Search results

  1. Snowdrop

    Nocebo and the contribution of psychosocial factors to the generation of pain, 2019, Benedetti et al

    I don't see any online presence for the "Innovative clinical training and trials healthcare worldwide initiative" that funded the 'research'. Certainly worth wondering what this initiative is about.
  2. Snowdrop

    Podcast: CBT for Chronic Fatigue Syndrome: Dr Lucy Maddox, Trudie Chalder

    I don't think TC et al have ever really grappled with dealing with anyone but the least severely ill (who are still very ill and deserve better than TC). I don't think they really know anything about the severely ill from any experience as health care providers/researchers. One of the things...
  3. Snowdrop

    Mayo Clinic Guide to Fibromyalgia: Strategies to Take Back Your Life By A. Abril M.D. & B.K. Bruce Ph.D. L.P., Mayo Clinic Press (2019)

    What I see in all this are things that looks superficially possibly correct. A whole story is built around how this supposedly works and for anyone who has no deep knowledge of the involved systems and/or is not capable of being aware of what it is that we don't know (what gaps there might be)...
  4. Snowdrop

    Daily Telegraph: Why do we tell women they're mad, when they're really ill? Nov 18 2019

    I think SW has taken quite the offense because he knows exactly that this charaterisation of people especially women is rife within parts of medicine and psychiatry. Although psychiatry will couch their language in rather softer tones and even believe (it's often all about their beliefs) they...
  5. Snowdrop

    Daily Telegraph: Why do we tell women they're mad, when they're really ill? Nov 18 2019

    I read 'mad' more to mean imaginary or moral weakness. In which case I think the headline is correct. Mad is slang and not a psychiatric category. That does open up a discussion though of what I consider an issue of how mental health labels are created--how accurate/meaningful they are. It...
  6. Snowdrop

    PEM for those who are, or were, mild sufferers, how would you describe it?

    When my illness was much milder long ago I had issues with cognitive PEM. It too was much milder but had bigger consequences (mostly). So I would forget where I put things, occasionally left my car keys locked in the car and would enthusiastically start some project that needed/wanted doing...
  7. Snowdrop

    Open letter to Dr Peter Fisher, Liverpool University, about a research survey on emotional distress and CFS. 2019

    Hi @Snow Leopard It's not so much the idea of being for or against psychology for me as it is that after a while hanging around with ME and seeing what is researched that it seems there is just an awful lot of it. And in terms of the big/main goal of getting well it is of limited (or no) value...
  8. Snowdrop

    Open letter to Dr Peter Fisher, Liverpool University, about a research survey on emotional distress and CFS. 2019

    My apologies. I've had my say but I don't seem to be finished with some other thoughts on this subject. To quote: On the face of it this seems very reasonable. Avoiding the pernicious effects of coercive therapy treatment to assistance with living-well. Sounds good. There are three...
  9. Snowdrop

    News from Scandinavia

    You know there seems to be a window for some therapy here. I find it disturbing when there are people out there who get excited about the idea of punishing people whose crime is to be in extreme pain and then take steps to alleviate it. And they are often loud (and IMO irrational) voices for...
  10. Snowdrop

    Open letter to Dr Peter Fisher, Liverpool University, about a research survey on emotional distress and CFS. 2019

    My problem with regard to this type of research is: Quote from text: The type of therapy that is described (ie the other types that don't posit a model of illness) is only about changing our cognitions as a way of improving emotional well-being. In my opinion having been ill for decades now I...
  11. Snowdrop

    Psychiatric conference in Norway nov. 2019 themed "Stressology" (Wyller among lecturers)

    Is it? Because I don't think so. I presume by ethically he means the UK Health Research Authority (IIRC) but does anyone know what he means by legally?
  12. Snowdrop

    Developing and pretesting a new patient reported outcome measure for paediatric CFS/ME: cognitive interviews with children, 2019, Crawley et al

    One conclusion of this study from an outside POV is that it took this paediatric "ME expert" at least 15 years of research to decide that patients and their carers should have some input into subjective measuring of outcomes in their illness. With the caveat as we well know that even this...
  13. Snowdrop

    Open letter to Dr Peter Fisher, Liverpool University, about a research survey on emotional distress and CFS. 2019

    That is a beautiful letter @Trish . Thank you for your effort. Clear and on point. I confess when I see this type of 'research' I am given to wonder at times how it is that the person has convinced themselves, in the interest of helping, that this will be of any benefit. And so the...
  14. Snowdrop

    What are the experiences of people living with functional movement disorders(FMD)? An Interpretative Phenomenological Analysis study, 2019, Dosanjh

    I have no idea but I wonder if the creators of the new-fangled methods in delivering psychological therapies understand that they are drifting ever closer to rather oppressive forms of social engineering? Under the guise of helping. Always the irony with this lot.
  15. Snowdrop

    The ME Association's continued support of the Sussex ME Society

    With all the stories of this nature finding their way into media I wonder if there might be some value in pushing for a new timeline for ME. Although it can't be good to suggest exercise regardless due to not knowing who might benefit and the harm that befalls those for whom it doesn't I...
  16. Snowdrop

    The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread

    This is just my opinion but Jen Brea is a big girl. As a woman on social media with a huge presence and following she must know that her public musings will come under scrutiny. There is a line to be drawn between discussion and possibly criticism of those views and ad hominem attacks...
  17. Snowdrop

    The ‘cognitive behavioural model’ of chronic fatigue syndrome: Critique of a flawed model, 2019, Geraghty et al

    Just as a side-bar for @AllenJB since you are new here you might not be aware of the History of ME and how it has been subverted by influential people on behalf of powerful interests (namely insurance). If you are interested (and don't already know) you could have a look here as a starting...
  18. Snowdrop

    The ‘cognitive behavioural model’ of chronic fatigue syndrome: Critique of a flawed model, 2019, Geraghty et al

    It's a bit of a nit-picky point but as there is now some good discussion on the divide between the biological and P-S model I'd like to see more discussion around the social aspect of BPS. All three of these components have some validity for illness (just not in the ways twisted by it's...
  19. Snowdrop

    Long-awaited cystic fibrosis drug could turn deadly disease into a manageable condition

    Even philanthropy isn't philanthropy anymore. It used to be an act that had no financial reward. Now here it simply means high risk-high reward.
  20. Snowdrop

    Status of CFS/ME (2019) Brinth et al Danish Medical Journal (Ugeskriftet.dk)

    I'm beginning to form an opinion that this way of thinking shows something else. When things are working more or less properly at the top echelons of power then those people who can't think for themselves (even if they think they can) will follow a herd that is not heading off a cliff. But...
Back
Top