ME/CFS AUSTRALIA (SA) INC
Registered Charity 698
PO Box 28,
South Australia 5007
Closed while relocating
1300 128 339
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 the various research projects, diets, medications, therapies 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.
Research: ME/CFS people and Second Life
Monday 28 September 2009
We have a policy of supporting research into ME/CFS. We encourage members to be involved if they can.
The most recent contact we have had about research is from Dr Mike Kent from the School of Media Communication & Culture at Murdoch University. Dr Kent's current research is centred around Second Life, a user-created 3D virtual world community.
Dr Kent says:
I am writing seeking your help in a research project working with people with ME/CFS. Currently I am working with Dr Kirsty Best at Murdoch University on a project called "Isolation, illness and the Internet: Exploring the possibility of a second life for sufferers of ME". This project has been funded through a Discovery Grant from the Australian Research Council.
The project is exploring if the online virtual world of Second Life can be used to help ease the isolation experienced by people who have Chronic Fatigue Syndrome or Myalgic Encephalopathy by providing an alternate place to make and maintain social networks and also to seek out information about their condition.
If you are interested, Dr Kent can be contacted via email (firstname.lastname@example.org) or his mobile phone 0412 442 808.
blog comments powered by Disqus