FYI. Interesting video that, if true, seems to implicate many of our healthcare leaders in a misinformation and censorship campaign to suppress Ivermectin use in preventing and treating Covid-19. Watch and reach your own conclusions.
A recent story, complete with a picture of dogs being subjected to sand fly bites and inflammatory lies by animal rights groups, is being used to disparage Dr. Anthony Fauci as a heartless, politically motivated scientist. There are a lot of reasons to judge Dr. Fauci harshly, but this is not one of them. Let me explain.
Drug development and testing involves multiple steps to ensure safety and efficacy of a proposed drug before it is given to humans to treat disease. In the case cited in the article from whitecoatwaste.org and echoed by PETA, lies include flies stripping flesh from bones. What is really happening is that anesthetized dogs are being infected with leishmaniasis parasites by bites from infected sand flies in order to test drugs to treat this dreadful tropical disease, which naturally infects dogs, cats, rodents, and humans by millions in tropical-subtropical regions of Africa, Middle East, southern Europe, South and Central America and even the United States. See Leishmaniasis Facts: below for more details about this disease.
The flies are not “stripping the flesh from the bones” as described in the article. Sand fly bites are like mosquito bites, not like being eaten by carrion or blow fly maggots, which this lie implies. After being infected with the parasite through several sand fly bites, the dogs will be treated for the disease by an experimental drug to see how effectively it cures them, and to determine any unpleasant or dangerous side effects of the drug.
Animal testing is a necessary, though disgusting, step in drug development. To ethically carry out this type of procedure, suffering of the animals must be minimized.[1.] That is why the dogs are anesthetized and only their heads are exposed to the sand fly bites. Dogs are the best model for this disease since it naturally infects dogs with a visceral form that can be fatal if untreated. This may be a part of development of veterinary treatment drugs, but it may be used for human drugs as well.
All drugs and cosmetics, as well as many other consumer products, are tested first on cell cultures and then on animals for both safety and effectiveness before graduating to human trials. Covid vaccines and treatment drugs were tested on animals such as genetically modified mice before human trials, but without outrage because there was no cute pet sentimental propaganda.
Animal testing is a necessary step that, though sensibly abhorrent, must be done. Eliminating testing of animal models would mean that drugs, cosmetics or other products would be given to humans without knowing if they might be harmful or be effective for the proposed purpose. Typical animal models used for product development include a variety of vertebrates including dogs, cats, monkeys, Guinea pigs, hamsters, rats and mice. Animal models used to gauge a product’s potential for environmental pollution also include fish, crustaceans like crabs, mollusks like snails, as well as single cell, colony and other microscopic animals.
If a cosmetic or household product advertises that it is not tested on animals, it only means that the ingredients underwent animal tested by others in the past. Re-blending of well-known ingredients may not need more animal testing for each new mixture within reasonable variability.
It is true that animal models are not perfect matches for reactions in humans. Each animal has unique metabolic systems that vary from species to species. What developers try to do is to match human systems as well as possible for the disease and the mechanism of the drug being developed. For instance, some products are affected by whether or not an animal can make its own vitamin C. Humans cannot and have that in common with hamsters, which are sometimes used for toxicology and other testing.
Both White Coat Waste and PETA (People for the Ethical Treatment of Animals) are advocacy groups that are dedicated to ending animal testing of all types. Ending animal testing would end drug, cosmetic and consumer product development. As much as I wish we could end animal testing, this is not possible unless we stop all progress, development or improvement of treatments for still orphaned diseases and conditions.
For example, the progress made by St. Jude in childhood leukemia and cancer treatment is remarkable. At one time, fatality was 80 to 90% for most types. Now, for most of these diseases, fatality is only 20%. This is still too high, but could not have been accomplished without new drug and treatment development. My daughter died over 40 years ago of a type of leukemia that is among those types that still have high fatality. Much research and development is still needed.
