I went to see Andrew Carnie’s exhibition ‘Seized out of this World‘ a couple of weeks ago in Winchester and came out with mixed feelings: I think because it was something so personal to me. What was most interesting for me was seeing somebody else’s artistic interpretation of temporal lobe epilepsy. It is the first time I have come across work on the subject in real life.

Using figurative, electrical and medical images projected onto layers of cloth, Carnie was able to engage more than just the visual sense. The hanging sheets rippled and undulated as fans blew air onto them from the sides, distorting the images as they merged. That he had used 6 slide projectors gave a rhythm to the piece. In the darkened gallery it was all encompassing.

It was a very different experience to mine although at times evocative of my own. I’m not sure whether Carnie has epilepsy himself or not, but it brought home to me that everyone’s experience is different. Of TLE and of seeing art.

The visitors’ book and the comments of other people while I was there was fascinating. I often think that the comments are as much part of the exhibition as the art. Ranging from ‘calming and meditative’ to ‘disturbing’ and ‘nightmarish in a Tim Burton kind of way’ the comments proved that this piece had moved them. Isn’t that what art is all about?


One response

  1. “Everyone’s experience is different. Of TLE and of seeing art.”
    I would very much like to experience art that grows from the experience of TLE.
    My writing — fevered as it is most of the time — is, I have decided, a picture
    of TLE. It’s not art, but it is an artifact. I dream of sometime organizing an
    exhibit, reading, soiree—whatever artistic expressions of TLE could be brought
    together, not so much to show anyone else, but so those of us who have this same
    condition, but who experience it in so many different ways, could get some sense
    of how our differences are the same.

    25/09/2009 at 2:19 am

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