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Invisibilia: For Some Teens With Debilitating Pain, The Treatment Is More Pain

Discussion in 'Other psychosomatic news and research' started by Andy, Mar 10, 2019.

  1. Mithriel

    Mithriel Senior Member (Voting Rights)

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    2,816
    Um, skin turning blue, hair changes that sounds like nerve damage to me. And these damaged nerves cause pain.... it doesn't need any more than that for an explanation.
     
  2. Woolie

    Woolie Senior Member

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    I think its difficult to judge the absolute incidence of something like pain across eras. Historically, large sections of the population would have remained silent about it, due to inability to afford doctors and/or fear of job loss. Those that had the economic capacity to speak up would have faced social obstacles (for men, reporting pain may have been seen as weakness, and for women, they may be dismissed as hysterical or otherwise psychologised - Freud's patients are a nice example). Plus, people are living longer now so there is are more average life years per person than in previous generations, so more opportunity for chronic issues to make themselves evident.

    But I think the real problem with evaluating the past is lack of records, and the likelihood of complaints being dismissed by either the patients themselves and/or others caring for them.

    I'm also very sceptical of the claim that were getting unhealthier as a society. We're getting fatter, sure, but paradoxically, the incidence of cardiovascular disease has gone down (average age is higher, gap between men and women is shrinking, mainly because men's risk has gone down). And of course, we're living longer. For me, those positives seem huge and do I don't think I could really say we're "getting unhealthier" overall.
     
  3. Jonathan Edwards

    Jonathan Edwards Senior Member (Voting Rights)

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    I agree. Think it is entirely appropriate to flag these sorts of studies up on S4ME because they illustrate the pervasive problem of bad scientific methodology in the wider field that gets put under MUS or whatever. I think it is reasonable to be emotional too because it is time this sort of thing stopped.I get increasingly angry when I see such poor science.

    As far as I can see from PubMed Sherry has never even attempted a controlled study. The general approach is eerily reminiscent of Wessely et al 1989 on how to do CBT in ME (before anyone has tested it).
     
  4. Jonathan Edwards

    Jonathan Edwards Senior Member (Voting Rights)

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    I am interested that you raise this defence, @shak8. I find it very hard to be that generous.

    The study seems to be from 1999. It was not an effort to see... because no valid study was done. It was introduction of a programme that was assumed would work.

    I cannot see what the plasticity of the young brain has to do with the theoretical basis being sound. Apparently Sherry blames the mothers. We don't really know what the basis is.

    Whether or not teens are legally able to give consent seems to me not relevant. They are too young to realise that health care workers may be interfering busybodies building empires.

    Encouraging people with CRPS teenage in painful activity sounds very much like torture to me.

    And dropping out is just regarded as being uncooperative by therapists.
    I spent twenty odd years working alongside physiotherapists and their lack of insight into their motivations terrified me. I pretty much gave up referring anyone for therapies.
    This may be S4ME but I think there is a much bigger problem with therapist-delivered treatments that the forum can legitimately try to address.
     
  5. Woolie

    Woolie Senior Member

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    I have to say, my view is the complete opposite to yours, @shak8. PwMEs are justifiably upset about how we have been treated, and are trying desperately to raise awareness of the problem with outsiders. Given the experiences we've had with our illness, we should be more aware than anyone how this type of paternalistic approach can cause harm. If we just take the view that our illness is "special", and readily buy into the same bullshit as long as its being dished out to other people, then what does that make us?
     
  6. Woolie

    Woolie Senior Member

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    Completely agree. Here at S4ME, we can be a voice for change that goes beyond our own illness.:thumbup:
     
    TrixieStix, shak8, Snowdrop and 10 others like this.
  7. Sarah94

    Sarah94 Senior Member (Voting Rights)

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    'Orwellian' is right.

    Torture is treatment
    Illness is recovery
    Scientific critique is harassment

    Orwell knew how language can affect thought. If we rename torture as "treatment" then it suddenly becomes acceptable! And if we rename scientific critique as "harassment" then it suddenly becomes unacceptable. And if we change the meaning of 'recovery' in a clinical trial... well, you know the rest.
     
    Last edited: Jun 17, 2019
    shak8, S-VV, EzzieD and 2 others like this.
  8. adambeyoncelowe

    adambeyoncelowe Senior Member (Voting Rights)

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    There's a really worrying comment here.
    This is not okay. He sounds like a sadist and there's a very real safeguarding issue here. It's beyond creepy.
     
    rvallee, Sarah94, EzzieD and 5 others like this.
  9. chrisb

    chrisb Senior Member (Voting Rights)

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    It is clearly OK so long as its not with a member of the department.
     
  10. rvallee

    rvallee Senior Member (Voting Rights)

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    I was thinking of this the other day and since the thread got bumped I'll try and make sense of it.

    This idea seems to be based on research that shows that unexpected pain feels worse when you anticipate it, when you are told that something will hurt but do not know how bad. In this research people anticipating an unknown level of pain, which could even be trivial, feel it more because of the anticipation. So not anticipating it would lessen the pain, which follows that avoiding thinking about it may help lower the pain.

    But this is only true of unexpected pain. Chronic pain is very much known, that's what makes it chronic. I personally find that anticipating and dealing with known pain makes it more bearable. Not easy, but this is very much like anticipating a side tackle, the impact is much lessened by muscle contraction and trying your best to deflect the worst of the hit. It's kind of a learned skill. It only works when the pain is known, but that is precisely the case with chronic pain.

    Resolve plays a huge role in enduring suffering, even if it does not make it disappear. People dealing with chronic pain have resolve in bulk, not by choice but sheer necessity.

    So the underlying assumption for this model is based on conditions that do not exist with chronic pain. The evidence simply does not translate to the different conditions, as it is strictly the surprise element that confuses the response. Take away the surprise, which is not present in chronic pain, and you are dealing with a different reality.

    This is more relevant to ideas like CBT and ACT and whatever in dealing with pain than this here with inflicting more pain, but it's relevant in that the whole thinking about pain within medicine is filled with invalid ideas that lead to all sorts of weird hypotheses like this one.
     
    Last edited: Jun 18, 2019
    shak8, Amw66 and Wonko like this.

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