"On receiving the proposals designated to me for review, I recall feeling completely inadequate and unprepared to review studies relating to extremely complex pure science. I felt that I had nothing to contribute to the debate. When considering this in more depth, discussing it with other RN members and research team staff, I realised that the training we had received had in fact prepared me for the job I needed to do. The focus was not on reviewing the scientific detail, but rather to assess the relevance to people affected by MS and to review the research methodology.

The realisation that I, as a person with MS, had a perspective the researchers could not share, helped me feel an essential part of the process, and resulted in a very positive experience. Throughout the process I have found the research team extremely supportive, willing and able to offer guidance whenever it was needed. This has helped develop a team in which everyone feels valued.

As a person with MS I feel that the advent of the Research Network offers the Society a truly inclusive approach to the appraisal of grant applications, in which all views are considered to create a truly holistic vision."