13 Reasons to abstain from emergency CΟVIDΙ9 vaϲϲines
Last updated: Mar 30 2021
#1 Experimental
Despite claims by the media, all CΟVID-Ι9 νaϲϲines available today are experimental νaϲϲines whose safety studies are ongoing. The νaϲϲines are NOT approved and are available only under emergency use authorization by the FDA and are not approved or licensed by the FDA. Phase 3 safety studies are still in progress and will not end for years to come.
A Study to Evaluate Efficacy, Safety, and Immunogenicity of mRNA-1273 Vaϲϲine in Adults Aged 18 Years and Older to Prevent CΟVID-Ι9
ModernaTX, Inc.
https://clinicaltrials.gov/ct2/show/NCT04470427
Actual Study Start Date : July 27, 2020
Estimated Primary Completion Date : October 27, 2022
Estimated Study Completion Date : October 27, 2022
FDA Emergency use authorization: https://www.fda.gov/media/144636/download
Moderna package information insert showing EUA authorization (unapproved product)
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e0651c7a-2fe2-459d-a766-0d59e919f058
Study to Describe the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaϲϲine Candidates Against CΟVID-Ι9 in Healthy Individuals
BioNTech SE/Pfizer
https://clinicaltrials.gov/ct2/show/NCT04368728
Actual Study Start Date : April 29, 2020
Estimated Primary Completion Date : August 3, 2021
Estimated Study Completion Date : January 31, 2023
FDA Emergency use authorization: https://www.fda.gov/media/144416/download
Pfizer package information insert showing EUA authorization (unapproved product) https://labeling.pfizer.com/ShowLabeling.aspx?id=14471
Federal law prohibits employers and others from requiring νaϲϲination with a CΟVID-Ι9 νaϲϲine distributed under an EUA
Feb 23 2021
...The abbreviated timelines for the emergency use applications and authorizations means there is much the FDA does not know about these products even as it authorizes them for emergency use, including their effectiveness against asymptomatic infection, death, and transmission of SARS-CoV-2, the virus that causes the disease.
...Given the uncertainty about the two νaϲϲines, their EUAs are explicit that each is “an investigational νaϲϲine not licensed for any indication” and require that all “promotional material relating to the CΟVID-Ι9 Vaϲϲine clearly and conspicuously … state that this product has not been approved or licensed by the FDA, but has been authorized for emergency use by FDA” (emphasis added).
Under Federal Law, Can Your Employer Make You Get the CΟVID Vaϲϲine?
Jan 29 2021
States and employers, under federal law, can’t mandate emergency use products such as the Pfizer and Moderna CΟVID νaϲϲines. But that doesn’t mean some won’t try.
For Now, US Troops Won't Be Required to Get New CΟVID-Ι9 Vaϲϲine
Nov 23 2020
...as the two departments sort out the details on who should receive the νaϲϲine and where, DoD officials stressed it will not be mandatory for U.S. service members...
According to officials, the νaϲϲine will remain voluntary as long as it is authorized under emergency conditions and doesn't have official approval from the FDA.
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#2 Long term safety unknown
Despite media claims of "safe" νaϲϲines, CΟVID-Ι9 νaϲϲines have been studied for safety for only a few months. In the past, νaϲϲines have taken years (sometimes up to a decade), to develop and study for safety. Because there are no long term studies, there is no data showing if problems will develop long term.
Moderna mRNA-1273 8 months
BioNTech SE/Pfizer BNT162b2 10 months
How long it took to develop 12 other νaϲϲines in history
https://www.businessinsider.com/how-long-it-took-to-develop-other-vaccines-in-history-2020-7
Researchers rush to test coronavirus vaccine in people without knowing how well it works in animals
Mar 11 2020
“The traditional vaccine timeline is 15 to 20 years. That would not be acceptable here,” said Mark Feinberg, president and CEO of the International AIDS Vaccine Initiative, whose work as chief public health and science officer at Merck Vaccines was instrumental in the development of the immunization against Ebola.
