Multiple Sclerosis Limited is the go-to provider of information, advice and support for people affected by multiple sclerosis.
We’re a combined entity of the ACT, NSW, Victoria and Tasmania with over 60 years' insight into how to live well with progressive neurological conditions. Multiple Sclerosis Limited (MSL) offers vital support and services for people living with multiple sclerosis while the search for a cure continues. We are here so no one has to face MS alone.
What Is Multiple Sclerosis
Multiple sclerosis is a chronic and often debilitating disease which attacks the central nervous system (the brain, spinal cord and optic nerves). There is currently no cure. It is the most common neurological disease in young adults and often attacks people at the time of their lives when they are planning families and building a career.
The average age of diagnosis is between 20 and 40 years of age, although symptoms may begin much earlier, and three out of four people living with multiple sclerosis are women.
No two cases of multiple sclerosis are identical and the severity and progression of the condition cannot be predicted.
Multiple sclerosis attacks the central nervous system (the brain, spinal cord and optic nerves).
Symptoms of multiple sclerosis include extreme fatigue, blurred vision and balance issues.
Multiple sclerosis is a lifelong disease for which there is no known cure...yet.
1 in 3 Australians will be directly impacted through a diagnosed family member, friend or colleague.
Difference You Make
The funds that you raise ensure that people living with multiple sclerosis get the vital support they need to meet their goals and live well, and ensure that no one has to face MS alone.
times last year, people reached out to our helpline MS Connect and were met with a caring person to listen and help them
people received specialised advice from the MS Nurse Advisor and Social Work Advisor Service last year
people registered for an MS Education and Wellbeing webinar in the past year to better understand multiple sclerosis
people joined the MS Peer Support Program throughout the last year to connect with others living with multiple sclerosis
“The information and support we received through MS Connect was absolutely invaluable, and we couldn’t be more thankful.”
Mr & Mrs Smith, parents of April, diagnosed 2017
“I can’t explain how much this has changed my life. I have my confidence back and a sense of control. I can hang out with my friends again.”
Jackie, 36, living with MS.
“Attending the MS Gym on a regular basis has allowed me to meet others in a similar position to myself and to discuss helpful aspects of this disease, while having a laugh. While attending the MS Gym I am assured that I am able to use the correct equipment and receive advice suitable to my needs.”
Gai, diagnosed 1999.
“It was really good to get some detail and clarity about the subject from an expert.”
Terri, diagnosed in October 2014.