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Startling Truths about Chemotherapy (Part One)

Over the years, I have repeatedly found that all medical recommendations are best treated with a large dose of scepticism.  Nowhere is this more true than in the treatment of cancer.

Patients who are diagnosed with cancer find themselves in a state of shock. And yet, while in a state of shock, they find themselves needing to make a number of vital decisions very quickly.

One of the big questions is often this one: “Should I have chemotherapy?”

Chemotherapy (or “systemic anticancer treatment”) might improve a patient’s chances of survival by three to five per cent, though that modest figure is usually over generous. For example, the evidence suggests that chemotherapy offers breast cancer patients an uplift in survival of little more than 2.5%.

When you consider that chemotherapy can kill and does terrible damage to healthy cells, and to the immune system, it is difficult to see the value of taking chemotherapy.

I don’t think it is any exaggeration to suggest that much of the hype around chemotherapy has taken the treatment into the area of fraud – far more fraudulent indeed than treatments which are dismissed as irrelevant or harmful by the establishment.

Chemotherapy is a cull, designed by the conspirators and the medical establishment to cut the cost of caring for cancer patients.

The chances are that the doctors looking after you – especially the specialist oncologists in hospital – will recommend chemotherapy. They may push hard to accept their recommendation. They may even be cross or dismissive or assume you are ignorant or afraid if you decide you don’t want it. Cancer charities often shout excitedly about chemotherapy. But they are also often closely linked to the drug companies which make money out of chemotherapy – which, in my view, makes them part of the large and thriving “cancer industry.” It is important to remember that drug companies exist to make money and they will do whatever is necessary to further this aim. They lie and they cheat with scary regularity and they have no interest in helping patients or saving lives. Remember that: the sole purpose of drug companies is to make money, whatever the human cost might be. They will happily suppress potentially life-saving information if doing so increases their profits. It is my belief that by allying themselves with drug companies, cancer charities have become corrupt.

Little or no advice is given to patients about how they themselves might reduce the risk of their cancer returning. The implication is that it’s chemotherapy or nothing. So, for example, doctors are unlikely to tell breast cancer patients that they should avoid dairy foods, though the evidence that they should is very strong.

The one certainty is that it is extremely unlikely that anyone you see will tell you all the truths about chemotherapy. The sad truth is that the statistics about chemotherapy are, of course, fiddled to boost the drug company sales and, therefore, drug company profits. And the deaths caused by chemotherapy are often misreported or underestimated. So, for example, if a patient who has been taking chemotherapy dies of a sudden heart attack, their death will probably be put down as a heart attack – rather than as a result of the cancer or the chemotherapy. There may be some mealy-mouthed suggestion that the death was treatment related but the drug will probably not be named and shamed. Neither the chemotherapy nor the cancer will be deemed responsible. What this means in practice is that the survival statistics for chemotherapy are considerably worse than the figures which are made available – considerably worse, indeed, than whatever positive effect might be provided by a harmless placebo.

Here’s another thing: patients who have chemotherapy and survive five years are counted as having been cured by chemotherapy. And patients who have chemotherapy and then die five and a bit years after their diagnosis don’t count as cancer-related deaths. And they certainly don’t count as chemotherapy deaths.

A 2016 academic study looked at five-year survival rates and concluded that in 90% of patients (including the commonest breast cancer tumours), chemotherapy increased five-year survival by less than 2.5%. Only a very small number of cancers (such as testicular cancer and Hodgkin’s disease) were treated effectively by chemotherapy.

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WHOA! DOGE Makes Three Major Findings Regarding Unemployment Benefits Fraud, Including One Discovery That Left Elon Musk Shocked: “So Crazy I Had to Read It Several Times”

The fraud within the United States government is so rampant that it is leaving Elon Musk shocked.

On Wednesday, The Department of Government Efficiency (DOGE) announced its findings from an initial survey of unemployment insurance claims since 2020 and uncovered three stunning discoveries regarding unemployment fraud.

There is one that even the Babylon Bee would find far-fetched.

What they found will leave you livid:

24,500 people over 115 years old claimed $59 million in benefits.

28,000 people under the age of five claimed $254 million in benefits.

9,700 people with birth dates over 15 years in the future claimed $69 million in benefits. In one case, a person with a birthday in 2154 who claimed $41,000 in benefits.

