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

    If abnormalities found in ME/CFS are found in clearly defined (post-)Covid-19 patients, that could be convincing for some people in the medical and scientific communities.
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    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    FWIW: https://blogs.bmj.com/bmj/2020/05/19/paul-garner-covid-19-and-fatigue-a-game-of-snakes-and-ladders/
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    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    And his views developing over time in public could even have an extra benefit.
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    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    Well I'm sorry if I misrepresented what you believe/said. I highlighted the bit I was referring to and believed that's what you were saying. --- Here are the paragraphs in question: Anyway, it doesn't look like my and other people's public challenging of him has had any negative effects...
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    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    You are entitled to your opinion but I don't know how you or others can be sure it isn't a postviral fatigue syndrome with a similar mechanism to ME/CFS/PVFS. As many others with ME/CFS have said, their symptoms at the start continued. There are 60+ day COVID groups. Dr Garner said the most...
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    #mylastnormalphoto with an ME spin

    Here's mine: Edited to add: A more long-winded version of this on Facebook:
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    #mylastnormalphoto with an ME spin

    Anil van der Zee started this: People could also do it on other social media platforms such as Facebook and Instagram. People can also make posts here if they wanted. Lots and lots of people have responded under Anil's post
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    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    It would definitely give useful data. However, if it wasn't part of her initial plans, it might add a lot to the costs. Anyway, I don't think I will get involved in passing on specific suggestions to her, at least at this stage. I think you are on Twitter, so you could always reply to her under...
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    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    Another way of looking at this is that warning people that they could be left with long term problems like ME and that they need to consider that pushing themselves or others could make things worse for the individual is not necessarily unethical. I think if an infectious disease doctor makes...
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    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    https://twitter.com/JTSglobalhealth/status/1262051298335174657
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    A general thread on the PACE trial!

    Australian ME/CFS advocacy award honours Alem Matthees https://may12th.org.au/australian-me-cfs-advocacy-award-honours-alem-matthees/
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    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    I have already tagged a number of entities and individuals on Twitter.
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    CDC create new page on how people with ME/CFS can be supported for May 12 and link to it in their weekly e-bulletin

    https://www.cdc.gov/Features/cfsawarenessday/index.html?deliveryName=USCDC_201-DM28478
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