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ME/CFS Australia Ltd
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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:
266 Port Road,
Hindmarsh,
South Australia 5007
Ph: 1300 128 339

Office Hours:
Wednesdays, 10am-3pm


FIBROMYALGIA HELP:
Contact
Fibromyalgia SA
at the
Arthritis Foundation of SA
118 Richmond Road,
Marleston 5033
Ph: (08) 8379 5711

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.

Become a Member
PDF Application Form 2014 (PDF, 290KB)
Why become a member?
 

ME/CFS Australian Patient Advocacy Network

Friday 25 March 2011

Helping handsA group of Victorian patients are setting up a new network:

 

Are you sick of our illness not being treated seriously?

Do you think we should expect more?

Join the ME/CFS Australian Patient Advocacy Network!

Who are we?

We are a group of ME/CFS patients whose ultimate wish is to recover. We are asking fellow patients to join with us in lifting our sights to advocate for appropriate medical research and treatment for our illness. Our approach is to establish a network of patients, carers and other interested people to draw on our skills, contacts and desire for change.

Our vision is that every ME/CFS patient in Australia has access to effective treatment and has a life with dignity, understanding and respect.

How do we plan to achieve our objectives?

We seek to work in partnership with ME/CFS Australia, State ME/CFS Societies and our doctors. We will also work in alliance with other groups with similar aims or independently where appropriate. Strategies may include: approaching scientific and medical institutions, politicians, government officials, research funding bodies and education organisations; to use publicity and awareness campaigns that support our goals; to leverage the recent retroviral findings into ME/CFS.

How do I join? Is there a cost? More information?

  • The network is free to join. Please register your interest at mecfsapan@gmail.com. We will forward more information and a membership form for completion.

What we are not

  • We are not a social group, provider of support services or support network for swapping treatment tips etc.
     
  • Not a forum for members or others to promote or sell their own services, books, or advance other outside interests.

 


 

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