COVID-19 / Malicious Medical Quackery
[Ed.: FEAR YOUR DOCTOR! Medicine is a disgraced profession. The Hippocratic Oath is no longer applicable… They cannot (and must not) be trusted any longer!
Cultivate Nosocomephobia and iatrophobia. Spread ‘vaccine hesitancy’! 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!
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]
DIED SUDDENLY: Official Documentary Film [1:17:21]
Inside mRNA Vaccines – The Movie [1:00:59]
Premiered Aug 11, 2025
This film explores the unprecedented global rollout of mRNA vaccine technology. www.insidemrnavaccines.com
00:00 Intro
02:53 Surgeon Joel Wallskog’s health issues
06:21 Operation Warp Speed initiative
06:38 Former CDC Director on mRNA vaccines
07:35 Regulators’ safety assessment
08:09 Calls to pause mRNA vaccines
09:32 mRNA researcher Robert Malone
12:56 Pathologist Ryan Cole on COVID vaccination
14:14 Cardiologist Aseem Malhotra on heart health
14:37 Cardiologist Peter McCullough on side effects
17:28 Scientist Jessica Rose on vaccine concerns
18:41 Critical care specialist Paul Marik on patient community
21:17 Explaining mRNA
23:45 How mRNA vaccines work
27:06 Spike protein and possible effects
30:57 Pathologist Arne Burkhardt’s biopsy findings
32:49 Health agencies’ safety stance
33:38 Vaccination in pregnancy and children
34:22 Artist Jessica Sutta’s health issues
39:03 Future uses of mRNA technology
42:55 Tobie Vergara’s health issues
45:12 History of mRNA vaccines
46:44 Modified mRNA technology
48:40 mRNA research status in 2017
49:07 Toxicity concerns in 2017
49:33 Progress in mRNA technology
49:50 mRNA vaccines during the pandemic
55:41 Support for post-vaccination syndrome
57:06 Doctors offering assistance
[Ed.: Other vaccine controversies include:
1. How the vaccines caused the paralysis of polio
2. How vaccines caused sudden infant death syndrome (SIDS)
3. How vaccines cause brain damage, but we call it autism
4. How we covered up brain damage and made it a mental condition
Bombshell Vax vs. Unvax Study Finally Sees the Light of Day — And the Results Are Staggering
[Ed.: An Inconvenient Study Full Movie [1:20:36]
Here is the link to the documentary An Inconvenient Study, which premiered tonight at the Malibu Film Festival. It is the brilliant true story of the suppression of a vaxed vs unvaxed children’s study and the Henry Ford Health Center–suppressed because it showed over several years 3-6 TIMES the incidence of chronic illness between children who had even ONE childhood vaccine compared with children compared with children who had NO vaccines. PLUS there was ZERO autism, ADHD and a couple of other things in the unvaxed cohort.
Watch the entire video and be sure to share it with everyone you think SHOULD KNOW about what it shows!
Over 1,100 Studies Reveal 12 Natural Compounds With Potent Anti-Cancer Effects Across All Major Tumor Pathways NICOLAS HULSCHER, MPH
Landmark analysis identifies 12 natural compounds with broad anti-cancer activity, consistently targeting core pathways such as cell death, immune evasion, metabolic dysfunction, and metastasis.
NOV 25, 2025
A landmark 2025 review titled, Natural anti-cancer products: insights from herbal medicine, published in Chinese Medicine, pulled together more than 1,100 scientific studies and uncovered something extraordinary: across cell, animal, and multi-omics research, 12 natural compounds repeatedly showed potent anti-cancer activity—triggering cancer cell death, blocking metastasis, cutting off tumor blood supply, disrupting tumor metabolism, and reversing drug resistance. Notably, the vast majority of this evidence comes from studies published since 2019, reflecting a rapid surge of new research in this field.
To build this analysis, they examined results from in vitro experiments (cancer cell lines), in vivo tumor models (mouse xenografts, orthotopic tumors, chemically induced cancers, zebrafish models), ex vivo mechanistic assays, and modern omics platforms including transcriptomics, proteomics, and metabolic profiling.
Their goal was to map how these compounds act at the molecular level. What emerged was a strikingly consistent pattern: a relatively small group of natural molecules repeatedly interferes with cancer’s core survival pathways — the very systems that support growth, spread, immune evasion, angiogenesis, and treatment resistance.