Leishmaniasis Facts: Leishmania is caused by a protozoan parasite carried and spread by infected sand flies. Sand flies are tiny, about half the size of mosquitos, and are silent. They are most active dusk to dawn. Only females need blood for egg and parasite development. Sand flies become infected by biting and taking a blood meal from infected dogs, cats, rodents or humans, so a few cases have now been acquired in Texas, probably by sand flies that had bitten immigrants from tropical countries.
Symptoms of visceral leishmania in humans, which may not be evident for months or even years, include fever, weight loss, enlarged spleen and liver, abnormal blood tests with low red and white cells and platelets and may cause kidney failure. The cutaneous form affects skin with nodules and ulcers that develop in a few weeks, but may progress to the visceral form even after the sores heal.
Symptoms in dogs include skin nodules, thickening of foot pads, dull and brittle hair and hair loss patches. Visceral symptoms include fever, loss of appetite, weakness, exercise intolerance, severe weight loss, diarrhea, vomiting, bleeding nose, tarry stools, swollen lymph nodes, enlarged spleen, kidney failure.
Treatment: No one treatment is effective for all cases. It varies with the form and the species/strain of the parasite, and even the geographical location. CDC offers advice for several possible treatments, but does not ensure success for any one of them. Some are not available in developing countries, and some are not available in the United States because the FDA had not approved them. There is a need for development of vaccines and better treatments with a more assured outcome for all strains in all areas.
Full disclosure: Most of my knowledge about drug development protocols was gained while I worked for a pharmaceutical company for five years in the 1990s. I was a supervisor in a chemical control lab that tested FDA approved prescription drugs. I was not directly involved in research and development or with testing experimental drugs on animals, but both were located at the same company site. Animal rights protests and violence prompted the company to build a high security fence that included parking lots in order to protect employees.
[1.] “In an emailed statement to MedPage Today, NIAID said the contract for “preclinical pharmacology and toxicology services” was conducted “as required in animal models by the FDA, in compliance with Good Laboratory Practice (GLP) guidelines and in a facility accredited by the Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) or its equivalent.” from https://www.medpagetoday.com/special-reports/exclusives/95275 Oct. 26, 2021
‘This Ends The Debate’ – Israeli Study Shows Natural Immunity 13x More Effective Than Vaccines At Stopping Delta
BY TYLER DURDEN- FRIDAY, AUG 27, 2021 – 07:39 AM
Dr. Anthony Fauci and the rest of President Biden’s COVID advisors have been proven wrong about “the science” of COVID vaccines yet again. After telling Americans that vaccines offer better protection than natural infection, a new study out of Israel suggests the opposite is true: natural infection offers a much better shield against the delta variant than vaccines.
The study was described by Bloomberg as “the largest real-world analysis comparing natural immunity – gained from an earlier infection – to the protection provided by one of the most potent vaccines currently in use.” A few days ago, we noted how remarkable it was thatthe mainstream press was finally giving voice to scientiststo criticize President Biden’s push to start doling…
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Science Norway reports Poor studies on long Covid are sensationalized by the media Excerpts in italics with my bolds.
Many recent reports in the media have given the impression that people are experiencing major long-term effects after having even mild Covid-19. This impression does not correspond with the knowledge we have accumulated so far.
We must dedramatise the long-term effects of Covid-19, often referred to as long Covid. The media have a responsibility in this regard. They must become more critical of the research methods used in the studies they refer to.
Most infectious diseases with severe symptoms will to some extent be accompanied by long-term effects. Most infectious diseases with mild symptoms will cause few short-term effects.
More and more studies are showing that this is probably also the case for Covid-19. It is vital that more high-quality studies are carried out to examine this problem.
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CDC is ending RT-PCR testing in favor of multiplex rapid antigen test to distinguish Covid from Flu. See CDC notice below. What they are not telling us is that the RT-PCR test has very high false positives, inflating the numbers. The rapid antigen test is more accurate and gives results in minutes, so medical care decisions can be made ASAP. Labs will start transitioning before the Dec 31, 2021 cutoff so numbers will start to drop, just in time for 2022 election year. England has been using the rapid antigen test for over a year.
07/21/2021: Lab Alert: Changes to CDC RT-PCR for SARS-CoV-2 Testing
Audience: Individuals Performing COVID-19 Testing
Level: Laboratory Alert
After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.
