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.

Yvonne Pettigrew, diagnosed with primary progressive MS (PPMS) in 2013, shares her experience of living with PPMS and reacts to the "exciting" news that Ocrevus has been approved by NICE for NHS treatment of early, inflammatory PPMS.

"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.

At the MS Trust we offer a range of benefits to our staff, including hybrid working options, a company pension, Employee Assistance Programme (EAP) and much more.

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