THE 12 NATURAL ANTI-CANCER COMPOUNDS
1. Apigenin (Chamomile)
- Helps immune cells detect tumors (reduces PD-L1)
- Slows growth signals inside cancer cells (inhibits PI3K/AKT, EGFR, ERK)
Improves chemotherapy responsiveness (reduces MDR1/P-gp activity) - Limits tissue invasion (suppresses NF-κB, MMP-2/9)
- Induces cell death through several pathways (apoptosis, autophagy, ferroptosis)
2. Artemisinin (Sweet Wormwood)
- Generates oxidative stress inside tumors (ROS, lipid peroxidation)
- Restricts blood vessel formation (anti-angiogenic)
- Slows cancer cell movement (reduces vimentin, N-cadherin)
- Helps counter drug resistance (affects STAT3, AKT, HSP90)
- Shows activity across many animal tumor models
3. Berberine (Coptis / Goldenseal)
- Disrupts major growth pathways (PI3K/AKT, HER2, TGF-β)
- Reduces tumor-fueling inflammation (NF-κB)
- Helps reverse drug resistance (P-gp, MRP1, NRF2)
- Lowers immune evasion signals (PD-L1)
- Reduces metastatic behavior (MMP-2/9)
4. Curcumin (Turmeric)
- Triggers cancer cell death (apoptosis, autophagy, ferroptosis)
- Lowers inflammation inside tumors (NF-κB, STAT3)
- Blocks blood vessel growth (VEGF inhibition)
- Helps reverse chemotherapy resistance (P-gp, BCRP)
- Reduces invasive behavior (Twist1, MMP-9, EMT markers)
5. Emodin (Rhubarb Root / Japanese Knotweed)
- Interferes with cancer cell communication (Wnt/β-catenin, STAT3, NF-κB)
- Initiates several types of cell death (necroptosis, ferroptosis)
- Disrupts cancer metabolism (GLUT1 reduction)
- Limits spread by reducing enzymes that break tissue barriers (MMP-2/9)
- Helps counter drug resistance (P-gp, GST)
6. EGCG (Green Tea)
- Slows growth by interrupting major pathways (PI3K/AKT/mTOR)
Promotes programmed cell death (Bax↑, Bcl-2↓) - Reduces inflammation (STAT3)
- Inhibits invasion and angiogenesis (MMP-2/9, VEGF)
- Decreases drug resistance (P-gp suppression)
7. Ginsenosides (Ginseng)
- Reduce metastatic behavior (EMT inhibition, MMP suppression)
- Improve immune responses (STAT3 downregulation)
- Promote cancer cell death (caspase activation)
- Help restore normal growth regulation (p53, PTEN)
- Some forms influence gut microbiota related to tumor microenvironments
8. Icariin / Icaritin (Horny Goat Weed)
- Support immune recognition of tumors (CD8+ T cells, CXCL9/10)
- Reduce PD-L1 (a key shield tumors use to hide)
- Inhibit tumor growth signals (PI3K/AKT)
- Counteract chemotherapy resistance (P-gp, MRP1)
- Improve cell adhesion and reduce invasiveness (E-cadherin upregulation)
9. Resveratrol (Grapes, Berries)
- Activates protective genes (p53)
- Reduces inflammation (NF-κB)
- Slows invasive behavior (vimentin↓, EMT↓)
- Initiates multiple cell death pathways (apoptosis, autophagy, ferroptosis)
Shows synergy with conventional treatments
10. Silibinin (Milk Thistle)
- Slows growth signals (mTOR, STAT3)
- Reduces tumor blood vessel development (anti-angiogenic)
- Limits spread (Wnt/β-catenin inhibition)
- Supports mitochondrial function
- Decreases PD-L1 expression
11. Triptolide (Thunder God Vine)
- Very potent at low concentrations (nanomolar range)
Blocks multiple tumor-promoting pathways (NF-κB, STAT3, AKT/mTOR)
Lowers immune evasion signals (PD-L1, CD47)
Promotes apoptosis and cell-cycle arrest
12. Ursolic Acid (Apples, Basil, Rosemary)
- Promotes cell death pathways (p53, ROS)
Slows tumor growth (AKT/mTOR inhibition)
Limits metastatic movement (CXCL12, FN1)
Helps reduce drug resistance
Activates stress pathways related to ferroptosis (NRF2 suppression)
Although the review does not provide detailed clinical trial outcomes, it assembles one of the most comprehensive collections of preclinical evidence ever compiled on how natural compounds act on cancer. Across cell studies, xenograft models, orthotopic tumors, and multi-omics analyses, the findings converge on a striking pattern: these molecules consistently disrupt the same core pathways that fuel tumor growth, immune evasion, metastasis, and treatment resistance.
Importantly, several of these compounds—such as curcumin, artemisinin derivatives, ginsenosides, icaritin, silibinin, and resveratrol—are no longer confined to laboratory research. Multiple early-stage and mid-stage clinical trials are already underway, and in the case of icaritin and certain ginsenosides, Phase II and Phase III studies are actively progressing. The scientific community is clearly beginning to take notice.
