Did you know that a cancer-causing monkey virus contaminated millions of batches of polio vaccine?
Did you know this virus has now been found inside people and inside their cancers?
The health authorities would like the American public to forget these facts. But it happened, and the repercussions are still with us today.
This known contamination took place at the end of the 1950s and the beginning of the 1960s, but may have continued for the next 40 years. In fact, over the last 60 years, cancer rates for every age group in America have continued to climb.
How did this vaccine contamination happen? And is there a link to the skyrocketing rates of cancer in the United States?
How were polio vaccines contaminated with cancer-causing monkey virus?
In the 1950s, scientists like Drs. Jonas Salk and Albert Sabin had isolated the poliovirus strains to make vaccines.
Salk’s strains would be inactivated with formaldehyde and injected into children. Sabin’s strains would be attenuated, or weakened, by transferring or passaging the live viruses through different host cells, and then fed to children orally.
Because his goal was to create a live attenuated vaccine, Sabin had to isolate the poliovirus strains and then passage the strains through various host cells in order to attain the right virulence — strong enough to illicit an immune response, but weak enough so as to not cause polio in the recipient.
Sabin’s oral polio vaccine (OPV) is a trivalent vaccine and was, therefore, comprised of three types – Type I, II, and III.
Here’s how Type I was created. In 1941, Drs. Thomas Francis and Thomas Mack isolated the Mahoney poliovirus “from the pooled feces of three healthy children in Cleveland.”
Then, to make his vaccine, Salk subjected the polio virus strain to passages through 14 living monkeys and two cultures of monkey testicular cultures. In 1954, the strain (now called Monk14 T2) was given to Drs. C.P. Li and M. Schaeffer, who subjected the virus to nine more passages through monkey testicular cultures.
Next, the strain (now called Monk14 T11) underwent 15 more passages in monkey testicular cultures, 18 passages in monkey kidney cells, two passages through the skin of living rhesus monkeys, and additional passages through African Green monkey skin and monkey kidney cell cultures.
This strain was now called MS10 T43 or LS-c.
In 1956, Sabin took this polio virus and passaged it through seven cultures of African Green Monkey kidney cells. That same year, the pharmaceutical company, Merck, Sharp & Dohme, passed the strain (now called LS-c, 2ab/KP2) through a rhesus monkey kidney cell culture.
The resulting material, called Sabin Original Merck (SOM), was provided to the pharmaceutical company Lederle in 1960, as the seed material to manufacture its polio vaccine.
Types II and III were created in a similar fashion.
Why was so much ‘passaging’ through animal cells necessary?
The theory of passaging is relatively simple. The idea is that as a virus becomes more adapted to a new animal species, that strain will become less adapted to its original host.
Putting the virus into various monkey tissues or cultures, including monkey kidneys, monkey testicles and monkey skin, was designed to adapt the polio virus to monkeys.
Once it was adapted to monkeys, so the theory goes, the polio virus would be less virulent for humans. While the idea made sense, what did not make sense were the risks of doing this.
Each time the polio virus was harvested from these monkey tissues and cultures, the scientists ran the risk of picking up extraneous monkey viruses mixed in with their polio virus.
This is, of course, what happened. In fact, since kidneys filter the blood and remove toxins, they are uniquely situated to be a potential source of viruses.
But the story gets even worse.
How was polio virus grown for vaccines?
Once their polio seeds were isolated, pharmaceutical companies needed a method to produce the vast quantities needed for nationwide immunization campaigns.
This required a medium or substrate upon which the poliovirus could be efficiently grown and harvested. Kidney cells from rhesus, and later African Green monkeys, were chosen because they were found to be an effective growth medium.
Monkeys were imported in large numbers from various countries. They were killed and their kidneys were removed. A small quantity of poliovirus would then be added to the minced kidneys, and within a few days, large quantities of poliovirus could then be harvested from these pulverized monkey kidneys cells.
There was a problem, however, with using monkey kidney cells to both create the original vaccine strains and grow the vaccine in large quantities: Monkeys are full of monkey viruses.
In fact, there were so many simian viruses identified in the polio vaccines that scientists started numbering them. Simian Virus 1, then 2, etc. Then they started abbreviating them: SV1, SV10, etc.
What is SV40?
SV40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This particular virus contaminated both the Inactivated Polio Vaccine (IPV) created by Salk, and the oral or “live” Polio Vaccine (OPV) created by Sabin.
As discussed below, SV40 was determined to be oncogenic, or cancer-causing.
SV40 is in the family Polyomaviridae, which includes JC virus (JCV) and BK virus (BKV). Polyomaviruses are small DNA viruses.
The SV40 genome encodes for various proteins, including “Large T-ag.” This protein stimulates host cells to enter the phase where the cell multiplies its genetic content prior to cell division. In addition, T-ag binds to various cellular tumor suppressor proteins.
In other words, SV40 helps stimulate human cells to multiply, and also stops the cellular machinery designed to stop cancer from starting. It’s a deadly “one-two punch.”
How was SV40 discovered in the polio vaccine? Dr. Bernice Eddy of the National Institutes of Health (NIH), Division of Biologics, discovered it when, in 1959, she took the material used to grow polio vaccines and injected it into hamsters.
Tumors grew in the hamsters, so Eddy wanted to isolate the causative agent — and it turned out to be SV40, the 40th simian virus contaminating the polio vaccines.
Her discovery was validated by Drs. Maurice Hilliman and Benjamin Sweet of Merck.
What did the scientists say?
Many scientists knew using monkey kidneys full of simian viruses was a dangerous way to make a vaccine.
As early as 1953, Dr. Herald R. Cox, a scientist working at Lederle Laboratories, one of the polio vaccine manufacturers, published an article in a peer-reviewed scientific journal in which he stated:
“[P]oliomyelitis virus has so far been cultivated only in the tissues of certain susceptible species — namely, monkey or human tissues. Here again we would always be confronted with the potential danger of picking up other contaminating viruses or other microbic agents infectious for man.”
In 1958, a scientific journal reported, “the rate of isolation of new simian viruses (from monkey kidney cells) has continued unabated.”
Additionally, in 1960, Merck wrote to the U.S. Surgeon General:
“Our scientific staff have emphasized to us that there are a number of serious scientific and technical problems that must be solved before we could engage in large-scale production of live poliovirus vaccine. Most important among these is the problem of extraneous contaminating simian viruses that may be extremely difficult to eliminate and which may be difficult if not impossible to detect at the present stage of the technology.”
What did the regulators do?
On March 25, 1961, the federal regulations that controlled the production of oral poliovirus vaccines were amended. These new regulations did not require the vaccine manufacturers throw away their SV40-contaminated poliovirus seeds, which were the source for all subsequent polio vaccines.
Instead, the rules required that “[e]ach seed virus used in manufacture shall be demonstrated to be free of extraneous microbial agents.”
The new regulations also required that each pair of monkey kidneys removed from a monkey for vaccine production “shall be examined microscopically for evidence of cell degeneration.”
Furthermore, fluid from the monkey kidney cells had to be combined with other tissue cultures in order to detect if there was any contaminating virus. The regulations required that “[t]he cultures shall be observed for at least 14 days.”
In essence, these regulations required an SV40 test that was comprised of taking the monkey kidney cells upon which the vaccine would be grown and:
- Look at them through a microscope to see if they demonstrated SV40.
- Take fluids from them.
- Introduce those fluids into other cell cultures.
- Wait 14 days.
- Determine if the other cell cultures were changed as a result of the presence of SV40.
What were some of the problems with the test?
These tests were not designed to detect the contaminating viruses themselves. One cannot see SV40 or any virus with a standard light microscope or the naked eye.
Instead, the government’s SV40 test relied on the observation of the presumed effect of an SV40 infection on certain tissue cells to demonstrate the presence of the virus.
In fact, the regulations required only a 14-day observation period, even though it was well documented that the effect they were looking for (“vacuolating change”) could take up to six weeks for SV40 to show itself with this method:
“In this laboratory in [Green Monkey Kidney] GMK cultures inoculated with small quantities of virus [(SV40)] (i.e., <100 TCID50), changes were not observed until five or six weeks after inoculation. Therefore to attain maximal accuracy with this method, a long period of observation is required.”
These quality control steps were designed to appease the pharmaceutical companies because they did not require that the companies throw anything away and start over.
The steps also did not protect the public because they did not ensure the removal of SV40 from the vaccines for a number of reasons, including:
- The original seed stocks that were known to be contaminated with SV40 were not thrown out, but instead used to make OPV for the next 40 years.
