As we approach World ME Day on 12th May, ANZMES have released a powerful national press statement

A big thank you to the librarians at Tūranga, the central Christchurch City Libraries Library, for helping us to profile ME/CFS for this World ME Day.

We are looking for another part time Registered Nurse

We are looking for another part time Work and Income Advocate to join our team.

Support a Cause with Every Cup

Nurse Wendy Dragt shares guidelines for managing our energy when we live with a broken energy system

The School of Health, Victoria University of Wellington, has published a new Long COVID resource for GPs. Epidemiologist, Dr Mona Jeffreys, talked to us about how the resource was developed and how GPs can access it.

Theme for this issue is Long COVID. We highlight recent articles in the media and a new Long COVID Primary Care Resource

Blue Sunday, created by Anna Redshaw, is a special day where people come together over a cuppa and some cake to raise awareness and funds for those living with ME/CFS.

Feeling creative and got some extra spoons? Turn them into something that speaks for our community with our Crash Wear Design Competition.

We’re looking for ME/CFS or Long Covid themed designs for our Crash Wear merch, something that captures the lived experience of ME/CFS and Long Covid.

Recording of a seated Tai Chi session for people with ME/CFS is now available

Today we want to congratulate the team involved in the establishment of Dysautonomia New Zealand and their progress in becoming a registered charity.  

A brief introduction to Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

Share your voice

Radical Rest Challenge - Nominate a friend or two (or yourself)

The 4th International Conference on ME/CFS, Long Covid and Gulf War Illness

Thank you to the individuals and funders who have supported our journey since we became a charity in 1985.

Dysautonomia often appears invisible, but it has a significant impact on daily life.

When living with chronic illness it is natural to grieve the losses and find it difficult to cope with at times.

Join our new facebook group for people affected my ME/CFS and Long Covid living on the West Coast