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New NMOSD medication to be considered at November PBAC meeting

NMOSD are forms of autoimmune demyelinating diseases that specifically attack and inflame...
Jen Willis and team on the way to Mount Everest Base Camp

Jen Willis: The trek to Everest Base Camp

Jen Willis, the first Australian with multiple sclerosis to attempt...
Rohan Greenland The May 50K

From our CEO

MS Australia CEO Rohan Greenland reflects on Chair Des Graham’s...
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MS Australia Chair Associate Professor Des Graham announces retirement

Associate Professor Des Graham has brought forward his previously announced...
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MS Australia funds innovative research projects addressing critical unanswered questions in MS 

New MS Australia research funding announced today aims to unlock...
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MS Australia funds groundbreaking projects to help revolutionise MS treatment and care

Three MS researchers have been awarded incubator grants, which aim...
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MS Neurologist and EBV researcher recognised in King’s Birthday Honours

In 2024, Emeritus Professor Michael Pender was made a Member...
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Improving sleep quality in Australians with MS by managing comorbidities

Analysis of data on sleep quality and the presence of...
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Count Us In: National Summit calls for a better deal for the millions of Australians living with neurological conditions.

NAA Chair, Rohan Greenland highlights the neglect of neurological conditions...
Rohan Greenland The May 50K

From our CEO

In his speech at the National Summit on Neurological Conditions,...
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Exploring Repetitive Transcranial Magnetic Stimulation (rTMS) as a Potential Treatment for Multiple Sclerosis

A new study has explored low intensity rTMS as a...
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A travel agent’s journey to support the MS community

For over 30 years, travel agent Lois Marshall has helped...
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Enlargement of a discrete brain region is providing clues on nerve damage in relapsing remitting MS

Australian researchers have identified a brain region that enlarges over...
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COVID-19: What did it do to quality of life in MS?

Australian researchers have found a link between COVID-19-related hardships and...
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Kate Casey

Entering adulthood with MS

Kate was diagnosed with MS in February 2006 at the...
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New report calls for faster MS diagnosis in Australia on World MS Day

A new report has revealed the prolonged time to diagnose...
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Sarah Flaim

My diagnosis brought relief

“At least it’s not a brain tumour…”  I vividly recall...
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Jessica Worsley

Self advocacy and a MS diagnosis

Following a challenging IVF journey and the traumatic birth of...

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