Fiscal year 2019 is over, and we can now examine how much NIH spent on ME research. In previous years, I’ve broken down the funding at a granular...
Dr. Francis Collins, Director of the National Institutes of Health, spoke to the ME community earlier this month at the meeting on Accelerating...
Small quote as it's a short blog. In the next two weeks, there are three important opportunities for the ME community to engage with NIH....
News is coming at the ME community at a crazy pace right now. Each time I go online, there is another controversial article that requires a...
One message dominates NIH’s talk about ME/CFS research: submit more high quality grant applications. Funding would increase if there were more...
Fiscal year 2018 is over, so now we can answer the question of whether ME research funding at NIH would go up or down. As I predicted back in...
NIH recently announced that it is forming a new Working Group on ME/CFS. The announcement is very low on specifics, but this Working Group has the...
I delivered these comments via telephone today at the CFS Advisory Committee meeting: My name is Jennifer Spotila. I will soon begin my 25th year...
Unrest, Jen Brea’s documentary about ME, will be shown on PBS stations around the United States on Monday night – January 8th. The film is already...
The Truth Is Not Always Nice Posted on November 1, 2017 by Jennie Spotila My parents used to tell me, “If you can’t say something nice, then...
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