Firing Up Disability Studies: A
Report from the Edges of the Human Community
Tanya
Titchkosky, Ph.D
Ontario
Institute for Studies in Education of the University of Toronto
Abstract
This
paper provides a report on first international Disability Studies Summer Institute
hosted by the Ontario Institute for Studies in Education (OISE) of the
University of Toronto, July, 2011.
This report, reflective in character, narrates some ways that the
Institute developed a critical understanding of “disability studies” that enabled
attendees to re-encounter current conceptions of “problem” and of “people” and to
re-think the relations between the two. This report discusses both keynote
material and the experience of an evacuation because of a fire during the
Institute. My aim is to reveal
some of the ways disability is conceptualized, lived, and theorized as food for
thought that can lead to further questions regarding the meaning of persons
within the human community.
Keywords
Interpretation;
Disability Studies Summer Institute; Recognition;
Human; Becoming; Crisis; Evacuation
Introduction
The first international
Disability Studies Summer Institute hosted by the Ontario Institute for Studies
in Education (OISE) of the University of Toronto occurred during the week of
July 18th, 2011.[1] As it so happened, a summer heat wave
accompanied us throughout our intense time together. Fifty emerging and
established scholars from Canada, USA and UK attended the Institute,
representing more than ten disciplines interested in exploring the significance
of disability studies for both academic and everyday life. In what follows, I provide a report on
the some of the understandings that arose through our time together.
The orienting aims for
this gathering were rather simple: to address the conceptions of disability at
work both in and out of disability studies so as to rethink them anew; to bring
conceptions of race and disability in touch with one another so as to revisit
their on-going separation; to do something other than celebrate disability
studies arrival into the academy or to proclaim its marginal status as
forgotten sister of those academic endeavours that preceded it. Basically, our aim was to make
disability studies matter differently by reflecting on what it is we are already
doing. Of course, there is already
an intense and long history of self-critique generated by and for those within
disability studies. Consider a few
examples: Mike Oliver’s (1999) characterization of disability studies research
as reproducing the self-interest of the “parasite people;” Rod Michalko’s (2002: 143) examination of disability studies as
it forgets it is imitating the conventions of belonging and thus forgets the
necessity of continued critique of such conventions; Corbett O’Toole’s (2004)
demonstration of the sexist and racist inheritance of disability studies; Tom
Shakespeare’s (2004) noting of various critiques of the pursuit of disability
rights as this leads to the wrong endeavor of patrolling the borders of
disability studies; or Chris Bell’s (2011: 4) demonstration of the whiteness of
disability studies. Without dwelling on any one of these critiques, the Summer
Institute grappled with the idea that some of the best-loved aspects of
disability studies may, ironically, perpetuate the understanding of disability
as a taken-for-granted problem over time and across various places around the
globe.
What
I intend in the pages of this report is to show some of the ways that we raised
the issue of how disability studies might encounter its own conceptions of
“problem” and of “people” so as to re-think the relations between the two. The following, then, is not a
conventional academic paper but a reflective report. I provide an account of the Summer Institute, including an
evacuation because of a fire, so as to show the ways disability is
conceptualized, lived, and theorized as food for thought for those oriented to
the continued need to question the nature of “problems” and “people.”
Key Notes in the Disability Studies Summer Institute
This intense week
involved three sessions a day where all present listened to a variety of people
offer their work and with plenty of time, albeit never enough, for all to
respond. I delivered the keynote
on the first morning with “The Becoming Crisis of Disability Studies:
Introductory Remarks,” which is related to my new book The Question of Access: Disability, Space Meaning (Titchkosky,
2011).
The other keynotes were
as follows:
Nirmala
Erevelles, The University of Alabama, “Disability as
"Becoming" in (Post/Neo) Colonial Context: Notes on the Political
Economy of the Flesh” and related to her new book Disability and Difference in
Global Contexts: Enabling a Transformative Body Politic (2011).
Dan Goodley,
Manchester Metropolitan University, “What is Critical Disability Studies? And,
Do We Need It?” and related to his new book, Disability Studies: An Interdisciplinary Introduction (2011).
Katherine McKittrick, Queens University, “On Blackness, Race, and the
Struggle to be Human” and related to her book Demonic Grounds (2006).
