No one should face MS alone
Nearly 38,000 Australians are living with MS. It is the most commonly acquired neurological disease in young adults, hitting during the prime of life. There is currently no cure.
But with your support, no one has to face MS alone.
Support MS nurses and expert care
Fund peer support and practical advice
Help families when they need it most
How your gift makes a difference
Aaron
Aaron was the first person to stay at Lidcombe Home supported disability apartments, next door to our MS Plus Wellbeing Centre. It was a life-changing experience.
Connie
When tests revealed it was likely Connie had MS, she faced a six-month wait to see a specialist to confirm her diagnosis. So she reached out to an MS Nurse through the Connect line. For the first time in years, Connie felt heard, understood and less afraid.
David
After 15 years of frustration and misdiagnosis, David was diagnosed with MS just before the Covid lockdowns. David found himself drawn into the Peer Support Program with MS Plus, and now runs his own group that meets every month.
Tamara
Diagnosed in the middle of Covid, Tamara felt lonely and scared. It took her a while to call the MS Connect team – but when she did, it changed the trajectory of her disease, and her life.
Why your support matters
37,000+ Australians
Living with MS today
70+ years
Supporting people living with MS, and their families
There is no cure
Your donation helps provide vital services, information and support
Still thinking about making a difference?
Your donation helps ensure no one has to face MS alone


