Autoimmune Inflammation and Disease Triggered by the Covid-19 Genetic Injections (Vaccines) an Interview with Panagis Polykretis, PhD

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Autoimmune Inflammation and Disease Triggered by the Covid-19 Genetic Injections (Vaccines) an Interview with Panagis Polykretis, PhD

…Alzheimer’s & the “Gut”; Aortic Dissection & Spike Protein; Cognition & Chlorella; UK Ivermectin Sales; Transient Global Amnesia & Covid Injection; The Value of the PSA Test; Stimulating T Cells..

Panagis Polykretis, PhD
“Allineare Sanità e Salute” Foundation
Milano, Italy
Independent Medical-Scientific Commission (CMSi)
Milano, Italy
panagis.polykretis@gmail.com
Dr. Panagis Substack
(https://substack.com/@panagispolykretis)
“Autoimmune Inflammatory Reactions Triggered by the COVID-19
Genetic Vaccines in Terminally Differentiated Tissues.”
Autoimmunity 2023 Dec;56(1):2259123. (2026)

Kirk Hamilton: Can you please share your educational background and current position?

Panagis Polykretis: I earned my degree in Biology at the University of Florence (Italy), followed by a PhD in Structural Biology at the Magnetic Resonance Center (CERM) also at the University of Florence. That training gave me a solid grounding in structural and molecular biology and in biophysics. After my PhD, I stayed on at CERM as a post-doctoral researcher, and then moved to the Institute of Applied Physics “Nello Carrara” of Italy’s National Research Council (CNR), in Sesto Fiorentino, where I worked as a researcher for four years — until, as I was told, “my views” and my publications on the COVID-19 vaccines closed off further progression in my career there. Today I work as a medical researcher at Ancestralize Ltd., a private company whose goal is to help revolutionize people’s health by addressing the drivers of chronic low-grade inflammation and metabolic imbalance — caused largely by ultra-processed foods and refined sugars, which have unfortunately become the main nutritional staple across much of the Western world — through targeted diet and lifestyle interventions. Furthermore, I am a member of the Scientific Committee of the “Allineare Sanità e Salute” Foundation, a member of the independent Medical-Scientific Commission – CMSi as well as a member of the International Advisor Board of Make Europe Healthy Again.

KH: What got you interested in studying the mRNA COVID-19 vaccine and autoimmunity in the first place?

PP: What first mobilized me was watching public health policy being implemented at the start of the pandemic without, in my view, adequate scientific grounding, and then seeing the genetic COVID-19 vaccines rolled out indiscriminately at massive scale on that basis. What struck me specifically was that their immunization mechanism intrinsically requires the body’s own cells to essentially sacrifice themselves (turning into factories that manufacture engineered viral antigen and, in doing so, becoming targets of the immune system themselves), and that this came with heightened risks tied to uncontrolled biodistribution. That is what prompted me to throw myself into this relentlessly, hoping to raise awareness within the scientific community about the potentially serious risks of autoimmune reactions against self-tissue, and about the need for thorough biodistribution studies as well as rational harm/benefit assessments.

Underlying all of that was a more basic immunology question I felt was not being asked publicly. We have known for decades that any nucleated cell producing a protein the immune system does not recognize as “self” is destined to be flagged as a threat and targeted for destruction. That is not controversial, it is how we fight viral infections and screen for cancerous cells. What struck me in late 2021 was that nobody seemed to be asking the obvious pharmacological follow-up: where in the body does this happen, in which tissues, and for how long? That is a biodistribution question, standard for any new drug or gene therapy, and it simply was not being asked for these vaccines. This is what compelled me to lay out this mechanism and its associated risks to human health in a 2022 letter to the Editor of the Scandinavian Journal of Immunology entitled “Role of the antigen presentation process in the immunization mechanism of the genetic vaccines against COVID-19 and the need for biodistribution evaluations” (https://doi.org/10.1111/sji.13160). “…The ‘traditional’ vaccines generally do not induce human cells to produce viral proteins, and thus, human cells do not expose viral antigens deriving from their proteosynthetic activity. On the contrary, the genetic vaccines against COVID-19 induce human cells to produce the spike protein, relying intrinsically to an autoimmune reaction, extended to all the cells that intake the genetic material and start the protein synthesis….”

