Family planning and MS: Understanding information needs

A new research study has explored the experiences of people living with MS around the concept of family planning. The study aimed to understand information needs and where opportunities might be to improve informed decision-making between patients and healthcare professionals to provide better support for people with MS.

Elena’s MS Legacy: A Gift for Care and a Cure

Elena Canu, a beloved daughter of Italian immigrants, had a fulfilling career working in Australian television. Having lived with MS for 30 years, Elena found it easy to help a cause close to her heart when writing her Will. Now her caring legacy lives on, funding crucial research and helping those affected by MS.

MS Australia President Des Graham

NDIS Interim Review gives cause for concern

This opinion piece by MS Australia’s President, Associate Professor Des Graham, was prompted by the recent release of the NDIS interim report, What we have heard report, and MS Australia’s ongoing campaign for improvements to the NDIS to better meet the needs of people living with multiple sclerosis.

Rohan Greenland The May 50K

From our CEO

CEO Rohan Greenland reflects on the remarkable progress made in MS therapies over the past three decades and emphasises MS Australia’s commitment to advocate and support the development of new and more effective treatments in the coming years.

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A Major Milestone for People with MS: Three MS Medicines added to World Health Organization’s Essential Medicines List