The following information and links are from my recent research. Please read all the way through to the end of this post so you don’t miss anything. Feel free to comment or add to anything here. Thanks for reading!

This famous and brilliant British doctor says: “We are victims of the greatest crime in history”:

https://www.youtube.com/watch?time_continue=1&v=EhYX8RzyMC4&feature=emb_logo

https://www.vernoncoleman.com/main.htm

FDA Recalls Dozens of Toxic Hand Sanitizers:

https://www.wakingtimes.com/2020/07/29/fda-recalls-dozens-of-toxic-hand-sanitizers/

Tucker Carlson: Coronavirus response is being driven by politics:

https://www.foxnews.com/opinion/coronavirus-response-is-being-driven-by-politicstucker-carlson

America’s Frontline Doctors SCOTUS Press Conference 27th July 2020:

https://www.bitchute.com/video/09K3kIwzeewO/

(NOTE: this video was censored from YouTube, and the frontline doctors website removed)

Nobel Laureate for science on Covid-19 lockdown – “The level of stupidity going on here is amazing”:

https://www.collective-evolution.com/2020/07/01/the-level-of-stupidity-going-on-here-is-amazing-nobel-laureate-for-science-on-covid-19-lockdown/

https://www.youtube.com/watch?v=AOUnO0cbhTA

Second Wave? Not Even Close!

https://off-guardian.org/2020/07/07/second-wave-not-even-close/

Professor Sucharit Bhakdi, MD (pictured above) is a Specialist in Microbiology, Professor at the Johannes Gutenberg University in Mainz, Germany, and Head of the Institute for Medical Microbiology and Hygiene. He is one of the most cited research scientists in German history. 

Here is what he has to say:

“We are afraid that 1 million infections with the new virus will lead to 30 deaths per day over the next 100 days. But we do not realise that 20, 30, 40 or 100 patients positive for normal coronaviruses are already dying every day.

[The government’s anti-COVID19 measures] are grotesque, absurd and very dangerous […] The life expectancy of millions is being shortened. The horrifying impact on the world economy threatens the existence of countless people. The consequences on medical care are profound. Already services to patients in need are reduced, operations cancelled, practices empty, hospital personnel dwindling. All this will impact profoundly on our whole society.

All these measures are leading to self-destruction and collective suicide based on nothing but a spook.”

In addition, Professor Sucharit Bhakdi has called lockdown measures “useless“, self-destructive“ and a “collective suicide.”

And here’s another:

“I have never seen anything like this, anything anywhere near like this. I’m not talking about the pandemic, because I’ve seen 30 of them, one every year. It is called influenza. And other respiratory illness viruses, we don’t always know what they are. But I’ve never seen this reaction, and I’m trying to understand why.

I worry about the message to the public, about the fear of coming into contact with people, being in the same space as people, shaking their hands, having meetings with people. I worry about many, many consequences related to that.”

~Joel Kettner, MD

Professor of community health sciences and surgery at Manitoba University

Former chief public health officer for Manitoba Providence

The Medical Director of the International Center for Infectious Diseases

And another:

“Patients who have been tested for SARS-CoV-2 are disproportionately those with severe symptoms and bad outcomes. As most health systems have limited testing capacity, selection bias may even worsen in the near future.

The one situation where an entire, closed population was tested was the Diamond Princess cruise ship and its quarantine passengers. The case fatality rate there was 1.0%, but this was a largely elderly population, in which the death rate from Covid-19 is much higher.

Could the Covid-19 case fatality rate be that low? No, some say, pointing to the high rate in elderly people. However, even some so-called mild or common-cold-type coronaviruses that have been known for decades can have case fatality rates as high as 8% when they infect elderly people in nursing homes.

If we had not known about a new virus out there, and had not checked individuals with PCR tests, the number of total deaths due to “influenza-like illness” would not seem unusual this year. At most, we might have casually noted that flu this season seems to be a bit worse than average.”

~John Ioannidis, MD

Professor of medicine, of health research and policy and biomedical data science at Stanford University School of Medicine

Professor of statistics at Stanford University School of Humanities and Sciences

Director of the Stanford Prevention Research Center

Co-director of the Method Research Innovation Center at Stanford (METRICS)

Quote taken from: “A fiasco in the making? As the coronavirus pandemic takes hold, we are making decisions without reliable data”, Stat News, 17th March 2020

And another:

“Italy is known for its enormous morbidity in respiratory problems, more than three times any other European country. In the US about 40,000 people die in a regular flu season and so far 40-50 people have died of the coronavirus, most of them in a nursing home in Kirkland, Washington.

In every country, more people die from regular flu compared with those who die from the coronavirus.

