#MEAction Network

The #MEAction Network is a grassroots global advocacy network for people living with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. The network was co-founded by Jennifer Brea and Beth Mazur on May 12th, 2015.

The organisation focuses on empowering grassroots activism to take action on all areas of ME/CFS, including research, treatment, diagnosis and management.

Go to the #MEAction Network website

Latest

Research Digest 30/07/21

Welcome to the 74th edition of the Research Digest. This edition features a systematic review of studies that investigate various sleep characteristics in ME/CFS and a pilot clinical trial of oral melatonin and zinc supplementation.
ME/CFS Pacing App

We would like to introduce to you the ME/CFS Pacing App created by our generous contributor, Mathew Blake.
Research Digest 16/07/21

Welcome to the 73rd edition of the Research Digest featuring a report investigating the availability of preventative programs and their economic benefits for patients with ME/CFS and a review on the use of lymphoblastoid cell lines in studies looking at ME/CFS and other neurological disorders.
COVID-19 Vaccine Information Hub

Information about COVID-19 vaccination is rapidly changing. That’s why we have created a hub to help you find the information easily.

Open Medicine Foundation Australia

Emerge Australia is proud to be launching the 5th addition to a global network of OMF-established Research Collaboration, with our partner, Open Medicine Foundation, seeing an Australian collaboration to join with those at Harvard, Stanford, Uppsala, and Montreal universities.
International Alliance for ME

The International Alliance for ME is a collaboration of ME organisations across the world