Please see this ‘Patient and Public Involvement’ poster.
PPI is now mandated for all medical research that affects patients. If you’d like to help, please get in touch with Dr Fiona Pearce to share your views on the topic. Dr Pearce needs to engage with a small group of people with rare autoimmune rheumatic diseases (of which Behçet’s is part) who would like to contribute to her research, by influencing the research questions, methods, interpretation and communication of results.