KH: Can you define what an autoimmune inflammatory reaction is? What are the mediators? Can you give an example of a human autoimmune condition?

PP: One nuance worth being careful about: what is described here with the vaccine-derived spike protein depends on the level at which the reaction is defined. If the determining factor is the tissue involved, the reaction can reasonably be called autoimmune, since it is macroscopically directed against a self-tissue (a cardiomyocyte, neuron, hepatocyte, or whichever cell type is affected). However, if the analysis is zoomed in to the molecular level (which is what the more modern definition actually requires), the antigen being targeted is not, strictly speaking, a self-antigen. It is a viral antigen, the spike protein of SARS-CoV-2, which however exploits the cell’s own protein-synthesis machinery to be produced. Under this narrower molecular definition, the reaction does not constitute autoimmunity, since it is not directed against a native self-protein. By the more modern standards, then, it would be more accurate to describe these events as immune reactions against self-tissues, rather than as autoimmunity.

As an example, multiple sclerosis is a case in point: autoreactive T cells target myelin, the insulating sheath surrounding nerve fibers in the central nervous system, causing demyelination and the neurological symptoms patients experience. This is, in fact, a condition I had worked on prior to turning to immune reactions against self-tissues triggered by genetic vaccines, specifically looking at how molecular changes to myelin antigens could make them appear foreign to the immune system.

KH: What is the hypothesized component of the COVID vaccine that triggers this autoimmune inflammatory reaction — the spike protein?

PP: It is not an hypothesis anymore, irrefutable histopathological evidence exist proving that mechanism. Across both the mRNA platforms (Pfizer/BioNTech, Moderna) and the adenoviral- vector platforms (AstraZeneca, Janssen), the vaccine’s purpose is to get human cells to manufacture the SARS-CoV-2 spike protein, so the immune system learns to recognize it. Once a cell does that, the spike protein is handled two ways: (i) the whole protein can “sit” on the cell surface, visible to B cells and helper T cells, and (ii) fragments get loaded onto MHC class I for display to CD8+ cytotoxic T cells. Both routes mark that cell as making something foreign (that’s the intended mechanism, it’s how the vaccine generates immunity). The question we’ve raised is what happens when that “marking for destruction” lands on a cardiomyocyte, a neuron, or a hepatocyte instead of a transient immune cell, and how widely throughout the body that occurs.

KH: Can a SARS-CoV-2 infection itself trigger a similar inflammatory autoimmune reaction, or is it just the mRNA vaccines?

PP: Both can, but through different mechanisms. With a natural infection, especially severe disease, the dominant route is what we describe in the 2026 paper (Detection of Vaccine-Derived Spike Protein “Associated with Immune Cell Infiltration in the Heart and Liver: A Report of Two Cases”, https://doi.org/10.3390/cells15110978): innate immune hyperactivation — a cytokine storm, with interleukin-6 and other mediators surging — that can activate pre-existing autoreactive B-cell clones or work through molecular mimicry, where a viral protein structurally resembles a human protein closely enough to confuse the immune system. That’s documented by studies performed before the rollout of genetic vaccines, so there’s no confounding overlap.

With vaccination, the mechanism is more direct: host cells are induced to manufacture the spike protein themselves and present it as an entire protein on the cell surface or as fragments on the Major Histocompatibility Complex I (MHC I), so the cell becomes a target by design, wherever the vaccine construct reaches.

KH: Do the four common coronaviruses that circulate globally and cause mild cold-like symptoms trigger any inflammatory autoimmunity?

PP: This is not an issue I have worked on, and I don’t have documented evidence. Therefore, I do not feel it is right for me to give a definitive answer in this case. I am aware of some scattered findings in the literature pointing toward a possible role for a couple of these viruses in immune-mediated processes, but I have not examined this closely enough to speak to it with real confidence, and I do not think it would be right for me to overstate a conclusion.

