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ME/CFS success story: Lightning Process on Youtube 2019

Discussion in 'Psychosomatic news - ME/CFS and Long Covid' started by John Mac, Aug 21, 2019.

  1. rvallee

    rvallee Senior Member (Voting Rights)

    Messages:
    12,461
    Location:
    Canada
    None of them had ME. Plenty of aimless people out there with poor motivation, looking for a meaning to their life. It's the same mechanism as cults. Some people find meaning in the weirdest things. It doesn't do anything that a motivational seminar would do. ME is often misdiagnosed so it's an easy target to exploit.

    Grifters gonna grift.
     
    Octogenarian, JoanNI and unicorn7 like this.
  2. Andy

    Andy Committee Member

    Messages:
    21,947
    Location:
    Hampshire, UK
  3. rainy

    rainy Senior Member (Voting Rights)

    Messages:
    207
    Location:
    Norway
    When I did the LP, one of the things we learned was to exaggerate the way we talk about our health in a positive way.

    After day one, we were told to go do something out of the ordinary, now that we had this great tool for health. We could do anything now!

    Then on day two we did an exercise were we had to get up in front of the group and talk about how much we had been able to do after the first day of LP, and how wonderful we had felt.

    We were told to use big, strong body language, and use words like "incredible, amazing, wonderful" - only strong positive words, about how great we felt and how much we had done. The rest of the group should judge if we had exaggerated strongly enough, and if they thought we didn't, we had to do it over again.

    When we were done, the LP pracitioner asked each of us "what could you have done differently in your presentation?" One person said: "well... I guess I could have lied a little more about what I had done."

    The LP practitioner then explained that we weren't supposed to exaggerate what we had done, just how we spoke about it. But I certainly had interperated it as the former, and I'm pretty sure most people in my group did.

    We had already been told to lie and say we're healthy and dont have ME anymore (we only do ME, sometimes, when we chose to), and to never say we have symptoms or that we feel bad. So it isn't surprising we thought we were supposed to lie about this too. Especially since most of us probably went home after day one feeling awful and not doing anything more than usual. Or if we did more than usual, we were now paying for it in PEM.

    The LP is like a course in training people to make great testimonies. You have to say you're cured, even if you aren't. You have to say everything is super amazing, even if it isn't. But just as long as you say it is, it might become true...
     
    Daisy, Dolphin, Hutan and 29 others like this.
  4. Keela Too

    Keela Too Senior Member (Voting Rights)

  5. Andy

    Andy Committee Member

    Messages:
    21,947
    Location:
    Hampshire, UK
    Earlier this year I met one of my wife's work colleagues who had been diagnosed as having ME years ago but had attended a LP course and had been 'cured'. The problem was that, amongst her anecdotes about her work, she spoke a number of times of how she would get to the end of the week and be completely exhausted. I kept my opinions to myself, no point arguing with the brainwashed, and I didn't want to make my wife's working relationship with her more difficult.

    Obviously the misdiagnosis rate for ME will work in the favour of LP, CBT, GET and all the other quack therapies. My wife, a number of years ago, went through about 9 months of post-viral fatigue that looked a lot like 'mild' ME, and I could have easily understood if she had ended up with an ME diagnosis. If she'd been sent to an ME clinic, or attended a LP course, they would have probably been delighted to claim her return to health as a success story for them.
     
    Dolphin, Octogenarian, wdb and 17 others like this.
  6. Trish

    Trish Moderator Staff Member

    Messages:
    52,310
    Location:
    UK
    Thank you @JoanNI and @rainy for sharing your experiences. I think this is vital in a world where most of us are without any treatment or proper care, and desperation can drive us into the hands of charlatans - I've wasted my money on a few in my time.
     
    Dolphin, Hutan, Octogenarian and 12 others like this.
  7. SallyC

    SallyC Senior Member (Voting Rights)

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    217
    The vast majority of the positive comments are from accounts with zero activity which is a bit suspicious.
     
    Dolphin, Sarah94, MEMarge and 12 others like this.
  8. DigitalDrifter

    DigitalDrifter Senior Member (Voting Rights)

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    894
    Reporting his video would not be in the spirit of free speech. Phil Parker has a right to make videos even if he is greatly misinformed on what ME is.
     
    Octogenarian likes this.
  9. JoanNI

    JoanNI Established Member (Voting Rights)

    Messages:
    29
    The advertised ‘3 day’ course is misleading, it’s actually 2days at 4 hours and 1day at 2 hours, so a total of 10 hours over 3 days. There’s minimum travel by taxi to the venue as the LP coach advises staying in a nearby hotel for your ‘life changing’ holiday.
     
