In this episode we want to banish toilet taboos! Tom from our Information Team explains a little bit about the science behind why these symptoms occur in MS; Helena, who lives with MS, shares her advice on how best to deal with these kinds of problems in the workplace, and we put some of your questions about bowel and bladder symptoms to MS specialist nurse Noreen Barker.

In this blog, Martin discusses the importance of raising awareness of caring and the contributions that carers make to the MS community.

Heather is now a full-time carer for her husband who lives with MS. Find out how they navigate inaccessible spaces, holidays and government support together.

"To forget the life where I once chose exclusion instead of inclusion would mean that I had learned nothing from a time when I chose to live MS and not life." Martin Baum looks at how MS prepared him for lockdown.

Chris shares his experience of being diagnosed with MS at the same time as starting hormone treatment and a surgical gender transition.

Dearbhla Crosse discusses her surprise feelings of empowerment when it comes to dating with MS during a global pandemic.

In this article, Julie describes the shock of both herself and her husband, Martin, receiving an MS diagnosis.

Discovering that the pattern of your MS is changing from RRMS to SPSM can be a distressing and confusing experience for you and your loved ones. We talked to MS Trust Chair of Trustees, Caitlin Sorrell, and her husband Tim, about his recent transition to SPMS.

Pete Davis tells us how he felt falling for someone with MS and that despite everything that MS throws at them, they still make things work.