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. As our Foundation Corporate Sponsor, we’re proud to have Fulton Hogan as part of the team making a difference by supporting our vision: Together, we provide … Read more
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 discuss the clinical needs of people living with Motor Neurone Disease in New Zealand. What became apparent throughout the day was that there are regional … Read more
To all participants and potential participants in our University of Auckland/ADHB MND genetics screening and MRI scanning studies, we hope you are well and thank you for your patience during the COVID-19 pandemic. Now that we are at Level One, we have resumed study enrolment and sample collection and imaging for both our MND genetics … Read more
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 by the beast that is MND, for the past three and a half years. For the first six months after receiving the diagnosis of MND, … Read more
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 others understand this, Jos from Wellington put pen to paper and came up with this piece entitled “Going for a walk”. “The sun is shining … Read more