Myalgic Encephalomyelitis Group Australia Ltd

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Myalgic Encephalomyelitis Group Australia Ltd ME Group Australia is a registered Australian charity whose purpose is to advance health for ME. Promoting knowledge and awareness of ME.
3.

Myalgic Encephalomyelitis Group Australia Ltd (ME Group Australia) is a registered Australian charity whose purpose is to advance health for people with Myalgic Encephalomyelitis (pwME) by undertaking any of the following activities:

1. Creating and or facilitating a network for ME patients and communities.
2. Promoting the official diagnosis of ME for Disability Support Pension, NDIS Access Request, and research participation.
4. Providing support for research into the causes, diagnosis, treatment and/or management of the disease.
5. Providing information for patients and medical professionals regarding the most recent developments in best practice for diagnosing, treating and/or managing ME.
6. Establishing and operating clinics for the diagnosis, management and treatment of ME, for research collaboration and the provision of support for sufferers.
7. Lobbying and facilitating the Application for the Recognition of Medical Specialty of ME under the Health Practitioner Regulation National Law.
* These activities may be undertaken on an Australia wide basis

We envisage the first ME Clinic as a small GP surgery style in Logan City, QLD which will provide โ€œofficial ME diagnosisโ€ and symptom management strategy until effective pharmaceutical treatment is introduced through research and trials. Until such time as better diagnostic criteria can be published, the company will adopt Myalgic Encephalomyelitis: International Consensus Criteria (ME (ICC)) for planning and operation of the company. The clinic will adopt International Consensus Primer for Medical Practitioners (ICP) as a guideline for diagnosis and management. Logan City is conveniently located between Brisbane and Gold Coast where participants of The National Centre for Neuroimmunology and Emerging Diseases (NCNED) is concentrated.

๐Ÿค“๐Ÿฅณ๐Ÿ…๐Ÿ™๐Ÿ’™They are also the longest   specialised Australian research centre. We are grateful for their commitment, dedicatio...
20/10/2026

๐Ÿค“๐Ÿฅณ๐Ÿ…๐Ÿ™๐Ÿ’™

They are also the longest specialised Australian research centre.

We are grateful for their commitment, dedication and progress in research on ME and ME/CFS.

14/10/2026

Sometimes it can feel like things are standing still. Especially for severe ME patients who can't easily participate in research. But in the Netherlands, they are being included.

"Patients with ME or postcovid are often so ill that they do not leave their home. That is why they hardly participate in scientific research. Doctors now drive through the country on a laboratory bus: โ€˜This experience cannot be described.โ€™"

"There, Dymphna's blood is stored in one of the largest biobanks in the world with body material from PAIS patients. She is almost the thousandth participant, says Bosch, who heads the research consortium that includes the biobank from the Amsterdam UMC and the LUMC. Scientists from home and abroad can request blood, cells, saliva, f***s and DNA and RNA samples from patients with ME or another post-acute infection syndrome for their research."

http://archive.today/8DqOm

Congratulations! ๐Ÿฅณ๐ŸŒŸ๐Ÿ…๐Ÿ’™
13/10/2026

Congratulations! ๐Ÿฅณ๐ŸŒŸ๐Ÿ…๐Ÿ’™

๐—ก๐—–๐—ก๐—˜๐—— ๐—ฅ๐—ฒ๐˜€๐—ฒ๐—ฎ๐—ฟ๐—ฐ๐—ต๐—ฒ๐—ฟ ๐—ช๐—ถ๐—ป๐˜€ ๐—–๐—ต๐—ฎ๐—ป๐—ฐ๐—ฒ๐—น๐—น๐—ผ๐—ฟ'๐˜€ ๐— ๐—ฒ๐—ฑ๐—ฎ๐—น ๐—ณ๐—ผ๐—ฟ ๐—˜๐˜…๐—ฐ๐—ฒ๐—น๐—น๐—ฒ๐—ป๐—ฐ๐—ฒ ๐—ณ๐—ผ๐—ฟ ๐˜๐—ต๐—ฒ ๐—ฃ๐—ต๐—— ๐—ง๐—ต๐—ฒ๐˜€๐—ถ๐˜€

We are thrilled to share that Dr. Sasso has been awarded the Chancellor's Medal for Excellence for the PhD Thesis of 2025 by Griffith University, recognising her as one of the highest-achieving PhD graduates and the Griffith Health Group's top-ranked candidate for 2025!

Presented by The Honourable Andrew Fraser, Chancellor of Griffith University, this award celebrates Etianne's outstanding contribution to research at the NCNED.

Her groundbreaking work on immune cell ion channel dysfunction is helping uncover the pathomechanism of ME/CFS, long COVID and GWI research that could shape future treatments for patients living with these debilitating conditions.

