COVID-19 / Malicious Medical Quackery
[Ed.: FEAR YOUR DOCTOR! Medicine is a disgraced profession. They cannot (and must not) be trusted any longer!
Cultivate Nosocomephobia and iatrophobia. Spread ‘vaccine hesitancy’! How Bad is My Batch?
If you know someone injured by the jabs, direct them to humanitysuit.com to become a plaintiff. Another great legal resource is: Freedom Council https://freedomcounsel.org; For Vaccine Exemptions: https://www.sirillp.com/vaccine-exemption-attorneys/ .
RESOURCE: VACCINE INFO COURSE All material from the course has been transferred to telegram. You can access everything here
How Bad is My Batch? Enter your batch number(s) and find out. Then take action and purge yourself of this shit to the extent possible. It’s do-able!]
DIED SUDDENLY: Official Documentary Film [1:17:21]
Inside mRNA Vaccines: The Movie [1:00:57]
This hard-hitting film rips the lid off the disastrous mRNA rollout — with stunning 3D animation and unfiltered testimony from the world’s leading experts.
AUG 11, 2025 Nicolas Hulscher, MPH
Today, we bring you the world premiere of the groundbreaking documentary Inside mRNA Vaccines — directed by Erki Tangsoo — in full, right here on Substack.
This powerful film pulls back the curtain on the rushed global rollout of mRNA vaccine technology, combining exclusive 3D animations and hard-hitting expert testimony from leading scientists and medical professionals.
“We turned the body into a factory, with no clear controls.” – Dr. Robert Redfield, former CDC Director
This documentary gives the public what mainstream media never will: an unfiltered second opinion.
Explore the science, sources, and timecodes featured in the film here.
Find out more about the film at: insidemrnavaccines.com
CDC Hit With Lawsuit Over Failure to Test Cumulative Effect of 72-Dose Childhood Vaccine Schedule
Texas AG Sues Eli Lilly for ‘Bribing’ Doctors to Prescribe High-Profit Drugs
The death cult continues hunting pregnant women and newborns. Moderna’s CMV vaccine will be approved soon. SASHA LATYPOVA
AUG 18, 2025
The strategy of eugenics and population control by “public health”, aka, poisoning by “vaccines” is not new, and mothers and children have always been its target. The “death care” drive to poison babies before they are born or on the first day of their life at the latest continues unabated, and yes, it is a critical agenda item that spans every administration, regardless of political party in charge. To recap just the most recent iterations, starting with Trump’s Operation Warp Speed:
- Early 2020: OWS mRNA vaccine development contracts specifically mentioned 4 million pregnant women in the US as a target, ahem, “for protection”, obviously. This was months before any non-evidence that SARS-Cov2 poses risk to pregnancy was compiled by the poisoners at CDC. I covered this non-evidence here. SARS-Cov2 (whatever that was) never posed any special risk to pregnant women, but the CDC still insists that it does, and insists that ALL pregnant women be shot with mRNA, per current FDA and CDC MAHA policy.
- The mRNA injections were never “officially” tested for safety in pregnancy. The strategy was to officially exclude pregnant women from clinical trials (which is the norm in drug development), but then “accidentally” get thousands of them injected anyway, collect the data and study the carnage, then lie about it to the public, coercing and manipulating pregnant women into injections at every turn. Examples of this include the infamous Shimabukuro et al study using fraudulent math. Applying the correct math showed 80%+ miscarriage rate and 300% increase in stillbirths in that dataset.
Note that JikkyLeaks, Arkmedic, Saidi, horse gambler OpenVAET + the assorted mouse crew (all of them have multiple online personas) try to misrepresent this finding and manipulate the public opinion away from it, by piling on other extraneous data. That’s bullshit. A published study is a dataset on its own, and it’s proper re-analysis is the way to demonstrate fraud on the public. Jikky crew are liars on behalf of the criminal cartel, don’t fall for their tactics.
- As I published in my review of Moderna’s animal studies submitted to the FDA and FOIAed in 2022, reproductive toxicity study in pregnant rats showed extreme maternal toxicity and fetal malformations. Moderna admitted to statistically significant increase in fetal skeletal malformations:The skeletal malformations were temporally associated to the days when highest toxicity was observed in the mothers: “Maternal toxicity in the form of clinical observations was observed for 5 days following the last dose (GD 13), correlating with the most sensitive period for rib development in rats (GDs 14 to 17)”.
The FDA included the following statement in the Basis for Regulatory Action Summary document (Section 4: Non-clinical Reproductive Toxicology, p.14):
“No vaccine-related fetal malformations or variations and no adverse effect on postnatal development were observed in the study. Immunoglobulin G (IgG) responses to the pre-fusion stabilized spike protein antigen following immunization were observed in maternal samples and F1 generation rats indicating transfer of antibodies from mother to fetus and from mother to nursing pups.”
I discussed this fact with RFK Jr on his podcast in 2022. The lie from the FDA is still there, they have not retracted it even though he is in charge of the agency now! - The CDC schedule today includes RSV shots for ALL pregnant women. Three vaxxes are approved for RSV, one of them – Moderna – is mRNA, discussed here. The others are just as poisonous. Robert Malone and Martin Kuldorff, new, MAHA co-chairs of ACIP just voted in the monoclonal antibody for RSV for ALL newborns whose mothers were not shot with RSV, which is “belt and suspenders” strategy, I guess. The RSV mAb for babies is an atrocity that killed more babies in clinical trials vs. whatever other poison was used as a “control”. Discussed in this post.
- Let’s not forget that MAHA-FDA approved the new Moderna shot mNexspike based on no placebo controlled trials and no long term safety. This is discussed in this post. In the same post I discussed the soon-to-be-approved Arcturus self-amplifying RNA shot (without placebo controlled trial, naturally), and quoted report from
Conspiracy Sarah on the $500M going to Jeffrey Taubenberger’s gold standard universal poison using BPL, and I separately discussed it here. All of these will be pushed on pregnant women per Makary-Prasad “new” mRNA policy.
You probably know this already – Prasad is back at the FDA as head of CBER, after a week of “spending more time with his family”. Does it mean he hates his family and wants to spend more time with the FDA?
