We got started in February 2018 as a small but growing grassroots group dedicated to advocacy for the tens of thousands of Coloradans affected by Myalgic Encephalomyelitis/CFS/SEID.
On May 12, 2018 we held our first public event when we joined thousands worldwide to make ME/CFS Awareness Day at the Colorado State Capitol. Following on the momentum from May 12th, we began reaching out to members of congress to raise awareness of ME and of our goals.
In addition to advocacy, we also have a Facebook group where members support eachother, talk about ME/CFS resources and form a community and sometimes meet eachother.