A place that feels like home: helping Beth reclaim confidence and mobility
Beth was diagnosed with MS in 2007 and has a long-standing goal to improve her core strength to reduce pressure on her legs and maintain her mobility as much as possible. She was at a bit of a loss when her previous exercise physiologist retired, until Beth was encouraged to visit MS Plus and the Hobart Wellbeing Centre, which offers a neuro friendly gym and a range of tailored services under one roof.
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- 10 March 2026
MS Plus Announces Sale of Blackburn Headquarters and Commences Search for New Accessible Location
MS Plus today announced its Victorian headquarters at 54 Railway Road Blackburn has sold.
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- 3 March 2026
My wife’s journey with MS by Ken Levien
"My advice for anyone navigating a new diagnosis, including family and friends, is that you can still live the life you want, even if adjustments need to be made and it may look a little different than you imagined."
- News
- 26 February 2026
2026 Fitzroy Mega Swim: Every lap for our clients
The 2026 Fitzroy MS Mega Swim has wrapped up – and what an extraordinary result. Together, our community has raised $156,331 (and counting!) to support people living with multiple sclerosis (MS). Every lap swum, every team formed and every dollar donated helps deliver practical, meaningful support for our clients across Australia.
- News
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- 24 February 2026
'My EP’s understanding of how people with neuro conditions need specific treatment has been incredible.' Marianne’s story
Marianne's weekly sessions with a neuro specialist EP have been life-changing. 'My EP went through all my history, my test results, I don’t think I’ve ever had such a thorough assessment. They really work on not just your MS but everything that’s going on in your life.'
- News
- 18 February 2026
Work, wellness and walking aids: Bec is redefining life with MS
A mother of three and public servant, Bec had always been active — commuting by bike, hiking with her family, restoring furniture. Post-diagnosis, she had to rethink how she moved through the world.
- News
- 4 February 2026
Connecting regional patients with vital neurological support
For many people living in regional areas, accessing the right healthcare and support services can be a significant challenge. This was the reality for Aaron, who was diagnosed with MS in 2007. Facing limited medical resources and growing frustration at the lack of specialist care in his hometown in regional New South Wales, Aaron recently became the first to stay at MS Plus’ newly developed Lidcombe Home supported disability apartments. His experience was more than just a break – it was life-changing.
- News
- 3 February 2026
A journey to living well and embracing life with MS: Brad’s story
‘While everyone was freaking out, I saw my MS diagnosis an important opportunity to reflect on myself — and spent those early days walking and thinking and reassessing my life to that point,’ Brad says
- News
- 20 January 2026
Finding strength in community: Denis’ story
Denis’ relationship with MS Plus spans more than 20 years — and includes the meeting of some lifelong friends.
- News
- 16 January 2026
Charlie’s cycling comeback: finding a way back on the bike after MS
Charlie discovered she had MS in 2010, however she suspects that the seeds of this condition were sown much earlier, as far back as 2004. At the time, she was deeply engaged in her passion for cycling, training a team for her third MS bike tour event.
- News
- 6 January 2026
“I’ve learned the value of taking care of myself,” Tarika reflects on being newly-diagnosed
“I realise now that the vision issue was my first episode, and my second ‘relapse’ was after my wedding three years later."
- News
- 22 December 2025
A sailing adventure with a difference: exploring Oceans of Hope
“That initial diagnosis was a shock and for about a year or so I was so depressed with it. Oceans of Hope was one of the things that really snapped me out of that.
- News
- 11 December 2025
