People with MS sometimes face legal problems in work, housing or access to services. These organisations can help you understand your rights and find ways to resolve these problems.

Read Amanda's practical tips for travelling on public transport when you live with MS. Find out how she plans trips and makes use of technology along the way.

"I would advise anyone in a similar situation to me to advocate for yourself.” For LGBTQ+ history month Victoria shares her MS diagnosis and treatment journey as a member of the LGBTQ+ community.

Antoinette takes her powered wheelchair for a trip across London. But will the journey be truly accessible? Read on to find out more.

Researchers in Sweden show evidence that a diet rich in fish and fish oils can reduce MS progression.

The MS Trust is committed to ensuring everyone with MS can access the treatments and services they need and deserve. We aim to represent and reach all people affected by MS. Find out more about equality, diversity and inclusion (EDI) at the MS Trust.

Find out how donating to the MS Trust helps us to support people with multiple sclerosis by providing information and supporting MS specialists.

Finding that the pattern of your MS is changing from relapsing remitting to secondary progressive can be a distressing experience. Many people report that it feels like being diagnosed with MS all over again. How can we improve the support available to people going through transition? Two years ago we commissioned a team of researchers at Cardiff University to explore people’s experiences and look at ways support could be improved. Dr Freya Davies explains what they found out.

The JC virus is a common infection unrelated to MS. Some MS drugs can weaken your ability to keep JC virus under control, which can lead to a rare but serious brain infection known as PML.