Eli Clare - Freaks & Queers
Eli Clare - Freaks & Queers
Eli Clare - Freaks & Queers
1. NAMING
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accident disabled her): in all its forms it means "unable," but where
does our inability lie? Are our bodies like stalled cars? Or does disability live in the social and physical environment, in the stairs that
have no accompanying ramp? I think about language. I often call
nondisabled people able-bodied, or when I'm feeling confrontational, temporarily able-bodied. But if I call myself disabled in order
to describe how the ableist world treats me as a person with cerebral palsy, then shouldn't I call nondisabled people enabled? That
word locates the condition of being non disabled, not in the nondisabled body, but in the world's reaction to that body. This is not
a semantic game.
Cripple. The woman who walks with a limp, the kid who uses
braces, the man with gnarly hands hear the word cripple every day
in a hostile nondisabled world. At the same time, we in the disability rights movement create crip culture, tell crip jokes, identify a
sensibility we call crip humor. Nancy Mairs writes:
I am a cripple. I choose this word to name me .... People-crippled or
nor---wince at the word cripple. as they do not at handicapped or disabled.
Perhaps I want them to wince. I want them to see me as a tough customer, one to whom the fates/gods/viruses have not been kind, but who can
face the brutal truth of her existence squarely. As a cripple, I swagger.'
Gimp. Slang meaning "to limp." Gimp comes from the wordgammy,
which hobos in the I8th century used among themselves to describe
dangerous or unwekoming places. Hobo to hobo, passing on the road:
"Don't go there. It's gammy." Insider language, hobo solidarity. And
now a few centuries later, one disabled person greets another, "Hey,
gimp. How ya doin?" Insider language, gimp solidarity.
Retard. I learned early that words could bruise a body. I have
been called retard too many times, that word sliding off the tongues
of doctors, classmates, neighbors, teachers, well-meaning strangers
on the street. In the years before my speech became understandable,
I was universally assumed to be "mentally retarded." When I started
school, the teachers wanted me in the "special education" program.
Differently abled is simply easier to say, easier to think about than disabled or handicapped or crippled.
Freak. I hold fast to my dictionary, but the definitions slip and slide,
tell half stories. I have to stop here. Freak forces me to think about naming.
Handicapped, disabled, cripple, gimp, retard, differently abled. I
understand my relationship to each of these words. I scoff at handicapped, a word I grew up believing my parents had invented specifically to describe me, my parents who were deeply ashamed of my
cerebral palsy and desperately wanted to find a cure. I use the word
disabled as an adjective to name what this ableist world does to us
crips and gimps. Cripple makes me flinch; it too often accompanied
the sticks and stones on my grade school playground, but I love
crip humor, the audacity of turning cripple into a word of pride.
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Gimp sings a friendly song, full of irony and understanding. Retard
on the other hand draws blood every time, a sharp, sharp knife.
In the world as it should be, maybe disabled people would be dif
ferentlyabled: a world where Braille and audio-recorded editions of
books and magazines were a matter of course, and hearing people
signed ASL; a world where schools were fully integrated, health
care, free and unrationed; a world where universal access meant
exactly that; a world where disabled people were not locked up at
home or in nursing homes, relegated to sheltered employment and
paid sweatshop wages. But, in the world as it is, differently abled,
physically challenged tell a wishful lie.
Handicapped, disabled, cripple, gimp, retard, differentlyabled,freak.
I need to stop here. Freak I don't understand. It unsettles me. I
don't quite like it, can't imagine using it as some politicized disabled people do. Yet I want freak to be as easy as the words queer
and cripple.
like cripple, is an ironic and serious word I use to describe myself and others in my communities.
speaks volumes
about who I am, my life as a dyke, my relationship to the dominant culture. Because of when I came out-more than a decade
after the Stonewall Rebellion-and where-into a highly politicized urban dyke community-queer has always been easy for me.
I adore its defiant external edge, its comfortable internal truth.
belongs to me. So does cripple for many of the same reasons.
and cripple are cousins: words to shock, words to infuse with
pride and self-love, words to resist internalized hatred, words to
help forge a politics. They have been gladly chosen-queer by many
gay, lesbian, bi, and trans peoples, cripple, or crip, by many disabled
people.
