Disability

Power, Prejudice, and Paradox

Published

7 years ago

February 5, 2015

I’ve recently changed how I describe myself or, more accurately, my experience. I now talk about “my paradoxical experience as a queer, caucasian, cisgender man with unique function (disability).”

Even doing this is paradoxical, given I argued the point in 2012 at TEDxAuckland that we need to decay labels to reveal diversity. But I’m doing it to explain a phenomenon of power, privilege and paradox, rather than to label myself.

Power and privilege have long been part of the politics of diversity and discrimination. Recently I heard another diversity expert, Leslie Hawthorne, encourage those with privilege to raise awareness of it by, for example, not using the word “lame” to describe something that is bad or stupid, because you are implying that people who can’t walk are bad or stupid.

There has also been the story of Ijeoma Oluo, a woman of colour, who experienced an instant reduction in racial slurs when she changed her Twitter profile picture to one that made her look caucasian.

These examples seem to me to slightly simplify the understanding of power and privilege — change a word here, look a bit different there. I think there are more complex subtleties at work, like context, subjectivity and objectivity, that paint a broader, more complex picture of power and privilege.

So back to me — let’s deconstruct those labels (or decay them) in terms of power and privilege (I’ll use P&P to save keystrokes).

Queer — not heterosexual (but not obviously so) — P&P comparatively low
Caucasian — not of colour — P&P unquestionably high
Cisgender — not transgender — P&P unquestionably high
Man — not woman — P&P unquestionably high
Unique function (disabled) — not non-disabled — P&P unquestionably low

So the question becomes, where do I sit in terms of P&P? We could do simple maths: 3 high P&P, only 2 low, ergo I have +1 P&P.

More complex maths — let’s give more points to unquestionably (2) than comparatively (1): -1+2+2+2-2=+3 — so I have +3 P&P? Or do I have +6 P&P as well as -3 P&P?

Of course this is where the paradox and complexity comes in, as well as context, subjectivity and objectivity (and other things I haven’t thought of but probably will do later). Let’s do some more decaying…

Context: As I said at TEDxAuckland, but to reframe it slightly, if I’m in a room of cisgender, caucasian men, they will not see my +6 P&P. They will see and/or sense my -3 P&P, feel awkward, discount me and I will lack P&P.

If, however, I’m in a room of indigenous, transgender and/or queer disabled people, chances are my +6 P&P will become very noticeable and my -3 P&P won’t be enough to save me. There goes my P&P. Again.

Similarly, if I’m in a recognised leadership role or on stage talking about P&P to a TEDx audience, I’ll have more of it than if I’m a stranger in the street.

Subjectivity: This works two ways. 1. The more people know me (i.e. the more subjective their experience of me), the more relative P&P I will have. They’re looking past the labels and seeing me for who I really am. 2. The more P&P I feel I have in different contexts, and the more I am aware of the behaviours and language that are commonly understood in the situation, the less threatening my perceived lack or abundance of P&P is likely to be.

Objectivity: I’ll refer back to Leslie Hawthorne, who recounted a story of an orchestra, which lacked female members. On becoming aware of this, “blind” (I’m not sure if that’s offensive or not to people who can’t see) auditions were held, so that decision-makers couldn’t tell the gender of the auditioning person.

Within a few years, female members had increased several-fold. So, ensuring some objectivity around P&P can decrease its impact.

So, where are we? Well, if you’re anything like me you’re likely in some state of confusion and uncertainty which, I would hazard to say, is a very good state from which to tackle diversity, not to mention leadership, complexity and change. Our human need to be sure and certain and to know the answers are precisely what leads us astray in the world, a world which is nothing like what we would like it to be.

In “A Short History of Stupid” by Helen Razer and Bernard Keane, Razer observes:

When you elevate lived experience to centrality in your socio- political critique and politics, you delegitimise the contribution to debate from other perspectives; if the traditional logical fallacy is appeal to authority, since the 1990s appeal to experience has come to rival it, creating a hierarchy of analysis with lived experience at the apex of authenticity. Moreover, as the phrase ‘check your privilege’ implies, it is not merely that a non- experience- based contribution to a discussion lacks legitimacy, the possession of other forms of experience creates an illegitimacy that is impossible to overcome: the scoring systems used to allocate ‘privilege points’ can be neatly flipped into a ‘how illegitimate is your opinion’ scale, depending on the colour of your skin, your sexual preference, your income and your gender. The result is a further fragmentation of public debate on issues, with fewer voices heard and greater unanimity among those voices given the imposition of dominant narratives even within sub- groups. The result is also a lesser willingness among generalists, and particularly media practitioners, to genuinely engage on policy issues arising from or including identity politics, for fear of being labelled racist/misogynist/homophobic/middle class/transgenderphobic/ableist/fattist/perpetrators of rape culture. They live in fear of fatally missing some critical nuance that would reveal them as inauthentic, or worse.

