Author Archive

13 Stillborn Deaths in 24 Hours – Mothers & COVID Shots

https://thephaser.com/2021/11/exposed-13-stillborn-deaths-in-24-hours-rally-lions-gate-hospital/ Video Here (Approx. 20 Min)

EXPOSED: 13 STILLBORN DEATHS IN 24 HOURS – LIONS GATE HOSPITAL B.C.

https://articles.mercola.com/sites/articles/archive/2021/11/30/surge-in-stillbirths-and-menstrual-changes

Nov. 30, 2021

Analysis by Dr. Mercola

Story at-a-glance

  • At Lions Gate Hospital in North Vancouver, British Columbia, 13 babies were allegedly stillborn in a period of 24 hours; all of their mothers had received a COVID-19 injection
  • At a rally outside the hospital, doctors launched an official complaint with the Royal Canadian Mounted Police against executives at the College of Physicians & Surgeons of BC, alleging conflicts of interest influencing their policies, decisions and statements made to the people of British Columbia
  • Scotland has also experienced an unusual rise in infant death rates; during September 2021, at least 21 babies under 4 weeks died — a rate of 4.9 per 1,000 births, up from an average of 2 per 1,000 births
  • As of November 12, 2021, there were 2,620 cases of fetal death or stillbirth among women who received a COVID-19 injection reported to the U.S. Vaccine Adverse Event Reporting System (VAERS)
  • The CDC-sponsored study that was widely used to support the U.S. recommendation for pregnant women to get injected “presents falsely reassuring statistics”
  • When the risk of miscarriage was recalculated to include all women injected prior to 20 weeks’ gestation, the incidence was seven to eight times higher than the original study indicated, with a cumulative incidence of miscarriage ranging from 82% to 91%

Excerpts:

Calls for Immediate Withdrawal of mRNA Shots

Not only does the IPAK data show COVID-19 injections prior to 20 weeks are unsafe for pregnant women, but 12.6% women who received it in the 3rd trimester reported Grade 3 adverse events, which are severe or medically significant but not immediately life-threatening. Another 8% also reported a fever of 38 degrees C (100.4 degrees F), which can lead to miscarriage or premature labor.13

Further, the study follow-up only continued for 28 days after birth, meaning the long-term effects of prenatal exposure to babies is unknown. The many concerns of mRNA COVID-19 injections during pregnancy and breastfeeding include transmission of mRNA and spike protein across the placenta and through breast milk, as well as the inhibition of synctyin-1, a protein essential for cell fusion and placental development.

Pregnant women were excluded from the mRNA injection clinical trials, but a Pfizer-BioNTech rat study revealed the injection more than doubled the incidence of preimplantation loss and also led to a low incidence of mouth/jaw malformations, gastroschisis (a birth defect of the abdominal wall) and abnormalities in the right-sided aortic arch and cervical vertebrae in the fetuses.14

Together, IPAK believes the data are compelling enough to withdraw the shots for vulnerable populations. Noting their advice in boldface, they say:15

“Considering the evidence presented here, we suggest the immediate withdrawal of mRNA vaccine use in pregnancy (Category X) and those breastfeeding, alongside the withdrawal of mRNA vaccines to children or those of child-bearing age in the general population, until more convincing data relating to the safety and long-term impacts on fertility, pregnancy and reproduction are established in these groups.”

Study: Borrelia burgdorferi Uses Evasion to Persist in Different Human Cell Lines

https://www.frontiersin.org/articles/10.3389/fmicb.2021.711291/full

Distinctive Evasion Mechanisms to Allow Persistence of Borrelia burgdorferi in Different Human Cell Lines

  • 1Department of Biological and Environmental Science, Nanoscience Center, University of Jyväskylä, Jyväskylä, Finland
  • 2Te?ted Oy Ltd., Jyväskylä, Finland

