In his latest blog post MS blogger Martin Baum, talks about his recent experiences with foot drop.

Anthony Chapman is a musician who was diagnosed with MS a few years ago. In this article we find out how he started streaming his beat making on Twitch and why he is helping the MS Trust make a theme tune for our new podcast series.

Having kept her MS secret for eight years, MS Trust supporter Jenna decided to open up about life with the condition earlier this year – and says it was the best decision she’s ever made. Here she tells us about the empowerment she felt sharing her story and raising awareness of MS.

Steph, 46, from London has faced many hurdles in her MS journey, but in her darkest moments, she has found hope and support through the MS Trust. This is her story.

People with MS report such a wide range of symptoms, that it's unlikely that any two people will have the same experience. In his latest blog, Martin Baum talks about a lesser known symptom, where it feels like he is being forcefully pulled backwards.

Jessica Ace is the host of the DISabled to ENabled podcast, which aims to inspire those living with chronic illness. Here she writes about her MS diagnosis and why she's determined to turn it into "something positive".

New MS Trust Chair of Trustees discusses what she is looking forward to in her new role.

As the lockdown restrictions begin to lift, and some kind of normality slowly resumes, many people may be feeling anxious and uncertain about life after lockdown. Here, blogger Elaine, who is one of the 2.5 million 'extremely vulnerable' people who have been asked to shield, writes about the apprehension she is currently feeling.

When Laura Goodall was diagnosed with MS in 2015, she thought her showjumping days might be over. But, four years later, Laura is back competing across the country and has recently been accepted onto the British Showjumping Para team.