…there is a very good example that we all forget: the swine flu in 2009. That was a virus that reached the world from Mexico and until today there is no vaccination against it. But what? At that time there was no Facebook or there maybe was but it was still in its infancy. The coronavirus, in contrast, is a virus with public relations.

Whoever thinks that governments end viruses is wrong.”

~Yoram Lass, MD

Israeli physician

Former Director General of the Health Ministry

Associate Dean of the Tel Aviv University Medical School

From: Interview in Globes, March 22nd 2020

And another:

“The ill-founded opinions expressed by international experts, replicated by the media and social networks repeat the unnecessary panic that we have previously experienced. The coronavirus identified in China in 2019 caused nothing less than a strong cold or flu, with no difference so far with cold or flu as we know…

Respiratory viral conditions are numerous and are caused by several viral families and species, among which the respiratory syncytial virus (especially in infants), influenza (influenza), human metapneumoviruses, adenoviruses, rhinoviruses, and various coronaviruses, already described years ago. It is striking that earlier this year global health alerts have been triggered as a result of infections by a coronavirus detected in China, COVID-19, knowing that each year there are 3 million newborns who die in the world of pneumonia and 50,000 adults in the United States for the same cause, without alarms being issued.

Our planet is the victim of a new sociological phenomenon, scientific-media harassment , triggered by experts only on the basis of laboratory molecular diagnostic analysis results. Communiqués issued from China and Geneva were replicated, without being confronted from a critical point of view and, above all, without stressing that coronaviruses have always infected humans and always caused diarrhoea and what people call a banal cold or common cold. Absurd forecasts were extrapolated, as in 2009 with the H1N1 influenza virus.

There is no evidence to show that the 2019 coronavirus is more lethal than respiratory adenoviruses, influenza viruses, coronaviruses from previous years, or rhinoviruses responsible for the common cold.”

~ Pablo Goldschmidt, MD

Argentine-French virologist specializing in tropical diseases, and Professor of Molecular Pharmacology at the Université Pierre et Marie Curie in Paris. He is a graduate of the Faculty of Pharmacy and Biochemistry of the University of Buenos Aires and Faculty of Medicine of the Hospital Center of Pitié-Salpetrière, Paris.

He currently resides in France, where he has worked for almost 40 years as a researcher in clinical laboratories developing diagnostic technology.

From an Interview on Clarin.com, 9th March 2020

AND:

The German Network for Evidence-Based Medicine is an association of German scientists, researchers and medical professionals.

The network was founded in 2000 to disseminate and further develop concepts and methods of evidence-based and patient-oriented medicine in practice, teaching and research, and today has around 1000 members.

Here’s what they had to say:

“Covid19: Where is the evidence?”, statement on their website, March 20th 2020

https://www.ebm-netzwerk.de/en/publications/covid-19

And yet another:

Dr Richard Schabas (author of the above article) is the former Chief Medical Officer of Ontario, Medical Officer of Hastings and Prince Edward Public Health and Chief of Staff at York Central Hospital.

AND:

“I am deeply concerned that the social, economic and public health consequences of this near-total meltdown of normal life — schools and businesses closed, gatherings banned — will be long-lasting and calamitous, possibly graver than the direct toll of the virus itself. The stock market will bounce back in time, but many businesses never will. The unemployment, impoverishment and despair likely to result will be public health scourges of the first order.”

~David L. Katz, MD

American physician

Founding director of the Yale-Griffin Prevention Research Center at Griffin Hospital in Derby, Connecticut

FROM:  “Is Our Fight Against Coronavirus Worse Than the Disease?”,

    New York Times 20th March 2020

Above article written by Peter C. Gøtzsche, MD, MS

Danish physician and medical researcher

Professor of Clinical Research Design and Analysis at the University of Copenhagen

Former leader of the Nordic Cochrane Center at Rigshospitalet in Copenhagen, Denmark

Co-founder of the Cochrane Collaboration

AND here is another chilling article:

All-cause mortality during COVID-19: No plague and a likely signature of mass homicide by government response

The following article, “Medical error—the third leading cause of death in the US” was originally published in 2016.

Introduction:

“2.6 million people die annually in low-and middle-income countries from medical errors, and that most of those deaths are related to misdiagnosis and administration of pharmaceutical products [and now, the financially incentivized and inappropriate mass use of deadly ventilators]. Medication errors alone cost an estimated $42 billion (US dollars) annually. Unsafe surgical care procedures cause complications in up to 25% of patients resulting in 1 million deaths during or immediately after surgery annually…Four out of every ten patients are harmed during primary and ambulatory health care. The most detrimental errors are related to diagnosis, prescription and the use of medicines.”