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#3 Promising and effective CΟVID treatments are already available, could be studied further or could be approved for emergency use but are suppressed
Peter McCullough, MD testifies to Texas Senate HHS Committee [on suppressed CΟVID treatments]
Mar 11 2021. 20m
https://www.youtube.com/watch?v=QAHi3lX3oGM
(backup: https://www.bitchute.com/video/jJe5BJwl6tdv)
https://aapsonline.org/covidpatientguide/
Dr. Pierre Kory testifies to Senate Committee about ivermectin
Dec 08 2020. 29m
The Story of Ivermectin
Feb 28 2021. 25m
https://tv.gab.com/channel/gordr/view/the-story-of-ivermectin-vs-remdesivir-603bc089f92a30bda575a1ed
Front Line CΟVID-Ι9 Critical Care Alliance (FLCCA)
https://covid19criticalcare.com/
Meta-analysis of randomized trials of ivermectin to treat SARS-CoV-2 infection
Jan 19 2021
https://www.researchsquare.com/article/rs-148845/v1
In six randomized trials of moderate or severe infection, there was a 75% reduction in mortality
Expanding Use of Ivermectin as Early Treatment for CΟVID
Feb 10 2021
https://www.americasfrontlinedoctors.com/expanding-use-of-ivermectin-as-early-treatment-forcovid/
A recent decision on the part of YouTube to remove two videos of expert testimony before the US Senate is part of a disturbing trend in which Big Tech firms act as commissars to suppress information they alone interpret as harmful to the public interest.
Common asthma treatment reduces need for hospitalisation in CΟVID-Ι9 patients, study suggests
Feb 09 2021
suggests that inhaled budesonide reduced the relative risk of requiring urgent care or hospitalisation by 90% in the 28-day study period. Participants allocated the budesonide inhaler also had a quicker resolution of fever, symptoms and fewer persistent symptoms after 28 days.
https://budesonideworks.com/validation-2/
Dr. Simone Gold - The truth about the CV19 νaϲϲine
Jan 04 2021. 56m
https://www.bitchute.com/video/cspP45qJChtf
20:50 Lancet hydroxychloroquine study and scientific and media corruption
HCQ is effective for CΟVID-Ι9 when used early: real-time meta analysis of 219 studies
Mar 13 2021
Early treatment is most successful, with 100% of 28 studies reporting a positive effect (12 statistically significant in isolation) and an estimated reduction of 64% in the effect measured (death, hospitalization, etc.) using a random effects meta-analysis, RR 0.36 [0.25-0.50].
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#4 New genetic engineering technology
All CΟVID-Ι9 νaϲϲines use new untested genetic engineering vaccine technology (mRNA/DNA), never used in any successful human vaccine before.
The story of mRNA: How a once-dismissed idea became a leading technology in the CΟVID νaϲϲine race
Nov 10 2020
...Although relatively easy and quick to produce compared to traditional νaϲϲine-making, no mRNA νaϲϲine or drug has ever won approval.
How the Johnson & Johnson [DNA] Vaccine Works
Jan 13 2021
https://www.nytimes.com/interactive/2020/health/johnson-johnson-covid-19-vaccine.html (bypass paywall: https://archive.is/RPPOx)
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#5 Not a νaϲϲine since it does not prevent infection or transmission
Despite media claims of CΟVID-Ι9 νaϲϲines being necessary to end the pandemic, CΟVIDΙ9 νaϲϲines have NOT been shown to prevent infection or prevent transmission. This is normally required to call a medical product a νaϲϲine. CΟVIDΙ9 νaϲϲines studies show only that they reduce moderate and mild symptoms. Hence, they are more correctly called experimental genetic engineering biologic treatments.
Vaϲϲinated people may still spread virus and are still required to social distance and wear masks.
