Find out what support is available for people caring for a person with MS and guidance on planning for the future.

The MS Trust will be holding an Estate Planning Live Talk in partnership with McClure Solicitors next Friday (June 26) to provide some guidance for those of you who would like to know more about how to get your affairs in order.

Stories from children and young people who have been diagnosed with MS.

Our executive summary lists key findings from the pilot wave of the Advanced MS Champions programme.

In this guest blog, Emily - aka The Wibbly Dinosaur, discusses Lhermitte's sign.

The MS Trust has launched a new awareness pack to help teachers and pupils raise awareness of MS in their schools and dispel some common myths and misunderstandings around the condition. MS Trust supporter Jenna Chudasama teaches at a secondary school in Leicester and recently used the pack to deliver an assembly to students about her own MS experience. “I hope that I inspired others to live their life to the full, no matter what challenges they are faced with,” Jenna tells us.

Maria was diagnosed with relapsing remitting MS last June. Here she shares her experience of choosing a disease modifying drug. "It’s scary being asked to make such a massive decision, so if you do feel afraid, that’s normal," Maria tells us.

Katherine Goulder is one of parkrun’s Outreach Ambassadors for MS. Here she tells us how parkrun very quickly became part of her own Saturday routine and why others with MS should get involved too.

Professor Basil Sharrack, a consultant neurologist, discusses a type of stem cell treatment called autologous haematopoietic stem cell transplantation (AHSCT), which is offered to a small number of people with MS on the NHS.