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  ME/CFS AUSTRALIA (SA) INC

Registered Charity 698

Email:
sacfs@sacfs.asn.au

Mailing address:
PO Box 28,
Hindmarsh,
South Australia 5007

Office:
266 Port Road,
Hindmarsh,
South Australia 5007
Ph: 1300 128 339

Office Hours:
Wednesdays, 10am-3pm


FIBROMYALGIA HELP:
Contact
Fibromyalgia SA
at the
Arthritis Foundation of SA
118 Richmond Road,
Marleston 5033
Ph: (08) 8379 5711

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.

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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.

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Vice-President’s Report
March 2001

1: Introduction
2: Who’s going to...?
3: Why a high turnover?
4: Independent teams
5: Issues to address
6: The way forward?
7: Conclusion


Reports
President’s report (AGM Nov 8, 2003)
Management Committee report (Jan 2003)
President’s end of year reports (2002)
President’s report (Mar 2002)
President’s report (Jan 2002)
President’s report (Nov 2001)
Nat. Assn. President’s report (Nov 2001)
President’s report (Sep 2001)
Miscellaneous reports (Jun 2001)
Vice-president’s report (Jun 2001)
Vice-president’s report (Mar 2001)

Vice-President’s Report (continued)

Who’s going to look out for us?

Unfortunately no-one. If we are going to make progress we are the ones who will have to forge the way ahead. I know it’s tough, but it’s time for us to pull together, and for ‘the tough to get going.’ We must actively seek to shape our destiny.

The people who shape world history, and actually make a difference are the determined ones – people willing to make a sacrifice. It’s not necessarily the ones who are the smartest, most-gifted or enjoy full health. I never met her but I hear our founding President, Lyn Drysdale, was a remarkable person. She would organise the society and counsel people from her sick-bed; and at all hours of the day and night. She wouldn’t let her poor health be a barrier to helping others – she is a great example to us all.

We have a big task ahead of us, and we are at a critical point in ME/CFS history in Australia – the revised clinical guidelines are due out sometime soon. We need to be ready to debate and critique them strongly. (They guide GPs in how to treat ME/CFS.) More about them in the next issue.

To move ahead we mustn’t ignore the difficulties we face in our society. Membership is down (and even when its been higher we had only the tip of the iceberg) and that places a financial strain on the society – especially as we now have to pay more rent for our office. And, as most members who take an interest in the running of the society would know, we have had a constant turnover of management committee members over the last few years.

This has meant a lack of continuity. I can’t express strongly enough how difficult it is for an organisation to grow/develop if every year its management committee has to re-invent the wheel. Frankly, whilst that wheel is getting re-invented, so much other stuff is not being worked on. And so this new management committee finds itself slowly working its way out of a big hole. Having been elected in February it will take several months for us to come to terms with our roles and responsibilities. It’s not an ideal situation.

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