We provide support, education & advocacy for people living with MECFS in Canterbury & West Coast, NZ Repeat offenders will be blocked from the page.
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PLEASE NOTE that MECFS Canterbury does not recommend any treatments. Any advice, either explicit or implied, is not intended to replace qualified medical advice. We do not accept any responsibility for any treatment undertaken by readers of any articles, or for any error or omission in connection with any article published on our social media. Any Comments on posts that are discriminatory will be removed.
16/04/2026
And for those who carry invisible pain — and for those who care for them — may these words serve as a quiet reminder:
13/04/2026
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.
Three winning designs will be featured on ME/CFS Canterbury “Crash wear” merchandise and the winners will receive one crash wear item of their choosing featuring their design.
Entries close Saturday, 31st May 2026, and winners will be announced on Friday 12th June 2026.
Our logo depicts a flying Kuaka, the Godwit. These birds show incredible endurance and are recognised for their tenacity and perseverance.
Now that winter is approaching, thousands of Kuaka have left Aotearoa and started their journey north to the breeding grounds of Alaska, stopping off in Korea and Japan for a rest and some food on the way. On the return journey, as our summer approaches, they fly directly to New Zealand, a trip of endurance with no food, water, or rest; nearly 12,000 km non-stop.
The Kuaka fly in flocks, with birds taking turns to lead and conserve their energy in the slipstream of others. Some banded birds have made that journey 20 times and some of them come to the Canterbury coast. The Kuaka arrive back at the Avon Heathcote Estuary every spring.
In the face of an enormous challenge, the Kuaka brings a spirit of endurance and cooperation, and that is what makes the Kuaka an appropriate symbol for MECFS Canterbury.
The Kuaka have been seen as birds of mystery: there is a saying: ‘Kua kite te kohanga kuaka?’,
‘Who has seen the nest of the kuaka?’.
The mystery of course was because the Kuaka makes their nests far away in Alaska.
There’s a parallel there with our experience with ME/CFS. The illness is as real as the Kuaka, but no one yet knows what is causing it. Hopefully one day, soon, the answer to the mystery will be as obvious as the location of the Kuaka’s nests is to us now.
There’s another evocative saying about the kuaka that can inspire our community:
‘Ka ngau ki te turi kakao te paringa o te tai, e tika te rere o te kuaka’
‘The spinifex wanders along the beach like the incoming tide, the kuaka flies direct’.
The big spiny seed heads of the spinifex plant move along the beach like tumbleweeds, backwards and forwards at the whim of the wind. But the Kuaka make their own way, working with purpose and as a group to achieve something remarkable.
It’s said that when Pacific explorers saw the flocks of Kuaka flying so determinedly and seeing that they weren’t sea-birds, they knew that there must be land to the south.
So, they set off, following the Kuaka flocks, and discovered Aotearoa.
We like to think that the scientists can be like those explorers, following the clues from people with ME/CFS, to make a great medical discovery.
18/03/2026
Dr Mona Jeffreys from Victoria University Wellington has shared a very useful new interactive Primary Health Care resource for adults with Long Covid for GP's.
Mona is speaking about it at our April Online Group meeting, keep an eye out for the event on our page.
Speaking to RNZ reporter Kathryn Ryan, Renee Dingwall shares her experience navigating the public health system with Long Covid, a complex chronic illness, highlighting the need for clear clinical pathways and coordinated care.
Long Covid Support Aotearoa's Larisa Hockey echoes the urgent need for structured care noting there has never been a publicly funded Long Covid Clinic and that the government has no plans to monitor Long Covid in New Zealand.
Meanwhile researchers like Mona Jeffreys (Victoria University of Wellington) are working to bridge the gap, developing resources for GP's to better support patients.
Six years after the country went into its first pandemic lockdown, new data shows the impact of Long Covid on hundreds of thousands of Kiwis, but what, if anything, has changed for Long Covid patients and their treatment?
18/03/2026
"Now that the scale of the problem is clearer, we want to know why there are still no plans to monitor it." - Larisa Hockey Long Covid Support Aotearoa
New data from the Ministry of Health estimates 185,000 New Zealanders experienced Long Covid symptoms in the 12 months ending July last year.
17/03/2026
Listen time: 7mins 02 sec
Larisa Hockey from Long Covid Support Aotearoa talks to RNZ’s Corrin Dann about the more than 400,000 New Zealanders experiencing Long Covid.
More than 400,000 Kiwis have reported experiencing long-covid in newly-released figures from Health New Zealand. Larisa Hockey from Long Covid Support Aotearoa spoke to Corin Dann.
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Established in 1985, MECFS Canterbury is a registered charity based in Christchurch and servicing the Canterbury and West Coast regions.
Our mission is to support and empower people with Myalgic Encephalomyelitis /Chronic Fatigue Syndrome and their whānau through inclusion, education, sharing and advocacy.
We aim to use our page to advertise our events and to share information, research, and experiences to raise awareness of this debilitating illness.
If you are a health professional or know someone that has ME/CFS, please follow us to learn more about ME/CFS.
If you are a person with ME/CFS and living in Canterbury, we invite you to join our community and receive our services. Please visit our website to become a member. You may also like to join our private facebook group for online peer support.
Please Note:
MECFS Canterbury does not recommend any treatments. Any advice, either explicit or implied, is not intended to replace qualified medical advice. We do not accept any responsibility for any treatment undertaken by readers of any articles, or for any error or omission in connection with any article published on our social media.
Any Comments made on posts that are discriminatory will be removed. Repeat offenders will be blocked from the page.
What is ME/CFS?
ME/CFS is a serious long-term illness. It affects people of all ages, ethnicities and both male and female. Overseas studies suggest the prevalence of ME/CFS is 4 in 1000 people, implying that there are 20,000 people affected in NZ, and 2,000 people in Canterbury (including 300 young people).
The causes and the specific pathologies of ME/CFS aren’t yet understood. It often starts after an infectious illness such as glandular fever. Researchers are finding issues with energy production, blood circulation and oxygen use.
Core Symptoms
Greatly lowered ability to do activities that were usual before the illness.
This drop in activity level occurs along with fatigue and must last six months or longer (3 months in children).
Worsening of symptoms after physical or mental activity that would not have caused a problem before the illness.
This is known as Post-Exertional Malaise (PEM). PEM is often delayed, typically happening 12 to 24 hours after exertion. People may be house-bound or even completely bed-bound during PEM.
Sleep problems.
People with ME may not feel better even after a full night’s sleep. At times, people with ME may have trouble falling asleep or staying asleep, may sleep for over 12 hours a day or may have a delayed sleep onset.
Problems with cognition.
Most people with ME/CFS have trouble thinking quickly and concentrating for periods of time compared to prior to illness onset; there may be trouble finding words or slurring of speech, particularly during PEM.
Worsening of symptoms while standing or sitting upright.
This includes feeling lightheaded, dizzy, weak, or faint while standing or sitting up. They may have vision changes like blurring or seeing spots. This is known as Orthostatic Intolerance.
Refer to our website for more information.
What are the impacts of having ME/CFS?
When someone develops ME/CFS, there is an enormous change in their life and that of their families.
Previously active people may be suddenly unable to work or attend school. Parents with ME/CFS may struggle to care for their children. The lack of energy and the flu-like symptoms means that many people are confined to their homes or even their beds. It is hard for family, friends and employers to understand, and many medical professionals and schools are not sufficiently well-informed to provide good support.