Poet Adina Burke on how the queer and disabled communities have more in common than not



Minneapolis poet Adina Burke, who identifies as a bisexual woman with Cerebral Palsy, has heard it all when it comes to how folks react to her identities. Some of the worst responses have come from folks she’s dated and even outsiders who comment about her relationships.

“My partner who is a cis male, gets high fives and thumbs up for doing things a normal loving boyfriend would do like help me with my coat and ex-girlfriends have gotten praise from their peers because of how inclusive they are being by dating me,” Burke says. “But I’m not a Mitzvah project.” While Burke’s partners are lauded for performing basic relationship duties, she has found that she frequently asks herself, “What do I have to offer?” and worries that she is burdening her partner with her disability.

“I’m a person with a lot of great qualities, and I’d like to live in a society one day that views my partner as lucky as I am to have them,” she says.

Outside of intimate spaces, being disabled sometimes excludes her from attending social events geared towards the queer community. Disability access in public spaces commonly caters to folks with impaired mobility, excluding folks with other types of needs the same level of access and agency in community space. Burke has found that the stigma of having Cerebral Palsy makes people treat her with pity as if she is fragile or to be avoided at all costs.

As an artist, Burke says one of her biggest challenges is facing the way folks with disabilities, especially in the queer community, are represented.

“In my opinion, they haven’t been represented so much as gawked at or used as a ‘super minority’ to check off some social justice box. I do believe this is changing, but I still see a lot of inspiration porn in my Facebook feed as well as within the local media, so I rightfully fear tokenism,” she says.

Burke defines “inspiration porn” as the propagation of photos, videos and other media which exploits people with “disabilities” in order to garner and capitalize on sympathy. This can be incredibly dangerous because it allows the whole person to be overshadowed by one identity or narrow attribute, their “ability.” Burke uses storytelling through spoken word poetry and punk music to confront this thinking.

“There’s this aura of rebellion. That’s why I’m drawn to [storytelling], and I now live in a world where those who have constantly held the mic are now passing it. Storytelling is wonderful for that,” she says.

Burke believes that storytelling is important for folks with disabilities in the queer community because it can provide a space to connect to voices that have not been heard in the past. “It allows the lifting of voices to echo, ‘you are not alone.’ And in a society that views and values what I like to call ‘Lone Wolf syndrome,’ this is vital. Storytelling is survival,” she says.

The Lone Wolf syndrome is explained by Burke as society’s pressure for people to live separately rather than jointly, which often allows transcendent stories and shared experiences to go unheard.

According to Burke, the queer community and the disabled community have more in common than not. Storytelling has allowed Burke to escape isolation and find people who do understand her lifestyle and have stories of their own to relate.

Angela Carter, a self-identified queer crip scholar and educator at the University of Minnesota says many of the public places for the queer community – such as bookstores, bars and coffee shops – are often not accessible to folks with disabilities.

Carter also says that sex has been limited for folks with disabilities in a historical context because many of these people have been represented as asexual or hypersexual due to a common misunderstanding of individuals with disabilities, especially in the queer community.

“People with disabilities and queer people have been medicalized, pathologized, criminalized and literally erased through so many of the same oppressive forces. This is also deeply racialized, so the experiences of queer white folks with disabilities can be very different than queer folks with disabilities who are people of color,” she explains. In general, Carter notes that folks with disabilities and the queer community overlap in that both have been regarded as “wrong” and “defective” and in need to be cured or fixed.

She has also seen a lot of positive overlap between the two communities. From the community outreach and solidarity to the artwork, writing and activism, the queer community and folks with disabilities both also use reclamation as a strategy to overcome oppressive language, like the terms “crip” and “queer.”

After being involved in the queer community and academia as an out queer crip person for the past ten years, Carter has seen studies around the community of folks with disabilities and the queer community change over the years.“I see my queer students thinking a lot more about disability, and I see my students with disabilities thinking a lot more about sexuality and queerness. They are building the queer community I wish I had when I came out fifteen years ago,” she says.

The importance of acknowledging the connections between disability and the queer community spans far outside of the classroom. According to Jay Wilson, Senior Access Consultant at the University of Minnesota Disability Resource Center (DRC), queer and trans folks with disabilities have been central to many queer and trans communities in the Twin Cities.

“A lot of times, the disability parts of our identities or experiences aren’t recognized. The ways in which we contribute may be different,” Wilson says. “For example, when we have a flare up of health disabilities, we may do activism from bed for 10 minutes a day, or we may participate by showing up to events and actions when we can.”

Like Burke, Wilson believes that it is up to able-bodied folks in the queer community to make events accessible for folks with disabilities, which will help center queer folks with disabilities to bring the communities together in a way that does not tokenize.

“Guardians and segregated living settings have the power to prevent people from going to a GLBT support group or event, date someone of any gender or physically or socially transition gender,” he says.

Whether people are being denied access to the queer community, are unable to attend events due to disability or are excluded from their own community due to lack of understanding of the intersections between disability and queerness, the use of storytelling can help everyone understand each other’s lived experiences a little better.

“I am not a trophy, Burke said. And hopefully through her stories society will know too.

Wilson recommends a number of resources, locally and nationally, for people who are members of the queer community and disabled community or for people who simply want to learn more about the intersection of the two.

These resources include:

ADAPT MN, local chapter of a national disability rights direct action advocacy group.

Glitterwurst Zines, publisher of zines about queerness and neuro-divergence.

Raymond Luczak, deaf, queer author and editor in Minneapolis.

hclouart, Heather C. Lou’s art on themes of resistance by people of color who are queer and disabled.

Rainbow Support Group at Wingspan, support group for queer and trans people with developmental or cognitive disabilities.

Sins Invalid, performance project on disability and sexuality.

Eli Clare, movement leader who first articulated much of the complexity in queer/trans disabled life.

Icarus Project, “grassroots support network and education project by and for people who experience the world in ways that are often diagnosed as mental illness.”

Madness and Disability, workbook for thinking about the ways that ableism, gender/sexuality oppression, racism and other oppressions impact mental and physical health.

Autistic Hoya, Lydia Brown’s blog about intersections of oppression.

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