PROBLEMATISING ‘ABLEIST’ EPISTEMOLOGIES IN HIGHER EDUCATION

By Ursula Mary Blythe

 

This post is available to download as a PDF here.

 

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The ‘body politic’ is an ancient metaphor by which nations, societies, and public institutions are envisioned through a performative body which fuels ‘ableism’. Whereas phenomenology examines the ‘first-person experience’ in order to navigate and resist ableism in social contexts. This short paper seeks to elaborate on the idea of the body politic in Western discourse whilst raising awareness of ‘ableist’ epistemologies in higher education (HE). My argument goes beyond the disability/impairment dichotomy of the ‘social model’ by drawing on philosophical theories of social constructionism and epistemic injustice, as well as revealing ableism as experiential for ‘all body types’ beyond disability (‘DIS’ hereafter).

 

Ableist paradigms were articulated through Plato’s conception of the ‘body politic’ which equated to the analogy between political and physical fitness over illness, where the latter was deemed as weakness. Political morality was mapped to body perfection, so political failure was associated with human defectiveness (Doonan, 2021). Hence, ableist thinking is as old as the Western philosophical canon which has led to epistemic injustice concerning ‘DIS’ over the course of humanity. A succinct way to explain epistemic injustice is ‘a wrong done to someone specifically in their capacity as a knower’ (Fricker, 2007: 1).

 

A growing number of contemporary philosophers argue that ‘the social’ may not be physically existent, but it is nevertheless real because it determines how we live (Haslanger, 2012). Owing to ‘ableism’ being a prevalent issue in the sociopolitical context, it has genuine educational significance. For example, HE students and staff find themselves having to overcome barriers that are the result of ableist norms and practices. Young people with ‘DIS’ are particularly vulnerable to epistemic injustice as their voices are often ignored (Barnes, 2016).

 

There  is no one who is not impaired in some way, but not everyone experiences the world as a person with ‘DIS’. According to social constructionism, ableism marginalises physically impaired people (Haslanger, 2012); but I would argue that it also standardises all students and staff within academia due to epistemologies (i.e. ways of knowing) that are deep-rooted in social norms that determine which bodies matter. In other words, ableism is ingrained in the ‘body politic’ which holds that normal abilities are superior, so ‘DIS’ needs correcting (Wieseler, 2020).

 

Dolmage (2017) argues that for too long ‘Disability has been constructed as the antithesis of HE, often positioned as a distraction, a drain, or a problem to be solved’  (audio ref.). Ableism reveals itself through the academy’s performative drive to ‘accentuate ability, valorise perfection, and stigmatise anything that hints at intellectual, mental, or physical weakness’ (ibid), even as we gesture towards the importance of equality, diversity, and inclusion (EDI). Moreover, Campbell (2009) asserts that ableism is maintained by patriarchal mechanisms, productive technologies, and social phenomena over time and space, resulting in renewed epistemologies and ways of categorising people.

 

The reason this is important in HE is because didactic practices are extremely performative which foster repressive epistemologies through attitudinal, physical, and structural norms. In educational contexts, digital technologies have the potential both to extend and to erase the body. Historically, media sources in the 1950s believed that technology was ‘a mere extension of bodily skills employed for the satisfaction of bodily appetites’ (Polanyi, 1958). Indeed, it has often been asserted that the online world makes life easier for students. However, the universal shift towards virtual self-management can limit epistemic communities.

 

Remote technologies can be both inclusive and exclusive, but either way they are changing how we experience academia. On the one hand, online learning equalises access to learning for anyone with the relevant technical resources. Likewise, assistive technology has been extremely productive for disabled students in plugging into HE via assistive devices and specialised software. This often equates to not having to travel to university which is beneficial if one is managing chronic pain. However, technologies have not reduced inequality of HE students with ‘DIS’, as well as resources being limited via the DSA (disability support allowance).

 

One could argue that technology reflects universal principles of standard design and ways of functioning, making the body redundant and removing one’s agency. Furthermore, virtual access to teaching is different from campus attendance and one’s experience of university life. The growing reliance on teaching via such platforms as Teams and Zoom could mean that bodily diversity is further marginalised. This brings us back to the importance of phenomenology in order to unify ‘DIS’ without side-lining the body (Jenkins and Webster, 2021), as well as reducing epistemic injustice in HE.

 

Collaboration is key to placing the voices of ‘DIS’ at the centre of the debate and decision-making processes in HE. The development of different epistemologies disrupts the ‘body politic’ that sustains academic ableism. Doing so can inform, even transform sociopolitical norms and create a more inclusive and nuanced phenomenology of ‘DIS’ within the wider epistemic community.

