The MS Trust were deeply saddened to hear that former Trustee and dear friend, Sandy Burnfield passed away at the end of last week.

After five years at the helm, the MS Trust’s Chair of Trustees is stepping down from her role. Here, Laura Chapman reflects on her time at the MS Trust.

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.

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.