Can a CΟVID-Ι9 Vaϲϲine Stop the Spread? Good Question.
Nov 20 2020
https://www.medscape.com/viewarticle/941388
"We don't know if people can become infected and thus also transmit even with νaϲϲination," said former US Food and Drug Administration Commissioner Margaret Hamburg, MD, in a November 18 briefing on CΟVID-Ι9 νaϲϲines sponsored by the American Public Health Association (APHA) and the National Academy of Medicine (NAM).
CΟVID-Ι9 Vaϲϲine Protocols Reveal That Trials Are Designed To Succeed
Sep 23 2020
...Prevention of infection is not a criterion for success for any of these νaϲϲines. In fact, their endpoints all require confirmed infections and all those they will include in the analysis for success, the only difference being the severity of symptoms between the vaϲϲinated and unvaϲϲinated. Measuring differences amongst only those infected by SARS-CoV-2 underscores the implicit conclusion that the νaϲϲines are not expected to prevent infection, only modify symptoms of those infected.
We all expect an effective νaϲϲine to prevent serious illness if infected. Three of the νaϲϲine protocols—Moderna, Pfizer, and AstraZeneca—do not require that their νaϲϲine prevent serious disease only that they prevent moderate symptoms which may be as mild as cough, or headache.
Fauci: Early CΟVID-Ι9 νaϲϲines will only prevent symptoms, not block the virus
Oct 26 2020
CΟVID: Vaϲϲinated people may spread virus, says Van-Tam
Jan 24 2021
https://www.bbc.com/news/uk-55784199
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#6 Manufacturers can never be sued for harm
All νaϲϲine manufacturers have immunity to lawsuits from any damages their νaϲϲines might cause now or from long term effects discovered years from now. This undermines any financial incentive for manufacturers to ensure long term safety now or to improve safety overtime.
You can’t sue Pfizer or Moderna if you have severe CΟVID νaϲϲine side effects. The government likely won't compensate you for damages either
Dec 16 2020
https://www.cnbc.com/2020/12/16/covid-vaccine-side-effects-compensation-lawsuit.html
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#7 Risks of CΟVID does not warrant risk of mass νaϲϲination of all people
Martin Kulldorff
Professor Harvard Medical School. Disease surveillance methods. Infectious disease outbreaks. Vaccine safety.
Mar 15 2021
https://twitter.com/MartinKulldorff/status/1371638485686358018
“...Thinking that everyone must be vaccinated is as scientifically flawed as thinking that nobody should. COVID vaccines are important for older high-risk people, and their care-takers. Those with prior natural infection do not need it. Nor children.”
Reconciling estimates of global spread and infection fatality rates of COVID-19: an overview of systematic evaluations
John P A Ioannidis
Mar 26 2021
https://pubmed.ncbi.nlm.nih.gov/33768536/
All systematic evaluations of seroprevalence data converge that SARS-CoV-2 infection is widely spread globally. Acknowledging residual uncertainties, the available evidence suggests average global IFR of ~0.15% and ~1.5-2.0 billion infections by February 2021 with substantial differences in IFR and in infection spread across continents, countries, and locations.
CΟVID-Ι9 Primary, Not Only, Cause of 94% of Deaths
Sept 01 2020
https://www.webmd.com/lung/news/20200901/covid-19-primary-not-only-cause-94-percent-of-deaths
About 94% of people who have died from CΟVID-Ι9 in the U.S. also had other contributing conditions listed on their death certificates, according to new data released by the CDC.
On average, patients’ records had 2.6 additional conditions. Only 6% of deaths listed CΟVID-Ι9 as the only cause.
CΟVID-Ι9 Has Claimed the Lives of 100,000 Long-Term Care Residents and Staff
Nationwide, deaths in long-term care facilities account for 40% of all CΟVID-Ι9 deaths.
