The PRIME Project is a collaboration between patients, carers, researchers and service providers who share a commitment to improving our understanding of ME/CFS.
The PRIME project aims to provide people with a deeper understanding of what it is like to live with CFS/ME. We are achieving this aim by using 'evidence-based public and patient involvement' methods to enable patients to steer the research agenda.
- You are reading the About Us section of the site, which contains background information about the project, our aims and vision, the people involved and how things are managed.
- Visit the Research section if you are interested in finding out how we are conducting the research for the project (what methodology we're using, how we are interviewing people, how we surveyed the existing literature, why we're running workshops etc).
- Visit the Database section if you want to read the experiences of people living with CFS/ME or browse our list of themes relating to the condition.
View a PDF document of all the CFS/ME groups involved in the PRIME project