 

KEYWORDS:

Ableism, body politic, ‘DIS’, epistemic injustice, higher education, phenomenology, social constructionism.

 

 

 

REFERENCES

  • Barnes, E. (2016) The Minority Body: A Theory of Disability Oxford: Oxford University Press.

 

  • Campbell F.K. (2009) Contours of Ableism: The Production of Disability and Abledness Basingstoke: Palgrave Macmillan.

 

  • De Beauvoir, S. (1949) The Second Sex Vintage Books: New York.

 

  • Dembroff, R. (2023) Real Men on Top: How Patriarchy Weaponizes Gender New York: Oxford University Press.

 

  • Dolmage, T.J (2017) Academic Ableism Disability in Higher Education USA: University of Michigan Press.

 

  • Doonan, C. (2021) Disabling the Body Politic Disability Studies Quarterly 41/No.3.

 

  • Fricker, M. (2007) Epistemic Injustice: Power and the Ethics of Knowing Oxford: Oxford University Press.

 

 

 

  • Haslanger S.A. (2012) Resisting Reality: Social Construction and Social Critique New York: Oxford University Press.

 

  • Jenkins, K. and Webster, K.A (2021) Disability, Impairment, and Marginalised Functioning Australian Journal of Philosophy 99/No.4. (pp.730-747).

 

  • Keller, R.M. & Galgay, C. E. (2010) Micro-aggressive Experiences of People with Disabilities In D.W. Sue (Ed.) Microaggressions and Marginality: Manifestation, Dynamics, and Impact (pp. 241-267) Hoboken, NJ: Wiley.

 

 

  • Merleau-Ponty, M. (1945) Phenomenology of Perception London: Routledge.

 

  • Polanyi, M. (1958) Personal Knowledge: Towards a Post-Critical Philosophy New York: Taylor & Francis.

 

 

  • Rasmussen, C. And Brown, M. (2005) The Body Politic as a Spatial Metaphor Citizenship Studies. Vol. 9/No. 5.pp (469-484).

 

  • Scuro, J. (2018) Addressing Ableism: Philosophical Questions via Disability Studies London: Lexington Books.

 

 

  • Wieseler, C. (2020) Epistemic Oppression and Ableism in Bioethics Hypatia: A Journal of Feminist Philosophy Vol. 35/No.4. (pp.714-732).

About the Author

Ursula Mary Blythe

As a humanities scholar, my interests include diverse epistemologies, ethics, and social philosophy. I am currently working on the phenomenology of gender and race. My dissertation research explores Ableism and Ways of Knowing. I facilitate philosophy in schools, public institutions, and community projects such as ‘Open Age’.

I have had some articles and blog posts published with the Wednesday Oxford Group, Philosophy Foundation, and MAP (minorities and philosophy) at Kings College London.

For me, philosophy in its contemporary form provides a lens to examine our ethical intuitions and sociopolitical praxis which encourages critique and human possibilities.


By this Author

    Comments

    1. Ursula M. Blythe

      Hello Ann, I have just read your remarks, thank you for taking the time to comment concerning the sociopolitical challenges in our current (somewhat troubling) discursive world! The key focus of this article was to raise awareness of ‘ableist attitudes’, in order to increase inclusion of different bodies and ways of navigating the world.

      All the best,
      Ursula

      Reply
    2. Ursula M. Blythe

      I would like to thank Ruth Heilbronn for reaching out concerning my blog article re. ‘Ableism’ in HE. She appreciates the use of the ‘body politic’ as a metaphor for performative praxis (i.e. ableism). However, Ruth questioned my argument about ‘remote technologies’ being somewhat exclusive and marginalising.

      In this short-written piece, I stated that there is an advantage of not having to travel to university when using remote technology, particularly if someone is managing chronic pain on a regular basis. However, there is also a massive risk of marginalising diverse bodies, minds, and social interactions. I would argue that what is missing from the current online meeting tech (e.g. Zoom) is the physical world of people, venues, and communal spaces that provide an opportunity to engage in human contact and social rituals, such as a coffee or a glass of vino (together). Basically, being present in the phenomenology of the world.

      In sum, I hope that such exchanges help to raise awareness of ‘ableist’ epistemologies in HE and beyond.

      Reply
      1. Sharon

        Not HE specific, but thinking about education more broadly. I found that the sudden rapid shift to online teaching led both to greater exclusion for my daughter (who has Down syndrome) but also greater visibility of existing exclusion too.