Now we are “up to date” on all or most of the poison shots that are being pushed on pregnant women and babies…
Not so fast! There is yet another mRNA miracle of gold standard science that Moderna will get an approval for quite soon:
Moderna’s mRNA injection for CMV
According to Enpoints News:
A pivotal readout of Moderna’s cytomegalovirus vaccine candidate is on the horizon, with enough cases now accrued in the Phase 3 study for a final analysis this fall.
But the company plans to add new secondary endpoints to the study “that we hope will increase the scientific value of the results,” president Stephen Hoge told analysts on the company’s second-quarter earnings call Friday.
Moderna took an early look at the trial at the start of this year, and said at that point that the vaccine hadn’t yet shown efficacy. The primary endpoints of the trial are prevention of cytomegalovirus infection and immunogenicity against antigens not encoded in the vaccine.
Hoge told analysts in February that with more cases accrued, it was still possible for the final efficacy endpoints to meet or exceed the company’s expectations. On Friday, Hoge reiterated that Moderna believes the vaccine will have an effect if the efficacy is better than 49.1%.
“If you think of all of the burden of disease associated with CMV over a lifetime, a 50% reduction in that would be a pretty profound benefit, we believe, on public health and for individuals,” he said.
What the heck is CMV, you may ask. It’s an imaginary computer model, duh. It’s called cytomegalovirus. Sounds scary, I know, that’s intentional. CMV is one of those asymptomatic but deadly things. First of all, everyone’s got it! It is claimed that ~50–80% of U.S. adults have been infected by age 40 but most infections are asymptomatic. m-kay…. Continuing with the usual bullshit virus tales, according to CDC:
symptomatic illness occurs more frequently in:
- Immunocompromised patients (e.g., transplant recipients, people with HIV/AIDS).
- Newborns with congenital CMV.
- Pregnant individuals (risk to fetus if primary infection occurs).
You see where this is going, right? “Congenital CMV”, aka the vax injury from all the shit the pregnant mother was jabbed with plus everything that the newborn was jabbed with has to be covered up with more “congenital” and “rare genetic” conditions!
Further quoting CDC:
- Incidence at birth: ~0.5–0.7% of live births (≈ 20,000–30,000 infants per year in the U.S.).
- Symptomatic at birth: 10–15% of infected newborns (~2,000–4,500 infants annually).
- Long-term sequelae:
- Hearing loss (most common)
- Vision impairment
- Developmental delay
- Hearing loss (most common)
- Estimated symptomatic cCMV‑related hospitalizations for infants < 1 year average 747 per year, corresponding to 18.6 per 100,000 infants combined (range ~17 to 19 per 100K). [PubMed Central].
OK, we got the number that Moderna juice is supposed to prevent in order to make the world a better, safer place for everyone who can still run and hide from “healthcare”! A whopping 700 cases of vaccine injured infants out of ~3.6-4 million newborns in the US that ended up hospitalized because they were poisoned before and at birth, also happened to “test positive” for CMV with a non-diagnostic fraudulent PCR test. Killing and maiming thousands of infants is the price they are willing to accept to Make America Healthier Again.
By the way, two studies – published NEJM and JAMA! – claim that they “validated” CMV PCR assays, but demonstrate no validation of anything. These are the usual circle-jerk exercises of virology: screenings of newborns with multiple unvalidated assays, finding the same computer model these tests are designed to find (but not finding it all the time however, since scientific reproducibility is not in vogue anymore) and then declaring that they validated the PCR assay! Got it.
I asked GPT about scientific validation of CMV as causative agent of any illness. It went into a tizzy, I thought it was going to fry my computer in despair. After many minutes of thinking very deeply and reporting me to several NSA databases for wrongthink and precrime it came back with some papers. I am beginning to enjoy using AI. It cited several “isolation” papers from the 1950’s and 60’s for which nothing except the title is available. Not even abstracts. Not even for money. It’s that important! Nothing says “trust the science” like hiding it extra hard. This paper was cited as “classic” for demonstrating causation of illness by whatever is deemed CMV. Not available. At all! One paper was found in open access claiming “isolation” of this virus from 3 infants who were sick with something. That’s it. Nothing else about proof of disease causality by this super-dangerous, world ending “pathogen” is available.
Yet, the gazillion-dollar valued Moderna is working extra hard to defeat the CMV pandemic before it starts! Do you think Moderna is planning to sell 700 injections per year? Heck no. This will be pushed again on ALL pregnant women and ALL newborns that don’t have the “correct CMV antibodies”. Bob Malone on MAHA-ACIP will see to it.
Do we know anything about the product Moderna is fighting so hard to bring to market? Turns out we do! That’s because I read 700+ mind-numbing pages from Moderna animal studies production under FOIA (and a lawsuit by Judicial Watch) and spent a couple of weeks deciphering that bullshit. Now I bring to you the gem of Moderna CMV vax, which was in development in 2017 and failed back then, since there was no way in hell, even under extremely corrupted and crony FDA relationship, that their gene therapy garbage was getting on the market. It required the global military faked pandemic and the PREP Act liability shield to do so. Back in 2020 Moderna included only one full report for a preclinical study in their Spikevax (mRNA-1273) submission to the FDA. That study was from 2017, a biodistribution study conducted with Moderna’s failed at the time mRNA-1647, the CMV vax!
Here is what we know:
This product is a construct of 6 different experimental mRNAs(!), none of which are approved for anything, nor studied separately. The study was a non-GLP (Good Laboratory Practice) biodistribution study in male rats only. Note that for some unspecified reasons they included no females! It’s like they knew they were going to target pregnant women even back then and wanted to avoid showing any damage to female reproductive system. The study was conducted at the Charles River facility in Canada.
The study was for mRNA-1674, formulated in the lipid nanoparticle (LNP) claimed to be substantially similar to the Spikevax LNP formulation. This study demonstrated distribution of the lipid nanoparticles throughout the entire body and accumulation in all major organ systems, except the kidney.
Notably, the study assessed only male animals and not females, therefore no information about biodistribution in females was made available to the FDA, and specifically, no information about exposure differences or accumulation in female reproductive organs was ever obtained.