In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test. CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Such assays can facilitate continued testing for both influenza and SARS-CoV-2 and can save both time and resources as we head into influenza season. Laboratories and testing sites should validate and verify their selected assay within their facility before beginning clinical testing.
- FAQ: CDC Distribution of COVID-19 Assays
- Guidance for SARS-CoV-2 Point-of-Care Testing
- Interim Guidance for SARS-CoV-2 Antigen Testing
- Interim Guidelines for Collecting, Handling, and Testing Clinical Specimens for COVID-19
- Frequently Asked Questions about COVID-19 for Laboratories
- Information for Laboratories about COVID-19
- CDC COVID-19 Website
- Clinical Laboratory COVID-19 Response Weekly Calls
- CDC Laboratory Outreach Communication System (LOCS)
If you have any questions, please contact us at LOCS@cdc.gov.
The Laboratory Outreach Communication System
Laboratory Outreach Communication System (LOCS) | Division of Laboratory Systems (DLS)
Center for Surveillance, Epidemiology, and Laboratory Services (CSELS)
Centers for Disease Control and Prevention (CDC)
The charts below are from Our World in Data, a global data tracker that combines the CDC, Johns Hopkins, WHO and the IMF world data to create a daily update of cases and deaths.
Since the U.S. media focuses on new cases, which are riddled with all kinds of misleading inconsistencies, including repeat testing (multiple testing per person), new cases also do not indicate level of sickness, only a positive result, and new cases are most likely from a PCR swab known to be 40-50% inaccurate depending on adjusted cycle thresholds which can produce false positives.
Fatalities are the truest measure real-word impacts of COVID-19.
So while the rest of the media is using new cases as a way to instill continued panic, let’s follow the science on the data that actually counts: how many people are dying in each State, on average per day. Below and current daily…
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BY TYLER DURDENMONDAY, JUL 26, 2021 – 06:11 AM
We have detailed(most recently hereandhere) thecontroversy surrounding America’s COVID “casedemic” and the misleading results of the PCR test and its amplification procedurein great detail over the past few months.
As a reminder, “cycle thresholds” (Ct) are the level at which widely used polymerase chain reaction (PCR) test can detect a sample of the COVID-19 virus. The higher the number of cycles, the lower the amount of viral load in the sample; the lower the cycles, the more prevalent the virus was in the original sample.
Numerous epidemiological experts have argued thatcycle thresholds are animportant metric by which patients, the public, and policymakers can make more informed decisionsabout how infectious and/or sick an individual with a positive COVID-19 testmight be. However,as JustTheNews reports,health departments across the country arefailing to…
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The article below from Epoch Times reveals the problem that inflates Covid-19 case numbers. PCR tests are great diagnostic tests for confirming the source of an illness; PCR is a terrible screening test for non-symtomatic people. You may also read the original article using the link at the end.
World Health Organization (WHO) Director-General Tedros Adhanom Ghebreyesus gives a press conference at Geneva’s WHO headquarters on Feb. 24, 2020. (Fabrice Coffrini/AFP via Getty Images)PUBLIC HEALTH INFORMATION
WHO Changes CCP Virus Test Criteria in Attempt to Reduce False Positives
BY MEILING LEE January 23, 2021 Updated: January 24, 2021
In updated guidance published on Jan. 20, the WHO said that lab experts and health care practitioners should also consider the patient’s history and epidemiological risk factors alongside the PCR test in diagnosing the CCP (Chinese Communist Party) virus.
The new guidance could result in significantly fewer daily cases.
“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,” the guidance says.
It’s unclear why the health agency waited over a year to release the new directive. The WHO didn’t reply to an inquiry from The Epoch Times.
Scientists and physicians have raised concerns for many months of an over-reliance on and a misuse of the PCR test as a diagnostic tool since it can’t differentiate between a live infectious virus from an inactivated virus fragment that is not infectious.
