London can feel like a daunting place to travel but since Caroline started using a walking stick she has found people to be more understanding. Although this piece focuses on travel around London, the experience and advice within can be applied to travelling around any major UK city.

Pain in MS can come in many different forms. Burning, throbbing, aching, stabbing, numbness and crawling are just some of the many ways that people with MS describe it. To shed some light on how pain is managed in MS, we put some of your questions to consultant nurse in pain management, Sue Barnes.

Treatment for MS may include medication, therapies, such as physiotherapy, and self-management techniques. Some people explore the use of complementary or alternative medicines (CAMs). Please consult with your neurologist, MS nurse or GP about the best treatments for you.

MS Trust responds to proposed changes to the benefits structure in England and Wales.

In this blog, Claire discusses the value of health comics and how she hopes her comic – Through the MS Looking Glass: Navigating the Unseen – will increase understanding and raise awareness of the hidden symptoms of MS.

We look at the government's proposals for reforming disability benefits, including Personal Independence Payment (PIP) and Universal Credit. Find out what it could mean and how you can have your say.

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Stephen Hodges has been supporting the MS Trust through fundraising and volunteering since 2013. Here, he tells us a bit about his experience

A US study has found that walking function is worse in Black people with MS.