OUR MISSION IS TO ADVOCATE FOR PEOPLE WITH MS IN NEW ZEALAND TO HAVE ACCESS TO FIRST WORLD TREATMENT, RESOURCES AND SERVICES TO IMPROVE THEIR WELL-BEING AND QUALITY OF LIFE

TOP READS

Multiple Sclerosis: Looking towards the future of MS treatments

Join us at our free public lecture as part of the 50th Anniversary celebrations of MSNZ

Mastering Mountains Grant helping Kiwis with MS achieve their dreams

Applications now open for the Mastering Mountains Grant to help achieve your outdoor adventure

Dorothy Newman Scholarship keeping people in employment

Past participant Anthony shares his story of how the Scholarship improved his employment prospects

MS Energise

New app developed by researchers at AUT to help PwMS self-manage their fatigue

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HERE TO HELP

Regional Support

Our Regional Societies offer a wide variety of support and services for people with MS, families, employers and carers affected by the condition. Each society employs trained Field Workers that offer support and guidance on a wide range of matters including:

    • Advice and information on Multiple Sclerosis symptoms and management
    • Access to information resources developed and provided by MSNZ
    • A range of support, social and exercise groups in your region
    • Advice on local services and supports
    • Guidance on work and income issues
    • Support with applications to the Lottery Individuals with Disabilities fund
    • Individual advocacy to ensure people with MS receive the best services in their community
FIND OUT MORE FIND A REGIONAL SOCIETY

WHAT WE DO

About MSNZ

WHO WE ARE AND WHAT WE DO

MSNZ is a non-profit organisation formed to support people with MS in NZ

Advocacy

OUR VISION AND MISSION

To advocate for people with MS in NZ to have access to first world treatment, resources & treatment

Research

RESEARCH AND STUDIES

News and updates

MS IN NEW ZEALAND

Read More About MS

SHARE YOUR STORY

I am immensely grateful for the MS Society and the Dorothy L Newman Scholarship’s assistance with my course fees this year, thank you!

Rachel Wellington

The MS Society successfully advocated for the funding of two new drugs…I know my treatment is not a cure, but now I am able to provide for my family

Anne Auckland