Additionally, the high cycle threshold values of most PCR tests—at 40 cycles or higher—increases the risk of false positives. A higher threshold value indicates less viral load and that the person is less likely to be infectious, while a person with a lower cycle threshold value has a higher viral load, or is more infectious.
The WHO did not specify what the threshold value cutoff should be for a positive diagnosis, but said to only “determine if [a] manual adjustment of the PCR positivity threshold is recommended by the manufacturer.”
However, it clarified that when the prevalence of the CCP virus is low, “the risk of false positive increases” meaning 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 [of the PCR test].”
SARS-CoV-2 is the scientific name for the CCP virus that causes the disease COVID-19.
The Centers for Disease Control and Prevention (CDC) says its PCR tests have a cycle threshold cutoff of 40 cycles. The federal agency finally included information on cycle threshold value in its Frequently Asked Questions about COVID-19 for laboratories on Nov. 12, 2020.
But many medical experts consider a threshold value cutoff of 40 cycles to only return false positives since samples that go through many amplification cycles will pick up negligible RNA sequences regardless if the virus is inactivate or the viral load is exceedingly low to pose any problem.
Prior to the CCP virus pandemic, for individuals to be considered a case, they must test positive and show clinical signs and symptoms. But to be counted as a CCP virus case, only a positive PCR test is required. And no matter how many times an individual is tested, each positive test is counted as a separate case.
The WHO is now advising that a positive PCR test that does “not correspond with the clinical presentation” should be verified by taking “a new specimen” and retesting it.
This advice may also help lower CCP virus cases in hospitals as it more clearly defines who is considered a hospitalized case.
The UK’s National Health Service (NHS) Director of International Relations Dr. Layla McCay confirmed to talkRADIO that a percentage of hospitalized patients officially counted as positive cases were actually being treated for different illnesses not related to COVID-19. They had only tested positive for the disease at the hospital without displaying any symptoms.https://platform.twitter.com/embed/index.html?creatorScreenName=EpochTimes&dnt=false&embedId=twitter-widget-0&frame=false&hideCard=false&hideThread=false&id=1346363750006317056&lang=en&origin=https%3A%2F%2Fwww.theepochtimes.com%2Fwho-changes-ccp-virus-test-criteria-in-attempt-to-reduce-false-positives_3668064.html&siteScreenName=EpochTimes&theme=light&widgetsVersion=ed20a2b%3A1601588405575&width=550px
Dr Layla McCay, NHS Confederation director, confirms to Julia that the hospital figures for “Covid patients” include patients who are not being treated for Covid but have simply tested positive while being treated for something else.@JuliaHB1 | @LaylaMcCay pic.twitter.com/xSud6LW13M
— talkRADIO (@talkRADIO) January 5, 2021
“It is correct that in hospital, people who tested positive for COVID will be the full range of symptoms,” McCay said. “Some will have it as an aside to some other problem for which they’re in the hospital.”
The day after the WHO released its new guidance, Chief Medical Adviser to President Joe Biden, Dr. Anthony Fauci, said the United States would rejoin the organization.
“As such, I am honored to announce that the United States will remain a member of the World Health Organization,” Fauci said. “Yesterday, President Biden signed letters retracting the previous administration’s announcement to withdraw from the organization, and those letters have been transmitted to the secretary-general of the United Nations and to you Dr. Tedros, my dear friend.”
Tedros Adhanom Ghebreyesus is the director-general of the WHO.
“The United States also intends to fulfill its financial obligations to the organizations,” Fauci added.
In July last year, the Trump administration pulled out of the WHO over its alleged role in helping the Chinese communist regime cover up the severity of the CCP virus.
There have been mixed responses from Congress over Biden’s decision to rejoin the WHO.
Rep. Lauren Boebert (R-Colo.) introduced a bill (pdf) on Jan. 21 to “prohibit the availability of United States contributions to the World Health Organization until Congress receives a full report on China and the COVID-19 pandemic, and for other purposes.”
She said in a statement: “The WHO is China-centric and panders to Beijing at every turn. There is no reason U.S. taxpayers should contribute more than $400 million annually to an organization that covered for China and failed to contain the spread of the COVID-19 pandemic.”
