The Myalgic Encephalomyelitis Action Network

Research and medical:we aim to grow The scientific field through outreach, education and patient-driven research so that treatments, diagnosis, and outcomes can improve for people with me.

#millionsmissing:#millionsmissing is our global effort to raise awareness and achieve rights for me/cfs patients. Since 2016, we have banded together every year to raise awareness and advocate for Action.

Digital advocacy and awareness:advocacy is a cornerstone of our work at #meaction. Every year, we take decisive steps to strengthen our voice with The us government through The national institute of health, The center for disease control & prevention, and The department of health and human services. We urge each agency to prioritize The health of people with me through accelerated research, clinical education, and a dedicated search for an fda-approved treatment. Influenced by The hiv/aids movement, our advocacy activities include participation in government committees, published petitions, open letters, meetings, peaceful protests, press conferences, advocacy days and more.