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News / Blog
News Archive by Month
Introducing our interim Chair – Natalie Thain
Following the recent resignation of our Chair Greg Horton, we are delighted to announce the appointment of Natalie Thain as interim Chair to our AGM on 30th October. Natalie brings...
Kiwis living with motor neurone disease to benefit from Emirates Team New Zealand’s charity partnership with MND New Zealand
Kiwis living with motor neurone disease (MND) are set to benefit from MND New Zealand being the official charity partner of Emirates Team New Zealand for the 36th America’s Cup....
Are you eligible for a tax refund? Make your donation to MND New Zealand go even further!
The end of the tax year is almost here! As we are a registered charity (The Motor Neurone Disease Association of New Zealand Incorporated - Registration Number: CC35320), if you...
Congratulations Fulton Hogan, this year’s recipient of the David Oliver Beacon Award!
Pictured: Caron Palmer (Deputy Chair, MND New Zealand) and Cos Bruyn (Fulton Hogan Managing Director). Fulton Hogan is this year’s recipient of the David Oliver Beacon Award. The decision was...
Celebrating one year with Fulton Hogan
A big thank you to our Foundation Corporate Sponsor Fulton Hogan as we celebrate the one-year anniversary of our partnership and The Fulton Hogan MND New Zealand Support Fund. It...
Organise a Walk 2 D’Feet MND in your community this summer!
Walk 2 D’Feet MND is MND New Zealand's national fundraising event series, organised and led by volunteer supporters. MND New Zealand provides guidance, resources, and support to organise a Walk...
Motor Neurone Disease Awareness Month – in review
Each week in New Zealand at least two people are diagnosed with MND. This devastating disease impacts hundreds of families throughout New Zealand, yet it’s something many kiwis have little...
MND Awareness Month: Our relationship with Fulton Hogan
It takes a team to live with the impacts of MND. Every member of the community plays a valuable part; friends and whānau, health professionals and researchers, volunteers and supporters....
Motor Neurone Disease Clinical Working Group aims to improve lives through standardised care
Last September, we held the first-ever MND Hui at Parliament. The hui offered the chance for people working in various disciplines across healthcare throughout the country to come together and...
The Seymour family story – ‘not just me’
David Seymour is living with MND and reflects on the vital role of his family and impacts on them. My family and I have been grappling with the devastation caused...
MND Awareness Month- Going for a walk
Sometimes it’s the simple pleasure in life that are the most enjoyable. For people living with MND, everyday things like going for a walk can be a challenge. To help...
COVID-19 Alert Level Two – what you need to know
Tomorrow New Zealand moves to Alert Level Two. It has been a long and challenging journey, so the easing of restrictions will be a relief to many, but the golden...
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