KH: Did SARS-CoV (2002) or MERS-CoV (2012) cause autoimmune inflammation in the host?

PP: To my knowledge, what has been documented in humans for both SARS-CoV and MERS-CoV is the innate immune hyperactivation mechanism, similar to the first mechanism described earlier from the natural SARS-CoV-2 infection. I am not aware, in this pre-pandemic literature, of any demonstration that the hyperactivation observed in these two outbreaks ever progressed to autoimmune reactions against tissues outside the respiratory tract, such as the brain for example, which by contrast, can occur following vaccination with genetic vaccines. This difference is also explainable by the distinct biodistribution that a virus can have within the organism compared with lipid nanoparticles, which were specifically engineered to optimize fusion with cell membranes and therefore have the ability to cross body compartments that a respiratory virus, largely confined to the lung and airway epithelium, would not as readily reach.

KH: Does this inflammatory autoimmunity result in more autoimmune conditions from the mRNA vaccines, as suggested by the study of Claudia Chaufan, MD, PhD?

PP: Dr. Chaufan and her co-authors, in their scoping review article “COVID-19 vaccines and autoimmune disorders: A scoping review”, report several mechanisms of action proposed in the literature linking COVID-19 vaccination and autoimmune disorders, including autoimmune inflammatory syndrome induced by adjuvants, molecular mimicry, bystander immune activation, and interactions with immunosuppressive and disease-modifying therapies. (Staying Healthy Today Interview,” Autoimmune Disorders and The Politics of Evaluating Covid-19 Vaccine Harm. An interview with Claudia Chaufan, MD, PhD”. “COVID-19 vaccines and autoimmune disorders: A scoping review, AIMS Medical Science, 2025, 12(4): 325-349.“

The mechanism described in my papers that were discussed earlier (i.e. the immune targeting of the body’s own cells when they synthesize the vaccine-derived spike protein) is a distinct pathway, it is supported by solid immunohistochemical evidence directly documenting vaccine-derived spike protein presence in specific tissues. This does not exclude the other mechanisms Dr. Chaufan catalogs. Several pathways can plausibly operate at once, or in different patients, and nothing about demonstrating one mechanism rules out the others contributing to the emergence of new autoimmunity or to the exacerbation of disease in people with pre-existing autoimmune conditions.

KH: Should the mRNA COVID-19 vaccines be taken off the market because of a lack of safety studies, in order to study issues like autoimmunity?

PP: As described in a presentation I delivered at the Italian Senate on October 27, 2025, titled “Evaluation of Safety Issues Associated with Genetic Vaccines Against COVID-19”, the risk of autoimmune reactions against the body’s own tissues is only one piece of a much larger set of unresolved safety questions surrounding these pharmaceutical products.

These products present so many open flaws that they are not limited to the risk of autoimmune reactions. The following questions remain, to this day, without a clear and documented answer:

– What exactly is contained in the vials, given the reported presence of residual, potentially replication-competent plasmid DNA contamination, including sequences derived from the SV40 oncovirus, in doses administered to billions of people?

– Where the vaccine-derived genetic material actually spreads within the body once injected, given evidence, including from the manufacturer’s own preclinical data, indicating broad biodistribution beyond the injection site within 48 hours?

– How long the vaccine-derived genetic material persists in cells and continues to induce spike protein synthesis, given documented cases of spike protein detected in human tissue many months after vaccination?

– Which tissues are capable of synthesizing the vaccine-derived spike protein, and what the potential health consequences of that synthesis are, particularly in organs such as the heart and brain?

– Does the residual DNA material have the ability to interact with the human genome in any way, an interaction that, to date, has not been ruled out through adequate genotoxicity testing?

– What the real, sustained protection offered by these vaccines actually is over time, given retrospective cohort data suggesting that protection not only wanes but can turn negative?

Given the number and the gravity of these open questions, none of which were resolved before mass vaccination campaigns proceeded my position is that these pharmaceutical products should be immediately withdrawn from the market.

KH: What do you suggest should be done to answer this question regarding inflammatory autoimmunity from the mRNA COVID-19 vaccine?

