Solve M.E. & Community Partners Denounce Misleading New York Magazine Article - Solve ME/CFS Initiative https://solvecfs.org/solve-m-e-community-partners-denounce-misleading-new-york-magazine-article/
@saminalberta
Unfortunately few things have helped me for more than a short time.
One of the best tools for optimizing my #mecfs has been pacing:
https://www.meaction.net/resource/pacing-and-management-guide/
For management of #mecfs and #longcovid, please consider pacing.
See the Pacing and Management Guide - #MEAction Network https://www.meaction.net/resource/pacing-and-management-guide/
My first post here. Tipping my toes into the water. I'm in my 8th year of being disabled by #mecfs. Interested in research and others with #mecfs and also #LongCovid.
@LongCovidAdvoc
Hopefully, on #mastodon, there will be progress made without the distractions of manufactured outrage from algorithms since we are no longer ourselves products being bought and sold.
Husband, Father, former software developer with myalgic encephalomyelitis, Living a limited life, missing from many places. #mecfs #pwme #longcovid #neisvoid
#MyalgicEncephalomyelitis #MyalgicE