Setting Priorities Together

Our peer researchers sharing the stories. You can read them here.

Over the past month, we ran two workshops, one in London and one in Bradford, to shape the next stage of our co-design work on inequalities in MS care. Each brought together people living with MS, our peer researchers, clinicians, MS nurses, charity staff and information providers.

The peer researchers opened each session by reading stories developed from the research. This was a powerful way to bring the data to life. These personal accounts helped frame the group discussions that followed, focused on identifying areas where change is most needed and most possible.

Together, we mapped out priorities and began to consider what kind of action might be needed, whether that’s new information resources, service adaptations, or advocacy work.

We’re now drawing together insights from both sessions to take forward into the next phase of co-design. Thank you to everyone who joined us and shared their time and experience.