> **Toni Nieminen:****Your book can be posited as an auto-ethnographic account in that your own experiences of living with cancer have shaped and enabled you to think about experience in a fragmented way, whereby change and contingency become the point of departure in experience and perception. Considering some criticisms of auto-ethnographic writing (who gets to say what, when and why), do you reserve impairment phenomenology for those living with impairments, or is it accessible also to the non-impaired? If so, how does the project change in the process? Further, and this is something you gesture towards in the concluding handbook, do you think that impairment phenomenology can be used as a research tool across disciplines?**
> **Jonathan Sterne:**This is a fantastic question! I think about this a lot. Who can and should write about impairment and disability? Anybody can. More people should. All are welcome. But as the saying goes, “nothing about us without us.” Writing about disability starts with reading work in disability studies. There is an awful lot of sanctioned ignorance among ableds, which is how you get neo-eugenic access policies and disability simulations, as well as scholarship that uses or engages with disability from an ableist frameworks. So, the first step is struggling to overcome that sanctioned ignorance.
> I don’t think there should be a passport for writing about anyone, but there is a responsibility to the group you are studying, and a moral requirement of social solidarity if you are in a privileged position with respect to them. In the humanities this is often personalized around the charisma and ethos of the intellectual—as in, to be wrong is to be morally deficient. I hate that, but I also understand it. For disabled people, the emotional stakes can be amplified because the personal and political are commingled, and we are so often represented by others against our will, especially in institutional contexts. Our challenge as scholars is to resist this impulse to completely personalize position-taking, while being attentive to the fact that universities and the field of academic writing are very ableist spheres, which often crowd out and systemically exclude disabled people. Right now in universities, we have a situation where most of the claims to putative expertise on disability come from nondisabled people. We have to ask how such a fucked-up result came to pass and what it will take to transform that situation. We need to deal with this in concert with other challenges our institutions are facing around their ongoing racist, colonialist, cis-sexist, and heterosexist histories. It is perennially unfinished work.
> As I mention above, I don’t use the label auto-ethnographic for_Diminished Faculties_, though I’m also a believer in Barthes’ “author is dead” thesis, and others will categorize me as they like and I’m fine with that. My resistance to the term is that I think all ethnography involves the position of the ethnographer (so ethnography without a reflexive turn on the ethnographer is bad ethnography). There’s also a systematicity and intentionality to ethnographic research that’s absent in_Diminished Faculties_. It’s a very fragmented text both in terms of subject matter and method.