- The substrate (monkey kidney cells) used to grow OPV were known to harbor SV40.
- The quality control step was completely inadequate. For example, a 14- day observation period would not detect a virus that could take six weeks to grow.
In fact, in the early 1960s there are multiple scientific papers calling attention to this and suggesting better technologies to detect SV40. The government and pharmaceutical industry ignored these concerns and suggestions.
How was the epidemiology flawed?
After SV40 was originally detected in the Salk and Sabin vaccines which had been administered to millions of children around the world, the scientific community held its breath and wondered if these children would be stricken with cancer when they were young, or later as adults.
Indeed, both the pediatric and adult cancer rates have climbed steadily over the last 60 years. But, the few epidemiological studies that looked for a direct link between SV40 and human cancer provided inconsistent conclusions.
Each of these studies suffered from major flaws, including the fact that no one knew who actually received the SV40-contaminated vaccines and who did not — so it was impossible to compare an SV40-exposed group with a non-exposed group.
Where is SV40 found today?
By 1999, numerous pathologists, microbiologists and virologists throughout the world had detected SV40 in a variety of human cancers, such as brain tumors, including medulloblastoma, bone cancer, mesothelioma and non-Hodgkin’s lymphoma.
Most of these were the very same cancers created when SV40 was introduced into animals.
The question left unanswered for decades now faced scientists again — was SV40 responsible for causing or contributing to human cancers?
Over the years, scientists from around the world have made startling and disturbing discoveries. They have found SV40 antibodies in a significant percentage of people, including children who were too young to receive the SV40-contaminated vaccines of the early 1960s.
Scientists also discovered SV40 is actually inside some human cancers. Furthermore, they determined that SV40 interferes with the genes, like p53, which are necessary for making cancer cells die.
Since genes like p53 help trigger apoptosis, SV40 can make chemotherapy and radiation therapy less likely to be effective.
What did the Institute of Medicine conclude?
In July 2002, the National Academy of Science Institute of Medicine (IOM) Immunization Safety Committee convened a study into SV40 and cancer, which culminated in a report published in October 2002.
According to the IOM report, “SV40 Contamination of Polio Vaccine and Cancer”:
“The committee concludes that the biological evidence is strong that SV40 is a transforming [i.e., cancer-causing] virus … that the biological evidence is of moderate strength that SV40 exposure could lead to cancer in humans under natural conditions, [and] that the biological evidence is of moderate strength that SV40 exposure from the polio vaccine is related to SV40 infection in humans.”
In other words, there was scientific evidence that SV40 wasn’t simply a bystander inside human cancer cells — the scientists concluded the monkey virus could be the cause of the cancer in the person.
What was the government’s response?
Nonetheless, the various U.S. government agencies such as the Centers for Disease Control and Prevention (CDC) and National Cancer Institute, disputed these conclusions.
According to the CDC, “SV40 virus has been found in certain types of cancer in humans, but it has not been determined that SV40 causes these cancers.”
According to the NIH, “the NCI is continuing to evaluate the possible link between SV40 infection and human cancers.”
While the government spends decades “evaluating” SV40, this monkey virus:
- Has already become prevalent in human populations and inside some human cancers.
- Is such a strong carcinogen that a search for scientific articles about “SV40 and cancer” reveals more than 6,100 different scientific articles.
- Makes orthodox cancer therapies less likely to be effective so they cannot save the life of the patient.
Conclusion
SV40 is a potentially deadly human carcinogen and it came from FDA approved and mandated vaccines.
To learn more about SV40, vaccines and cancer read “The Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus, Contaminated Polio Vaccine, and the Millions of Americans Exposed” and visit SV40 Cancer Foundation and Our Alexander.
© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
October 1, 2021
Posted by aletho |
Book Review, Science and Pseudo-Science, Timeless or most popular | CDC, National Cancer Institute, NIH, United States |
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The purpose of this report is to document how all over the world millions of people have died, and hundreds of millions of serious adverse events have occurred, after injections with the experimental mRNA gene therapy.
We also reveal the real risk of an unprecedented genocide.
F A C T S
Our aim is to only present solid facts, and stay away from unfounded claims. The data is clear and verifiable. References can be found with all presented information, which is provided as a starting point for further investigation.
C O M P L I C I T Y
The data shows that we are currently witnessing the greatest organized mass murder in the history of our world. The severity of this situation compels us to ask this critical question: will we rise up to the defense of billions of innocent people? Or will we permit personal profit over justice, and be complicit?
Networks of lawyers all over the world are preparing class action lawsuits to prosecute all who are serving this criminal agenda. Hundreds of millions of people worldwide are rising up against this criminal operation. To all who have been complicit so far, we say: There is still time to turn and choose the side of truth. Please make the right choice.
W O R L D W I D E
Although this report focuses on the situation in the United States, it also applies to the rest of the world, as the same type of experimental injections with similar death rates – and comparable systems of corruption to hide these numbers – are used worldwide. Therefore we encourage everyone around the world to share this report. May it be a wake up call for all of humanity.
AT LEAST 5 TIMES MORE DEATHS
VACCINE DEATHS ARE SEVERELY UNDERREPORTED
VAERS data from the American CDC shows that as of August 26, 2021 already half a million people suffered severe side effects, including stroke, heart failure, blood clots, brain disorders, convulsions, seizures, inflammations of brain & spinal cord, life threatening allergic reactions, autoimmune diseases, arthritis, miscarriage, infertility, rapid-onset muscle weakness, deafness, blindness, narcolepsy and cataplexy.
Besides the astronomical number of severe side effects, the CDC reports that approx. 16,000 people died as a result of receiving the experimental injections. However, according to a CDC whistleblower who signed a sworn affidavit, the actual number of deaths is at least five times higher. This is what the CDC healthcare fraud detection expert Jane Doe officially stated in a sworn affidavit:1
‘I have, over the last 25 years, developed over 100 distinct healthcare fraud detection algorithms, both in the public and private sector. (…) When the COVID-19 vaccine clearly became associated with patient death and harm, I was inclined to investigate the matter. It is my professional estimate that VAERS (the Vaccine Adverse Event Reporting System) database, while extremely useful, is under-reported by a conservative factor of at least 5 (…) and have assessed that the deaths occurring within 3 days of vaccination are higher than those reported in VAERS by a factor of at least 5.’
The CDC is also vastly underreporting other adverse events, like severe allergic reactions (anaphylaxis). The Informed Consent Action Network (ICAN) reported that a study showed that the actual number of anaphylaxis is 50 to 120 times higher than claimed by the CDC. 2, 3
On top of that, a private researcher took a close look at the VAERS database, and tried looking up specific case-ID’s. He found countless examples where the original death records were deleted, and in some cases, the numbers have been switched for milder reactions. He says:
‘What the analysis of all the case numbers is telling us right now is that there’s approximately 150,000 cases that are missing, that were there, that are no longer there. The question is, are they all deaths?’4
How criminal the CDC is, was also revealed a few years ago, when researchers investigated the link between vaccines and autism. They found that there indeed is a direct connection. So what did the CDC do?
All the researchers came together and a large dustbin was placed in the middle of the room. In it they threw all the documents that showed the link between autism and vaccinations. Thus, the evidence was destroyed.
Subsequently, a so-called ‘scientific’ article was published in Pediatric, stating that vaccinations do not cause autism. However, a leading scientist within the CDC, William Thompson, exposed this crime. He publicly admitted:
‘I was involved in misleading millions of people about the possible negative side effects of vaccines. We lied about the scientific findings.’ 5
Maybe the worst example of criminal methodology used to hide vaccine deaths is the incredible fact that the CDC doesn’t consider a person vaccinated until two weeks after the injection.
Therefore everyone who dies within the first two weeks after being injected, is not considered a vaccine death, further skewing the data. 6,7
MODERNA: 300,000 ADVERSE EVENTS
HUNDREDS OF THOUSANDS IN THREE MONTHS TIME
A whistleblower from Moderna made a screenshot of an internal company notice labeled “Confidential – For internal distribution only”, showing there were 300,000 adverse events reported in only three months time.” This is a quote from this confidential notice:
‘This enabled the team to effectively manage approximately 300,000 adverse event reports and 30,000 medical information requests in a three month span to support the global launch of their COVID-19 vaccine.’
https://alexberenson.substack.com/p/some-actual-news
LESS THAN 1% IS BEING REPORTED
STUDY SHOWS REAL NUMBER OF ADVERSE EVENTS IS 100X HIGHER
All this information already shows us that the number of adverse events and deaths is a multitude of what is being told to the public. The situation is however still far worse, than most of us can even imagine.