Rod Michalko
and Rinaldo Walcott, Ontario Institute for Studies in Education of the
University of Toronto, “The Pleasure of the Humiliated Body,” and related to Michalko’s (2002) The
Difference that Disability Makes and Walcott’s (2000) Rude: Contemporary Black Canadian Cultural Criticism.
There
was also one evening session open to the general public where the question “Why
Disability Studies?” was addressed.
With an audience of over 130 people, we put this question into
conversation with audience members’ interests in how differences in learning,
in language, in accessibility requirements resulted in forms of disablement as
well as a growing desire to question disability as a form of social devaluation
particularly poignant in the lives of new immigrants. The formal presentations were short, the extended audience
conversation was lively, and the event managed to generate a sense of the
necessary inter-relation between wider community concerns and the DSSI
concerns.
Overall,
the DS Summer Institute provided a means for scholars to question what
disability studies is and what it needs to be in order for it to better address
the on-going cultural production of disability as a “naturally excludable type”
(Titchkosky 2007:149). It is, however,
not easy to ask how to generate a crisis in our own understanding by
researching the key concepts or critical analytic moves already at work in
disability studies. It is also
difficult to restlessly return to reflect on disability studies’ current
procedures and beliefs in order to face embodiment itself as a dynamic scene
for social inquiry that is already related to, yet distanced from, other areas
of cultural studies. Moreover,
from the point of view of common sense, it would seem that problems of disability,
and thus disability studies, are simply a little too obvious to fret
about.
With
the DS Summer Institute as background, and drawing upon aspects of my keynote, I
turn now to a discussion of how disability is taken as problem that, regarded
as obvious, may itself cause a variety of troubles. I will show how disability studies addresses this obvious
character of disability-as-problem in ways that attempt to rupture the typical
interpretive flow that moves from impairment, to disability, to disadvantage,
to discrimination and danger for disabled people. I then provide an account of a fire evacuation during the
final day of the Disability Studies Summer Institute as a way to further pursue
a disability studies perspective that simultaneously questions what we are and
are not doing with this perspective.
I provide this account as a way to question what it is we react to when
faced with those institutional social scenes that position disabled people
precariously on the edges of what is imagined as the ordinary order of the
human community. In other words,
while my report does not take the shape of a conventional social science paper,
it nonetheless provides a narrative structure within which we, reader and
writer, can reflect on the movement of meaning as it is accomplished and
enforced by the flow of daily academic life.
The Obvious Sense of Disability as a Problem
In the everyday academic
culture, as Paul Abberley (1998) reminds us, it is
ordinary to be interested in disability only as a problem and many disciplines
work “on” this problem taken-for-granted as such. Let us turn to an obvious
example of understanding disability as a problem and toward which disability
studies holds some affinity. The World Report on Disability, recently
released by the World Health Organization and the World Bank, certainly
confirms the obviousness of disability understood as a problem. This new Report suggests, as has the UN in the past, that the “silent
crisis” of the global state of disability is worse than first imagined:
What do
we know about disability?
Higher
estimates of prevalence
More than a billion
people are estimated to live with some form of disability, or about 15% of the
world’s population (based on 2010 global population estimates). This is higher
than previous World Health Organization estimates, which date from the 1970s
and suggested around 10%.
According to the World
Health Survey around 785 million (15.6%) persons 15 years and older live with a
disability, while the Global Burden of Disease estimates a figure of around 975
million (19.4%) persons. Of these, the World Health Survey estimates that 110
million people (2.2%) have very significant difficulties in functioning, while
the Global Burden of Disease estimates that 190 million (3.8%) have “severe
disability” – the equivalent of disability inferred for conditions such
as quadriplegia, severe depression, or blindness. Only the Global Burden of
Disease measures childhood disabilities (0–14 years), which is estimated
to be 95 million (5.1%) children, of whom 13 million (0.7%) have “severe
disability”. (WHO, World Report on
Disability, 2011: 7-8)
What
do we know now about the problem of
disability? According to the World Report, we know it to be located
in certain bodies and to be more prevalent than previously thought. We know, too, that disability is a
special some-thing; a thing that
conditions the body; it is a measurable entity of rank-able and count-able
severity; it is a billion conditions giving rise to difficulties for
individuals; these difficulties may also be burdensome to others; disability is
lack of function, disease, debilitating.
