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Tag Archives: DHHS
Charter Changes
It came down to the wire, but HHS Secretary Sylvia Burwell has renewed the charter of the CFS Advisory Committee. While there are no sweeping changes to the charter, some of the changes may have you scratching your head. CFSAC … Continue reading
Posted in Advocacy
Tagged CFSAC, DHHS, government, politics, recommendations, speaking out
Comments Off on Charter Changes
Why You Should P2P
My concerns about the NIH’s Pathways to Prevention Workshop on ME/CFS are legion, and I’ve been quite vocal about them. But today I am asking you to participate in the P2P Workshop on December 9-10, 2014. Registration for attending in … Continue reading
Posted in Advocacy
Tagged action, DHHS, funding, government, NIH, occupy, P2P, politics, recommendations, researchers, speaking out, suffering, testimony
35 Comments
Turnover
Multiple sources have confirmed that Dr. Nancy Lee is stepping down as Designated Federal Officer of the CFS Advisory Committee. Also departing is her assistant DFO, Marty Bond. Dr. Lee was a lightning rod for criticism and controversy. During her … Continue reading
Renewal?
Will the CFS Advisory Committee be back this fall? Not many people seem to be paying attention to the fact that it could potentially disappear. The CFSAC is a chartered federal advisory committee, and by law it must be renewed … Continue reading
La La La, I Can’t Hear You
On May 28th, Mary Dimmock and I sent NIH Director Dr. Francis Collins a 38 page packet outlining our concerns that the P2P Workshop will not advance the ME/CFS research field, and may even set it back. We finally got … Continue reading
Posted in Advocacy
Tagged action, case definition, DHHS, government, NIH, P2P, politics, priorities, recommendations, researchers, speaking out
19 Comments
P2P: The Question They Will Not Ask
by Mary Dimmock and Jennie Spotila The most important question about ME/CFS – the question that is the cornerstone for every aspect of ME/CFS science – is the question that the P2P Workshop will not ask: How do ME and … Continue reading
Posted in Advocacy, Commentary, Research
Tagged case definition, DHHS, government, IOM, NIH, occupy, P2P, politics, researchers, speaking out
38 Comments
Parsing CFSAC
I feel like a broken record, saying that the June 16-17th CFS Advisory Committee meeting was frustrating. This meeting struck me as a tangle of threads that can only be understood by teasing them apart. There were signals buried in … Continue reading
Posted in Advocacy, Commentary
Tagged case definition, CDC, CFSAC, DHHS, government, NIH, occupy, P2P, politics, priorities, recommendations, researchers, speaking out, testimony
17 Comments
P2P: Taking Shape
The P2P ME/CFS Workshop has been approved and is scheduled for December 9-10th, 2014. The focus of this post is on analyzing four components of the information released by NIH yesterday: P2P is describing our disease as fatigue, without post-exertional … Continue reading
Posted in Advocacy
Tagged biomarkers, case definition, CBT, CPET, DHHS, drugs, funding, GET, government, NIH, P2P, politics, priorities, researchers, speaking out, treatment
13 Comments
Guest Post: CFSAC Testimony of Andrew Bokelman
Andrew Bokelman was scheduled to deliver public comment to the CFS Advisory Committee on June 17th and was the first telephone commenter. His call was terminated by the operator prior to his 3 minutes being up. After protest on Andrew’s … Continue reading
Posted in Advocacy
Tagged case definition, CDC, CFSAC, DHHS, government, IOM, politics, speaking out, testimony
5 Comments
Burning Underground
Just over a year ago, advocate Leela Play noticed something odd on a federal contracting website. What she found was a notice of intent to award a sole source contract to the Institute of Medicine to create clinical diagnostic criteria … Continue reading →