In the biodistribution study, high LNP concentrations were observed in lymph nodes and spleen and persisted in those organs at 3 days after the injection. The study was stopped before full clearance could be observed, therefore, no knowledge exists on the full-time course of the biodistribution. Other organs where vaccine product was detected included bone marrow, brain, eye, heart, small intestine, liver, lung, stomach, and testes. Given that the LNPs and mRNA-1647 were detected in all these issues, it is reasonable to assume that the LNPs carrying mRNA-1273 likewise would distribute in the same way, and therefore, the spike protein would be expressed by the cells in those critical organ systems with unpredictable and possibly catastrophic effects.
All of this brings us to current day and Moderna running a Phase 3 clinical trial for the CMV mRNA vax.
Moderna mRNA-1647 clinical trial design:
The study is conducted ONLY in females of childbearing potential. Wow. As we have just discussed, the preclinical biodistribution study EXCLUDED females. Therefore, we don’t know whether female reproductive organs are being damaged, however, given the evidence from all mRNA shots currently on the market, we certainly do know! The LNPs accumulate in the ovaries, and destroy them.
While Moderna’s trial design states that pregnancy is an “exclusion” criterion, as we discussed above, they bet on having some significant number of “accidental” pregnancies during the study.
Furthermore, the study has 296 worldwide locations! This is a massive number of clinical sites for any study. I don’t know what the target enrollment is (no info available), however, this number of sites is typical for studies that are “fishing expeditions” – i.e. designed for extremely rare conditions or extremely slow progressing conditions, or both. The slow progression here doesn’t apply, since we are talking about fraudulent PCR tests finding “positive” or “negative”, i.e. a binary test, not a progression test. CMV is an imaginary product of a fraudulent PCR test, therefore it is quite rare. The fraudulent PCR tests for CMV are designed to paint a target on pregnant women and infants (see the reported incidence below, it is truly a very evil joke).
Study design:
The language about placebo is confusing. I don’t know what “biological placebo” means, and I highly suspect that this is the usual deception, i.e. not a real placebo. However, I can’t verify yet until the study is published.
The “endpoints”, i.e. what is being studied include – you guessed it – nothing about CMV-induced illness! They study “seroconversion”, i.e. can our jab generate the “correct antibodies” to a fake computer model. That’s because CMV is a fake computer model, of course, but also because the fake computer model is alleged to cause illness in 700 babies, yet the study is conducted in “females of reproductive potential”! If this gold standard science doesn’t dazzle you, what will? Apparently that’s what Moderna’s SCO Hodge lied about to the investors, telling them they “added” this endpoint for extra special science goodness. In fact, this is the only efficacy endpoint they are studying – and hilariously, producing those “correct” antibodies in only 49% of the injected women.
This would be hilarious if it weren’t so evil. The study probably has 10,000-20,000 participants, young women, who may want to be mothers some day. This mass sterilization effort disguised as a “clinical trial” will destroy those dreams for many of them, and possibly that’s the reason these pointless poisonings include so many subjects. That’s the way to maximally poison, jab, jab, jab, as many as you can catch!
To put this in a broader perspective, here is a comment from one of the readers that explains why pregnant women or women who plan to have children are such a key target for the poisoning cabal:
If you truly want to understand the true source of all this fakery, double talk, and redefinition of language to serve the agenda of the communist-fascists sons of bitches that are currently ruling the world, then you must read, and reread until you truly fathom the depths of evil, the 1952 book by the British philosopher Bertrand Russell, called: The Impact of Science on Society – except “science” ain’t science, it is as he defines it “social engineering” – and he only does that in one sentence in the whole book – then he tells us the true source of the modern tyrannies, Karl Marx, because Marx’s allegedly “great contribution” was to redefine the meaning of philosophy to be the active pursuit of ALTERING SOCIETY to serve the elites, who Russell in his book defines as the “rich, privileged oligarchs” – But wait, it gets worse. Russell also redefines THEORY and says that it shall now be treated as fact if it serves the elites agenda of SOCIAL ENGINEERING – and if this wasn’t enough already he goes on to tell us that TRUTH is now redefined to mean PROPAGANDA that serves the elites agenda of social engineering – apart from these heinous redefinitions of “science” “truth” “theory” and “philosophy” we also see from Russell’s book that the TRUE DEFINITION of NET ZERO is a NET ZERO BIRTH RATE ACROSS ALL MANKIND – Yep, he spells it out – he wanted 95% of men sterilized and 70% of the women sterilized so the useless breeders could not breed. Karl Marx was the turning point which is EXACTLY why the morons of the western academic world and establishment love him. He didn’t just put forward the heinous evils of communism he spelled out how the western elites could change all the language to be double talk, to deceive the public and attack them relentlessly with SOCIAL ENGINEERING – Bertrand Russell’s book is more correctly stated as: “The Impact of Social Engineering on Society.” – and it is all negative for the 99%.
Is this mRNA shot going to be approved by the MAHA-FDA that publicly states “mRNA is not viable” while approving more mRNA? Does a bear crap in the woods?
Was Executive Order on Homelessness Intended to Expand Forced Psychiatric Treatment?
August 17, 2025 AbleChild
The President’s recent Executive Order (EO), Ending Vagrancy and Restoring Order, broadens the definition of “mental illness” to include the homeless, funneling the homeless back into the psychiatric industry that most likely played a role in the crisis.
The EO is not reform. Recycling human lives through a profit-driven machine that exploits human desperation, trapping millions in a relentless cycle of abandonment has been tried and failed. One must wonder who is advising the President to take such extreme and inhumane measures? Could it be the very industry that will benefit from the increased funding that comes with the EO?
The failure of America’s behavioral health industry is not just a policy flaw—it is a catastrophic betrayal. A ruthless monopoly has taken hold, placed profits far above human lives and left hundreds of thousands of vulnerable Americans abandoned and homeless on the streets. Behind this broken system, major vendors, policymakers, and entrenched interests wield legal shields to evade accountability while pushing dangerous psychiatric drugs that devastate lives.
