Multiple Sclerosis (MS) is a long-term health condition affecting over 130,000 people in the UK.

The experience of living with MS from the perspective of a person from a minoritised ethnic group is not well understood. These groups are poorly represented in all aspects of MS research conduct and planning.

We plan to tackle this by having people from these groups help lead our research. This way, we can better understand and focus on what matters most to them.