Our Story:

We are a group of patients and advocates who volunteer our time to raise awareness for Myalgic Encephalomyelitis.  Due to the severity of our illness, our activities, writings and meetings take place from our homes and beds.

Our current focus is to raise awareness to ask Congress to increase funding into research for severe ME patients, use the term Myalgic Encephalomyelitis (instead of CFS) along with more accurate criteria that is recommended and supported by ME experts, advocates, and patients.