This is a response to @nymag
For the poorly researched piece this past week. The tone of the author on social medial has been very dismissive of the people who suffer from these incurable diseases.
#pwME #LongCovid #MECFS #MyalgicE
https://www.meaction.net/2022/11/10/elementor-59066/
I am experiencing this as well. It doesn't take much for my narrow cognitive bandwidth to be overtaxed and trigger #mecfs PEM.
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/
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.
Husband, Father, former software developer with myalgic encephalomyelitis, Living a limited life, missing from many places. #mecfs #pwme #longcovid #neisvoid
#MyalgicEncephalomyelitis #MyalgicE