Lyme borreliosis is a multisystemic disease caused by the pleomorphic bacteria of the Borrelia burgdorferi sensu lato complex. The exact mechanisms for the infection to progress into a prolonged sequelae of the disease are currently unknown, although immune evasion and persistence of the bacteria in the host are thought to be major contributors. The current study investigated B. burgdorferi infection processes in two human cell lines, both non-immune and non-phagocytic, to further understand the mechanisms of infection of this bacterium. By utilizing light, confocal, helium ion, and transmission electron microscopy, borrelial infection of chondrosarcoma (SW1353) and dermal fibroblast (BJ) cells were examined from an early 30-min time point to a late 9-days post-infection. Host cell invasion, viability of both the host and B. burgdorferi, as well as, co-localization with lysosomes and the presence of different borrelial pleomorphic forms were analyzed. The results demonstrated differences of infection between the cell lines starting from early entry as B. burgdorferi invaded BJ cells in coiled forms with less pronounced host cell extensions, whereas in SW1353 cells, micropodial interactions with spirochetes were always seen. Moreover, infection of BJ cells increased in a dose dependent manner throughout the examined 9 days, while the percentage of infection, although dose dependent, decreased in SW1353 cells after reaching a peak at 48 h. Furthermore, blebs, round body and damaged B. burgdorferi forms, were mostly observed from the infected SW1353 cells, while spirochetes dominated in BJ cells. Both infected host cell lines grew and remained viable after 9 day post-infection. Although damaged forms were noticed in both cell lines, co-localization with lysosomes was low in both cell lines, especially in BJ cells. The invasion of non-phagocytic cells and the lack of cytopathic effects onto the host cells by B. burgdorferi indicated one mechanism of immune evasion for the bacteria. The differences in attachment, pleomorphic form expressions, and the lack of lysosomal involvement between the infected host cells likely explain the ability of a bacterium to adapt to different environments, as well as, a strategy for persistence inside a host.

(See link for full article)

For more:

Deer Ticks Parasitizing Big Brown Bats in NY

https://academic.oup.com/jme/advance-article-abstract/doi/10.1093/jme/tjab174/6425286?redirectedFrom=fulltext

Ixodes scapularis (Ixodida: Ixodidae) Parasitizing an Unlikely Host: Big Brown Bats, Eptesicus fuscus (Chiroptera: Vespertilionidae), in New York State, USA

Journal of Medical Entomology, tjab174, https://doi.org/10.1093/jme/tjab174
Published:  11 November 2021

Abstract

Ixodes scapularis Say is a three-host tick that has been recorded feeding on over 150 different species of terrestrial vertebrates (mammals, birds, and reptiles). This tick is found throughout the northeastern, coastal southeastern, and upper midwestern United States and is considered the most significant vector of tick-borne pathogens to humans in North America. Despite its ubiquity and broad host range, I. scapularis previously has not been reported feeding on bats (Chiroptera). However, during 2019 and 2020, larvae and nymphs of I. scapularis were recovered from big brown bats, Eptesicus fuscus (Palisot de Beauvois), at four locations in rural New York State, USA. All Ixodes infested bats were injured and found on the ground; therefore, parasitism by I. scapularis was likely opportunistic. Nonetheless, the large number of pathogens known to be associated with bats and the frequency with which I. scapularis bites people suggest that this host–tick relationship is of at least potential epidemiological significance.

AHA Data Confirmed: Whistleblowers State COVID Shots Lead to Increased Heart Attacks

https://www.bitchute.com/video/tuuurhjzi3Bn/  Video Here  (Approx. 1 Min)

Dr. Aseem Malhotra, a British Cardiologist, discusses the recent American Heart Association study linking COVID-19 shots to increased heart attacks.

He shares that British authorities in the field of Cardiology confirm that this is happening, but they are afraid to go public because they will lose their research funding from the Drug Companies.

Full article: https://healthimpactnews.com/2021/march-of-the-vaccine-dead-protest-in-italy-british-cardiologist-confirms-aha-study-that-covid-19-shots-causing-heart-attacks/

The article points out that this is not Dr. Aseem Malhotra’s first rodeo. He has been featured multiple times over the years at Health Impact News because he is one of the few doctors worldwide that is not afraid of exposing the fraud in the pharmaceutical industry, as he has exposed the false lipid theory of heart disease that claims cholesterol causes heart disease which then created a 100 billion dollar cholesterol-lowering drug business led by Pfizer.

