One of the (many!) challenges of having an unpredictable and unique condition like MS is you can never be quite sure if a symptom is related to your MS or something else entirely.
Our Research Network member Sarah Rees spoke to Dr Ana Manzano and Professor Helen Ford. They discussed designing an online disease modifying therapy (DMT) decision aid to support people with relapsing MS.
Sarah Rees lives with MS and is a member of our Research Network. She’s been taking a look back at some of the highs and lows for MS research during this exceptionally challenging year.
Online dating is always something of an adventure. For every person who met their life partner on an app, you will hear ten horror stories of unsuitable, awkward or downright odd experiences.
Sarah Rees is a member of our Research Network. She caught up with researcher and occupational therapist Colette Beecher (pictured above) to find out how her experiences with an MS treatment called HSCT inspired her PhD project.
For those of us with MS who are usually able to live full and active lives, life under lockdown is a serious shrinkage. But it's a rare opportunity to realise what really matters.
This week we launched our online fatigue management course. Research Network member Sarah Rees caught up with Dr Sarah Thomas, the researcher behind the course.
Alasdair Coles is a researcher from the University of Cambridge. He told Research Network member Sarah Rees about his vision of a future where everyone with MS has access to effective treatments.
In June this year, I ‘celebrated’ my fourth MS anniversary. For me, marking the moment matters because it is a chance to take stock of myself and my progress.