PP: Immunohistochemical studies are sufficient to describe the mechanism and the cell types involved. These are, fortunately, techniques well established for decades, requiring instrumentation that is fairly standard and readily available in many hospitals that perform routine histopathology. Accordingly, thorough histopathological examination should be performed during autopsies and biopsies, specifically looking for the vaccine-derived spike protein.

KH: Do you have any other comments on this very interesting subject?

PP: What follows is not really a comment but an exhortation. I would like to encourage physicians to look objectively for the causes of the harm their patients have suffered, and to follow the evidence all the way through, specifically testing for the vaccine-derived spike protein, because this phenomenon could be occurring far more commonly than is currently believed. Every unexplained adverse event, every unexpected death in a recently vaccinated patient, deserves that level of diagnostic rigor, rather than being dismissed by default as unrelated or coincidental. Only through this kind of systematic, tissue-level investigation, case by case, will the magnitude of this issue ever become clear.

KH: Do you recommend a specific lab to test for the actual spike protein in living patients? Right now, like others, I am using the surrogate marker of IgG Spike Protein Antibodies?

Without pointing to any one specific laboratory, since I would rather not appear to be endorsing a particular provider, I can say that this type of testing (direct detection of spike protein in plasma, in circulating exosomes, and within peripheral blood mononuclear cells, alongside residual vaccine mRNA testing) does exist and is offered by specialized labs, including at least one in the UK that sources the analysis out to a partner lab in Germany. I would expect that similar testing is available through comparable specialized laboratories in other countries as well.

That said, I want to be honest about how I personally view the clinical value of this kind of testing. For me, confirming whether one’s own body is still producing spike protein months after vaccination has more of an “academic” value, than a direct bearing on what to actually do about it clinically. It can even be counterproductive in some cases, if it pushes patients into a state of stressful health-related anxiety without giving them a correspondingly clear and validated intervention to act on, since they do not provide information regarding which tissue is actually producing the vaccine-derived spike protein, and there is no way to act directly against their own cells that are producing it, without harming their own body.

I have to admit that I remain fairly skeptical of the various protocols and techniques currently marketed as detoxification from the spike protein, including mechanical approaches. I want to emphasize, though, that this is just a “gut feeling” on my part, not a position based on any time actually invested in researching or evaluating the efficacy of the various existing detoxification protocols.

As I have always maintained, my primary recommendation, for someone who has the misfortune of still having cells producing vaccine-derived spike protein months after vaccination, is to focus on keeping the body’s overall systemic inflammation as low as possible through a genuinely healthy diet and lifestyle. Though, I suspect this advice, prioritizing diet and lifestyle, holds true in general for anyone, regardless of vaccination status.

KH: In patients who have died are you talking about looking for the spike protein in autopsy tissue samples?

PP: Yes. I consider this an essential step, absolutely necessary for science to understand the mechanisms through which genetic vaccines can cause adverse reactions, and it should have been standard practice from the very beginning, in order to gather as much information as possible and allow for rational risk-benefit assessments, potentially preventing the loss of lives.

Beyond the scientific value, there is also a human one. For a considerable number of families who have unfortunately lost a loved one through these mechanisms, this kind of investigation would have meant something very different from a report simply reading “sudden death from unknown causes”. It would have meant actually knowing what their loved one died of.

KH: Thank you very much Dr. Polykretis for taking the time to share this potentially lifesaving information?

PP: Thank you very much for your invite, it has been a true pleasure.