He is calling for an immediate end to vaccine mandates.

https://articles.mercola.com/sites/articles/archive/2021/11/30/covid-vaccine-acute-coronary-syndrome

mRNA Vaccines Put You at Risk for Acute Coronary Syndrome

Analysis by Dr. Joseph Mercola
Nov. 30, 2021

Story at-a-glance –

  • Using the PULS cardiac test, researchers have found Pfizer and Moderna mRNA COVID shots dramatically increase biomarkers associated with thrombosis, cardiomyopathy and other vascular events following vaccination
  • Pre- and post-injection PULS tests for 566 patients were compared. On average, their PULS scores went from an 11% five-year risk for acute coronary syndrome, to a more than double, 25%, five-year risk
  • Those who got the injection for fear that COVID-19 might adversely affect their heart now face the grim reality that they’ve exchanged a potential risk for a more certain one
  • Another paper details how the mRNA shot can cause thrombocytopenia (low platelet count) through a mechanism that involves the activation of platelets by antibodies against the spike protein (anti-spike antibodies)
  • A mystery that remains to be solved is why only certain people with antibodies to the spike protein (anti-spike antibodies) go on to develop symptoms of platelet activation and thrombocytopenia. One hypothesis is that only a subset of the anti-spike antibodies formed after vaccination can activate platelets and cause thrombocytopenia

Excerpts from article:

In a November 21, 2021, tweet, cardiologist Dr. Aseem Malhotra writes:1

“Extraordinary, disturbing, upsetting. We now have evidence of a plausible biological mechanism of how mRNA vaccine may be contributing to increased cardiac events. The abstract is published in the highest impact cardiology journal so we must take these findings very seriously.”

Signs and Symptoms to Watch For

ACS (Acute Coronary Syndrome) is an umbrella term that doesn’t just include heart attacks, but also a range of other conditions involving abruptly reduced blood flow to your heart. Signs and symptoms of ACS typically begin very suddenly, and include:5

Chest pain/discomfort, often described as aching, pressure, tightness or burning sensations Pain that radiates from your chest to your shoulders, arms, upper abdomen, back, neck and/or jaw
Nausea and/or vomiting Indigestion
Shortness of breath Sudden heavy sweating
Lightheadedness, dizziness and/or fainting Unusual or inexplicable fatigue
Restlessness and/or apprehensiveness

If you suspect ACS, do not drive yourself to the hospital. Call for an ambulance, as it is a true medical emergency that may need prompt medical attention. (See link for full article)

_________________

Lastly, Dr. Mercola discusses “vaccine”-induced thrombocytopenia, or low platelet count, caused by antibodies against the spike protein, resulting in depletion of platelets by activating them. Platelet activation can lead to DIC (disseminated intramuscular coagulation), exhausting the coagulation system causing the low platelets which in turn causes hemorrhaging. Dr. Hoffe states that after testing those who got the shots with a D-dimer test, at least 62% had microscopic blood clotting.

As of November, there were over four thousand cases reported to VAERS, which is notoriously low at capturing adverse events so the true numbers are much, much higher.

Five Studies on mRNA “Vaccine” Spike Protein Pathogenicity. Share With Your Doctor

https://popularrationalism.substack.com/p/five-studies-on-mrna-vaccine-spike

Five Studies on mRNA Vaccine Spike Protein Pathogenicity. Share With Your Doctor.

Ignore the “Fact Checker” Opinion Web Sites. Here’s a Collection of Resources on Spike Protein Pathogenicity for Your Use. Add Your Own in the Comments.
Don’t believe the opinion blog article websites that tout themselves as “Fact-Checkers” when all they do is cite so-called “experts” who offer zero evidence and only provide their subjective, and in many cases, misleading, opinions.

This is a short collection of studies that show that they SARS-CoV-2 spike protein itself pathogenic. These are just a sample. Remember: putting a spike protein into the human body by injection does not magically change its ability to cause disease: pathogenicity.