— The World Health Organization

Below is this medical online article that concluded that medical errors are the third leading cause of death in the US. The study, published in 2016 in the British Medical Journal, was authored by researchers from the Johns Hopkins University School of Medicine. The authors calculated that medical errors accounted for > 250,000 deaths every year in the US, which made iatrogenic (= physician, drug or vaccine-caused) deaths the third leading cause of death in the US, surpassed only by #1 heart disease (647,457) and #2 cancer (599,108) (2018 CDC data).

It is important to note that medical errors and adverse effects from prescription drugs that have caused deaths or illnesses are rarely listed by physicians on death certificates or in rankings of causes of death or illnesses. The online article calls for better reporting by physicians.

Also be aware that the study – as has been the case of ALL such studies of causes of death, acute illnesses, chronic illnesses or adverse drug effects – did NOT evaluate vaccine-induced deaths or injuries, mainly because virtually every physician, in every country (where powerful, for-profit pharmaceutical/vaccine corporations control the practice of medicine, most medical school curricula and most major media outlets), consistently fails – or refuses to acknowledge – even the most obvious vaccine injuries or deaths as worthy of being reportable diseases or worthy of being listed in their differential diagnostic impressions, discharge diagnoses or death certifications.

https://www.hcp.med.harvard.edu/sites/default/files/methodsmakarydaniel_2016_bmj%20%281%29.pdf

How Google Censors Health News:

https://articles.mercola.com/sites/articles/archive/2019/11/08/google-censorship-buries-mercola.aspx

INVESTIGATION: Google Manipulates Search Suggestions To Promote Pharma, Discredit Natural Health:

https://www.greenmedinfo.com/blog/investigation-google-search-autosuggestions-program-users-pro-pharma-anti-health-

“Propaganda is to a democracy what violence is to a dictatorship.

It’s a mechanism of control.

It’s the “manufacture of consent”.

~Edward Bernays

“There is little value in insuring the survival of our nation if our traditions do not survive with it.  And there is a very grave danger that an announced need for increased security will be seized upon by those anxious to expand its meaning to the very limits of official censorship and concealment.” ~John F. Kennedy

1984: YouTube Will Demote Conspiracy Videos In Its Recommendation Algorithm — A Scary Prospect For Freedom Of Thought:

https://www.activistpost.com/2019/01/1984-youtube-will-demote-conspiracy-videos-in-its-recommendation-algorithm-a-scary-prospect-for-freedom-of-thought.html

CRITICAL:  Please watch the hugely important 2015 video embedded in the article featuring world class journalist Naomi Wolf

https://www.youtube.com/watch?time_continue=533&v=GuB6wavzcww&feature=emb_logo

Read carefully:

According to an amendment to the 2013 National Defense Authorization Act (NDAA), the House Bill H.R 5736 (now law), the federal government of the United States can now legally propagandize the domestic public.

Arguably, this makes staged theatrical presentations, featuring crisis-actors, and purporting to be ‘reality’, legal.

And, as if that isn’t enough, Don North writes in “US/NATO Embrace Psy-ops and Info-War” that,

“As reflected in a recent NATO conference in Latvia and in the Pentagon’s new ‘Law of War’ manual, the U.S. government has come to view the control and manipulation of information as a ‘soft power’ weapon, merging psychological operations, propaganda and public affairs under the catch phrase ‘strategic communications.”

Mark Taliano, “Fake threats and engineered fears.” 16 July, 2016. (https://ahtribune.com/politics/1073-engineered-fears.html?fbclid=IwAR0qHlFivL8c1QIqMxZsiQO43qYN0R-ITQCPa9jUXAWjU9v8_LjzMFiGlJE) Accessed 18 April, 2019.

In truth, none of this is about Trump.

The focus on Trump is a mistake. You could look at anywhere–any newspaper or public commentator and you can see all of the criticisms of the Tump policies, administration, etc and all of the issues that they have. He is almost universally vilified. Google is doing all it can (unscrupulously, btw) to unseat Trump in November.  Trump is surrounded by a media frenzy of utter contempt. The presidential alternative we have for November is literally no better a choice (but at least would be more easily malleable by those pulling the marionette strings. Trump has too many strings loose for them). Biden is clearly suffering from some form of rapidly advancing dementia. We should all be concerned, if not terrified if he ends up in the Oval Office.

But what should we actually be looking at?

Faith in elected leaders to fix our problems is the mistake that we keep repeating. 

When President Obama was elected to the White House he said all of the right things:  He said he was going to create a more equal America, into a period of cooperation instead of partisanship, he said he was going to “close Guantanamo on day one of his administration”…. and it was still open on the last day of his presidency.  He said that “there was going to be no more warrantless wiretapping in America….We  don’t do that.  That is NOT WHO WE ARE”…. And in fact he expanded it.  He made it worse. It went deeper. it got more sophisticated  and more pervasive. He even signed into law ’The National Defense Authorization Act’ back in 2013—making LEGAL (albeit 100% unconstitutional) the propagandizing of the American public through the use of all forms of media without Americans’ knowledge or consent.   And it all continues.  Now mass propaganda AND mass surveillance it is at a fever pitch and picking up speed. And the likes of Google, Facebook, YouTube and all other social media platforms and “smart” technologies (including your cell phone) are surveillance, social engineering and control tools for the state (which is controlled by the interests of corporate and mega financial interests).  Today, what is being termed “Contact tracing” (control seized by authoritarian government agencies is always presented as being for “our own good”) is merely a euphemism for mass surveillance and control of the population.  It must be resisted with every fiber of our beings.