All told, there was $382M worth of employment benefits fraud.

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Profits Over Patients: How Big Pharma Weaves Its Web Of Corruption And Drug Dependency

 I never set out to be an advocate. I wasn’t a doctor, scientist, or policy expert. I was just a regular person who, like so many, blindly trusted that our healthcare system was designed to protect us.

But life has a way of pulling us into the arena when we least expect it.

After the tragic and unexpected loss of my husband Woody to the antidepressant Zoloft he was prescribed for insomnia, I was thrust into a world I never imagined—one where medicine wasn’t solely about healing, but deeply entangled in a system that prioritizes profit over safety, buries harms, and keeps the public in the dark.

For over two decades, I’ve had a front-row seat to how this system truly operates—not the illusion of rigorous oversight we see in medical journals or glossy pharmaceutical ads, but the reality of how industry influence is woven into every stage.

I’ve met with regulators, testified before the FDA and Congress, filed a wrongful death and failure-to-warn lawsuit against Pfizer, and earned a seat on the FDA’s Psychopharmacologic Drugs Advisory Committee as a consumer representative.

I’ve also spoken at and participated in global conferences like Selling Sickness, Too Much Medicine, and the Harms in Medicine meeting in Erice, Italy—where some of the world’s leading experts acknowledge what few in mainstream medicine dare to say:

Our healthcare system isn’t about health—it’s about business.

And in this business, harm isn’t an accident. It’s built into the system.

The more I uncovered, the more I realized:

We aren’t just patients. We are customers.

And we are all trapped in Big Pharma’s spiderweb of influence.

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House to Vote on SAVE Act to Require Proof of Citizenship for Voting

The House of Representatives is scheduled to vote on the Safeguard American Voter Eligibility (SAVE) Act this morning. 

The bill, championed by Republicans who want honest elections, will mandate documentary proof of citizenship to vote in federal elections. Currently, one does not need to provide proof of citizenship, such as a driver’s license or a passport, to vote in races for President, the House, and the Senate.

Under the proposed law, states would be barred from processing voter registration applications unless applicants present “documentary proof” of citizenship, such as a REAL ID-compliant driver’s license, a U.S. passport, or a certified birth certificate paired with a government-issued photo ID.

The bill doesn’t stop there. It mandates states to actively purge noncitizens from voter rolls, leveraging federal databases like the Department of Homeland Security’s Systematic Alien Verification for Entitlements (SAVE) system and the Social Security Administration’s verification tools. States would also be required to set up programs within 30 days of enactment to root out ineligible voters.

The SAVE Act also takes aim at federal agencies, requiring them to share citizenship data with state election officials within 24 hours of a request—no fees allowed.

Any election official caught registering non-citizens could face criminal penalties, including federal charges. The Department of Homeland Security would even be tasked with investigating and potentially deporting any noncitizen caught unlawfully registered.

Congress previously failed to pass the SAVE Act before the 2024 election. But now, with President Trump in the White House and a majority in both chambers of Congress, Republican lawmakers have no excuse to allow illegal aliens and fictitious individuals to vote without proving they’re a lawful voter.

As revealed by Elon Musk and the Department of Government Efficiency, entitlements fraud in Social Security, disability, and Medicare is benefiting millions of people aged 110 years old or older and illegal aliens. How many of these people are voting in our elections?

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The Media Playbook for Measles Looks a Lot Like Its COVID Playbook — This Time, Kids Are the Pawns

There are moments in the history of a movement that test its resolve. For the medical freedom movement, this is one of those moments.

We are in the midst of another full-on attack by the pharmaceutical-industrial complex, aided and abetted by a beholden mainstream media united around its allegiance to a $69 billion vaccine industry.

Five years ago, we fought back as our government, Big Media and Big Pharma orchestrated and executed a COVID-19 fear campaign — a campaign built on lies, deception and censorship — and then parlayed the public’s fear into dangerous and deadly medical mandates and hospital protocols that continue to cause profound harm.

The upside to COVID-19 global disaster?

It opened the eyes of millions more people to the dangers of shoddily tested vaccines, regulatory agency hubris and one-size-fits-all “medicine.”

As our movement has grown exponentially, so has our threat to Big Pharma.

