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.

Alison Chubb was diagnosed with primary progressive MS in 2006. Despite the challenges her MS brings, last summer Alison competed in Riding for the Disabled’s prestigious National Championships. Here she talks about how she’s following her horse riding dream and learning to make the most of every opportunity that comes her way.

Paula tells us how she has turned to mindfulness over the years to help her manage both her relapsing remitting MS symptoms and anxiety.

James and Lianne Carvell were inspired to set up Monkey Sox, a community interest company raising funds and awareness for multiple sclerosis, following James’ diagnosis in 2016. We caught up with the husband and wife team to chat about James’ journey with MS, the importance of raising awareness, and how Monkey Sox has given the couple a new way “to think and feel about 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.