The famous Lazarus report from Harvard Pilgrim Health Care inc. in 2009 revealed that in general only 1% of adverse events from vaccines is being reported:
‘Adverse events from drugs and vaccines are common, but underreported. Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA). Likewise, fewer than 1% of vaccine adverse events are reported.’
LESS THAN 1% IS BEING REPORTED
STUDY SHOWS REAL NUMBER OF ADVERSE EVENTS IS 100X HIGHER
All this information already shows us that the number of adverse events and deaths is a multitude of what is being told to the public. The situation is however still far worse, than most of us can even imagine.
The famous Lazarus report from Harvard Pilgrim Health Care inc. in 2009 revealed that in general only 1% of adverse events from vaccines is being reported:
‘Adverse events from drugs and vaccines are common, but underreported. Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA). Likewise, fewer than 1% of vaccine adverse events are reported.’
See: https://digital.ahrq.gov/sites/default/files/docs/publication/r18hs017045-lazarus-final-report-2011.pdf
REASONS FOR UNDERREPORTING
THE POPULATION IS UNAWARE AND MISINFORMED
The reason that less than 1% of adverse events is reported, is first of all because the vast majority of the population is not aware of the existence of official reporting systems for vaccine adverse events.
Secondly, the pharmaceutical industry has been waging an unrelenting media war the past decades against all medical experts, who attempted to inform the public about the dangers of vaccines.
One deployed strategy is name calling, and the negative label ‘anti-vaxxer’ was chosen to shame and blame all scientists, physicians and nurses who speak truth.
Because of this criminal campaign of aggressive suppression of adverse events data, the majority of the population is clueless that vaccines can cause any harm at all.
The message the general public constantly hears and sees, couldn’t be further from the truth: ‘Vaccines are safe and the best way to protect yourself from disease.’ The thousands of books, scientific studies, and reports documenting the devastating effects of vaccines in general, have been suppressed by all possible means. The undeniable fact that children (and people of all ages, for that matter) are far more ill today than ever before in history, while at the same time they are the most vaccinated population in all of history, is flatly denied.
The widespread propaganda by the vaccine companies, who use government agencies as their main carrousel, simply told humanity for decades that adverse events are a very rare occurrence.
When vaccinated people therefore suffer from serious adverse events, it doesn’t even occur to them that this could be from previous injections, and therefor don’t report it as such.
During the current world crisis the attacks on medical experts who are warning about vaccines, have gone to an even higher level. Medical experts are now being completely deplatformed from all social media, their websites are deranked by Google, entire YouTube channels are deleted, many have lost their jobs, and in some countries medical experts have been arrested, in an attempt to suppress the truth about the experimental covid injections.
Scientists who speak out against vaccines are even labeled ‘domestic terrorists’. All means are deployed by the criminal vaccine cartel to suppress the truth.
As a result countless medical professionals are afraid to report adverse events, which further contributes to the underreporting of these side effects. Additionally, the amount of scientific information warning for these dangerous biological agents, and the number of medical experts warning humanity, is so overwhelming and almost omnipresent – despite the aggressive attempts to silence them – that it is virtualy impossible for any medical professional to not be at least somewhat aware of the risk they are taking, by administering an untested DNA altering injection, without even informing their patients of what is being injected into their body.
If they then see their patients suffer or die, they are naturally afraid of being held accountable, so they refuse to report it.
Lastly: many medical professionals receive financial incentives to promote the vaccines. In the United Kingdom for example nurses get ₤10 per needle they put into a child. That again is a reason for them to not report adverse events.
They see large numbers of patients come in with serious adverse reactions, like heart failure, and they notice how the authorities of their hospitals are not reporting any of these vaccine injuries. Dr. Maria Gonzales, ER doctor from the U.S. Dept. of Health and Human Services, expresses her outrage about this in the Phoenix Indian Medical Center.
She discusses with a colleague how a patient was vaccinated and as a result got heart failure:
‘They’re not going to blame the vaccine. But he has an obligation to report that, doesn’t he? They are not reporting!’ – ‘Right!’ – ‘Because they want to shove it under the mat. The government doesn’t want to show that the vaccine is full of shit.’
PROJECT VERITAS WHISTLEBLOWERS
DOCTORS AND NURSES SPEAK OUT: ‘THEY ARE NOT REPORTING!’
Project Veritas is a journalistic organization that has been exposing crime and corruption in our world for years. They often receive video footage from hidden cameras, that reveal what is going on behind closed doors. They were contacted by several federal doctors and nurses, who can no longer be silent.
In an interview with James O’Keefe from Project Veritas, the nurse Jodi O’Malley testifies:
‘I’ve seen dozens of people come in with adverse reactions.’
She adds that none of these are being reported. When asked if she isn’t afraid for repercussions for speaking the truth, she answers:
‘I am not afraid, because my faith is in God. This is evil at the highest level.’
The video also shows nurse Jodi talking to a doctor, who is desperate to break the silence:
‘It is bullshit. I am about tired of it. So what we’re going to have to do, cause we’re on the inside… I’ve been thinking about it.’ – ‘And, what do we do?’ – ‘I don’t know, but there’s so much I want to blow up.’ – ‘So much. How do we do that?’ – ‘You know Project Veritas?’
There are thousands of doctors and nurses like this, whose hearts are burning to speak out, but who are afraid. I have personally been contacted by different groups of hundreds of medical professionals. If you are a medical professional and want to speak out, please contact Project Veritas veritastips@protonmail.com or Stop World Control: network@stopworldcontrol.com
You will be not be alone, but you will find a vast army of freedom fighters, worldwide, who will stand with you. Please come forward and share your story. Humanity needs you!
Watch the videos from Project Veritas with the medical whistleblowers here:
https://www.projectveritas.com/news/federal-govt-whistleblower-goes-public-with-secret-recordings-government/
THOUSANDS OF STORIES
FACEBOOK POST REVEALS TSUNAMI OF ADVERSE EVENTS
A local ABC News Station posted a request on Facebook for people to share their stories of unvaccinated loved ones that died. They wanted to make a news story on this. What happened was totally unexpected. In five days time over 250,000 people posted comments, but not about unvaccinated beloved ones. All the comments talk about vaccinated loved ones that died shortly after being injected, or that are disabled for life. The 250,000 comments reveal a shocking deathwave among the population, and the heartwrenching suffering these injections are causing. The post was already shared 200,000 times, and counting…


Notice in the last comment how the lady says that everybody in the hospital is afraid to report this as a vaccine reaction, and another person says ‘the doctors can’t report it’. That is proof of what I explained earlier: Most medical professionals are terrified to report adverse events, which causes the true prevalence of vaccine injuries to remain hidden from the world.
The 250,000+ comments show that once people find a safe place to report their suffering caused by the injections, we see a tsunami… This is only one single Facebook post, that is getting no media attention whatsoever. What would we see if this was announced on the news, and everyone was allowed to report their stories?
https://www.facebook.com/80221381134/posts/10158207967261135/?d=n
VACCINE DEATHS SUMMARY
WHAT IS HAPPENING IS FAR WORSE THAN WE THINK
- VAERS published 16,000+ deaths and 450,000+ adverse events, as of August 28, 2021
- CDC fraud expert says that number of deaths is at least five times higher 150,000 reports have been rejected or scrubbed by the VAERS system.
- The actual number of anaphylaxis is 50 to 120 times higher than claimed by the CDC
- Vaccinated people who die within two weeks, are not listed as vaccine deaths
- Moderna received over 300,000 reports of adverse events in only three months-time
- The Lazarus Report shows that only 1% of adverse events is being reported by the public
- The majority of the population is not aware of the existence of systems where they can report vaccine adverse events
- Aggressive censorship and propaganda told the public that adverse events are rare, causing people to not understand how their health problems stem from past injections
- The shaming and blaming of medical professionals who say anything against the vaccines, cause many in the medical community to avoid reporting adverse events
- The fear of being held accountable after administering an injection that killed or disabled patients, further prevents medical personnel from reporting it
- Having accepted financial incentives to promote, and administer the covid vaccines, also stops medical personnel from reporting adverse events
- Profit driven vaccine manufacturers have every reason not to report the destruction their untested experimental products are causing 250,000+ Facebook users comment about vaccine deaths and serious injuries
- Nurses and doctors testify how their hospitals are hiding vaccine injuries.

