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.

21 January 2020

Thanks to MS, I'm learning to ride!

Alison Chubb was diagnosed with primary progressive MS in 2006. Despite the challenges her MS brings, last summer Alison competed in Riding for the Disabled’s prestigious National Championships. Here she talks about how she’s following her horse riding dream and learning to make the most of every opportunity that comes her way.

15 January 2020

Why I wanted to become a Friend of the MS Trust

Sam Bromfield is our Friend of the MS Trust in Norfolk. Here she tells us why she wanted to get involved and why she'd encourage others to become part of our Friends network too.

8 January 2020

Effect of vitamin D supplements on MS activity

Two research studies assessed the effect of high doses of vitamin D on relapses and brain lesions.

24 December 2019

Mission 100 is back for 2020!

Wesley Thompson tells us about his Mission 100 challenge and why he signed up to support the MS Trust.

18 December 2019

Christmas presence not presents

MS blogger Martin Baum was diagnosed with MS nearly forty years ago. Here he reflects on the impact his diagnosis has had on the festive period over the years.

13 December 2019

An MS diagnosis inspired me to set up my own business

An MS diagnosis back in September turned out to be the 'push' Samantha Cooper needed to start her own dream business. "Like everybody with MS, I have no idea what my future with the condition looks like but I hope to keep a positive mindset and overcome it the best way that I can," she tells us.

9 December 2019

Tysabri: reducing the risk of PML with extended interval dosing

This research compared the risk of PML on Tysabri (natalizumab) extended interval dosing with standard interval dosing.

2 December 2019

The pulling power of MS

People with MS report such a wide range of symptoms, that it's unlikely that any two people will have the same experience. In his latest blog, Martin Baum talks about a lesser known symptom, where it feels like he is being forcefully pulled backwards.

27 November 2019

"I can’t remember what a healthy body feels like, but that’s ok, because I love my body and all it can still do"

When Evie was diagnosed with MS aged just 16, she felt "shock, grief and uncertainty". But, 10 years later, she feels determined to deal with whatever MS throws at her. Evie has decided to share her story to raise awareness and help others going through something similar.

20 November 2019

BMA award honours for MS Trust resources

We’re delighted that a number of MS Trust resources have been recognised at the 2019 British Medical Association Awards.

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.