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ME/CFS Australia Ltd
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Registered Charity 3104


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PO Box 322,
Modbury North,
South Australia 5092

1300 128 339

Office Hours:
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ME/CFS South Australia 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 South Australia 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.

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Jane Gill
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This article originally appeared in the June 2000 issue of Talking Point.

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Jane Gill

From Bute, South Australia

Jane has helped start up a new Northern Yorke Peninsula Support Group for CFS sufferers and carers, which meets at the Wallaroo Community Health Centre.

I first became ill nearly six year ago. I’d had glandular fever and wasn’t getting any better. I struggled on for 18 months going back to the doctor and getting nowhere with him. As I read articles in magazines and newspapers about CFS I virtually diagnosed myself, with confirmation from a couple of friends. I took the initiative and booked an appointment with a specialist in town who said I had a rather severe case of CFS and proceeded to record a letter to be sent back to the local GP stating that fact.

It was terribly difficult for me in those first 18 months. I had no name for what was wrong with me. I couldn’t say to anyone, “Well, I have this or that.” It was a little like a nightmare that had no end.

I became a member of the ME/CFS Society. They gave me the name of a contact, Marjorie Turner, at Port Pirie who was like a light to me. To be able to ring her and talk for ages about how I felt and to hear she knew how I felt was such a relief. It turned my life around and gave me the start I needed.

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