Prior to former President Donald Trump withdrawing from the WHO, the United States contributed the most money to the health agency, according to State Department statistics.
What is real and what is agenda driven misinformation, disinformation and confusion? Here are the basic facts in plain language, followed by a few of the lies and conspiracy theories that you may be concerned or confused about.
So far, there are three vaccines approved under Emergency Use Authorization (EUA) by the FDA for use in the US, and one approved for England, EU and other countries. Many companies in several countries entered the race to develop vaccines when President Trump made the funds available and announced Operation Warp Speed to develop vaccines as quickly and safely as possible. Several other companies are still doing research or trials. Merck dropped out when it determined that its vaccine was not as effective as the others that were being developed, but partnered with Johnson and Johnson, which lacked capacity, to manufacture their vaccine. Other independent efforts include Sputnik 5 from Russia and Convidicea from China.
Pfizer and Moderna (US) used gene sequencing techniques to create a short segment of the Covid-19 single stranded mRNA (messenger RNA) molecule that codes for the Covid-19 surface spike protein. To produce immunity, the vaccine mRNA first uses ribosomes inside the host’s cells to build the Covid-19 spike protein. Ribosomes are molecular machines that build proteins by reading the genetic information of mRNA. When injected, the mRNA enters the host’s cells and uses ribosomes, to read the genetic code and make copies of Covid-19 spike protein. The new copies of the Covid-19 spike protein then can be used by your immune system to evoke an immune response that produces antibodies and other defenses to Covid-19. Note that, contrary to rumors and scare stories, the small segment of mRNA never enters the nucleus of the cell so it cannot interact with or change the DNA, which is protected inside the nucleus.
AstraZeneca (UK & EU) and Johnson & Johnson (US) developed their vaccines using a more conventional method. Each used a non-replicating, weakened adenovirus combined, through recombinant gene engineering techniques, with laboratory created Covid-19 genes coded for Covid-19 spike proteins. The Covid-19 spike proteins are expressed on the adenovirus surface, giving them the ability to evoke an immune response in the human body and produce antibodies to Covid-19. An adenovirus is a double stranded DNA virus that normally causes the common cold. The corona type viruses like Covid-19 are single stranded RNA viruses.
Research and Approvals
The research itself was expedited because the companies already had the information provided by China, WHO and CDC for the virus RNA genetic sequence and the protein structures, including surface and spike proteins. Each company used well established genetic sequencing techniques to build copies of genes and/or proteins to make their vaccines. In addition to gene recombinant technology and gene and protein sequencing techniques, Pfizer and Moderna took advantage of a very recent patented breakthrough in stabilizing the Covid-19 spike protein against early immune system attack in order to design their mRNA molecules. None of this would have been possible just a few years ago.
Each of the vaccines went through a series of tests and double-blind clinical trials to determine safety and effectiveness. Even for FDA Emergency Use Authorization (EUA), the complete series of trials (in vitro, animals, humans in three phases) double blind clinical trials were completed on tens of thousands of volunteers and thoroughly documented. All possible negative effects were thoroughly documented on the various populations involved. The trial participants included a wide range of ages, races and backgrounds. No shortcuts were taken. The only reason they were approved so quickly is that they got priority by the government agencies, and the documentation was expedited, so that they did not wait months or years to get approval of each trial design and permission to run each phase of the trials.
The process was further expedited by running some of the trials concurrently, not in series, which would have required waiting between trials for approval and permission to run each new phase. After early trials showed promise, bulk manufacturing was begun so that vaccines would be available immediately if and when they were approved. Manufacturing before final approval was a gamble the Warp Speed team was willing to fund in order to get the vaccines out as quickly and safely as reasonably possible. At the same time, a distribution system was developed to make the vaccines available throughout the country.
The efficacy of all three US approved vaccines is high, compared to flu shots. Fifty percent is considered a good result. Pfizer’s or Moderna’s COVID vaccine was 80% effective in preventing infections. That number jumped to 90% two weeks after the second dose. Moderna’s vaccine reported 94.1% effectiveness at preventing COVID-19 in people who received both doses. The Pfizer-BioNTech vaccine was said to be 95% effective.
