Sarah lives with MS and shares her experience of living with long term pain, discussing management techniques to help with the psychological impact long term pain can have.

The Is MS care fair? report found that while almost 80% of people with relapsing remitting MS had seen their neurologist and MS specialist nurse in the past year, around 40% of people with progressive MS hadn’t seen either of these key health professionals. 12% of people with progressive MS reported receiving no specialist support at all in the last year.

Since being diagnosed with MS, Tim has run the London Marathon in support of MS Trust twice. He tells us why he runs and why he believes it’s important to support our work.

Andy Merry, a Yeoman Warder at the Tower of London, tells us about his mission to scale Mont Blanc and raise £60,000 for MS Trust and The Royal Marines Charity.

Paralympic champion Kadeena Cox, who was diagnosed with MS in 2014, talks sport, MS and the people who inspire her.

We all know how important it is to get a good night’s sleep, especially if you suffer from fatigue. But if you wake several times during the night needing to get up for a wee, having a full night's sleep is really difficult. In this blog Helena from the MS Trust's information and engagement team explains what nocturia is and what you can do to to help with it

After an MS diagnosis you’re bound to have worries about how the condition might impact your independence and freedom: will you still be able to do those ‘normal’ everyday things you always have done? One of the most common questions that our information team gets asked is: ‘Can I still drive?’ For most people with MS the answer is ‘Yes’, but there are some things you need to be aware of

Neve she shares her experience of being diagnosed with multiple sclerosis aged 17, telling family and friends, life at school, and the transition from child to adult MS services in the NHS.

Sometimes MS can feel like a barrier to our relationships, making it harder to maintain the ones that matter or develop new ones. In this episode we talk about these issues with Billy from Shift.ms, who lives with MS himself, and Flora from our helpline.