I’m sat in Copenhagen airport feeling extremely tired, but also very lucky to have been able to attend the NNDR Conference this year, and present some reflections from my ongoing research project. Like previous disability studies conferences I have been to, this conference was welcoming, mostly accessible, and thought-provoking. I had the chance to meet new colleagues from across the globe, share ideas, and gain an insight into the many different areas of research currently situated somewhere under the broader and intersectional umbrella of disability studies.
The hashtag #NNDR2019 is the best place to reflect upon, or catch up on the conversations shared throughout this conference. In this blog, I hope to write some of my own reflections from the event, which will regrettably cover only a small proportion of the diverse papers presented over the last few days.
Wednesday 8th May, 2019
The first paper of the conference was a keynote delivered by Prof. Jesper Vaczy Kragh. In this, he presented a history of institutionalisation in Denmark and introduced us to some key figures in this push towards the medicalisation of disability, such as Keller and Steincke. Both of whom, were also early proponents of forced sterilization and castration under the premise of eugenic logic, that ‘the existence of tainted individuals will deteriorate the fit, and accordingly, the average intelligence of the population’ (Steincke). He traced developments in the 1900’s, as well as the seeming shift back towards reinstitutionalization.
In the Gender, Body and Sexuality stream, Rebecca Fish and Yani Hamdani offered gendered perspectives of autistic girls and women, and experiences of violence in locked wards. These papers raised important questions considering the way that women are perceived to, and do experience different forms of violence and behaviour management.
The symposium, Troubling the Best Welfare State There is, asked important questions about how discourses and practices surrounding welfare were contributing to particular ideas around disability identity. Lill Hultman discussed some of the issues relating to the assessment process of personal assistance (PA) in Sweden, Lina Palmqvist considered the intersection between age and disability within the context of austerity, and Niklas Altermark criticised the discursive construction of PA funding as a problematic, burdensome cost.
Thursday 9th May, 2019
In the first keynote of the day, Prof. Katherine Runswick-Cole drew upon critical disability studies as a means of thinking about the construction of the family within ‘neoliberal-ableism.’ She highlighted the discursive construction of ‘us’ against ‘them’ through the rhetoric of ‘hardworking families’ and ‘troubled families.’ While ‘hardworking families’ are bolstered as adaptable, and the site to challenge societal ills, so-called ‘troubled families’ are marginalized as the cause of such social problems. Katherine drew upon the possibilities and risks associated with mother activism, and recommended the need to resist individualisation, to use and reuse the norm, and to engage with ‘advocacy-activism’ as a form of resistance.
In the session, ‘Society and Disability in Exclusion/Inclusion Perspective, speakers considered how disabled people were both included and excluded within particular contexts. Scott Avery presented an intersectional analysis of discrimination across the life trajectory, Mariela Yabo and Dori Rivkin described and evaluated a project to include young disabled people in Adult centres in Israel, and Elise Milot presented some reflections on a social inclusion and community participation project for ‘adults with intellectual disability’ in Quebec. Finally, Ian Matthews analysed the representation of disability within media stories, drawing upon stereotypes of vulnerability and innocence.
In the symposium, Disablist Hate Speech, editors and authors of an upcoming book presented understandings and findings relating to experiences of disablist hate speech. Opening the symposium, and providing an overview of the book, Mark Sherry outlined some tensions inherent within hate speech law, particularly thinking in terms of an international context. Following this, Mark discussed some of the unique ways that online hate speech was targeted disabled people, with the explicit motivation of causing physical and emotional harm. Next, Erin Pritchard drew attention to the problematic use of the word ‘midget’ in media and everyday language. Erin challenged continued representations of people with dwarfism as the subject of humour, and called for a ban on dehumanizing and derogatory representations. Line Melboe gave examples of the experiences of Sami disabled people, drawing attention to the complex intersections of identity. Finally, Terge Olsen engaged with Carol Thomas’ work on psycho-emotional disablism to document the way in which hate speech can contribute to barriers to doing and barriers to being.
Friday 10th May, 2019
In a session titled ‘Disability, Stigma and Coping Strategies,’ I delivered my paper on some preliminary reflections on my ongoing PhD project. I focused on three key analytical questions concerning how hate is understood, how it hurts, and how it is negotiated in everyday life. I wanted to draw attention to the importance of recognising everyday hate, but also to the intricate ways that disabled people are negotiating and resisting these. Next, Alise De Bie explored some of the coping strategies enacted by services users of mental health services. Alise emphasized the importance of reading for resistance within data to better understand the different ways that people are challenging mainstream discourses. Finally, Patrick Jachyra positioned and problematised medicalised discourses surrounding autism, and then shared research findings that shed light on why some young people diagnosed with ASD may become disengaged with physical activity. Specifically, he detailed some of the dangers associated with engagement with physical activity, such as being bullied in changing room spaces.
Final Thoughts
Unfortunately, after the morning’s presentations my energy levels dipped and I was unable to make any comprehendible notes. I am, however, left with many thoughts that I try to make sense of over the next few weeks. In particular, I have been thinking about the values and motivations underpinning disability research, and how this influences the ways in which disabled people are included (or not) in the research process. I have been thinking more about the importance of recognising and indeed, harnessing, the diverse forms of resistance that disabled people enact within the context of their everyday lives. And I am thinking about the potential for international collaborations, and in particular, how I myself can engage more with growing disability studies literature in the Global South, and the values that such perspectives would offer.
Special thanks to everyone involved in the organisation of NNDR 2019, and to all of the wonderful researchers, activists, advocates, and policy-makers that attended.

