J&J/Janssen vaccine was 66.3% effective in clinical trials at preventing COVID-19 illness in people who had no evidence of prior infection 2 weeks after receiving the vaccine. Analyses of secondary endpoints demonstrated vaccine efficacy against central laboratory confirmed and blind-adjudicated severe/critical COVID-19 occurring at least 14 days and at least 28 days after vaccination of 76.7% (54.6, 89.1) and 85.4% (54.2, 96.9), respectively.
Lies, Conspiracy Theories and Confusion
Claim #1. – Aborted Baby Parts – None of the vaccines contain aborted baby parts as claimed by conspiracy theorists. The truth is that before going on to animal and human tests, the vaccines were tested in vitro on a cell line, originally derived from an aborted fetus in 1966, to determine if the vaccine is safe before testing on animals and then humans. Some of those spreading this lie produced a video and apparently did some study of the AstraZeneca trial documentation, but misunderstood or intentionally distorted the information. The MRC5 cell line was mistakenly claimed to be part of the vaccine, and the word “recombinant” was misinterpreted as “human recombinant.” It really refers to combining the vaccine adenovirus genes with genes coded for Covid-19 spike protein. This may be one source of the next conspiracy theory.
Claim #2. – Vaccines will change your DNA – None of the vaccines change human DNA, but ordinary viruses do. Because viruses lack the ability to reproduce on their own, they hijack the host cell’s DNA to make copies of themselves. Unlike viruses, the vaccines never enter the cell nucleus where DNA is found. The Pfizer and Moderna vaccines were created by gene sequencing techniques to produce short segments of mRNA (messenger RNA) coded for the Covid-19 virus coat spike protein. The vaccine is designed to enter the cell cytoplasm and use the cell’s ribosomes (outside the nucleus) to make the virus coat protein, which then causes an immune response, forming antibodies.
The AstraZeneca and Johnson & Johnson vaccines use nonreplicating, weakened adenoviruses whose DNA have been modified to include Covid-19 coat protein instructions. The vaccine adenovirus carries the protein on its surface to produce the immune response. It never needs to enter the cell so it can’t affect the cell’s DNA. Note that “nonreplicating” means it has been “killed” by heat or other means and cannot reproduce by making copies of itself.
Claim #3. – Experimental Vaccines – The claim is that the vaccines are experimental so they haven’t been tested and can’t be trusted. See above for a brief summary of testing and trials. No steps were skipped or ended early. The only part that is not completed is long term follow up for length of time that the immunity lasts, and any possible rare, chronic or extended reactions to it.
Claim #4. – Vaccines kill people – Some people have died days of weeks after getting the shot. In each case, investigations found no clear cause-and-effect link between the deaths and the vaccine. The high number (25) reported from Norway were among elderly, frail nursing home residents and could not be linked directly to the vaccine. Other deaths investigated are found to have other causes, but may continue to be associated statistically even weeks after the injection.
There is a US database called VAERS (Vaccine Adverse Effects Reporting System, https://vaers.hhs.gov) that documents any adverse reactions to vaccines. In the Covid-19 part of the databases, I chose to study the first two weeks in January, 2021 as a manageable sample. In that time, there were 9676 adverse reactions and 106 deaths reported of 444,753 vaccinations administered. Most of the adverse reactions were either allergic reactions (treated with Benadryl or epi pen) or mild flu-like symptoms or injection site soreness, infection or itch. Adverse reactions were 2.2% of those vaccinated, and deaths were 0.02%. These percentages are higher than those in later periods because of the age and condition of people permitted to get the vaccine at that time. To assure myself that this was representative of the overall pattern, I later checked late March entries and found a similar pattern.
