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Tag Archives: stigma
NIH Obstacles Thwart ME Research
After I published my post on the NIH Obstacle Course (November 2018), readers’ reactions made clear that a shorter version of the article could be useful. Today, STAT published that shorter article in the First Opinion section. You can read … Continue reading
Posted in Commentary
Tagged accountability, action, bias, experts, frustration, funding, government, grants, NIH, politics, priorities, recommendations, researchers, RFA, SEP, speaking out, spending, stigma, strategy
5 Comments
NIH’s Obstacle Course to Success for ME/CFS Researchers
A shorter version of this article was published on STATNews on January 10, 2019. One message dominates NIH’s talk about ME/CFS research: submit more high quality grant applications. Funding would increase if there were more high quality grant applications. Give … Continue reading
Posted in Advocacy, Commentary, Research
Tagged accountability, action, bias, experts, frustration, funding, government, grants, NIH, politics, priorities, recommendations, researchers, RFA, SEP, speaking out, spending, stigma, strategy
9 Comments
The Death Threat Myth Exposed
Update April 7, 2021: Further comment from Dr. Vicky Whittemore added to the end of this post. Last week, an old story was recounted to a new audience. During the March 30, 2021 NIH telebriefing with the ME/CFS community, Dr. … Continue reading →