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