WORLD EXPERTS WARN HUMANITY
LEADING SCIENTIFIC VOICES ISSUE GRAVE WARNINGS
This alarming data leads world experts, like the Nobel Prize Winner in Medicine, Dr. Luc Montagnier, to issue a grave warning that we are currently facing the greatest risk of worldwide genocide, in the history of humanity. Even the inventor of the mRNA technology, Dr. Robert Malone, warns against these injections that are using his technology.
The situation is so severe that former Pfizer vice president and chief scientist Dr. Mike Yeadon came forward to warn humanity for these extremely dangerous injections. One of his best known videos is titled ‘A Final Warning’.
Another world renown scientist, Geert Vanden Bossche, former Head of Vaccine Development Office in Germany, and Chief Scientific Officer at Univac, also risks his name and career, by bravely speaking out against administration of the covid shots. The vaccine developer warns that the injections can compromise the immunity of the vaccinated, making them vulnerable for every new variant.
WWII holocaust survivors wrote to the European Medicines Agency demanding the injections to be stopped, which they consider to be a new holocaust.
REFERENCES:
1: https://renzlaw.godaddysites.com/45k-whistleblower-suit
2: https://www.icandecide.org/wp-content/uploads/2021/03/Letter-to-Dr.-Walensky-re-anaphylaxis.pdf1: https://renzlaw.godaddysites.com/45k-whistleblower-suit
3: https://jamanetwork.com/journals/jama/fullarticle/2777417
4: https://centipedenation.com/first-column/150k-records-deleted-from-vaers-covid-database/
5: https://www.forbes.com/sites/emilywillingham/2015/08/06/a-congressman-a-cdc-whisteblower-and-an-autism-
tempest-in-a-trashcan/?sh=47819f145396
6: https://rumble.com/vm1yrt-wow-vaccine-caused-deaths-reported-as-un-vaxxed-covid-deaths.html
7: https://dissident.one/2021/08/29/18311/
September 29, 2021
Posted by aletho |
Deception, Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular, War Crimes | CDC, COVID-19 Vaccine, United States |
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Centers for Disease Control (CDC) Director Rochelle Walensky has overridden the recommendations of the FDA vaccine advisory committee and authorized booster shots for individuals who took the Pfizer vaccine. The boosters are for anyone who took the Pfizer vaccine six months ago or more, in addition to all those with underlying medical health conditions that make them susceptible to the COVID-19 variants. [CDC Announcement HERE]
Additionally, all healthcare workers and basically all those who were previously designated as “essential workers”, including those in the food supply chain, are authorized to receive the vaccine. According to Joe Biden’s speech that followed the unilateral declaration of the CDC, this decision means, “60 million Americans are now eligible for a booster six months after their second shot. And up to 20 million who will receive their — received their earlier Pfizer shot at least six months ago are eligible today.”
The unilateral booster declaration does not include authorization for Moderna or Johnson and Johnson, only Pfizer. Apparently, the Pfizer lobbying group has deeper pockets and is more politically connected. The Moderna and J&J decision will be made at a later date. “We will also evaluate with similar urgency available data in the coming weeks to swiftly make additional recommendations for other populations or people who got the Moderna or Johnson & Johnson vaccines.” (link)
September 29, 2021
Posted by aletho |
Timeless or most popular, War Crimes | CDC, COVID-19 Vaccine, Rochelle Walensky, United States |
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Very, very few physicians are courageous enough to stand up against the vaccine-but-not-early treatment with generics tyranny pushing mass COVID vaccination.
Few will prescribe ivermectin. Few acknowledge the many vaccine risks that for most people outweigh the benefits.
Few accept the science that natural immunity is better than vaccine immunity and people with it should not get the jab.
When Americans see the data on COVID deaths of over 600,000 who or what should they blame? The truth is this: Better than blaming the virus they should blame hospitals and the vast majority of physicians. Why?
Because the medical establishment has never had the courage to stand up to the medical tyranny engineered by Fauci and implemented by the CDC and FDA.
People still are dying from COVID because their physicians refuse to genuinely follow the science and prescribe cheap, safe and proven generics like ivermectin.
Of course, there have always been a minority of doctors who have since March 2020 been curing their patients of COVID by using a variety of protocols that hospitals and their doctors refuse to use.
Why are so many nurses and physicians refusing to be vaccinated? Because they have seen on a daily basis large numbers of patients suffering and dying not from the virus but from the COVID vaccines.
Now one of the most respected physicians and medical researchers, Dr. Robert Malone, has spearheaded a movement to combat medical tyranny by organizing physicians from all over the world and creating just days ago a Physicians Declaration. Here are some key highlights from this historic action.
— There is an unprecedented assault on our ability to care for our patients.
— Public policy [think Fauci] has chosen to ignore fundamental concepts of science, health and wellness, instead embracing a “one size fits all” treatment strategy [think COVID vaccines] that results in too much illness and death when the individualized, personalized approach to health care is safe and equally or more effective.
–Thousands of physicians are being denied the right to provide treatment to their patients [think ivermectin], as a result of barriers put up by pharmacies, hospitals, and public health agencies, rendering the vast majority of healthcare providers helpless to protect their patients in the face of disease. Physicians are now advising their patients to simply go home (allowing the virus to incubate) and return when their disease worsens, resulting in hundreds of thousands of unnecessary patient deaths, due to failure-to-treat [other than using vaccines].
— Physicians must defend their right to prescribe treatment, observing the tenet FIRST, DO NO HARM. Physicians shall not be restricted from prescribing safe and effective treatments [other than vaccines]. These restrictions continue to cause unnecessary sickness and death. The rights of patients, after being fully informed about the risks and benefits of each option [especially vaccines], must be restored to receive those treatments [such as ivermectin].
— We invite patients, who believe in the importance of the physician-patient relationship and the ability to be active participants in their care, to demand access to science-based medical care.
That last point is where you the reader must join this revolt and demand from your physicians and hospitals your right to get access to generic medicines like ivermectin. Print the Declaration and give it to your doctor.
If this Declaration simply remains words but not profound changes in the practice of medicine in this pandemic, then all hope for saving lives will be lost.
We are rapidly approaching the point where more people will die from COVID vaccines than the virus.
Fauci and his allies will not easily admit their many evil wrong actions. If you want to examine extensive medical science details on the emerging Vaccine Dystopia, then read this truth-telling article.
September 28, 2021
Posted by aletho |
Full Spectrum Dominance, Science and Pseudo-Science | CDC, Covid-19, COVID-19 Vaccine, FDA, United States |
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1. Marion Gruber, the #2 person in CBER, who has been there for decades and her deputy, Phil Krause, announce their resignations in August, just after Biden administration announces its plan to offer 3’d vaccine doses beginning the week of September 20.
2. FDA issues a license for the Pfizer vaccine on Aug 23, for only two doses while permitting a 3d dose only for those who are immunocompromised. FDA fails to hold an advisory committee meeting around this decision.
3. FDA is caught out for a “bait and switch:” licensing Comirnaty when only the EUA vaccine, named Pfizer-BioNTech, is actually available in clinics. The “license” provides legal cover for mandates, while the EUA provides broad liability cover to the manufacturer. I was the first person to publicly identify this fraud.
4. FDA schedules an advisory committee meeting for Sept. 17, the Friday before Biden’s Sept. 20 date to start offering boosters to the public.
5. Gruber and Krause publish an article in the Lancet noting boosters are not necessary.
6. Pfizer presents to the advisory committee a very small and inadequate data collection to justify the requested broad license expansion for boosters, almost as if they don’t want it. Or perhaps they were told it would be a shoe-in. Israeli data are presented to buttress the argument for boosters. The advisory committee votes against the broad expansion of boosters to the general population, 16-2. And this is a hand-picked committee, most of whom are temporary members, chosen, it seems, to help usher in the shots with the least difficulty.
7. A new question is quickly created and put to the advisory committee, asking whether they will approve boosters for those over 65 and those at high risk of severe disease. They give a unanimous vote yes.
8. FDA leadership has the right to make decisions that go against the advisory committees, but there is a political and prestige cost when this is done. On Wednesday evening 9/22/21, just before the CDC’s advisory committee, the ACIP was to vote on which demographics would get a recommendation for a booster dose the FDA announced its decision to go against its advisory committee and, with weasel words I explained yesterday, opened the booster dose to a broad swathe of Americans. However, they did not license the vaccine for this; instead, they expanded the EUA.
6. ON 9/23/21 the ACIP committee met, were briefed, and were posed 4 questions to vote on. They assented to 3, but, like the FDA advisory committee, refused to approve a recommendation for a broad expansion of the third dose. (It should be noted that all members of the advisory committee work at medical schools, where a third dose would probably become mandatory in the near future.)