If we’re hoping for a champion or waiting for a hero we will be waiting FOREVER.  Because it’s not a politician that you’re looking for.  We need to look in the mirror.

There are no heroes that will save you. There are only heroic actions and heroic choices. The moment you wonder if you are the one you’ve been waiting for, you’ll realize that you are. ~ Nora

Some States Are Now Police State: Camps and Ankle Bracelets:

https://www.youtube.com/watch?v=fBkKAVfiaIA

https://www.technocracy.news/masks-are-neither-effective-nor-safe-a-summary-of-the-science/

“The foregoing data show that masks serve more as instruments of obstruction of normal breathing, rather than as effective barriers to pathogens. Therefore, masks should not be used by the general public, either by adults or children, and their limitations as prophylaxis against pathogens should also be considered in medical settings.”

Endnotes

1  T Jefferson, M Jones, et al. Physical interventions to interrupt or reduce the spread of respiratory viruses. MedRxiv. 2020 Apr 7.

https://www.medrxiv.org/content/10.1101/2020.03.30.20047217v2

2  J Xiao, E Shiu, et al. Nonpharmaceutical measures for pandemic influenza in non-healthcare settings – personal protective and environmental measures.  Centers for Disease Control. 26(5); 2020 May.

https://wwwnc.cdc.gov/eid/article/26/5/19-0994_article

3  J Brainard, N Jones, et al. Facemasks and similar barriers to prevent respiratory illness such as COVID19: A rapid systematic review.  MedRxiv. 2020 Apr 1.

https://www.medrxiv.org/content/10.1101/2020.04.01.20049528v1.full.pdf

4  L Radonovich M Simberkoff, et al. N95 respirators vs medical masks for preventing influenza among health care personnel: a randomized clinic trial.  JAMA. 2019 Sep 3. 322(9): 824-833.

https://jamanetwork.com/journals/jama/fullarticle/2749214

5  J Smith, C MacDougall. CMAJ. 2016 May 17. 188(8); 567-574.

https://www.cmaj.ca/content/188/8/567

6  F bin-Reza, V Lopez, et al. The use of masks and respirators to prevent transmission of influenza: a systematic review of the scientific evidence. 2012 Jul; 6(4): 257-267.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779801/

7  J Jacobs, S Ohde, et al.  Use of surgical face masks to reduce the incidence of the common cold among health care workers in Japan: a randomized controlled trial.  Am J Infect Control. 2009 Jun; 37(5): 417-419.

https://pubmed.ncbi.nlm.nih.gov/19216002/

8  M Viola, B Peterson, et al. Face coverings, aerosol dispersion and mitigation of virus transmission risk.

https://arxiv.org/abs/2005.10720, https://arxiv.org/ftp/arxiv/papers/2005/2005.10720.pdf

9  S Grinshpun, H Haruta, et al. Performance of an N95 filtering facepiece particular respirator and a surgical mask during human breathing: two pathways for particle penetration. J Occup Env Hygiene. 2009; 6(10):593-603.

https://www.tandfonline.com/doi/pdf/10.1080/15459620903120086

10 H Jung, J Kim, et al. Comparison of filtration efficiency and pressure drop in anti-yellow sand masks, quarantine masks, medical masks, general masks, and handkerchiefs. Aerosol Air Qual Res. 2013 Jun. 14:991-1002.

https://aaqr.org/articles/aaqr-13-06-oa-0201.pdf

11  C MacIntyre, H Seale, et al. A cluster randomized trial of cloth masks compared with medical masks in healthcare workers.  BMJ Open. 2015; 5(4)

https://bmjopen.bmj.com/content/5/4/e006577.long

12  N95 masks explained. https://www.honeywell.com/en-us/newsroom/news/2020/03/n95-masks-explained

13  V Offeddu, C Yung, et al. Effectiveness of masks and respirators against infections in healthcare workers: A systematic review and meta-analysis.  Clin Inf Dis. 65(11), 2017 Dec 1; 1934-1942.

https://academic.oup.com/cid/article/65/11/1934/4068747

14  C MacIntyre, Q Wang, et al. A cluster randomized clinical trial comparing fit-tested and non-fit-tested N95 respirators to medical masks to prevent respiratory virus infection in health care workers. Influenza J. 2010 Dec 3.