        As her teachers moved to online teaching, she was ignored. No work differentiated. Left to navigate the online spaces with no support, from her own bedroom. Expected to keep up with her peers, with no support assistant or visual resources. When raised with the school, the only solution they could offer was 121 sessions with learning support assistants (who I guess are her default teachers in school when her teachers are addressing the rest of the class). No teachers contacted us during lockdown, her work was set by LSAs. She had zero interaction with her peers except for potentially bullying messages in the chat during an art lesson. Moving online made her even more isolated and left out than usual

        Reply
    3. James MacAllister

      Hi Ursula,
      Thanks for writing this and for sharing it – it was good to get your perspective on how some canonical political philosophy has perhaps been part of the problem in shaping ableist ways of knowing. You are raising some important practical issues too and I agree that collaborating and listening to the voices of all is the way to go in terms of decision making in the future in HE contexts that aspire to be less ableist.

      Reply
    4. Ursula Blythe

      Hi James,

      Thank you for your valuable comments, particularly as you have a personal interest in accessibility and ‘DIS’ inclusion.

      I look forward to meeting you on the new PESGB Disability Working Group, and good luck with your nomination for a position on the PESGB executive board. I think you would make a real difference.

      Reply
    5. Rachel

      Firstly, well done Ursula.

      As a support worker I have worked with both children and mature students. Currently I’m helping to support students in Higher Education who have physical or ‘hidden needs’. It’s important to understand that individuals who have a specific need are people just like everybody else. This is something that is often overlooked. If we spent more time getting to know the person, we’d be able to support them better and help them to feel more valued and cared for. My students never fail to show how hard working, resilient and focused they are in their goals. Even when times get really tough, they are there still aiming to be the best that they can be. I learn from them a great deal, not just from a work perspective, but a personal perspective as well. I admire them, and the courage they have to always keep going.

      Reply
    6. Ursula Blythe

      Good evening Rachel,

      Thanks for taking the time to highlight the importance of care and appreciation of students with ‘DIS’, including mature students with complex needs.

      Such advocacy helps to challenge the ‘body politic’ and ‘ableist’ epistemologies in HE and beyond.

      Reply
    7. Ursula M. Blythe

      Dear members & prospective members,

      Just a short, but important note to say that the PESGB have set up a ‘Disability Working Group’. The committee members have a range of different experiences and research expertise in ‘DIS’ studies, particularly concerning philosophy of education.

      The members agreed that Ruth Wareham will facilitate the group and the rest of us will be active participants, in order to improve accessibility and inclusion, particularly when organising the Oxford Conference and ‘all’ other PESGB events.

      We had our first meeting yesterday, so we discussed accessibility for the forthcoming Oxford conference and other communications relating to disability and epistemic inclusion, such as ‘audio’ submissions. If you have any disability adjustments for the 2023 conference, please let us know asap, so we can assist you appropriately.

      Reply
    8. Sharon

      thank you for writing this piece Ursula – not least highlighting issues that are often invisible apart from to those with lived experience of ‘DIS’ either personally or through relationships with loved ones. I hope that the Disability working group will be able to instigate a shift both in attitudes and the inclusion of disability within our philosophising about education – something I feel is often completely missing.

      Reply
      1. Ursula M. Blythe

        Respect Sharon, as a carer/parent of a disabled child which presents a maze of challenges, particularly concerning public support services. Also, your theoretical research focuses on disability, education, and philosophy.

        I suggest you have a look at Prof. Fiona Kumari Campbell who is an Australian scholar-activist based at the University of Dundee. She is an inspirational voice in comprehending ‘Ableist Praxis’ ingrained in our society. For me, Kumari Campbell is a phenomenal interdisciplinary scholar-activist, who also draws on philosophy and phenomenology.

        I look forward to working with you on the newly formed PESGB ‘DIS’ Working Group. As you said, our initial focus should be on accessibility and shifting ableist attitudes.

        Reply
    9. Ursula M. Blythe

      Good evening Sophie,

      Thanks for your recent voice message. You had some queries re. philosophical terminology (i.e. Epistemology and Phenomenology) relating to my ‘Ableism’ article above. In real terms, epistemology is about ‘knowledge’ and how we know things, and who’s knowledge counts such as an ‘ableist’ authority or the person with ‘DIS’.

      Phenomenology relates to research of ‘lived experience’, and how this can inform other epistemologies and inclusion of ‘DIS’ in the public domain.

      As suggested, I welcome the opportunity to discuss academic ableism, particularly in relation to EDI. Otherwise, good luck with your new role at KCL.

      Reply
    10. Ursula M. Blythe

      Thanks Sophie, I got your voice message about philosophical concepts re. epistemology (i.e. ways of knowing) and phenomenology (i.e. lived experience) of ‘DIS’.

      As suggested, lets meet to discuss these ideas in the context of understanding ableist practices in HE.

      Good luck with your new EDI role at KCL. Well deserved.

      Reply