The World Report tells us that we should know disability
is difficulty … it has struck a large number people who, if one reads on, are
nonetheless regarded as though they are unexpected and unanticipated, as if
disability was rare. We now know
that disability is a ‘they’ who should be included, who should receive aid and
assistance, but unfortunately do not. By mapping disability as individual difficulty, we are
shown that there is much disability but little participation by disabled people
in routine areas of daily life, such as learning, labour, leisure, and even
love. We should also note that
there is a strange over-representation of disability in some locales: in all
forms of incarceration, in locales that have offices of social assistance or
mental health or welfare regimes, in separate or special education classrooms,
and anywhere there is poverty, war, or state brutality… these locales are very inclusive
of disabled people.
This
is what we “know” now from this new report and it is this knowledge of the
silent crisis of disability that the president of the WHO as well as the
President of the World Bank “invite” us “to use this evidence in this report”
to build an “inclusive world in which we are all able to live a life of health,
comfort, and dignity” (World Report on
Disability, 2011: 5). And yet,
the world remains fairly quiet about its response to include the dysfunctional
burden of the difficulty called individual impairment even when the world is
responsible for its production through colonial exploitation; through war,
technological advancements, and manufacturing; through environmental
degradation as well as normal educational practices, etc.
Part
of this lack of response is tied to the on-going social act of charting bodies
from above, a kind of Archimedean point that (re)forges a notion of disability
as a product of nature. Thus, disability is something that simply and obviously
is and, just as obviously, what it is is a
problem, and a difficult one at that.
It comes to seem as though culture is far removed from the production of
the entity called “person with a disability.” This removal of culture results in the typical Western
assumption that impairment is more or less caused by an individual’s
unfortunate fate (bad luck, bad genetics, injury, malnutrition, war, accident,
wear and tear, job requirements, technological advancement, stress, trauma,
difference). Such unfortunate
fates, imagined as if natural, lead rather directly to the conclusion that
disability “is” an “inability to do” in a “way considered normal” for a human
being (WHO, 1980). Put in the
language of the new Report (2011:7)
the nature of impairment is such that it causes “difficulties functioning,” as
well as “activity limitations, and participation restrictions.” A belief that these fates as well as
their consequences are manufactured “as if” by nature provides a depiction of
disability as somewhat unrelated
to the culture within which it appears.
Disability appears not as itself a cultural production but instead
appears as an already given problem for
cultures and towards which there are various responses (good and bad, enabling
and disabling).
It
is interesting that the Report
remains curiously uninterested in the ways in which it conceives of disability
as a problem in the first place.
And so it comes to pass that the major solution to the problem is that
the nation state and its people should learn to treat the problem that
disability always already is in a
“better” way – with more assistance and less discrimination. Thus, around the globe we have a rather
cohesive research and administrative endeavour that teaches all involved,
including disabled people, to believe that disability is already a problem; it
is not culturally manufactured as such, but “we” should do “more” with what
will forever be “less” which is the ruling definition of the condition of impairment. Strangely enough, it rarely comes to
the fore for questioning that societies continue to make some people represent
“the less-than of humanity” within a project that aims to build a more
inclusive world.
Stranger
still is that this dominant version of inclusion suggests that what we can know about disability is dependent
on the body remaining a distinctly individual problem not configured as a
collective one. Disability as a
billion individualized nodes of difficulty, some representing the edges of
humanity itself, becomes knowable as a burden for others. Mapped from above as though disability
is simply a biological or functional calamity that has befallen a large number
of an unfortunate few, it becomes millions of individual natural disasters to
which others are being asked by the Report
to respond and respond better.
This
most ordinary and accepted, even normal and normalizing, conception of
disability can still serve, though, as food for thought.
The Obvious Sense of Disability Studies
From the perspective of
disability studies, attending to this prevalent cultural representation of
disability-as-problem begins to move us toward the need to develop a sense of a
crisis, not in bodies, but in our ways of conceptualizing our
bodies together in social space and over time. It was this understanding that grounded the organizing of
the Disability Studies Summer Institute on the theme of a “becoming crisis” so
as to address how disability is taken as problem in the first place.
Disability studies itself represents the potential to offer a becoming
crisis to current ways of understanding disability since it suggests ways to
question the obviousness of “problem.”