A stark example is Henderson Behavioral Health in Florida. For years, Henderson treated Nikolas Cruz, the Marjory Stoneman Douglas High School shooter in Parkland Fla., with powerful psychiatric drug cocktails but ignored repeated warning signs, labeling him “not a risk.” After years on toxic psychiatric drugs, Cruz turned to street Xanax (benzodiazepine) before murdering 17 innocent people. Families who sued faced cold court dismissals protecting providers from liability—even when negligence was clear. This immunity is no accident—it is an impenetrable systemic shield for the behavioral health industry.
One of behavioral health’s most shameful abuses is patient dumping. In 2013, Rawson-Neal Psychiatric Hospital in Las Vegas was found to have discharged over 1,500 psychiatric patients. It was dubbed “Greyhound Therapy” where psychiatric patients were given one-way bus tickets out of Nevada between 2008 and 2013. The discharge orders for one patient should be given a three-day supply of Thorazine, Klonopin and Cymbalta to treat his schizophrenia, anxiety disorder and depression, plus “Ensure and snacks for a 15-hour bus ride.” Dozens ended up in New York and California. Other states participated in the patient dumping practice as well when benefits ran out. In New York, hospitals discharged psychiatric patients onto the streets, sometimes clad only in paper gowns, with no follow-up care. Courts condemned these acts as unlawful and inhumane, yet liability shields still remain and penalties are very low and contracts are almost never cancelled. In fact Rawson-Neal Psychiatric Hospital did not lose their Medicaid Contract. The broad neglect continues in new forms. This is a major contributing factor to homelessness.
No one denies the problem of homelessness is urgent and painful. But turning to the same industry that helped create the crisis to “solve it” is insanity. The EO removes legal barriers to forced commitment and expands mental illness to cover homelessness. There is no doubt that some were diagnosed mentally ill in school and put on psychiatric drugs that contributed to the inability to fully function in society and will probably continue given that one in four Americans take at least one prescription mind-altering psychiatric drug.
The dark history of mental health institution shutdowns goes back to the Willowbrook State School Supreme Court ruling in New York. Willowbrook was a hellscape exposed in the 1970s for abuse and neglect. It closed with promises of humane community care, but psychiatry only rebranded. Walls fell, but endless drug cocktails and soaring costs remained. Behavioral health companies grew, went public, ousting local clinics, hiking costs, and lowering care quality. Emergency rooms overflowed; jails became mental institutions. Homelessness among treated patients rose.
Whistleblowers call this the “quieter horror”—vulnerable people dying alone in waiting rooms or overdosed on dangerous drugs while billions are spent annually on ineffective psychiatric drug treatments.
Military and veteran mental health care is not spared. Robert Card, under military oversight, was ordered to undergo a psychiatric evaluation and treated with mind-altering drugs just weeks before committing a mass shooting. The military faces lawsuits for failed care—not the vendor, Four Winds Hospital. The state of Montana even outsources rebuilding its mental health department to China, raising alarming concerns about oversight and sovereignty.
Central to these crisis’s are entrenched legal shields. Courts affirm mental health providers owe no special duty to protect third parties from patient violence. These protectors embolden a ruthless monopoly prioritizing profit and survival over patient safety and public welfare.
Patient dumping, once condemned, still haunts this system. The U.S. Second Circuit Court ruled hospitals must ensure safe transitions—not just clear beds. Yet liability protections persist, allowing neglect to continue.
Today’s so-called “solutions,” embodied by sweeping executive orders, deepen forced, profit-driven treatment and expand government control. The EO betrays dignity and traps millions in coercive systems protecting monopolies, not healing humans.
In the 1970s, Dr. Loren Mosher’s Soteria Project offered a humane, home-like treatment for first-episode psychosis using minimal medication. It outperformed hospitals but was defunded for threatening pharmaceutical profits. Mosher resigned from the American Psychiatric Association, calling it the “American Psychopharmacological Association.”
The way forward is to elevate humane perspectives, including those of Mosher, Dr. Peter Breggin, and the dissenting voices raised at the recent FDA’s SSRI and pregnancy hearings, that highlighted the dangers of the psychiatric drug model.
The industry’s legacy is a ruthless cycle of abandonment and addiction. Providers take taxpayer money, maximize profits, and destroy lives with impunity. Until liability shields like those protecting Henderson are removed, true provider competition enforced, psychiatric drug violence tracked, and proven community models funded, this tragedy will repeat.
History shows what happens when psychiatry and government unite: rights vanish, lives are controlled, and the powerless silenced. This EO reeks of powerful pharmaceutical insider intervention, not care. Instead of truly addressing homelessness, this executive order expands forced psychiatric control under the guise of care, driven by profit and coercion.
Be the Voice for the Voiceless
AbleChild is a 501(3) C nonprofit organization that has recently co-written landmark legislation in Tennessee, setting a national precedent for transparency and accountability in the intersection of mental health, pharmaceutical practices, and public safety.
What you can do. Sign the Petition calling for federal hearings!
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Airline Pilot Incapacitation Crisis After Illegal mRNA Shot Mandates Nicolas Hulscher, MPH
With 33 years in the cockpit, Dr. Kevin Stillwagon reveals how mRNA mandates endangered pilots, grounded careers, and put aviation safety at risk.
AUG 17, 2025
Today we’re joined by Dr. Kevin Stillwagon — retired airline captain with 33 years of experience, chiropractor, and immunology educator — who exposes the shocking rise in pilot incapacitations and deaths since the rollout of COVID-19 mRNA injections.
Key Findings
- 40% increase in early pilot deaths (before retirement age) since 2021
- Pilot long-term disabilities tripled starting in 2021
- Near-miss aviation events exploded — from just 1 per year pre-2021 to 28 per year at Washington National Airport alone
- The FAA’s Incapacitation Data Registry was discontinued in 2022, leaving no centralized tracking of pilot health
How mRNA Mandates Jeopardized Aviation Safety
- mRNA shots illegally forced on pilots violated FAA medical rules banning experimental products.
[Ed.: If jabbed pilots have been incapacitated in significant numbers, shouldn’t we be all the more on alert for vehicle drivers on the roads who have been jabbed? This would be 8 out of every 10 drivers!]
Canada to Begin Euthanizing Disabled Citizens Frank Bergman
August 16, 2025
In Canada, the liberal government’s dangerous expansion of euthanasia laws is set to open the floodgates to state-sponsored discrimination against people with disabilities.
