ME/CFS is poorly understood, including by medical practitioners. It often falls upon sufferers themselves to undertake research into treatment and support. The Web is already overflowing with information, and navigating through it to find what is current can be extremely tiring. We have brought together links to what we consider to be the most user-friendly and accessible ME/CFS resources available, providing up-to-date information about research, treatment protocols and online support groups.

• Research

• Treatment protocols

• Online support groups

• National support organizations

• Member-contributed resources