Highlights…

AORTIC DISSECTION – RISK FACTORS – COVID VACCINE – The Predictable Catastrophe: Why Aortic Dissection Should Never Be a Surprise. Death of Senator Lindsey Graham should be reviewed for antecedent predictors to inform others at risk. Peter A. McCullough, MD, MPH, Focal Points, Jul 14, 2026.
1) An autopsy case report of aortic dissection complicated with histiolymphocytic pericarditis and aortic inflammation after mRNA COVID-19 vaccination. “…Microscopic examination revealed pericarditis with predominantly macrophage and lymphocyte infiltration. These histological findings were compatible with those of post-vaccination myocarditis…In the present case, extended inflammation of the aortic adventitia was a possible cause of aortic wall fragility followed by dissection…”

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Nutrition, Prevention and Integrative Medicine…

ALZHEIMER’S DISEASE – GUT – For Years We Searched for Alzheimer’s in the Brain. Now, Researchers Suggest It May Begin Elsewhere. A large-scale genetic study suggests some of the processes driving Alzheimer’s disease may begin in the lungs, gut, and blood, years before reaching the brain. Rakefet Tavor, Epoch Times, 7/6/2026.
1) Genomic partitioning of Alzheimer’s disease in humans reveals non-CNS etiology. “…We observed limited genetic enrichment in the CNS, with brain-resident microglia emerging as the sole enriched cell type. Instead, AD risk loci were predominantly enriched in peripheral immune compartments and immune-enriched barrier tissues, such as the lung and the digestive tract, and particularly within myeloid-lineage cells…”

ALZHEIMER’S DISEASE – PREVENTION – Alzheimer’s Runs in the Family; Smart Move to Start Prevention Measures Now. Why waiting for symptoms is a losing strategy — and what to do about it today. Peter A. McCullough, MD, MPH, Jul 14, 2026.

AORTIC DISSECTION – SPIKE PROTEIN – FIBROSIS – Could spike protein-mediated fibrosis predispose to aortic dissection? Implications for histopathological evaluation and differential diagnosis. Jessica Rose, Unacceptable Jessica, Jul 13, 2026.

COGNITIVE DECLINE – CHLORELLA – EXERCISE – Simultaneous Multicomponent Exercise and Chlorella Intake Improve Information Processing Function and Prevent Decline in Executive Function among Community-Dwelling Older Adults in Japan: A Randomized Controlled Trial. Dr. Kojiro Ishii, Faculty of Health and Sports Science, Doshisha University, Kyo-Tanabe, Japan, Tel: +81-774-65-6724; kishii@mail.doshisha.ac.jp

IVERMECTIN – UNITED KINGDOM – SALES – Ivermectin Prescriptions Soaring In England. The latest on this little old medicine with a variety of uses. Tess Lawrie, MBBCh, PhD​, A Better Way with Dr Tess Lawrie & Friends, Jul 14, 2026.

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Cancer…

BREAST CANCER – IVERMECTIN – MEBENDAZOLE – CBD OIL – 53 year old woman in GEORGIA with Early Stage TNBC Breast Cancer, poorly differentiated, reports after 8 months: Cancer Free headed into Surgery! William Makis, MD, Covid Intel, July 08, 2026

BREAST CANCER – MEMORY LOSS – Katie Couric: Vaccine Evangelist, Breast Cancer, and a Brain That Forgot. Tragedy of COVID-19 vaccination playing out in public figures as audiences connect the dots. Peter A. McCullough, MD, MPH, Focal Points, Jul 11, 2026. ”…Then she got breast cancer. Then, in July 2026, she suffered an episode of transient global amnesia (TGA) so severe she forgot what year it was, who was president, and hours of her own life…”

CANCER – PREVENTION – What the Public Is Not Told About Cancer Prevention. The Hidden Role of Metabolism, Lifestyle, Inflammation, and Environmental Exposure in Modern Cancer. Paul Marik, MD, Cancer & Metabolic Healing. Jul 08, 2026.

CANCER – IMMUNOTHERAPY – T CELLS – T-Cell Immunity: The Holy Grail of Cancer (and COVID-19) Prevention? Immunosenescence is a primary driver of the increased risk of cancer in older adults. An inactivated, nonpathogenic bacterium shows promise in stimulating T-cell production. John Leake, Focal Points, Jul 13, 2026.
1) Rook GA, Dalgleish A. Infection, immunoregulation, and cancer. Immunol Rev. 2011 Mar;240(1):141-59. Graham A. W. Rook, Department of Infection, University College London (UCL), 46 Cleveland Street, London W1T 4JF, UK e-mail: g.rook@ucl.ac.uk “…Dysregulated chronic inflammation can drive oncogenesis and also provides growth and angiogenic factors that enhance the subsequent proliferation and spread of tumor cells. Thus, a modern failure to down-regulate inappropriate inflammation could underlie increases in some cancers in parallel with the increases in chronic inflammatory disorders…”

