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.

Evie and Alec both got special books about multiple sclerosis which carefully told them what it is, why some people have it and also what it makes people with MS feel like.

Ian Daly takes a light-hearted look at the increasingly bizarre 'cures' for MS.

In her latest blog for the MS Trust, Carla King looks at how to cope with homeschooling when you have MS.

In his latest blog, Ian Daly speaks candidly about his own experience with depression and urges others to seek help if needed.

2020 has been far from a normal year. In his latest blog for the MS Trust, Martin Baum reflects on the impact lockdown has had on MS care across the country.

Nigel Bartram, diagnosed with primary progressive MS (PPMS) in 2009, tells us why despite living in France, he is supporting the 'MS Trust...in us' campaign