Quality of Life for ME/CFS Patients


This is what researchers have to say about our place in society. Looks and feels accurate to me based on my personal experiences over the last decade+. What do you think fellow ME/CFS warriors? Are we some of the most marginalized, misunderstood, sickly lot of loners in this world? It’s way past time to make changes and that’s what things like #millionsmissing a

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