COLON CANCER – COLONOSCOPY – FLEXIBLE SIGMOIDOSCOPY – Colonoscopy Versus Flexible Sigmoidoscopy for Colorectal Cancer Screening: An Evidence-Based Review. Paul Marik, MD, Cancer & Metabolic Healing, Jul 12, 2026.

COLON CANCER – PREVENTION –Preventing Colo-rectal Cancer – Keeping your POOP Healthy. Cancer & Metabolic Healing, Paul Marik, MD, Jul 12, 2026.

COVID mRNA VACCINE – CANCER INCREASE – COVID vaccination and post-infection cancer signals: Evaluating patterns and potential biological mechanisms. Oncotarget. 2026 Jan 3;17:1-29. “…Across reports, several recurrent themes emerged: (1) unusually rapid progression, recurrence, or reactivation of preexisting indolent or controlled disease, (2) atypical or localized histopathologic findings, including involvement of vaccine injection sites or regional lymph nodes, and (3) proposed immunologic links between acute infection or vaccination and tumor dormancy, immune escape, or micro-environmental shifts…” (Charlotte Kuperwasser, PhD, Department of Developmental, Molecular and Chemical Biology, Tufts University School of Medicine, Boston, MA 02111, USA; email: charlotte.kuperwasser@tufts.edu / Wafik S. El-Deiry, MD, Legorreta Cancer Center at Brown University, The Warren Alpert Medical School of Brown University, Providence, RI 029121,USA email: wafik@brown.edu )

COVID 19 mRNA VACCINE – TURBO CANCERS – “…The observations of oncologists from around the world as well numerous published peer- reviewed case reports (1-12) and epidemiological data from the US, UK , S. Chorea and Japan indicate that there has been an abrupt increase in the incidence of cancers beginning in 2021 and continuing into 2023, following the widespread use of the COVID-19 vaccination. (13-19)…” Paul Marik, MD and Justus Hope MD., Cancer & Metabolic Healing, Jul 09, 2026.

ENDOMETRIAL CANCER – IVERMECTIN – FEBENDAZOLE – 62 year old FLORIDA woman with Early Stage Endometrial cancer reports after 6 months – Cancer Free! William Makis, MD, Covid Intel, Jul 09, 2026.

PARKINSON’S DISEASE – CHLORELLA – RESEARCH for Parkinson’s – CHLORELLA. William Makis, MD, Covid Intel, Jul 13, 2026.

PROSTATE CANCER PREVENTION – Preventing Prostate Cancer. Take action Now. Cancer & Metabolic Healing, Jul 13, 2026.

PSA – CANCER – SCREENING – PSA Screening: Promise, Pitfalls, and the Future of Prostate Cancer Detection. Paul Marik, MD, Cancer & Metabolic Healing, Jul 14, 2026.
”…Elevated PSA levels may occur with:

  • benign prostatic hyperplasia (BPH),
  • prostatitis,
  • urinary retention,
  • infection,
  • recent ejaculation,
  • prostate manipulation,
  • aging,
  • and prostate cancer.

Thus, PSA is best viewed not as a cancer test, but as a marker of prostate gland activity and disruption…”

