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My partner developed ME/CFS after a COVID infection in 2023. They‘ve been sick for two years now, a year of that spent fully bed-bound. They spend all of their time in the dark, unable to do anything — including watch TV, listen to podcasts, play a video game. Even talking is often too much and must be kept to a minimum. ME (myalgic encephalomyelitis) is no joke. It’s a post-viral illness that was historically activated via Epstein-Barr Virus (mono) or Lyme Disease, and has now been included as one of the possible forms of “long COVID”. ME has been described as “the living death” because of the way it destroys your quality of life but does not directly kill you. There is still no meaningful treatment and no cure, as many patients have been gaslit and told the illness is all in their heads. With a rise of cases after COVID, this illness has become harder to ignore. This May 12th, take some time to learn about ME, its symptoms, the current lack of funding. Help raise awareness for this illness and discover how you can support those currently suffering from this illness. Link at the top for more info.
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