The final kill switch is transparent noncoerced consent. Instead of taking “a share of the loot” from the drug-DOPE game, we need our universities, the National Institutes of Health, and our medical system to enshrine the principle of non-coerced consent.
Four targets — blood pressure, blood sugar, cholesterol, and BMI — the Four Horsemen of the Apocalypse, four ways to medicalize you, four ways to apply a disease-mongered label to you, and four avenues for you to start living under a dark cloud.
Among pre-exposure, when you take it to prevent contagion, or post-exposure, when you take it after having contact with an infected person to try to avoid the disease, there are 18 studies. And all of the prophylaxis studies are positive.
What Would a Brutally Honest Man Look Like? Continue Reading
I look around at the people I love and I’m not always sure who I’m talking to anymore. Half of them seem to be on something. More docile than they used to be. I miss them and they’re standing right there.
There are many more hidden Vioxxes in our medicine cabinets, which exist due to systemic flaws in drug regulation that allows dangerous medications to flood the market, harm millions, and linger far too long before reluctant regulators pull the plug.
An Ode to Remembrance on Prescribed Harm Day Continue Reading
The FDA’s first EUA for a Covid-19 vaccine rested on its determination that the benefits of the Pfizer–BioNTech vaccine outweighed its risks. Yet the trial report did not bring those together within a common framework. I did—and what I found was startling.
The Full Risk–Benefit Balance Behind the First Covid-19 Vaccine Continue Reading
The grift goes wide and deep. Many influencers and physician-educators have financial ties through sponsored content or brand partnerships, sometimes pushing lines of supplements, telehealth services, books, or their appearances on the speaking circuit.
The most infuriating part of the VRBPAC meeting was that the members actually acknowledged and discussed some of these concerns, but instead of postponing its recommendation, the committee simply recommended further studies be done after malflusiva’s approval.
The FDA possesses the legal authority, institutional framework, and technical expertise necessary to solve this problem. What is missing is leadership’s willingness to demand the standards that once defined American drug regulation and legacy records of a low number of recalls.
FDA Leadership’s “Blind Spots” Lead to a Surge in Medical Device and Drug Recalls Continue Reading
To believe it, given that it involves an enormous number of people, institutions, medical societies, scientific bodies all in sync to cover up and steer people away from valid treatments, you have to believe something else: that humanity doesn’t care.
Buried Before Ivermectin: Meet Chlorine Dioxide Continue Reading
Unless this system is forced into the open, selective reporting will continue to be standard practice in even the most prestigious journals. And the public will keep receiving a polished marketing story instead of the full scientific truth.
Major Journal under Fire for Omitting Pfizer’s Failed Flu Data in Seniors Continue Reading
Predictably, Moderna has secured up to $60 million from the Coalition for Epidemic Preparedness Innovations (CEPI) to accelerate development of an Ebola “vaccine” amid an ongoing outbreak in eastern Democratic Republic of Congo.
Moderna Is Building a Modified mRNA “Vaccine” for Ebola Bundibugyo Continue Reading
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