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.
Society meeting reminder
Friday 6 November 2009
A reminder that the Society's next meeting will be held tomorrow (7 November).
It's the last meeting of the year, and a lot will be happening.
Dr Ian Buttfield is speaking at the meeting about the lactic acid and ME/CFS research project.
We're sure that Dr Buttfield will give an enlightening and entertaining address.
This is also the Annual General Meeting.
(Our AGM's are quite "safe" because we don't ask for nominations from the floor, so you won't be dragooned into a committee.)
It is Peter Cahalan's last meeting as President, so it would be good to get a decent crowd along to farewell Peter, who has given so much to the Society over the past decade.
We will also be farewelling committee members Lynda Brett and Adrian Hill.
And to add to the importance of the occasion, we will be thanking the young men who participated in the Ride for CFS this year, and became our major fund-raisers for the year.
So please consider. We are in the meeting room at 80 Payneham Road, Stepney, behind the Catholic church, so there is very easy parking and access.
Details of the meeting can be found on the Society's Facebook page.
View Larger Map
blog comments powered by Disqus