For decades, the Canadian government has imposed a Nazi-style lethal ableism.
Over 90% of babies diagnosed with Down syndrome are aborted before birth.
Other disabled children often face the same fate.
But the upcoming change, set for 2027, is far worse.
Canada plans to expand its euthanasia policies to include those suffering solely from disability or mental illness.
This move has been met with near-unanimous condemnation from disability groups.
Even the United Nations Committee on the Rights of Persons with Disabilities has raised alarms.
The group is accusing Canada of engaging in Nazi-style “state-sponsored eugenics.”
Disability rights organizations, including Inclusion Canada, have been sounding the alarm for years, warning that people with physical disabilities are increasingly being pushed toward euthanasia due to the lack of adequate care or support.
Tragically, these warnings have gone ignored by the government.
One harrowing story circulating on X from victim advocate Samantha Smith reveals the horrifying reality of Canada’s slippery slope.
In it, a nurse performed several assisted suicides at a care home, including one case where the family of a mentally disabled man chose euthanasia for him, even though he didn’t want to die.
The man wasn’t terminally ill, wasn’t elderly, and wasn’t dying.
Nevertheless, he was forced into death against his will because his family deemed him expendable.
Smith’s account paints a grim picture: “They held his hand while he told them ‘I’m hungry’ and ‘I’m thirsty.’
“That poor man didn’t understand what was happening to him as he was pumped full of medication that would end his life.”
Despite the nurse’s moral objections, they were told that it was their “legal duty” to carry out the “assisted suicide” procedure.
The nurse couldn’t continue and refused, but Smith points out that not everyone will have the moral strength to resist.
What started as a push for “choice” and “dignity” has turned into a nightmare of coercion and loss of life.
In countries where euthanasia is already legal, such as the Netherlands, 40% of euthanasia deaths occur without the patient’s consent.
In Canada, the situation is no better.
The government has already offered euthanasia to Paralympians who only requested a mobility aid.
Euthanasia has also been carried out on individuals like Alan Nichols, who was euthanized after visiting his doctor with hearing loss.
Leaked documents reveal that Ontario’s euthanasia providers have tracked hundreds of possible criminal violations.
Yet, not one case has been referred to law enforcement.
Canada’s medical establishment is already embracing lethal ableism.
Once euthanasia eligibility expands to include those with disabilities and mental illnesses in 2027, it will likely only get worse.
For now, there is still time to stop this dangerous expansion, but the clock is ticking.
The lives of people with disabilities depend on halting this cruel and unjust eugenics policy before it spreads even further.
READ MORE – Canada Moves to Begin Euthanizing Children Without Parental Consent
Germany Confirms Covid ‘Vaccines’ Laced with Cancer-Causing DNA Frank Bergman
August 16, 2025
A team of leading German researchers has confirmed that Covid mRNA “vaccines” are laced with cancer-causing DNA contaminants.
The findings emerged during a major investigation into reports of dangerous levels of DNA contaminants in Pfizer’s Covid mRNA injections.
Experts have been sounding the alarm about the presence of DNA contamination in Covid shots for some time.
However, this latest study uses advanced techniques for more reliable quantification, making it the most significant investigation to date.
As Slay News has previously reported, leading scientists have been warning for some time that surges in deadly cancers among the Covid-vaccinated were caused by DNA fragments in the mRNA injections.
The study was led by Jürgen O. Kirchner, an Independent Researcher in Hamburg, and Professor Brigitte König of the University of Leipzig.
The results of the study were published in the Preprints journal.
The researchers hypothesized that residual DNA contaminants in multiple batches of Pfizer’s Covid mRNA “vaccine” significantly exceed regulatory safety thresholds.
They used advanced Qubit fluorescence spectroscopy to analyze vials for the “vaccines.”
Kirchner and König conducted an extensive critique and defense of their May 2024 study, which quantified residual DNA in Pfizer injections using Qubit fluorometry.
The authors challenge competing claims, most notably from Kaiser et al. (2024–2025).
Kaiser et al. argue that DNA measurements were inflated due to high mRNA concentrations interfering with Qubit readings.
To verify accuracy, the authors followed the Qubit DNA High Sensitivity Assay Kit protocol.
They tested multiple Pfizer mRNA shot batches, using standard additions and dilution controls.
They also examined fragment length distributions via the Agilent 2100 Bioanalyzer and analyzed the impact of RNA interference based on data from Qubit’s manufacturer, Thermo Fisher.
Independent laboratory testing of multiple Pfizer “vaccine” batches revealed residual plasmid DNA concentrations.
The contaminations range from 12 to 17.8 ng/µL, far exceeding the European Union’s legal threshold of 0.033 ng/µL per dose.
The researchers confirm that their findings reveal that DNA contamination exceeded safe levels by approximately 300 to 500 times.
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The Qubit fluorometric quantification method used in the analysis was confirmed to have minimal interference from residual RNA.
It was well below 1 ng/µL, falling within the instrument’s ±15% accuracy range.
These findings challenge prior claims by Kaiser et al. that “vaccine” batches complied with DNA safety limits.
The researchers behind the latest study argue that those earlier estimates relied on non-validated extraction techniques such as phenol-chloroform and ethanol precipitation, which are known to underrepresent true DNA content.
The specificity of the Qubit system was supported by both manufacturer documentation and internal validation using standard addition experiments.
Further reinforcing the findings, a December 2024 study by a U.S. FDA laboratory independently confirmed the presence of residual DNA in Pfizer’s Covid mRNA “vaccine” batches at concentrations ranging from 6 to 470 times above the FDA’s 10 ng/dose threshold, as Slay News reported.
Together, these results raise significant regulatory concerns about the accuracy of DNA quantification methods used during vaccine quality assessments.
They also suggest that DNA contamination in mRNA “vaccine” products has been massively underestimated.
This latest study reignites debate over residual DNA impurities in gene-based products such as Covid “vaccines.”
It raises urgent questions for regulators and public health agencies.
If the Kirchner-König findings are accurate and reproducible, Pfizer’s mRNA “vaccine” could contain DNA contaminants at levels that breach regulatory safety thresholds by orders of magnitude.
