Myalgic Encephalomyelitis/Chronic Fatigue is exhausting. No matter how much sleep you get, you never feel rested. Below are some pages filled with information about ME/CFS and the latest research. I will add more as I find them.
I could write a whole lot more about this, but there are already many pages out there that do a great job of explaining, so I decided to link a few of those, instead. Be sure to check out the Chronic Illness Good Stuff section to see good websites and social media accounts to follow.
ME Action Network– Info about ME/CFS
Millions Missing– Stories from those living with ME/CFS
Since the pandemic started, there have been many reports of people who have been infected with the virus experiencing symptoms long after having “recovered,” and testing negative for COVID-19. This isn’t a new experience to many of us. Post-viral illness is a very real problem, and has many of the same symptoms experienced by those living with ME/CFS. Below is the newest research as of January 2021, and the Millions Missing Facebook Page that has been posting consistent updates about both ME/CFS and long-haul covid19.
Sites & accounts that I have found to be helpful, comforting, informative, & very relatable for anyone living with ME/CFS.
Lori Madeira- @mecfswarrior
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