Italian Leader Slams ‘False Coronavirus Numbers: 25,000 Did Not Die, It’s a Way To Impose a Dictatorship’
On Friday, April 24, 2020, Vittorio Sgarbi, a member of the Italian Chamber of Deputies, denounced what he claims are false coronavirus death statistics. Sgarbi feels that fake statistics are being propagated by the government and the media to terrorize the citizens of Italy and establish a dictatorship.
The member of the Forza Italia party slammed the closure of 60% of Italian businesses for 25,000 Chinese-Coronavirus deaths from the floor of the legislature.
“It’s not true,” he said. “Don’t use the deaths for rhetoric and terrorism.” According to the National Institute of Health, 96.3% did not die of coronavirus, but of other pathologies stated Sgarbi – which means that only 925 have died from the virus and 24,075 have died of other things claimed Sgarbi, “….the virus was little more than an influenza. Don’t lie! Tell the truth!”
Sgarbi’s controversial speech was delivered during ‘Cura Italia’ decree law discussions. The proposal intends to develop measures to strengthen the national health service based on what he claims is false data. Sgarbi challenged his colleagues to investigate the real numbers themselves and be united in the reporting the truth:
“Let us be united in liberation against hypocrisy and lies, against falsifications, against the false numbers that are given to terrorize Italians. The 25,000 dead, as Professor Bassetti said, died of heart attacks, cancer and other…Let’s not use them to humiliate Italy. Let’s not use them to give citizens false news. Give the numbers, check them out, and I challenge you before a jury of honor, Trizzino, to look at the numbers…”
Shedding Light On The Dishonorable Record Of Dr. Fauci – A Real Mengele
By F. William Engdahl
In 2008, US President George W. Bush presents the Presidential Medal of Freedom to Fauci “for his determined and aggressive efforts to help others live longer and healthier lives.”
Dramatic political and social decisions are being made across the United States and around the world on what emergency quarantine measures and other steps must be taken. In many cases the radical and severe measures, such as shutting down the world economy, are being justified by COVID-19 case projections of morbidity into the future. If there is one person who is the face of the current strategy of dealing with the coronavirus in Washington it is the Director of the US National Institute for Allergy and Infectious Diseases (NIAID) of the NIH, Dr. Tony Fauci. What major media conveniently leave out in discussing Fauci’s role is his highly controversial and conflicted history since he first joined NIAID in 1984 during the beginnings of the AIDS panic. His role then sheds valuable light on his remarkable and highly controversial actions today. (See link for article)
_________________
**Comment**
Summary of infractions by Fauci:
Dismissed hydroxychlorquine as “anecdotal” for severe COVID-19 patients but 7 years earlier backed the same drug.
Took COVID-19 projections from institute backed by the Gates Foundation, who virtually owns the WHO and owns major stakes in the leading vaccine manufacturers.
Fauci stated COVID-19 was about 10 times more lethal than the seasonal flu but in a medical journal stated it was similar to seasonal flu in morbidity.
AIDS researcher Robert Gallo worked under Fauci. Gallo proclaimed he “discovered” the AIDS virus called HIV – but completely disregarded scientific procedures of prior peer-reviewed published scientific evidence including the required electron microscope analysis.
Fauci claimed AIDS was highly contagious despite scientific evidence.
NIAID had been studying poppers/nitrates which are proven immune-suppressants, in the earliest AIDS patients. They dropped this like a hot-potato for the more lucrative “cure” for AIDS.
Under Fauci, Gallo made millions on his patented HIV blood test despite the fact it didn’t directly test for the virus but for active antibodies, something immunology practice said was invalid. Antibodies merely suggest a past infection response, not necessarily presence of HIV. It too often gave false positives.
Fauci and Gallo widely promoted their deeply flawed antibody test(sound familiar?)
Gallo stated, “A PCR test for the presence of the virus itself can accurately determine a child’s HIV status.” Fauci endorsed this claim. Please see: https://madisonarealymesupportgroup.com/2020/05/07/was-the-covid-19-test-meant-to-detect-a-virus/ The creator of PCR states the test was never meant to diagnose patients but was for research and manufacturing purposes. Dr. David Rasnick, bio-chemist, protease developer, and former founder of an EM lab called Viral Forensics stated, “I’m skeptical that a PRC test is ever true. It’s a great scientific research tool. It’s a horrible tool for clinical medicine.”