During
the Institute, however, seeking this crisis in understanding came with a
twist. Could we encounter, or even
generate, a crisis in disability studies’ own
understandings of impairment, disability, and embodiment? Could we address what we already know
in order to wonder about it? For
example, does the obviousness of exclusion and discrimination faced by disabled
people, especially through the primacy of medicalized
definitions of our situation, have something new to say to us other than, once
again, that disabled people experience exclusion and discrimination? If the exclusion of disabled people is
understood as caused by failed social responses to different forms of
embodiment (Oliver, 1996), and if it is common to narrate these exclusions as
somewhat expected since disability is “naturally” too difficult, too severe,
too burdensome, then are we not facing the very boundaries of the question of
what it means to be human, or the edges of community sensibilities? In short, do we need to re-think what
we are doing when offering critiques and explanations of exclusion, i.e., when
we are doing disability studies?
The
Disability Studies Summer Institute can be characterized as an oriented entanglement
with these sorts of questions.
Such questioning helped us forge some new pathways to understanding
disability as a dramatic and complex scene where critical interpretations
regarding the cultural production of the meaning of persons can be encountered
as part of embodied existence in everyday life. This cultural scene included our own conflicting
orientations toward what disability studies is as well as how we imagine the
social significance of bodies in social space over time. This prompted the Institute participants
to ask about disability studies own institutionalized role in addressing
disability as a “thing to be studied” that can end up reproducing so many lives
as problem objects that are talk-about-able but nonetheless outside the play of
mutual recognition or the interplay of co-constitution necessary to found human life.
But,
we also imagined that disability is not best understood as a million natural
disasters striking so many unfortunate few since it can be better addressed as
a dramatic cultural scene where the question of what is human and what is natural
are often asked. (This suggests
that humanity can be uncovered through engaging with its denial.) Disability studies, if it is to examine
the answers to such questions, or even raise them, needs to gear itself into a
consideration of what counts as human in a culture that insists that the
encounter with some bodies is an encounter of pure limit (not-quite-human) and
as though limit can be split from possibility by those who count as
all-too-human. To learn something
new about the lives of disabled people without reflecting on the undergirding
concepts of embodiment grounding this new knowledge production can reproduce
the taken-for-granted sense of problem that provoked the research project in
the first place. If, for example, disability is the problem of a lack of
participation and is studied as such, what does disability studies need to do
and be in order to do and be more than a confirmation of the current state of
affairs? Moreover, among other
arenas of critical studies of social exclusion (critical race studies, queer
studies, gender studies) where disability still serves as a “naturally”
exclude-able other, or serves as a taken-for-granted cut-off point of critical
engagement, addressing embodiment may reinvigorate the desire to question any
social practice that normalizes what counts as mainstream knowledge
production. These ways of
questioning suggest that what we know can become an occasion to put into crisis
the question of how we know it.
Another
twist: exploring the meaning of human and its resultant knowledge regimes are
hardly possible if disability studies cannot question its own use of the
categories of impairment, question its own identity politics and boundary
building, and engage its celebrations of crip
community. After all, the terms of
our own engagement with discriminatory and able-ist
culture also participate in that culture thus making some others into an unquestioned
background against which the disabled figure arises as a problem. Yet another
twist: recognizing the need for critical self-reflexive analysis, is not to
invite complacency toward critical cultural research that refuses to avail
itself of a disability studies perspective and instead continues to make
“disability” a cut-off point for the nature/culture distinction. If we do not include a consideration
of what critical work does with
bodies, minds, senses and comportments that seem not to fit either in everyday
life or in academic knowledge production, what remains of disability will
always be that which is made to teeter on the edge of danger, degradation, and
death.
The
Disability Studies Summer Institute made clear that without an analysis of current
cultural conceptions of embodiment, disability will pop up only as an impending
emergency understood as its own self-contained crisis. War, storms, fire, economic downturns
will continue to be occasions where societies position the disabled body precariously. Disability again and again triggers
calls to “Flee,” “Take cover,” “Evacuate,” “Tighten up your resources,” or,
“Get real, disability is beyond inclusion.” Yet, how these manoeuvres are
actually accomplished in the face of an almost universal desire to sustain a
myth of normalcy as a collective Real with its liberal values of “inclusion,”
will continue to make some lives questionable and will continue to make human
community precarious (Frazee, 2009).
Thus we need to nurture a collective desire to re-think normalcy itself.
