Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in New Zealand affects about 0.4% of the population. There will be up to 100 affected...
Moderator note: Thread moved from 'General ME/CFS News'. It’s interesting to listen to the last 2 minutes of this short 9 minute video, so...
https://mro.massey.ac.nz/bitstream/handle/10179/14653/02_whole.pdf?sequence=2&isAllowed=y New Zealand study of PEM using 2xCPETs at 48 or 72...
My very supportive dr has suggested perhaps applying for the Supported Living Payment (WINZ benefit type that appears to cover 2 years instead of...
@Ravn brought this article in a NZ magazine to our attention in the New Zealand thread. Marc Wilson is a regular columnist in the Listener, a...
"Dr. Rosamund Vallings Talks The Irish ME/CFS Association is pleased to announce that it has arranged for Dr Ros Vallings, a leading international...
Paul Milner & Berni Kelly (2009) Community participation and inclusion: people with disabilities defining their place, Disability & Society, 24:1,...
I saw this posted on the "ME/CFS-Evolving Science" facebook page... Changes in the transcriptome of circulating immune cells of a New Zealand...
The main paper in NZ is running a series of articles on people getting diagnosed with fictitious illness disorder. It seems to be people with EDS...
At the ANZMES (Association of NZ ME Societies) annual general meeting yesterday, Dr Ros Vallings gave a research update. Dr Vallings is NZ's only...
Superb article for psychologists originally published in the June 2018 edition of the Journal of the New Zealand College of Clinical Psychologists...
The Royal Australasian College of Physicians Annual Congress was held in May in Sydney...
May 13 2018 "Christchurch resident Melissa Bailey shares how she copes with the debilitating disease M.E." "I've learned a lot about the human...
I saw this in the ME Global Chronicle. I haven't watched it myself. I am interested to hear people's thoughts about whether it is worth sharing....
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