Congratulations also to her supervisory team, Professor Sonya Marshall-Gradisnik, Dr Natalie Eaton-Fitch, and Dr Kiran Thapaliya, for their guidance and support along the way.

Best wishes,
Sonya and the NCNED team

NCNED would like to express our gratitude and appreciation to all the volunteers, Support Groups and the following Organizations:
โ€ข The Stafford Fox Medical Research Foundation
โ€ข National Health and Medical Research Council
โ€ข MERUK
โ€ข Dr John Hamwood
โ€ข The McCusker Charitable Foundation
โ€ข Mr Adrian Flack
โ€ข Talei Stewart
โ€ข The Alison Hunter Memorial Foundation
โ€ข The Buxton Foundation
โ€ข The Henty Community
โ€ข The Blake Beckett Foundation
โ€ข Change for ME Charity
โ€ข QLD ME/CFS/FM Support Association
โ€ข WA ME/CFS and Lyme Association
โ€ข Fibromyalgia ME/CFS Gold Coast Support Group Inc
โ€ข Tweed ME/CFS/FM Lyme Support Group
โ€ข ME/CFS South Australia Inc
โ€ข ME/CFS & FM Association NSW Inc
โ€ข ME/CFS Australia

Griffith University, Griffith Health, , , , , , , , , , , , , , , , , , Tom Kindlon's ME CFS & related page: News, Research and more, ME/CFS Australia, ME Australia, ME CFS and Lyme Association of WA, ME/CFS/FM Support Association QLD Inc, Fibromyalgia me/cfs Gold Coast Support Group Inc., Chronic Fatigue Syndrome & Fibromyalgia NSW, Australia, My QoL, ME/ CFS South Australia Inc, Myalgic Encephalomyelitis Group Australia Ltd, ME Research UK, Me/cfs San Diego, Myalgic Encephalomyelitis M.E Chronic Fatigue Syndrome CFS Science, Leeds ME Network, Stichting ME Research, Bristol ME Support Group, Oxfordshire ME Group for Action, ME Long Covid unite SA, May 12th International ME CFS FM Awareness Day Australia, FJD/Robotech Robot line markers Australia

๐Ÿฅณ๐Ÿ’™
08/10/2026

๐Ÿฅณ๐Ÿ’™

๐—ก๐—–๐—ก๐—˜๐—— ๐—ฅ๐—ฒ๐˜€๐—ฒ๐—ฎ๐—ฟ๐—ฐ๐—ต๐—ฒ๐—ฟ๐˜€ ๐—œ๐—ป๐˜ƒ๐—ถ๐˜๐—ฒ๐—ฑ ๐˜๐—ผ ๐—ฃ๐—ฟ๐—ฒ๐˜€๐—ฒ๐—ป๐˜ ๐—ฎ๐˜ ๐—ก๐—ฎ๐˜๐—ถ๐—ผ๐—ป๐—ฎ๐—น ๐—ฉ๐—ฒ๐˜๐—ฒ๐—ฟ๐—ฎ๐—ป๐˜€ ๐—›๐—ฒ๐—ฎ๐—น๐˜๐—ต ๐—–๐—ผ๐—ป๐—ณ๐—ฒ๐—ฟ๐—ฒ๐—ป๐—ฐ๐—ฒ

The National Centre for Neuroimmunology and Emerging Diseases (NCNED) is proud to announce that Distinguished Professor Sonya Marshall-Gradisnik and Dr Natalie Eaton-Fitch were recently invited speakers at the National Pro Patria Centre Conference in Canberra, a leading forum focused on advancing the health and wellbeing of Australian veterans.

During the conference, Professor Marshall-Gradisnik presented NCNED's research examining the significant and long-lasting impacts of Gulf War Illness on the health and wellbeing of Gulf War veterans. Her presentation highlighted the ongoing challenges faced by veterans and the importance of continued scientific investigation to better understand the biological mechanisms underlying chronic illness following military service.

Dr Eaton-Fitch delivered a presentation showcasing the latest findings from NCNED's epidemiological research involving veterans who served during the 1990-1991 Gulf War. Her presentation provided valuable insights into the long-term health outcomes, disease burden and lived experiences of this veteran population, reinforcing the need for ongoing research and evidence-based support services.

The invitation to present at this prestigious national conference reflects NCNED's growing leadership and expertise in veteran health research. Through multidisciplinary investigations and strong stakeholder engagement, NCNED continues to contribute important knowledge that informs clinical practice, policy development and future research directions for veterans living with complex chronic health conditions.

We extend our sincere thanks to the National Pro Patria Centre for the opportunity to share our work and engage with researchers, clinicians, policymakers and veteran advocates from across Australia.

