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.

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

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.

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”.

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.

10 October 2019

Can standing frames improve mobility in progressive MS?

This study set out to assess improvements in mobility from using a standing frame at home for people with progressive MS.

6 October 2019

Gemma's story - "All I remember him saying were the words ‘MS in your brain’ "

Gemma was diagnosed with MS in June 2019. Here she writes about how her world was turned upside down in just two short weeks.

2 October 2019

Sophia's story - "I always try to look to the positives"

Sophia Roth was diagnosed with MS in 2015.

2 October 2019

MS nurse takes on 2020 London Marathon to raise money for the MS Trust

MS Clinical Nurse Specialist, Gail Shore, has decided to take on the Virgin Money London Marathon in 2020 to raise money for the MS Trust. Despite being apprehensive (she has not run more than 10k), she explains why she is taking on this iconic event to help the MS Trust to continue to support other MS health professionals and those living with MS today.

29 September 2019

Changing your life one step at a time

Stuart Mold and Debbie Simpson took part in our China trek, and Stuart writes about their incredible adventure.

16 September 2019

Stuck with my MS like glue

In his latest blog post MS blogger Martin Baum, talks about his recent experiences with foot drop.