AUTHOR

Louise Mckinlay

https://www.msnz.org.nz

POSTS

MS Voice e-Newsletter – June 2025 Edition

June 24, 2025 | MS Voice, My Story, News, Newsletter

Welcome to our June 2025 Edition of MS Voice, your go-to place for the latest news, updates, and real life stories from Multiple Sclerosis New Zealand. In this edition we highlight the urgent need for neurological care investment and introduce […]


MS Diagnosis Surges 67% in NZ: Māori Disparities Highlight Urgent Need for Neurological Care Investment

June 17, 2025 | Advocacy, Media, News

Neil Woodhams, President of Multiple Sclerosis New Zealand, joined Dale Husband on Waatea News to discuss the recent study which showed a 67% surge of MS diagnoses in New Zealand since 2006 and the Māori disparities that highlight the urgent […]


MS Voice e-Newsletter: World MS Day Special Edition – May 2025

June 3, 2025 | MS Voice, News, Newsletter

In our World MS Day special edition, we sound the alarm on the worsening shortage of neurologists across the country, share a promising breakthrough for Progressive MS, shed light on MS prevalence gaps in Aotearoa and introduce you to Angus, […]


The Need is Urgent: Critical Shortage of Neurologists as MS Cases Rise

June 3, 2025 | Media, News, Uncategorised

Multiple Sclerosis New Zealand is calling for more governmental investment in specialist neurologists, clinical nurse specialists and allied healthcare workers to better diagnose and treat the growing numbers of people with MS in Aotearoa New Zealand. Listen to MSNZ National […]


I May Have MS, But I am Lucky – Chris Lord’s Story

May 31, 2025 | Life with MS, My Story, News

Today is World Multiple Sclerosis (MS) Day. Seeing the reminder in my calendar pop up prompted a moment of reflection. It made me think about not just my experience (circa 2 years), but the experiences of over 4000 Kiwis who […]