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:
HOMECFS.SolveCFS.org
SOS: Save our Science
April 11, 2025
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People disabled by ME and Long Covid across the UK send out an SOS. It’s time to send out our SOS signal, if we want to have funded research. May 12th, is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing of people with myalgic encephalomyelitis (ME) gather to demand an increase in research and
