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    No Causal Effects Detected in COVID-19 and ME/CFS: A Two Sample Mendelian Randomization Study 2023 Xu et al

    Sounds to me like they're clueless and they elected to punt. Persistent muscle soreness? Interesting that they characterize Covid as an infection and not so ME/CFS. They do seem to reduce ME/CFS to pain with fatigue, so, you know, clueless. Give the ball to someone else.
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    Long-term high-dose immunoglobulin successfully treats LC patients with pulmonary, neurologic, and cardiologic symptoms, 2023, John S Thompson et al

    What are case reports if not a trial run for a clinical trial? Besides, I am a bit familiar with this sort of NIH group think. Three months is like code for long-term. If this were an abx treatment RCT, three months is a lock for whatever result they want.
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    (CDC) Diagnosis and Treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), 2023

    CDC really is more advertising agency than medical research entity, right? The NIH is the research arm, or at least what passes as research.
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    USA: NIH National Institutes of Health news - latest ME/CFS webinar 14 Jan 2025

    I think I will apply for their research roadmap working group. Hope my name doesn't throw up any red flags. It might. I've some history there. :)
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    Long-term high-dose immunoglobulin successfully treats LC patients with pulmonary, neurologic, and cardiologic symptoms, 2023, John S Thompson et al

    Six patients for three months. Six. For how long again? Three months? In what fantasy world is three months "long term"? I think of long term from the patients' perspective, which means years. I'm not sure three years qualifies as long term. Maybe. Thirty does; thirty would qualify. Three...
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    Endothelial dysfunction in ME/CFS patients, 2023, Sandvik, Mella, Fluge et al

    "However, we suspect that in ME/CFS the endothelial dysfunction is related to an abnormal immune response...." Why abnormal? Why not simply an immune response. There are several infections that can target endothelial cells, not the least of which is Covid...
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    No Causal Effects Detected in COVID-19 and ME/CFS: A Two Sample Mendelian Randomization Study 2023 Xu et al

    So, I have ME. I just got over Covid a week ago. Some of my symptoms right now are imo covid-related. They're different than my ME/CFS ones. In a month or two or six, could those symptoms qualify me as LC, and who in the world would make that call? I also qualify as chronic Lyme, but there...
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    Psychology Today: Learning About Long COVID From Other "Invisible" Illnesses

    Sometimes it's the system, or part of it, that renders the illness invisible. A 1983 paper on Lyme, for example, purportedly had that very affect by reducing subjective symptoms to "minor" status. The result was that if clinicians could resolve the handful of overt "major" symptoms, the disease...
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    No Causal Effects Detected in COVID-19 and ME/CFS: A Two Sample Mendelian Randomization Study 2023 Xu et al

    Can pwME get long covid? Anyone looking? I'd suspect Hanson or Levine, but don't really know if anyone has published anything. But I'd be curious to see that math.
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    USA: NIH National Institutes of Health news - latest ME/CFS webinar 14 Jan 2025

    Good to see they're not rushing into anything....
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    No Causal Effects Detected in COVID-19 and ME/CFS: A Two Sample Mendelian Randomization Study 2023 Xu et al

    Until we can demonstrate conclusively that there are absolutely no Covid remnants in any patient who presents with persistent symptoms, "causal" studies such as this cannot rise above definitional white noise.
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    No Causal Effects Detected in COVID-19 and ME/CFS: A Two Sample Mendelian Randomization Study 2023 Xu et al

    Oh good. Statistics and semantics conjoined in a single piece highlighting two confusing and contested diseases. What could go wrong?
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    Article: We Might Have Long Covid All Wrong (covers FND,ME/CFS,includes Sharpe,Garner, Carson and more).

    "There is zero credible evidence that she ever had Lyme Disease (by her own admission, she tested negative based on established, mainstream CDC criteria), let alone a chronic manifestation that was alleviated in any way by multiple rounds of long-term antibiotics, which have been decisively...
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    List of rare and uncommon diseases: differential and mis – diagnosis in ME/CFS

    I can appreciate this sentiment. But there may be rare or fringe cases that might not be considered as such if they are tested for - and found - more often. When my wife tested positive for her rare channelopathy gene she was only one of less than 100 in the entire world. Five years later and...
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    List of rare and uncommon diseases: differential and mis – diagnosis in ME/CFS

    Perhaps an alternative co-thread might be common diseases with inadequate diagnostics that could be misdiagnosed as ME/CFS. :)
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    List of rare and uncommon diseases: differential and mis – diagnosis in ME/CFS

    Babesiosis is considered rare. It can mimic ME/CFS. Ditto for B Miyamotoi, which is a relapsing fever and I believe is still considered rare. I second channelopathies.
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    Rubio Sends Letter to Pfizer CEO on Alleged Gain-of-Function Research

    But strains are a different species. When it comes to new strains, humans got a history with nudging nature.
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    Rubio Sends Letter to Pfizer CEO on Alleged Gain-of-Function Research

    Sometimes it is relevant. Sometimes accountability needs to matter. And the arrogance of it all can be terrifying.
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    Myalgic encephalomyelitis/chronic fatigue syndrome: an overview of current evidence 2023 Ludwig et al

    Give me a medical discipline and I will give you a discipline that has demonstrated a willingness to use psychology as a get-out-of-jail card. Cardiology. Pediatrics. Infectious disease. Rheumatology. I've personally experience it in three of the four. It seems to me, however, the most...
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    Myalgic encephalomyelitis/chronic fatigue syndrome: an overview of current evidence 2023 Ludwig et al

    Why qualify "muscle weakness" at all? Any qualifier here runs the risk of introducing a bias. It's like if I were to say "hillfolk-trained" neurologists, that qualifier may introduce a bias.
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