Freak is another story. Unlike queer and crip, it has not been
widely embraced in my communities. 4 For mefreak has a hurtful,
scary edge; it takes queer and cripple one step too far; it doesn't feel
good or liberating.
This profusion of words and their various relationships to
marginalized people and politicized communities fascinates me.
The history of freakdom extends far back into western civilization. The court jester, the pet dwarf, the exhibition of humans in
Renaissance England, the myths of giants, minotaurs, and monsters all point to this long history, which reached a pinnacle in the
mid-I8oos to mid-I900s. During that century, freaks were big entertainment and big business. Freak shows populated the United
Since '999, I've been taken to task by folks in BOSM and leather communities
more than once for my analysis of the word pervert. In my '999 endnotes, I try to
soften my analysis by claiming that the word hasn't been "used to construct both
individual and communal identities." But my reasoning is exactly wrong when seen
from inside BOSM communities where claiming pervert has in truth been central
to building a communal identity. The ways I have misread the word as an outsider
to the BOSM world is a great example of how reclaiming the ugly words has so
much to do with context. My original intent to find words in LGBT communities
that were analogous to the word retard in disahility communities becomes extraordinarily complex.-E.C.,
2009
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States, and people flocked to the circus, the carnival, the storefront
dime museum. They came to gawk at "freaks," "savages," and "geeks."
They came to be educated and entertained, titillated and repulsed.
They came to have their ideas of normal and abnormal, superior and
inferior, their sense of self, confirmed and strengthened. And gawk
they did. But who were they gawking at? This is where I want to
start.
Whatever these paying customers--rubes in circus lingo-believed, they were not staring at freaks of nature. Rather, the freak
show tells the story of an elaborate and calculated social construction that utilized performance and fabrication as well as deeply
held cultural beliefs. At the center of this construction is the showman, who, using costuming, staging, elaborate fictional histories,
marketing, and choreography, turned people from four groups
into freaks. First, disabled people, both white people and people
of color, became Armless Wonders, Frog Men, Giants, Midgets,
Pinheads, Camel Girls, Wild Men of Borneo, and the like. Second,
nondisabled people of color-bought, persuaded, forced, and kidnapped to the United States from colonized countries allover the
world-became Cannibals and Savages. Third, nondisabled people
of color from the United States became Natives from the Exotic
Wilds. And fourth, nondisabled people with visible differencesbearded women, fat women, very thin men, people covered with
tattoos, intersex people-became wondrous and horrifying exhibits. Cultural critic and disability theorist Rosemarie Garland
Thomson argues that the differences among these sometimes
overlapping groups of people melded together:
Perhaps the freak show's most remarkable effect was to eradicate distinctions among a wide variety of bodies, conflating them under a single
sign of the freak-as-other.... [A}U the bodily characteristics that seemed
different or threatening to the dominant order merged into a kind of
motley chorus line of physical difference on the freak show stage .... [A}
non disabled person of color billed as the "Fiji Cannibal" was equivalent
to a physically disabled Euro-American called the "Legless Wonder."6
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unknown African men and women did not slide into the world as
infant freaks. They were made freaks, socially constructed for the
purposes of entertainment and profit. This construction depended
not only upon the showmanship of the "freaks" and their managers. It also capitalized on the eagerness of rubes to gawk at freaks
and on the ableism and racism, which made the transitions from
disabled white person, disabled person of color, nondisabled person of color, to freak even possible. Without this pair of oppressive
ideologies, the attendant fear and hatred of all disabled people and
all people of color, and the desire to create an Other against whom
one could gauge her/his normality, who could ever believe for even
one farcical moment that William Johnson was Darwin's missing
link; Barney Davis, a wild man from Borneo; Ann Thompson, an
armless wonder?
Ann, in that photo ofyou with your husband and son, you sit on a rug
decorated with crosses, a rug you crocheted. The showmen made a big deal
ofyour dexterity. But did you learn to crochet as afreak show stunt? Or did
you, like so many women ofyour time, sew and knit, embroider and crochet,
simply as a necessity and a pastime?