By focusing on the cultural production of disability around the world as a
crisis of exclusion as well as focusing on the cultural processes of peculiar
inclusions of disability in the academy today, we can continue to uncover the
ways normalcy remains a social phenomenon in need of further examination
(Titchkosky and Michalko, 2009:1).
As
a way to demonstrate the importance of re-thinking the “Real” of normalcy in key
scenes of disablement and able-ism, I turn to an account of an evacuation that
the DS Summer Institute participants underwent on our final day together. Of particular interest is not only what
happened but, also, conflicting interpretations of what happened. An account of both the affront of the
happening and how it can be interpreted will be pursued in what follows as a
way to exemplify the “becoming crisis” offered by a disability studies
perspective that orients to exposing conceptions of disability at work which
help to sustain the normal and the ordinary.
Evacuate!
It is Saturday
afternoon, July 23rd, 2011, the sixth day of the Disability Studies
Summer Institute. Around 2:00 pm,
we are having our final meeting in a fifth floor classroom of a twelve story downtown
building of the University of Toronto.
Organizing for this final meeting, I had expected only a small portion
of the group of fifty to show up in order to plan for future projects. There were about 30 participants
present, two of whom brought their young children. We were beginning to discuss
projects that could arise from this intense week when our meeting, and as it
turned out our Summer Institute, came to an abrupt end.
Through
the open doors of the classroom we noticed firefighters proceeding down the
hallway outside our classroom. They were calling out to each other, it sounded
like they were looking for something on the large fifth floor outdoor balcony,
or for keys to get out there. Two people from the Institute moved to where
their children were playing outside the classroom. Soon, I also left the
classroom and realized it was access to the balcony the firefighters were
seeking. I began to look for the
security phone since I knew Security would have the balcony door keys. I did not find the security phone. I did, however, find that the pay phone
outside the accessible washroom was missing from the wall – a shaded
paint stain indicating to me that a phone was once here. Despite no phone and just as
firefighters started using the butt of an axe to break through the glass
balcony door, a Security person showed up who was pressed into service to
straightforwardly open the doors.
No
fire alarm was sounding but more firefighters were arriving. The fifth floor was filled with the
sound of firefighters’ loud voices issuing directions to each other as well as
the electronic clatter of voices over walkie-talkies; there had also been the
thudding sound of their attempt to break through locked doors; and then, once
the balcony was accessed, the smell of smoke flowing into the hallway near our
classroom. While no one was
speaking to our group, all these unusual sounds, sights, and smells, led me to
believe that I should talk to someone in charge.
One
firefighter was standing near a red fire hose box near the balcony door. This hose box, like the doorway to the
balcony, was in close proximity to our classroom. To this firefighter who was semi-stationary unraveling a
fire hose, I said, “Should we evacuate?”
“Yes,”
he said.
I
said that there were many people in our classroom who had mobility and other
impairments. He said that the fire
was out on the balcony. The firefighter did not appear too concerned, and I
began to glean the impression that soon the fire would be under control, after
all no alarm was sounding. So,
stating more than asking, I said, “Oh, so we don’t have to evacuate…”
“No.
Evacuate,” was the reply.
I
repeated my prior comment and said that many people in our classroom have
mobility impairments. This did not
seem to make an impression on him as he did not respond. I got more specific, saying that there were
wheelchair users, people with visual impairments. There were people who, if forced to use stairs, would face
danger. I said very emphatically
that we needed assistance and the firefighter said that he would send someone over. But the walky-talkies so frequently in
use in the hallway, as well as the loud voices among the firefighters, remained
silent on this issue. I continued… given that the fire is outside the building,
could we use the elevators? “No,”
said the firefighter, since the elevators were under the control of the fire department. He continued with his work of
unraveling the hose.
The
smell of smoke was not as strong as the growing sense of threat that there
would be no assistance. Repeating
myself, I said that evacuating by stairs would be a problem. A different firefighter said, while
moving out of the building on to the balcony, that he would send someone
over. This never happened.
I
returned to the elevator area, thinking that perhaps I simply missed locating
the security phone. Still, there
was no phone, but there was a blue poster that read:
MOBILITY-IMPAIRED
FIRE PROCEDURES
When stairs are not an option.
Know what to do. Be safe.
