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Spirits Of Another Sort Workshop Journal #4- An Assumption of Competence

8/10/2014

2 Comments

 
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After a week off, this past Monday we began rehearsals with the entire ensemble of "Spirits of Another Sort." If you missed our last post about the casting of this project, you can check it out here-

Spirits of Another Sort Workshop Journal #3- Where Are All The Actors?

One of my goals in documenting this process was to work towards the development and creation of a practical model for educators and fellow artists who interface with these particular populations. Sara Buffamanti and Becky Leifman are both teaching artists, Will Dickerson (our Oberon/Theseus), is a special education teacher in addition to being both an actor and director.

For me, the Disability Community is not exclusively comprised of people with disabilities. The community also includes doctors, physical therapists, occupational therapists, medical professionals, family members, friends, lovers, teachers- anyone who might enter that particular sphere of influence. This makes it one of the most diverse, complicated and inclusive communities in existence.

I met Jan Valle several years ago. A professor at The City College of New York in the field of Disability Studies, Jan was one of the first people I told about the project. I was eager to have her sit in on the process and get her perspective on the work. She came to one of our initial Rude Mechanical rehearsals and sat in on our first read-through with the full ensemble earlier this week. I am grateful for her participation and appreciate the fact that she was able to contribute something to this series.
-Gregg Mozgala, Artistic Director      

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“You have NO idea what you are doing!” I blurted out in admiration to Gregg Mozgala, Artistic Director of The Apothetae, immediately after observing a three hour rehearsal with the Rude Mechanicals. Gratefully, Gregg laughed in recognition of my clumsy attempt to express what I really meant to be an acknowledgment of the highly transgressive nature of this work and its larger contribution to publicly redefining cultural meanings of Disability. As Gregg can attest, I was so blown away by the rehearsal that I initially could not articulate a response to it with any real coherence. It honestly took me a few days to process what I had seen.

I am a professor in the School of Education at The City College of New York. I have worked in the field of special education for over three decades; however, I currently teach and write from the theoretical perspective of Disability Studies in Education (DSE). In contrast to the conceptualization of Disability as a deficit, disorder, or dysfunction that undergirds special education, DSE scholars are interested in the social construction; what constitutes Disability in any given society and conversely what reinforces constructed notions of ability. In other words, if we reframe Disability as natural human variation rather than pathology, we shift away from a deficit model in which persons with disabilities are viewed for what they cannot do and move toward a strengths-based approach that assumes competence and values individuals for what they can do. DSE explicitly troubles widely accepted notions of what constitutes “normalcy” and its oppression of many individuals who cannot or choose not to conform to culturally determined standards of “normalcy.”

So, it is through a DSE lens that I viewed rehearsal with the Rude Mechanicals. (I am particularly interested in theatre and disability because I teach a course on inclusive theatre practices for CCNY’s graduate educational theatre program.) That evening, I entered an inclusive theatre space where able-bodied actors and actors with disabilities worked together in genuine community. This was no “special arts program” designed to meet “the needs” of the disabled as defined by non-disabled professionals. This was a rehearsal like any other rehearsal for professional actors. An assumption of competence was evident throughout every aspect of the rehearsal. The expectation was that every actor could and would participate meaningfully. Actors with and without disabilities thoughtfully considered character motivations and what “actions” might best represent those motivations. I was struck not only by the level of conversation initiated by those labeled as cognitively disabled, but also by the various and sophisticated ways they engaged in “sense-making.” While the able-bodied actors offered much in regard to experience, background, and leadership, the contributions made by the Rude
Mechanicals legitimately enhanced understanding of the work for everyone. This was the conversation of ACTORS and a model for what is possible when we commit to a paradigm of competence.

Gregg’s conceptualization for this piece—Athenians as able-bodied actors, fairies as actors with physical disabilities, and the Rude Mechanicals as actors labeled with cognitive disabilities—is provocative in its inclusion and reflection of all of us who make up the human condition. I am reminded of a journal entry written by a student in my inclusion theatre class last semester. I think her words speak eloquently to the significance of Gregg’s ongoing work: 

"The artist tries to portray and bring an understanding and meaning to the human experience, and what is that human experience without everything and everyone who is part of the human experience? It is not just about some of us. It is about all of us. So reflecting the experience of all of us is exactly what art is there to do. It is always pushing boundaries, exposing the truth, reflecting back at society what society is doing, making sense of the world’s petty problems by turning them into art. So without disability included, the art is incomplete."



2 Comments
Margot link
8/11/2014 01:19:36 am

I love this post Gregg! I'm so glad you consider people like family members,therapists,doctors,and friends as part of the disabled community. When I used to dabble in "disability rights" events what I would see is that the able bodied members of the community would be completely excluded from all conversations. It sickened and saddened me. Somebody's able bodied wife once told me "I feel like the enemy", yet it was because of her that her disabled husband could live at home independently. I would never want somebody to feel like an enemy for doing something good. I often see caregivers and disabled people going in opposite directions for resources/help and I wish this would change.

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Mama
8/18/2014 12:30:03 am

That was right on, Gregg. It takes someone living 'it'everyday, be the person with the disability or the parent, friend or caregiver who REALLY knows the entire picture. Sometimes the caregiver actually is out in front of the disabled person because they can often sense what is coming on before the disabled person. These people often do background work to help minimize the effects on the disabled person that never come to light.
Love you, mama

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