Within this context of able ism and racism, the people who
worked the freak show did not live only as victims. Many of the
"freaks" themselves---particularly those who were not cognitively disabled or brought to the United States from Africa, Asia, South and
Central America, the Pacific islands, and the Caribbean-controlled
their own acts and displays, working alongside their managers to
shape profitable shows. Many of them made decent livings; some, like
Charles Stratton, Mercy Lavinia Warren Bump, and William Johnson, even became wealthy. When P T. Barnum lost all his money in
a bad business deal, Stratton came out of semi-retirement and rescued him by agreeing to go on yet another lucrative European tour.
Others, like the Hilton sisters, conjoined twins who worked in the
mid-I900S, became their own managers, or, like Bump and her Lilliputian Opera Company, formed their own performing groups,
which were employed by dime museums and traveling vaudeville
companies. In other words, white, nondisabled freak show owners
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and managers didn't only exploit "their freaks." The two groups
also colluded together to dupe the audience, to make a buck off the
rube's gullibility. Within the subculture of the freak show, rubes
were understood as exploited victims-explicitly lied to, charged
outrageous sums for mere trinkets, pickpocketed, or merely given
incorrect change at the ticket counter.
Charles, there is a picture ofyou, taken during a visit with the
of England. You have a miniature sword drawn and are staging a fight
with a poodle. Your wife, Mercy, writes ofembarrassment and outrage. Of
presidential candidate Stephen Douglas, she remembers: "He expressed
great pleasure at again seeing me, and as I stood before him he
took my hand and, drawing me toward him, stooped to kiss me. I
instinctively drew back, feeling my face suffused with blushes. It
seemed impossible to make people at first understand that I was
not a child."8 Did you share her embarrassment and outrage as you
faced that poodle.? Or didyou and Barnum laugh long and hard as you
concocted your stunts?
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times the job was lousier than others. The African women and
men who performed as "Ubangi savages" made a nickel on every
photograph they sold, nothing else; whereas their manager, Ludwig
Bergonnier, made $1,500 a week renting "his display" to the Ringling Brothers Circus. In contrast, Charles Stratton became rich,
owning a horse farm and a yacht. Still others, like William Johnson,
found community among the people who worked the freak show.
You who ended up in the history books named only "Ubangi Savages,"
no names ofyour own: night after night, you paraded around the circus tent,
air sticky against your bare skin, burlap prickly against your covered skin.
Did you come to hate Bergonnier?
What did the people who worked as freaks think of their jobs,
their lives? I want to hear their stories, but like the stories of other
marginalized people, they were most often never told, but rather
eaten up, thrown away, lost in the daily grind of survival. Some of
these people didn't read or write, due to their particular disabilities or to the material/social circumstances of their lives. Or, as in
the case of many of the people brought here from other countries,
they didn't speak English and/or didn't come from cultures that
passed stories through the written word. A few people who worked
the freak show did write autobiographies, but these pamphlets or
books were mostly part of the whole production, sold alongside
the handbills and photos. These stories ended up being part of the
showmen's hyperbole. So, in order to reconstruct, celebrate, and
understand the lives of the people who worked the freak show, I
rely on historians, like Robert Bogdan, who have sifted through
thousands of handbills, posters, newspaper articles, and promotional garbage used to create The Armless Wonder, The Wild Men
of Borneo. In large part, I will never truly know their lives but
can only use my imagination, political sensibilities, and intuition
to fill the holes between the outrageous headlines in the New York
Times and other newspapers and the outrageous handbills sold at
the carnival.
The historians who moralize about the freak show frustrate
me. These academics will take a detail, like the fact that Hiram and
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During the freak show's heyday, today's dominant model of disabilitythe medical model-did not yet exist. This model defines disability
as a personal problem, curable and/or treatable by the medical
establishment, which in turn has led to the wholesale medicalization
of disabled people. As theorist Michael Oliver puts it:
Doctors are centrally involved in the lives of disabled people from the
determination of whether a foetus is handicapped or not through to
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It was all too easy for white people to gawk at people of color,
using the image of dog-eating savages from far-away "uncivilized"
islands both to create and strengthen their sense of white identity
and white superiority.