I agree. I don’t see myself (or anyone else) as absolutely either owning or lacking P&P — I don’t think it’s a useful paradigm. Sometimes we have, it sometimes we don’t. Sometimes we can influence it, sometimes we can’t. Sometimes we’re prepared, sometimes we’re not. Sorry kids, it’s messy out there.

And — hate to say it — it’s getting messier.

Philip Patston

Philip Patston began his career 25 years ago as a counsellor and social worker, and he is the founder of DiversityNZ. Philip lives in New Zealand and is recognised locally and overseas as a social and creative entrepreneur with fifteen years’ experience as a professional, award-winning comedian. His passion is working with people when they want to explore and extend how they think about leadership, diversity, complexity and change.

Culture

What Do You Know About Disability Cultural Competence?

Published

2 weeks ago

November 19, 2021

Elspeth Slayter

Recently, I had the opportunity to give a webinar on disability cultural competence to social service workers, but was met with many blank stares. As a disabled social worker myself, I often notice that the disability community is not recognized as a cultural group. Disability is also not considered as a social identity in diversity considerations, despite the ways the community feels about it. Frankly, our field has a long way to go when it comes to developing disability cultural competence. Let’s see if we can change that.

Why the We Need to Prioritize the Disability Community

You may be asking yourself, why all the focus on disability? Well, the disability community comprises 26 percent of the adult U.S. population – that’s one in four Americans according to the Centers for Disease Control. Among children under the age of 18, estimates suggest that 4.3 percent of the population is disabled according to the U.S. Census from 2019. This means that social services workers are interacting with the disability community all over! It’s also important to note that disability transcends race, ethnicity, gender and other social identities, as seen in the graphic below (courtesy of Courtney-Long, Romano, Carroll, et al., 2017). So we need to remember to be intersectional in our practice – these are not siloed communities.

Courtesy of Courtney-Long, Romano, Carroll, et al., 2017

Importance of Disability Identity

I’d like to transition now to talking about the importance of having a disability identity. Some people identify as disabled from a cultural perspective. Some people are not even aware that this is an option and you can open their eyes to the world of disability as a resource for them. In other words, for some, this is a missed opportunity to connect to a supportive network. For others, it’s a choice not to identify as disabled either due to stigma, internalized ableism or other beliefs. The idea is that developing a strong disability identity is super helpful with your long-term well-being. And in order to do this, you have to both connect with the disability community and with disability culture. So what is that?

What is Disability Culture?

In short, disability culture is the “sum total of behaviors, beliefs, ways of living, & material artifacts that are unique to persons affected by disability.” It’s essential for social service workers to be tuned in to disability culture so they can leverage it to connect with their clients. And let’s be clear, disability culture does NOT consist of disability service programs. Where we really see disability culture come alive is on social media sites, such as Twitter and Instagram. You can follow some of the major disability culture hashtags to see the dialogues and debates that are hot in our community right now, such as: #DisabilityTwitter; #DisabilityVisability; #DisabilityAwareness; #IdentityFirst; #DisabilityLife; #Spoonie,#SpoonieLife, and more.

You may notice that the last two hashtags included the word “spoonie.” This derives from “spoon theory,” which is an actual theory based on a metaphor about how much mental and physical energy a person has to accomplish their activities of daily living (ADLs) and instrumental activities of daily living (IADLs). The disability community talks about how many “spoons” they have as a unit of measurement of energy – and sometimes refers to themselves as spoonies. Please note that in teaching you this, I am helping you to develop your disability cultural competence.

How Build Disability Cultural Competence

Other ways to build up your disability cultural competence are to check out the Disability Visibility Project, which tells the stories of diverse members of the community in wonderful ways. And there are a range of organizations, such as Sins Invalid, which founded the disability justice movement. You can also read the 10 principles of that movement in this short document. This will help you to tune in to the disability pride movement. We have a pride month and a pride flag too, it happens in July.

