A Study Gives Mysterious Chronic-Fatigue Syndrome Some Legitimacy - The Atlantic
"The new Stanford discovery provides some verifiable evidence that CFS sufferers can begin to start cashing in on for increased social legitimacy. So while this research gets medicine no closer to relieving sufferers’ physical symptoms, it takes a step toward alleviating the social maladies of people with CFS."
Not so sure about the phrase "cashing in", to finally be treat by medical professionals without negative preconceptions would be almost a miracle for all of us with M.E.
Has anyone else experienced offhand, discriminatory treatment?