News & stories

Stay in the know with the latest news, research and stories from the MS community. Find information on things that matter to you, from tips on managing symptoms, through to stories about different drugs and treatment options. Want to share your story with us? We'd love to hear from you.

8 July 2024

Hot and bothered: how heat makes MS symptoms worse

It's common for MS symptoms to get worse when you are hot. This temporary effect can be brought on in busy, heated rooms, outdoors in the sun or when exercising. But what can you do to beat the heat?

8 July 2024

Demystifying MS diets pt 2: What is a healthy MS diet?

We chew the fat with registered dietician Claire Fenlon (Chilterns Neuro Centre) about the importance of healthy eating with MS and explore the research behind MS diets.

4 July 2024

Advanced MS at 23 years old: my story

Jasmine lives with advanced MS at just 23 years old. Find out how she finds joy in the connections with her family, friends and healthcare professionals.

1 July 2024

Demystifying MS diets pt 1: the Wahls Protocol and Overcoming MS

We’re sinking our teeth into the world of MS and diet and digesting the facts in a two-part podcast series. First up, we tuck in to two of the most popular MS diets: The Wahls Protocol and the Overcoming MS diet and lifestyle.

27 June 2024

Rolling with it: MS and wheelchair Ju Jitsu

Determined not to tap out of exercise, wheelchair user Christopher discovered a form of Ju Jitsu that was just right. Find out how it improves his mental and physical health.

20 June 2024

Recalculating: MS and Tube troubles

Travelling by Tube isn’t always straightforward for people living with MS. Find out how Antoinette’s flexible mindset helps her journeys.

13 June 2024

Fighting for access to family life: being a full-time carer

Heather is now a full-time carer for her husband who lives with MS. Find out how they navigate inaccessible spaces, holidays and government support together.

10 June 2024

Young carers in MS – Oritsé Williams' story

Artist Oritsé Williams has been in the limelight since 2008. But long before the dazzling, bright lights of fame, Oritsé began his journey as a young carer for his mum, who was diagnosed with MS when he was 12 years old. Find out about the challenges that he and his siblings faced, his mother’s MS journey and why he’s passionate about supporting other young carers out there

28 May 2024

Yvonne talks about having MS and volunteering

Yvonne talks about having MS and volunteering for us

28 May 2024

Anna's volunteering experience with the MS Trust

Anna began volunteering with the MS Trust in 2023. Here she talks about how she was able to use her professional skills to make a difference in the service of others.

28 May 2024

Limbo land - what you can do while you wait for an MS diagnosis

Waiting for a potential multiple sclerosis diagnosis can be daunting. In this episode, we explore the "limbo land" time during your first appointments and a possible MS diagnosis. We discuss the roles of neurologists and the tests you might go through. Plus, we cover some top tips for preparing for each appointment and what to do next.

21 May 2024

MS bladder issues: the power of talking

Battling MS bladder issues, Heather sought support from the MS community. Find out how opening up to others changed her perspective.