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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:
Closed while relocating

Phone:
1300 128 339

Office Hours:
Wednesdays, 10am-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.

Disclaimer

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.

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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Australian funding for ME/CFS

Friday 6 November 2009

MoneyPaul Leverenz, chairman of the ME/CFS Association of Australia, has written about the state of national funding for ME/CFS:

Readers will be interested to know that the Australian Government through its National Health and Medical Research Council funds CFS research to a value of approximately $1.17* per patient per annum. That's about one (decent) cup of coffee for every three patients. This can be compared to approximately $400 spent per HIV patient per annum.

Read a little more about the funding situation in our new blog entry "ME/CFS Research Funding Needs Boost".

(Already the privately funded Mason Foundation awards grants to ME/CFS research far in excess of the Government.)

It is interesting to note that if even if one in ten patients donated $10 to research, we'd match Government research spending. Let's put them to shame.

* Based on information provided on the NHMRC website and assuming 100,000 people with ME/CFS.

ME/CFS Australia's blog can be found here.

 


 

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