During this same period of time, imperialism had intensified
to a fevered pitch, both abroad in places like the Philippines and
at home as white people continued to subjugate and destroy Native peoples and cultures. By the time of the 1904 World's Fair,
the United States had won the Spanish-American War and gained
control over the Philippines. In explaining his decision to solidify
the United States' colonial rule there, President McKinley referred
to "our civilizing mission." What better way to justify that mission,
than to display Filipino people as "uncivilized savages"?
This interplay between politics and the freak show also occurred on the national level. For instance, the missing-link evolutionary theory, used so profitably by showmen, supported slavery
before Emancipation and the suppression of civil rights after. But
the freak show didn't only use this ideology. The display of Black
and white cognitively disabled people and nondisabled people of
color as the "missing link" and the "What Is It?" actually bolstered
the theory. The scientists and politicians could point to William
Johnson and say, "See, here is living proof. Look at this creature." In
doing so, they were reaffirming the less-than-human status of people of color and rationalizing much of their social and political
policy. Simply put, the freak show both fed upon and gave fuel to
imperialism, domestic racist politics, and the cultural beliefs about
"wild savages" and white superiority.
The decline of the freak show in the early decades of the 20th century coincided with the medicalization of disability. As pity, tragedy, and medical diagnosis/treatment entered the picture, the
novelty and mystery of disability dissipated. Explicit voyeurism
stopped being socially acceptable except when controlled by the
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Robert Waldow and Violet and Daisy Hilton tell. All of them lived
during the freak show's decline as medicalization took hold.
Robert Waldow, a tall man born in the 1920S, resisted becoming a giant, a freak. He wanted to be a lawyer, but unable to get the
necessary education, he turned to shoe advertising. And later, after being pursued for years by showmen, he worked for the circus,
earning a large salary and refusing to participate in the hype that
would have made him appear taller than he really was. At the same
time, doctors also pursued Robert, reporting him to be the tallest
man in the world-this being medical hype, not circus hype. They
refused to leave him alone. In 1936 a Dr. Charles Humberd showed
up uninvited at the Waldow's home. Robert refused a physical exam
and wouldn't cooperate with the interview. Humberd left disgruntled and the next year, unbeknownst to the Waldows, published
an article in the Journal of the American Medical Association called,
"Giantism: A Case Study," in which Robert became a case study of
a "preacromegalic giant." Because of the article, which cast him as
a surly brute, Robert and his family were deluged with unwelcome
attention from the media, the general public, and the medical establishment. In the biography The Gentleman Giant, Waldow's father reveals that Robert was far more disturbed and angered by his
dealings with doctors than with showmen.
Conjoined twins Daisy and Violet Hilton echo this reaction.
These women worked the circus, carnival, and vaudeville circuits
from the time they could talk. Early on, their abusive guardians
controlled and managed the show. They would lock Daisy and Violet away for days at a time to ensure that no one but rubes paying
good money could see them. Later, after a court order freed the
sisters, they performed on their own. The cover of one publicity
pamphlet has Daisy playing the saxophone, Violet, the piano, and
both of them smiling cheerfully at the viewer. Much of their lives
they spent fighting poverty as the freak show's popularity waned.
And yet in their autobiography, they write about "loathGngJ the
very tone of the medical man's voice" and fearing that their guardians would "stop showing us on stage and let the doctors have us to
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punch and pinch and take our picture always."20 Try telling Robert
Waldow and the Hilton sisters how enlightened today's medical
model of disability is, how much more progressive it is than the
freak show, how bad the bad old days were. Try telling Coco Fusco
and Guillermo Gomez-Pefia that the freak show is truly dead.
The end of the freak show meant the end of a particular kind of
employment for the people who had worked as freaks. For nondisabled people of color from the United States, employment by
the 1930S didn't hinge heavily on the freak show, and so its decline
didn't have a huge impact. And for people from Africa, Asia, South
and Central America, the Pacific islands, and the Caribbean, the
decline meant only that white people had one less reason to come
kidnap and buy people away from their homes. But for disabled
people-both people of color and white people-the end of the
freak show almost guaranteed unemployment, disability often being codified into law as the inability to work.