Robert A Giraldo, MD and Etienne de Harven, MD, (produced the first electron micrograph of a retrovirus) pointed out that both the ELISA and Western Blot, and a genetic test, the PCR or ‘viral load’ test – the two major tests to determine AIDS, are not valid. “None if these tests detect the HIV virus itself, nor do they detect HIV particles.” They go on to state that over 70 conditions including influenza, leprosy, and even pregnancy, can cause antibody tests to be positive without HIV infection. The same is true for COVID-19. BTW: the Giraldo & de Harven 2006 article was mysteriously retracted in 2019, right before the Wuhan outbreak.
While the CDC requires a positive HIV antibody test to determine AIDS, the WHO in ruling for Africa requires no testing, but only symptoms: weight loss, chronic diarrhea, prolonged fever, persistent cough, etc. – all symptoms common in poverty, squalor, and malnutrition.
Fauci has taken millions from the Gates Foundation and the Clinton Foundation as well as tens of billions from US taxpayers for this bogus research.
Fauci recommended AZT, a chemotherapy drug which failed for leukemia, for HIV patients even without symptoms. The manufacturer of AZT handed NIAID a biased study on the drug they manufactured. Please see this article on how Fauci is now recommending another failed drug for COVID-19: https://madisonarealymesupportgroup.com/2020/05/08/update-cdc-playbook-learning-from-lyme/ Remdesivir failed for Ebola but has been dug out of the drug graveyard just like AZT was. Reason? Nine of the 19 NIH experts on the COVID-19 panel recommending treatment have financial ties with Gilead Science the manufacturer of Remdesivir.
Fauci recommended AZT, highly toxic drug, for pregnant women despite fetal risk.
Fauci’s MO is his continued refusal to explore the role of lethal drugs and other toxins in disease and insists upon a single-germ theory.
Fauci collaborated with Gilead Science on PrEP (pre-exposure prophylaxis) experiments: testing toxic HIV drugs on healthy people to supposedly protect them from AIDS. (4 tests of at least 2,000 and up to 5,000 people were in each test).
The FDA ignored 2 of the 4 Truvada tests that failed and were stopped and approved Truvada for PrEP. Gilead lists side-effects which can lead to death. (This same authority is bad-mouthing HCQ for COVID-19 for side-effects despite its wide usage, initially over the counter, for travelers and its clinical success in COVID-19. In fact it’s banned for COVID-19 in 3 U.S. states and in France)
In 2019 Fauci and NIAID got $100 million from the Gates Foundation for developing “gene based” therapies for HIV and sickle cell disease. Fauci was named 1 of the 5 Leadership Council of the Gates Foundation Global Vaccine Action Plan.
No one has isolated and purified samples of patients tested SARS-CoV-2 positive for COVID-19. No electron microscope analysis exists.
The triad of Fauci, Redfield, and Birx hold the future of public health and the entire world economy in their hands. Don’t you think we’ve given them a bit too much power?
Don’t you think with the evidence presented they should be arrested for criminal fraud?
You may be wondering why I am discussing COVID-19 during an Inside Lyme podcast. I am concerned for my children, grandchildren, and my patients. I want to share my understanding of COVID-19 through my eyes as a clinical epidemiologist.
COVID-19 is now a pandemic. We need an effective and safe drug to treat this virus.
Researchers have turned to existing drugs that might be effective without causing significant side effects. Hydroxychloroquine and chloroquine have been prescribed for the treatment and prophylaxis of malaria in addition to the treatment of autoimmune diseases. Hydroxychloroquine and azithromycin have also been prescribed for Lyme disease patients. Hydroxychloroquine and azithromycin have been marketed under the name Plaquenil and Zithromax, respectively in the US.
Both chloroquine and hydroxychloroquine have side effects. The most common side effect of hydroxychloroquine is nausea and diarrhea. In rare cases, hydroxychloroquine can lead to reduced white blood cells, platelets count, anemia, and retinopathy. Retinopathy can lead to color blindness and loss of vision. Both hydroxychloroquine and azithromycin can lead to sudden death from a prolonged QT interval.
ANTIVIRAL EFFECTS OF HYDROXYCHLOROQUINE AND CHLOROQUINE
Hydroxychloroquine and chloroquine have shown some antiviral benefits in vitro(Wang, 2020, letter) Both have been studied for other related viruses, including Severe Acute Respiratory Syndrome (SARS) and Middle East Respiratory Syndrome (Mers).