https://onlinelibrary.wiley.com/doi/epdf/10.1111/j.1750-2659.2011.00198.x?fbclid=IwAR3kRYVYDKb0aR-su9_me9_vY6a8KVR4HZ17J2A_80f_fXUABRQdhQlc8Wo

15  M Walker. Study casts doubt on N95 masks for the public. MedPage Today. 2020 May 20.

https://www.medpagetoday.com/infectiousdisease/publichealth/86601

16  C MacIntyre, Q Wang, et al. A cluster randomized clinical trial comparing fit-tested and non-fit-tested N95 respirators to medical masks to prevent respiratory virus infection in health care workers. Influenza J. 2010 Dec 3.

https://onlinelibrary.wiley.com/doi/epdf/10.1111/j.1750-2659.2011.00198.x?fbclid=IwAR3kRYVYDKb0aR-su9_me9_vY6a8KVR4HZ17J2A_80f_fXUABRQdhQlc8Wo

17  N Shimasaki, A Okaue, et al. Comparison of the filter efficiency of medical nonwoven fabrics against three different microbe aerosols. Biocontrol Sci.  2018; 23(2). 61-69.

https://www.jstage.jst.go.jp/article/bio/23/2/23_61/_pdf/-char/en

18  T Tunevall. Postoperative wound infections and surgical face masks: A controlled study. World J Surg. 1991 May; 15: 383-387.

https://link.springer.com/article/10.1007%2FBF01658736

19  N Orr. Is a mask necessary in the operating theatre? Ann Royal Coll Surg Eng 1981: 63: 390-392.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2493952/pdf/annrcse01509-0009.pdf

20  N Mitchell, S Hunt. Surgical face masks in modern operating rooms – a costly and unnecessary ritual?  J Hosp Infection. 18(3); 1991 Jul 1. 239-242.

https://www.journalofhospitalinfection.com/article/0195-6701(91)90148-2/pdf

21  C DaZhou, P Sivathondan, et al. Unmasking the surgeons: the evidence base behind the use of facemasks in surgery.  JR Soc Med. 2015 Jun; 108(6): 223-228.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480558/

22  L Brosseau, M Sietsema. Commentary: Masks for all for Covid-19 not based on sound data. U Minn Ctr Inf Dis Res Pol. 2020 Apr 1.

https://www.cidrap.umn.edu/news-perspective/2020/04/commentary-masks-all-covid-19-not-based-sound-data

23  N Leung, D Chu, et al. Respiratory virus shedding in exhaled breath and efficacy of face masks Nature Research.  2020 Mar 7. 26,676-680 (2020).

https://www.researchsquare.com/article/rs-16836/v1

24  S Rengasamy, B Eimer, et al. Simple respiratory protection – evaluation of the filtration performance of cloth masks and common fabric materials against 20-1000 nm size particles. Ann Occup Hyg. 2010 Oct; 54(7): 789-798.

https://academic.oup.com/annweh/article/54/7/789/202744

25  S Bae, M Kim, et al. Effectiveness of surgical and cotton masks in blocking SARS-CoV-2: A controlled comparison in 4 patients.  Ann Int Med. 2020 Apr 6.

https://www.acpjournals.org/doi/10.7326/M20-1342

26  S Rengasamy, B Eimer, et al. Simple respiratory protection – evaluation of the filtration performance of cloth masks and common fabric materials against 20-1000 nm size particles. Ann Occup Hyg. 2010 Oct; 54(7): 789-798.

https://academic.oup.com/annweh/article/54/7/789/202744

27  C MacIntyre, H Seale, et al. A cluster randomized trial of cloth masks compared with medical masks in healthcare workers.  BMJ Open. 2015; 5(4)

https://bmjopen.bmj.com/content/5/4/e006577.long

28  W Kellogg. An experimental study of the efficacy of gauze face masks. Am J Pub Health. 1920.  34-42.

https://ajph.aphapublications.org/doi/pdf/10.2105/AJPH.10.1.34

29  M Klompas, C Morris, et al. Universal masking in hospitals in the Covid-19 era. N Eng J Med. 2020; 382 e63.

https://www.nejm.org/doi/full/10.1056/NEJMp2006372

30  E Person, C Lemercier et al.  Effect of a surgical mask on six minute walking distance.  Rev Mal Respir. 2018 Mar; 35(3):264-268.

https://pubmed.ncbi.nlm.nih.gov/29395560/

31  B Chandrasekaran, S Fernandes.  Exercise with facemask; are we handling a devil’s sword – a physiological hypothesis. Med Hypothese. 2020 Jun 22. 144:110002.

