Advocacy & Action
We are a group of advocates for people with the neurological disease Myalgic Encephalomyelitis (ME). Our aim is to encourage the use of robust scientific research methods and objective scientific diagnosis to end the false debate that ME is a fatigue disorder that is treatable with CBT and GET. To help foster a research community that has funding and the desire to undertake high quality scientific research into ME. To further expand the knowledge of scientists and clinicians by suggesting scientific research that should be undertaken. To empower the ME community through science education on symptomology, diagnosis and research analysis. And to bring about effective treatments and work toward a cure.