Candice shares her experience of one of the most debilitating symptoms of MS, known as trigeminal neuralgia. Before MS, life for Candice was busy and somewhat normal but over the space of a few months, everything changed.

James Townsend is co-founder and CEO of Mobilise, an online community supporting thousands of carers across the country. James shares his personal connection to MS and insights into the challenges and rewards of caregiving.

What is advanced MS? In this section we look at the realities of living with advanced multiple sclerosis, who can help, and sources of support for carers and people living with advanced MS.

Using hand grip strength to investigate upper body function and muscle fatigue in people with multiple sclerosis.

Beccy Huxtable from The Scott Mills Show on BBC Radio 1 talks about how she turned to the MS Trust for help and support when diagnosed with MS in 2012.

Researchers have investigated how the risk of developing long term disability has changed over the last three decades for people whose MS begins in childhood.

Looking for a fundraising experience you’ll never forget? Get ready for the flight of a lifetime with Wing Walks for MS Trust!

This World MS Day 2026 we are joining the campaign to highlight our information for people newly diagnosed with MS. We strive for our free Making Sense of MS booklet and supporting resources to be available to the 135 people diagnosed each week.

Welcome to the May 2025 TiMS newsletter! We think that it is important to keep you up-to-date with the work we are doing. This newsletter will tell you about the things discussed at the last meeting and update you on our latest projects.