The Solve ME/CFS Initiative has launched a campaign to help increase awareness of —and ultimately research funding for—ME/CFS. The campaign, “Humans of ME/CFS,” is a takeoff of the popular “Humans of New York” photoblog and Facebook page.
The aim of the campaign is to show the faces and stories of those suffering from ME/CFS worldwide so that those who are in charge of allocating research funds cannot deny the widespread devastation this disease has inflicted on so many for so long.
To submit your 500-word story and photo or read those shared by others, go to:
In August, we shared with you that we and six other ME/CFS organizations had submitted a proposal to the National Center of Health Statistics (NCHS) to fix the coding of ME/CFS in the US International Classification of Diseases (ICD-10-CM). Today, we are writing with an update on that proposal and asking that you sign the