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.

14 November 2019

Why I'm marking my MS anniversary by fundraising for the MS Trust

To mark the one year anniversary of her MS diagnosis, our supporter Lauren Walsh has enlisted 30 friends and family members to fundraise for the MS Trust in all sorts of different way ways, from gin and yoga nights to mountain climbing! Here, Lauren shares her MS story and her reasons for fundraising for the MS Trust.

12 November 2019

Sleep problems in MS

It's thought that sleep disturbances are experienced by around half of people with MS. We speak to consultant neurologist Dr Kirstie Anderson, who has a special interest in sleep problems. Here she talks about which sleep disorders are more common in MS and shares her tips for getting a better night's sleep.

12 November 2019

Susan's story - My nurse gave me hope that I can actually have a life

Susan was diagnosed with secondary progressive MS aged 51, here she talks about the positive impact her MS nurse has had on her wellbeing.

12 November 2019

MS Trust launches new campaign highlighting the vital need for more MS specialist nurses

Today the MS Trust launches its #FairMSCare campaign, aimed at raising awareness of the vital need for more multiple sclerosis specialist nurses across the UK.

1 November 2019

Why I’m releasing a charity Christmas song for the MS Trust

Ruth Green is a singer from Letchworth Garden City and supporter of the MS Trust. This Christmas she will be releasing a song, Share Christmas with Someone, with all the money raised going towards our work supporting everyone affected by MS. This is Ruth’s story.

30 October 2019

MRI reveals smouldering MS lesions

This study used new MRI techniques to visualise smouldering lesions, to see how they change over time and how they are linked with different types and stages of MS.

30 October 2019

"It is my chance to give back!"

Fundraising for the MS Trust isn't just about skydiving or taking on a marathon, there are lots of different ways you can support our work making sure a life with MS isn't a life defined by MS. Take our fantastic supporter Beth, who will be holding a Be Bold in Blue quiz and charity raffle at her local pub. Here she writes about her MS diagnosis, dealing with the fear of the unknown, and why she wants to give something back to the MS Trust.

28 October 2019

Meet Mr and Mrs Monkey Sox

James and Lianne Carvell were inspired to set up Monkey Sox, a community interest company raising funds and awareness for multiple sclerosis, following James’ diagnosis in 2016. We caught up with the husband and wife team to chat about James’ journey with MS, the importance of raising awareness, and how Monkey Sox has given the couple a new way “to think and feel about MS”.

28 October 2019

The MS that tried to steal Christmas

Along with the mince pies, mulled wine and general merriment, Christmas can also bring with it rather a lot of stress, particularly when you’re dealing with the unpredictability of MS. In her latest column, Emily – AKA The Wibbly Dinosaur – reveals her top tips for surviving the festive season.

28 October 2019

I play underwater rugby for Team GB

Did the Rugby World Cup have you hooked this autumn? Well, did you know there’s an underwater version of the game? Jo Wood, diagnosed with MS in 2013, plays for the Great Britain team and competed at the Underwater Rugby World Championships earlier this year. “I came back with a new resilience and realisation that I have MS, but MS doesn’t have to have me,” Jo tells us.

22 October 2019

Focus on: sleep problems in MS

Consultant neurologist, Dr Kirstie Anderson, talks about which sleep disorders are more common in MS and shares her tips for getting a better night’s sleep.

21 October 2019

Ask the expert: Disease modifying drugs

There are now 14 disease modifying drugs (DMDs) being used to treat MS in the UK with more in the pipeline. With such a wide range of drugs available, finding one that’s right for you and your MS can be a challenge.To answer some frequently asked questions about DMDs we spoke to MS nurse advisor, Nikki Embrey who sheds light on how you know whether a DMD is working and talks about some of the side effects people worry about most.