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ME/CFS Australia Ltd
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Registered Charity 3104


Mailing address:
PO Box 322,
Modbury North,
South Australia 5092

Suite 506,
North Terrace House,
19 North Terrace,
Hackney, SA, 5069

1300 128 339

Office Hours:
Wednesdays, 11am-3pm

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.

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Stigmatized Chronic Fatigue Syndrome Sufferers Seek Recognition

Wednesday 14 September 2016


From Canada's CTV News:


CTV News

Stigmatized Chronic Fatigue Syndrome sufferers seek recognition Staff 
Published Saturday, September 10, 2016 10:33PM EDT
© 2016 Bell Media All rights reserved.

As many as 400,000 Canadians suffer from Chronic Fatigue Syndrome, or Myalgic Encephalomyelitis. But according to a federal review, their condition is all in their minds.

Canada's largest scientific funding agency recently decided that ME/CFS is not deserving of research funding because it is not a legitimate disease, and more likely made up by patients.

That has infuriated patients such as Vancouver's Jasmine Sanchez-Ziller. For the past decade, the once athletic 25-year-old has been losing energy, leaving her housebound and mostly bedridden.


Full article…


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