Latest News

Carers…How are you?

May 15, 2020 | Advocacy, Life with MS, Research, Support

The Carers Alliance wants to know how you, family carers, have been during Covid-19. Feedback received so far has shown that carers generally have come through the weeks of lockdown well, but it has been tiring. No respite, early reductions in […]


[Updated] COVID-19 – Advice for Patients

April 9, 2020 | Advocacy, Life with MS, Research, Support, Treatments

NOTE: This post was updated on the 9/04/2020, to reflect the requirements of Alert Level 4 and emerging data. Key updates: Updated information based on very early emerging data Updated information about your upcoming appointments Latest travel advice Information for […]


The Good Service Project

December 17, 2019 | Advocacy, Education, Funding, Research

“Is it reasonable to wait four months for my neurology referral or MRI?” It’s a surprisingly common question, and that worries us. We regularly receive calls from distressed people experiencing multiple sclerosis (MS) symptoms for the first time or in […]


The Cost of MS Study

December 17, 2019 | Advocacy, Education, Funding, Research, Uncategorised

New Zealanders with multiple sclerosis (MS) face undue restrictions to life-altering drug treatments and valuable social supports. The cost and consequences of this lack of access are enormous. We believe this needs to change. New Zealanders with MS need better […]


Join us at the MS Research Day 2019

September 27, 2019 | Event, Research

Our friends the New Zealand Multiple Sclerosis Research Trust are delighted to host MS Research Day 2019 in conjunction with MS Auckland. The event will cover a range of stimulating topics relevant to people with MS, their families, and their […]