Kirk’s Comment: PSA’s have significant value if done serially like once per year along with a digital rectal exam. A slow steady rise is normal. A singular PSA elevation when there hasn’t been any serial testing doesn’t necessarily mean its cancer. It could be an infection or prostatitis, a “trauma” (like riding bicycle or sex), just an enlarge prostate, or a variety of things. A sudden spike should be recheck to confirm. If I see a “jump” in over a point in a year I pay attention and recheck in three months. If you feel an irregularity you might do a prostate MRI. A prostate MRI is a great diagnostic tool. It also is a good tool to identifying areas to do a biopsy and REDUCE the number of biopsy “pokes”. If you are a patient and you are going to have a biopsy after a prostate MRI for suspicious areas the interventional radiologist or whoever is doing the biopsy SHOULD TELL YOU HOW MANY SAMPLES they are going to take. And it shouldn’t be 12, 15 or 19 some patient told me the other day. The prostate MRI should help the radiologist “target” biopsies just to the suspicious areas. It should be more like 2-4 targeted samples. Just shotgunning 12-15 samples into the prostate after a prostate MRI is inappropriate and a waste of the technology. For more than 25 years I have referred patients to Prostate Oncology Specialists a group of oncologists only dedicated to preventing and treating prostate cancer with the least and most “quality of life” medical interventions possible. They do color Doppler ultrasound on most all their patients initially in the office and are very skilled at it. They can see the suspicious area (s). If they need greater clarification before a biopsy they would get a prostate MRI and do “targeted” biopsies. Usually 2-4 samples not 12 plus. And the last conversation I had with they have never had to refer someone for a prostatectomy. They treat prostate cancer medically and do a significant amount of active surveillance or “watchful” waiting.

SALIVARY CANCER – MESOTHELIOMA – IVERMECTIN – MEBENDAZOLE – FENBENDAZOLE – 63 year old Louisiana woman with Mesothelioma and Salivary Gland Cancer reports after 9 months – Cancer Free! Oncologist shocked! William Makis, MD, Covid Intel, Jul 12, 2026.

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Covid Syndrome…

COVID VACCINE – CARDIAC EVENTS – ATHLETES – DEFIBRILLATORS – They Died During Sports Competition and Came Back Wired. Inside the S-ICD revolution that’s letting athletes like Eriksen and Bauer compete through the unthinkable. Peter A. McCullough, MD, MPH, Focal Points, Jul 13, 2026.

COVID VACCINATION – POLICY – CANADA – COVID-19 vaccination decisions and impacts of vaccine mandates: a cross-sectional survey of COVID-19 in Alberta, Canada. “…Our findings contribute to a growing body of empirical work—now spanning three Canadian provinces—examining the effects of COVID-19 vaccine mandates on the healthcare workforce. While these policies were framed by their proponents as necessary to protect patients and preserve healthcare system capacity, the experiences reported by respondents in this and prior studies do not align with those stated rationales. Instead, the data document consistent and recurring reports of workforce destabilization, constraints on professional judgment, and limitations on informed consent under conditions of mandate enforcement….”

COVID VACCINE – SPIKE PROTEIN – Covid mRNA Persistence of Vaccine mRNA, Plasmid DNA, Spike Protein, and Genomic Dysregulation Over 3.5 Years Post-COVID-19 mRNA Vaccination. We report the longest documented persistence of COVID-19 vaccine-derived material to date following YEARS of investigation spanning 200+ specialist evaluations and 200+ advanced lab/imaging tests. Nicolas Hulscher, MPH, Focal Points, Jul 09, 2026.
1) HULSCHER, Nicolas et al. Persistence of Vaccine mRNA, Plasmid DNA, Spike Protein, and Genomic Dysregulation Over 3.5 Years Post-COVID-19 mRNA Vaccination. Medical Research Archives, [S.l.], v. 14, n. 6, july 2026.

COVID VACCINE INJURY – INJURY TABLE – RFK Jr. Announces Plan To Create COVID-19 Vaccine Injury Table, Died Suddenly News, Jul 13, 2026.

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Societal and World Health…

GENOCIDE – CHRISTIANS – NIGERIA – ‘35 Christians Are Killed a Day’: Inside Jihadi Violence in Nigeria | Judd Saul, Jan Jekielek, American Thought Leaders, Epoch Times, Jul-14-2026.

VIOLENCE – ANTIFA – Antifa in 2026: More Trans. More Terrorism. Andy Ngo | “ANTIFA Is Not Dead”: Terrorism, Corruption, and Violence | Michael Knowles Interviews Andy Ngo, Ngo Comment, Jul 12, 2026.

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