Now, with an
established ensemble, The Sharing Circle is support group and creative
incubator. The actors' attachment to the project and to each other
is fixed as much by the chairs they pull in a circle before rehearsal
as by the communal mission they share.
The DisAbility
Project is a theater ensemble of disabled and nondisabled actors.
In a society that once cast people with disabilities as destined
for a lifetime of institutionalization -- or even sterilization
-- the project gives people with disabilities a voice.
Onstage, the
company seeks to create art that is interesting and fresh. The project
asks its actors to reinvent themselves, just as people with disabilities
do in a world weighted in favor of those without disabilities.
But here, art
intersects with reality. The theater ensemble is about change, as
in changing perceptions about people with disabilities. They want
audiences to applaud them for what they can do rather than what
they can't. They want to be seen the way they see themselves.
As differently
abled.
And they want
society's fittest to see that people with disabilities are not so
different. Disability can happen any day to anybody through accident,
age or ancestry.
Within their
circle on one Saturday in May, Edith Ritterband breaks the ice by
informing the group she has taken her exam to become a paramedic.
Ritterband,
the company's community outreach coordinator, left Memphis, Tenn.,
on a Greyhound bus for St. Louis at 5 a.m. so she could make rehearsal.
"If I'm
tired, I have a better excuse than all of you," she says, teasingly.
"At Edith's suggestion I went to a Jewish singles speed-dating
thing," says Stuart Falk, with a nasal, self-deprecating delivery
similar to that of comedian Richard Lewis.
"There
were eight women and eight men. The women stayed put and the men
rotated from table to table. We only had about eight minutes with
each other. So then we had to go home and wait expectantly, while
we found out who we matched with. I matched with three women.
"Three
out of eight. Not bad for a guy in a chair."
Dating is hard
enough. But at 38, Falk has been married twice, divorced twice.
Empathetic smiles blossom around the circle.
"I spoke
with one of them," he continues. "She was kind of tops
on my list and I'm thinking, 'I hope she does call. I hope she does.'
So she did. And we have a tentative date Monday night."
He grits his
teeth and wipes imaginary sweat from his brow. The smiles around
the circle turn hopeful.
"I'll
keep you posted."
Anybody else?
Lipkin asks.
"I'm sorry
I missed last week," Katie Rodriguez begins. "I tried
on my dress. I've got six more days as a single woman."
"I bet
you look just like Julia Roberts," Rich Scharf says.
Need more teeth
for that, says Rodriguez, 35, who has a well-deserved reputation
for being perpetually perky and very well-organized. She is often
the first to arrive for rehearsal.
"I've
planned this so well I think I can actually enjoy the event,"
she announces to a smattering of applause.
In a week,
Rodriguez will marry. Not bad for a woman on wheels.
Actors and
advocates
The Sharing
Circle helps them shed the shrouds of their self-consciousness for
the comfortable cloak of trust. "People can take real artistic
risks when they know each other and are committed to a project greater
than themselves," Lipkin says.
The Sharing
Circle connects them, but it also provides inspiration for their
performance pieces. There's not exactly a whole body of theater
work out there for disabled actors or, for that matter, on the subject
of disability. So they draw from personal experience.
Lipkin, whose
edgy work with That Uppity Theatre Company has been acclaimed here
and abroad, has long written about those who know the pleasure and
pain of being different.
Project pieces
"Parking," "Coffeehouse" and "Attendant
Care -- What a Scare" speak directly to disability issues.
Falk delivers "Club Med" -- the name alludes to medicine,
not a posh resort -- with the battle-hardened humor of a veteran
of many hospital stays.
Jim Tuscher's
astonishment at seeing a televangelist's showy production inspired
the satirical "Healing Ministries." Another piece is universal:
the unleashed oppression of a doctor's waiting room. They're choreographing
a number to the Prince song "Kiss."
Two pieces
show the personal side of disability: One is a reflection on growing
up with asthma and another is about a quadriplegic's first sexual
experience since her car accident.
Everyone works
within his or her range of motions. In the piece on asthma, Rodriguez
thumps her chest playing asthmatic Marcia LaCour-Little's heart
and Colleen Gilmore and Nick Kalfas fan their arms as Marcia's imaginary
lungs. In a mirroring exercise, they begin a pretend day, regardless
of ability, by washing faces. They brush their teeth, their hair.
All the pieces are tweaked and picked apart till they are acted
to some elusive perfection, with actors learning more than one part
in case someone isn't able to be there. Lipkin can't tell you when
the pieces reach that perfect pitch where they are fresh, thoughtful
and sometimes irreverent -- but never preachy. She likes the way
a friend once described the sound of a club head's sweet spot striking
a golf ball. Ping! It's like that.
The players
always wind up a performance on the same note.
"We are
of you," they say in unison. "We are among you. We are
you. Do not be afraid."
Building
blocks
The Sharing
Circle segues into breathing exercises and shoulder massages by
Lipkin. The lights go down, the music up. The troupe tunes out the
rest of the world.
