Merged thread Long COVID highlights why we need to overhaul the term ‘psychosomatic’ This is a rather embarrassing article (for the authors) in...
This is an article about the lack of recognition and support for people with LC in Australia. There's no mention of ME/CFS although 'chronic...
ME Advocacy Network Australia have launched a campaign to get Australia's harmful ME/CFS clinical guidelines updated. There's a handy graphic to...
As I've said elsewhere on the forum, my ferritin has also been very high since I came down with ME/CFS. After tests for haemochromatosis and fatty...
Disgraceful.
Moved post An article about the recent Griffith MRI study.
Some good publicity: [MEDIA]
I'm sure sufferers of the relapsing-remitting form of MS will be very pleased to hear that they can overcome their illness with a quick phone call...
The transcript for the recent Canberra public hearing for the Inquiry has been released. ME/CFS patient advocates Michelle O'Brien and Penelope...
This sort of pseudoscientific nonsense is so prevalent, the American Cancer Society has a very unequivocal statement on their website:
I suppose this article is a step in the right direction, however it completely glosses over the fact that there are virtually no specialists for...
According to the RACGP, it is based on "NHMRC Level 1 evidence" which would be Cochrane's flawed exercise review.
An interesting statistic (see figure also): [ATTACH] These figures relate just to private health insurance (which most Australians do not...
In one of the Australian ME/CFS groups, I'm noticing an increasing number of people who have been given an FND diagnosis. Almost all have an...
Which demonstrates to me that everyone involved in this study does not know anything about PEM.
The announcement of this study caused a firestorm on Twitter and continues to do so: [MEDIA] With the exception of a "clever" acronym, nothing...
[MEDIA] [MEDIA]
Separate names with a comma.