https://pubmed.ncbi.nlm.nih.gov/32590322/

32  P Shuang Ye Tong, A Sugam Kale, et al.  Respiratory consequences of N95-type mask usage in pregnant healthcare workers – A controlled clinical study.  Antimicrob Resist Infect Control. 2015 Nov 16; 4:48.

https://pubmed.ncbi.nlm.nih.gov/26579222/

33  T Kao, K Huang, et al. The physiological impact of wearing an N95 mask during hemodialysis as a precaution against SARS in patients with end-stage renal disease.  J Formos Med Assoc. 2004 Aug; 103(8):624-628.

https://pubmed.ncbi.nlm.nih.gov/15340662/

34  F Blachere, W Lindsley et al. Assessment of influenza virus exposure and recovery from contaminated surgical masks and N95 respirators. J Viro Methods.  2018 Oct; 260:98-106.

https://pubmed.ncbi.nlm.nih.gov/30029810/

35  A Rule, O Apau, et al. Healthcare personnel exposure in an emergency department during influenza season.  PLoS One. 2018 Aug 31; 13(8): e0203223.

https://pubmed.ncbi.nlm.nih.gov/30169507/

36  F Blachere, W Lindsley et al. Assessment of influenza virus exposure and recovery from contaminated surgical masks and N95 respirators. J Viro Methods.  2018 Oct; 260:98-106.

https://pubmed.ncbi.nlm.nih.gov/30029810/

37  A Chughtai, S Stelzer-Braid, et al.  Contamination by respiratory viruses on our surface of medical masks used by hospital healthcare workers.  BMC Infect Dis. 2019 Jun 3; 19(1): 491.

https://pubmed.ncbi.nlm.nih.gov/31159777/

38  L Zhiqing, C Yongyun, et al. J Orthop Translat. 2018 Jun 27; 14:57-62.

https://pubmed.ncbi.nlm.nih.gov/30035033/

39  C MacIntyre, H Seale, et al. A cluster randomized trial of cloth masks compared with medical masks in healthcare workers.  BMJ Open. 2015; 5(4)

https://bmjopen.bmj.com/content/5/4/e006577

40  A Beder, U Buyukkocak, et al. Preliminary report on surgical mask induced deoxygenation during major surgery. Neurocirugia. 2008; 19: 121-126.

http://scielo.isciii.es/pdf/neuro/v19n2/3.pdf

41  D Lukashev, B Klebanov, et al. Cutting edge: Hypoxia-inducible factor 1-alpha and its activation-inducible short isoform negatively regulate functions of CD4+ and CD8+ T lymphocytes. J Immunol. 2006 Oct 15; 177(8) 4962-4965.

https://www.jimmunol.org/content/177/8/4962

42  A Sant, A McMichael. Revealing the role of CD4+ T-cells in viral immunity.  J Exper Med. 2012 Jun 30; 209(8):1391-1395.

https://europepmc.org/article/PMC/3420330

In this Mercola interview video Patrick Wood credibly, brilliantly and systematically connects all the key dots and supplies an approach (the only approach) to addressing the events of our time and showing us our way out:

https://www.technocracy.news/dr-mercola-reveals-technocracy-as-masterplan-for-the-great-reset/

https://articles.mercola.com/sites/articles/archive/2020/08/09/patrick-wood-technocracy.aspx

Resources:  https://cspoa.org/

https://www.technocracy.news/

Patrick Wood YouTube: “Technocracy News and Trends”

Why COVID-19 Clinical Trials Cannot Be Trusted The “Gold Standard” for Science Is Gold for the Drug Companies:

https://breggin.com/why-covid-19-clinical-trials-cannot-be-trusted/

Why COVID-19 Clinical Trials Cannot Be Trusted The “Gold Standard” for Science Is Gold for the Drug Companies

By Peter R. Breggin MD and Ginger Ross Breggin

Science! We have been told that science must be relied upon to make our decisions when dealing with the pandemic called COVID-19. We must in effect bow down to science, no matter how humiliating and painful it may feel.

But science has an Achilles heel—a fatal flaw that can completely ruin it and frequently does.

What is the fatal flaw of science? It is conducted by human beings. Where serious science controversies exist, science is no more reliable than politics…or heaven forbid…no more reliable than religion. Science is only as dependable as the people who conduct and disseminate it. The adage for judging opinions still holds true—consider the source!

When Anthony Fauci announced the rollout of his initial clinical trial for remdesivir as the great hope for knocking out the coronavirus epidemic, he boasted about the clinical trial’s importance: “A randomized, placebo-controlled trial is the gold standard[1] for determining if an experimental treatment can benefit patients.”