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#8 Risk of later immune overreaction due to incomplete and flawed animal studies
All prior coronavirus νaϲϲines resulted in death and serious harm when vaϲϲinated animals were exposed to the live virus, an effect called antibody dependent enhancement (ADE). Animal trials for CΟVID-Ι9 νaϲϲines did not rule out ADE.
Note: ADE is also called "pathogenic priming" or "immune enhancement" or "paradoxical immune enhancement"
Immunization with SARS Coronavirus Vaϲϲines Leads to Pulmonary Immunopathology on Challenge with the SARS Virus
Apr 20 2012
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335060
Because of a concern for reemergence or a deliberate release of the SARS coronavirus, νaϲϲine development was initiated. Evaluations of an inactivated whole virus νaϲϲine in ferrets and nonhuman primates and a virus-like-particle νaϲϲine in mice induced protection against infection but challenged animals exhibited an immunopathologic-type lung disease.
Informed consent disclosure to νaϲϲine trial subjects of risk of CΟVID-Ι9 νaϲϲines worsening clinical disease
Oct 28 2020
https://pubmed.ncbi.nlm.nih.gov/33113270
...Conclusions drawn from the study and clinical implications: The specific and significant CΟVID-Ι9 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in νaϲϲine trials, as well as those being recruited for the trials and future patients after νaϲϲine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.
Pfizer CΟVID νaϲϲine trial shows alarming evidence of pathogenic priming in older adults
Dec 11 2020
https://www.lifesitenews.com/opinion/pfizer-covid-vaccine-trial-shows-alarming-evidence-of-pathogenic-priming-in-older-adults (backup: https://archive.is/qVXC5)
Researchers fast-track coronavirus νaϲϲine by skipping key animal testing first
Mar 13 2020
https://www.livescience.com/coronavirus-vaccine-trial-no-animal-testing.html
A clinical trial for an experimental coronavirus νaϲϲine has begun recruiting participants in Seattle, but researchers did not first show that the νaϲϲine triggered an immune response in animals, as is normally required.
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#9 Pharmaceutical industry has a long history of corruption
Pfizer
https://violationtracker.goodjobsfirst.org/parent/pfizer
Penalty total since 2000: $4,712,210,359
healthcare-related offenses $3,373,675,000
Pfizer faces DOJ, SEC foreign bribery probes for China, Russia operations
Nov 09 2020
Justice Department Announces Largest Health Care Fraud Settlement in Its History
Pfizer to Pay $2.3 Billion for Fraudulent Marketing
Sep 02 2009
Tough on Crime? Pfizer and the CIHR
May 2010
https://pubmed.ncbi.nlm.nih.gov/21532766/
Pfizer has been a "habitual offender," persistently engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results. Since 2002 the company and its subsidiaries have been assessed $3 billion in criminal convictions, civil penalties and jury awards.
Johnson and Johnson
https://violationtracker.goodjobsfirst.org/prog.php?parent=johnson-and-johnson
Penalty total since 2000: $4,247,999,381
healthcare-related offenses $3,136,511,000
Johnson & Johnson Has a Long Rap Sheet — Why Should We Trust Its Vaϲϲine?
Mar 01 2021
https://childrenshealthdefense.org/defender/johnson-johnson-why-trust-vaccine/
Johnson & Johnson to Pay More Than $2.2 Billion to Resolve Criminal and Civil Investigations
Allegations Include Off-label Marketing and Kickbacks to Doctors and Pharmacists
Nov 04 2013
Opioid Crisis Fast Facts
Mar 16 2021
https://www.cnn.com/2017/09/18/health/opioid-crisis-fast-facts/index.html
August 26, 2019 - Oklahoma wins its case against Johnson & Johnson in the first major opioid lawsuit trial to be held in the United States. Cleveland County District Judge Thad Balkman orders Johnson & Johnson to pay $572 million for its role in the state’s opioid crisis. The penalty is later reduced to $465 million, due to a mathematical error made when calculating the judgment.
...