  10. JoanNI

    JoanNI Established Member (Voting Rights)

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    29
    Yes that’s correct, ‘think only positive thoughts and speak only positive words with great enthusiasm’ if I remember rightly.
    They don’t actually say ‘fake it till you feel it’ but that’s the idea.
     
  11. JoanNI

    JoanNI Established Member (Voting Rights)

    Messages:
    29
    Yes, I noticed that too. Phil Parker must have a little band of people he alerts to make positive and supportive comments on all ’ME recovery’ videos perhaps?
     
  12. JoanNI

    JoanNI Established Member (Voting Rights)

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    29
    The sad thing is, I had read good and bad stories about LP but the desperation to get well overcame all reasoning.
     
  13. NelliePledge

    NelliePledge Moderator Staff Member

    Messages:
    13,277
    Location:
    UK West Midlands
    Which would be fine if he wasn’t actually selling a product. In which case it’s entirely appropriate to report something making misleading claims.
     
    sea, Dolphin, Octogenarian and 7 others like this.
  14. EzzieD

    EzzieD Senior Member (Voting Rights)

    Messages:
    547
    Location:
    UK
    Don't know if everyone here is aware that Parker was reported to the Advertising Standards Agency in 2012, and their conclusion was:

    https://www.asa.org.uk/advice-online/health-the-lightning-process.html

    https://www.asa.org.uk/rulings/Phil-Parker-Group-Ltd-A11-158035.html

    Parker said in his defence:
    LOL. He thinks being an osteopath, psychotherapist and hypnotherapist makes him suitably qualified to deal with serious medical conditions, and that personally training other LP practitioners makes them qualified too.

    But despite the ASA's rulings, he merrily carries on pushing the same crazy and potentially dangerous nonsense. Seriously needs reporting again, but would it make any difference this time either?
     
    sea, Dolphin, Octogenarian and 12 others like this.
  15. NelliePledge

    NelliePledge Moderator Staff Member

    Messages:
    13,277
    Location:
    UK West Midlands
    I’ve found it quite helpful when I used to respond to stuff on Facebook when theLP evangelists come on to post a link to advertising standards ruling it seems to be quite effective at shutting down exchanges.
     
    Dolphin, MEMarge, Annamaria and 6 others like this.
  16. DigitalDrifter

    DigitalDrifter Senior Member (Voting Rights)

    Messages:
    894
    Phil Parker tries to silence critics with threats of legal action, let's not stoop to his level.
     
    Octogenarian likes this.
  17. NelliePledge

    NelliePledge Moderator Staff Member

    Messages:
    13,277
    Location:
    UK West Midlands
    He needs reigning in to limit the risk of his bogus approach causing harm to people. I fully support ME Associations actions in complaining to Advertising Standards and if people highlight that to social media platforms all to the good.
     
    sea, Dolphin, Mithriel and 13 others like this.
  18. Caroline Struthers

    Caroline Struthers Senior Member (Voting Rights)

    Messages:
    833
    Location:
    Oxford UK
    I just had a look and disliked it. As you say, the number of likes and dislikes is not showing, and there are maybe one or two short negative comments (not yours) but the majority are positive and refer to negative comments you can no longer see. Awful.
     
    Dolphin, Mithriel, Hutan and 9 others like this.
  19. Adrian

    Adrian Administrator Staff Member

    Messages:
    6,486
    Location:
    UK
    I have come across a couple of people who have recovered but I suspect that is a post viral thing (one was ill for a couple of years).

    One of the things I think happens is as people start to feel a bit better they try stuff to improve and then the credit things tried with further improvements. So natural fluctuations can lead to credit to interventions tried at the time. This is why clinical trial are needed and trials that are robust enough to produce solid results (unlike Smile in this case).
     
  20. Barry

    Barry Senior Member (Voting Rights)

    Messages:
    8,385
    I think that in the future, when ME/CFS is much better understood, it may be that a good many present day ME/CFS diagnoses might include quite a lot of variants, and/or maybe several conditions with strongly overlapping symptoms. I suspect that somewhere within that confusing mix there may well be a subgroup who actually might be helped by gentle exercise, possibly even by very carefully increasing it; with future understanding, these patients might be diagnosed with something different. But I'm certain that better understanding will also show many people with present-day diagnoses can be harmed with that approach, and most will not benefit at all.

    So it does not surprise me there are some apparent present day successes to crow about. But for every success, how many people get harmed by this throw-enough-sh*t-against-a-wall-and-some-of-it-will-stick approach.
     
    Octogenarian, Sarah94, JemPD and 3 others like this.

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