Image: used with kind permission of Clare Norton, mother of Merryn Crofts (pictured) who died shortly after her 21st birthday in 2017 as a result of ME

Kathy Dallest

NAAC Chair

Senior Health Informatician, Queensland Facility for Advanced Bioinformatics, Queensland Cyber Infrastructure Foundation, The University of Queensland,  https://www.qcif.edu.au/

About our council 
Our Members are connected leaders and influencers of the researcher agenda nationally and globally for ME/CFS. We connect people with a passion for furthering understanding of ME/CFS through research and the translation of robust findings to healthcare practice and consumer self-management for improved quality of life.  

Our Mission 
 To provide a reference point for patients, consumers health practitioners and researchers to find up to date information on ME/CFS research. 

 To provide a robust communication and collaboration platform between researchers, consumers, carers, healthcare practitioners, service delivery leaders, educators and policy makers in state and federal governments to enable relevant and high quality translatable research to deliver outcomes of value to consumers and carers and governments.  

Who we are 
Our diverse membership represents researchers, citizens, consumers, carers, healthcare practitioners, service delivery leaders, educators, policy makers and others; all with a special interest in quality research in ME/CFS including translation of research findings into healthcare delivery and care services. 

 Our Values  
The NAAC values are shared understanding, respect, transparency and commitment. 

Image: used with kind permission of Clare Norton, mother of Merryn Crofts (pictured) who died shortly after her 21st birthday in 2017 as a result of ME

Kathy Dallest

NAAC Chair

Senior Health Informatician, QCIF Bioinformatics, Queensland Cyber Infrastructure Foundation  https://www.qcif.edu.au 

 



About our council 
Our Members are connected leaders and influencers of the research agenda nationally and globally for ME/CFS. We connect people with a passion for understanding ME/CFS through research and the translation of robust findings to healthcare practice and consumer self-management for improved quality of life.  

Our Mission 
 To provide a reference point for patients, consumers health practitioners and researchers to find up to date information on ME/CFS research. 

 To provide a robust communication and collaboration platform between researchers, consumers, carers, healthcare practitioners, service delivery leaders, educators and policy makers in state and federal governments to enable relevant and high quality translatable research to deliver outcomes of value to consumers and carers and governments.  

Who we are 
Our diverse membership represents researchers, citizens, consumers, carers, healthcare practitioners, service delivery leaders, educators, policy makers and others; all with a special interest in quality research in ME/CFS including translation of research findings into healthcare delivery and care services. 

 Our Values  
The NAAC values are shared understanding, respect, transparency and commitment. 

NAAC Monthly International Research Update

A monthly review on literature published on ME/CFS. 

Latest News

Myalgic encephalomyelitis and Long COVID have overlapping presentation Authors Professor Sonya Marshall-Gradisnik and Dr Natalie Eaton-Fitch were invited to contribute a perspectives article reflecting on decades of research on ME/CFS. Myalgic encephalomyelitis and Long COVID have overlapping presentation. Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) presents as a […]
This original research from the Australian National Centre for Neuroimmunology and Emerging Diseases (NCNED) found impaired TRPM3 ion channel activity in post COVID-19 condition patients. The methodology employed in this study was the result of a ground breaking development over the past 7 years identifying the pathophysiology in ME/CFS. Globally it is recognised that the symptoms of post-COVID-19 overlaps significantly with ME/CFS.
Professor Sonya Marshall-Gradisnik and the team at Griffith University’s National Centre for Neuroimmunology and Emerging Diseases (NCNED) have found a link in the pathology between Long COVID and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Latest News

Myalgic encephalomyelitis and Long COVID have overlapping presentation Authors Professor Sonya Marshall-Gradisnik and Dr Natalie Eaton-Fitch were invited to contribute a perspectives article reflecting on decades of research on ME/CFS. Myalgic encephalomyelitis and Long COVID have overlapping presentation. Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) presents as a […]
This original research from the Australian National Centre for Neuroimmunology and Emerging Diseases (NCNED) found impaired TRPM3 ion channel activity in post COVID-19 condition patients. The methodology employed in this study was the result of a ground breaking development over the past 7 years identifying the pathophysiology in ME/CFS. Globally it is recognised that the symptoms of post-COVID-19 overlaps significantly with ME/CFS.
Professor Sonya Marshall-Gradisnik and the team at Griffith University’s National Centre for Neuroimmunology and Emerging Diseases (NCNED) have found a link in the pathology between Long COVID and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).


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