Thank you for visiting.
We provide support and information for people affected by Myalgic Encephalomyelitis (ME) /Chronic Fatigue Syndrome (CFS) and Fibromyalgia Syndrome (FMS) in the Canberra region.
ACT ME/Chronic Fatigue Syndrome Society is a not for profit, self help organisation which provides support services such as monthly support group meetings, a self help course and Telephone Information and Support Service (TISS). We provide information about ME/CFS and FMS to members, medical practitioners and the public. We also raise funds for research into ME/CFS and hold information sessions and events to raise awareness in the ACT region. If you think you could benefit from any of our services please get in touch.
ACT ME/Chronic Fatigue Syndrome Society does not provide counselling services or either systemic or individual advocacy.
The Support Group generally meets on the first Tuesday of the month at the Pearce Community Centre. Meetings are informative, interactive sessions usually led by a guest speaker. As well, there is time for a friendly chat over a cup of tea or coffee.
Adults of any age with an interest in ME/Chronic Fatigue Syndrome and/or fibromyalgia are welcome.
Tuesday 1 August 2017 @ 12:45pm
Making the most of your visit to the GP
*Preparation *At the surgery *After the visit
Speaker: Claudia Cresswell
Project Officer, Health Literacy Program
Health Care Consumers' Association
Time: 12:45pm for a 1:00pm start - finish 2:00pm
Venue: Large meeting room, Building 1
Pearce Community Centre, Pearce
Tea and coffee provided
For more information please email or phone 6290 1984.
Support Group meetings are not held in December or January.
♦ Breakthrough in ME/Chronic Fatigue Syndrome Testing
♦ Institute of Medicine (IOM) Report
♦ International Consensus Primer for Medical Practitioners (ICP)
♦Carer Gateway - national online and phone service for carers