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.

27 May 2020

Sew-cially distanced fundraising ideas

Over a discussion on the MS Trust Community Facebook group, we discovered that MS Trust supporters Anne (from the North East) and Anna (from London) have been spending their time in lockdown creating beautiful face masks for friends in their area. We were even more thrilled to hear that they had made this into a great socially-distanced fundraising opportunity, exchanging the masks for donations to the MS Trust. Here, Anne and Anna share why they decided to get creative for the MS Trust…

18 May 2020

MS inspired me to write supernatural thrillers

From poetry to photography, many people find a creative outlet can help them make sense of MS. Emma Warhurst, diagnosed with MS five years ago, writes supernatural thrillers and uses her MS symptoms as inspiration! She shares her story.

18 May 2020

How mindfulness has helped me to be kinder to myself

Studies have shown that practicing mindfulness can have benefits for people with MS, helping with symptoms like pain, stress, anxiety and depression, as well as general quality of life. Here, Helen Petley, writes about her experiences of mindfulness, how it's helped her to be kinder to herself and the new group she's set up to help others with MS practice mindfulness during the Covid-19 pandemic.

11 May 2020

Should I be preparing now in case I catch coronavirus?

Should I be preparing now in case I catch coronavirus? How to be as resilient and ready to fight off infection. Helpful advice from Megan Roberts, MS Nurse and Head of the HP programme.

5 May 2020

Taking on their own 10k

Siblings Helen and Ian share why they are still supporting the MS Trust despite the cancelation of their running event.

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.