The Research Network is a group of people affected by MS who are helping to shape our research programme.
They make sure that the research the Society funds reflects the needs and interests of people living with MS, and helps us communicate research in a way that’s accessible to everyone affected by MS.
Activities might include reviewing research applications, meeting researchers and taking part in a research panel or steering group.
"I believe the research community should know that we have a part to play in what they do and that our opinion matters".
Any questions? Email firstname.lastname@example.org or call 020 8438 0718 for more details.
Read members' experiences of involvement within the Research Network and the impact this has made.