Chloroquine improved outcomes in a series of small studies in China. Gao and colleagues discussed the finding in the journal BioScience Trends .
“Thus far, results from more than 100 patients have demonstrated that chloroquine phosphate is superior to the control treatment in inhibiting the exacerbation of pneumonia, improving lung imaging findings, promoting a virus negative conversion, and shortening the disease course according to the news briefing.”
These findings led the State Council in China to approve chloroquine for COVIID-19
FIRST FRENCH CLINICAL TRIAL BY GAUTRET AND COLLEAGUES
Gautret and colleagues published a French trial evaluating the benefit and risks of hydroxychloroquine and Zithromax for the treatment of COVID-19.
The authors prescribed 600 mg of hydroxychloroquine to 26 patients with COVID-19. Two were asymptomatic. Ten had upper tract respiratory infections, and six had lower tract respiratory infections. The doctors prescribed azithromycin to 6 of their patients with COVID-19 to prevent bacterial superinfection.
The authors were able to show a significant reduction in the viral load in nasopharyngeal samples of their COID-19 patients treated with hydroxychloroquine compared to COVID-19 patients who were not treated.
The authors were able to show even a greater reduction in viral load in the six COVID-19 patients when Zithromax was added.
Only one of the 26 patients treated with hydroxychloroquine was dropped from the study due to an adverse event. That patient dropped out due to nausea.
The authors explained why they decided to share their findings early.
“For ethical reasons and because our first results are so significant and evident, we decide to share our findings with the medical community, given the urgent need for an effective drug against SARS-CoV-2 in the current pandemic context.”
FLAWS IN THE FIRST FRENCH TRIAL BY GAUTRET
The Gautret trial was small and flawed. They should have used controls from the same hospital with the same characteristics as the 26 treated patients. Instead, they enrolled 16 controls were from other centers.
The Gautret trial did not evaluate whether a reduction or elimination of the COVID-19 virus in saliva would prevent outcomes important to patients such as a transfer to an intensive care unit or death. Four of the 26 patients treated with hydroxychloroquine did poorly. Three were transferred to the intensive care unit. One died. None of the patients with a COVID—19 infection developed a QT prolongation.
The Gautret trial was not designed to determine if the absence if COVID-19 from the saliva meant the absence of COVID-19 from other tissues.
The Gautret trial could not determine if the benefits seen for the six COVID-19 patients treated with azithromycin were from an antiviral effect or an antibiotic effect.
SECOND FRENCH TRIAL
A recently published second French trial by Gautret and colleagues added further support for the hydroxychloroquine with azithromycin.
“In 80 in-patients receiving a combination of hydroxychloroquine and azithromycin we noted a clinical improvement in all but one 86 year-old patient who died, and one 74-year-old patient still in intensive care unit.”
PLANNED TRIALS
Researchers at the University of Minnesota are planning on a trial “to see whether malaria treatment hydroxychloroquine can prevent or reduce the severity of the coronavirus disease (COVID-19)” writes Gabe Gutierrez and Dennis Romero in NBCNews.
COULD CUTTING THE COVID-19 VIRAL LOAD BE HELPFUL?
Yes, according to Gautret. “hydroxychloroquine and azithromycin “can play a role in controlling the disease epidemic by limiting the duration of virus shedding, which can last for several weeks in the absence of specific treatment.” write Gautret.
COULD HYDROXYCHLOROQUINE AND AZITHROMYCIN FOR INDIVIDUALS WITH COVID-19 BE HELPFUL?
Yes, according to both Gautret trials. Hydroxychloroquine and azithromycin lowered the COVID-19 viral load patient. Moreover, most of the patients with a COVID-19 infection were improved or discharged in the second Gautret trial.
COULD HYDROXYCHLOROQUINE AND AZITHROMYCIN PREVENT COVID-19 INFECTION?
Neither Gautret trials assessed whether hydroxychloroquine with azithromycin would be effective for prophylaxis before an infection. The study only enrolled hospitalized patients already infected with the COVID-19 virus.
WHAT NOW?
For now, researchers and politicians are divided on whether to recommend hydroxychloroquine and azithromycin for the prevention and treatment of COVID-19. There is growing pressure on doctors to wait for science.
Doctors have patients who are sick now. Doctors have patients who want to prevent getting COVID-19.
“The Food and Drug Administration (FDA) on Sunday issued an emergency-use authorization for a pair of anti-malaria drugs as health officials work to combat the rapid spread of the novel coronavirus.” writes Jusin Wise in The Hill.
