![]() 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. Disclaimer 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. 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. |
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Shedding Light On An Invisible IllnessThursday 24 May 2018
From New Zealand newspaper the Otago Daily Times:
Shedding light on an invisible illness It all started with a headache. My skull throbbed, and every joint felt like it was encased in hot lead armour. I didn't know it at the time, but I had a pretty bad case of glandular fever. Evidently my tendency to kiss strange boys in nightclubs had caught up with me. Most people suffering from glandular fever feel better after six weeks or so. It's been three and a-half years, and I still feel like I'm trudging through Chelsea golden syrup, with my battery on 10%, and my mind thick and foggy. For the last three and a-half years, I've been shuffled from doctor to doctor, and have been poked, prodded and prescribed all number of different ''remedies'' for my strange condition. I've been told that my bone-deep tiredness is ''all in my head'', that it's a side-effect of depression, that I'm just overreacting. For a while, I believed them. I thought that I was just imagining the never-ending fatigue, the headaches, the sore joints. But then a month ago, I was finally diagnosed with myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS).
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Registered Charity 3104
Email:
sacfs@sacfs.asn.au
Mailing address:
PO Box 322,
Modbury North,
South Australia 5092
Phone:
1300 128 339
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