1998: Wessely playing down differences between himself and Showalter

Esther12

Senior Member (Voting Rights)
This leads on from a discussion elsewhere, so might seem odd out of context, but there you go.

https://www.lrb.co.uk/v20/n16/sarah-rigby/diary

I was just reading this letter from Wessely, and thought it was of interest, as he now will now emphasise how different Showalter's views were from his own (although in this letter he only talks of "the research I described in the Guardian":

In her account of her struggle to overcome chronic fatigue syndrome (CFS), Sarah Rigby (LRB, 20 August) suggests that a recent article of mine in the Guardian ‘silently contradicted’ the views of Elaine Showalter. In fact there is no contradiction between the research I described in the Guardian and the position taken by Showalter in her book Hystories or in the Diary she wrote for the LRB. Our work showed that the majority of those who come to a specialist clinic such as the one I run at King’s College Hospital do indeed come from the professional classes. Nearly all believe they are suffering from myalgic encephalomyelitis (ME), and many do not fulfil established international criteria for CFS. An illness which preferentially affects the successful middle classes is inherently implausible, and provides the basis for Showalter’s critique. However, when we looked outside the clinic, we found the opposite. Operationally-defined CFS was more common in lower socio-economic groups, but most of those affected did not use terms such as ME to describe their illness. There is thus no discrepancy between our epidemiological studies of CFS and Showalter’s historical analysis of ME – we are describing different constructs and concepts, so it is not surprising that we reach different conclusions.

Simon Wessely
King’s College School of Medicine, London SE5

He gets a fairly sharp response from Sarah Rigby:

Vol. 20 No. 20 · 15 October 1998

Simon Wessely (Letters, 17 September) now claims that he sees a distinction between ME and CFS, two years after his instrumental role in the Royal Colleges committee whose final report specifically (and, many felt, inappropriately) recommended that ‘ME’ should be renamed ‘CFS’. Even if he now makes a distinction between the two terms, he certainly did not do so in his Guardian article, on which I based my assumption that he disagreed with the position Elaine Showalter took on CFS and class in Hystories.

In that book Showalter suggested that, CFS, like neurasthenia, ‘was most commonly seen among the upper social classes’. In the Guardian, using the same historical parallel, Simon Wessely said that in Victorian times CFS was, ‘oddly enough’,

thought to be an illness that predominantly affected the upper echelons of society. So is it yuppie flu, then? The Victorians gradually learnt that it wasn’t, and we are slowly finding the same. My clinics do contain rather more teachers, doctors and nurses than one would expect, but when we extended our studies to general practice and the community we found that CFS was common in all social classes.

In his letter Wessely suggests that in his Guardian article he was writing about CFS, and that Elaine Showalter had been giving an account of ME. In his article, however, he uses the two terms as though they were interchangeable, and writes under the title ‘No-name illness’. The only distinction he made between them was this: ‘ME is the term that dominates the clinic and the media, but doctors talk and write about CFS. Encephalomyelitis … is a misnomer while chronic fatigue syndrome is instead neutral … but is it, whatever we call it, new?’ The implication must surely be that he sees (or then saw) the two terms as different names for the same thing, not as ‘different constructs and concepts’, as he now claims.

In her book Showalter also used the two terms as though they were synonymous, noting that ‘ME’ is the name ‘used in the UK’. ‘Whatever the official definition or name of the syndrome,’ she went on to say, ‘doctors use it in lax and general ways.’ This last point certainly seems to be true, and it’s the reason for the British ME charities’ aversion to the term ‘CFS’, which they see as a large and unspecific category, consisting of many sub-groups with different causes and symptoms. Their point has usually been that as it is already widely used in Britain, the term ‘ME’ should continue to be used here until a more satisfactory alternative can be agreed on. However, neither Showalter nor Wessely mentioned sub-groups in what they wrote. The symptoms Showalter described, as well as her historical account of the illness, clearly indicate that she was writing about CFS as a whole and was not making the distinction Simon Wessely now makes in his letter. In print, if not necessarily in intention, there can be no doubt that Wessely did contradict Showalter’s views on this issue.

Sarah Rigby
Norwich

I've not been able to find the Guardian article of Wessely's that Rigby refers to. Anyone have a copy?
 
I could not find the Grauniad article but it is perhaps significant that this 1997 paper referred to the fact that "chronic fatigue had become invisible" with "no name...."
https://www.researchgate.net/publication/13774809_Chronic_fatigue_syndrome_A_20th_century_illness

Unfortunately you have to put in a request for the full document.

"Understanding somatisation can still shed some light on the meaning of chronic fatigue at the end of the 20th century."

Has anyone ever understood it?
 
Thanks. It's currently on sci hub here: http://www.sjweh.fi.sci-hub.hk/download.php?abstract_id=239&file_nro=1

You might need to be quick to dl from that link though, as lots of scihub domains are being shut down at the moment.

Just making a note that I'm onto the page marked as 24 on this. I'm sure I've already read it anyway, but it's full of the usual Wessely stuff of implying more than he says, and so taking a long time to say very little. I might try to finish it tomorrow.
 
First impressions.

One comes away from this with the sense that sense that Wessely feels the overwhelming need to say something, but is not quite sure what he wants to say.

Now here is an interesting quote.

"Goldberg and Bridges have suggested an influential definition of somatisation, seeing it as a process by which patients gain access to medical care.They define somatisation as occurring when a patient with a psychiatric disorder seeks consultation for physical symptoms attributed by the patient to a physical cause. Finally treatment of the psychiatric disorder would be expected to reduce or eliminate the physical symptoms."

This is a little unfair. He goes on to discuss other definitions, but there seems to be no overt criticism of this underlying idea.

He finishes with:

" I have also shown how the genuine fear and stigma of mental illness and the need for explanations that are both protective of self esteem and in keeping with modern views on sickness and health are also important..........etc."

It needs reading a couple more times. It needed editing a couple more times.
 
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