Read more about the latest developments in MS research, treatments and specialist care, plus the latest updates on our work and the efforts of our amazing supporters
The MS Trust sends out a weekly news alert which includes the latest updates from the MS Trust, latest news, blogs and a news feed from MS in the Media.
Read our latest news
Spencer Bull was the vice-captain of the GB squad at last month’s Invictus Games. Here the British Army Lieutenant Colonel talks to us about “taking back control” following an MS diagnosis.
What do you do when the disease modifying drug (DMD) you've chosen isn't working? In this guest blog, Lauren shares her thoughts around choosing an MS treatment and what it is like having to change to a new one.
The Scottish Medicines Consortium (SMC) has decided that fampridine (Fampyra) will not be made available on the NHS in Scotland for people with MS-related walking problems.
Kate guest blogs about her experiences taking part in a clinical trial for the drug bexarotene.
- The effect of pregnancy on MS
- Ocrevus for PPMS decision paused
- Coexisting conditions affect atrophy
- Medical cannabis rule change in Jersey
Spasticity and spasms are a common symptom of MS and can have a big impact on your daily life. To find out how they can be successfully treated and managed, we put some of your questions to physiotherapist, Katrina Buchanan.
25 years ago, the MS Trust was founded on Christmas card sales and they still play a crucial role today in enabling us to support everyone affected by MS.
When MS Trust supporter Tim Sorrell signed up to his first parkrun, somewhat reluctantly, he could never have imagined the positive difference it would make to his life. He explains what makes it so special.
Since the first event back in 2004, parkrun has grown into something of a national phenomenon, with hundreds of thousands of people taking part every Saturday, come rain or shine. Now parkrun wants more people with disabilities and long-term health conditions to get involved, be it through running, wheeling, walking or volunteering. Katherine Goulder is one of parkrun’s Outreach Ambassadors for MS. Here she tells us how parkrun very quickly became part of her own Saturday routine and why others with MS should get involved too.
Radio 1 DJ Scott Mills, whose mum has MS, recently presented our BBC Lifeline Appeal. Here he tells us how his family have adapted to his mum’s MS diagnosis, the importance of speaking out about MS, and why his mum is his biggest inspiration.
From 1 November, specialist clinicains will be able to legally prescribe cannabis-derived medicinal products to patients with exceptional clinical need.
A new report published this week by the MS Trust finds that many MS specialist nurses are routinely managing more patients than the recommended caseload. As a result, people with MS are missing out on the vital care and support they need and deserve.
From 1 November, medicinal cannabis can be prescribed by specialist doctors. We look at what is meant by medicinal cannabis, how legislation is changing and what this means for people with MS.
NICE has announced that it is pausing the publication of final guidance on ocrelizumab for PPMS while further discussions take place between drug company and NHS England.
Car enthusiast Nico has organised a rather unique driving challenge to raise funds for the MS Trust. Here he tells us what the challenge involves, the inspiration behind it, and how you can sign up.
What causes MS? This is something we yet don't know, but there are a lot of theories out there. In this blog guest blogger Emily, takes us through some of them.
- MS-SMART trail unsuccessful
- People with progressive MS need early support
- PIP rules protest
- Is cannabis effective?
- The role of vitamin D unclear
- Pregabalin and gabapentin restrictions
- Statue by sculptor with MS unveiled
- More MS risk genes identified
- Gut enzyme potentially linked to MS
Back in September, a group of friends took on a gruelling canoe challenge in the Lake District, raising nearly £4,000 to support the MS Trust's vital work. Here, supporter Caroline Horton writes about the inspiration behind the challenge and the sense of achievement she felt after completing it.
Choosing a disease modifying drug (DMD) is an individual decision and it can be important to weigh up your options and think about what might work best for you. In this guest blog, Toni shares her experiences of choosing an MS treatment and explains what it was like to start on Plegridy.