Australia
ME International lists all ME and ME/CFS organizations regardless of any diagnostic criteria that they might promote because people may want to learn about ME or CFS organizations around the world.
ME International, however, wants to clarify that ME International specifically supports the ICC diagnostic criteria. ME International feels the fastest way for ME patients to get proper care is by adopting the ICC.
See button below for other criteria organizations.
ME International, however, wants to clarify that ME International specifically supports the ICC diagnostic criteria. ME International feels the fastest way for ME patients to get proper care is by adopting the ICC.
See button below for other criteria organizations.
ICC Organizations
ME Australia
"ME Australia focuses on Australian activities and research to inform people of developments involving Myalgic Encephalomyelitis (ME) and chronic fatigue syndrome (CFS)."
Scientists: Dr Christopher Armstrong, Julie Hughes, Chelsea Bartlett and Dr Laura Miller, ACU, Dr. Elisha Josev, Dr Sarah Knight, Assoc Prof Brett Lidbury, Prof Sonya Marshall-Gradisnik, Dr Neil McGregor, Fane Mensah, Dr Ranjit Menon, Rhiannon Morris, Dr Michael Musker, Dr Alice Richardson, Prof Donald Staines
Not a Registered Charity
"ME Australia focuses on Australian activities and research to inform people of developments involving Myalgic Encephalomyelitis (ME) and chronic fatigue syndrome (CFS)."
Scientists: Dr Christopher Armstrong, Julie Hughes, Chelsea Bartlett and Dr Laura Miller, ACU, Dr. Elisha Josev, Dr Sarah Knight, Assoc Prof Brett Lidbury, Prof Sonya Marshall-Gradisnik, Dr Neil McGregor, Fane Mensah, Dr Ranjit Menon, Rhiannon Morris, Dr Michael Musker, Dr Alice Richardson, Prof Donald Staines
Not a Registered Charity
Other ME Organizations**
The Hummingbirds' Foundation for M.E. (HFME)
"The HFME is dedicated to fighting for the recognition of Myalgic Encephalomyelitis based on the available scientific evidence, and for patients worldwide to be treated appropriately and accorded the same basic human rights as those with similar disabling and potentially fatal neurological diseases such as Multiple Sclerosis." (Archived) Some of the information is outdated due to the death of the founder on 14 June 2016. ~MEI
Founder: Jodi Bassett (deceased)
**ME as described by Ramsay & Dowsett. HFME info created prior to ICC.
"The HFME is dedicated to fighting for the recognition of Myalgic Encephalomyelitis based on the available scientific evidence, and for patients worldwide to be treated appropriately and accorded the same basic human rights as those with similar disabling and potentially fatal neurological diseases such as Multiple Sclerosis." (Archived) Some of the information is outdated due to the death of the founder on 14 June 2016. ~MEI
Founder: Jodi Bassett (deceased)
**ME as described by Ramsay & Dowsett. HFME info created prior to ICC.
To find additional ICC orgs, see our International page.
