MS: Busting the Myths
August 20, 2020 | Education, Research
We’re really excited to hear the latest in MS Research via the NZ MS Research Trust’s new webinar series. Replacing their Research Day in Auckland, this series of online webinars means we can hear the latest, from the experts, from […]
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 […]
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 […]
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 […]
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 […]