Since controlled clinical trials involving drugs and vaccines are very expensive, require access to sick and often highly infectious patients, and must be approved by the Institutional Review Boards (IRBs) and the FDA—they can only be conducted with funding from Big Pharma and Big Government or occasional other large institutions. We will see that the tragic result of this hegemony was remarkably demonstrated in Fauci’s government trial on behalf of his favorite drug company, Gilead.[2]

Meanwhile, the People’s Drug Is Running Ahead

As we have documented in earlier reports, here[3] and here[4] and on our Coronavirus Resource Center,[5] hydroxychloroquine and zinc as a prophylactic, and hydroxychloroquine plus azithromycin and zinc for patients developing COVID-19 could right now greatly improve the treatment of patients in the US, as it has done elsewhere.

Doctors and entire nations have been and are continuing to use this drug successfully, especially in combination with azithromycin and zinc. The Association of American Physicians and Surgeons has shown that the countries which actively use hydroxychloroquine have significantly lower death rates than those that do not.

Meanwhile, the so-called “gold standard” of controlled clinical trials has been vastly ramped up by the pharmaceutical industry and we can expect a deluge of supposedly scientific studies pouring from them. This report warns the world not to trust the Pharmaceutical Empire’s forthcoming tsunami of evidence for the safety and effectiveness of their products.

Bias Already Controls Ongoing and Planned Clinical Trials

You can see the drug company bias in a recent list of all current and planned registered trials of remdesivir for the treatment of Covid-19. Many of the trials have “arms” or comparator studies for chloroquine or hydroxychloroquine. There are fourteen of these chloroquine and/or hydroxychloroquine trial arms; but all of them are set up so that they are doomed to fail. Only one adds azithromycin to the hydroxychloroquine and none adds zinc. Yet, the combination of hydroxychloroquine, azithromycin and zinc[6] is considered the most successful treatment for COVID-19 by experienced clinicians.[7] In addition, several studies compare remdesivir to the older drug chloroquine rather than to hydroxychloroquine which is considered safer. Put simply, every single registered remdesivir clinical trial has been rigged to make hydroxychloroquine fail in comparison.

We cannot take seriously any of the in-progress or planned remdesivir studies!

Meanwhile, a search of ClinicalTrials.gov[8] shows only three ongoing or proposed trials for the combination of hydroxychloroquine, azithromycin and zinc. Their outcome will probably be determined by whether or not they are intended to show that the medication works. Meanwhile, it is likely that some clinical trials of “Trump’s Wonder Drug” will be conducted by researchers who are hostile toward the President. Almost all clinical trials are conducted by researchers with vested interests in the pharmaceutical industry, what we call The Pharmaceutical Empire. Nearly all will be conducted by experienced researchers with long histories of working for drug companies. They are likely to be interested in knocking hydroxychloroquine out of the competition in favor of more financially rewarding drugs and vaccines or simply to please those in the Pharmaceutical Empire who have been paying their salaries and giving them bonuses for years.

Perhaps in the crucible of the epidemic, some institutions will courageously conduct genuinely scientific studies of the hydroxychloroquine’s rug’s safety and effectiveness in combination with azithromycin and zinc; but that is an idealistic longshot. The world that awaits the clinical trial results should be warned that most of the trials will be showcase trials for those who sponsor them.

Science is a process. To develop genuine or more lasting scientific validity often takes many trustworthy and honest scientists and institutions working independently and separately in many settings, publishing numerous papers, over a long period of time. I doubt that “Trump’s Wonder Drug” will ever be given a fair scientific review, at least in the United States. It is more likely to occur in other countries where the Pharmaceutical Empire has somewhat less influence. And when that happens, the research will get scant airing in the US.

Science in the Public Arena

Whenever science has huge financial, political, and social impacts—that is, when science becomes especially important to us human beings—it is instantly seized upon by unscrupulous human beings and industries for their own purposes. Often the science becomes wholly corrupted and at other times it is vastly distorted and misinterpreted as it passes through the media to the unwitting people.

I will never forget Neil Cavuto self-righteously attacking[9] President Trump’s personal use and support of hydroxychloroquine. The Fox News anchor cited a ridiculously flawed, unofficial and still unpublished study of VA patients which purportedly showed hydroxychloroquine increased the death rate, when a more accurate analysis[10]showed that in combination with azithromycin it was saving lives. The study itself was rejected by the VA as unauthorized and misleading.

Cavuto accused Trump of killing people! One of the doctors that Cavuto later interviewed disappointed him by saying he had been using the drug for 40 years to treat other diseases, and he had never seen a single death. The media rarely slips up like that but Cavuto was in a rush that day to use science to prove Trump was not only wrong, but dangerous.

Recently, Stella Emmanuel MD, a black African doctor who immigrated to the US and practices medicine in Texas, defended hydroxychloroquine as part of a group presentation by American doctors assembled for that purpose. The major media picked her to ridicule for her Christian beliefs and social media cancelled her enormously popular video. Her clinical experience treating hundreds of COVID-19 patients without a single death was uniformly ridiculed by the conventional media, while similar opinions by other doctors in the group were ignored. Only occasional media gave her a chance[11] to express her well-informed views.