In the '30S when Franklin Roosevelt's work programs employed many people, the federal government explicitly deemed
disabled people unable to work, stamping their work applications
"P. H. Physically handicapped. Substandard. Unemployable,"
sending them home with small monthly checks. The League of the
Physically Handicapped protested in Washington, DC, occupying
the Work Progress Administration's offices, chanting, "We want
jobs, not tin cups."" In this climate, as freak show jobs disappeared, many disabled people faced a world devoid of employment
opportunities.
Listen for instance to Otis Jordan, a disabled African American
man who works the Sutton Sideshow, one of the only remaining
freak shows in the country, as "Otis the Frog Man." In 1984, his exhibit was banned from the New York State Fair when someone
lodged a complaint about the indignities of displaying disabled
people. Otis responded, "Hell, what does she {the woman who
Now with this history in hand, can I explain why the word freak
unsettles me, why I have not embraced this piece of disability
history; this story of disabled people who earned their livings by
flaunting their disabilities, this heritage of resistance, an in-yourface resistance similar to "We're here, we're queer, get used to
it"? Why doesn't the word freak connect me easily and directly to
subversion? The answer I think lies in the transition from freak
show to doctor's office, from curiosity to pity, from entertainment
to pathology. The end of the freak show didn't mean the end of
our display or the end of voyeurism. We simply traded one kind of
freakdom for another.
Take for instance public stripping, the medical practice of
stripping disabled children to their underwear and examining them
in front oflarge groups of doctors, medical students, physical therapists, and rehabilitation specialists. They have the child walk back
and forth. They squeeze her muscles. They watch his gait, muscle
tension, footfall, back curvature. They take notes and talk among
themselves about what surgeries and therapies they might recommend. Since the invention of video cameras, they tape the sessions.
They justify public stripping by saying it's a training tool for students, a way for a team of professionals to pool knowledge!3 This
isn't a medical practice of decades gone by. As recently as 1996, disability activist Lisa Blumberg reported in The Disability Rag that
"specialty" clinics (cerebral palsy clinics, spina bifida clinics, muscular dystrophy clinics, etc.) at a variety of teaching hospitals regularly
schedule group-rather than private--examinations and conduct
surgery screenings in hospital amphitheaters!4 Excuse me, but isn't
public stripping exactly what scientists and anthropologists did to
"Maximo" and "Bartola" a century ago? Tell me, what is the difference between the freak show and public stripping? Which is more
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quarter. My life story. Pay me. You think I'm being exploited? You pay to
go to a baseball game, don't you?"
Today's freakdom happens all the time, and we're not even paid for
it. In fact disabled people have, as a group, an astounding unemployment rate of 71 percent. ,6 When we do work' we make 64 cents
In 1999 I incorrectly cited the unemployment rate for disabled people. I assumed
that the unemployment rate equaled the employment rate subtracted from
100
percent.
However the two rates are calculated in entirely different ways. The employment
rate for disabled people factors in all non-institutionalized disahled people between
the ages of 18 and 64; whereas, the unemployment rate factors in only the disahled
people who are actively in the labor force. In
2002,
abled people was 21 percent; the corresponding number for nondisabled people was
78 percent. In the same year, the unemployment rate for disabled people was 14
percent, while for nondisabled people, it was 6 percent. Underlying these numbers
is the reality that a far greater percentage of the total nondisabled population is in
the labor force (83 percent) than of the disabled population (24 percent). For more
information, see www.i1r.comeII.edu/edilDisabilityStatistics/issues.cfm (accessed May
20, 2009).-E.C., 2009
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which pieces of that history we want to make our own, and develop
a self-image full of pride. The women and men who worked the
freak show, the freaks who knew how to flaunt their disabilitiesthe tall man who wore a top hat to add a few inches to his height,
the fat woman who refused to diet, the bearded woman who not
only refused to shave, but grew her beard longer and longer, the
cognitively disabled person who said, "I know you think I look like
an ape. Here let me accentuate that look"-can certainly teach us
a thing or two about identity and pride.
