Tag: big pharma

Pro-Vaccine Panelists: ‘We’re Losing the PR and Communications Battle’

The medical industry is losing control of the vaccine narrative, according to participants in a webinar moderated by Chelsea Clinton and organized by Unity Consortium — a group of pharmaceutical companies and pro-vaccine organizations.

Vaccine makers GSK, Merck and Sanofi, along with Big Tech platforms Reddit and Snapchat, and Spanish-language media giant Televisa Univision sponsored Wednesday’s event: “Who Influences Young People’s Health Choices? The New Conversations About Vaccines.”

Unity Consortium lists Pfizer, Merck, GSK and Sanofi among its members. Vaccine inventor Dr. Paul Offit is a member of its board of directors.

During the hour-long conversation, Clinton and the panelists criticized the growing number of parents and teens who are starting to question the safety of vaccines. They blamed the trend on increased access to what they characterized as online “misinformation” — and on organizations like Children’s Health Defense (CHD).

“What’s different today … is that people have access to a lot more information,” said Dr. Margot Savoy, chief medical officer of the American Academy of Family Physicians. “The part that makes me nervous is that, more and more, we’re getting into this odd space where people are feeling a little more polarized.”

Jessica Steier, founder and CEO of Unbiased Science and author of “The Playbook Used to ‘Prove’ Vaccines Cause Autism,” said pro-vaccine voices are “losing the PR and communications battle.”

Elisabeth Marnik, Ph.D., executive director of The Evidence Collective and author of “I Grew Up Unvaccinated. Now I’m an Immunologist,” said the circulation of and public access to such information is “one of the hardest parts about social media.”

“The more somebody sees these false claims circulating, the more likely they are to start to question their own understanding. And that’s one of the dangers of social media,” Marnik said. She said that parents’ decisions not to vaccinate their children are “a product of [this] information ecosystem.”

Clinton suggested that the ecosystem acts as a barrier to sustaining trust in the medical profession and public health. “The algorithms are part of the challenge of both … the corrosion of trust and … the barriers to replenishing and sustaining that trust,” Clinton said.

According to Marnik, the public health establishment is losing public trust because “public health and science aren’t always good storytellers.” The “anti-vaccine side” is “really good at spreading these stories that are really compelling and very scary and [that] can motivate people in ways that are harmful.”

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New York Times does it again, pushing pro-vaccine narrative over journalism

A recent New York Times article examining Robert F. Kennedy Jr. and developments at the CDC is drawing criticism over what some describe as one-sided vaccine coverage.

The article, published March 23, relied heavily on interviews with former CDC officials and presented commonly cited claims that vaccines are safe and effective, while offering little perspective from those who question that view.

It also highlighted Kennedy’s work and advocacy, including claims that he has spread misinformation about vaccines.

The coverage pointed to a 2025 measles outbreak in a Texas community with low vaccination rates, attributing reported deaths to measles. Other accounts cited by Children’s Health Defense have raised questions about those conclusions.

The article also addressed statements about vaccine ingredients, including the use of fetal cell lines in some vaccines. Kennedy has raised concerns about the presence of human DNA fragments, which some individuals cite as a religious or ethical issue.

On autism, the article echoed the widely held view that rising diagnosis rates are largely due to expanded screening and reporting. Critics argue that explanation does not fully account for the increase.

The article further referenced concerns about what it described as “spurious harms” linked to vaccines. However, federal data show billions of dollars have been awarded through the vaccine injury compensation program.

It also cited public health positions on issues such as fluoridated drinking water and routine vaccination schedules recommended by major medical organizations.

The broader debate over vaccine mandates and informed consent was also raised, including whether individuals should have the right to decline vaccines for religious or personal reasons.

The discussion comes as vaccination rates for some vaccines have declined, religious exemptions have increased, and lawmakers consider changes to vaccine policy, including liability protections and exemption laws.

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End of Federal Childhood Vaccine Incentives

Doctors will no longer receive financial rewards tied to childhood vaccination rates under key government programs. The announcement, first detailed in a December 30 memo from the Centers for Medicare & Medicaid Services (CMS), states that the agency “does not tie payment to performance on immunization quality measures in Medicaid and CHIP [the Children’s Health Insurance Program] at the federal level.” CMS urged states to discontinue similar incentives and eliminated mandatory reporting of childhood immunization data, though voluntary reporting remains an option. The memo also signaled efforts to strengthen informed consent and accommodate religious exemptions.

