anzmes

Copied post Petition for NZ govt to recognise ME as a disability. https://www.parliament.nz/en/pb/petitions/document/PET_125649/petition-of-associated-myalgic-encephalomyelitis-society

Posts consolidated from a number of threads - apologies if the posts do not completely flow Covid-19 vaccination experiences News from Aotearoa/New Zealand and the Pacific Islands

Copied post Watching at the moment but I think it should be an interesting watch. https://youtu.be/ZZGlVJYyAO4 Discussion here Video: Professor Warren Tate's Update on His Research into ME/CFS - 11th November 2017

The recently revised Auckland clinical guidance document is not officially available to the public (just medical professionals) but has been circulated by some advocates; this is how I first obtained a copy of the document. Some of the issues are: Name: Chronic Fatigue Syndrome - does not give...

At the Association of New Zealand ME Societies (ANZMES)'s AGM on 10 November 2018, Dr Ros Vallings presented an ME Research Update. Dr Vallings is the Medical Advisor to ANZMES and is the only specialist ME doctor in New Zealand. A summary of the AGM itself is on the New Zealand thread. One...

The News from Scandinavia is such an interesting and useful thread, so I thought it could be worth seeing if we could sustain a similar one for New Zealand. We do have some good research being done, some active advocates and even a suggestion from David Tuller that he might get here in the next...

Watching at the moment but I think it should be an interesting watch. https://youtu.be/ZZGlVJYyAO4