News

From our CEO

25 July 2023

Rohan Greenland The May 50K

You could be forgiven if you missed World Brain Day on July 22.

It certainly deserves much more attention, especially by our politicians. An initiative of the World Federation of Neurology, it helps promote the concept of brain health.

Here in Australia, we know that around one-in-six people have a neurological or neuromuscular condition.

Despite these very significant numbers, we don’t have a national neurological action plan, nor do we know what the Australian Government is doing to implement the 2022 Global Action Plan for Neurological Disorders.

The need for action is clear.

The Neurological Alliance Australia, which we currently Chair, and MS Australia are calling for:

  • A national neurological research mission within the Medical Research Future Fund (neurological research is under-funded)
  • A national minimum data set for neurological conditions (unbelievably, there is no national data set)
  • A neurological advisory group to improve access and equity to the NDIS
  • Better investment in public health, including a focus on brain health, and
  • An urgent boost in the number of MS nurses.

Most of the major disease groups have dedicated action plans, research initiatives and data collections. But neurological conditions are being left behind, even though more than four million Australians are living with one or more of these disorders.

Time for change. Time for action.

Related News

MS News

In LEEPs and Bounds: Lived Experience Shaping Change

20 October 2026

Over the past 3 years, MS Australia’s Lived Experience Expert Panel (LEEP) has grown quickly and made a real difference across the organisation.

MS News

Hearing lived experience voices on mental health and MS

8 October 2026

This World Mental Health Day 2026 (10 October), members of our Lived Experience Expert Panel (LEEP) share their experiences of managing mental health while living with MS, including seeking professional support, staying active, connecting with others and adapting to changing circumstances.

LEEP

Julie Lonsdale-Light

29 September 2026

LEEP member, Julie shares her experience of MS diagnosis and how she's learned to manage her health over the years. "Having MS means I am constantly “assessing” my body and listening to how I feel. I try not to do too much and take rest breaks as needed."

Read More
WHO three MS medicines added to EML

Newsletter subscription

  • This field is for validation purposes and should be left unchanged.

From our CEO