U.S. Health and Human Services Secretary Robert F. Kennedy, Jr. welcomed the directive, posting: “Government bureaucracies should never coerce doctors or families into accepting vaccines or penalize physicians for respecting patient choice. That practice ends now.” Advocates such as Children’s Health Defense CEO Mary Holland called it a welcome step toward treating vaccines like other medical interventions, free from metric-driven pressure. Pediatrician Dr. Michelle Perro noted that tying compensation to specific decisions can erode trust in care.

Promoting Preventive Care or Distorting Judgment?

This change comes after years of scrutiny over financial incentives in pediatric medicine. An October 2025 clip from Dr. Suzanne Humphries on The Joe Rogan Experience claimed some doctors could lose up to $250,000 annually by not meeting vaccination targets, including for Covid shots in infants. These incentives stemmed from value-based payment models under Medicaid, CHIP, and private insurers. Practices received bonuses or higher reimbursements for hitting coverage benchmarks (e.g., percentages of patients vaccinated). One analysis of an Oregon pediatric practice projected more than $1 million in annual losses for declining CDC-scheduled vaccines, largely from administrative fees. Roughly 40 percent of U.S. children are on Medicaid, amplifying the program’s reach. During Covid, specific per-dose payments (around $45 plus administration fees) added to the structure.

Proponents of the incentives argued they promoted preventive care and reduced disease outbreaks, with insurers — not pharmaceutical companies — providing payments to lower long-term costs. Critics, however, contended the metrics distorted clinical judgment and pressured families, contributing to eroded trust and reports of patients being dismissed for declining shots.

The CMS policy applies only at the federal level; some states or private insurers may retain incentives. It is telling that pediatric organizations are pushing back against broader vaccine-policy shifts under the current administration.

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Vaccine Amnesia: Why Did The Media Stop Covering Vaccine Disasters?

A key theme I’ve tried to highlight in this publication is that the same medical catastrophes keep repeating (because those responsible are never held accountable), so by understanding what happened in the past, you can see and understand what is happening now and what will likely happen in the future.

For example, because vaccines are “risky but necessary,” the medical profession and government, again and again, concluded that they needed to tell the public all vaccines were “safe and effective” as the potential injuries a mass vaccination campaign would cause were outweighed by “necessary” benefit the vaccines could offer. As such, examples can be found again and again of severe injuries being systematically covered up for the “greater good” (e.g., the earliest documented example I know of this happened in 1874 with the smallpox vaccine) and health authorities concocting the same set of excuses we’ve seen since smallpox as to why those vaccines failed to prevent the diseases they were supposed to.

Since the risks outweigh the benefits for most vaccines (detailed here), a mass vaccination paradigm can only be sustained by censoring all evidence of harm, and then using that absence of evidence as proof the vaccines are safe. As such, over the decades, we’ve seen more and more be done to conceal those harms.

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FDA Grants Speedy Approval to Eli Lilly’s Weight-Loss Pill for Obesity

Federal regulators on Wednesday approved Eli Lilly’s new weight-loss pill, a second daily oral medication to treat obesity and other weight-related conditions.

The Food and Drug Administration granted expedited approval to orforglipron, a GLP-1 drug that works like widely used injectable medications to mimic a natural hormone that controls appetite and feelings of fullness.

The drug, which will be branded as Foundayo, is expected to begin shipping Monday. The company said people with insurance may be able to get the drug starting at $25 per month with a Lilly discount card. Prices for people paying cash will range between $149 per month to $349 per month, depending on the dose.

The new pill joins drugmaker Novo Nordisk’s oral Wegovy pill, which has spurred more than 600,000 prescriptions in the United States since it was approved in December.

The FDA authorized Eli Lilly’s drug as part of a new program aimed at cutting drug approval times. The agency said it reviewed the company’s application in 50 days.

