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Hand
& Eye: Fifteen Years of the Dorothea Lange–Paul Taylor
Prize
September 19, 2005–January 8, 2006
Juanita Kreps and Lyndhurst Galleries

The Garden of Eden:
Living with Schizophrenia on Coney Island
DONA ANN MCADAMS AND BRAD KESSLER (2002)
Over the past few decades, institutional homes for adults with schizophrenia
and other mental disorders have multiplied on or near Coney Island
in Brooklyn, New York, making the area a kind of clearinghouse for
Manhattan’s mentally ill. The group homes, generally private
institutions run for profit, remain the twenty-first century’s
equivalent of the “back wards” of years gone by. Dona
Ann McAdams has photographed in day programs, adult homes, and homeless
shelters throughout the New York City area for nearly two decades,
and she continues this work today. McAdams and Brad Kessler’s
project focuses on a community of schizophrenics who live in a group
home called the Garden of Eden.
PHOTO GALLERY
Photographs by Dona Ann McAdams
Hand Coloring by Workshop Participants at Brooklyn Day Program
WRITING
Garden of Eden
By Brad Kessler
Catch the Culver Local at 42nd or
34th, Broadway or Delancy, and you can count the stops there. Thirty-one
in all, each ticking by like tacks on a wheel of fortune. The train
empties as it goes, so the only ones emigrating in the early dawn
are those who’ve slept the night in their seats.
In Brooklyn, you’re in the air, staring into the upper stories
of walk-ups, at people in positions of repose, sleeping in beds
or combing hair or pulling on pairs of socks for the weekday. Their
windows are wide in June, or scalloped by spinning fans. Soon the
alphabet begins, Avenue A, B, and C, and runs the entire stretch
of Brooklyn, until X leads to Y and then to Z, and you’re
left with no letters, no words, no language. Nothing but the ocean
and the air at the terminal tip of New York, where the city peters
into a strand of sand and the buildings are broken and sinking back
to the sea. Here is the end of the line. Coney Island. The last
and final stop.
Fog breathes over the park, lifts and swirls, blows down avenues
and dissolves off Coney Island Creek. A dog barks somewhere beside
the ocean. There is moisture in the air, on sewer caps, on the boardwalk
benches. The world is evaporating this morning. The fog owns everything.
We’ve been coming out here for some time now. Each Friday
in the early morning we make our way to a building at the end of
Surf Avenue. The building, which used to house the local Y, now
holds the Brooklyn Day Program; it is a place for people with mental
illness. People come here from all over Brooklyn but most arrive
from the institutional homes nearby: The Garden of Eden up Stillwell
Avenue, Surf Manor, next door; Seabay, Seaport, or Mermaid Manor,
all a short bus ride away. People come to Brooklyn Day for medication
and meals, for counseling and group therapy, for classes in music,
art, social, and daily life skills. They come to Brooklyn Day to
pass the hours and stay off the streets. They come, in most cases,
because they’ve nowhere else to go.
The fog has not yet lifted off the island, and a bank of fluorescent
lights burn above. Twenty-five people have shown up for Dona’s
Friday art workshop, and they’re settling into seats, choosing
crayons, pencils, and pads of paper. The participants all suffer
from an assortment of illnesses (including schizo-affective, bipolar,
and compulsive disorders), yet most have been diagnosed with schizophrenia.
Many have been institutionalized before, some for decades, others
for shorter stays, and nearly all are on heavy medication, usually
anti-psychotics (such as Mellaril, Prolixin, Haldol, or Clozaril).
Jacob T. is walking around the classroom taking a survey. He’s
trying to find out who makes more money, Dean Martin or Jerry Lewis.
Jacob is in his early sixties, wears a gray wool cardigan and glasses
as thick as bottle bottoms.
“Dean Martin or Jerry Lewis,” he asks at one table.
“Who you think makes more money?” He waits for someone
to answer, but no one pays any attention and he moves on to the
next table.
Out the opened windows, we can hear buoys ringing in the bay, the
surf breaking beyond the boardwalk. It is a soothing sound, and
everyone seems to be at ease this morning. Arthur B. is in his corner
sketching an electrical flow chart on a piece of manila paper. On
good days, Arthur always draws electricity, creating intricate maps
of how a current moves in a system, through armatures and transformers,
the current turning positive then negative. He carefully draws in
the voltage and the values of the electricity. He used to be an
electrician, and now lives nearby in a large institutional home
for adults. On bad days, Arthur doesn’t do electricity at
all. On bad days, he draws flowers.
Over the centuries, the severely mentally ill have garnered a variety
of names: lunatics, hysterics, the insane, the demented, the deranged.
