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    Blog - Hypothesis: ME/CFS as a Breakdown in Homeostasis, 2021, Marks

    I agree with arewenearlythereyet: this 'Nobel-candidate' hypothesis seems to boil down to: "something in the body is malfunctioning!". Unless there's an effective "repair homeostasis" treatment, it's not a useful hypothesis.
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    The faecal metabolome in COVID-19 patients is altered and associated with clinical features and gut microbes, Lv et al, 2021

    Someone should do some studies of microbiomes of patients with broken bones, gunshot wounds, or other such trauma. Will they find changes in the microbiome? I expect they will. Eventually, they can come up with some methods for determining when microbiome changes are actually caused by a...
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    Effect of neuromuscular electrical stimulation on the recovery of people with COVID-19 admitted to the ICU: A narrative review, Burgess et al, 2021

    I think that (testing whether PEM can be triggered by electrical muscle stimulation) would be worthwhile. There are other possibilities, such as the cognitive effort to get those muscles moving being responsible for triggering PEM. I'm pretty convinced that muscle damage, and the consequent...
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    New Garmin “High Intensity Exercise” monitoring and what it showed my body is doing

    I think that just indicates that the device isn't measuring what you think it's measuring. Extreme physical exertion probably raised heart rate and resistance to blood flow. I suppose it's possible to have a fast heart rate and low resistance to flow, which would be the same 'power level' as a...
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    Open Analysis of Post-exertional Malaise Using a Two-day CPET in People With ME/CFS, 2021, Ithaca College

    Not every PWME gets PEM from physical exertion either, or even gets it to the same degree from the same exertion. I could hike or bike for hours without triggering PEM, yet climbing a ladder once would trigger it. I expect that a lot (most?) of us have both triggers to some degree (although I...
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    Open Analysis of Post-exertional Malaise Using a Two-day CPET in People With ME/CFS, 2021, Ithaca College

    This study came up on PR, and my comment was that researchers should look into using cognitive triggers for PEM. Maybe socializing for 10 minutes will produce the same level of PEM, but with less harm to the patient. It would also avoid extraneous factors resulting from the physical exertion...
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    Dysregulated Provision of Oxidisable Substrates to the Mitochondria in ME/CFS Lymphoblasts, 2021, Missailidis et al

    It wasn't easy. I knew that something in high-protein foods was making my symptoms worse. Peanut and soy butter had the same effect, so it wasn't meat-only. Then I remembered that I had some gelatin in my cupboard. That was the worst trigger yet, and it's essentially amino acids, and three...
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    Dysregulated Provision of Oxidisable Substrates to the Mitochondria in ME/CFS Lymphoblasts, 2021, Missailidis et al

    I was suspicious of Complex V long before I knew about ME. I thought I had some problem with kynurenine production, which involved superoxide and Complex V. There were some other factors, now forgotten, that kept me suspicious. Now I've become sensitive to proline, which reduces activity of...
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    Open Cardiovascular Analysis of PEM, 2021, Natelson

    That doesn't help with understanding the impact of cognitive exertion. :thumbsdown: Experiments with cognitive exertion could lead to less-harmful methods of triggering PEM for research projects. That's assuming that cognitive-induced PEM actually is less harmful, which we don't know for...
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    Open Cardiovascular Analysis of PEM, 2021, Natelson

    They could also induce PEM via cerebral exertion. Does anyone know whether socializing or other cerebral exertions are as likely to cause crashes as 'maximal exercise tests' are? I was going to suggest this to the researchers, but I couldn't find a way to contact them.
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    Reality of ME. How would you get this across (briefly) using words or graphics?

    I think of it as being in prison for something I didn't do, with no idea when, if ever, I'll be released. I certainly don't have the freedom to do what I would like to do.
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    Exploratory study into the relationship between the symptoms of CFS/ME and fibromyalgia using a quasiexperimental design, 2021, McKay et al

    I think "quasiexperimental" means "We'll start with the results we want and make up the experiment to provide them." :rolleyes:
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    What if they find a biomarker?

    Researchers should put out a call for anyone who is able to trigger temporary remissions reliably, even if it's only for a few times. Get the patient in a lab, do extensive testing, trigger the remission, then redo the tests and see what's changed (and redo again when switched back out of...
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    What if they find a biomarker?

    I feel that an even stronger argument for ME being reversible is temporary remission. I had several, more frequently at the start, with the last one maybe in year 5 or so, with none in the last 14 or so years, alas. :( These were an abrupt switch from full ME to apparently fully healthy...
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    Dental implants

    I have one (molar), gotten several years into my ME. I didn't have any problems healing quickly, or any other problems with it. My ME doesn't keep me inactive or horizontal though.
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    PEM: Swimming compared to other activities?

    I didn't notice and difference in PEM between +30C and -40C. Swimming in my creek in winter would require considerably more effort. That water is hard! :D
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    Exercise modifies glutamate and other metabolic biomarkers in cerebrospinal fluid from Gulf War Illness and [ME/CFS], Baranuik et al, 2021

    I didn't notice any difference during PEM. For me it was just 'fatty meal without carnitine = worse symptoms. With carnitine = no extra symptom severity'. I didn't need 3000 mg either; I think I took half a level tsp or so.
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