With cancer rates rising worldwide, these well-tolerated, multi-pathway natural compounds should be advanced into rigorous clinical testing to fully determine their therapeutic potential in human disease.
Nicolas Hulscher, MPH Epidemiologist and Foundation Administrator, McCullough Foundation
Support our mission: mcculloughfnd.org
Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.
[Ed.: I’ve noticed that the Horny Goat Weed does not make you any hornier…]
BREAKING: Dr. Rima Laibow Calls Out RFK Jr. for Failing to Withdraw the Ultra-Deadly Covid Jabs LIONESS OF JUDAH MINISTRY
She argues that ongoing mRNA approvals under his leadership amount to “Crimes Against Humanity.”
NOV 23, 2025
⚡ What aren’t they telling you? Please Join Exposing the Darkness News on Telegram.
Dr. Rima Laibow unloads on RFK Jr., claiming he’s backpedaling on vaccine truth and refusing to use his emergency powers to halt new mRNA authorizations.
Pointing to FDA pipelines and a shift in rhetoric, she asks bluntly:
“What the hell is going on here?”
Source: Sense Receptor
“Just look at the approval of the mRNA vaccines… that’s not, ‘Give him time, he’s working with a complex organization.’ That’s crimes against humanity and complicity.”
Laibow adds, “He’s gotta tiptoe and pussyfoot and condemn children, adults, and old people to illness and death because he’s afraid of somebody? Really?”
This clip of Laibow, a psychiatrist, is taken from an interview with Dr. Bill Lionberger posted to the Vaxxchoice Rumble channel on November 20, 2025.
Partial transcription of clip
“Kennedy allegedly came into his office, his HHS office, on day one already knowing what causes autism. He’s written about it, he’s given interviews, he’s made documentaries, he’s done bus tours, he’s written books. He’s made his mark on that particular issue. And now we hear it’s Tylenol? Okay, so that, that causes my eyebrows to go up as high as the back of my neck.
“Really? It’s Tylenol, is it? Okay. And maybe we’ll take a look at vaccines too, because golly gee, could be something else too, you know, that’s, that’s twinkle toes nonsense. Let’s just look at the mRNA vaccines… I listed all of the vaccines that have been— injections called vaccines, that have been approved since Kennedy took office on the 13th of February. And I listed the ones that are in the pipeline, and there are the FDA pipeline for approval, fast approval, and there are several mRNA and a couple of mRNA replicon ones.
“Well, that’s not, ‘Give him time, he’s working with a complex organization.’ That’s crimes against humanity and complicity. And I don’t understand how you put those two things together. We got a guy who understands all of these things, who’s well informed, who’s been brought up to speed, and who has the power and authority, more power than the President of the United States in terms of health emergency, by the way.
“His declaration of health emergency overrides that of the head of the executive branch of the government of the United States. Immense power. And he’s, he’s gotta tiptoe and pussyfoot and condemn children, adults, and old people to illness and death because he’s afraid of somebody? Really? Oh, gosh, we have to wait while children are rendered autistic, while he’s being afraid of people?
“Were you in that office, would you really condemn children? Would you really condemn old people? Would you really condemn young people to drop dead on the field of play with silent myocarditis from the vaccine that they were assured was safe and effective? No, you would not. And you would take the consequences, run the risk, and do what was right.
Well, what the hell is going on here? You tell me.”
Study Finds Nattokinase Dissolves 84% of Amyloid Microclots Within 2 Hours In Vitro NICOLAS HULSCHER, MPH
A natural enzyme potently degrades the same amyloid microclots recently found in 100% of COVID-19 vaccinated individuals tested.
NOV 22, 2025 The Focal Points
As I reported a few days ago, a recent peer-reviewed study revealed a deeply alarming finding: 100% of the vaccinated participants examined had amyloid fibrin(ogen) microclots circulating in their blood.
BREAKING STUDY: Anomalous Amyloid Microclots Found in 100% of the COVID-19 Vaccinated NICOLAS HULSCHER, MPH NOV 17, 2025 Read full story
These are the same Thioflavin-T–positive, β-sheet, fibrinolysis-resistant clots now widely observed in Long VACCINE and Long COVID patients due to spike protein exposure. The anomalous microclots also appear to be behind the long white fibrous clots being pulled out of corpses by the majority of embalmers worldwide.
Their presence in every vaccinated individual tested underscores a crisis that the medical establishment has yet to acknowledge — and one that now demands immediate scientific attention.
If they are as widespread as early data suggests, then the most urgent question now becomes: How do we degrade them?
Nattokinase Breaks Down Amyloid Microclots
A recent peer-reviewed study by Grixti et al, published in the Journal of Experimental and Clinical Application of Chinese Medicine, used purified recombinant nattokinase and a high-resolution automated microscopy system to observe exactly what happens when the enzyme directly contacts amyloid fibrin(ogen) microclots.