March 15, 2021 - According to court documents, Purdue files a restructuring plan to dissolve itself and establish a new company dedicated to programs designed to combat the opioid crisis. As part of the proposed plan, the Sackler family agrees to pay an additional $4.2 billion over the next nine years to resolve various civil claims.
Medical Journals Are an Extension of the Marketing Arm of Pharmaceutical Companies
2005 May
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1140949/
“Journals have devolved into information laundering operations for the pharmaceutical industry”, wrote Richard Horton, editor of the Lancet, in March 2004 [1]. In the same year, Marcia Angell, former editor of the New England Journal of Medicine, lambasted the industry for becoming “primarily a marketing machine” and co-opting “every institution that might stand in its way” [2]. Medical journals were conspicuously absent from her list of co-opted institutions, but she and Horton are not the only editors who have become increasingly queasy about the power and influence of the industry. Jerry Kassirer, another former editor of the New England Journal of Medicine, argues that the industry has deflected the moral compasses of many physicians [3], and the editors of PLoS Medicine have declared that they will not become “part of the cycle of dependency…between journals and the pharmaceutical industry” [4]. Something is clearly up.
The Illusion of Evidence Based Medicine
Mar 09 2021. 42m
https://www.youtube.com/watch?v=UAEAWyfuEWY
As much of the world rushes to receive a lightly-tested pharmaceutical product, we thought it was high time to look again at the (very) big business of medicine. Leemon McHenry, PhD, guides us to the fraudulent core of ghostwritten studies, captured legislators, revolving-door regulatory agencies, pay-to-play medical journals, and the "key opinion leaders" who lend their academic credentials to giant corporations...for a price.
With every stage in the process seemingly structured for corruption, we can only wonder along with Professor McHenry: "Who's looking out for scientific integrity?"
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#10 PCR test is flawed and allows false positives to be manipulated
Most cases, deaths, hospitalizations and all νaϲϲine studies use the experimental PCR test for diagnosing CΟVIDΙ9 whose false positive rate can be effectively controlled by the PCR test lab/manufacturer by setting the test's cycle rate (which they are not required to disclose). Many asymptomatic people were, and continue to be, tested using only the PCR test to diagnose CΟVIDΙ9, a fundamental redefinition of the term 'case'. This problem was corrected by the WHO Jan 20 2021 (US presidential inauguration day).
If more than 35 cycles are used then the test returns 100% false positive rate. Additionally, a positive PCR test is misrepresented as an active infection "case" when this was, in every prior year, only determined by doctor diagnosis using observed symptoms and tests. The PCR test does not detect active virus but instead detects genetic material which could be from a prior infection, from another coronavirus or from the body itself. A positive PCR test by itself is insufficient to diagnose disease.
PCR test FDA emergency authorization
March 31 2020
https://www.fda.gov/media/136598/download
https://www.nytimes.com/2020/08/29/health/coronavirus-testing.html
...The Food and Drug Administration said in an emailed statement that it does not specify the cycle threshold ranges used to determine who is positive, and that “commercial manufacturers and laboratories set their own.
2007 article that explains the known problems with PCR testing and how it led to a false epidemic and the compulsory and unnecessary νaϲϲination of thousands of health care workers:
https://www.nytimes.com/2007/01/22/health/22whoop.html
...“The big message is that every lab is vulnerable to having false positives,” Dr. Petti said. “No single test result is absolute and that is even more important with a test result based on P.C.R.”
As for Dr. Herndon, though, she now knows she is off the hook.
“I thought I might have caused the epidemic,” she said.
CΟVID Testing Fraud Uncovered. 24m
https://thehighwire.com/videos/covid-testing-fraud-uncovered
As cases of coronavirus rise across America, shouldn’t death rates be going up too? Del breaks down how CΟVID tests may be seriously flawed by providing less than accurate results and why the majority of positive cases could be false.
