MECFSnet, the website of the ME/CFS Collaborative Research Centers and the Data Management Coordinating Center, is now live. https://mecfs.rti.org/
They have a page, https://mecfs.rti.org/get-involved/, with the parts of the studies at all centers that are open for recruitment. I've either updated or created new threads for these in our recruitment sub-forum, https://s4me.info/forums/recruitment-into-current-me-cfs-research-studies.129/
That is the right message. If people understood that they basically have a 1% risk of losing everything and there is nothing they can do about it except ending the denial and systemic discrimination, much more would be done. People pay significant sums to insure themselves against much less serious and less likely threats, like losing your house to fire.
