Science for ME

Welcome

A warm welcome to the Science for ME forum! We’re glad you found us.

Science for ME is an independent, patient-led, international forum for people with ME/CFS and the carers, clinicians, scientists and advocates who support us.

ME/CFS is a debilitating disease or group of diseases, often apparently triggered by an infection. A core feature is Post-Exertional Malaise, a reaction to exertion that results in an exacerbation of symptoms that include flu-like symptoms, fatigue, cognitive difficulties, muscle weakness and pain.

Our goal is to provide an international platform to discuss all aspects of ME/CFS, with a special focus on science, support, and advocacy.

ME/CFS has many names including Myalgic Encephalomyelitis (ME) and chronic fatigue syndrome (CFS). A number of specific post-infectious syndromes such as post-Covid-19 syndrome (Long Covid), Q fever-fatigue syndrome and post-Lyme disease, as well as Gulf War Illness, have similarities and may overlap with ME/CFS, and are served by the forum. There is also some coverage of other poorly understood and 'invisible' illnesses including fibromyalgia.

We value four things especially:
· high quality scientific research, which will be necessary to produce effective treatments;
· open, critical discussion of claims and ideas;
· mutual support and respect;
· equality.

To browse the forum, click here (link to the forum page).
To see a summary of recent news, click here
To become a member of the forum and access the Members Only part of the forum, click here