A conversation in the 'News from New Zealand and the Pacific Islands' thread led to the idea that 'we'* work together on ensuring that people with...
Would you be interested in helping M.E. Awareness NZ to prepare content for an online petition. I see we can create one on...
Thanks for the feedback on the challenging read. We will try to do better! Yes, if you would take a picture of some shoes for the Millions...
Invitation to join M.E. Awareness NZ and our Online MillionsMissingNZ Campaign Hi All, Our invitations… Join our M.E. Awareness NZ closed...
We have shared on our M.E. Awareness NZ facebook page. [MEDIA]
Just found this 2015 article on NZ Doctor. Sharing to help piece the links together of what the thinking is in various parts of the country....
This worries me, as our local pain clinic believes that the pain of ME/CFS & fibromyalgia is brain handling messages incorrectly....
Wendy Matthews in Whitford, Auckland is behind this. Yes, as @Daisybell said, the trust is in it's infancy, but very determined, and is developing...
@Ravn Thanks - I presume it is okay to share it on various networks? Do you think it is okay to use the term "Myalgic Encephalitis"?
Just reporting back. The sponsorship has been accepted by an awesome GP who has some ME/CFS patients, so has some awareness already. She has been...
@SamF Have you seen this thread /research?
The appointments are officially 15 minutes long - which includes the writing up notes time. We are normally there for 20 mins. We go monthly....
How did you react to this bit... frank isn't he. "Persons with ME/CFS (PWCs) are admittedly very complex and challenging but eternally grateful...
I saw this posted on the "ME/CFS-Evolving Science" facebook page... Changes in the transcriptome of circulating immune cells of a New Zealand...
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