The “millions missing” from life due to myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are coming together worldwide to fight for their future, and you can help.
To recognize ME/CFS Awareness Day, people with ME/CFS and their allies will hold public demonstrations and participate in a social media campaign on May 12 to raise awareness of the seriousness of the condition and call on government health officials to finally begin dedicating real strategy and funds to research and treatment.
The event, a global campaign of advocacy organization #MEAction, is called #MillionsMissing. The hashtag represents the
estimated 15 to 30 million people around the world who have ME/CFS and are prevented from living full lives due to symptoms like extreme mental and physical fatigue, post-exertional malaise, pain, immune dysfunction and sensory sensitivity. The disease has no FDA-approved treatments or cure.
Now in its third year, #MillionsMissing is a collaboration between #MEAction and Stacy Hodges, a patient from North Carolina who came to the organization with the idea to do a protest in Washington, D.C. In 2016, protests were held in 24 cities. This year, there are more than 95 public events planned around the world, including the U.S., U.K., Australia, New Zealand, Mexico, Canada, Japan and more. (
Click here to find a demonstration near you.)