Society Logo
ME/CFS Australia Ltd
Please click here to donate ME/CFS South Australia Inc

Registered Charity 3104


Mailing address:

PO Box 322,
Modbury North,
South Australia 5092

1300 128 339

Office Hours:
Monday - Friday,
10am - 4pm

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.

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.

Become a Member
DOCX Application Form (Word, 198 KB)
Why become a member?

A Trial Of ME – Elizabeth's Story

Tuesday 26 November 2019


From #MEAction:


Elizabeth Thorne
Elizabeth Thorne


By Elizabeth Thorne
November 21, 2019
© 2019 The Myalgic Encephalomyelitis Action Network, All Right Reserved.

This is me, my story, I am one of the millions missing. I may not look ill to you, but if you see me, it will be because I am having a ‘good’ day because I am well enough to be able to get dressed and leave the house. The rest of the time I am missing from society, you will not see me as I am in bed, resting and sleeping, but never feeling rested or refreshed. I have missed out on so much of life… The nursing career I should have had… The children I should have had… The normal life I should have lived.

Getting sick

I’m now 39 and I have had myalgic encephalomyelitis (ME) for almost 20 years, I was just starting out in life with my boyfriend (now husband), having just moved out of my parents’ home for the first time. It was supposed to be the start of our life together. I had started a job that I loved and was hoping to train to be a nurse in the future. We were planning to get married and start a family, doing all the normal things that young couples take for granted. This was all pulled out from under me when I developed ME.


Full article…



blog comments powered by Disqus
Previous Previous Page