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.

3 May 2020

Being diagnosed with MS during lockdown

Receiving a diagnosis of MS is never easy. But being told you have MS in these extraordinary times could mean a whole new level of uncertainty and worry to deal with. We hear the experiences of people who have been diagnosed with MS during lockdown, and share some tips to help.

30 April 2020

Preliminary research on Covid-19 in people with MS in Italy offers some reassurance

People with multiple sclerosis who contracted Covid-19 did no worse than the general population according to preliminary results from Italy.

30 April 2020

Mental health and MS: An emotional balancing act

In his latest blog on mental health and MS, Will Berard writes about how MS can affect your balance emotionally, as well as physically.

29 April 2020

Why I'm supporting the MS Trust's Emergency Appeal

In these uncertain times, people with MS need us more than ever. And we need your support to ensure we can continue to provide the vital services people like Carla rely on. MS doesn't stop, and neither will we.

28 April 2020

Mental health and MS: Dealing with my Black Dog

In his latest blog on MS and mental health, Will Berard writes candidly about the impact depression has had on him, and why we need to get better at recognising depression as a symptom of MS, and not just "because MS is a bummer. Man"

28 April 2020

I have challenged myself to walk 150 miles throughout the month of May

Holly shares why she is taking on her Miles for MS challenge to support the MS Trust.

23 April 2020

Mental health and MS: Managing anxiety

In the second blog of a new series focusing on mental health and MS, Will Berard writes about his experience of managing anxiety.

21 April 2020

Dealing with MS as a family

The emotional impact of an MS diagnosis can be hard to deal with for the whole family. The Bunby’s (Natasha, Marc, Deon and London) tell us about the ups and downs of living with MS, how they support each other and their advice for other families.

21 April 2020

How a sailing adventure inspired Robert Munns to get others with MS out on the water

An epic sailing adventure gave Robert Munns “a new perspective on life” and inspired him to help other people with MS experience the joy of sailing too. This is his story.

21 April 2020

Mental health and MS: Understanding your mind

Will Berard is a stand-up comedian who lives with MS. In the first of a new series of blogs on mental health and MS, Will urges us all to value our mental health as much as our physical health.

21 April 2020

"I am jumping for joy with all the happiness it has brought"

Julie Stevens - AKA Jumping Jules - turned to poetry to help her make sense of MS and, over 100 poems later, she says it has brought her incredible happiness. Here she tells us about her MS journey and her dream to publish her own book of poems.

20 April 2020

Why I'm raising awareness of MS and mental health

When former professional cricketer Chris Paget was told he had MS in 2017, he didn’t know which way to turn. Feeling isolated and alone, he spiralled into depression, refusing to open up even to the people closest to him. Thanks to the love and support of his family and friends, Chris was able to emerge from the darkness and today, three years later, he says he’s “never felt stronger”. It’s been quite the journey to get to this point and one that’s inspired Chris to launch Milestone, a new initiative to help normalise the conversation around mental health. We caught up with Chris to find out more.