Society Logo
ME/CFS Australia Ltd
Please click here to donate ME/CFS Australia (SA) Inc

Registered Charity 3104


Mailing address:
PO Box 322,
Modbury North,
South Australia 5092

Suite 506,
North Terrace House,
19 North Terrace,
Hackney, SA, 5069

1300 128 339

Office Hours:
Wednesdays, 11am-3pm

ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.


ME/CFS Australia (SA) Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.


Printer-friendly version

Research Update
1: Introduction
2: Psychological or organic?
3: Digestive problems
4: Diversity in CFS
5: Fatty acids
6: Conclusion

Talking Point
June 2001
In this issue:

Vice-President’s Report
Pesticide Blues
Was it something you ate?
Research Update
Medical Seminar (Aug 25)
Support Groups

An update on ME/CFS research at the University of Newcastle

Summary of lecture delivered May 12

By Dr Hugh Dunstan

Dr Hugh Dunstan spoke at a public meeting on May 12, 2001, at Urrbrae Education Centre


What I would like to talk about today are new advances in CFS research in symptom presentation, homeostasis and the host response in the body, and a new way of thinking about the disease entity in terms of common aspects that occur in the majority of patients. This leads to concepts of nutrient support and effective patient management. I would like to finish by presenting some concepts of evolution and infection.


Many of the core symptoms of CFS, like fatigue and muscle pain, are non-specific in nature, indicating a generalised host response to pathogenic challenge. While these symptoms are associated with an infection, none are useful in characterising a disorder. The definition of CFS is one of exclusion, but there are many general features of this host response system that are relevant to CFS patients.

In our work with multivariate statistics, we look at the whole range of symptoms and try to group people in terms of complex symptom profiles. A graphic analysis of this data shows the controls all clustered together. The CFS patients with fatigue only can be separated, but specifically those patients with fatigue and pain can be very well separated. Different symptoms can be grouped to reduce the amount of information to help construct a clinical management program for the patient.

Next: Psychological or organic? Next
Previous Previous Page