How to take part in ME/CFS research
Registers and biobanks make research possible. Here is what they are, how access works, and how patients contribute.
A comprehensive, open-access medical documentation of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome — a severe, chronic, multi-system neuroimmune disease affecting an estimated 0.89–2.5% of the global population.
A structured reference work spanning five parts, with an epistemic classification system (achievements, hypotheses, speculations, predictions, warnings, recommendations). Available as a navigable website and downloadable PDF.
Use the sidebar to browse chapters and sections. Each page has its own table of contents. Use the accordion below to open each part, then the carousel to browse the chapters it contains and see what each one covers.
Short, accessible articles exploring specific ME/CFS topics — mechanisms, treatment reasoning, and patient-facing explanations.