, affecting
everyone directly or indirectly and revealing our obligations to one
another as members of a democratic society. Issues of accessibility can be
fully addressed only through public institutions and collective effort. For
the disability community, there is no answer but politics.

But politics need not be repulsive. That’s the beauty of Mouffe’s
agonism: By legitimating clashing arguments and welcoming them into the
political fold, unproductive antagonism becomes constructive, and
compromises emerge.

And success here could yield broader insights. I believe there is great
potential for a new disability politics to provide a positive blueprint for
dealing with our partisan divide and other identity issues that goes beyond
the unhelpful political correctness frame.
Thinking seriously about precisely why disability maintains a moral
consensus might allow us to harness any advantages (e.g. a common moral
vocabulary) while discarding what’s unhelpful. What if we could construct a
model of politicization that doesn’t entail bitter partisanship, and rescue
authentic disagreement from stultifying consensus? The resulting practices
and mentalities could be revolutionary for disability politics, and for
democracy itself.

I’m still thinking through how this might work, and I recognize that any
such efforts will require real trade-offs and difficult conversations.
Politics — when put into action — always does.

Jay Ruckelshaus is a Rhodes Scholar and graduate student in political
theory at the University of Oxford, and the founder and president of Ramp
Less Traveled, a nonprofit organization that helps students with spinal
cord injuries pursue higher education.

Disability is a weekly series of essays, art and opinion by and about
people living with disabilities. The entire series can be found here.

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-- 
Shilpaa Anand
Assistant Professor, Department of English
Convener, Committee for Cell for Persons with Disabilities
Maulana Azad National Urdu University
Hyderabad 500 032.

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