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.

Natasha, who lives with MS, tells the MS Trust why she thinks the Advanced MS Champions programme is so important.

When Emma was diagnosed with MS aged 27, she admits it was a 'devastating' time. But, 10 years later, she is determined to focus on the positives. In this blog, Emma writes about her MS diagnosis, life as a farmer, and why she won't let MS beat her.

Fee was diagnosed with MS over 10 years ago. Here she tells us how her daily strength, balance and stretch exercises help with her MS symptoms.

Josh Astley has used his own experience of an MS diagnosis to design a companion robot for people living with MS. Here, the University of Sheffield student tells us about the inspiration behind his design.

As he gets set to take on his biggest challenge to date, we caught up with our intrepid supporter Kenny Smith to find out more about the inspiration behind his fundraising.

Danielle MacGillivray talks to us about coming to terms with her MS diagnosis and learning to "appreciate the little things" every single day.

When Lara was diagnosed with MS, she suddenly felt like “the light had changed from green to red.” But now, two years on from that diagnosis, she’s determined to focus on what she can do and not what she can’t. This is her story.