7. Unlike the FDA, which issues the rules for drugs and vaccines, the CDC claims to allow its advisory committee to make the decisions about how vaccines should be used. I could not recall a time that the CDC Director had tried to overrule its advisory committee. Helen Branswell of Stat says it happened only once before, in 2003 over the smallpox vaccine. But on 9/24/21 CDC Director Walensky overruled the advisory committee to broaden the recommendation for a third dose to practically all Americans aged 18 and over. The smallpox vaccine decision was totally political, designed to scare Americans into going to war against Iraq, where no smallpox was ever found.
How will CDC be able to hide behind ACIP’s skirts, claiming that ACIP makes the vaccine decisions, when this time ACIP didn’t?
8. The Biden administration eventually got what it said it wanted, but at the cost of revealing it didn’t give a damn about the Science. Both the FDA and CDC leadership were forced to publicly ignore the evidence as well as their own advisers.
9. A usual suspect was trotted out to applaud the tyrants:
“American Medical Association President Gerald E. Harmon, M.D., applauded Walensky’s leadership and said that his organization believes the recommendation “is a critical step to preserve our nation’s health care capacity and prevent illness among those who have continued to put their own health and safety at risk to care for patients.”‘
As I noted a few days ago, Harmon, a 2-bit family practitioner from South Carolina, rode to fame and fortune as a flight surgeon by exposing and punishing anthrax vaccine refusers with an iron hand, eventually making Major General. This is a ‘leader’ who knows on which side his bread is buttered.
10. Lots of boosters are coming, since the US Government and other governments have already purchased them. New vaccines are a super conduit for graft and corruption.They are sold for several times more than what they cost to make; the profits are incalculable; and so there is an awful lot of money available to pay for “lobbying,” i.e., lobbing cash at politicians.
September 24, 2021
Posted by aletho |
Deception, Science and Pseudo-Science | CDC, COVID-19 Vaccine, FDA, United States |
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Last Friday, FDA’s advisory committee (VRBPAC) voted 16 to 2 against giving a license to a third Pfizer booster shot for everyone age 16 and up.
Although a second vote at Friday’s meeting had not been planned, another question was hastily developed. That question asked whether the vaccine could be licensed for a third booster dose for high risk people under the age of 65. That vote got a unanimous yes.
The panels decisions are not final. The FDA is obliged to take the panels advice into consideration, but it is not required to adopt it. So yesterday, the FDA issued a license for the Pfizer vaccine for the booster dose.
But in doing so, FDA added an additional category of people for the booster dose, a category that had not been included in the Advisory Committee’s vote:
- “individuals 18 through 64 years of age whose frequent institutional or occupational exposure to SARS-CoV-2 puts them at high risk of serious complications of COVID-19 including severe COVID-19.”
This is what I call weasel wording. This statement does not make sense. People whose occupation puts them at high risk of exposure to COVID are no more likely to be at high risk of serious complications or severe COVID-19 than anyone else. They are at higher risk of developing COVID, but not at higher risk of serious COVID.
What FDA did (and you know who did this: Peter Marks, head of CBER and Janet Woodcock, acting Commissioner, are the only people with the authority to come up with this BS) was to take the VRBPAC approval for people with underlying conditions that put them at high risk for severe COVID, and twist it into an approval for all health care workers, staff at schools and colleges, grocery store workers, big box employees, etc.
Why? Because a license is necessary to impose a mandate, that’s why.
It looked like the weasels had won again. However, there was a small hoop left to jump through before any mandates came down.
While FDA determines how a drug or vaccine should be licensed or authorized for use, the CDC’s ACIP committee is the group responsible for creating the recommendations for use of the vaccine in different demographic groups.
And so ACIP did what it never does. It rejected the CDC’s proposal to widen the license for the third dose to all with potential occupational exposures. the ACIP limited their approval to what the FDA advisory committee had voted for last Friday. As CNBC noted,
“The panel struggled over a controversial proposal to give boosters to a wide swath of the U.S. population, rejecting the plan by a vote of 9-6.“
… Dr. Leana Wen [member of the Council on Foreign Relations and the World Economic Forum], an emergency physician and former Baltimore health commissioner, on Twitter called the CDC panel’s vote to reject boosters more widely a “mistake.”
“Really, we are not allowing healthcare workers, many of whom got vaccinated in back in December, to get a booster? What about teachers in cramped classrooms where masks aren’t required?” she tweeted, adding CDC Director Dr. Rochelle Walensky should overrule the recommendation.
… In a paper published days before an FDA advisory meeting last week, a leading group of scientists said available data showed vaccine protection against severe disease persists, even as the effectiveness against mild disease wanes over time. The authors, including two high-ranking FDA officials and multiple scientists from the World Health Organization, contended in the medical journal The Lancet that widely distributing booster shots to the general public is not appropriate at this time.
I think 2 things happened. The propaganda that the vaccines still prevent serious disease while perhaps not preventing mild disease stood in the way of approving boosters to prevent mild disease. Why give a potentially dangerous booster to prevent a cold? It doesn’t make sense.
Second, everyone on those committees knew that if the vaccine’s third dose did get approved for a huge swath of the general public, it would be mandated for themselves in no time. A third dose would have been required for every member of both FDA’s and CDC’s advisory committees. I don’t think they were ready for that. And maybe they weren’t ready for the resistance from those who took the 2 shots thinking they were done… and now, it seems they could get into a situation where they could be fired for not having a third dose. What about more and more doses?
Or maybe the large demonstrations in Australia and Europe were influencing those advisory committee members…
September 23, 2021
Posted by aletho |
Aletho News | CDC, COVID-19 Vaccine, FDA, Human rights, United States |
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We are in the fight against the greatest evil forces ever known, as the Coronavirus is much more than a weaponized guise by the elite, for this sinister agenda is to entrap the masses by mandated and forced vaccination genocide.
Is the CDC playing global political and military chess with the nation and the world because we question the fact-gathering of how an American Congress could have the power and leverage to “mobilize philanthropic and private-sector health challenges to more than 140 countries from 1,200 health protection programs?”
The Centers for Disease Control and Prevention is known as the national public health agency of the United States; it’s a federal agency under the Department of Health and Human Services located in Atlanta, Georgia. They were founded July 1, 1946, and interesting to note that as the successor to the WWII Malaria Control in War Areas program of the Office of National Defense Malaria Control Activities.
Proceeding its founding and the fox guarding the henhouse, there was a global influence of the Malaria Commission of the League of Nations and the Rockefeller Foundation, which sought government takeovers through collaborative efforts with the agency; which only grew more powerful through the decades against the ignorance of Americans and those global entities.
The Center for Disease Control (CDC) believes they can amplify, impact and improve the safety of America and the world; their narrative states they are an independent nonprofit and the sole entity created by Congress to mobilize philanthropic and private-sector health challenges.
They claim they “are a catalyst for unleashing the power of collaboration between CDC and philanthropies, private entities and individuals to protect the health, safety, and security of America and the world.”
They are a strategy for implementing philanthropy as an opportunity in contributing to breakthrough collaborations and innovations when addressing complex health challenges.
Collectively they align themselves with partnerships of diverse interests and resources, government agencies, corporations, and foundations; they use the narrative “that our support saves and improves lives-right now and in the future,” through donors, and more than 1,200 health protection programs that have raised over 1.2 billion dollars which support the CDC’s work over two decades.
Their bragging rights proclaim that they’ve managed to enlist hundreds of programs in the United States and more than 140 countries through their capability of keeping people healthy, safe and secure, through world-class scientific expertise, and networks of extended philanthropic reach, collaborating with supposed experts to focus on science.
But how do we know this isn’t a TROJAN HORSE, and these mechanisms weren’t created to capture the trust of innocent Americans and more than 140 countries through false narratives pushing an agenda against the hearts and minds of humanity? After all, the most awakened souls can connect the dots and see the weaponization of health is taking root through some form of mass genocide.
Many top medical experts are speaking out against the vaccines and note that the ramifications of this experimental COVID-19 vaccine are imposing serious health problems onto the population as a potential biohazard.
This den of thieves is made up of the corrupted governments and corporations who strategically push mandates while they target 100% of the American population unlawfully, and against the U.S. Constitutional rights of all Americans.
According to the Worldometer, as of September 14, 2021, the American population totals about 333 million-plus souls, out of which two-thirds of this population have been vaccinated, one-third of the population totaling about 100 million people remain unvaccinated for many personal and Constitutional reasons.