The term “schizophrenic” is a relatively new one. It
was coined in 1911 by the Swiss psychiatrist Eugene Bleuler. Bleuler
took a whole set of aberrations and “conditions” and
created a catch-all phrase to describe them. The resultant disease
(for it was now considered, like syphilis or polio, a disease) was
schizophrenia. Though Bleuler’s disease was not based on any
medical evidence, it nonetheless caught on as a convenient tool
for defining what the severely mentally ill suffered from. Schizophrenia
(contrary to popular belief) had nothing to do with split-personalities.
Instead, it described a whole range of baffling behavioral disorders:
delusions, hallucinations, catatonia, inappropriate emotions, “disordered”
thinking. In short, it meant the schizophrenic had lost his or her
grip on known reality, that they were living under a different set
of assumptions than the rest of the world. It meant they had entered
a country of their own which had its own language and logic, a place
where they heard voices and saw things no one else had seen.
Today, medical science still cannot say what causes schizophrenia,
but a few things are certain: that schizophrenia is global, that
it shows up in just about every culture, and that it is very widespread.
One out of every one hundred people in a given population are afflicted
by schizophrenia (there are 2.5 million schizophrenics in the United
States today). That we come into contact with so few schizophrenics
in our daily life does not mean they do not exist; it means, simply,
we’ve done a good job in hiding them. They’ve been sent
to homes and hospitals and halfway houses where they are less visible—and
less troubling—to the rest of the population. A small percentage
(and those generally whose family’s have money) are treated
effectively and are functioning. Yet for the most part, in the United
States at least, schizophrenics are completely ghettoized.
Most of the people who attend the Friday workshop have been diagnosed,
at one time or another, with schizophrenia. When and where they
first developed symptoms of the disease varies with each person,
yet it is safe to say that it first struck in their late adolescence,
specifically between the ages of fifteen and twenty-six. Before
that, several of the people in the workshop may have had personality
disorders, but otherwise there may not have been any unusual signs
that they were “different” or “odd.” At
a certain point (because they had locked themselves in a room and
refused to come out, or because they left the house stark naked
one afternoon, or because they tried to drink a bottle of nail polish
remover) they were taken (often forcibly) to the hospital. There
a psychiatrist interviewed them (and probably shot them with a strong
sedative) and there they were given a diagnosis (schizophrenia)
and from that day on, their life, and the lives of those closest
to them, was never the same again.
Many years ago, when Dona first started coming to Brooklyn Day,
she brought with her half a dozen inexpensive cameras and taught
the participants how to take photographs. Although they never really
warmed to the technology, they enjoyed posing for pictures and sending
the prints to their families or pinning them to the walls of their
adult homes. One week, that same year, a woman in the class picked
up a crayon and began drawing on a photograph of herself. Everyone
looked on, fascinated. Soon, the whole class took crayons in hand
and started scribbling on the surface of their prints, coloring
in their faces, arms, legs, foreheads, creating characters of themselves
and adding their own interpretation to their images. As the weeks
went by, the workshop participants settled into a routine. They
would set up portraits of themselves, directing McAdams how they
wanted to be shot. Afterward, they’d edit her contact sheets,
deciding which pictures they wanted her to print (and which they
didn’t).
Not so many years ago, most of the people in the Friday art workshop
would have been, quite literally, locked away. They would have been
incarcerated in places like Pilgrim State, Creedmore, Kings County
Hospital—the large state mental health institutions whose
reign lasted for decades (until as late as the 1970s, and early
’80s). Some people who come on Friday mornings are veterans
of the state institutions, and they bear the scars (sometimes literally)
of their years of incarceration. They are elderly now, and their
generation is dying off and a younger generation of schizophrenics
are filling the classroom. And though much has changed since the
bad old days of the state institutions, much has remained the same.
The myth of the “violent schizophrenic” still looms
large in the public imagination, and the stigma of the severely
mentally ill, the schizophrenic, has not lessened over the years,
but has been made greater by deinstitutionalization, and homelessness,
and general lack of awareness. One day in class, a workshop participant
picked up a book on Vincent Van Gogh and read out loud a passage.
“During his lucid periods,” she read, “Van Gogh
was quite extraordinary.” She put the book down and said:
“If only they could describe us that way. If only they thought
we were like Vincent Van Gogh. Extraordinary. Instead, they think
we’re shit.” She closed the cover of the book and shook
her head, and we thought, yes, if only they were thought of as so
many Vincent Van Goghs, troubled and alienated, yes, suffering from
a severe brain disease, yes, but also sensitive and vulnerable and
artistic—even heroic in their daily struggle for a way to
survive in this world.
banner image:
Installation view of Hand & Eye:
Fifteen Years of the Lange–Taylor Prize. Photograph
by Christoper Sims.
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