Dr Mike Yeadon - PCR Testing
Nov 20 2020. 33m
https://www.youtube.com/watch?v=D1onx7LaNio
WHO issued new PCR test guidance that requires re-testing positives without symptoms on Jan 20 (which will cause cases to fall due to less false positives)
Nucleic acid testing (NAT) technologies that use polymerase chain reaction (PCR) for detection of SARS-CoV-2
Jan 20 2021
https://www.who.int/news/item/20-01-2021-who-information-notice-for-ivd-users-2020-05
***Where test results do not correspond with the clinical presentation, a new specimen should be taken and retested using the same or different NAT technology.***
WHO reminds IVD users that disease prevalence alters the predictive value of test results; as disease prevalence decreases, the risk of false positive increases (2).
This means that the probability that a person who has a positive result (SARS-CoV-2 detected) is truly infected with SARS-CoV-2 decreases as prevalence decreases, irrespective of the claimed specificity.
Most PCR assays are indicated as an aid for diagnosis, therefore, health care providers must consider any result in combination with timing of sampling, specimen type, assay specifics, clinical observations, patient history, confirmed status of any contacts, and epidemiological information.
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#11 Suspicious deaths and injuries following νaϲϲination
There have been suspicious deaths following CΟVIDΙ9 νaϲϲination in elderly in nursing homes around the world. There is no process in place to investigate if the νaϲϲines are contributing to these deaths. Despite having been recently vaϲϲinated, it is presumed by authorities these deaths are either coincidences or a CΟVIDΙ9 outbreak.
Reports of Deaths After CΟVID Vaϲϲines Up by 259 in 1 Week, CDC Data Show
Mar 12 2021
https://childrenshealthdefense.org/defender/vaers-reports-death-up/
CΟVID-Ι9 outbreak at Auburn nursing home infects 137 residents, kills 24
Jan 09 2021
...The outbreak at The Commons on St. Anthony in Auburn started Dec. 21 as a wave of post-Thanksgiving CΟVID-Ι9 cases began hitting the county
...The nursing home began vaϲϲinating residents Dec. 22. So far 193 residents, or 80%, and 113 employees, or less than half the staff, have been vaϲϲinated.
Death by Coincidence?
Jan 14 2021
https://childrenshealthdefense.org/defender/death-by-coincidence
Tip of the Iceberg? Thousands of CΟVID Vaϲϲine Injuries and 13 U.S. Deaths Reported in December Alone
Jan 14 2021
55 People Have Died in US After Receiving CΟVID-Ι9 Vaϲϲines: Reporting System
Jan 14 2021
23 Die in Norway After Receiving Pfizer CCP Virus Vaϲϲine
Jan 14 2021
...Norway has changed its CΟVID-Ι9 νaϲϲination guide to state that “very frail” people should no longer receive the jab, citing 13 post-νaϲϲine deaths in the country from side effects that appear to be linked to Pfizer and partner BioNTech’s mRNA νaϲϲine.
53 Dead in Gibraltar in 10 Days After Experimental Pfizer mRNA CΟVID Injections Started
Jan 24 2021
Deaths of Elderly Who Recovered From CΟVID-Ι9, but Died After Vaϲϲine, Raise Questions
Feb 10 2021
One-Third of Deaths Reported to CDC After CΟVID Vaϲϲines Occurred Within 48 Hours of νaϲϲination
Feb 19 2021
https://childrenshealthdefense.org/defender/latest-data-cdc-vaers/
Urgent Open Letter from Doctors and Scientists to the European Medicines Agency regarding CΟVID-Ι9 Vaϲϲine Safety Concerns
Feb 28 2021
We note that a wide range of side effects is being reported following νaϲϲination of previously healthy younger individuals with the gene-based CΟVID-Ι9 νaϲϲines. Moreover, there have been numerous media reports from around the world of care homes being struck by CΟVID-Ι9 within days of νaϲϲination of residents. While we recognise that these occurrences might, every one of them, have been unfortunate coincidences, we are concerned that there has been and there continues to be inadequate scrutiny of the possible causes of illness or death under these circumstances, and especially so in the absence of post-mortems examinations.