Stay tuned.
References:
Wang M, Cao R, Zhang L, Yang X, Liu J, Xu M, Shi Z, Hu Z, Zhong W, Xiao G. Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro. Cell Res. 2020 Mar;30(3):269-271.
Gautret P, Lagier JC, Parola P, Hoang VT, Meddeb L, Mailhe M, Doudier B, Courjon J, Giordanengo V, Vieira VE, Dupont HT, Honoré S, Colson P, Chabrière E, La Scola B, Rolain JM, Brouqui P, Raoult D. Hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an open-label non-randomized clinical trial. Int J Antimicrob Agents. 2020 Mar 20:105949.
Cai J, Xu J, Lin D, Yang Z, Xu L, Qu Z, Zhang Y, Zhang H, Jia R, Liu P, Wang X, Ge Y, Xia A, Tian H, Chang H, Wang C, Li J, Wang J, Zeng M. A Case Series of children with 2019 novel coronavirus infection: clinical and epidemiological features. Clin Infect Dis. 2020 Feb 28. pii: ciaa198
Gao J, Tian Z, Yang X. Breakthrough: Chloroquine phosphate has shown apparent efficacy in treatment of COVID-19 associated pneumonia in clinical studies. Biosci Trends. 2020 Mar 16;14(1):72-73.
Gautret P, Lagier JC, Parola P, and colleagues. Clinical and microbiological effect of a combination of hydroxychloroquine and azithromycin in 80 COVID-19 patients with at least a six-day follow up: an observational study. To be published as of 3/20/20.
Clinical trials on coronavirus drugs may take only months, researcher says. Gabe Gutierrez and Dennis Romero, From NBCNew.com Last accessed 3/29/20.
_____________
**Comment**
I posted this recently, but “authorities” have been bad-mouthing HCQ because many of them are getting financial kick-backs from Gilead Science, the manufacturer of the anti-viral Remdesivir, which bombed for Ebola, so they dug it out of the drug graveyard and are repurposing it for COVID-19. HCQ is a direct competitor and the CDC/NIH won’t have it. They diss any test or treatment that competes with their own. It’s all about profits. This is why nothing will change until these people can not have patents and conflicting interests. See: https://madisonarealymesupportgroup.com/2020/05/08/update-cdc-playbook-learning-from-lyme/
Approximately $70 million in U.S. taxpayer funding began Gilead’s partnership with the U.S. Army, Centers for Disease Control and Prevention (CDC) and National Institutes of Health (NIH) to develop remdesivir. Initially for treating Ebola, it failed to show benefit and was shelved. If remdesivir is used to treat COVID-19, Gilead shareholders, not the taxpayers, will profit.
Gilead’s own press release revealed the side effect of acute respiratory failure in 6% of patients in the remdesivir five-day treatment group, and 10.7% of patients in the 10-day treatment group, clearly ominous findings with a drug designed to treat respiratory failure caused by COVID-19.
Dr. Steven Nissen, a Cleveland Clinic cardiologist who has conducted dozens of clinical trials, explained to The New York Times:
“The disclosure of trial results in a political setting, before peer review or publication, is very unusual. Scientists will need to see figures on harms associated with the drug in order to assess its benefits. … This is too important to be handled in such a sloppy fashion.”
Going back to 1997, Donald Rumsfeld chaired the Board of Directors at Gilead and after 2001 he held share packages valued at $5-25 Million. Gilead originally developed Tamiflu.George P Shultz, US Secretary of State also was on the board. He sold stocks at a value of more than $7 million. CA governor’s Pete Wilson’s wife also sat on the board.
“‘I don’t know of any biotech company that’s’ so politically well-connected [as Gilead],‘ Andrew McDonald, of the analyst firm Think Equity Partners, told Fortune.” (Source: “Virus Mania, How the Medical Industry Continually Invents Epidemics Making Billion Dollar Profits At Our Expense”)
It’s looking very much like the CDC is helping Gilead reclaim its losses on Remdesivir’s failure in Ebola. Let’s just whip it back out for COVID-19, the public won’t notice!
The recent discovery of a secret, illegal, Chinese-linked lab in California will now make more sense when you read the following information. 20 Infectious agents were discovered in the lab including COVID and malaria.
Approx. 13 Min. (You can click on subtitles to read in English)
April 27, 2020
By Dr. Harry Ambrose
What Are SARS COVID2 Patients Really Dying From?
