MS: Busting the Myths
January 7, 2020 | Life with MS, Support
I have multiple sclerosis (MS), and I know that when I get stressed, I feel more unwell. Stress makes MS symptoms worse in my own body. It is interesting to note that studies show that the better you cope with […]
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 […]
