Sophia Roth was diagnosed with MS in 2015.

Paula tells us how she has turned to mindfulness over the years to help her manage both her relapsing remitting MS symptoms and anxiety.

James and Lianne Carvell were inspired to set up Monkey Sox, a community interest company raising funds and awareness for multiple sclerosis, following James’ diagnosis in 2016. We caught up with the husband and wife team to chat about James’ journey with MS, the importance of raising awareness, and how Monkey Sox has given the couple a new way “to think and feel about MS”.

MS doesn’t need to mean giving up the things that make you who you are. Whether it’s picking up a paintbrush or baking a cake; digging out your old sewing machine or playing an instrument, taking up a new hobby, or rediscovering an old one, can help you retain a sense of self following an MS diagnosis. Here, five people with MS tell us about their respective passions.

Will Berard is a stand-up comedian who has MS. In this blog he talks about fatigue,"perhaps the most invisible of invisible disabilities".

Did the Rugby World Cup have you hooked this autumn? Well, did you know there’s an underwater version of the game? Jo Wood, diagnosed with MS in 2013, plays for the Great Britain team and competed at the Underwater Rugby World Championships earlier this year. “I came back with a new resilience and realisation that I have MS, but MS doesn’t have to have me,” Jo tells us.

When Ewan, a keen cyclist, was diagnosed with MS in 2015, he worried that he might not be able to get on a bike again. But, four years later, he's cycled over 50,000 miles and released a book all about his cycling experiences and adventures. This is his story.

Following nearly six years as the CEO of the MS Trust, David Martin has announced his plans to reitire early in 2024.

Remyelination has been appearing more and more in the latest MS news. We spoke to Dr Nick Cunniffe who is involved in the research, to find out more.