Karen Kirke
Established Member (Voting Rights)
I have had a letter published in the Journal of the Royal Society of Medicine entitled
‘Measuring improvement and deterioration in myalgic encephalomyelitis/chronic fatigue syndrome: the pitfalls of the Chalder Fatigue Questionnaire’
You can read the letter here (see posts below if you are unable to access it):
https://journals.sagepub.com/doi/10.1177/0141076820977843
It is in response to Adamson et al’s audit of the ‘South London and Maudsley Persistent Physical Symptoms Research and Treatment Unit’ published earlier this year:
https://journals.sagepub.com/doi/full/10.1177/0141076820951545
The Adamson et al audit was discussed here:
https://www.s4me.info/threads/cogni...in-the-uk-2020-adamson-wessely-chalder.16242/
Thank you to my sister, Ciara Kirke, for proofreading a draft and pointing out where it didn’t make sense. Thanks also to @Tom Kindlon for having a look at the final draft and crossing his fingers for me.
I hope the letter will spark discussion of outcome measures here and among the researchers looking to measure fatigue over time post-Sars-Cov-2 infection and other infections.
As some will already know, I have had ME/CFS since 2008 following viral meningitis. I was a Speech & Language Therapist at a hospital. My ME/CFS is severe – I am completely housebound – and unfortunately is worse than when I last posted about it.
[Edited to correct my sister's name to the one she uses for work, Twitter.]
[Edited to signpost people to posts below if they are unable to access the letter.]
‘Measuring improvement and deterioration in myalgic encephalomyelitis/chronic fatigue syndrome: the pitfalls of the Chalder Fatigue Questionnaire’
You can read the letter here (see posts below if you are unable to access it):
https://journals.sagepub.com/doi/10.1177/0141076820977843
It is in response to Adamson et al’s audit of the ‘South London and Maudsley Persistent Physical Symptoms Research and Treatment Unit’ published earlier this year:
https://journals.sagepub.com/doi/full/10.1177/0141076820951545
The Adamson et al audit was discussed here:
https://www.s4me.info/threads/cogni...in-the-uk-2020-adamson-wessely-chalder.16242/
Thank you to my sister, Ciara Kirke, for proofreading a draft and pointing out where it didn’t make sense. Thanks also to @Tom Kindlon for having a look at the final draft and crossing his fingers for me.
I hope the letter will spark discussion of outcome measures here and among the researchers looking to measure fatigue over time post-Sars-Cov-2 infection and other infections.
As some will already know, I have had ME/CFS since 2008 following viral meningitis. I was a Speech & Language Therapist at a hospital. My ME/CFS is severe – I am completely housebound – and unfortunately is worse than when I last posted about it.
[Edited to correct my sister's name to the one she uses for work, Twitter.]
[Edited to signpost people to posts below if they are unable to access the letter.]
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