In response, we’re seeing the same tactics rolled out again. This time, it’s measles. This time, children are the pawns in pharma’s playbook.

Children’s Health Defense (CHD) stood strong and stayed true to our mission during COVID. We’re standing just as strong now. We remain just as committed now to the truth, informed consent and medical freedom as we were during the pandemic.

As pharma ramps up its measles playbook, our No. 1 job is to dismantle the vaccine industry’s lies — broadcast far and wide through the industry’s most reliable and faithful megaphone: mainstream media.

The media would have you believe that measles is a “deadly” disease. But any suggestion that MMR (measles-mumps-rubella) vaccines are safer than measles infection isn’t supported by facts.

In fact, between 2000 and 2024, nine measles-related deaths were reported to the CDC. During the same period, 141 deaths following MMR or MMRV vaccination were reported in the U.S. to the Vaccine Adverse Event Reporting System (VAERS) — suggesting the MMR vaccine can be deadlier than measles.

The media echo the same familiar refrain: The MMR vaccine is “overwhelmingly safe.”

In fact, the MMR vaccine is associated with serious health risks. The package insert for Merck’s MMRII says, “M-M-R II vaccine has not been evaluated for carcinogenic or mutagenic potential or impairment of fertility.”

Research also shows the MMR vaccine causes febrile seizures, anaphylaxis, meningitis, encephalitis, thrombocytopenia, arthralgia and vasculitis. In 2004, researchers at the Centers for Disease Control and Prevention found that boys vaccinated with their first MMR vaccine on time were 67% more likely to be diagnosed with autism compared to boys who got their first vaccine after their 3rd birthday.

The media insist there’s no viable treatment for measles — hence prevention, with the MMR vaccine, is the sole solution.

In fact, as CHD reported, doctors in West Texas are successfully treating measles with budesonide and vitamin A. Even the World Health Organization recommends vitamin A.

Yet some hospitals and doctors are refusing to treat measles patients with budesonide. Texas health officials rejected pleas by a treating physician to endorse the treatment and get the word out to hospitals about its effectiveness.

Sound familiar?

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Trump White House holds Hamas ‘entirely responsible’ for Israeli execution of Palestinian medics

The Trump administration has doubled down on its position that Hamas is to blame for Israeli troops executing 15 Palestinian medical workers in Gaza, even after a video showed that the Israeli military was lying about the incident.

The Israeli army initially claimed its forces opened fire on vehicles that were advancing “suspiciously” and had no headlights or flashing emergency lights. But a video recorded by one of the executed paramedic’s phone showed the ambulances they were driving had emergency lights on when the Israeli army opened fire.

“Forgive me, mother. This is the path I chose. To help people,” said Palestinian medic Refaat Radwan moments before he was killed.

The Israeli soldiers tried to cover up the crime by burying the 15 medics and their ambulances in a shallow grave. The army has since changed its story, acknowledging the lights were flashing and that they opened fire on unarmed men but claiming six of them were linked to Hamas while offering no evidence.

Despite the clear evidence of a war crime, the US is still backing the Israeli army’s conduct. “Hamas uses ambulances and more broadly human shields for terrorism,” White House National Security Council spokesman Brian Hughes told Reuters. “President Trump understands the impossible situation this tactic creates for Israel and holds Hamas entirely responsible.”

Before the video came out, State Department spokeswoman Tammy Bruce was asked about the executions and also said that Hamas was to blame. “Every single thing that is happening in Gaza is happening because of Hamas. Every single dynamic,” she said.

On Monday, Hamas responded to Hughes’s statement and denied that it uses ambulances for military purposes. Hamas wrote on Telegram that the statement represents “a horrific example of unethical solidarity with the Nazis of our time, in their brutal war against innocent civilians and humanitarian organizations.”

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COVID Could Have Been Engineered in Wuhan Lab, U.S. Intelligence Agency Concluded 5 Years Ago

An analysis by the U.S. Department of Defense’s intelligence agency concluded five years ago that the virus that caused COVID-19 could have been engineered in a Chinese laboratory and later escaped to spawn the pandemic that eventually killed millions of people, recently released documents obtained by U.S. Right to Know show.

