Category Archives: Actor-Network

Actor-Network, ethnomethodology, on assessment, on schooling policy, parentings

Policy? or Politics?

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Could the hegemony of “policy” be coming to an end?

For many years state officials, “private” foundations, benevolent billionaires, academia and a certain elite media have been telling everyone else what is what in “education”.  (For one sense of this set look at Brill’s 2010 story in  the New York Times magazine).  In the world of academia where I live, this will have been the decade of “data-driven” “policy” “studies.”  We keep being told, repeatedly, such “narratives” (stories? fiction?) as:

In Rhode Island schools, a multidisciplinary effort helps teachers to quickly understand what skills their students have already grasped and which subjects need more attention. In Houston, a regional alliance has noticed signs of students going off-track on higher-level math skills and acted to intervene.

What do these stories have in common? Success here derives from access to data, or big data as it’s sometimes called. The examples above come from the Data Quality Campaign, a nonprofit effort driving education outcomes through hard numbers.
(GovTech November 2014, retrieved in December 2015)

What interests me here, of course, is the hint of an “actor-network” of local schools and a corporation “e.Republic, Inc.” “The nation’s only smart media and research company focused exclusively on public sector innovation for state and local government and education” (retrieved in December 2015)

One problem with just sketching an actor-network (an excellent thing to do) is that it can end with an altogether static map and little sense of the movements through it, or the temporalities that assemble and then sometimes dissemble the network.

So, recently, I have tried to write about such networks as acting (and revealing themselves) through crowded conversations (deliberations).  I am experimenting with generalizing conversational analyses (somewhat like Latour generalized ethnomethodology when he moved from looking at the production of knowledge in short interactions among a few people (Garfinkel et al. 1981;  Goodwin 1995), to looking at a laboratory (Latour 1979), to looking at the scientific enterprise as a whole (Latour 1987).

And so, once upon a time, we had Senator Kennedy and President Bush (as symbolic leaders) producing “No child left behind” after very long conversations that started at least 20 to 30 years earlier –unless it is 200 years (Varenne 2007, 2011).

And then, a few years later, President Obama and Arnie Duncan, his secretary of education, started new conversations which, among other things,  privileged “data-driven policy.”  I am necessarily wrong in suggesting that they were the sole authors who literally started these long-turn taking sequences.  But they can stand as markers of a new sequence with somewhat different participants and discursive order as the original metaphor (a child is like a sponge) developed into practical conceit (regulations, the attendant bureaucracies, the texts to be produced among the various actors, etc.).
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Actor-Network, applying anthropology, autoethnography, health, medecine, of the body

An actor-network of consequential consociates: applying anthropology to one’s personal case

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In this post, I am doing something somewhat different from the usual.  I am maintaining the order I think I have established (at least as I look at it, retrospectively): this is an experiment in anthropological theorizing and teaching.  But I am delving further into parts of my life that I have not brought out.

So here it goes: applied medical anthropology

A few years ago, my wife, Susan, was diagnosed with a form of cancer known as “myelofibrosis” (who may not know it under that name might be a topic for another post as the exact name can be consequential—see below).  The “official” diagnosis was made, not surprisingly by an oncologist, the acknowledged, state approved, expert who can transform speech (this is myelofibrosis) into not simply an act, but a sequence of new moves a particular set of others, from the patient, to her family, to insurance companies, must now make. [This would be easy to model as a special case of entry into a particular kind of polity of practice.]

The oncologist told us, as I remember it four years later, something like: “People live with this for 15 years or more … You are likely to die of something else … It will change your everyday life as you will now have to schedule regular medical visits.”  I remember she was altogether good at telling us something that we knew, and much that we did not know: we had certainly never heard of this cancer or of its treatment.  Of course we went to the Internet and learned what we could, talked to her further, and settled into what I am experimenting in calling, for various theoretical reasons, a “new normal.”  Actually, what we learned was not extremely bad news for people entering in their 70s.  The oncologist then (and I will keep emphasizing conversational and interactional temporality) tried a drug that would alleviate the symptoms of a cancer that affects the production by the bone marrow of red blood cells: profound anemia and the attendants limits on mobility.

Susan’s body, in its thinginess and peculiarities, was leading us to various particular disabilities that can be mitigated or expanded depending (de Wolfe 2014).

So, this was actually a good time for us to adopt the car culture of suburbia.  The long walks in Manhattan to which we were accustomed would not have been possible anymore.  We escaped one disability.

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