Stretching
and warm-ups are over. Lipkin wants to try a piece new to many of
them. She calls it "Waking in the Forest." Explore the
possibility of movement and the world around you, she directs them.
Think of yourselves,
she says, as single cell organisms. On that most basic biological
level, they are equals.
What's my motivation?
The theater
ensemble was Lipkin's idea.
Her ideas evolve
with the complexity of the atmospheric conditions -- clashing fronts,
cumulus clouds and electrical currents -- that converge to produce
lightning.
Personal trauma
does not make one compassionate, Lipkin insists. But she endured
her share of trauma growing up. She grew up in a middle-class, progressive,
ethnically diverse neighborhood on Chicago's south side. Her parents,
Evelyn and Stanley Lipkin, say their daughter was an intellectually
curious, shy and "not physically strong" child. They don't
remember her without a pen and a piece of paper in her hand. She
spun a fourth-grade assignment on state capitols into a play.
At age 7, a
neighbor's dog attacked her. When she returned to school, the other
kids taunted her. The scar is still visible, running from her right
temple down to her cheek.
"I think
she realized that there's potential for aggressiveness and violence
in the world," her mother says.
Lipkin once
marched home after school and demanded to know what her parents
had done to thwart Sen. Joe McCarthy, the Communist-hater.
In the past
four years, Lipkin has undergone four surgeries, at times sidetracking
her dream of a theater company of able-bodied and disabled actors.
In the fall of 1996, she was diagnosed with breast cancer.
Survival bestowed
on her a greater sense of urgency about her life and work, and a
personal revelation about what she calls the "fluidity of our
identity."
"This
is such a physical, external culture we live in, so that it's frequently
difficult to get through the packaging," Lipkin, 46, says.
"But what happens when some of that packaging is stripped away?
Who are we when some of those qualities are altered in some major
way. Who are we to other people?
"That's
not to say I'm idealizing people with disabilities," she says.
"There are people with disabilities who are heroic and there
are those with disabilities who are mean-spirited. But when circumstances
are altered, it seems like our souls can be seen more clearly.
"If you
think about it from the point of view of a person who can't speak,
or from somebody who is in a wheelchair, it would seem that certain
physical attributes are just that. They're certain physical attributes
and yet, we're so reliant on them. But someone doesn't cease to
be a person because they can't walk."
This spring,
Lipkin's conversations have been lightning riffs on the relevance
of theater, gigs coming and gone, arts funding, publicity for their
fledgling troupe and the delicateness of an ensemble. She worries
over Colleen Gilmore, whose multiple sclerosis -- the relapsing,
remitting type -- has flared up. But Colleen continues to work as
a nurse and act.
Lipkin is also
trying to figure out where the company goes from here.
When she first
conceived of the DisAbility Project, she imagined they would do
one major production and then move on. Since February, when the
Project did its first public performance before mostly family and
friends, requests have come in almost weekly, most of them from
social service, educational and religious groups. The biggest one
looms: a performance for the eighth annual International Post-Polio
and Independent Living Conference.
Now, Lipkin
wonders whether they should continue to tour. And if they do, where
can they find fit theater space to rehearse and perform in?
Lipkin is looking
for a space different from the standard proscenium setting. The
project's space has to accommodate more than the typical few accessible
seats. She imagines a space with no fixed seats, where the actors
could make of it what they will.
A new vocabulary
After watching
the exercise on organisms, Lipkin asks for impressions. She was
drawn to Rodriguez's movements, the lilt of her arms and the tilt
of her head. Graceful. Rodriguez says she feels more comfortable
about moving, even with her limited mobility, than she used to.
Lipkin: "You
were finding a new movement vocabulary."
Instead of
being pushed, they're pushing society's boundaries.
"Because
people look at people with disabilities and say, 'Hmm, well, I don't
think these people really have anything going on," Rodriguez
says. "But here we are as a group. We're going to force society
to look at us and we're doing the things that society doesn't normally
think we can do.
"Hell,
years ago, we wouldn't have been alive. We'd be shut in an institution.
But here we are. We're not only going to act and say things, we're
going to do things with our bodies."
********
Americans
with Disabilities Act
The Americans
with Disabilities Act prohibits discrimination on the basis of disability
in employment, state and local government, public accommodations,
commercial facilities, transportation and telecommunications. It
also applies to Congress.
To be protected
by the ADA, one must have a disability or have a relationship or
association with an individual with a disability.
Who is covered?
An individual with a disability is defined by the ADA as a person
who has a physical or mental impairment that substantially limits
one or more major life activities, a person who has a history or
record of such an impairment or a person who is perceived by others
as having such an impairment. The ADA does not specifically name
all of the impairments that are covered.
Source:
"A Guide to Disability Rights Laws," U.S. Department of
Justice. This booklet also is available in large print, Braille,
audio tape and computer disk.