Diagnosis
The Canadian ME/CFS Clinical Case Definition and Guidelines for Medical Practitioners (Overview) provides a comprehensive breakdown of the symptoms, diagnosis and management of ME/CFS. While aimed at medical practitioners, it is also of great value to people who have ME/CFS, assisting with a greater understanding of the condition.
Diagnosis of ME/CFS
Diagnosis is based on:
- Physical examination;
- The type, pattern and severity of symptoms;
- The history and length of illness; and
- Laboratory and other tests.
A medical practitioner will carry out routine laboratory tests and, following assessment of the person's symptoms, case history, physical examination and his/her test results, may request a number of additional laboratory tests and investigative procedures, depending on the individual's specific illness profile.
Although there is no specific test available yet to diagnose ME/CFS, routine laboratory and other investigations are important to eliminate other diseases that have symptoms in common with ME/CFS. Abnormalities may be found in a number of non-routine tests and, in some circumstances, may be of diagnostic assistance. Some non-routine tests are showing promise as potential diagnostic tools.
A diagnosis of ME/CFS will involve a number of visits to the diagnosing practitioner over a period of time. The diagnosing practitioner is usually able to make the diagnosis, although in individual cases the practitioner may refer the person to a specialist.
For a positive diagnosis of ME/CFS to be made, symptoms need to correspond with a Case Definition of ME/CFS and to have been present for at least six months, although a diagnosis may be made after three for children. Excluding other illnesses is an important part of the diagnostic process.
It is not uncommon for people with ME/CFS to consult a number of doctors before receiving a diagnosis of ME/CFS because some practitioners are unfamiliar with ME/CFS. In these circumstances a clear diagnosis can be a relief for the person with ME/CFS as it removes the uncertainty and allows the person to focus on treatment and illness management.
For more information on the diagnostic procedure for ME/CFS, refer to the following pages of the Canadian Guidelines (Overview):
- Clinical evaluation of ME/CFS, pages 7-8;
- Routine tests, pages 8-9; and
- Non-routine tests for abnormalities in ME/CFS, page 18.
News
![]()
Dr. Byron Hyde in Australia
Dr. Byron Hyde will be visiting Australia in September 2010 to make presentations on ME and CFS in …
Read more![]()
XMRV virus and related virus 'MLV' confirmed in CFS
Researchers have found murine leukemia viruses (MLV) related gene sequences in blood samples …
Read more![]()
'Exploring ME/CFS' on ABC national radio, 'Nightlife' with Tony Delroy, Aug 23
'Exploring ME/CFS' was the topic of a national radio interview on Tony Delroy's ABC 'Nightlife' …
Read moreDid you know?
As many as 180,000 Australians are directly affected by ME/CFS
Research
Research into ME/CFS is occuring across the globe. Follow the links below for research resources.
Alison Hunter Memorial Foundation
Australian Research Institutions
International Research Institutions
Support Organisations by State
ME/CFS Australia directs enquiries from members of the community about frontline support for people with ME/CFS to independently run state organisations.
Resources
Nutrition and ME/CFS: Download a PDF, available in the following languages:
Chinese(717 kb)Croatian(880 kb)Dutch(680 kb)French(740 kb)German(865 kb)Greek(821 kb)Italian(735 kb)Spanish(679 kb)Vietnamese(741 kb)
