I am committed to educating people about ME/CFS.

 

ME is not a mental disorder. Those of us who live with it mourn every day for our former lives that have been dismantled by this illness. We dream of a cure that can give us our lives back. We have become physically disabled. Because this illness is invisible, the scientific and medical communities have largely used the archaic practice of sweeping it all under the rug. To this I say enough already!

 
 

I offer a wide range of specialized medical writing and manuscript editing services:

Read about my struggle with Myalgic Encephalomyelitis: