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.

“I want to encourage people who are not confident in the kitchen to stick on that apron and get cooking” James Coke, diagnosed with MS over 20 years ago, tells us about the inspiration behind his blog The Disabled Chef and shares some top tips for cooking with a chronic condition.

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.

An MS diagnosis left Phil, 33, feeling ‘stunned and scared’, but writing about some of the emotions he experienced in a poem helped him come to terms with the diagnosis.

How your children will cope with your MS, is an ongoing concern for the majority of parents following diagnosis. Here Martin Baum, who was diagnosed with MS over 20 years ago and his son Josh, discuss how they coped and the impact it has had on them over the years.

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.