This
poster had a little plastic slot that holds cards stamped with a big University
of Toronto icon on one side and security phone numbers on the opposite side in
tiny, eight font
(perhaps smaller) lettering. When
this card system was installed a few months earlier, there were complaints at
faculty council about its inaccessible features. Now, I was simply sorry to find that the cards were
missing. I did not have a pen on
me and given my dyslexia, I did not attempt to memorize the security phone
number posted outside the elevators.
Only
a few minutes had passed. No fire alarm was sounding. No public announcement was made. Still, on my way back to the classroom, I heard a voice
behind me say “Evacuate.”
Back
in the classroom, people had already begun to collect up their belongings. They
told me that someone walking by the classroom had called into the classroom,
“Take the stairs.” I told the
group that the firefighters do not seem too worried about the fire which was
outside on the fifth floor balcony, but that they did want us to evacuate.
Then
-- it all happened fast and without guidance -- but this is what participants
reported to me: People carried
their colleagues down the stairs, one person slid down on their bum which could
have exacerbated a health condition, while colleagues carried a wheelchair,
others risked their own safety, e.g., sliding their foot down while grasping a
rail in one hand a colleague in the other. Anxiety in the midst of so many unknowns abounded. For some, unfamiliar with the
stairwells and reaching what they assumed was the exit door and finding it to
be locked, a deep sense of dread ensued.
From
my perspective, back in the fifth floor hallway, firefighters were still
striding by the rest of us who continued to move toward the stairwell of the
building to wait our turn down the stairs. The last four of us to evacuate
represented the distinctive diversity of various sensory, emotional, physical,
learning differences. Entering the
stairwell, we were met by two people walking down the stairs and about to exit
on to floor five. We told them of
the fire and the evacuation. They
hurriedly re-entered the stairwell and who they may have passed on the stairs
below or what that passing may have looked like, I can only imagine.
We
were ignored by all who had professional responsibility for security and safety
that day. We also faced a series
of environmental barriers such as missing phones and signage. Moreover, no one was willing to wait
behind as per university protocol.
Instead, the Disability Studies Summer Institute participants feared for
each other’s safety throughout the evacuation process and risked their own
safety too, in favour of mutual support.
This expectation for mutual support in times of trouble was not,
however, shared by the authorities.
Upon reaching the ground floor, many in our group encountered unhelpful
campus police. The people who
first left the building did not know if everyone made it down and tried to
inform the firefighters of this fact via the campus police. Facing a lack of official recognition
and response, while holding a basic but growing concern for one’s colleagues, only
added to a building sense of collective alarm. It is counter-intuitive that a lack of mutual recognition
could be ‘good’ for anyone involved in emergency work but, somehow, this lack
of response held together as a reasonable and universal response from
authorities that day.
As
a group, we eventually figured out that everyone was out of the building. As a group, we continued to wait
outside during a heat wave, insisting that we needed to talk to the fire
department about this dangerous evacuation experience, long after they may have
believed the “crisis” had passed.
No one wanted to leave without letting authorities know how dangerous
the evacuation had been, and how unacceptable their response had been. We patiently waited, trying to engage
police and security to discuss the events and learn more about both what had
happened and what would happen next. Upon returning for the third time to the
front door of the building, and as I saw fire-fighters heading toward the back
exit door, I was told by campus police, to “Keep my ideas in my head,” since
this was now a fire investigation.
I said that we, as a group, were part of what needed to be investigated. Facing only hostility, I returned to
the group and continued to wait in the extreme afternoon heat. In the meantime, we were not asked any
questions nor were any ones’ health needs assessed by anyone officially
involved in this evacuation. Some
people had headaches, some were crying, some were sweating profusely, some were
talking and others taking notes or pictures. From my perspective, it seemed we shared a troubled sense of
a profound lack of recognition by officials regarding what we had undergone as
well as a peculiar sense of camaraderie as a group toward whom such treatment
is possible.
Perhaps
this is why everyone remained to express their thoughts both to campus police
representatives and to the fire department’s District Chief who came out to
talk to us after the building was cleared for re-entry. Many spoke not only of a lack of
assistance but also of a radical lack of understanding for the danger that was produced for us with this call to
evacuate. There was, we insisted,
a general failure to acknowledge us in our particularity, exacerbated by the
failure to acknowledge what we had just gone through. Thus, our point, put most succinctly by one participant: “Not
the fire, but instead the evacuation itself was the danger!” Emergency officials, processes, as well
as the missing or impoverished emergency structures all worked together to fan
this little fire into a blazing display of voided mutual recognition, including
a lack of recognition for embodied differences.
