Fibromyalgia ME CFS Australia Bridges & Pathways

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Fibromyalgia ME CFS Australia Bridges & Pathways We work collaboratively to fasttrack change. All Australians have the right to best practice medical care. On this page we share useful information and research.

Bridges & Pathways Institute/ Fibromyalgia Australia is an Australian charity working towards solutions, services/research for all Australians living with poorly understood complex chronic condtions. Bridges & Pathways/Fibromyalgia Australia works in partnerships to improve daily care, early diagnosis and management of Fibromyalgia and ME/CFS in primary care settings We particularly focus on consumer priorities and improving health outcomes by fast tracking research into affordable daily care. We facilitate provider training, clinical research, with best practice resources and case assessments and management. Australians urgently need immediate access affordable multidisciplinary management to limit their condition and improve quality of life. Just because there is not cure does not mean nothing can be done to improve, health, wellbeing and quality of life. There is a let of emerging research that give us hope.

13/10/2026
13/10/2026

Here is a 10-month update on my attempts to get dextro-naltrexone d...

09/10/2026
08/10/2026

The team at La Trobe University in Australia, including Dr Sarah Annesley and Dr Daniel Missailidis, have published a study acknowledging funding from ME Research UK, which provides evidence of altered lipid metabolism in ME/CFS.

Read more: https://tinyurl.com/yv4mmvtn
Read the research paper: https://tinyurl.com/5d3hbs7v

Don’t forget to select Bridges and Pathways or Fibromyalgia Australia when want you last minute tickets
07/10/2026

Don’t forget to select Bridges and Pathways or Fibromyalgia Australia when want you last minute tickets

Only $2 per ticket

💬 Help us change the conversation.Share this post with someone who needs to know that no cure does not mean no care. ...
06/10/2026

💬 Help us change the conversation.
Share this post with someone who needs to know that no cure does not mean no care. Together, we can build greater understanding of what it really means to live with Fibromyalgia and ME/CFS

01/10/2026

As the autonomic nervous system (ANS) is so far-reaching in function, it is no surprise that the symptoms of dysautonomia (dysregulation of the ANS) are so varied. These can include, but are not limited to, brain fog, vision problems, palpitations, nausea, and temperature dysregulation. Many of these symptoms overlap with ME/CFS, and often individuals with ME/CFS have a co-existing dysautonomia diagnosis, commonly PoTS (a form of orthostatic intolerance with elevated heart rate).

Read more: https://tinyurl.com/dysauto2026

Western Australian Opportunity
01/10/2026

Western Australian Opportunity

27/09/2026

I thought this 8-minute video on pacing was excellent

"Pacing is the balance between rest and activities. This video describes pacing, provides tips on how to pace when living with an energy-limiting condition, and identifies some of the common barriers people may encounter when trying to successfully pace."

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