MS: Busting the Myths
November 25, 2020 | Research
MS Brain Health are running a survey to capture the value of their work on individuals in developing their approach to MS care – both in terms of personal impact and the wider health and care environment. If you are […]
April 2, 2020 | Support
MS data sharing during the coronavirus pandemic The MS Data Alliance (MSDA) and the MS International Federation (MSIF) with its members, have teamed up to lead a global data sharing initiative for COVID-19 in people with MS. They are calling […]
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 […]