The never-before-published analysis by the Defense Intelligence Agency (DIA) points out that the lab in question — the Wuhan Institute of Virology — was highly capable of genetic manipulation, and includes an assessment that the genome of the coronavirus strain that caused COVID-19 is “consistent with the hypothesis” that it was “a lab-engineered virus” that “escaped from containment.”

The analysis by scientists in the DIA, which is charged with collecting and analyzing medical and health intelligence as part of its operations, also concluded that the virus that became known as SARS-CoV-2 could have come from “a bank” of bat coronaviruses in the Wuhan lab that was under the research of senior virologist, Shi Zhengli.

The DIA referred questions about the analysis to the Office of the Director of National Intelligence, which did not respond to requests for comment for this story. Shi, who also did not respond to interview requests, previously denied in news reports that her lab held the virus strain that caused the pandemic.

The DIA has not publicly recognized the analysis as its official position on the matter. But, unlike other federal assessments that provide few details to back up their findings that COVID-19 likely emerged from a lab, the DIA assessment offers the most detailed U.S. agency scientific analysis made public to date supporting why such a conclusion was drawn.

The DIA analysis appears to be the work of reputable government scientists whose findings, made during the first months of the pandemic, were kept secret while a competing hypothesis that COVID-19 emerged by natural means gained traction and became widely accepted.

“The slides are highly significant because they show that a strong scientific basis supporting a potential lab leak was identified early on,” said Steve Massey, a University of Puerto Rico bioinformatics professor and researcher for DRASTIC, a group of scientists investigating COVID-19 origins.

“Much of that basis has subsequently been fortified by new information, such as the absence of furin cleavage sites in newly sequenced coronaviruses related to SARS-CoV-2,” he added.

The DIA analysis, which is dated June 25, 2020 —  about three and a half months after COVID-19 was declared a pandemic — has not been previously disclosed to the public.

The documents consist of a 46-page slide deck and are labeled with the classification “secret/noforn” — or, not releasable to foreign nationals. Eight pages of the analysis remain classified and were withheld from disclosure.

The analysis was part of a batch of documents — some heavily redacted and one marked “top secret” — recently released to U.S. Right to Know after it filed a Freedom of Information Act (FOIA) request and later sued to get the records.

The DIA analysis does not prove how the pandemic began. Rather, it argues that the virus could have come from a lab, and shows that multiple features in its genome are consistent with genetic manipulation. The analysis also offers a plausible scenario for how the virus could have been made in the lab and then escaped.

Over the past two years, U.S. agencies, including the FBI, the U.S. Department of Energy and the CIA, have publicly acknowledged assessments concluding that COVID-19 could have emerged from a lab, though most intelligence agencies assess that the virus likely occurred naturally by passing from an infected animal to a human.

Neither scenario has been disproved.

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Whistleblower Drops Bombshell During Senate Hearing: Accuses Facebook (Meta) of Secretly Aiding China in Undermining U.S. National Security 

A former Meta executive turned whistleblower just dropped a political nuke that has rocked Capitol Hill and should terrify every American who values freedom, privacy, and national sovereignty.

Sarah Wynn-Williams, once Facebook’s director of global public policy (now Meta), appeared before the Senate Judiciary Subcommittee on Crime and Counterterrorism on Wednesday and leveled jaw-dropping allegations against her former employer.

That Meta knowingly briefed the Chinese Communist Party on advanced U.S. technologies, including artificial intelligence, beginning in 2015—just to get a seat at Beijing’s lucrative tech table.

“These briefings focused on critical emerging technologies, including artificial intelligence – explicit goal being to help China outcompete American companies,” said Wynn-Williams, who worked at the social media giant from 2011 to 2017, according to the New York Post.

“There’s a straight line you can draw from these briefings to the recent revelations that China is developing AI models for military use, relying on Meta’s Llama model,” she added.

Project Aldrin, as it was known internally, was Meta’s covert initiative to worm its way into the Chinese market. But according to Wynn-Williams, it wasn’t just about business—it was about compromise.

Her testimony details how Meta’s briefings helped the CCP leapfrog U.S. competitors by giving them insights into emerging technologies meant to secure America’s future.

Her disclosures didn’t stop at AI. Wynn-Williams also revealed that Meta built a censorship engine for the CCP in 2015, and in 2017, willingly took down accounts belonging to Chinese dissident Guo Wengui after pressure from Beijing.

