An MS diagnosis can be a lot to get your head around. There’s the unpredictability to navigate, the invisible symptoms, the different treatment options, and the emotions that come with knowing you’re going to have to deal with the condition for the rest of your life.

The MS Trust are delighted to welcome Caitlin Sorrell as the new Chair of trustees from December 2020.

Being diagnosed with MS can sometimes affect your sex life, but we know that people can often feel too embarrassed or awkward to seek out support. This Sexual Health Week (14-20 September 2020), we want to normalise the conversation around sex and MS and break down some of those taboos. Here, MS nurse Shamayne Evetts, who works in the Dorset area, writes about what her service is doing to offer support and shares some advice for people with MS who may be experiencing problems with sex and intimacy.

When farmers Emily Padfield and Mark Warner applied for a new TV show promising an “off-grid experience in the Alaskan wilderness", they never once imagined they would actually end up appearing on the show, let alone winning it! We caught up with Emily to hear more about the couple’s experience on the BBC2 show ‘Win the Wilderness’ and why it was her MS that persuaded them to take on this ‘crazy’ adventure.

Jess tells the MS Trust about her husband, Neil, and how she believes an Advanced MS Champion in her area would support her with Neil's advanced MS.

John, who lives with Primary Progressive MS, tells the MS Trust why he thinks the Advanced MS Champions programme could benefit people living with advanced MS.

Peter shares why he thinks an Advanced MS Champion could have improved the quality of life for his late wife, who had advanced MS.

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.