When it comes to engaging in disability competent practice, we need to develop knowledge about disability culture and disability history. We can also consider taking the following steps to round out this competence:

First, we need to examine our own attitudes about disability and engage in reflective practice around that. You can consider your own implicit bias about the disability community through Harvard University’s Project Implicit test about ableism, or through social worker Vilissa Thompson’s guide to checking your own ableism.

Second, developing disability cultural competence over time also includes a careful look at the terminology we are using and respecting disabled people’s choice of identity-first language in many cases. You can read more about that here and throughout that site. The Harvard Business Review also has a thoughtful essay on why you need to stop using particular words and phrases. It’s a great resource and helpful read for many.

Third, we also need to think respectfully about disability etiquette and how ideas play out in different parts of the disability community. One should presume competence about us – all of us! We ask that you respect our bodily autonomy, speak to the person and not their companion/interpreter, ask before you help, be sensitive about physical contact/equipment contact, don’t make assumptions about capacity, listen to us, don’t assume you know better and if you are in doubt about what to do, ask! Writer Andrew Purlang sums up his disability etiquette request as follows:

Don’t be afraid to notice, mention, or ask about a person’s disability when it’s relevant — but don’t go out of your way!
Offer to help, but make sure to listen to their response, respect their answer, & follow their directions
Don’t tell a disabled person about how they should think about or talk about their own disability
Don’t give unsolicited medical, emotional, or practical advice
Don’t make a disabled person responsible for managing your feelings about their disability, or for your education on disability issues
If you make a mistake, just say you’re sorry and move on. Don’t try to argue that you were right all along.

Now What?

Taken together, these steps, learning disability culture, and examining our own attitudes about disability, go a long way towards the development of disability cultural competence. But none of it will do any good if we are not fighting for disability access and disability inclusion, which are central issues for the disability community. Many people think that issues of access were solved by the passage of the Americans with Disabilities Act of 1990. But the implementation of that law is fraught and embattled, and there is lots of work to be done on the access front. Take a look at these simple guides below. They will go a long way in helping to engage the disability community and making us feel welcome! Above all, remember our movement’s rallying cry, “nothing about us, without us!”

Website Accessibility

Accessible Social Media Guide

Meeting Accessibility

Webinar Accessibility

Public Event Accessibility

Disability

New Analysis: More U.S. Adults Identify as Disabled; Ethnic and Socioeconomic Disparities Persist

Published

4 weeks ago

November 10, 2021

SWHELPER

A new analysis led by Johns Hopkins Medicine researchers finds that the number of U.S. adults who report they have a disability is 27%, representing 67 million adults, an increase of 1% since the data were last analyzed in 2016. In this new study, which used data collected in 2019, before the COVID-19 pandemic, the researchers found a wide array of disparities between socioeconomic and demographic factors that persists among those who identify as disabled and those who do not.

“To reduce ableism and create more inclusive communities, our country must be equipped with data on the prevalence of disabilities and who is most impacted by them,” says Bonnielin Swenor, Ph.D., M.P.H., director of the Johns Hopkins Disability Health Research Center and associate professor of ophthalmology at the Johns Hopkins University School of Medicine and Wilmer Eye Institute.

Swenor and her research team analyzed survey data from the Centers for Disease Control and Prevention’s 2019 Behavioral Risk Factor Surveillance System, a collection of health and behavior information from annual telephone surveys of more than 400,000 U.S. adults.

Results of the analysis were published Oct. 21 in JAMA Network Open.

Approximately 27% of American adults reported a disability. When compared with the U.S. adult population, this represents 67 million adults. An additional 6 million people reported a disability since data on disability prevalence were analyzed and reported in 2016.

In the current study, approximately 12% of American adults reported more than one disability. Mobility was the most often reported disability type, followed by cognitive/mental, independent living (requiring help for daily tasks and outings), hearing, vision, and self-care (needing help with bathing, dressing and other personal care tasks).

In addition, the researchers analyzed socioeconomic and demographic data to better understand the prevalence of disability across intersecting groups.

“Developing effective measures and policies to include people with disabilities in all aspects of life needs to account for the variability in how people among different ethnic, socioeconomic, demographic and geographic groups experience disability,” says Swenor. “With robust data, we can strengthen the foundation of our knowledge about disability and develop tangible solutions.”

