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.
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During the month of May, over 100 people walked, ran, swam, jogged, rowed, arm cycled, wheeled and more as part of Miles for MS. We find out why they wanted to get involved and how exercise has helped them live well with MS.
It’s that time of year when everyone is jetting off on holiday, but when you have MS there’s often a bit more planning involved before you can pack up your suitcase and head to the beach. Where can you find accessible accommodation and attractions? How do you organise travel insurance? What are the rules around travelling with medication? These are just some of the many questions you may face. So whether you’re planning a holiday overseas or a last minute trip somewhere in the UK, this article goes through a few key things to think about in advance.
“I want to encourage people who are not confident in the kitchen to stick on that apron and get cooking” James Coke, diagnosed with MS over 20 years ago, tells us about the inspiration behind his blog The Disabled Chef and shares some top tips for cooking with a chronic condition.
If you have MS, it’s likely you’ve experienced that overwhelming feeling of tiredness or sudden lack of energy that defines MS fatigue. It’s one of the most common symptoms of MS and many people find that the heat can make it worse. So with temperatures rising and the 2018 summer scorcher in full swing, we put your questions on fatigue to occupational therapist, Kate HaywardIf you have MS, it’s likely you’ve experienced that overwhelming feeling of tiredness or sudden lack of energy that defines MS fatigue. It’s one of the most common symptoms of MS and many people find that the heat can make it worse. So with temperatures rising and the 2018 summer scorcher in full swing, we put your questions on fatigue to occupational therapist, Kate Hayward
Last summer, thanks to our incredible supporters, the first MS Trust-funded MS specialist nurses arrived at Leicester Hospitals. Since then, we’ve also helped to bring new nurses to Bradford and Lanarkshire, and soon Hull. Together, they’ve made a world of difference to thousands of people living with MS. We caught up with Leicester nurse Jon Maisey to find out about his first year in post, and Jenna Chudasama, to hear about the invaluable support he’s given her.
Having hidden her MS for a number of years, Lisa Murray-Lang decided to put pen to paper and write a book about her life with the condition as a way of letting others know. This is Lisa’s inspiring story.
Trust representatives were treated to a wonderful evening of Morris dancing with the Towersey Morris who have raised £720 for the Trust.
MS Trust supporter Kenny Smith is going to cycle around the UK for 50 consecutive days to celebrate what would have been his sister Kathleen’s 50th birthday.
In a new blog, a person with MS chronicles her journey taking part in a clinical trial for the drug bexarotene. In part three of Hellie's Clinical Trial Adventures, Hellie gets an MOT at the hospital and officially joins the trial.
In a new blog, a person with MS chronicles her journey taking part in a clinical trial. This is part one in which Hellie goes to the hospital for tests to see if she is eligible for the trial .
- Doctors should be allowed to prescribe medical cannabis
- Early warning signs of MS
- Iron levels in brain may predict future disability
When Diane Green was diagnosed with progressive MS, she thought her riding days were over. But now, 17 years later, Diane and her horse Winnie have their sights set on the Paralympics in 2020.
In a new blog, a person with MS chronicles her journey taking part in a clinical trial. This is part one in which Hellie spots a request for people to participate in a clinical trial.
Ian, diagnosed with primary progressive multiple sclerosis last August, tells us about his journey with MS and offers some advice for others in a similar situation.
The MS Trust is very disappointed that the Scottish Medicines Consortium is unable to recommend ocrelizumab as an NHS treatment for relapsing remitting MS.
Carole has been living with MS for 15 years. She tells us how channelling her creative side has helped her “see the good in things again”.
- Ocrelizumab not approved for PPMS
- Solvents, smoking and MS risk
- Air pollutants not linked to MS
- Cannabis review finds benefits