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    Prevalence of Aspergillus-Derived Mycotoxins (Ochratoxin, Aflatoxin, and Gliotoxin) and Their Distribution in the Urinalysis of ME/CFS, 2022, Yu Wu

    It doesn't show whether it's a cause or an effect. ME-affected bodies are abnormal, so there's no reason why it can't result in less ability to remove various toxins.
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    Coining a term for being limited in your interrelated energy and time.

    I think you're on the wrong pathway. I never experienced that sort of 'energy limitation'. My physically-induced PEM was triggered by what I believe was muscle microtears (caused by using muscles in ways other than usual daily activities), not by general exertion*time. My cognitively-induced...
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    Cognition, emotion, and the central autonomic network, 2022, Quadt et al

    The abstract certainly doesn't entice me into reading the full article. It sounds like they didn't find anything new, so they put their efforts into making it look impressive, or at least to intimidate readers into not asking questions.
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    The Pathobiology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: The Case for Neuroglial Failure, 2022, Renz-Polster et al

    https://osf.io/ef3n4/ The newsbrief posting reminded me that this paper wasn't mentioned. I think it may be a pretty important hypothesis for ME's root cause. It fits what I believe is the root cause of ME: that neuroglia are involved. I'm not sure whether there are any ME symptoms that...
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    What ME/CFS research, funded by UK sources, is currently in process (as of end Jan 2022)?

    All those projects, and I only like the one studying brain inflammation.
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    Big improvement after period of dry weather?

    I haven't noticed any changes in my ME due to weather. I have a Type I allergy to something in the air in winter around evergreen trees when certain conditions are met involving temperature and humidity (and probably other factors). My guess is that something is releasing spores. Your...
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    Association between vaccination status and reported incidence of post-acute COVID-19 symptoms in Israel

    How does one factor in the fact that people who get 2 doses have different mindsets than those who get one dose, who have different mindsets than those who haven't gotten vaccinated? Strong belief in the protection of 2 doses is likely to make those people underreport any symptoms.
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    Article : What’s the Difference Between Chronic Fatigue Syndrome and Fibromyalgia?

    I had, and still occasionally have, what seems to be neuropathic pains due to my ME. I consider that a symptom of ME that some but not all PWME have. I certainly don't believe that neuropathic pain is the cause of ME. Besides, I don't think they understand central sensitization either, so...
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    Complaints from patients with [FND]s: a cross-sectional UK survey of why patients complain and the effect on the clinicians..., 2018, Bolton

    Doctors don't know how to treat FNDs, so these patients are less satisfied with healthcare services than patients with treatable disorders. Makes sense to me. Doctors who are unable to satisfy patients are less satisfied than doctors who are able to satisfy patients. Is anyone else noticing a...
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    Poll: Does taking supplements to 'support' mitochondria at a particular time of day improve your sleep?

    Your poll should have allowed multiple selections for 'didn't improve' or just had one selection for 'didn't improve regardless of when taken'. None of the supplements listed affected my sleep. What has had a positive effect is CLAs (conjugated linoleic acids). Without them, I generally wake...
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    Medscape: Fast Five Quiz: Chronic Fatigue Syndrome (Myalgic Encephalomyelitis)

    Well, I scored zero. :facepalm: It's all guessing what the 'experts' guess is correct, since they don't actually know for sure.
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    No signs of neuroinflammation in women with [CFS] or Q fever fatigue syndrome using the TSPO ligand [11C]-PK11195, 2021, Raijmakers, Knoop et al

    It may not be as simple as standard neuroinflammation, but I'm still convinced that it's part of my ME. My ME symptoms always increased with infections or exertions that would produce IFN-g, which would in turn activate glial cells. So far there's no definitive study (large, proper controls...
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    ME/CFS progression in years and stages

    21 years, constantly mild with varying degrees of feeling a bit better or worse. I've had quite a few symptoms and sensitivities occur and change or disappear. I managed to cure my PEM, persistent neuropathic muscle aches, and another problem that required treating with T2, and an intolerance...
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    Male vs. Female Differences in Responding to Oxygen–Ozone Autohemotherapy (O2-O3-AHT) in Patients with ME/CFS, 2021, Chirumbolo et al

    Did they compare this to any other pain reduction techniques? Maybe females are simply more likely to check 'improved' rather than 'no change' on these sorts of questionnaires.
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    Article: How to Tell if Sitting in Front of a Computer All Day Is Making You Fatigued

    Aside from the psycho-nonsense issue, different brain activities have different effects on overall feeling. Playing a strategy game past 2:30 PM gives me insomnia that night, but playing a first-person shooter game (mindless shooting of zombies) doesn't. Maybe some neurons deplete something or...
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    Can Understanding Gut-Brain Axis Biopsychosocial Pathways Improve Clinical Reasoning?, 2021, Ford et al

    The amazing thing: there's probably someone out there who is actually proud of creating this nonsense. :rolleyes: Oh, and if it doesn't result in a major accolade for transforming patient care, it will of course be the fault of the nurses for not implementing it properly, or the patients for...
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    What differentiates ME/CFS from known primary mitochondrial diseases; could mitochondrial disease cause PEM?

    It could be, but it could also be just a malfunction that evolution hasn't weeded out yet. If your computer stops working because a single transistor ot trace failed, it isn't because it's trying to protect itself from further damage.
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