To generate true amyloid microclots, the researchers mixed fibrinogen with LPS, triggered clot formation with thrombin, and labeled the resulting structures with Thioflavin-T — producing the same β-sheet, ThT-positive fibrinaloid clots seen in human Long COVID and post-vaccine samples.
Nattokinase was then added at two concentrations: 14 µg/mL and 28 µg/mL — levels that fall within the range achievable in humans following high-dose oral administration.
The Results Were Clear and Quantitative
At the higher dose (28 µg/mL), nattokinase reached peak activity at around 2 hours and produced:
- ~84% reduction in total clot number
(Figure 4A: 920 → 150) - ~52% reduction in total amyloid fluorescent intensity
(Figure 4B: 2500 RU → 1200 RU) - ~20% reduction in median clot size
(Figure 4C: 15 µm → 12 µm — though this metric underestimates true digestion because the smallest clots disappear first)
At the lower dose (14 µg/mL), nattokinase still produced substantial, dose-dependent effects:
- ~67% reduction in total clot number
(920 → 300) - ~20% reduction in total amyloid intensity
(2500 RU → 2000 RU) - ~7% reduction in median clot size
(15 µm → 14 µm)
In other words: nattokinase directly digested amyloid fibrin(ogen) structure.
The authors state this explicitly:
We show that recombinant nattokinase is effective at degrading the fibrinaloid microclots in vitro.
This is the strongest biochemical evidence to date that a natural fibrinolytic enzyme can break down the same amyloid microclots now found in the blood of vaccinated individuals and Long COVID patients.
Potent Dual-Activity
Amyloid fibrin microclots are not ordinary clots. They are structurally misfolded, β-sheet amyloid constructs that resist plasmin, resist rtPA, and trap inflammatory proteins in a dense mesh. Their resistance to dissolution means they can persist in circulation, obstruct capillaries, and contribute to a long list of chronic symptoms.
Adding to this, nattokinase has already been shown in studies to degrade the SARS-CoV-2 spike protein itself (in-vitro) —the same protein that drives amyloid transformation of fibrinogen and accelerates the formation of fibrinaloid microclots. This was one of the primary reasons nattokinase was incorporated into McCullough Protocol Base Spike Detoxification:
This dual activity is significant: nattokinase appears to be able to break down both the trigger (spike) and the pathological result (amyloid microclots). No pharmaceutical thrombolytic therapy has demonstrated this combined effect.
This makes nattokinase one of the few agents with a plausible mechanism to reduce amyloid clot burden without requiring invasive procedures, mechanical devices, or hospital-grade thrombolytics.
Secondary Evidence: Mechanical Clot Destruction via Ultrasound
Alongside this nattokinase study, another recent paper by Rasouli et al demonstrated that amyloid microclots can also be physically fragmented using low-frequency ultrasound, gas microbubbles, and rtPA in a microfluidic vein model. In the strongest condition — low-frequency ultrasound combined with microbubbles and rtPA — large amyloid microclots (>30 µm) were reduced from ~550 to ~20 (Figure 5F), representing a >90% reduction. This demonstrates that cavitation-enhanced ultrasound can physically shatter nearly all large amyloid microclots in a controlled microfluidic model.
However, this approach requires specialized ultrasound equipment, precise acoustic dosing, and close monitoring to avoid cavitation-related tissue damage. While the study clearly shows that amyloid microclots can be mechanically shattered with sufficient low-frequency ultrasound and microbubble–mediated forces, translating such a protocol into human clinical practice would demand extensive safety trials, controlled environments, and expert oversight. These methods may ultimately prove valuable for individuals with severe or refractory amyloid microclot burden.
The Path Forward
If amyloid microclots are present in 100% of COVID-19 vaccinated individuals in some cohorts, then the first priority is determining the true population prevalence. We urgently need large-scale, unbiased studies using standardized Thioflavin-T microscopy, flow cytometry, or advanced microfluidic analysis to map how widespread this pathology is.
Equally urgent is the need for human trials of nattokinase, evaluating:
- pharmacokinetics at different dosing levels
- optimal timing and duration
- real-world effects on amyloid microclot/spike burden
- symptom improvement
- combination strategies with other natural fibrinolytics
The scientific path forward is becoming clear: the amyloid clots can be detected, measured, and in controlled settings, broken down.
Whether the wider scientific community chooses to act on this knowledge will determine how many people suffer long-term consequences from a serious problem that is now plainly visible.
Nicolas Hulscher, MPH Epidemiologist and Foundation Administrator, McCullough Foundation
Support our mission: mcculloughfnd.org
Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.
Read previous articles https://krakennews.us/daily-shmutz-covid-19-malicious-medical-quackery-11-21-25/
