My Op-Ed: Maine senators should abide by Constitution, OK release of torture report/ Portland Press Herald
Special to the Press Herald
https://www.washingtonpost.com/health/2021/09/17/covid-booster-shots-fda-recommendation/ Fauci said some scientists seem to believe “it is okay” for vaccinated people to get infected as long as they experience only mild or moderate symptoms and don’t end up in the hospital. But he said, “As a clinical person who sees a lot of patients, that isn’t okay,” adding that even mild infections…
This post is a continuation of the article by Will Jones posted recently about the origin of COVID, adding my own spin. From Vincent Munster’s lab page (NIAID Hamilton Montana) we find the following. It indicates that his entire career has been spent promoting the lie that pandemics arise from animal spillover (when this…
Thank goodness for Jeremy Hammond, who can call out the CDC on their lies and withholding of data. The NY Times added to his reportage 10 days later. As Apoorva Mandavilli wrote in the NY Times 2 days ago, But the C.D.C. has been routinely collecting information since the Covid vaccines were first rolled out…
https://aapsonline.org/delicensing-doctors-for-harmful-misinformation/ Delicensing Doctors for ‘Harmful Misinformation’ By Jane M. Orient, M.D. In addition to being subjected to various forms of censorship, for the first time in living memory American doctors are getting threat letters from licensure boards warning them against distributing “harmful misinformation.” Medical boards in 12 states have disciplined doctors because of this allegation. While it…
Review of the Emerging Evidence Demonstrating the Efficacy of Ivermectin in the Prophylaxis and Treatment of COVID-19 Kory, Pierre MD1,*; Meduri, Gianfranco Umberto MD2; Varon, Joseph MD3; Iglesias, Jose DO4; Marik, Paul E. MD5 American Journal of Therapeutics: May Jun 2021 – Volume 28 – Issue 3 – p e299-e318 Conclusions: Meta-analyses based on 18 randomized…
Recall that FDA’s Device Center was recently shown to make political decisions re medical device approvals, and to grandfather in devices on the basis of earlier approvals of very different devices. GAO wrote several damning reports including this one from June 2009: Shortcomings in FDA’s Premarket Review, Postmarket Surveillance, and Inspections of Device Manufacturing Establishments. …