Myalgic Encephalomyelitis Action Network

To build a global movement to fight for recognition, education, and research so that one day, all people with m.e. Will have access to compassionate and effective care.

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.

#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.

Myalgic Encephalomyelitis Action Network is a 501(c)(3) nonprofit (EIN 47-4011296) based in Santa Monica, CA.