All the facts seem to point out that the death of the patients by the Sars Cov-2 virus is not an interstitial pneumonia that has been talked about so much in the media. There is a real cause which we explain in detail and chronologically in this chapter, and about which not much is said in the official journalistic media.
___________________
**Comment**
I’ve loosely transcribed the audio from Spanish to English. In short, SARS COVID2patients are not dying from interstitial pneumonia (which is why ventilators aren’t working and often cause more harm than good) but rather from DIC(disseminated intravascular coagulation) – a medical term for blood clotting causing a lack of oxygen.
Here’s the loose transcript:
Autopsies revealed a number of micro-thrombi, generalized venous, this means that in the capillaries, blood clotting occurred with obstruction blood flow, this caused the inability of oxygen to reach the alveoli, and for more mechanical respirator than the patient had, he was going to die anyway, because he had occluded blood vessels that carry oxygenated blood to the lungs, they also found micro throbs, in the heart, brain, and kidneys.Which means the patients did not die of interstitial pneumonia as told initially, they died from a blood condition called disseminated intravascular coagulation (DIC) also found in the x-rays of the lungs that interstitial pneumonia can be easily confused with images caused by micro thombus.
These discoveries of Italian pathologists in more than 50 autopsies performed in Bergamo and Milan Italy, center of the largest number of cases in that country, was corroborated by another more recent study in the U.S. by the doctor specializing in pathology, Sharon Fox and collaborators, in April in New Orleans, but only in 4 patients.
So in total 74 autopsies and other Chinese studies by Dr. Ning Tang etal., between Feb and March that confirm these facts.Increased D-dimers in the blood and coagulopathy indicators are related with worse prognosis of hospitalized patients.
SARS, COVID2 was invented in a British lab (Pirbright Institute) from a U.S. patent (Bickerton et al.) which has 4 genetic inserts:
HIV
Malaria
TB
most likely Dengue or Zika, which most likely were carried out in the biosafety lab in Wuhan China, and then escaped or were released.
Of these diseases Malaria, Dengue, Zika, and HIV can cause Thrombocytopenia, which means decreased platelets and formation of micro clots or thrombus, which produces purpuric lesions on the skin, which results in red dots on the limbs, that have been reported in some patients asymptomatic but infected with COVID-19 – mainly in young people, and the worst cases are capable of inducing coagulation, Disseminated Intravascular, which is a systemic event triggered by damage in the blood vessels, caused by inflammation.This has two consequences:
Severe, localized micro thrombus formation OR
Generalized or localized bleeding
The video states that while some scholars will say “severe infections can trigger DIC,” which is true, but among those infectious processes are HIV, Malaria, ZIKA, and Dengue, which is irrefutable.
It shouldn’t be surprising that the genetic codes inserted into the new SARS invention, COVID2 are those of these pathologies.
The first action when the patient stops being asymptomatic and before hospitalization should be blood studies to analyze coagulation because DIC must be avoided at all costs.
Prothrombin time or PT, which measures the external path of the cascade of coagulation
Partial thromboplastin time, of PTT, which measures intrinsic and common pathway, the amount of D-dimers,
Level of fibrinogen, platelet count and hematocrit will show quickly what is happening.
This clotted blood is mainly in the lungs, heart, brain and kidney.It is feasible that many died of hemorrhagic vascular brain ischemia, others with kidney failure, and others with heart disease such as myocardial infarction or failure of cardiac dilation of the heart.
Pathologist Sharon Fox found dilation of the right ventricle that means the heart was dilated, by the effort of pumping blood to the lungs that were occluded by micro thrombus, covered by platelet accumulation, and exudates inflammatory, characteristic of coagulopathy or DIC.
Another study just published by Wuhan General Hospital by Zhang et al., in more than 300 hospitalized patients from Jan 1999 to March 2020, the scale levels, D-dimers like prognostic factor of higher or lower mortality, and the conclusion was that patients with increased elevation of this blood factor had a greater risk of dying.
All of this evidence points to the fact patients are dying of micro thrombus (DIC) in the lungs, mainly, without ruling out heart, brain, and kidneys, NOT by interstitial pneumonia as reported and continues being reported today.
These studies raise a very suspicious question:
Who told these researchers in Wuhan, China to studyD-dimers specifically just 12 days after the pandemic was declared?This is suspicious and indicates they already knew it was a disease that causes DIC and had probably done autopsies prior to December and they knew which blood element was indicated.