Pride is not an inessential thing. Without pride, disabled people are much more likely to accept unquestioningly the daily material conditions of ableism: unemployment, poverty, segregated and
substandard education, years spent locked up in nursing homes, violence perpetrated by caregivers, lack of access. Without pride, individual and collective resistance to oppression becomes nearly
impossible. But disability pride is no easy thing to come by. Disability has been soaked in shame, dressed in silence, rooted in isolation.
In 1969 in the backwoods of Oregon, I entered the "regular" first grade after a long struggle with the school officials who
wanted me in "special education," a battle won only because I
had scored well on an IQ test, my father knew the principal, and
the first grade teacher, who lived upriver from us, liked my family
and advocated for me. I became the first disabled kid to be mainstreamed in the district. Eight years later, the first laws requiring
public education for disabled kids, Individuals with Disabilities
Education Act (IDEA) and Section 504, were signed. By the mid1980s, mainstreaming wasn't a rare occurrence, even in small, rural
schools, but in 1969 I was a first.
No one-neither my family nor my teachers-knew how to
acknowledge and meet my particular disability-related needs while
letting me live a rather ordinary, rough-and-tumble childhood. They
simply had no experience with a smart, gimpy six-year-old who
learned to read quickly but had a hard time with the physical act of
writing, who knew all the answers but whose speech was hard to understand. In an effort to resolve this tension, everyone ignored my
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that happens so regularly I rarely even notice. I don't see peoplecurious, puzzled, anxious-turn their heads to watch my trembling
hands, my jerky movements. I don't see people strain to understand
me, then decide it's impossible. Long ago I learned to block all
those visual intrusions. I only know it happens because my friends
notice and tell me. Yet I know I store the gawking in my bones. Today's freakdom happens every time some well-meaning stranger or
acquaintance suggests a certain combination of vitamins, crystals,
or New Age visualization techniques that she knows will cure my
CPO I always want to retort, "Yeah right, like I'm looking for a cure,
like my brain cells that died some time before birth will magically
regenerate," but the moment inevitably passes before I can even
think of the words. This is my personal history of freakdom.
In addition,freak is shadowed for me by the complicated collective history of exploitation and subversion at the freak show. I relish
the knowledge that there have been people who have taken advantage of white people's and nondisabled people's urge to gawk. I love
that disabled people at one time were paid to flaunt, perform, and
exaggerate their disabilities. At the same time I hate how the freak
show reinforced the damaging lies about disabled people and nondisabled people of color. I despise the racism, ableism, capitalism,
and imperialism that had showmen buying and kidnapping people
into the freak show. I rage at how few choices disabled people had.
To infuse the word freak with pride, I would need to step
through my personal history of freakdom into the larger collective history of the freak show. Stepping through the last slivers of
my self-hatred, through the pain I've paired with gawking and the
word retard, I could use Charles Stratton's strut, Ann Thompson's
turning of the ordinary into the extraordinary, to strengthen my
own resistance. I could name myself a freak alongside Daisy Hilton, William Johnson, and Otis Jordan. I want it to work.
Instead the two histories collide in a madcap wheelchair race.
My personal history isn't so easy to step through; the slivers tear
my skin; the old familiar pain leaves me guarded and cautious. And
the collective history is hard to reduce to a pure story of resistance
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To unravel the relationship of the word freak to pride and witness, let me step back for a moment, move to the word queer, to
the LGBT community. I think it no accident that I've paired the
words queer and freak in this examination of language, pride, and
resistance. The ways in which queer people and disabled people
experience oppression follow, to a certain extent, parallel paths.
Queer identity has been pathologized and medicalized. Until 1973,
homosexuality was considered a psychiatric disorder. Today transsexuality and transgenderism, under the names of gender dysphoria
and gender identity disorder, are classified as psychiatric conditions. Queerness is all too frequently intertwined with shame, silence, and isolation. Queer people, particularly LGBTyouth, often
live cut off from other queer folk, alone in our schools, neighborhoods, and families of origin. Queer people deal with gawking all
the time: when we hold hands in public, defy gender boundaries
and norms, insist on recognition for our relationships and families.
