by mssystems2 | Dec 14, 2022
Since my MS diagnosis in 2005, I’ve experienced numerous debilitating symptoms (including leg weakness, optic neuritis, nerve pain, sensory loss, bladder instability). In 2018, my fatigue and brain fog were so bad that I had no quality of life and was forced to resign...
by mssystems2 | Dec 14, 2022
My family,Partner and friends.I was told I had Multiple Sclerosis not back problems when I went and got it checked.I went from a walking stick to a wheelchair pretty quick.My thoughts are to let people know live your life to the fullest as you never know when your m.s...
by mssystems2 | Dec 14, 2022
I have been volunteering with the MS Community Visitor Scheme at Princess Court Homes, Mildura since the 25th August 2016. I have had the pleasure of regularly visiting an older couple for the last four years. My role is to visit them for friendship and companionship....
by mssystems2 | Dec 14, 2022
I found myself in a deep depression wanting to end my life. I had enough of being sick and enough of the multiple sclerosis. I called MS CONNECT and three words saved my life ARE YOU OK?. After my darkest day, I made it a personal promise to give back to Multiple...
by mssystems2 | Dec 14, 2022
My husband was diagnosed with Muscular Dystrophy (MD) before our marriage in 1972. At that stage there was no MD Association in Victoria. His cousin who is a General Practitioner advised some Physiotherapy. Since there was no help from MD then — the only one was in WA...
