MS: Busting the Myths
February 27, 2025 | Advocacy, Carer, Carers, Event, Life with MS, MS Voice, News, Newsletter
Welcome to the February edition of MS Voice—your trusted source for the latest news, updates, and real-life stories from Multiple Sclerosis New Zealand and the MS community. This year promises to be a dynamic one as we continue our commitment to […]
February 25, 2025 | Advocacy, News, Treatments
Over the last decade, we have seen the needs of people with MS are changing. This is largely due to the availability of higher efficacy DMTs in NZ, and ever-advancing research is also telling us even more about the importance […]
February 25, 2025 | Advocacy, Carer, Carers, Event, Funding, Life with MS, News, Survey
Consultation is underway across the country to help shape future disability funding and service models. This is your opportunity to have your say and we encourage you to do so, now more than ever. Note: This consultation is for people […]
February 25, 2025 | Advocacy, Carers, Life with MS, News, Support
The Ministry of Disabled People – Whaikaha is calling for expressions of interest to join the Working Groups they are planning to set up to help with the refresh of the New Zealand Disability Strategy. The current strategy is nearly […]
February 24, 2025 | Advocacy, News
Recently, Multiple Sclerosis New Zealand (MSNZ) wrote to Pharmac to express our immense disappointment with their Health Technologies Assessment (HTA) process, the treatment funding assessment process, and the impact this is having on the MS community. The varicella zoster virus, […]