In a clinical trial of more than 3,000 adults with obesity, participants who received the highest dose of orforglipron, 36 milligrams, lost 11.2% of their body weight — about 25 pounds on average — over more than 16 months. That compared with a 2.1% weight loss, or less than 5 pounds, in patients who received a placebo, or dummy pill, according to the New England Journal of Medicine.

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Big Pharma Giants Pfizer and BioNTech Forced to Shut Down COVID-19 Booster Shot Trials After Americans Refuse to Be Guinea Pigs

Major Big Pharma companies have abruptly halted their latest COVID-19 mRNA “booster” trial because they literally couldn’t find enough willing participants.

After years of gaslighting the American public, raking in hundreds of billions in profits from experimental shots that were shoved down our throats under the guise of “public health,” the same corporations that partnered with the Biden regime, Anthony Fauci, and the lying mainstream media are now facing the cold, hard reality: Americans are done being lab rats.

According to internal letters sent to trial investigators and obtained by Reuters, Pfizer is ending its study of “updated” shots in healthy adults aged 50 to 64.

The company admitted it was “unable to generate relevant data” because recruitment had effectively hit a brick wall.

Reports indicate that more than 80% of potential recruits didn’t even make it past pre-screening, or simply refused to participate.

The trial, which aimed to enroll a massive 25,000 to 30,000 participants, folded after failing to meet even the most basic enrollment targets.

This comes at a time when the “science” is being scrutinized like never before. Under the current administration, the FDA has been pressured to actually require randomized placebo-controlled trials, the very thing skeptics have been demanding for years.

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FDA Warns of Deaths Linked to Drug It Wants Removed From Market

The Food and Drug Administration said in a March 31 alert that it has learned of eight deaths linked to a drug called avacopan that is used to treat blood vessel inflammation.

A review of studies, documents from avacopan manufacturer Amgen, and reports to the FDA’s adverse event reporting system resulted in the identification of 76 cases of drug-induced liver injury “with reasonable evidence of a causal association with avacopan use,” the FDA said in a drug safety alert.

Fifty-four of the cases led to hospitalization, and eight ended in death.

Some of the cases involved a syndrome that features the destruction of bile ducts in the liver, which can lead to permanent liver damage.

“Patients should contact their health care professional immediately if they develop any signs or symptoms that may indicate liver injury, such as: feeling more tired than usual; nausea; vomiting; unusual itching; light-colored stools; yellowing of skin or eyes; dark urine; swelling in the stomach or abdomen; or pain in the right upper abdomen,” the FDA stated. “Patients should talk to their health care professional about the safety risks associated with Tavneos and whether to continue therapy or switch to alternative treatments.”

Avacopan, also known as Tavneos, was approved by the FDA in 2021 for the treatment of severe active anti-neutrophil cytoplasmic autoantibody-associated vasculitis, or blood vessel inflammation.

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The American Mind Has Collapsed: How Vaccine Damage and Tribal Stupidity Created a Nation of Gullible Fools

How Mainstream America Became Dumb… and then Dumber

I’ve spent years observing, documenting, and sounding the alarm about the erosion of American intelligence and discernment. Today, I believe we are witnessing not just a cultural or political decline, but a mass cognitive collapse — a deliberate, engineered stupidity that has rendered a once-critical populace into a nation of gullible fools.

This is not an accident. It is the culmination of a multi-front war on human cognition, waged through toxic vaccines, processed food poisons, electromagnetic pollution, and a relentless propaganda machine that celebrates mediocrity and punishes truth. The evidence is everywhere, from the halls of government to the checkout line at the grocery store. We have crossed a cognitive event horizon, and the path back to reason seems all but lost [1]. Here’s how we got here, and why it matters for the survival of freedom itself.

The Unprecedented Decline of American Intelligence

The data is in, and it’s grim. Across all ages and demographics, test results show Americans are getting dumber [2]. This isn’t a minor dip in scores; it’s a systemic plunge. I believe this mass cognitive decline is largely driven by physical and chemical assaults on the brain, with vaccine damage playing a central role. The adjuvants in vaccines, particularly aluminum, are a silent, pervasive threat [3]. Studies have found high aluminum levels in patients with Alzheimer’s, autism, and epilepsy, and this neurotoxic substance is directly injected into the population, especially infants [3].

Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction [4]. This is not speculation; it is documented science that the corrupt medical establishment desperately wants you to ignore. When you combine this with the brain-damaging effects of other environmental toxins like lead [5], glyphosate in food, and electromagnetic fields from 5G, you have a perfect storm for neurological decay. The once-critical American mind, capable of innovation and self-governance, has been replaced with a gullible, tribalistic stupidity that I find unprecedented in our history. We are becoming a population of psychological zombies, primed to believe anything our tribal leaders tell us [6].

The Artemis Moon Farce: A Case Study in Celebrating Nothing

Nothing exemplifies this collapse of basic reasoning more than the public’s reaction to NASA’s Artemis program. Celebrating a flight that’s merely planned to go around the moon as “going back” to the moon reveals a total failure of logic and an embrace of empty symbolism. This manufactured triumph is a perfect symbol of an empire that can no longer distinguish reality from propaganda, nor achievement from theatrics.

This isn’t about space exploration; it’s about the degradation of meaning. A society that celebrates a symbolic loop as a monumental return has lost its ability to assess value and substance. It eagerly consumes the spectacle while ignoring the substance — or lack thereof. This willingness to applaud a non-event is a symptom of a deeper sickness: a population so cognitively damaged that it cannot perform the most basic reality checks. It is ready to be sold any story, no matter how hollow, as long as it’s wrapped in the flag and accompanied by a press release. The provided sources on this specific NASA mission are limited, but the pattern of celebrating engineered narratives over tangible reality is a hallmark of our cognitive decline.

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FDA Launches New AI-Powered System to Track Drug and Vaccine Side Effects

For decades, the system designed to catch dangerous side effects from drugs, vaccines, and consumer products has been failing. Not because the problems weren’t happening — but because the infrastructure meant to track them was too fragmented, too slow, and too burdensome to keep up.

The result was a growing gap between what patients experienced and what showed up in federal safety records. Patterns of harm went undetected or took far too long to surface, and the public was left making health decisions based on an incomplete picture.

Now the U.S. Food and Drug Administration (FDA) is attempting to close that gap with a sweeping technology overhaul — one that could fundamentally change how quickly you see safety signals and how much control you have over your own health choices. Here’s what the new system does, what it replaces, and why it matters.

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Biden officials pushed COVID booster harder after surveillance found stroke increase: Sen. Johnson

The Biden administration pushed COVID-19 boosters for elderly people even harder after its vaccine safety surveillance systems discovered, as early as November 2022, “statistically significant safety signals for ischemic stroke” in that age group following uptake of the Pfizer bivalent, Sen. Ron Johnson, R-Wis., told Secretary of Health and Human Services Robert F. Kennedy in a letter Monday, disclosed Wednesday.

The Permanent Subcommittee on Investigations chair released nearly 2,000 pages of “relevant HHS records” in conjunction with the letter, in 10 batches, documenting the stroke signal and internal communications between officials “acknowledging significant statistical limitations in their ability to detect safety signals through their data analyses.”

The Biden White House next made edits to a draft Centers for Disease Control and Prevention and Food and Drug Administration “communications plan” to increase booster uptake, in January 2023, that “downplayed the significance of the safety signal, changing a sentence that stated that the ‘signal is moderately elevated’ to the ‘signal is slightly elevated,'” Johnson told Kennedy.

“Biden health officials posted on FDA’s website that ‘no change is recommended in COVID-19 vaccination practice,'” the same month, even as they “initiated multiple studies and statistical analyses — including a so-called ‘Stroke Project” — to investigate the validity of their assertion” through at least September 2025, Johnson’s office said.

He asked Kennedy for more information about detection of ischemic stroke following the booster because “the full extent of HHS’s awareness of the ischemic stroke safety signal remains incomplete and key records are still missing.”

Biden officials downplayed the risk of ischemic stroke they found in coadministered COVID and flu vaccines in fall 2023.

Several months earlier they approved “additional investigation” of the booster stroke signal even while emphasizing they weren’t changing vaccine recommendations, but quickly dismissed the signal after using a “different methodology.“

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