Whatever
else this account might be, it is the stuff of everyday life that is good to
think with; that is, it was “borne of the aporia that engenders the
interrogation of what it means to be human both individually and collectively”
(Michalko, 2002:167). It is also a way to explore an array of circumstances which,
combined, ironically enough to make a vivid illustration of one of our primary
areas of interest at the Disability Studies Summer Institute, namely, the
social constitution of the edges of humanity and its outsiders. Thus, I turn now to explicate some of
this story from a disability studies perspective as a way to show the differing
forms of “crisis” that are in play.
Engaging the Evacuation
It may seem obvious
enough that a fire on an outside balcony that prompted no Official to sound the
building’s fire alarm represents only a little crisis poorly managed. However,
from a disability studies perspective there are other ways to conceive of the
crisis especially as this relates to understanding bodies in social space. For
example, my account of the evacuation references bodies, specifically
impairments, but to what end? Bodies
described as impaired or different might be read as if they caused the danger
of this evacuation. Recall too
that disability is typically conceptualized and documented as a problem and
this ubiquitous social act lends sense to the otherwise peculiar idea that
embodied differences are a reasonable place to locate the problem of this
evacuation. It is possible that by noting bodies I reproduce them as the
problem and I do not draw to our attention to the unimaginative version of the “normal
evacuee” that was being perpetuated by this scenario. But instead of reproducing a taken-for-granted sense of
disability-as-problem, let us continue to examine it.
Starting
from a most basic sense that disability is a social, not natural, phenomenon
the danger of the evacuation is not located in our bodies. Neither emergency processes nor the
bodies involved are signifiers of nature -- there is nothing “natural” to be
found in this evacuation. Inadequate
and as wrong as they were, the physical environment, the evacuation procedures,
the forms of engagement by the firefighters, security, campus police, are social; they are social practices
not predetermined by nature, not even by the nature of fires. The social
practices and structures of evacuation interacted with this particular group of
people transforming our differences or impairments into disabilities, and
further transforming disabilities into dangers. To believe otherwise is simply to decontextualize the body. Thus, not bodies but rather their
de-contextualization can now be understood as part of the crisis that caused
the dangerous evacuation scenario.
Understanding the evacuation in this way can put into crisis the
taken-for-granted sense of disability-as-problem that the evacuation relied on
and certainly reproduced.
But
what sort of problem was disability made to be? Given that none of the protocols, procedures, or
environmental structures actually address the people who were asked to
evacuate, or the actual people who work and learn in this University space
every day, bodily differences were made into potentially deadly threats. Neither
fires nor bodies need to be understood as “naturally” dangerous, but finding
fires in contexts they are not expected, as well as making some bodies
unexpected in some environments, makes for danger. The production of disability-as-danger
that day teeters on the edge of human rights violation as well as serious
health and safety issues. Insult
was added to injury when this did not appear to be immediately obvious to the
officials involved who stood unconvinced that they had participated in the
production of danger, thus repeating the degradation.
I
can also report, however, on a further strange turn of events. A refusal to understand disability as a
natural disaster waiting to happen, a refusal to take disability as a strange
outsider that is impossible to include, and instead insisting on the necessity
of human recognition between disability and non-disability, makes for a
different sort of crisis in understanding that leads to immediate changes. “Job
competency” and the “ordinary environment,” for example, appear much
differently when disability is not regarded as grounds for inaction and indifference.
Suspending a belief in disability as always-already the problem, comes with a
different set of consequences; it has led to framing the evacuation as
catastrophically dangerous and not as a minor mis-hap;
taking the perspective that disability belongs, has led to the Dean of OISE
launching investigations and complaints and thereby changing environmental
structures, protocols and personnel.
When understood only as problem, however, impairment and differences end
up framed by social processes that turn human embodiment against itself,
displacing people from the space of mutual human recognition.
But
there is more to this crisis. Just
as it turns out that the fire was not as dangerous as the evacuation was, so
too the evacuation might not be as dangerous as are some of the other ways we
now interpret it. For example, it
is possible, even tempting, to say:
What
a horrible thing to have happened – it could have been a lot worse. But perhaps the fire department and
others did not know about disability, and thus they failed to do the right
thing. Maybe now they will undergo
disability awareness training.