I went through many of the reactions and all of the deaths reported in these time periods to determine any links, if present. All but a few of the deaths were among the elderly with other serious conditions, many in long term care facilities or hospice. The average age was 74, with a range of 40s to 90s and one 104 for the January set. The one exception was a 25-year-old man that died 20 days after injection; His death is unlikely to be vaccine related because of the elapsed time. Although there were no details, he may have been chronically ill, judging from the fact that he got the vaccine very early when mostly vulnerable people were getting vaccinated. Unfortunately, details of factors contributing to death for some were sketchy or missing. Also company identification was uncertain for the second set. Some listed one company in that column but stated a different company in the text, so no conclusions could be drawn connecting any one company to deaths or adverse effects. The VAERS reporting system is voluntary and transcribed from entries by healthcare personnel and untrained family members.
Claim #5. – Vaccines will sterilize people – Not sure where this one came from, but it is pure fantasy. There is no mechanism for it to do this. There is no secret ingredient added to sterilize people. By the way, this is a common propaganda theme used by population control and anti-vax activists to scare poor people in developing countries from getting much needed vaccines such as polio and measles.
Claim #6. – Vaccines contain specific antibodies that overwhelm and deactivate natural nonspecific antibodies. This is totally false and is probably just anti-vaccine propaganda to prevent people from getting the protection of vaccines. Our bodies make and retain in reserve antibodies for hundreds of substances, both specific and nonspecific. There is no way that antibodies from any vaccine can deactivate any antibodies naturally produced by our bodies.
Claim #7. – Microchips are inserted with the vaccine – this conspiracy theory gets quite elaborate with Bill Gates, Anthony Fauci and Moderna sometimes woven into the narrative about tracking, monitoring and controlling every person on earth. Every word of it is false, including Gates and Fauci as roommates at Harvard (attended a decade apart), Fauci founding Moderna (not), and Gates, a software guy, inventing RFID microchips.
An RFID (Radio Frequency Identification Device) chip is a radio receiver and transmitter. It transmits only when it receives a signal from a reader that then reads the transmitted signal. RFID technology has been used to track shipments for over 70 years. RFID chips are attached to the vaccine containers to track them and make sure they are delivered to the correct facilities. Maybe that’s where this story came from. Microchips that are used in animals are about the size of a grain of rice and need a special applicator to insert under a pet’s skin, not the tiny needle used for vaccinations.
NOTE: Tiny RFID chips, called Smart Dust, that are the size of a grain of sand are being developed for the military. These are experimental (read expensive and unavailable) and require other equipment such as external sensors, antennae, communication nodes and networks to operate. A larger version, ¼ – ½ inch, which contains a tiny computer is called a Mote. It also requires other equipment to operate.
Claim #8. – Nanoparticles are in the vaccine and may contain tiny robots or machines – The “nanoparticles” in the Pfizer and Moderna vaccines are actually very fine lipid (oil) droplets that protect and help the mRNA segment enter the cell in order to make Covid-19 proteins. Nano is a measure of size and does not imply functionality or complexity. From Wikipedia: “A nanoparticle or ultrafine particle is usually defined as a particle of matter that is between 1 and 100 nanometers in diameter.” A nanometer is 1 billionth of a meter. Although many nanoparticles are solids and may be made of metals, etc., the “particles” in these vaccines are simply very fine oil droplets, similar in size to the colloidal fats in milk, (ranging in size from 1 to 1000 nanometers). Like the colloidal fat in milk, the tiny size of the oil droplets in the vaccines helps keep the oil suspended without separating and settling out. For comparison, the Covid-19 virus is 120 nanometers in diameter, which is large for a virus.
Claim #9. – Nanoparticles are on the testing swab and are inserted into the blood brain barrier – one version says the swab used to take the sample deep in your nose is used to insert nanoparticles in the “blood brain barrier” there. First of all, sterile swabs are mass produced and readily available from medical supply companies. They are not specific to the test. The blood brain barrier is not a membrane located in your nose. It consists of membranes covering all of the capillaries of the brain that protect the brain from contaminants. From Wikipedia: “The blood-brain barrier (BBB) is a highly selective semipermeable border of endothelial cells that prevents solutes in the circulating blood from non-selectively crossing into the extracellular fluid of the central nervous system where neurons reside.” (“Solutes” refers to solids.)
