MS: Busting the Myths
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 […]
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 […]