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  1. Aimossy

    Typing myalgic encephalomyelitis by infection at onset: A DecodeME study, 2023, Bretherick et al

    One of the things that surprised me was the percentage that said they had IBS being as low as it was. I was personally actually ok about that separations at this time @Trish because more in-depth work on the cohort can happen with questionnaires. They can look further into the things your...
  2. Aimossy

    Typing myalgic encephalomyelitis by infection at onset: A DecodeME study, 2023, Bretherick et al

    Woah. I have waited so long to see work like this and it's starting. I actually cried I was so relieved to see this pre-print paper and genuinely surprised by some of the findings. Well written and important. The beginnings of fundamental work that is so badly needed. Thank you DecodeME team...
  3. Aimossy

    (2022) "Weʼre raising £16,000 to Continue Dr Geraghty's Vital ME/CFS Research"

    I won't donate because it is very unclear what he is researching specifically therefore I have no idea what impact if any it would have. If he wants to advocate as he has been thats great but I am not funding single person paid advocates.
  4. Aimossy

    Predictors for Developing Severe Myalgic Encephalomyelitis/Chronic Fatigue Syndrome following Infectious Mononucleosis, 2022, Jason et al

    I agree with this and think all ME/CFS needs a proper standardised measurement for severity that includes symptoms and disruption of activities of daily living.
  5. Aimossy

    Preprint Medrix: Dynamic Epigenetic Changes during a Relapse and Recovery Cycle in ME/CFS - Helliwell, Tate et al -2022

    I am pretty sure he was inspired by another scientist that did a very long expensive study on himself in the States. With limited funding this was a very smart study in my opinion. I hope he does another one with Male subjects due to sex differences. It is good to see in-depth longitudinal work.
  6. Aimossy

    My opinion on the topic “angry posts by patients on social media are harmful and something should be done about it”

    I agree with @Andy on everything including the above but I would like to add that as @TiredSam says twitter is a cesspool and a place for many to vent at times. I have vented on there myself to be honest. Not sure if at times it has been constructive when I have. I am sure that Andy did not mean...
  7. Aimossy

    Applicants needed for Columbia ME/CFS Research Center Community Advisory Committee

    The Microbe Discovery Project FB just posted this: "CII need more applications for their ME/CFS Community Advisory Committee. Experience in epidemiology is a particularly important area of need. Please share widely and reach out to folks you know that have this experience. Open to people...
  8. Aimossy

    New biomedical PhD funding, T cell receptors (Chris Ponting)

    This is great news @Simon M A big thankyou to you and especially Chris! I think this could be be game changer in the UK. Prof Ponting is quite specialised in this area of work isn’t he?
  9. Aimossy

    S4ME Q&A with Prof Chris Ponting - Question Collection Thread

    Is it possible the CMRC can form a collaborative research hub or center a bit like the ones just funded by the NIH?
  10. Aimossy

    S4ME Q&A with Prof Chris Ponting - Question Collection Thread

    Is it possible to make the CMRC produce a larger conference in the UK through gaining funding considering they have no funds? With the idea of helping to build more interest and a stronger base.
  11. Aimossy

    S4ME Q&A with Prof Chris Ponting - Question Collection Thread

    What does the CMRC need to do to create a stronger biomedical base and bring in more researchers who are specialists in their own fields?
  12. Aimossy

    S4ME Q&A with Prof Chris Ponting - Question Collection Thread

    What is Chris's vison for the CMRC going forward and how can this be acheived?
  13. Aimossy

    What is Action for ME's current (March 2018) position on the PACE trial?

    Was nice to see the quotes from Chris Ponting too and other helpful links.
  14. Aimossy

    What is Action for ME's current (March 2018) position on the PACE trial?

    Thanks for this. Some more simplified clarity around PACE version CBT and GET which is very different from standard CBT and appropriate GET for ME which is more like pacing, could help confusion as it's also quite a long read. David Tuller had explained this more simply and well many times. His...
  15. Aimossy

    Australia - Mason Foundation to investigate viability of ME/CFS Biobank - update - funding awarded for biobank

    Maybe NCNED? The only researchers in Aus flushed with cash... Would seem a bit unfair for other biomed researchers keen to get funding for work who can already access cohorts. It is possible to access the UK biobank already anyway I think. Its set up and well characterised and NIH supported.
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