Thanks to @BBC_Future for running this adapted excerpt from #DoingHarm on the longer—and sometimes deadly—diagnostic delays women face: https://t.co/z1nz5DxZG3
On May 12th, over 100 cities worldwide will call on governments and health officials to take action for people living with Myalgic Encephalomyelitis (ME). #MillionsMissing is a global day of protest to demand health equality for people with ME. https://t.co/fyygpZD8Sn
“Transparency is essential in scientific research. In this case, the Archives paper failed to disclose salient and relevant information about the composition of the study sample, the outcome-swapping, and the official school attendance records.” https://t.co/QJOlfxyx8W
Wow. Amazing, thorough, understandable summary of the current ME situation. I think this is the best article on M.E. I have ever read. a million thanks to @_NathalieWright https://t.co/nSBEIwE7d8
@Shrink_at_Large@scotjess3@keithgeraghty Yep. If you are interested there is a good overview of the issue here: https://t.co/evg7Cz6L1F
and here: https://t.co/NPg1jIUgD6
"Because of the ignorance of ME/CFS in the medical profession, the minuscule funding for research from the government, through the National Institutes of Health and the big foundations, I salute the arrival of a movie that may shake up a complacent world"
https://t.co/QsVKwfFzRH
Our parent non-profit, The Center For Scientific Integrity, is pleased to be able to help @davidtuller1 raise funds for this effort. https://t.co/jkc64977Y2