Out of the majority of 52% or two-thirds of the population that have been fully vaccinated, this leaves 48% who have experienced receiving at least one jab, and many of these people will not take another shot as they have experienced some measure of health problems or changed their mind against a 2nd dose.
The power of networking should never be underestimated, whether good, bad or indifferent, so if you’re wondering what affiliations are connected with the CDC through partnerships of Corporations, Foundations & Organizations, look no further, you will see a pattern emerge, and why the push for vaccinations is everywhere we go, there are so many groups doing business with the CDC.
Corporations: Our Partners: Corporations | CDC Foundation
Foundations: Our Partners: Foundations | CDC Foundation
Organizations: Our Partners: Organizations | CDC Foundation
The CDC is facing some legal issues regarding false reporting on vaccines, and yet we are supposed to trust them with safeguarding the protection of our personal wellness?
> CDC Gets Called Out In Federal Court Over Lack Of Scientific Studies
There’s a silent rage building across the country over the hot subject of mandatory vaccinations; depending on where you reside within the U.S., you will get a quick lesson on the politics involved in the economics of the American workforce and various corporations, schools, and other institutions, organizations, and business that try to create UNCONSTITUTIONAL mandates against those not complying with the questionable vaccinations.
One state that doesn’t play politics with the lives of its citizens is Florida. It’s the reason why so many northerners from democratic cities are relocating to the sunshine state and be mindful that the governor of Florida has protected the state’s citizens against the obtuse mandates of the CDC and other rogue agencies who seek to go against the sovereign rights of Americans.
Governor, Ron DeSantis of Tallahassee, Florida, signed a bill earlier in the year protecting Floridians by banning vaccine passports. DeSantis states for the record that starting September 16, 2021, the great state of Florida will start issuing $5,000 fines to businesses, schools, and government agencies that require people to show proof of a COVID-19 vaccination.
As part of “promises made, promises kept,” the statute reads that a business entity….may not require patrons or customers to provide any documentation certifying COVID-19 vaccination or postinfection recovery to gain access to, entry upon, or service from the business operations in this state.” The same rules apply to governmental entities and educational institutions.
The statute continues by stating that it does not otherwise restrict businesses, government entities, or educational institutions “from instituting screening protocols consistent with authoritative or controlling government-issued guidance to protect public health.”
Humanity is going through a major transformation regarding every aspect of the human experience here on earth; breakdowns become breakthroughs and revelations trigger revolutions as the collective consciousness awakens from its deep state of slumber, we are recognizing a clearer lens into who the monsters are that have been hiding in the shadows.
As mankind awakens, we connect the dots into the nefarious agendas created by the three-letter government agencies and challenge their unethical policies and procedures created by the morally corrupt working deep within the political and military systems.
It is up to every individual to do their own research, question everything, get involved in making a difference in the world, as it’s ordinary people who make extraordinary differences in the world.
Sources:
DeSantis Warns Businesses Who Follow Biden’s Vaccine Mandate Will Be Fined $5K Per Employee (newsweek.com)
The Coronavirus: A Global Pandemonium & 2nd American Revolution – America Out Loud
Coincidence or More Deep State Interference Concerning Coronavirus – America Out Loud
September 17, 2021
Posted by aletho |
Civil Liberties, Deception, Timeless or most popular | CDC, COVID-19 Vaccine, Human rights, United States |
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There is now a growing body of literature showing natural immunity not only confers robust, durable and high-level protection against COVID, but also provides better protection than vaccine-induced immunity.
Yet, the Centers for Disease Control and Prevention (CDC) is ignoring the long-standing science of natural immunity when it comes to COVID — while acknowledging the benefits of natural immunity for other diseases — according to an expert who accused the agency of providing contradictory, ‘illogical’ COVID messaging.
Dr. Marty Makary, professor of surgery and health policy at John Hopkins University, on Tuesday accused the CDC of “cherry-picking” data and manipulating public health guidance surrounding vaccines and natural immunity to support a political narrative.
Makary joined the “Clay Travis and Buck Sexton Show” to discuss the clinical impact of natural immunity as it compares to the vaccine.
During the show, Travis pointed out the CDC’s guidance on COVID is inconsistent with its vaccine recommendations for other contagious viruses, like chickenpox.
The CDC’s current guidance for chickenpox, for example, does not encourage those who have contracted it to vaccinate themselves against the virus. The CDC only recommends two doses of chickenpox vaccine for children, adolescents and adults who have never had chickenpox.
“So why doesn’t the CDC say the same thing about those of us who already had COVID?” Travis asked.
Makary called the conflicting guidance “absolutely illogical,” and accused the agency of “ignoring natural immunity.”
“It doesn’t make sense with what they’re putting out on chickenpox,” Makary said. It’s like they have adopted the immune system for one virus, but not for another virus, he said, and “cherry-picking the data to support whatever they’ve already decided.”
“They salami slice it — something we call fishing in statistical techniques,” Makary said. “That is when you look for a tiny sliver of data that supports what you already believe.”
According to a Sept. 13 article in The BMJ, when the COVID vaccine rollout began in mid-December 2020, more than a quarter of Americans — 91 million — had been infected with SARS-CoV-2, according to CDC estimates.
As of this May, that proportion had risen to more than a third of the population, including 44% of adults between the ages of 18 and 59.
However, the CDC instructed everyone, regardless of previous infection, to get fully vaccinated as soon as they were eligible. On its website, the agency in January justified its guidance by stating natural immunity “varies from person to person” and “experts do not yet know how long someone is protected.
By June, a Kaiser Family Foundation survey found 57% of those previously infected got vaccinated.
Dr. Anthony Fauci, President Biden’s chief medical advisor, was asked Sept. 10 by CNN’s Dr. Sanjay Gupta whether people who have tested positive for the virus should still get a vaccine.
Gupta cited recent data from Israel suggesting people who recovered from COVID had better protection and a lower risk of contracting the Delta variant, compared to those with Pfizer-BioNTech’s two-dose vaccine-induced immunity.
“I don’t have a really firm answer for you on that,” Fauci said. “That’s something we’re going to have to discuss regarding the durability of the response.”
The research from Israel did not address the durability that natural immunity offers. Fauci said it is possible for a person to recover from COVID and develop natural immunity, but that protection might not last for nearly as long as the protection provided by the vaccine.
“I think that is something that we need to sit down and discuss seriously,” Fauci said.
Numerous studies, however, have shown people who recovered from COVID have robust, durable and long-lasting immunity.
Evidence of natural immunity
As early as November 2020, important studies showed memory B cells and memory T cells formed in response to natural infection — and memory cells respond by producing antibodies to variants at hand.
A study funded by the National Institutes of Health and conducted by the La Jolla Institute for Immunology, found “durable immune responses” in 95% of the 200 participants up to eight months after infection.
One of the largest studies to date, published in Science in February 2021, found that although antibodies declined over eight months, memory B cells increased over time, and the half-life of memory CD8+ and CD4+ T cells suggests a steady presence.
In a study by New York University published May 3, the authors studied the contrast between vaccine immunity and immunity from prior infection as it relates to stimulating the innate T-cell immunity — which is more durable than adaptive immunity through antibodies alone.
The authors concluded:
“In COVID-19 patients, immune responses were characterized by a highly augmented interferon response which was largely absent in vaccine recipients. Increased interferon signaling likely contributed to the observed dramatic upregulation of cytotoxic genes in the peripheral T cells and innate-like lymphocytes in patients but not in immunized subjects.”
The study further noted:
“Analysis of B and T cell receptor repertoires revealed that while the majority of clonal B and T cells in COVID-19 patients were effector cells, in vaccine recipients, clonally expanded cells were primarily circulating memory cells.”
This means natural immunity conveys much more innate immunity, while the vaccine mainly stimulates adaptive immunity — as effector cells trigger an innate response that is quicker and more durable, whereas memory response requires an adaptive mode that is slower to respond.
According to a longitudinal analysis published July 14 in Cell Medicine, most recovered COVID patients produced durable antibodies, memory B cells and durable polyfunctional CD4 and CD8 T cells –– which target multiple parts of the virus.
“Taken together, these results suggest broad and effective immunity may persist long-term in recovered COVID-19 patients,” the authors said.
In other words, unlike with the vaccines, no boosters are required to assist natural immunity.
In a May 12 study conducted by the University of California, researchers found natural immunity conveyed stronger immunity than the vaccine.
The researchers wrote:
“In infection-naïve individuals, the second [vaccine] dose boosted the quantity but not quality of the T cell response, while in convalescents the second dose helped neither. Spike-specific T cells from convalescent vaccinees differed strikingly from those of infection-naïve vaccinees, with phenotypic features suggesting superior long-term persistence and ability to home to the respiratory tract including the nasopharynx.”
