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.

15 July 2020

"I want to share my story in the hope that it will help people"

Two years after her mum was diagnosed with MS, Sian Spence received the same diagnosis. Here, Sian shares her journey and what's she learnt along the way.

14 July 2020

I adore 'the Proclaimers' and 500 miles was a fitting tribute to them

Back in May, Kate completed her Miles for MS challenge by cycling 500 miles over the month. Here she shares why she took part and how she hasn’t stopped cycling since!

9 July 2020

People with neurological conditions are missing out on vital treatment and support during the pandemic

People living with neurological conditions like MS are missing out on vital treatment and support as a result of the COVID-19 pandemic, according to a recent survey by the Neurological Alliance.

2 July 2020

Letisha's diagnosis story

Letisha Charles-Thomas received her diagnosis of MS (multiple sclerosis) in May 2019 after numerous appointments and tests.

1 July 2020

MS was my wake-up call to start living life to the full

Lauren was diagnosed with MS in June last year. Here she shares how MS was the wake-up call she needed to start living life to the full - and to write her first book!

28 June 2020

Round-up of research on coronavirus, Covid-19 and multiple sclerosis

A round-up of coronavirus and multiple sclerosis research.

22 June 2020

We are planning to make it an annual event!

Claire took part in Miles for MS this May to raise money for the MS Trust. Here she shares why her team 'the Movers & Shakers' got involved to support the MS Trust.

18 June 2020

MS Trust to team up with McClure Solicitors for estate planning live talk

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.

15 June 2020

David's Diary: Supporting the 'forgotten many'

Are people living with Secondary Progressive MS being forgotten? Yes, says a new report. MS Trust CEO David Martin, who was involved in putting together the report, writes about what must be done to help the 'forgotten many'.

14 June 2020

My fear of returning to a 'new normal'

As the lockdown restrictions begin to lift, and some kind of normality slowly resumes, many people may be feeling anxious and uncertain about life after lockdown. Here, blogger Elaine, who is one of the 2.5 million 'extremely vulnerable' people who have been asked to shield, writes about the apprehension she is currently feeling.

11 June 2020

The World of Now: Health and safety in a time of shielding

Over 2 million people in the UK are currently shielding from COVID-19. A small number of people with MS are considered extremely vulnerable and are part of this group. Here, Kate Swinburn shares a poem she's written about her experience of shielding and life under lockdown.

3 June 2020

How my MS experience shaped my research career

Hannah Morris-Bankole, researcher and PhD student at University of Reading, talks about psychological support in the early days following a diagnosis of MS. Multiple sclerosis and mental health issues. Newly diagnosed people may not know what they are entitled to and where to turn for help.