Kylie’s grown up with multiple sclerosis being a part of her everyday life. When she was just four years old, her mother was diagnosed with the condition and when she was 20, her older sister Bronwyn was told she too had MS. Bronwyn was just 25. “I missed out on having a mum,” Kylie says. […]
Family matters: Kylie’s story Read More »
Jess Worsley remembers exactly how she felt when she received her MS diagnosis four years ago. She had just welcomed her daughter in the world, and rather than living blissfully in the newborn bubble, she was navigating a world of living with MS. “I felt as if I was drowning, and every time I managed
Friendship and support for the newly diagnosed Read More »
We are challenging Australians to walk, run or move 50 kilometres throughout the month of May to raise funds for life-changing research into MS. All funds raised will support life-changing research into the prevention, treatment and finding a cure for multiple sclerosis. Register today and join us at the May 50k this year! It’s completely
Leave your limits behind with The May 50K Read More »
The MS Society SA & NT hosted its first ever World MS Day Dinner on Saturday 27 May, 2023 at the Adelaide Convention Centre, and what an amazing night it was! Hosted by iconic Australian comedian, screenwriter, director and disability advocate, Tim Ferguson, 175 guests were treated to a spectacular night of fine dining and
World MS Day Dinner 2023 – oh what a night! Read More »
The winner of the Game Changer Lottery’s (GCL) $60,000 Super Early Bird prize, Owen Lampe, is a long-time supporter of the MS Society SA & NT. “As a kid I used to do the MS Readathon,” Owen says. “I think it’s a great way to get the kids to sit down and read while raising
$60,000 Super Early Bird winner ‘buzzing’ about win Read More »
