Sins Invalid

Sins Invalid was founded in 2005 by Patricia Berne and Leroy F. Moore Jr. The organization, which Berne has described as "a hybrid between a community-based organization and a performance," originated in the San Francisco Bay Area and tours nationally.[2] Berne and Moore, who are old friends, have both had disabilities since birth, and they started the project upon realizing the paucity of venues dedicated to celebration of their work and their bodies.[2] Berne serves as Director of the organization, and she has been involved in work surrounding asylum claims, youth incarceration alternatives, the LGBTQIA community, and mental health support for survivors of violence, among other fields.[3] Moore is Sins Invalid's Community Relations Director. His work extends to writing, poetry, lecture series, and hip-hop/music. He has worked, studied, and lectured internationally and is considered a "leading voice" regarding police brutality toward and wrongful incarceration of people with disabilities.[3]

According to a Huffington Post interview conducted by Cory Silverburg with Berne and Moore, Sins Invalid's (pronounced as in "not valid") name came from the idea that a disabled child is a manifestation of "the sins of the father being cast upon the son".[4] As Berne articulates, there is a pervasive societal norm that validates bodies according to beauty, hygienic, health, and other sets of standards. The Sins Invalid framework asserts that humans have a wide variety of embodiments, and all bodies are valid and worthy of celebration.[4] It is also a play on words, since people with disabilities have historically been referred to as "invalids".[4]

Since its creation, Sins Invalid has held annual major theater performances and an artist-in-residence performance, which have all received critical acclaim.[1] In 2012, the project launched a Kickstarter campaign, culminating in the 2013 release of a 32-minute documentary titled Sins Invalid: An Unshamed Claim to Beauty in the Face of Invisibility, directed by Berne, which details its disability justice efforts and the value of artistic expression. The documentary also elucidates the need for inclusion of sex and sexuality in disability rights discourse.

In the Cory Silverberg interview, Berne said, "I can experience my sexuality as a crip, as someone who fully occupies a non-normative physical space. And part of that movement to fully living in one's own experience is naming and resisting dehumanization."[4] Acknowledging the full history of disability in the United States requires a deconstruction of the dehumanizing practices that have plagued the community. All types of experiences are included in the show, and the denial of sexuality is part of that dehumanization. In the same interview, Moore said, "…we’re sharing these stories in a way that hopefully connects us to our past and also allows us to change our future."[4] The medicalized framing of disability has framed it as a problem to be cured, a pathology that decides, alongside doctors, the future of its host.[8] People with disabilities are often told what their futures will look or feel like, and part of gaining agency involves the decision one makes when deciding one's future for oneself. Sins Invalid aims to reinforce this agency and choice in the futures of people with disabilities, including an audience in order to expand the message and so that people with and without disabilities might internalize it.

Sins Invalid's celebration of the multiplicity and diversity of identities is an iteration of intersectionality in practice. The human body is not permanent and unchanging; rather, it is a non-static being that can change based on nature, the environment, or perception. Since disability does not discriminate, it is useful as a category of analysis in terms of its potential to create, as disability studies scholar Simi Linton puts it, "a prism through which one can gain a broader understanding of society and human experience".[9] Since Sins Invalid includes performers with disabilities who are also people of color, queer, etc., intersectionality is woven into its performances and guiding ideology. In the documentary, Sins Invalid member Leah Lakshmi Piepzna-Samarasinha comments on the freedom that the space provides for various manifestations of difference, such as queerness. She says, "No one has to closet themselves," and this applies to any identity.[2] This ties into Berne's idea of being able to "orient the gaze," or the position the audience occupies as consumers of the performance.[2] Since the project is conscious of so many diverse lenses and does not limit the frame to disability, performers and audience members alike have the opportunity to feel empowered by the acknowledgement of identities.

In order to understand the idea of embodiment, of occupying the body, Berne states, one must have an understanding of the body as situated within a historical, political, cultural, and social context.[10] Feminist disability studies scholar Rosemarie Garland-Thomson argues that, "integrating disability as a category of analysis and a system of representation deepens, expands, and challenges feminist theory".[11] For Garland-Thomson, the "shared human experience of embodiment" provides a framework in which all individuals should be able to understand the way systems affect or do not affect them based on their bodies.[11]