https://www.theatlantic.com/science/archive/2017/11/how-the-zombie-fungus-takes-over-ants-bodies-to-control-their-minds/545864/
(totally unrelated to ME/cfs, absolutely no parallels with the physical immobility & brain dysfunction of ME, nothing to see here ...)
the clinic is still connecting their (competently diagnosed) patients with researchers - i'm hoping that will continue in the short term.
maybe the proposed biobank might have a dual role - to hold biological specimens - and to hold contact details for 'competently diagnosed' patients who are...
coincidentally, for me, faecal testing, some specific antibiotics, then specific bowel flora, minimised my POTS for about 3-6 months. later, another round achieved the same result, which partly faded over time. bowel-cleanse fluids (for a gastroendoscopy?) gave a similar beneficial effect...
the existing "Australian (medical) Guidelines" mentioned are still based on the GET/CBT/hysteria model.
it will probably take some time and a lot of effort, for the NHMRC report to be finalised, for the existing medical guidelines (GET/CBT/hysteria model) to be updated with actual science, and...
another small anomaly in the "ME Australia" blog / recommendations
it seems that the blog is discussing the relevant scientific knowledge of the NHMRC committee members, while the linked citation is discussing diagnostic criteria for research & clinic.
is it possible that the citation is...
it's a proposal, not a done deal.
the date for the next federal elections hasn't been announced yet (will be soon) - and it would need support from other parties, in both houses, because Greens are a minority party.
there are other national issues that need to be addressed urgently, and any...
it's a wonderful policy. extra gold stars for ex-senator Scott Ludlam, who got the ball rolling many years ago.
three cheers for the collaborative efforts of many many australian advocacy groups & individuals, who contacted their local politicians, attended advocacy events, etc.
this draft report (Dec 2018) DOES NOT claim the recovery rate is 99%.
the section that mentions "99% recovery" in "post infectious fatigue" is a review of existing australian research (admittedly sparse, possibly includes Dubbo study) - AFAIK post infectious fatigue is not the same as ME/cfs...
is there a way to estimate the cost of publishing these articles, in these newspapers, as if they were an advertisement, rather than favour-for-mates propaganda ?
if we replace 'fatigue' with 'cough', 'itch', etc - this study remains equally meaningless,
because a common symptom can have a multitude of different biomedical causes.
do UK doctors still do differential diagnosis - or is that superceded by a BPS pamphlet,
and being sent home to think...
#1 The use of the Chalder Fatigue Scale suggests they're studying general fatigue, not ME/CFS. (https://me-pedia.org/wiki/Chalder_fatigue_scale)
Mainland China prefers FS-14 items. UK prefers FS-11 items (excludes items 5, 10 & 14). (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730538/)...
Oxford criteria is NOT similar to CCC/ICC. :banghead:
Could be multiple pathogens, could be novel pathogens, could be lack of ability to detect the pathogens, etc. Our current knowledge of human pathogens, is only a fraction of the truth. (recent example -...
another confounding factor would be inter-generational poverty
low income families -> financial stressors, less able to afford safe clean housing, warm clothes, healthy food, medical care, child care, transport, education.
longer work hours, less recreation, lesser satisfaction in their work...
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