According to The BMJ, studies in Qatar, England, Israel and the U.S. have found infection rates at equally low levels among people who are fully vaccinated and those who have previously had COVID.
As The Defender reported in June, the Cleveland Clinic surveyed more than 50,000 employees to compare four groups based on history of SARS-CoV-2 infection and vaccination status.
Not one of more than 1,300 unvaccinated employees who had been previously infected tested positive during the five months of the study. Researchers concluded the cohort “are unlikely to benefit from COVID-19 vaccination.”
In the largest real-world observational study comparing natural immunity gained through previous SARS-CoV-2 infection to vaccine-induced immunity afforded by the Pfizer vaccine, researchers in Israel found people who recovered from COVID were much less likely than never-infected, vaccinated people to get Delta, develop symptoms or be hospitalized.
“Our results question the need to vaccinate previously infected individuals,” they concluded.
Experts speak out on natural immunity
In a recent letter to the editor of The BMJ, Dr. Manish Joshi, a pulmonologist at UAMS Health; Dr. Thaddeus Bartter, a pulmonologist at UAMS Health; and Anita Joshi, BDS, MPH, said data demonstrate both adequate and long-lasting protection in those who have recovered from COVID, while the duration of vaccine-induced immunity is not fully known.
The authors of the letter said the “SIREN” study in the Lancet addressed the relationships between seropositivity in people with previous COVID infection and subsequent risk of severe acute respiratory syndrome due to SARS-CoV-2 infection over the subsequent seven to 12 months.
The study found prior infection decreased risk of symptomatic reinfection by 93%.
A large cohort study published in JAMA Internal Medicine which looked at 3.2 million U.S. patients, showed the risk of infection was significantly lower (0.3%) in seropositive patients compared to those who were seronegative (3%).
A recent study published in May in the journal Nature demonstrated the presence of long-lived memory immune cells in those who have recovered from COVID-19 suggesting durable and long-lasting immunity.
“This implies a prolonged (perhaps years) capacity to respond to new infection with new antibodies,” the authors wrote.
© [Sept. 2021] Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
September 16, 2021
Posted by aletho |
Science and Pseudo-Science | CDC, Covid-19, COVID-19 Vaccine |
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Antibody testing is the gold standard for determining immunity, says immunologist and physician Dr. Hooman Noorchashm. Yet, the CDC and FDA are actively deterring people from testing their immunity. Why?
In May 2021 the FDA issued an advisory discouraging Americans from testing the status of their antibody immunity to COVID-19, Noorchashm wrote in an editorial on his blog. “Those who are adequately immune to COVID-19 are rarely, if ever, getting reinfected — regardless of whether this immunity comes from vaccination or from a natural infection,” Noorchashm said.
Meanwhile, “those who are NOT immune to SARS-CoV-2 are susceptible to being infected,” he said. He surmises that to end the pandemic upward of 90% of the population need to become immune.
As far as testing for immunity, according to Noorchashm, the FDA advisory prevents people from obtaining critical information necessary to protect themselves during the pandemic. “ … by not encouraging liberal COVID-19 antibody testing, especially in fully vaccinated Americans, the FDA and CDC are preventing vaccinated, but inadequately immune, persons from finding out that they remain susceptible to infection,” he wrote.
Citing his own experience as a physician, he said “patients who hesitate to undergo vaccination are far more likely to do so when they are confronted with a negative antibody test demonstrating they are susceptible.”
SOURCES:
Noorchashm.medium.com August 27, 2021
Epoch Times August 19, 2021
September 4, 2021
Posted by aletho |
Science and Pseudo-Science, War Crimes | CDC, COVID-19 Vaccine, FDA |
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In a nutshell: Yesterday CDC asked its advisory committee to “recommend” the Comirnaty vaccine for 16 and 17 year olds. And it agreed, unanimously. Or pusillanimously.
The vote may seem silly or superfluous, because it had already been recommended for this age group as an EUA.
But this vote was anything but superfluous. This seemingly minor recommendation, which did not get headlines, moves the licensed Comirnaty vaccine from a place where the manufacturer is legally liable for injuries, to a berth within the Childhood Vaccine Injury Compensation Program, for which there is no manufacturer liability. Instead a $0.75 excise tax is charged per dose, which goes into a fund administered by DHHS to pay for injuries, if one is lucky enough to convince the special masters (judges) in the program that a vaccine caused your injury. Once a vaccine is recommended for children, its liability is waived no matter who receives it.
But the important part is that once this process is complete (which I expect to be only a very few weeks), Pfizer can roll out stocks of the licensed vaccine while still having its liability waived. That means that the loophole I told you about last week is being backfilled by the USG, with the help of the supine and spineless ACIP committee members, and will soon disappear.
I say spineless with true conviction, because the briefings they received yesterday were a load of fraud and hogwash. Yet no one challenged the data nor the conclusions. It is hard to believe that the lot of them are really that stupid that they believed what they heard. It is also hard to believe that none of them had a conflict of interest, which they all asserted along with their vote.
Furthermore, no one ever actually said why the vote was held: which was for liability purposes, nor that the vote would lead to mandates, which could not be implemented under the EUA.
So, it is disappointing.
Children’s Health Defense went to court today in Tennessee to challenge the FDA on issuing both a license and EUA for the same product. AFLDS also went to court today in Colorado challenging the mandate. More on these cases later.
September 1, 2021
Posted by aletho |
Civil Liberties, Deception, Science and Pseudo-Science | CDC, COVID-19 Vaccine, Human rights, United States |
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The Biden administration is on the precipice of announcing mandatory six month booster shots for people who have already had the vaccine. The reason? Data from Israel is showing that vaccinated populations are, for yet unknown reasons, more susceptible to even worse infections from the Delta variant.
It appears, from the early data, that once you take the vaccine you put your immune system into a state of perpetual dependency requiring booster shots to chase the variants every six months. Without the boosters, the hospitalization rates amid the vaccinated population appear worse than non-vaccinated. Delta hits the vaccinated population harder than Alpha, and Lambda will likely hit the vaccinated population harder than Delta…. and so it goes, and so it appears it will continue.

The Daily Beast outlined a foreboding article yesterday with the overarching message that America had better prepare for this quickly based on the Israeli data. The Israeli scientists call the population who have taken the vaccine+booster the “ultra-vaccinated”, and unfortunately it appears those ultra-vaccinated patients are now on course to require frequent booster updates as their immune system is now mRNA dependent to battle the evolving COVID variants.
FTA – […] Asked what has brought Israel to peak transmission even as the country has already provided third doses of vaccines to 1.5 million citizens, Rahav, who has become one of the best known faces of Israel’s public health messaging, sighed, saying, “I think we’re dealing with a very nasty virus. This is the main problem—and we’re learning it the hard way.” (read more)
Metaphorically, a drug user chasing a “high” trains his/her brain to become dependent or addicted in order to retain that altered mental state, so too does the COVID vaccination regime appear to place the patient into an dependent state for their immune system.
However, on the positive side (for those vaccinated) the Biden administration appears to be gearing up to deliver this booster process on a long-term basis.
The Biden administration is planning to announce updated guidance recommending a third dose of Pfizer or Moderna’s vaccine be given to Americans very six months after their second dose (instead of eight months), according to The Wall Street Journal. Right now, the final plan is still being worked out, and will need to be approved by the CDC’s vaccine advisory team, essentially controlled by vaccine makers, along with the FDA (also controlled by vaccine makers).
As soon as the pharmaceutical industry tells the Biden administration what to do, the CDC will begin pushing the booster shots onto the vaccinated population.
There is no actual science behind this process, but then again, there hasn’t really been any science behind any of it; so don’t worry, just take the next shot and await further instructions. However, if this process is put into place, it would appear that the vaccination passports will have an expiration date.
WASHINGTON DC – […] The Biden administration and vaccine companies have said that there should be enough supply for boosters that they plan to begin distributing more widely on Sept. 20. The U.S. has purchased a combined 1 billion doses from Pfizer and Moderna.
A White House spokesman declined to comment. An FDA spokeswoman declined to comment on interactions with vaccine manufacturers. (read more)
You will notice the institutions of Healthcare have now stopped using the term “follow the science.” One of the reasons they have dropped that terminology is apparently because they change the ‘science‘ on a week to week basis.
CDC Director Rochelle Walensky was recently asked if her agency was giving current guidance to the public based on “the data” or based on arbitrary “hope” that they will be correct and their guidance will help people.
