This is a place for young Australians suffering from ME (and ME equivalent CFS) to connect with eachother, and to discuss issues that uniquely affect young people living with this disease in this country.

Feel free to discuss anything in relation to your experience with this illness, especially that relating to -
-dealing with your diagnosis and prognosis
-school/TAFE/university/other study and work
-family and friends
-management and day to day life
-symptoms
-activism and advocacy
-test results and pathology
-treatment and medications
-diet
-Disability Support Pension (DSP) and dealing with Centrelink
-And anything else you feel is relevant!

Know any other young Australian's on MySpace with ME? Send them an invite!