The authors argue that alternative measurement techniques underestimate contamination due to flawed extractions and methodologically unsound assumptions.
These underscore a critical gap in regulatory oversight and methodological standardization for nucleic acid-based vaccines.
Weighing in on the previous FDA study, Kevin McKernan, a former director of the Human Genome Project, described the findings as a “bombshell.”
McKernan has been sounding the alarm about the cancer-causing mechanism of DNA contamination in the vaccines.
He explained that plasmid DNA fragments entering the cell’s cytoplasm with the help of lipid nanoparticles could overstimulate the cGAS-STING pathway.
The cGAS-STING pathway is a crucial component of the innate immune response.
“Chronic activation of the cGAS-STING pathway could paradoxically fuel cancer growth,” McKernan warned.
“Repeated exposure to foreign DNA through COVID-19 boosters may amplify this risk over time, creating conditions conducive to cancer development.”
During the FDA study, traces of the SV40 promoter were detected among the DNA fragments.
While the authors concluded that these fragments were “non-replication-competent,” meaning they cannot replicate in humans, McKernan disagreed.
“To assert that the DNA fragments are non-functional, they would need to transfect mammalian cells and perform sequencing, which wasn’t done here,” McKernan stated.
“Moreover, the methods used in this study don’t effectively capture the full length of DNA fragments,” he added.
As Slay News previously reported, McKernan issued a warning to the public last month after discovering traces of Covid mRNA “vaccines” in the rapidly developing cancerous tumors of turbo cancer patients.
Dr. McKernan, a genomics scientist with 25 years of experience in his field, made the discovery during experiments in his Boston lab.
McKernan gene-sequenced a cancerous tumor, matching the genetic sequence to Pfizer’s Covid mRNA injection.
The discovery is being hailed as definitive proof that Covid mRNA “vaccines” cause cancer.
“We’re in the stage where we’re scanning through tumors to look for integration events and looking for evidence of this in cancer biopsies,” McKernan said.
“And we can find them now.
“They found one that had really high spike [protein] sent to us for sequencing.
“And we can find components of Pfizer’s vaccines inside this thing a year after vaccination.”
READ MORE – Major Study Links Covid ‘Vaccines’ to ‘Sudden Unnatural Death’ Surge
Why Synthetic mRNA is So Dangerous [6:33] PETER A. MCCULLOUGH, MD, MPH
Killing 22 Government mRNA Programs Should be Just the Start
AUG 17, 2025
Please enjoy this brief summary I did for Amanda Head and John Solomon on Real America’s Voice Just The News on why synthetic mRNA is so dangerous. The inability to shut off a potentially dangerous or lethal antigen like the SARS-CoV-2 Spike protein is the Achilles Heel of the failed biotechnology.
COVID-19 ‘Vaccines’ Estimated to Have Killed More People Than 121 Hiroshima Nuclear Bombings NICOLAS HULSCHER, MPH
FDA criteria for Class I recall and market withdrawal far exceeded.
NOV 03, 2024
Since the global roll-out of the COVID-19 injections in late 2020, substantial data has surfaced linking them to a catastrophic number of deaths. Below is a working list of some of the strongest evidence to date:
- Rancourt et al: estimated 17 million COVID-19 vaccine deaths worldwide by September 2023 .
- Mostert et al: estimated 3.1 million excess deaths likely attributed to COVID-19 vaccination/lockdowns among 47 countries of the Western World from 2020 to 2022.
- Vaccine Adverse Event Reporting System (VAERS): 37,966 reported COVID-19 vaccine deaths – under-reporting factor of 31 yields 1,176,946 COVID-19 vaccine deaths among countries that use VAERS.
- Skidmore: estimated 278,000 Americans may have died from the COVID-19 vaccine by December 2021.
- Pantazatos and Seligmann: estimated 146,000 to 187,000 possible vaccine-associated deaths in the United States by August 2021.
- Hulscher et al (I): estimated 49,240 excess cardiac arrest deaths possibly due to COVID-19 vaccination in the U.S. from 2021-2023.
- Hulscher et al (II): found a high likelihood of a causal link between COVID-19 vaccines and death from analysis of 325 autopsies.
- Aarstad and Kvitastein: found a higher COVID-19 vaccine uptake was associated with increased all-cause mortality.
- Alessandria et al: found all-cause death risks to be higher for those vaccinated with one and two COVID-19 vaccine doses compared to unvaccinated individuals. The subjects vaccinated with 2 doses lost 37% of life expectancy compared to the unvaccinated population during follow-up.
- 10.Lataster: found a positive correlation between COVID-19 vaccination rates and excess mortality for every month examined.
Regardless of methodology used, far too many suspected deaths have occurred due to the experimental COVID-19 injections. For reference, approximately 140,000 people were killed from the Atomic Bombing of Hiroshima in 1945. Therefore, the COVID-19 injection campaign may have killed the equivalent of at least 121 Hiroshima nuclear attacks.
COVID-19 ‘vaccine’ death acknowledgment by federal agencies may mirror the same path as finally declaring smoking harmful in 1964 after years of claiming cigarettes to be healthy.
Among 462 medicinal products that were withdrawn from the market between 1953 and 2013, the median interval between the first reported adverse reaction and the year of first withdrawal was 6 years. Unfortunately, the time elapsed from the first reports of serious adverse events to withdrawal of products has not improved consistently over the last 60 years. Since 1950, 95 medicinal products were withdrawn from markets due to causing death. 83% of withdrawals due to death utilized evidence drawn from case reports. Most withdrawals occur more than 1 or 2 years after the first reports of deaths begin to appear. Thus, COVID-19 vaccines are now long overdue for market withdrawal.
The continuation of advertising and recommending deadly medical products (COVID-19 injections) for all ages flagrantly violates The Precautionary Principle:
“When an activity raises threats of harm to human health or the environment, precautionary measures should be taken even if some cause-and-effect relationships are not fully established scientifically.”
The U.S. Food and Drug Administration defines a Class I recall as:
“A situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”
This indicates that the COVID-19 injectable products must undergo an immediate Class I recall by the FDA to protect public safety. This should be priority #1 of the next presidential administration, as COVID-19 injections remain an immediate threat to the entire U.S. population aged 6 months and older.