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The pink triangle functions now as a symbol of identity, witness, and pride in queer communities. As a sign of identity, it communicates both covertly and overtly. That pink triangle graphic
worn on a button or stuck on a bumper may not have much meaning to many straight people-particularly those not connected to
or aware of queer culture-but among LGBT people, especially
in urban centers, it readily signals queer identity to other queer
people. In this fashion, the pink triangle functions as an insider's
language, a language attempting to include a marginalized people
while excluding the oppressor. It is also used more overtly to speak
of identity, sometimes incorporated into educational work about
the historical oppression of gay people, other times into activist
work. As a symbol of witness, it remembers and memorializes the
gay men who died in the Holocaust. It keeps the memory of Nazi
atrocities alive in our consciousness. It serves as a reminder of the
extremity of queer oppression. And as a symbol of pride, the pink
triangle neutralizes and transforms hatred, following a similar political path as the words queer and cripple. It is worn by out and
proud queer people. These functions-marking identity, expressing pride, insisting upon witness-go hand in hand, all three important for any marginalized community. In our search for liberation,
we can sometimes turn the language and symbols most closely reflecting our oppression into powerful expressions of pride. And yet
that equation sometimes betrays history; blurring the difference
between witness and pride.
As a symbol of pride, the pink triangle has frequently been
divorced from its history. In one ahistorical explanation of this
symbol, the owner of a Minneapolis gay bookstore tells his customers that pink triangles represent white gay men/lesbians and black
triangles-used by the Nazis to mark people deemed anti-social,
including, it is assumed, lesbians, as well as sex workers, cognitively
disabled people, and homeless people, during the Holocaustrepresent black gay men/lesbians. Divorced from its history; the
pink triangle becomes a consumerist symbol, used to sell T-shirts
and keychains; it becomes a lie. It is not and never will be the rain-
And now I can come back to freak. The disabled people who use
the word freak, are they, like many queer people, betraying witness
in their creation of pride? A disabled person who names herself
pridefully a freak draws on the history of freakdom and the freak
show to strengthen her sense of resistance, to name a truth, to
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bolster her identity. But in using history this way, is she remembering only Ann Thompson, Violet Hilton, and the cognitively disabled girl who, while on display, took to swearing at the rubes?
What about "Maximo" and "Bartola"? What about the nondisabled people of color who died at the freak show, desolate for their
homelands? When we name ourselves freaks, are we forgetting the
part of history that calls for witness, not pride? Are we blurring
the two?
How does the history of the freak show interact with the history of today's freakdom? How do our personal histories enter our
collective history? If I had not internalized nondisabled people's
gawking to the point that I no longer notice it, ifinstead I felt pissy
and uppity about it, would I be more able to imagine flaunting my
CP? Would I be more willing to take the resistance of the people
who worked as freaks as my own? Would I gladly use the word to
acknowledge a simple truth: that the world considers me a freak?
What about people disabled as adults, people who make it
relatively smoothly through the first rounds of denial, grief, and
rehab and maybe find the disability rights movement and disability
community? They don't have a long personal history of freakdom.
Hopefully shame, silence, and isolation haven't been buried deeply
in their bodies. What might their relationship to the history of the
freak show, to the word freak, be? Do they ache toward assimilation, not wanting to approach freakdom? Or does freakdom make
immediate sense? I don't know, but their relationships to freak
probably differ from mine. What about cognitively disabled people? What does freak mean to them? Where is the pride in a legacy
of being owned by showmen who exhibited you as non-human?
Again their relationships to freak show history are bound to differ
from mine.
I think of the disabled people I know who call themselves
freaks. Many of them are performers, helping to build disability
culture and/or working to break into mainstream culture. In using the name freak, they claim freak show history both as disabled
people and as showmen and -women. They shape pride out of a
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that whether I call myself freak or not, I share much with Ann
Thompson and William Johnson, Otis Jordan and Daisy Hilton. I
want to refigure the world, insisting that anthropologists never
again construct lies like the ones they built around the bodies of
"Maximo" and "Bartola," that doctors never again publicly strip
disabled children. I want to sharpen my pride on what strengthens
me, my witness on what haunts me. Whatever we name ourselves,
however we end up shattering our self-hatred, shame, silence, and
isolation, the goal is the same: to end our daily material oppression.