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Thoughts About M.E.
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Myalgic Encephalomyelitis (M.E.) Advocacy
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Thoughts About M.E. | Myalgic Encephalomyelitis (M.E.) Advocacy Thoughts About M.E. Myalgic Encephalomyelitis (M.E.) Advocacy Skip to content Home About Quotes ← Older posts A New Direction Posted on September 21, 2016 by Jeannette Burmeister When I published my blog post last week, “ The #CoyneEffect: Is the ME Community Stepping Up or Backing Down? ” following my hiatus from advocacy, I did not intend for that to be my return to ME advocacy. I simply felt compelled to make use of this space to express my grave concern about the chilling effect of organizations and individuals with a sizable platform enabling Coyne’s attempted silencing of courageous dissenting voices criticizing the unconscionable neglect of, and misconduct relating to, ME by the federal health agencies. We sorely need those voices to counter potentially harmful government activities. The absence of these voices clearly weakens the community. I also wanted to set the much-distorted Coyne ...
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