Best wishes,
Sonya and the NCNED team

NCNED would like to express our gratitude and appreciation to all the volunteers, Support Groups and the following Organizations:
โ€ข The Stafford Fox Medical Research Foundation
โ€ข National Health and Medical Research Council
โ€ข MERUK
โ€ข Dr John Hamwood
โ€ข The McCusker Charitable Foundation
โ€ข Mr Adrian Flack
โ€ข Talei Stewart
โ€ข The Alison Hunter Memorial Foundation
โ€ข The Buxton Foundation
โ€ข The Henty Community
โ€ข The Blake Beckett Foundation
โ€ข Change for ME Charity
โ€ข QLD ME/CFS/FM Support Association
โ€ข WA ME/CFS and Lyme Association
โ€ข Fibromyalgia ME/CFS Gold Coast Support Group Inc
โ€ข Tweed ME/CFS/FM Lyme Support Group
โ€ข ME/CFS South Australia Inc
โ€ข ME/CFS & FM Association NSW Inc
โ€ข ME/CFS Australia Ltd

Griffith University, Griffith Health, , , , , , , , , , , , , , , , , , Tom Kindlon's ME CFS & related page: News, Research and more, ME/CFS Australia, ME Australia, ME CFS and Lyme Association of WA, ME/CFS/FM Support Association QLD Inc, Fibromyalgia me/cfs Gold Coast Support Group Inc., Chronic Fatigue Syndrome & Fibromyalgia NSW, Australia, My QoL, ME/ CFS South Australia Inc, Myalgic Encephalomyelitis Group Australia Ltd, ME Research UK, Me/cfs San Diego, Myalgic Encephalomyelitis M.E Chronic Fatigue Syndrome CFS Science, Leeds ME Network, Stichting ME Research, Bristol ME Support Group, Oxfordshire ME Group for Action, ME Long Covid unite SA, May 12th International ME CFS FM Awareness Day Australia, FJD/Robotech Robot line markers Australia

โ—Final Reminderโ—โ€๐Ÿ™๐Ÿ“ข Health Professionals, we want to hear from you! ๐ŸงHi everyone,Iโ€™m Lydia, a 4th-year Occupational Ther...
30/09/2026

โ—Final Reminderโ—โ€๐Ÿ™

๐Ÿ“ข Health Professionals, we want to hear from you! ๐Ÿง

Hi everyone,

Iโ€™m Lydia, a 4th-year Occupational Therapy student at Australian Catholic University (ACU), currently completing a project with ME Group Australia (MEGA).

Iโ€™m developing a resource to support Health Professionals in safely assessing and prescribing assistive technology (AT) for people with Myalgic Encephalomyelitis (ME).

Iโ€™m particularly interested in hearing from Health Professionals with experience working with ME, as well as Health Professionals who donโ€™t have extensive experience with ME. Both perspectives are valuable in identifying gaps and understanding what information and guidance would be most useful when working with this population.

โฑ๏ธ Estimated completion time: 5-15 minutes
๐Ÿ”— Survey links

๐Ÿค“ Health Professionals with ME expertise: https://forms.gle/zUQ1iHsHk47aS7RU8

๐Ÿง Health Professionals with limited ME expertise: https://forms.gle/NpJGb4eHo76cune67

We'd love to hear back by 2nd October, with the survey closing on this date.

Thank you to anyone who can contribute! Your experience and perspective would be greatly appreciated and will help inform the development of the resource.



Your OT Tutor ME & CFS Exhaustion Management by Telehealth Melanie Weeks Occupational Therapy

โ—Final Reminderโ—๐Ÿ™๐Ÿ“ข Do you live with Myalgic Encephalomyelitis (ME)? Weโ€™d love to hear from you! ๐Ÿ’™Hi everyone,Iโ€™m Lydia, ...
30/09/2026

โ—Final Reminderโ—๐Ÿ™

๐Ÿ“ข Do you live with Myalgic Encephalomyelitis (ME)? Weโ€™d love to hear from you! ๐Ÿ’™

Hi everyone,

Iโ€™m Lydia, a 4th-year Occupational Therapy student at Australian Catholic University (ACU) , currently completing a project with ME Group Australia (MEGA).

Iโ€™m developing a resource to support Health Professionals in safely assessing and prescribing assistive technology (AT) for people with ME.

As part of this project, Iโ€™m seeking people with lived experience of ME to share their experiences of accessing, trialling, using or being prescribed assistive technology.

Your perspective can help identify what worked well, what could have been better, and what information or support may be helpful for others when working with Health Professionals around assistive technology.

โฑ๏ธ Estimated completion time: 10-30 minutes

๐Ÿ”— Complete the survey here:
https://forms.gle/w3s4Arn8TLYWhJf68

๐Ÿ“… Survey closes: 2 October 2026

Your experience is valuable, and Iโ€™d really appreciate you taking the time to contribute.

Please also feel free to share this post with others who may have relevant lived experience.

