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MS Trust staff, MS health professionals and people with MS offer their perspectives on hot topics in the world of MS
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Former Royal Marine Andy Merry works as a Yeoman Warder at the Tower of London. He was diagnosed with MS last year and has since raised over £27,000 to support the work of the MS Trust by climbing the highest mountain in the Alps. We caught up with Andy just after he returned from his challenge in June to ask him about his experience of climbing Mont Blanc for MS.
MS health professionals are invited to enter or nominate colleagues in the third annual QuDoS in MS recognition programme.
The MS Trust’s first fundraiser with The October Club took place on Friday (July 27), raising over £25,000 for people with advanced MS.
When Kimberley was diagnosed with MS in February, she was scared to open up about the condition. But then a few months later, on World MS Day, she decided to ‘come out’ about her MS in a rather public way – and was overwhelmed by the support she received from friends and strangers alike.
A night of celebration with Towersey Morris who have raised almost £13,000 to help people with MS.
Interested in organisations or tools that help you make your world more adaptable? Denise suggests three of her favourites
First Susan in Neighbours, then Nancy in Hollyoaks and now Johnny in Coronation Street: a series of soap characters have been diagnosed with MS. But is this a good way of raising awareness, or an unhelpful misrepresentation? We asked people on social media for their views.
More and more people with MS are signing up to Pilates classes to improve both their physical and emotional wellbeing. Open Door went along to a class at the MS Therapy Centre in Norwich to find out why this type of exercise is proving so popular among the MS community and to meet some of the men and women reaping the rewards
Since Mental Health Awareness Week took place back in May, we’ve received a number of questions about how MS can affect your mental health and how you can manage these challenges more effectively. We put your questions to consultant neuropsychologist Jo Johnson
Relationships are full of ups and downs – it’s a fact of life. But when your partner has a long-term health condition like MS, there may be some extra bumps in the road for you both to navigate. Here are a few ways you can support your loved one along the way
When Denise Stephens was diagnosed with MS at the age of 24, she was disappointed to find that a lot of equipment recommended to her made her feel like she was “living in a hospital”. Determined to find things that worked for her, and share her discoveries with others, she founded Enabled by Design, a community of people passionate about design for all
- Access to disease modifying drugs
- The cost of MS
- Protecting cognitive reserve
- Diet and childhood MS
- Vitamin D and bone health
- Depression risk factors
After deciding to move on from running an accessible holiday centre, David Tucker started to experience many 'strange' symptoms. Five years later he was diagnosed with MS. Here David reflects on the journey he's been on and shares his hopes for the future.
- EMA restricts use of Zinbryta
- Kadeena Cox interview
- Breastfeeding, menstruation and risk of MS
A year on from his London to Paris cycle ride, Dave Evans reflects on the life-changing experience of cycling 300 miles alongside 40 other MS Trust supporters.
When Carla was diagnosed with MS in 2008, she felt like she’d lost control of her “body and future.” Here she explains how the Kubler-Ross Curve helped her come to terms with her MS diagnosis and to stay positive.
Alex did a presentation at her school assembly during MS Awareness Week to help her fellow students understand more about MS.
Christina McDonald was diagnosed with MS last November, just a few weeks before her 27th birthday. Here Christina tells us about the different emotions she’s experienced in the past few months and how she’s learnt to accept and process her diagnosis.