This proves that this plague came long before they gave the alert, allowing it to spread widely.
And, they already knew about the micro thrombus and coagulopathies as the vital element in the the cause of mortality.
It took 3 months and thousands of people dying until the studies presented in this video happened.A harsh reality of what went on.
Most of these issues are involved with COVID2, showing why HCQ would be a good choice.
I must also point out that Lyme/MSIDS patients often struggle with hypercoagulation/thrombosis and blood clots.
For Portal vein thrombosis (PVT) doctors recommend anticoagulant drugs — blood thinners such as heparin. If PVT, as in this case, is caused by an infection, antibiotics will also be prescribed to cure the source of the problem. This is also the treatment used by Lyme literate doctors (LLMD).
Heparin helps many MSIDS patients:
http://aac.asm.org/content/48/1/236.full.pdf Similarly with Bartonella, some respond miraculously to Heparin, which is a blood thinner. In the above link, heparin was found to inhibit Babesia growth. Horowitz also found it helps clear the parasites from the body.
Malaria and Babesia are cousins.
Heparin helped my husband immensely. His blood looked like snot and continually clotted in catheters.
Interestingly, the authors state that vein thrombosis caused by borreliosis has not been studied, yet emphatically state that the combination of thrombosis and borreliosis is rare.
THIS IS THE BIZARRE DISCONNECT PATIENTS LIVE THROUGH.
Absence of proof, is not proof of absence
And rarely reported is far different than rarely occurs.
The following video created by a Canadian does an excellent job of editing multiple videos together showing the big picture of what’s going on with COVID-19. After the article I show Fauci’s patents – which are numerous and include patents regarding OspA –which should perk up ears of Lyme/MSIDS patients.Nearly every Lyme vaccine to come out revolves around OspA(outer surface protein A).
Here is my latest video on the uncovering of millions of $$ sent to the Wuhan lab under the control of Dr. Fauci and in Canada, Trudeau sent hundreds of thousands of $$ which helped create the crisis we are facing. Dr. Tam continues to mishandle the situation as she places her loyalty to the World Health Organization over the citizens of Canada. Where does her loyalty lie? It’s time to fire Dr. Fauci … and … Dr. Theresa Tam.
________________
**Comment**
Dr. Fauci doesn’t need to only be fired. He needs to be held accountable for his crimes and put in jail.
Fauci’s patent for the treatment of OspA-stuck-on-anything: U.S. Patent No. 5,696,079He also makes a decent salary in this business of abusing sick and disabled people: Fauci salary
Lastly, the media has been complicit in all of this. They are not questioning the draconian measures being taken or the disagreement in the medical community. If they do show the “other side” they cast a bad-light upon it. In fact, much has come out showing they continue to twist facts or make them up entirely(falsely showing footage taken in Italy and claiming it was taken here as well as staging an event to make it look worse than it is). They claim it was an “editing” mistake. I’ve worked in TV and that type of mistake isn’t made!https://madisonarealymesupportgroup.com/2020/05/06/expose-cbs-michigan-health-center-workers-stage-fake-patients-in-covid-19-testing-watch-it-quickly-before-its-yanked/
Recently I posted another fantastic Canadian article which discussed Event 201, a global pandemic exercise simulation of a factitious new coronavirussponsored by Bill and Melinda Gates, World Economic Forum and the Center for Health Security at Johns Hopkins. They discussed what to do about “misinformation” on the internet.
Excerpt:
Hasti Taghi chief of staff capacity at NBC Universal, noted that the anti-vaccine movement was very strong due to social media and therefore, they need to disseminate “the right information….to ensure the public has trust in the vaccines that we’re creating” against COVID-19. Harrington agreed stating this recent strong resistance was a “beta” test for dealing with resistance to COVID-19 vaccines. Also in attendance at Event 201 was Avril Haines, past assistant to the president and Principal Deputy National Security Adviser for the Obama administration, Deputy Director of CIA, Legal Advisor to National Security Council, who suggested daily briefings would work better than trying to control information to “flood the zone” from “trusted sources”at every level by community and faith based leaders and health care officials. Harrington agreed and added the need to educate trusted local leaders in advance of a pandemic to ensure readiness.
Four months after Event 201 COVID-19 information started flowing simultaneously from the media showing COVID-19 to be the most serious threat to humanity.
Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history.
This is not a conspiracy theory. It’s a conspiracy. Period.
Madison Area Lyme Support Group 