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85-Million-Person Study Finds Increased Risks of Stroke, Heart Attack, Coronary Artery Disease, and Arrhythmia Following COVID-19 Vaccination

This comprehensive Bayesian multivariate meta-analysis included 15 studies, with 11 controlled observational studies forming the basis of the primary analysis. In total, the analysis evaluated over 85 million individuals, including nearly 46 million vaccinated individuals (with first, second, or third doses) and nearly 40 million unvaccinated or control participants. Vaccines studied included BNT162b2 (Pfizer), mRNA-1273 (Moderna), and ChAdOx1 (AstraZeneca), spanning multiple countries across Asia, Europe, and North America. Moderna (mRNA‑1273) was not prominently featured in the primary risk estimates due to limited availability of controlled studies specifically isolating its cardiovascular effects. As a result, the main metrics focus on outcomes associated with Pfizer, AstraZeneca, and dose-specific pooled data.

Here’s what they found:

Increased Risks Following COVID-19 Vaccination

(Compared to unvaccinated/control group)


Coronary Artery Disease (CAD)

  • Overall: OR 1.70 (95% CrI: 1.11–2.57) → 70% increased risk
  • BNT162b2 (Pfizer): OR 1.64 (95% CrI: 1.06–2.55) → 64% increased risk
  • Second dose (all vaccines): OR 3.44 (95% CrI: 1.99–5.98) → 244% increased risk

Myocardial Infarction (MI)

  • Second dose (all vaccines): OR 3.86 (95% CrI: 2.28–6.60) → 286% increased risk
  • BNT162b2 (Pfizer): OR 1.87 (95% CrI: 1.22–2.89) → 87% increased risk
  • Second dose of BNT162b2: OR 3.84 (95% CrI: 2.21–6.66) → 284% increased risk

Stroke

  • BNT162b2 (Pfizer): OR 2.09 (95% CrI: 1.36–3.21) → 109% increased risk
  • First dose of BNT162b2: OR 3.69 (95% CrI: 2.13–6.37) → 269% increased risk
  • First dose (any vaccine): OR 3.40 (95% CrI: 1.98–5.86) → 240% increased risk

Arrhythmia

  • First dose (any vaccine): OR 2.99 (95% CrI: 1.20–7.44) → 199% increased risk
  • ChAdOx1 (AstraZeneca): OR 8.11 95% CrI: 3.67–17.99) → 711% increased risk
  • First dose of ChAdOx1: OR 4.89 (95% CrI: 1.21–19.38) → 389% increased risk

This large-scale analysis of over 85 million individuals shows that COVID-19 vaccines are associated with significantly increased risks of stroke, heart attack, coronary artery disease, and arrhythmia. Pfizer’s mRNA injections (BNT162b2) were specifically linked to substantial increases in stroke, myocardial infarction, and coronary artery disease—particularly following the first and second doses. Arrhythmia risk was elevated following the first dose of any vaccine, with the strongest signal observed after AstraZeneca’s ChAdOx1.

As each day passes, a new study is published that reveals the serious harms of the COVID-19 genetic countermeasures. They must be removed from global markets immediately.

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Largest US Egg Producer Cal-Maine Under DOJ Price Investigation

Cal-Maine Foods Inc., the nation’s largest egg producer, on Tuesday acknowledged that it is being investigated by the Department of Justice’s Antitrust Division over the national increase in egg prices.

The brief admission in its newest financial report made headlines and the company’s shares fell by about 4 percent in after-hours trading.

“In March 2025, the Company received a civil investigative demand in connection with a widely publicized investigation by the Antitrust Division of the Department of Justice into the causes behind nationwide increases in egg prices,” Cal-Maine said in its financial report for its third quarter on Tuesday. “The Company is cooperating with the investigation.”

Egg prices have hit record highs in recent months, largely due to a bird flu epidemic that has forced farmers to slaughter more than 166 million birds, mostly egg-laying chickens.

One dozen Grade A eggs cost an average of $5.90 in U.S. cities in February, up 10.4 percent from a year ago. That eclipsed January’s record-high price of $4.95.

The Ridgeland, Mississippi-based Cal-Maine accounts for roughly 20 percent of the nation’s egg supply.

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