A public records officer at the NIH is at the centre of a scandal involving FOIA requests. Subpoenaed emails belonging to a former advisor to Fauci revealed that someone had taught him to avoid emails being captured by FOIA requests.
The FOIA Lady Pleads the Fifth Continue Reading
The FDA has approved hundreds of drugs without proof they work—and in some cases, despite evidence they cause harm. That’s the finding of a blistering two-year investigation by medical journalists Jeanne Lenzer and Shannon Brownlee, published by The Lever.
FDA Exposed: Hundreds of Drugs Approved without Proof They Work Continue Reading
The Kalfas study falls short. By relying on short-term, industry-funded data and ignoring the lived reality of withdrawal, it downplays a public health crisis hiding in plain sight. Starting an antidepressant is easy. But stopping can be the hardest part.
Antidepressant Withdrawal: Why Do Researchers Keep Downplaying It? Continue Reading
In recent congressional hearings, it was revealed that top US public health officials created ‘secret’ back channels for communications on federal business in order to avoid prying eyes. David Morens, a former top advisor to Anthony Fauci, allegedly destroyed public documents and boasted to colleagues that he would communicate with Fauci on personal Gmail accounts to circumvent FOIA requests.
The Great FOIA Dodge Continue Reading
Drug regulators and public health agencies have saturated the airways with claims that serious harms following covid vaccination are “rare.” There has been very little scrutiny of that claim by the media, and I could not find an instance where international agencies actually quantified what they meant by the term “rare” or provided a scientific source.
Sorry but Serious Harms from the Vaccine are Not Rare Continue Reading
Kansas is the latest US state to file a lawsuit against Pfizer, accusing the pharmaceutical giant of misleading the public about the safety and effectiveness of its Covid-19 vaccine.
Another State Sues Pfizer Continue Reading
While relief matters deeply for those who need it, we should be wary of the growing trend to over-medicalise women’s health—turning a normal biological transition into a lifelong pharmaceutical dependency.
Are We Over-Medicalising Menopause? Continue Reading
Some members have raised concerns that the drug regulator has repeatedly moved ahead with decisions on booster doses without holding open public discussions and say the agency is relying less and less on its independent experts for advice before approving drugs.
The FDA’s Audacious Move to Boost Kids Aged 5-11yrs Continue Reading
“It’s time for regulators to restore public trust and release these sorts of data. Until then, why should we inject anyone, especially children, with a vaccine without disclosing these, and other kinds of data?” says Wiseman.
Drug Regulators are Hiding RNA Stability Data Continue Reading
True, Kennedy is not a psychiatrist. But as a lawyer who has spent decades exposing the failures of public health institutions, he understands where scrutiny is needed. Moreover, Kennedy is not issuing medical directives—he is demanding accountability.
RFK Junior Attacked for His Stance on Psychotropic Meds Continue Reading