Claim #10. – 5G cellphone radiation either causes Covid-19 or makes it worse – This is related to anti-technology fears and is totally unfounded. An earlier claim that cellphone radiation causes cancer has been thoroughly debunked by numerous scientific studies, but is still believed by many. This new iteration claims that the 5G, which operates at higher radio wave frequencies, is more harmful to health than previous cellphone Generations, e.g. 4G, 3G. Current 4G networks, operate in the 700 MHz-2500 MHz range, and 5G operates in a higher frequency range in two bands, either less than 6GHz or greater than 24 GHz. (Hertz means cycles per second, MHz is million and GHz is billion cycles per second). Radio waves are non-ionizing “radiation” and are harmless at frequencies and power levels encountered. The 5G broadens the band width so it can support more users and transfer data faster. Since the higher frequency radio waves don’t travel as far, more cell towers are needed to fill the gaps in the 4G network.
Another version of this conspiracy theory is that 5G cellphone technology is intended to track people with embedded RFID chips. If you have a cellphone, you can be and are already “tracked” by GPS; no embedded RFID chip needed. Although extremely unlikely, this is more likely than the scenario above, and is probably responsible for Hong Kong riots just before China’s 5G system was completed and turned on. Unlike most free countries, China can require its people to get RFID chips embedded in order to access social services, hospitals, schools or employment. 5G short-range and closer towers could, in this case, locate people more accurately.
Over many decades, the anti-vaccine movement has done great damage and cost many lives, especially in poor countries. Celebrity activists such as Robert F. Kennedy, Jr. and his Children’s Health Defense foundation, are either innocent true-believers or sinister liars with an evil agenda. The antivaxxers join a cadre of antitechnology groups that want to scare people about anything that is not “natural.” Natural doesn’t make it’s safe; arsenic and death cap mushroom are “natural” but deadly. By “not natural,” they mean anything that was not practiced in ancient times. i.e., technology of any kind, including fertilizers, pesticides, hybrid and GMO foods, most modern medicines, electronics, vehicles, and industries.
Their purpose is to control us by keeping us scared of everything from our food and water to electric lights, pollution and climate change. Their goal is to cripple modern societies and take us back to simpler times of the past. Secret: the good old days were terrible, with high infant and childhood mortality, short, disease ridden and painful lives, hunger, filth, pollution. Like all good lies, they are spiced with truths and half-truths as well as so-called “science” and “authority” to make them believable. Our world is just fine without limiting population and life spans. Overpopulation and limited natural resources are myths, as are most of the climate change claims. Not that it does not exist, but that it is not an emergency, and we can do very little to change it other than adapt to it.
Among many targets of the modern anti-vaccination movement are vaccines of all types. MMR (measles, mumps, rubella) vaccine was among early targets, claiming that either the shot overwhelmed the immune system or the preservative thimerisol (containing an organo-mercury preservative) was responsible for autism and autoimmune diseases. This has been thoroughly studied and debunked but it is still claimed, even when the thimerosal was replaced by another preservative. Every vaccine since then has been targeted by their scare stories and propaganda, and it has caused misery and death worldwide.
It makes no sense for pharmaceutical companies to invest billions of dollars and years of research to produce a product that will kill or maim their customers. Even most of the believers in the overpopulation myth and the zero-growth movement have not gone that far, but they may have spread the antivaxxers scare stories in poor countries to keep children from being protected. Their usual methods involve providing or requiring abortion and physical sterilization of poor people, while keeping them poor, sick and ignorant by denying them modern development.
One thing is certain, once a conspiratorial claim is made, it never dies. Regardless of overwhelming scientific evidence to the contrary, some people will continue to believe and spread it. Behind it is a general distrust of authority and government that has been fostered by these groups and promoted by actual government failures and misinformation.
 See my book Saving Africa From Lies That Kill: How Myths about the Environment and Overpopulation are Destroying Third World Countries, Kay Kiser, 2018, or my blog www.savingafricafromliesthatkill.com
Click on the link above to view video of Part 2 of Steve Hilton’s investigation into the origins of Covid-19.