“The Untold Vaccine Story” w/ John Leake [59:09] Naomi Wolf
AUG 15, 2025
“A thought-provoking interview with John Leake exploring his new book Vaccines: Mythology, Ideology, and Reality, co-authored with Dr. Peter McCullough, diving into the myths, politics, and hidden truths shaping global vaccine narratives.”
Scrutinizing violence’s ties to antidepressants DR. PETER AND GINGER BREGGIN
“In too many cases, psychiatric drugs cause or contribute to horrendous acts of violence.”
AUG 11, 2025
Click here to watch the interview.
Dr. Breggin and Tamara Scott discuss the New York shooter, motivation and mental illness.
In addition to sharing the interview, above, we are reprinting an article by Dr. Breggin, below, that was published by Variety in 2013. The information is as important now as it was over a decade ago. Sadly, nothing has changed regarding psychiatry’s reliance on drugs to treat human distress and trauma.
Published in Variety Jan 18, 2013
Scrutinizing violence’s ties to antidepressants by Peter R. Breggin, MD
Peter R. Breggin, MD, is a psychiatrist and the author of many books and scientific articles dealing with adverse drug effects, including “Medication Madness” (2008). His latest book is “Psychiatric Drug Withdrawal: A Guidebook for Prescribers, Therapists, Patients and Their Families” (2013).
Huge efforts have been made by the pharmaceutical industry to prevent the public and the health professions from knowing that antidepressant drugs can cause violence and suicide.
Joe Wesbecker had threatened his co-workers in the past, but had never been violent. In 1989, Wesbecker was placed on Prozac (fluoxetine). One month later, he became agitated and delusional. Suspecting Prozac as the cause, his psychiatrist stopped the antidepressant. Two days later, with most of the drug remaining in his system, a heavily armed Wesbecker walked into his former place of work in Louisville, Ky., where he killed eight people and wounded many others.
Survivors and families of the deceased sued Eli Lilly for negligence in developing and marketing Prozac, and the case went to trial in 1994. A consortium of lawyers and an Indiana court had appointed me to be medical and scientific expert for more than 100 combined product liability suits against Eli Lilly concerning violence and suicide caused by Prozac. In that role, I became the scientific and medical expert in the Wesbecker case.
The lawyer handling the Wesbecker case died, and when the new attorney took over, he seemed to thwart every attempt I made to help us both prepare for trial. He did not tell me about huge amounts of new information, wouldn’t talk with me on the phone. The night before the trial, he still refused to discuss anything with me, and in frustration, I shoved a carefully prepared series of notecards into his hand, saying, “You must ask me these questions or we’ll lose the trial.”
When I testified the following day, the attorney tried to stifle some of my most telling testimony in support of his case against Eli Lilly. Several jurors voted to find the company negligent, but Lilly won the trial by a 9-3 vote. One more vote against the company, and it would have been a hung jury. Eli Lilly and the major media reported the trial as if it had wholly and forever exonerated Prozac and the company.
“In too many cases, psychiatric drugs cause or contribute to horrendous acts of violence.”
Afterward, I couldn’t figure out if the lawyer in the Wesbecker case was incompetent or, as my wife Ginger suspected, he had been bought in advance by Eli Lilly to throw the case. The trial judge, John Potter, later discovered that the trial had indeed been fixed.
Judge Potter threw out the rigged jury trial and changed the result to settled “with prejudice” by the drug company. This time major media failed to cover the incredible turnabout in the case. Although I have written about it extensively in my book “Medication Madness” (2008), the real outcome of the trial to this day remains relatively unknown even among psychiatric and legal experts.
Columbine
In 1999, Eric Harris, along with Dylan Klebold, slaughtered students and a faculty member at Columbine High School in Colorado. I was a psychiatric expert in several cases surrounding the Columbine massacre, none of which went to trial. From the medical records, I discovered that Harris had been prescribed the antidepressant Luvox one year earlier, before he became profoundly disturbed. Harris remained on Luvox over the next year, becoming increasingly filled with hate and violence. On autopsy, he had a significant level of Luvox in his bloodstream.
A 16-year-old boy in Manitoba, Canada, abruptly plunged a knife into the chest of one his best friends, killing him. The youngster, with no history of violence or serious mental illness, had been put on Prozac three months before the murder. When his mother told the psychiatrist that Prozac was making her son worse, the doctor increased the dose. Seventeen days later, with no significant provocation, the teenager killed his friend.
Aurora
Before he committed the massacre in the theater in Aurora, Colo., in 2012, James Holmes was in psychiatric treatment at his university clinic. Given that he was in treatment with a psychiatrist who was worried about his dangerousness, it is almost certain that Holmes was either taking psychiatric drugs or in withdrawal from them at the time he committed murder.
We do not know if the Newtown shooter, Adam Lanza, was taking psychiatric medication at the time of the shootings, although a Dec. 14 Washington Post article reported that a family friend said “he was on medication.” There are many suggestions that this socially withdrawn individual had been psychiatrically diagnosed and treated.
Notice that all five individuals (Wesbecker, Harris, Holmes, Lanza, and the Canadian teenager) were already under psychiatric care shortly before or when they committed violence. In addition, the Virginia Tech shooter was psychiatrically hospitalized a year before he murdered his classmates.
These events confirm that involvement in psychiatric treatment, with its emphasis on prescribing psychoactive drugs, is no protection against violence perpetrators. Instead, in too many cases, psychiatric drugs cause or contribute to horrendous acts of violence. Psychiatry is a cause and not a cure for mass violence, and looking for help from psychiatry will only distract us from seeking genuinely effective solutions.
Michael Yon: HORROR IN JAPAN — At Least 600,000 Dead from Covid Jabs LIONESS OF JUDAH MINISTRY
A massive Japanese database points to a loss of life so large it’s hard to fathom.
AUG 10, 2025
Combat correspondent Michael Yon delivers a bone-chilling warning: a Japanese science team, led by Dr. Yasufumi Murakami, has poured through 25 million vaccination records, and believes at least 600,000 lives were lost to Covid injections.
