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  1. Kalliope

    Podcast: Episode 37: Finding Answers for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

    This was very good. My impression it that this is the first time the journalist is covering ME, and he's really done his homework! ETA: Thank you for warning about the loud music in the start!
  2. Kalliope

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    Thank you! That helped me find this summary of a talk by dr. Harsha Master from the Royal College of General Practitioners annual conference 2021 with more details of how they work: https://www.rosecottagedoc.co.uk/post/red-flags-in-long-covid
  3. Kalliope

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    She explains a bit more at 30 minutes into the podcast. I was not able to work out the name she uses for this model, perhaps someone else can. Developed by a dr. Master?
  4. Kalliope

    Blog: The Science Bit by Brian Hughes

    The Science Bit "The problem may well be that some of our treatments are too evidence based" quote: Colleagues on the Science For ME forum drew my attention to this little gem of a passage — removed from the internet just last month, but preserved for posterity by the Wayback Machine — which...
  5. Kalliope

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    Dr. Amy Small was interviewed in the last episode of the podcast Talking General Practice. The interview begins at 11.45 minutes into the podcast. She talks about her infection with Covid-19 and developing Long Covid. Then of how she improved with dietary changes (like cutting out sugar)...
  6. Kalliope

    Lightning Process - discussion thread

    Another article from Nina E. Steinkopf who tells the story of a parent of a child who underwent LP. The article was first published in July 2021, but has now been translated into English. Treating children with the Lightning Process quote: It was a scary experience for me as a parent. How bad...
  7. Kalliope

    UK NICE 2021 ME/CFS Guideline, published 29th October - post-publication discussion

    Fantastic opinion piece in the Norwegian newspaper Aftenposten by the professors Ola Didrik Saugstad and Rolf Rønning. They start with sharing the news about the NICE guideline, and then provide some history (as Wessely, the psychosomatic approach), present research into ME, how ME patients...
  8. Kalliope

    Lightning Process - discussion thread

    good question. This is a google translation of the argumentation from the LP association from Nina E. Steinkopf's article: The decision was based on the LP association's view on the matter: “LP must be regarded as a teaching activity where stress-regulating and performance-enhancing knowledge...
  9. Kalliope

    Lightning Process - discussion thread

    Nina E. Steinkopf with interesting news from Norway. The Norwegian Directorate of Health and the Consumer Ombudsman defined LP coaches as practitioners of alternative treatment in 2018. This year, LP coaches asked the Norwegian Directorate of Health to review that definition. The Directorate...
  10. Kalliope

    UK NICE 2021 ME/CFS Guideline, published 29th October - post-publication discussion

    From twitter. Sharpe criticises Kunst for getting a thread about lack of evidence behind GET/CBT wrong:
  11. Kalliope

    Prevalence of fibromyalgia 10 years after infection with Giardia lamblia: a controlled prospective cohort study, 2021, Hunskar et al

    Here's an article from 2004 where it states that 100 people still felt fatigued after having contracted the Giardia parasite in the outbreak in Bergen in 2004. Over 20 of them got diagnosed with ME according to same article and the researchers wanted to study ME as part of this. google...
  12. Kalliope

    Prevalence of fibromyalgia 10 years after infection with Giardia lamblia: a controlled prospective cohort study, 2021, Hunskar et al

    Until the pandemic, this outbreak of Giardia in Bergen, Norway, was said to be the first time researchers knew for sure what had initiated ME, which made this particular patient group very interesting to study. Now it seems the researchers have moved away from "ME" to FM and "chronic fatigue"...
  13. Kalliope

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    This refers to the NICE guidelines, but as dr. Asad Khan brings in the aspect of Long Covid in his tweets, I figured this was the best thread. Interesting, but not surprising, what he's saying about silent colleagues who have worried about linking ME to Long Covid and the reason why. I hope he's...
  14. Kalliope

    UK NICE 2021 ME/CFS Guideline, published 29th October - post-publication discussion

    This refers to the NICE guidelines, but as dr. Asad Khan brings in the aspect of Long Covid in his tweets, I figured this was the best thread. Interesting, but not surprising, what he's saying about silent colleagues who have worried about linking ME to Long Covid and the reason why. I hope he's...
  15. Kalliope

    UK NICE 2021 ME/CFS Guideline, published 29th October - post-publication discussion

    only vaguely. it will be interesting to see if they'll adjust anything. I'm not holding my breath. When it comes to @Jonathan Edwards 's question, there are two articles so far in Denmark about the NICE guideline. Haven't seen anything yet from Sweden or Denmark. One of the Danish articles is...
  16. Kalliope

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    The New York Times Another Struggle for Long Covid Patients: Disability Benefits I have a temporary subscription to NYT so the article is open for me, but I don't know whether it is for everyone. If it's not, and you want to read it, just send me a PM and I'll copy/paste it to you. Quote: Long...
  17. Kalliope

    News from Scandinavia

    I am so sorry to read what St. Olavs hospital put you through, @rainy :broken_heart: I completely understand why you don't trust them to be able to make a proper plan of care for ME patients. I'm worried as well about this. Once again there's been a rather positive initiative from politicians...
  18. Kalliope

    News from Scandinavia

    I assume that is the standardised plan of care which has been promised for several years to be developed for ME patients. But they've expanded it to be a plan for fatigue-conditions in general, so I fear it will end up with a biopsychosocial approach and be more suited for other conditions than ME.
  19. Kalliope

    USA: Mount Sinai PACS clinic and Dr David Putrino

    Moved post That was a really nice podcast. Very interesting to hear about dr. Putrino's work. Here's a transcription of what is said between 26-33 minutes into the podcast (hope I got most of it right): Amy Proal Overall, I can understand how when a clinician first sees a patient like this...
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