...
Should all such evidence not be available, we demand that approval for use of the gene-based νaϲϲines be withdrawn until all the above issues have been properly addressed by the exercise of due diligence by the EMA.
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#12 Unknown effects on fertility, pregnant women, unborn children and breastfeeding
Pfizer CΟVID19 Vaϲϲine: “Reg 174 Information for UK Healthcare Professionals” (used for informed consent in UK)
...4.6 Fertility, pregnancy and lactation
Pregnancy
There are no or limited amount of data from the use of CΟVID-Ι9 mRNA Vaϲϲine BNT162b2. Animal reproductive toxicity studies have not been completed. CΟVID-Ι9 mRNA Vaϲϲine BNT162b2 is not recommended during pregnancy.
For women of childbearing age, pregnancy should be excluded before νaϲϲination. In addition, women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose.
Breast-feeding
It is unknown whether CΟVID-Ι9 mRNA Vaϲϲine BNT162b2 is excreted in human milk. A risk to the newborns/infants cannot be excluded. CΟVID-Ι9 mRNA Vaϲϲine BNT162b2 should not be used during breast-feeding.
Fertility
It is unknown whether CΟVID-Ι9 mRNA Vaϲϲine BNT162b2 has an impact on fertility.
Suspicions grow that nanoparticles in Pfizer’s CΟVID-Ι9 νaϲϲine trigger rare allergic reactions
Dec 21 2020
Potential adverse effects of nanoparticles on the reproductive system
Dec 11 2018
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294055
...In medicine, nanoparticles (NPs) can be used as nanoscopic drug carriers and for nanoimaging technologies....
NPs can pass through the blood–testis barrier, placental barrier, and epithelial barrier, which protect reproductive tissues, and then accumulate in reproductive organs. NP accumulation damages organs (testis, epididymis, ovary, and uterus) by destroying Sertoli cells, Leydig cells, and germ cells, causing reproductive organ dysfunction that adversely affects sperm quality, quantity, morphology, and motility or reduces the number of mature oocytes and disrupts primary and secondary follicular development. In addition, NPs can disrupt the levels of secreted hormones, causing changes in sexual behavior.
Dr. Wodarg and Dr. Yeadon request a stop of all corona νaϲϲination studies and call for co-signing the petition
Dec 01 2020
...The νaϲϲinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a νaϲϲine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaϲϲinated women.
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#13 Military propaganda, psychological manipulation and censorship are being used to increase νaϲϲine uptake
5 ways they’re trying to trick you into taking the CΟVID “νaϲϲine”
Mar 04 2021
https://off-guardian.org/2021/03/04/5-ways-theyre-trying-to-trick-you-into-taking-the-covid-vaccine
Before CΟVID, Gates Planned Social Media Censorship of Vaϲϲine Safety Advocates With Pharma, CDC, Media, China and CIA
Mar 12 2021
https://childrenshealthdefense.org/defender/gates-planned-social-media-censorship-vaccine-safety/
Psychological Attack on the UK
Jan 03 2021
https://www.ukcolumn.org/article/psychological-attack-uk
CΟVID and the New Age of Censorship
Dec 07 2020
https://www.wsj.com/articles/covid-and-the-new-age-of-censorship-11607381415
Cyber War Declared in U.S. and UK to Quash Vaϲϲine Hesitancy as Nations Prepare for Mass Inoculations
Nov 16 2020
How SAGE and the UK media created fear in the British public
Jun 27 2020
https://evidencenotfear.com/how-sage-and-uk-media-created-fear-in-the-british-public
The British Army’s Information Warfare Unit Is Helping Combat Coronavirus Misinformation
Apr 22 2020
https://www.buzzfeed.com/joeydurso/coronavirus-british-army-information-warfare-77-brigade
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