The scale of the tragedy is almost beyond human comprehension.
WATCH [2:44]
Source: Sense Receptor
“A science team… led by… Dr. Yasufumi Murakami…ha about 25 million records. And the deaths from the Covid injection in Japan are at least 600,000, they believe—that they know about.”
This clip of Yon is taken from a discussion with Joe Oltmann posted to the Untamed Nation Rumble channel on July 23, 2025.
Partial transcription of clip
“The science team is led up by by our mutual friend, Dr. Yasufumi Murakami. He’s a, an expert on this and he’s been pulling together the key people in Japan. And now they have up to about 25 million records. A week or so ago it was 21 million that they had, that they were talking about. But now that they’ve, they’re satisfied with the most latest records they’ve released. It’s about 25 million records. And the deaths in Japan are at least 600,000 they believe, that they know about.
“I’ve been in on the calls and the meetings and that sort of thing, but this is not actually, I’m cautious. At the end of the day, about 600,000 and counting. And it’s clearly getting worse. And so, it’s quite severe. It makes me wonder of course, what the numbers are like across the United States and in Europe. You know, Dr. Murakami, he’s living this night and day, you know, with his team. There’s a lot of volunteers. I think it’s about 350 volunteers who have been helping assemble the data.
“Of, course the Japanese are still going down that direction of more jabs. Not all of them, but you know, they’re like we are, except even more intensely jabbed than we are. And last year Dr. Murakami and Masako and I, we drove up to Fukushima, which is in a different part of Japan. A lot of people know Fukushima from the tsunami and the nuclear reaction. So they’ve actually built a jab plant there. I mean this thing is unbelievable. We went to it and published footage from it and this, this thing is, what’s it called? Arcturus, I think it was the name. They, they, we were right there, we were right at the front gate and again I published it. It’s on my Substack.
“But they were building another rep, what they call replicons. What Dr. Murakami calls replicons. These are the ones that will replicate, right, like, right out of the movie. And so if somebody else gets the jab, they would spread to unjabbed people.”
Government Records Obtained via FOIA Reveal Catastrophic Death Toll Hidden from the Public
GENOCIDE CONFIRMED: Japan Admits Covid Shots Killed Over 600,000
August 9, 2025
Here’s what’s simple—and profound:
When you undergo chemotherapy, the first casualty is your red blood cells, leading to anemia (treated with Epogen). Next, it wipes out neutrophils, leaving you vulnerable to infection (treated with Neupogen).
But the most devastating effect? It destroys your NK and T cells—your body’s elite cancer-fighting forces.
Think about that: The very treatment meant to kill cancer also annihilates the only cells that can actually protect you from it.
For 35 years, medicine has ignored this paradox. We replace red blood cells and neutrophils—but not the lymphocytes that matter most. The result? A weakened immune system, vulnerable to relapse and secondary cancers.
Now, consider long COVID. The virus is cunning—it targets the same NK and T cells, crippling immunity. The parallel is undeniable: Weakening these cells leaves the body defenseless, whether from chemo or chronic infection.
Dr. Soon-Shiong’s message is clear: “We’ve been treating cancer wrong.” The future lies in restoring immune function, not just attacking tumors.
The fight isn’t just against cancer or viruses—it’s for the immune system itself. And after 20 years of challenging the status quo, Dr. Soon-Shiong is leading that revolution.
It’s time to rethink everything.
WATCH [1:47]
August 9, 2025
“The purpose of the pandemic… was to damage the economy, to get us used to doing what we’re told under a mock emergency, and to roll up our sleeves to receive these dangerous materials.”
“Some self-appointed group of very rich people have decided they don’t like 8 billion people being on the planet, and want it to be a much smaller number.”
WATCH [2:20]
BREAKING NEWS: Alberta Premier Danielle Smith’s govt files Court Application to criminalize and eliminate the use of IVERMECTIN in Alberta! DR. WILLIAM MAKIS MD
AUG 09, 2025
The Court Application was brought by Danielle Smith’s bureaucrat, top Pedophile Leader and Registrar of College of Physicians and Surgeons of Alberta:
Dr. Scott McLeod, who has been attacking IVERMECTIN use in Alberta since COVID began (and reinstating the medical licenses of child rapists involved in Alberta’s Pedophile and Child Pornography Communities).
Scott McLeod was a doctor in the Canadian Armed Forces before he was appointed by the Trudeau-Notley alliance to the leadership of CPSA in 2017. He has controlled the medical licenses of 11,000 Alberta doctors since 2017 and sabotaged my original Cancer Program at Cross Cancer Institute.
I have just hired a Military Specialist lawyer with extensive background in Healthcare (Catherine Christensen, Valour Law)
The College (CPSA) has no legislative authority to attack our Health Coaching or Ivermectin Cancer Clinic, legislative authority given to them by the Provincial Government of Alberta under Health Professions Act.
They are overstepping their legal limits and if they get a corrupt Judge to sign off on any Court Order, they will criminalize and shut down ANY health practitioner who tries to help anyone with IVERMECTIN, FENBENDAZOLE or MEBENDAZOLE.
This is how @ABDanielleSmith will criminalize the use of Ivermectin in Alberta and she is doing it quietly under everyone’s noses.
You MUST fight this.
Flood Danielle Smith’s Office with phone calls on Monday: 780-427-2251.
Flood CPSA Scott McLeod’s Office with phone calls on Monday: 780-969-4969.
Scott McLeod, as a key Leader in Alberta’s Pedophile Community, has been targeting doctors who use Ivermectin since 2020 while simultaneously protecting doctors who engage in child sex abuse, child sex trafficking and child pornography.
Call Danielle Smith and tell her not only is this unacceptable, but Scott McLeod must be IMMEDIATELY removed and this Court Application withdrawn.
For those of you Albertans, who still worship Danielle Smith, realize that not only is Danielle responsible for the actions of CPSA by law, she also has a legal duty to ensure CPSA is serving the best interests of Albertans.
If CPSA is harming thousands of Cancer patients who use Ivermectin and may possibly get some of these patients killed, the responsibility lies squarely with Alberta Premier Danielle Smith, who is responsible for all of CPSA’s actions under law, as Premier of Alberta.