Director Walensky was honest in her reply: “… So there’s actually hope, [because] we don’t have data yet…”
It is very comforting to know that “hope” is guiding the decision-making of those who are injecting substances into the global population without any idea what the long-term ramifications might be….
… Then again, if you really believed that human existence was the cause of harm to this planet; and saving the planet was the #1 priority of your community; then removing the harm would be for the greater good. Personally, while I hate to be argumentative, I would respectfully disagree with people who prefer my death in order to save the world. But, to be fair, that’s just me being selfish.
I am reminded of the words from a carnival operator I heard as a child as we approached the turnstiles of the roller coaster. Apparently the young lady at the front of the line had said something to him as we all waited for the next car to arrive. I did not hear the question, but his reply was:
“… Well Miss, once you get on the ride – you ain’t getting off ’til the ride’s over.“
Those words stuck in my mind as I pulled down the retaining bar. And as my life has rattled, wobbled and squeeked toward unknown destinations, I have often found a reason to reference them.
August 30, 2021
Posted by aletho |
Science and Pseudo-Science | CDC, COVID-19 Vaccine, United States |
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As a number of politicians push for ‘vaccine passports’ amid fears that a new brand of medical apartheid is coming, a re-surfaced CDC publication advocating internment camps for the ‘high-risk’ has some people fearing the worst.
Last year, the Centers for Disease Control and Prevention (CDC) released a paper that floated the totally not suspicious idea of relocating “high-risk” individuals into green zone “camps.” While the proposal didn’t attract much attention at the time, as draconian anti-Covid measures are beginning to ramp up, and basic human rights and liberties are coming under attack, the document has attracted newfound attention. And not without reason, it seems.
The very first line of the document discusses the implementation of a “shielding approach in humanitarian settings… focused on camps, displaced populations and low-resource settings.” Essentially, and this will be important later on, ‘humanitarian settings’ is just another way of saying ‘camps’. Many people are quick to associate the idea of camps with the containment of refugees, for example, or illegal aliens who have breached the border. Yet the only time the word ‘refugee’ is mentioned in the paper is in reference to a camp in Kenya. At the same time, ‘camp’ and ‘camps’ are referred to about 20 times.
There is another ambiguous thing about this document, and that involves its description of “high-risk” individuals and the “general population.”
The paper reads: “In most humanitarian settings [i.e. camps], older population groups make up a small percentage of the total population. For this reason, the shielding approach suggests physically separating high-risk individuals from the general population to prioritize the use of the limited available resources and avoid implementing long-term containment measures among the general population.”
In other words, the CDC is saying that older people being held in camps (humanitarian settings), because they are in the ‘high-risk’ category, should be separated from the ‘general population’ in these facilities so as to reduce the ‘containment measures’. OK, fine. But the document never explains who makes up the general population inside the camps, and why these ‘low-risk’ individuals are being held in these humanitarian ‘green zones’ in the first place.
Either due to a careless lack of clarity or deliberate deceptiveness on the part of the CDC, it is not difficult to see how some people could interpret the inclusion of high-risk groups into these ‘humanitarian settings’ to mean the unvaccinated. But even if there is no evil intent to intern the anti-vax crowd in camps, the conditions set down for these humanitarian settings leave much to be desired. Indeed, to be avoided at all costs.
In one passage, it is stated that “monitoring includes both adherence to protocols and potential adverse effects or outcomes due to isolation and stigma. It may be necessary to assign someone within the green zone, if feasible, to minimize movement in/out of green zones.”
Would that ‘someone’ by any chance be the local police or even the US military? The document offers no clues. However, several lines later, the CDC advises that “isolation/separation from family members, loss of freedom and personal interactions may require additional psychosocial support structures/systems.”
Admitting that confinement in these settings would entail “the loss of freedom and personal interactions” strongly suggests that these individuals are being held in these facilities against their will. In fact, reading through the document, one might get the impression the CDC is talking about a maximum-security prison for the criminally insane.
Anyone who thinks being detained in one of these facilities for the ‘high-risk’ would be all fun and games may wish to take particular heed from this line, which warns: “this shielding approach may have an important psychological impact and may lead to significant emotional distress, exacerbate existing mental illness or contribute to anxiety, depression, helplessness, grief, substance abuse, or thoughts of suicide among those who are separated or have been left behind.”
Left behind? Left behind from what, exactly? The Rapture?
Finally, the authors of this document seem fully aware that their warm and cuddly humanitarian setting, which seems to more resemble a gulag than a health retreat, will not be welcomed by all members of the general population. Gee, I wonder why.
“While the shielding approach is not meant to be coercive, it may appear forced or be misunderstood in humanitarian settings,” advises the CDC, which appears overly concerned about public perceptions. “As with many community interventions meant to decrease COVID-19 morbidity and mortality, compliance and behavior change… are difficult in developed, stable settings; thus, they may be particularly challenging in humanitarian settings which bring their own set of multi-faceted challenges that need to be taken into account.”
The CDC paper references heavily from a March 2020 study authored by one Caroline Favas, entitled ‘Guidance for the Prevention of COVID-19 Infections among High-Risk Individuals in Camps and Camp-like Settings.’ Once again, any hope for clarity is dashed, as this paper, which mentions the words ‘camp’ and ‘camps’ 73 times, is written for “the displaced community itself, humanitarian actors and camp coordination/management authorities.” Few details are given as to who the ‘displaced community’ may be.
(Note: The Favas study provides a broad definition of ‘camp’ or ‘camp-like settings’ as “forcibly displaced population, including refugees and internally displaced living in high density formal or unformal settlements, under collective or individual shelters”).
What follows in the Favas study, which was published by the London School of Hygiene & Tropical Medicine, occasionally comes off as one of those jargon-riddled medical tracts that are almost as painful to read as a doctor’s handwritten medical prescription. Yet, just as with the CDC paper, the Favas study is crystal clear when it acknowledges that these camps will be viewed negatively by many members of the population.
“Conversely, it is likely that the approach will not be successful if it is perceived as coercive, misunderstood or used by authorities as a pretext for forms of oppression.”
So, who will get to determine who is at high risk of Covid infection and who is not? On this tricky point, Favas, as well as the CDC, wash their hands of the process, leaving it up to ‘community members’ to decide who should be detained in these ‘humanitarian settings’.
“Identification of high-risk community members should be a community-led process, which supports and promotes community ownership of the approach,” Favas avers. “The purpose of the shielding approach and the inclusion criteria should be clearly communicated and explained to the community, so that each household can identify who among them is at risk and should be shielded, on a voluntary basis.”
Favas provides some options for how the detainees could be isolated from their families and communities, none of them terribly comforting. The first involves providing a green zone at the household level. While it may not seem so bad keeping grandma confined to a back room, the author describes the “household shelter” as either a “single shelter” or a “multi-shelter compound.”
The next type of facility is a group of shelters (with maximum 5-10 households), within a small camp area.
Finally, there are the full blown “sector” camps that would accommodate 15,000 or more people. It would be difficult to imagine a camp of such scale that would not require a high police presence, as well as virtually all of the rules and regulations of a prison.
Many people would probably scoff at the thought of Covid camps, dismissing them as the fevered dream of a ‘conspiracy theorist’. And perhaps they would be right. After all, just last month, the Associated Press debunked the claim floated in a satirical publication that Joe Biden was planning to send the unvaccinated to quarantine camps until they agreed to take the shot. Yet the increasingly befuddled US leader has made false claims in the past, like promising that Americans would be free from their mask bondage if they agreed to be vaccinated. That promise evaporated last month as the CDC backtracked, mandating mask wearing in places experiencing spikes in Covid levels, even among the vaccinated.
While some may find it irrelevant to discuss a paper that was released by the CDC last year, they may want to ask why the CDC and Caroline Favas were already discussing the possibility of ‘humanitarian settings’, i.e. camps for high-risk individuals, in early 2020, when the outbreak was still in its early stages. Some might say that was jumping the gun.
In any case, now that the CDC document has made a splash one year after its release, it would be a good time for an explanation regarding some of its more ambiguous and even outrageous suggestions. At a time when a feeling of general distrust and even paranoia of Covid measures is sweeping the globe, people need assurances that their real enemy is not the very people they elected to protect them.
Robert Bridge is an American writer and journalist. He is the author of ‘Midnight in the American Empire,’ How Corporations and Their Political Servants are Destroying the American Dream.
August 11, 2021
Posted by aletho |
Civil Liberties, Timeless or most popular | CDC, Covid-19, COVID-19 Vaccine, Human rights, United States |
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