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Hi there I’m from Australia, moved to the UK in 2018. In 2009, following a bout of extended vertigo (originally suspected to be labrynthitis) an MRI found a number of MS like lesions. Neurological examination was normal, and a follow up MRI several months later found no changes. Neurologist recomme...

I've had symptoms for the past 8 years but was only officially diagnosed in February. I thought I was handling it ok - wasn't looking to change anything I'd been doing just maybe not push myself as hard - then Covid-19 hit. Again was ok at the start but now my fatigue is hitting me earlier and earli...

I’ve recently just been diagnosed and have been given the option of which medication I could try out the most promising one is Tecfidera but has some unpleasant side effects and I was just wondering if you are on this medication, how long did the symptoms last or do you still have them?

Finding a way to get the human nervous system to grow back the myelin, the nerve covering that MS attacks and causes the symptoms, be they minor or major, we all experience is the next huge hurdle. - I link to a total science paper here: https://www.cell.com/cell-reports/pdf/S2211-1247(20)30611-2.pd...

I need some advice on disclosing my symptoms #symptoms

Belong is a short film that sees Dave, who has recently been diagnosed with MS, meet with others affected by the condition for the first time. They discuss MS symptoms, how MS has affected their relationships and how MS can also have a positive effect on a person's life. What good out of bad have yo...