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  1. Simon M

    Post-exertional symptoms distinguish myalgic encephalomyelitis/chronic fatigue syndrome subjects from healthy controls, 2020, Mateo et al

    Has this been published yet? It would be good to have more detail. E.g. anything over 3 months to recovery I woulc call a relapse. But I am pleased they are finally reporting data. I'd also be interested to see the severity of people who volunteer for CPETs - how representative are they of PwME?
  2. Simon M

    Post-exertional symptoms distinguish myalgic encephalomyelitis/chronic fatigue syndrome subjects from healthy controls, 2020, Mateo et al

    Despite being in the field for at leat a decade, CPET researchers are still failing to collect and publish harms data. That is as unacceptable for biomedical research as it is for psychosocial research.
  3. Simon M

    Differences in Symptoms among Black and White Patients with ME/CFS 2022, Jason and Torres

    I think this is the first specific study looking at ethnic differences, which is is a very important area. but I'm not sure how much we can conclude from these results. It's a very small study, and we don't know if patients of different ethnicities are equally representative of their ethnic groups.
  4. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    The Jason 1999 community prevalence study was based on just 32 CFS cases: 0.42% prevalence with an overall 95% confidence range of 0.29%-0.56%. The confidence intervals for male and female prevalence separately will be even wider than this so that the sex ratio can tell us nothing reliable. I...
  5. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    [Re my comment about GWAS and the 'role' of IL-10 in rheumatoid arthritis and other autoimmune diseases] Oh dear, I can clearly no longer rely on my memory to accurately recall stuff like this! Thanks for pointing out my error. I should have referrd more broadly to the iL-23 pathway, where...
  6. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    those are all good points. I'm not at all wedded to Norway or any particular country. The big advantage Norway does have is a well respected health and health data collection system. This would make it faster and cheaper to set up any study, but the most important thing is to get reliable data...
  7. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    I agree that the priority is finding core mechanisms and I understand the scepticism over genetic studies But people have been following hypotheses for mechanisms for decades and we've got nowhere. Genetic studies are different because any DNA differences are causal, so provide better clues...
  8. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    2. Getting serious about epidemiology We need to kneel down the epidemiological findings to date on prevalence and incidence (onset). Personally, I think Norway might be the ideal place for this because of its comprehensive health system and quality of health reporting (many cohorts, e.g...
  9. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    Here are my two suggestions. 1. Prospective study: infectious mononucleosis (and Covid?) As suggested above. Think of this as Dubbo 2, recruiting people at the point of diagnosis with glandular fever/infectious mononucleosis. Then follow-up detailed follow-up for two years, checking people's...
  10. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    As for any other rare variant whole genome/exome study, the aim is to find mutations with a big effect, usually affecting the protein normally made by the gene. That then provides a massive clue as to the underlying biology: 1. It could point to the biology in rare cases, tiny sub-groups of ME...
  11. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    Agreed. Can you say how that would work? I've been tracking this in studies for decades and have never seen good evidence for anything much below 80%. Could you explain more? I think the Bakkens study had over 5,800 cases, taken from a retrospective analysis of the entire Norwegian health...
  12. Simon M

    Suppose you have €5-10 million for ME/CFS research, what would you spend it on?

    DecodeME is banking half of every DNA sample so that a future whole genome sequencing study can be done that will pick up these rare mutations. And I agree, spending some of the hypothetical buddies on this would be a smart move. I agree and include prospective studies of glandular fever etc in...
  13. Simon M

    Poem based on Anthony Komaroff ME/CFS article is a finalist in US poetry contest

    No, really: @Veronica Ashenhurst is a poet with severe ME. Her poem “Redefining Her” was chosen as a finalist in Health Affairs’ poetry contest. It’s a “found poem,” meaning that text from another source is used to create poetic meaning. Specifically, in writing the poem, Veronica restricted...
  14. Simon M

    Single-cell transcriptomics of the immune system in ME/CFS at baseline and following symptom provocation, 2022, Ahmed, Hanson et al.

    Thanks :) To be fair to the authors, they used an omics approach as a broad sweep (given how little we know), as a way of identifying areas to worth pursuing. The discussion section says: "our analysis discovered upregulation of chemokine/cytokine pathway genes in patientderived monocytes as...
  15. Simon M

    Single-cell transcriptomics of the immune system in ME/CFS at baseline and following symptom provocation, 2022, Ahmed, Hanson et al.

    3. Platelets: slightly off at baseline, normal after exercise Platelets are plate-shaped cells whose primary role is to plug blood vessels that are punctured to promote clot formation. The authors looked at the impact of exercise on the expression of individual genes (their main method), and...
  16. Simon M

    Single-cell transcriptomics of the immune system in ME/CFS at baseline and following symptom provocation, 2022, Ahmed, Hanson et al.

    2. The big story: gene expression indicates "primed" monocytes in ME Monocytes are large immune cells, and their role is to migrate to where they are needed and become macrophages. Macrophages engulf and neutralise invading pathogens like bacteria, viruses and even yeast. They can also Hoover...
  17. Simon M

    Single-cell transcriptomics of the immune system in ME/CFS at baseline and following symptom provocation, 2022, Ahmed, Hanson et al.

    Comments 1. Overview This is a small sample of only 30 patients (I'm pretty sure they took blood samples from 90 people with ME). Two findings stand out: for monocytes and platelets At baseline, they found big differences between patients and controls for monocytes. (They found smaller...
  18. Simon M

    Office of National Statistics: Prevalence of ongoing symptoms following coronavirus (COVID-19) infection in the UK: Updates

    So, we are now up to 333,000 people reporting their daily activities have been “limited a lot“. It wasn’t so long ago this was around 230,000. Approximately 600,000 people have had long Covid for between one and two years, and half a million have had it for two years or more. What would be...
  19. Simon M

    Published poems by Veronica Ashenhurst, who has Severe ME

    Welcome to the firm, Veronica, it’s great to have you here. Congratulations on making the “best of the Net“.
  20. Simon M

    Published poems by Veronica Ashenhurst, who has Severe ME

    I had assumed that amber was a reference to the colour of a country on fire.
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