Then, things will be better.
I am sure it won’t happen again.
This
seems to be a reasonable way interpret the evacuation but, still, a basic
premise of a disability studies analysis is to consider what “reasonable
responses” make of disability. The above expresses the idea that it is
a lack of knowledge that is the problem and that disability awareness training might
be the solution. Something about
disability appears to be unknown.
But what is it and what especially needs to come to be known?
People
certainly need to know that stairs are not always an option. But this is known. The poster on every floor of the
building that reads, “When stairs are not an option… be safe” announces, among
other things, the common knowledge that stairs are not always a safe evacuation
option. Perhaps the unknown is
more precise, namely, that stairs are not an option for some people. But is
this then an invitation to imagine yet another crisis located “in” certain bodies?
Reasoning
that the production of danger occurred through a basic lack of disability
knowledge suggests that it is not stairs as a mode of evacuation that needs to
be re-thought but, instead, that there is something about bodies that needs to
be learned. This potentially enforces an understanding of disability as “far
out,” since it is reasonable to assume that disability disrupts even the most
common of lived experiences, namely, that every environment has limits and everybody
moves ambiguously within these environmental limits. The inescapable reality of embodied existence as a
context-dependent phenomenon is shared by every living person whether disabled or
currently non-disabled. Put more
basically, in evacuations sometimes non-disabled people cannot take the stairs
thus revealing that the doing and the meaning of an evacuation is not dependant
on bodies alone. To ignore or forget non-disability’s tie to embodied ambiguity
situated in the context of environmental limits and to make disability’s tie to
this ambiguity so “far out” that mutual recognition disappears is to erect a (mythical)
dividing line. Disability may even be made to represent a line of no
return. Moreover, the assumption
that professionals need more awareness of disability as a
really-far-out-alien-location-of-disruptive-ambiguity is unlikely to change the
social processes at play that throw disability on to one side of the line
between mutual recognition of the human community and its opposite. Still, thrown
to one side, it then becomes reasonable to conceive of disability-knowledge
itself as a barrier to other people competently accomplishing their jobs.
Lessons Learned
Interpretive responses
to the evacuation attest to at least two lessons. There are social processes in play that serve to transform difference
or impairment into disability-as-danger.
There are also social processes at play that transform seemingly reasonable
responses to embodied differences into a place for questioning and
inquiry. Sometimes this latter
form of transformation is called “disability studies” and as a transformer of
normal reasoning into a space of questions it plays a role in undoing the
normalization of injustice and human degradation. It is this perspective that animates my need to regard dangerous
events not only as in need of documentation but also in need of analysis. The sense we make of difficult
disability events can be examined for how it plays a part in the production of the
crises that make some people count as less than human. It is not simply that
some bodies do not matter. It is
instead that disability is made to matter as if it is decontextualized from the
human community that both causes the crisis that disability is made to be and itself
needs to be put in crisis through critical inquiry.
A
failure to consider the conceptions of disability that already inform our
engagement with our bodies, minds, senses, comportments, is to risk… no, is to enforce
the status quo. This solidifies the normalization of human
diminishment. Disability as
currently conceived and governed – almost always as problem and never as
promise (Titchkosky, 2011b) – normalizes the notion that there are some
humans too questionable to live with, or to imagine including, hanging out with,
or building into collective everyday realities. Disability studies invites a consideration of the versions
of (non)human that are difficult to include into our physical and imaginative
structures as anything but crisis, burdensome, or dangerous in order to reconsider
cut-off points for participation, worth.
Thus we also perhaps revisit conceptions of the human itself. We need not only celebrate the arrival
of disability studies into the academic scene, or rehearse its internal
critiques, but also regard our work as an occasion to focus on the margins of
the question of the human.
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[1] The
Disability Studies Summer Institute was funded by the Dean of OISE, Julia
O’Sullivan, and supported by Rinaldo Walcott the Chair of Sociology and Equity
Studies in Education at OISE, as well as by my SSHRC grant, “The Cultural
Production of Disability as an Excludable Type in University Life,” held with
Rod Michalko. The full schedule of
presentations, other related texts as well as some presentations are archived
at Manchester Metropolitan University http://disabilitystudiessummerinstitute.posterous.com/