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    Recovery from Myalgic Encephalomyelitis/Chronic Fatigue syndrome developed after [SARS-CoV-2] vaccination: A case report, 2025, Kurotori et al

    Not all truths of medicine are scientifically proven so a useful therapy may not yet be deemed science based but it may be real in effect and have a sound but unknown mechanism. What was her condition? If inflammatory, many would say then not ME anyway, if sth to do with serotonin, possibly...
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    Future healthcare for ...the common pain disorder ‘fibromyalgia...’ – fundamental changes based on the discovery of an immune cause, 2025, Goebel

    But any phrase will do in that world and it is the "Royal College of Psychological Medicine" and to be fair to the FNDer they are looking at brain waves nowadays. When I say medical I mean psychological, functional, biomedical, when some say medical they exclude psychological and FND, when...
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    Future healthcare for ...the common pain disorder ‘fibromyalgia...’ – fundamental changes based on the discovery of an immune cause, 2025, Goebel

    Very interesting. Meanwhile sarcoidosis patients with an established and recognised immune condition accompanied very often by fatigue and pain are getting FM diagnoses on the "symptom list" basis. Infact it may not be a bad diagnosis as the immune disruptions may be similar to those found in FM...
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    Future healthcare for ...the common pain disorder ‘fibromyalgia...’ – fundamental changes based on the discovery of an immune cause, 2025, Goebel

    I take your point but psychology is not ipso facto not medical, as BPS/Wezza etc repeatedly (and correctly) assert@ nor are functional disorders non medical. So a functional and/or psychological diagnosis is still a medical diagnosis and could easily therefore be an overdiagnosis or a wrong...
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    May I ask your view (if any) on this? https://aonm.org/mitochondrial-testing/ aonm is associated with at least one person who is not favoured by many on here, but the tests as far as i recall overlap with those Julia Newton used in Newcastle (UK) to investigate mit function in pwME (diagnosis)...
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    Interrogating pulmonary diffusing capacity in long COVID: insights from DLCO and DLNO testing, 2025, Parks et al.

    Yes there are a fair few sarcoid doctors who consider decline to be important in causing symptoms .
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    Interrogating pulmonary diffusing capacity in long COVID: insights from DLCO and DLNO testing, 2025, Parks et al.

    Sorry if this question is slightly off topic. Can anyone tell me how "normal %" is arrived at in PFT's? Is it that ca 100% of the general population with say 80% expected TLCO etc are asymptomatic or is it that 80% of healthy controls are asymptomatic or is it that 80% of the pateint population...
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    Recovery from Myalgic Encephalomyelitis/Chronic Fatigue syndrome developed after [SARS-CoV-2] vaccination: A case report, 2025, Kurotori et al

    promoted sth like that , enhanced, sped up. provided optimal conditions, removed obstacle to recovery. I think you will get the picture. The Japanese herbal is anti inflammatory and promotes mito function, the -one drug affects serotonin . Tilled the land abit to help recovery "grow" There are...
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    Recovery from Myalgic Encephalomyelitis/Chronic Fatigue syndrome developed after [SARS-CoV-2] vaccination: A case report, 2025, Kurotori et al

    Don't you think remission can be encouraged through appropriate support and treatment? That is commonplace in medicine and does not relegate a given condition to a biophysical nonentity, just one can get better more easily if the conditions are optimal. She was given both herbal and pharma...
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    United Kingdom: Sussex & Kent ME/CFS Society News

    Miller, as I read him , considers long coviders in the absence of evident organic damage to have ME ( without, as far as I can discern, considering the possibility of damage not yet evidenced ). It's just a symptoms game and matters such as 2 day CPET worsening found in some with ME but not so...
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    Recovery from chronic fatigue syndrome: a reflexive thematic analysis of experiences of people before, during and after treatment, 2025, Chalder+

    Reminds me of the doc that was on Scottish TV about ME some years ago, where they had one or two Mickell patients , one of whom at least had clearly not recovered and was cogitating on redefining his concept of health. There are one or two similar cases on the Recovery website which Garner...
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    Peripheral Levels of Selected Biomarkers in Patients with Post-Sarcoidosis Chronic Fatigue Syndrome, 2025, Małujło-Balcerska et al

    Quite a few sarcoid sufferers are being given a CFS diagnosis but as if it were an alternative cause for fatigue , which is questionable, or on the other hand as if it were merely a list of symptoms and if you have then you can pile in, with aetiologies counting for little of anything. It's...
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    Peripheral Levels of Selected Biomarkers in Patients with Post-Sarcoidosis Chronic Fatigue Syndrome, 2025, Małujło-Balcerska et al

    Markers of immune disturbance have been found up to 27 yrs before sarc diagnosis in a Swedish study. Numerous sarkies will say they ahve felt unwell for years and it makes me wonder if this is rooted in pre sarc phenomena.
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    Peripheral Levels of Selected Biomarkers in Patients with Post-Sarcoidosis Chronic Fatigue Syndrome, 2025, Małujło-Balcerska et al

    May have been me. CS or another ME Assoc Rep has met up with some sarkies and was impressed by the degree of similarity between PEM as reported in ME/CFS and post exertional fatigue reported by current sarkies. Post sarc fatigue is certainly debilitating and may be accompanied by myalgias so it...
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    Who is Simon Wessely?

    Did they in their world of non dualism give any regard to the fact that aluminium poisoning itself might increase propensity to anxiety whether as part of specific mechanisms or by inducing stress of general dysfunction and the experience thereof. https://thescipub.com/abstract/amjnsp.2011.65.69
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    Specific Antibody Deficiency

    I have not dome the vaccine provocation test, only baseline. Some UK immunology depts would only diagnose after provocation In my case the question arises of vacine provoked sarcoidosis and/or hemophagocytosis so I ahve to be cautious.
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    Is the key pathology of ME/CFS in bone marrow?

    Would hemophagocytosis be of any relevance to this?
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    Is ME/CFS something to do with Butyrate?

    I thought clonazepam is in NM disorder rather than diazapam for effect on GABA in muscles.
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    A look at my whole genome sequencing results

    I looked through my raw data on 23nMe and could not find any ClinVar reported polymorphism relating to the list from Decode. I am a monozyg for HLA DRB1 1501 which is a hit for chronic, esp pesticide and organic dust induced sarcoid and for fatigue states but found nothing else. I have a shed...
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    Guardian piece on"Lyme"

    "Persistent physical symptoms arise when biological defence systems, evolved to keep us safe, go awry. If we all shout "not always, why not?" and "not in every case displaying such symptoms" they will come out with "we didn't say always..." "Approaches that work for many are based on...
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