"I thought I was dying, but little did I know it was a new beginning." Dominika shares her MS diagnosis experience and outlook on life.

We caught up with MS Trust fundraiser, Olivia to talk about her MS journey and her new event, The Twelve Day Marathon.

In today's episode we are joined by Claire Winchester, MS Trust Head of Info and Engagement. She shares insights from a recent survey exploring how MS affects travel and transportation.
We also hear from Motability's Ross Smith to learn more about their scheme and how it can help people with MS stay independent.

As the final data from the MS Risk-Sharing scheme (RSS) is published in the BMJ, we reflect on how this pioneering scheme has changed the landscape for people living with MS.

Researchers from the University of Plymouth have developed ‘The Telerehab Toolkit’ to support health and social care practitioners in the remote assessment and management of people with movement impairment and physical disability.

For many, MS nurses are a lifeline but, sadly, we know that some people are missing out on the vital care and support they provide, simply because there are currently not enough of them. The MS Trust recently published a report into nurse provision across the UK, this blog looks at some of the key findings.

Briumvi (ublituximab) has been approved by NICE and the SMC for people with relapsing remitting MS in England, Wales and Scotland.

The MS Trust wishes Blessing Oluwasanmi the best of luck in her new role as an MS Nurse at the Walton Centre in Liverpool and looks forward to having a new MS nurse in post at Plymouth.

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