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The
ACT Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Society
The Society exists to give support and help to people with ME/CFS, provide
information about ME/CFS, Fibromyalgia and related illnesses and their
treatment to members, medical practitioners and the public; and promote
research.
The ACT ME/CFS Society is purely a voluntary organisation. We receive
a grant from the ACT
Government and the rest of our finances comes from membership subscriptions,
donations and fundraising ventures.
We have an office at SHOUT
(Self Help Organisations United Together), in the Pearce
Community Centre, Collett Place.
Summary
of services offered:
For more about the Society go here.
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HOME > A.C.T. ME/CFS Society
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Coming up: |
| The Next Support Group |
| The next Support Group meeting, a tour of the Independent Living Centre, is scheduled the 6th of March. The meeting will start at 10:20am, and will be at the Independent Living Centre, 24 Parkinson Street, Weston. It will be followed by a morning tea at 11:30am at nearby Coolamon Court shopping centre. Phone Roz at SHOUT on 6290 1984 for more information. |
Drs
Guidelines for ME/CFS
The South Australian Department of Health in collaboration with
medical professionals and the SA ME/CFS Society have developed guidelines
for GPs.
Also read guidelines
for psychiatrists.
Overviews of the Canadian Consensus clinical guidelines for ME/CFS
(2003) and Fibromyalgia (2004) can be downloaded from here.
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 Visit
the Alison Hunter Memorial Foundation website for detailed information
on ME/CFS Research. |
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