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Poem: Thanks a shitload, Karen Armstrong

Posted on January 13, 2012October 17, 2022 by David Barker

Thanks a shitload, Karen Armstrong.
I mean, I’m happy for your diagnosis
and all. I mean, not knowing is worse
than floating in medical limbo.

I get the stigma of epilepsy: how
people can be cruel, even smart ones,
with puppy words that never bite,
at least not until they grow teeth.

“No Karen,” she agreed, adding …
“Hospitals are not for intelligent people.”
Woof. I must be super stupid, thinking
illness was the cause for my admissions.

I wish you could have met my friend
who was so smart he hanged himself.
If only he could have been stupid
and gotten the help he needed.

I get the freedom of diagnosis: how
it drops the scales from your eyes
and lets you see you are not mad,
your mind, not “irretrievably flawed”:

the world has been given back to you.
Has it been taken away from me?
Don’t make me the baby you toss
out with your tepid bath water.

The Spiral Staircase, by Karen Armstrong - book cover

This is a poetic response to some passages I read in The Spiral Staircase: My Climb out of Darkness, a memoir by Karen Armstrong. I read it as research for a novel I’m writing in which one of the characters is an ex-nun. As I had hoped, the memoir gave me insight into the experience of transitioning from convent to the secular world. I admire Armstrong’s writing and her work to promote understanding amongst the world’s major religions. However, I tripped over something that I couldn’t ignore. Armstrong recounts mysterious episodes of fainting, forgetfulness, finding herself in strange places, experiences of anxiety and panic. The sisters of her order believed she was hysterical and engaging in attention-seeking behaviour. Later, as an academic outside the convent, she was referred to a psychiatrist and even hospitalized for psychiatric treatment. Eventually, she received a correct diagnosis: epilepsy. However, her relief was accompanied by an “it could have been worse; I could have been mentally ill” sentiment. To which I respond: so what if you were? In the long run, would it have made any difference? Should it make any difference?

I suppose what bothers me is that, although she is sensitive to the problem of stigma, at least in relation to epilepsy, she nevertheless writes in a way that contributes to stigma in relation to mental illness.

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