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Guardian: Long Covid is very far from ‘all in the mind’ – but psychology can still help us treat it - by Carmine M Pariante, April 2021

Discussion in 'Psychosomatic news - ME/CFS and Long Covid' started by Kalliope, Apr 27, 2021.

  1. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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  2. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    Did anyone manage to listen to this? I can't seem to find an option on the BBC London site to listen back.
     
    MEMarge likes this.
  3. Arnie Pye

    Arnie Pye Senior Member (Voting Rights)

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    I think this is what you are looking for : https://www.bbc.co.uk/programmes/p09dw1l8

    They really don't make it easy to find! I haven't looked for the particular segment of the program involving Pariante.
     
    MEMarge, Andy and InitialConditions like this.
  4. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    They really don't! But thanks.
     
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  5. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    Edit [Pariante interview] starts at 2:19:00 - the segment is much longer and involves a long Covid patient before Pariante.
     
    Trish, MEMarge, Andy and 1 other person like this.
  6. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    I don't think we learned much. As I said to David Tuller yesterday—and others may disagree, but this is my personal opinion—I think there's enough biomedicine and biology in Pariante's work for it to be taken seriously. Any work on brain inflammation and central fatigue may prove important to ME/CFS, even if to just a subset of patients. I certainly don't lump him in with the likes of Chalder and Crawley, who are not serious scientists.
     
    Last edited: May 6, 2021
  7. Andy

    Andy Committee Member

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    My concern would be that his support for, and his misrepresentation of patient's concerns about, CBT for ME would suggest that he would be open to interpreting any biomedical results that he might find into that framework. The results of his work might prove to be useful; his interpretation of it, possibly not so much.
     
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  8. Trish

    Trish Moderator Staff Member

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    Pariante 2:19 to 2:39
    More or less repeats his arguments from the article.
    Goes on and on about personalised treatment/ help with management. pacing, pushing at your limits gently etc etc. Seems to think that the NHS clinics are getting it right with their usual mix of therapists to provide this personalised help.

    He argues that it's important for psychosocial approaches to be included in all research studies of Long Covid.

    He also made what to me seems a very superficial statement that as far as the body and brain are concerned psychological stressors and infections have exactly the same effect on the body and brain - ie stimulating the immune system, so from that he seems to deduce that ME/CFS and Long Covid can be treated by psychosocial treatments.

    The interviewer says her mother has ME/CFS and has experienced clinicians and friends saying it's all in her mind. Pariante tried to dismiss this as belief from over 50 years ago. He didn't acknowledge that it's still going on.

    The interviewer was very respectful and didn't challenge him at all.
     
  9. petrichor

    petrichor Senior Member (Voting Rights)

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    He's right that psychological stress isn't good for ME/CFS, as it isn't good for many other conditions. Maybe I'm wrong, but I don't think that anyone has challenged the idea that psychological stress can be bad for ME.

    The problem is this ambiguity with whether that's treated as a central perpetuating mechanism of ME or whether it's just something seen as a factor as it is in many other conditions, including physical ones. He isn't making that clear, isn't talking about evidence for what he's saying, and keeps talking about various analogies and comparisons which basically amount to truisms.

    It's a bit of a dogs breakfast, which is frustrating, because although he seems like a nice and respectful guy, that all makes it hard to have a good dialogue with him.
     
  10. Midnattsol

    Midnattsol Moderator Staff Member

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    There was an interview/story with Helland from the Norwegian Competence Center, where she said something along the lines of "Some people only hear psychosocial when we talk about the biospychosocial approach". I could have given her the benefit of the doubt that she also included healthcare workers in this, but then she went to say that we now know that illness is influenced by many factors, and we must treat it holistically or something similar. IE, the healthcare workers know what this means, but patients misunderstand.

    Sorry, no. Some healthcare workers really do believe it's psychosocial, supported by the type of statements such as the one above.
     
  11. Mithriel

    Mithriel Senior Member (Voting Rights)

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    I have never found psychological stress bad for my ME. I have had nights when I could not sleep for worry, but that is universal with extreme stress even if you don't have ME.

    My symptoms depend on how much I do whether life is good or bad.
     
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  12. dave30th

    dave30th Senior Member (Voting Rights)

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    Did Pariante discuss the cancer analogy as he did in his article?
     
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  13. rvallee

    rvallee Senior Member (Voting Rights)

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    He seems to straddle both. But he needs to pick a horse and soon because everyone still clinging to the wrong horse will find themselves to be entirely irrelevant before they get a chance to get back in the barn.

    Association with the ME-BPS world is the same as being associated to HIV deniers in the AIDS world. It's as clear as it gets. That stink won't come off.
     
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  14. rvallee

    rvallee Senior Member (Voting Rights)

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    And that disqualifies him as a serious person. Being unable to acknowledge reality always should be.
     
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  15. shak8

    shak8 Senior Member (Voting Rights)

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    When Pariante says (2:22 in the BBC interview) that it is the same effect on the body, whether you suffer grief or a virus, that is a misleading exaggeration.

    I've had experiences with grief (divorce because I was ill, death of parents) and it never put me in bed (I have primarily fibro). I experienced pain, but it was the emotional pain specific to grieving, and ultimately of limited duration. I knew my body to be in good condition during those times.
     
    Last edited: May 6, 2021
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  16. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    but he (Pariante) is very tight with SW and a lot of his work is on depression. All of the bPS group are just dying for something that 'proves' the correlation between ME and depression.
     
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  17. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    I think they'd have found that correlation by now if it existed. Pariante's talk at the 2018 CMRC conference included reference to the finding of low cortisol levels in ME/CFS patients and he then compared it with high cortisol found in depressed patients.
     
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  18. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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  19. Sid

    Sid Senior Member (Voting Rights)

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    Tbh the fact that he is reduced to fighting a rearguard action so blatant and pathetic is a sign that we’re making progress. They’ve fallen back very far from their original position in the 1990s (there is no disease, CBT/GET is curative) to now saying that CBT is somewhat helpful as an adjunct treatment whose mechanism action is placebo.
     
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  20. Jonathan Edwards

    Jonathan Edwards Senior Member (Voting Rights)

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    Well, that would be drivel - pure psychobabble. Pariente has done some meaningful biological studies but he seems to have no idea in terms of overall theoretical framework. Personalised treatment is bullshit, as we know. I have n'tween the presentation but it is no good being half a scientist.
     

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