Thank you for helping inform the development of this resource!



MillionsMissing Australia ME Advocacy Network Australia Fibromyalgia ME CFS Australia Bridges & Pathways ME/CFS Australia ME/ CFS South Australia Inc Emerge Australia Inc Not Just Tired ME/CFS/FM Support Association QLD Inc ME CFS and Lyme Association of WA

๐Ÿฅณ๐Ÿ’™
29/09/2026

๐Ÿฅณ๐Ÿ’™

๐—–๐—ฒ๐—น๐—ฒ๐—ฏ๐—ฟ๐—ฎ๐˜๐—ถ๐—ป๐—ด ๐—•๐—ฟ๐—ฒ๐—ฎ๐—ป๐—ป๐—ฒ ๐—”๐—ฟ๐—ฐ๐—ต๐—ฒ๐—ฟโ€™๐˜€ ๐—›๐—ผ๐—ป๐—ผ๐˜‚๐—ฟ๐˜€ ๐—ฅ๐—ฒ๐˜€๐—ฒ๐—ฎ๐—ฟ๐—ฐ๐—ต ๐—ฆ๐˜‚๐—ฐ๐—ฐ๐—ฒ๐˜€๐˜€

We are delighted to congratulate Breanne Archer on the successful completion of her Honours research project at the National Centre for Neuroimmunology and Emerging Diseases (NCNED) that investigated immunological and cellular mechanisms in long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).

Throughout her Honours candidature, Bree demonstrated exceptional dedication, scientific curiosity and research excellence. Her work has contributed important new knowledge to the understanding of both long COVID and ME/CFS, two complex and debilitating conditions that continue to impact millions of people worldwide. Through meticulous laboratory investigation and data analysis, Bree reported significant novel findings, advancing our understanding of the immunological and cellular changes associated with these illnesses. Her research has generated valuable insights that will help inform future studies and support ongoing efforts to improve diagnosis, treatment and patient outcomes. These research findings will be presented at conferences and submitted for publication in the coming months.

Beyond her scientific achievements, Bree has been a highly valued member of the NCNED research team, consistently demonstrating professionalism, enthusiasm and a commitment to high-quality research. Her ability to translate complex scientific questions into meaningful research outcomes reflects the qualities of an emerging research leader.

Adding to this remarkable achievement, Bree has been awarded the opportunity to undertake a research scholarship in Switzerland, where she will be working within a leading Swiss research laboratory until early December. This international placement represents a significant milestone in her research career and will provide invaluable opportunities to further develop her scientific expertise, collaborate with international researchers, and broaden the impact of her work on a global stage.

We are incredibly proud of all that Bree has accomplished and excited to see what she achieves during this next chapter of her research journey. We wish her every success in Switzerland and look forward to hearing from her in the coming months.

Best wishes,
Sonya and the NCNED team

NCNED would like to express our gratitude and appreciation to all the volunteers, Support Groups and the following Organizations:
โ€ข The Stafford Fox Medical Research Foundation
โ€ข National Health and Medical Research Council
โ€ข MERUK
โ€ข Dr John Hamwood
โ€ข The McCusker Charitable Foundation
โ€ข Mr Adrian Flack
โ€ข Talei Stewart
โ€ข The Alison Hunter Memorial Foundation
โ€ข The Buxton Foundation
โ€ข The Henty Community
โ€ข The Blake Beckett Foundation
โ€ข Change for ME Charity
โ€ข QLD ME/CFS/FM Support Association
โ€ข WA ME/CFS and Lyme Association
โ€ข Fibromyalgia ME/CFS Gold Coast Support Group Inc
โ€ข Tweed ME/CFS/FM Lyme Support Group
โ€ข ME/CFS South Australia Inc
โ€ข ME/CFS & FM Association NSW Inc
โ€ข ME/CFS Australia Ltd

Griffith University, Griffith Health, , , , , , , , , , , , , , , , , , Tom Kindlon's ME CFS & related page: News, Research and more, ME/CFS Australia, ME Australia, ME CFS and Lyme Association of WA, ME/CFS/FM Support Association QLD Inc, Fibromyalgia me/cfs Gold Coast Support Group Inc., Chronic Fatigue Syndrome & Fibromyalgia NSW, Australia, My QoL, ME/ CFS South Australia Inc, Myalgic Encephalomyelitis Group Australia Ltd, ME Research UK, Me/cfs San Diego, Myalgic Encephalomyelitis M.E Chronic Fatigue Syndrome CFS Science, Leeds ME Network, Stichting ME Research, Bristol ME Support Group, Oxfordshire ME Group for Action, ME Long Covid unite SA, May 12th International ME CFS FM Awareness Day Australia, FJD/Robotech Robot line markers Australia

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Suite 2. 03 120 Chalk Street
Tanah Merah, QLD
4030

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