Funding signals new hope for multiple sclerosis treatment

Hunter researchers will help advance vital prevention and treatment methods for thousands of people living with multiple sclerosis (MS) following a funding announcement today from MS Research Australia.

Professor Rodney Scott and Associate Professor Saadallah Ramadan
Professor Rodney Scott and Associate Professor Saadallah Ramadan

Typically affecting young adults between the ages of 20 and 40, MS is an incurable chronic neurological disease that damages nerves and interrupts electrical messages to the rest of the body, eventually resulting in loss of motor function.

Laureate Professor Rodney Scott and Associate Professor Saadallah Ramadan rom the University of Newcastle and the Hunter Medical Research Institute (HMRI*) will lead two separate projects into areas of MS research that have not been previously explored.

Professor Scott received $211,000 to investigate whether disease severity is associated with differences in the epigenetics of patients with MS.

“Epigenetics is essentially a mechanism to turn genes on and off in different tissues without changing the actual DNA sequence and is a way of regulating gene activity. These mechanisms are also influenced by environmental factors such as sunlight exposure, and could explain why some people have mild disease and others more severe disease,” Professor Scott said.

“This project is a new frontier in MS research that will assess epigenetic differences in people with mild disease and compare it to those with more severe disease to determine whether increased epigenetic change can explain these differences.

“This information will help identify new ways of predicting MS progression and could be used to develop better treatment strategies that prevent or reverse its debilitating symptoms.”

Associate Professor Ramadan was awarded $25,000 to investigate an effective treatment option to combat fatigue.

“Fatigue and depression are very common, highly significant symptoms of MS and are major causes of reduced quality of life. Fatigue affects up to 80% of people and often presents early in the disease course,” Associate Professor Ramadan explained.

“Fatigue management in MS is yet to be achieved, but we hope our proposed oral intervention containing selected vitamins and nutrients will improve the function of mitochondria, which are parts of the cell that produce energy.

“Improving this function might slow the neurological damage and have a protective effect, therefore allowing MS sufferers to return to some normality in life by eliminating fatigue.

“The project will also use magnetic resonance imaging (MRI) to measure the neurological response to our oral treatment and assess whether it is a viable method to manage fatigue.”

The funding was part of MS Research Australia’s 2018/19 grant round where $1.75 million has been committed to MS researchers across the country.

Not just another Multiple Sclerosis Survey – help a clinical psychologist with MS at the University of Pretoria, with her research


University of Pretoria - Multiple Sclerosis Research

University of Pretoria – Multiple Sclerosis Research

Isabelle Swanepoel, a clinical psychologist and lecturer at the University of Pretoria, South Africa.

She says of herself “I am currently busy with my PhD study in MS, I myself was diagnosed in 2004 and has been blessed with good health. This is not just another MS survey, using the members and moving on. I have MS myself and therefor know the experience and the journey. I want to make a difference and I believe I will. ”

Swanepoel invites you to help her with that research by taking part in her survey.  She says ” Dear fellow MS Experts – by – Experience

I was diagnosed with MS (RR) in 2004 and have been blessed for the last 10 years. From my hospital bed in 2004 I made a promise to myself that I will help other with MS in this struggle…
Today 10 years and 2 beautiful kids later, my dream, promise and vision is coming true!!!
I am currently busy with my PhD study in MS and the results will be used internationally to help and improve the lives of fellow MS survivors all over the world. I realize that the MS community is tired of being used for research; however this is not the same. This is for US.

I am not ignorant for all the criticism and judgement that may follow… staying positive.

I have a gut feel that I can be supported in getting this message through to MS survivors, that nothing can stop us from health!
Waiting in anticipation to hear from you how I can take this journey forward.
Isabelle

https://www.surveymonkey.com/s/FB32T9K

Thanks in advance.  Please use the comment box below to ask Ms Swanepoel  any questions about the research.