The survey data showed that, compared with adults without a disability, disabled adults were more likely to be older, female, Hispanic, have less than a high school education, have low income, be unemployed, and be bisexual, transgender or gender nonconforming. Digging deeper, the team found differences in disability prevalence based on sociodemographic groups. For example, Black females had a higher prevalence of disability than females of other races, and Black adults identifying as gay or bisexual had a lower prevalence of disability compared with gay or bisexual adults of other races.

Swenor and the research team note that an aging population and other factors may contribute to the increase in reported disability. The data include information from before the COVID-19 pandemic, and Swenor says there may be an increase in people reporting a disability resulting from long-term symptoms of COVID-19.

The research team aims to use these data to continue studying the experiences of disabled populations, including identifying and finding support and resources for people with disabilities and ascertaining the capabilities of schools and employers in supporting disabled communities.

In addition to Swenor, researchers who contributed to the report include Jessica Campanile, Jennifer Deal, Ph.D., Nicholas Reed, Au.D., and Varshini Varadaraj, M.D., M.P.H.

Disability

Zoom Differentiation and Accommodations

Published

4 weeks ago

November 10, 2021

Wendy Taylor

Though virtual learning is seemingly becoming less commonplace across the country, it’s still certainly around and likely will be for some time. And we all know that virtual learning has its challenges. Especially when it comes to differentiating in the virtual classroom. For students with special education accommodations, teachers will need to get creative in order to account for every student’s unique needs and optimize learning opportunities. Thankfully, there are strategies and methods for providing special education accommodations in Zoom—we just need to think outside the box and modify what each accommodation looks like in the virtual realm. Let’s take a look.

Zoom Chat

Since some are no longer physically in the classroom, proximity, prompting, and cueing accommodations pose a bit of a challenge for instructors. Yet, nothing has changed in terms of the student’s needs. In fact, students who struggle to focus and/or stay on task may need the prompting and proximity accommodations even more now that they are sitting in front of a screen. Online learning does not allow for physical proximity; however, teachers can utilize the chat function to maximize student engagement and provide an alternative form of proximity, prompting, and cueing.

Reaching out: The Zoom chat can be used to individually reach out to specific students with prompting accommodations to spur participation and to rephrase a question when necessary.

Clarifying: The chat also allows teachers to check for understanding by providing a platform for asking clarifying questions, follow-up questions, etc.

Advocating: Teachers should remind students of their chatting capabilities so that students with accommodations can advocate for themselves and speak up when they need assistance.

Tracking: The chat also acts as a data tracker; teachers can modify their settings in Zoom so that chats are saved. This allows for teachers to review correspondence with students and share questions and check-ins with parents. Teachers can also use saved chats to track the number of times a student initiates a task, asks clarifying questions, responds to polls or exit responses, etc.

Reminding: Teachers can use the Zoom chat as a method for reminding students of their extended time or reduced workload accommodations as well. This allows teachers to discreetly remind a certain student that his due date is extended without drawing attention to the student’s accommodations in front of the whole class. **Just be certain that, when chatting with specific students about these accommodations, you have selected the student’s name from the dropdown so that the chat remains a private, 1:1 conversation.

Breakout Rooms

The grouping function in Zoom can also be beneficial when ensuring certain special education accommodations are offered. Teachers have the option to manually assign groups, which means that students with special education services can be grouped with a para-educator or with other students who have the same accommodations.

Variance: Teachers should try to avoid always grouping special education students together, however, as to avoid drawing attention to certain small groups or stigmatizing students who need additional support.

Oversight: Teachers can randomly assign groups using the “automatic” option when creating breakout rooms. Then, while students work, the “host” can pop in and out of groups to act as a “check-in” for students with that accommodation.

Mobility: Teachers can also move the para-educator from group to group during breakout room sessions so that every student receives supports throughout the collaborative activity.

Discretion: Breakout rooms also offer opportunities for differentiation. Teachers can modify assignments and link adapted materials in the chat to send to specific breakout rooms. From the chat link, students can click on the shared Google doc to access the modified material. This function can provide students with resources such as word banks, sentence starters, outlines, graphic organizers, glossaries, etc. The key is that each student who receives these accommodations will have access in a discreet manner and can choose to use the materials as needed.

In short, there are many steps educators can take to ensure virtual learning provides differentiation and accommodation on a platform like Zoom. Though virtual learning may not be around forever, it still remains for some, and with that, educators must ensure they enhance the learning experience as much as possible.