  1. “Our in vitro V(D)J reporter assay shows that the spike protein intensely impeded V(D)J recombination.” Jiang & Mei, 2021.
  2. “The data presented here indicate the need of a strict and thorough clinical surveillance on the future effects of the mass vaccination against the current SARS-CoV-2 pandemic.” Kanduc, 2021 (Lyons-Weiler, 2020 was first to conclude the Spike protein was autoreactogenic – and likely to affect the heart protein Titin.)
  3. “Researchers created a “pseudovirus” that was surrounded by SARS-CoV-2 classic crown of spike proteins, but did not contain any actual virus. Exposure to this pseudovirus resulted in damage to the lungs and arteries of an animal model—proving that the spike protein alone was enough to cause disease. Tissue samples showed inflammation in endothelial cells lining the pulmonary artery walls.” (Salk.edu). (Lei et al., 2021)
  4. “In conclusion, these experiments reveal that Spike-induced degradation of endothelial junctional proteins affects endothelial barrier function and is the likely cause of vascular damage observed in COVID-19 affected individuals.”(Raghavan et al, 2021). (Okamoto and Suzuki, 2017 for the importance of intact endothelial junctions.)
  5. “We show that intravenously injected radioiodinated S1 (I-S1) readily crossed the blood–brain barrier in male mice, was taken up by brain regions and entered the parenchymal brain space. I-S1 was also taken up by the lung, spleen, kidney and liver.” (Rhea et al., 2021)

Have additional studies? Help a scientific out – drop them in the comments with a quote from the study w/their conclusions. Have a doctor? Give them a gift subscription, and I’ll keep these articles coming.

References

Kanduc, 2021. Anti-SARS-CoV-2 Immune Response and Sudden Death: Titin as a Link. Adv. Stud Biol 13:37-44. http://www.m-hikari.com/asb/asb2021/asb1-2021/p/kanducASB1-2021.pdf

Jiang H, Mei YF. SARS-CoV-2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro. Viruses. 2021 Oct 13;13(10):2056. doi: 10.3390/v13102056. PMID: 34696485; PMCID: PMC8538446. https://www.mdpi.com/1999-4915/13/10/2056

Lei Y, Zhang J, Schiavon CR, He M, Chen L, Shen H, Zhang Y, Yin Q, Cho Y, Andrade L, Shadel GS, Hepokoski M, Lei T, Wang H, Zhang J, Yuan JX, Malhotra A, Manor U, Wang S, Yuan ZY, Shyy JY. SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2. Circ Res. 2021 Apr 30;128(9):1323-1326. doi: 10.1161/CIRCRESAHA.121.318902. Epub 2021 Mar 31. PMID: 33784827; PMCID: PMC8091897. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091897/pdf/res-128-1323.pdf

Raghavan S, Kenchappa DB, Leo MD. SARS-CoV-2 Spike Protein Induces Degradation of Junctional Proteins That Maintain Endothelial Barrier Integrity. Front Cardiovasc Med. 2021 Jun 11;8:687783. doi: 10.3389/fcvm.2021.687783. PMID: 34179146; PMCID: PMC8225996. https://www.frontiersin.org/articles/10.3389/fcvm.2021.687783/full

Okamoto T, Suzuki K. The Role of Gap Junction-Mediated Endothelial Cell-Cell Interaction in the Crosstalk between Inflammation and Blood Coagulation. Int J Mol Sci. 2017 Oct 27;18(11):2254. doi: 10.3390/ijms18112254. PMID: 29077057; PMCID: PMC5713224. https://www.mdpi.com/1422-0067/18/11/2254

Rhea EM, Logsdon AF, Hansen KM, Williams LM, Reed MJ, Baumann KK, Holden SJ, Raber J, Banks WA, Erickson MA. The S1 protein of SARS-CoV-2 crosses the blood-brain barrier in mice. Nat Neurosci. 2021 Mar;24(3):368-378. doi: 10.1038/s41593-020-00771-8. Epub 2020 Dec 16. PMID: 33328624. https://www.nature.com/articles/s41593-020-00771-8.pdf