What Are Placebo-Controlled Clinical Trials?

But what about placebo-controlled clinical trials? In a placebo-controlled double-blind randomized clinical trial, the drug is randomly given to one group of people while a harmless inert pill or saline injection is randomly given to the other group, called the placebo control. If a portion of the drug group develop encephalitis, for example, and none of the placebo group contract the disease, then the study may generate statistically significant data indicating the drug or vaccine causes encephalitis.

To eliminate doctor or patient bias in evaluating the trials, they are double-blind. That is, neither the patient nor the doctor, or anyone evaluating the trials, know who are the subjects getting the treatment and who are the placebo controls.

Despite how it sounds, controlled clinical trials are not science. Pure science is a search for objective truth or improved theories about reality based on observation and empirical facts. At their best, clinical trials are applied science—the use of the scientific method for achieving certain ends, such as convincing the FDA to approve the next blockbuster drug to make the company even wealthier.

Clinical trials are not in search of truth or improved theories—they are the application of a superficially scientific method toward a specific goal. In this, they are more like engineering—applying science to achieve practical goals—in this instance, getting the FDA to approve a potentially valuable product.

If We Lived in Utopia

In theory, it might be possible to create and to conduct a clinical trial more in search of the truth than in the interest of creating wealth. In practice, it is not possible. Placebo-controlled randomized double-blind clinical trials are extremely expensive to conduct. They need an institutional base and an Institutional Review Board (IRB) to approve it. They require recruiters and managers, along with scientists, statisticians and healthcare providers. If they are intended to gain FDA approval, the process becomes bureaucratically overwhelming, requiring years and tens of millions of dollars. Most drug or vaccine clinical trials are sponsored (paid for and controlled) by the pharmaceutical industry. Clinical trials are like music and art in the Renaissance—they needed wealthy sponsors like a king or prince—so they rarely challenged the monarchy.

Fauci and his NIH Institute for Allergy and Infectious Diseases collaborated with his favorite corporation,[12] Gilead, to get expedited approval for Remdesivir. Gilead is estimated to have spent one billion dollars[13] on developing and promoting Remdesivir on its own and Fauci’s institute is estimated to have contributed 70 million more dollars to implementing the NIH clinical trial of the drug.

When so much time, effort and money are being spent on a project, can we expect the sponsors to admit they have come up empty-handed—or worse, that they have created a monster that will do far more harm than good? Can we expect Tony Fauci to tell us, “Oops, I’ve been completely wrong in touting this drug long before we had clinical trials and now I have to confess I’ve wasted a fortune, untold man hours, and a lot of precious time on promoting it, and it is making many patients worse. Oh, yes, and I was wrong about hydroxychloroquine, too, because it is a very good drug with sixty years of safe prescribing behind it, it costs almost nothing, and should be given very early to every suspected COVID-19 patient and used as prophylaxis, too. Even the World Health Organization says they know of no deaths associated with it. And, yes, in addition, I apologize to President Trump for undermining his support for hydroxychloroquine.”

Because of this horrendous partnership—the most power-hungry in the government in combination with the greediest in industry—Fauci’s remdesivir “gold standard” clinical trial became a monstrous demonstration of political corruption masquerading as science.

But before I go into more detail about the undisclosed failure of Fauci’s long-expected clinical trial for Remdesivir, let me tell you more about my professional background and the origins of my disillusionment about clinical trials. In the early 1990s, I was the one doctor in the world who threatened the success of the blockbuster drug, Prozac, and here’s what happened.

The Prozac Clinical Trials

Prozac (fluoxetine) changed the world of psychiatry and medicine, promoting a false theory of biochemical imbalances causing mental disorders and paving the way for multiple new psychiatric drugs with revenues in the multiple billions of dollars.

As a clinical and forensic psychiatrist and the author of many scientific articles and medical books, I have considerable experience in independently evaluating clinical trials.

In the early 1990s, I was chosen by a consortium of several dozen attorneys and approved by a federal judge to become the sole scientific investigator for approximately 150 lawsuits against Eli Lilly for the allegedly fraudulent development and marketing of its drug, Prozac (fluoxetine). My first task was to determine if there was a scientific basis for the lawsuits, and if there was, my next task was to develop that scientific basis for the all cases against the company. I got started by taking the courses that drug company executives take to learn about making drug applications to the FDA. I went to relevant conferences put on by the FDA and other organizations. I interviewed key FDA officials on the phone and in person. I read a great deal and I began to evaluate the first case given to me. Then I prepared to give a deposition and to testify in court against Eli Lilly.

Early in my research as the forensic psychiatric expert for the combined Prozac cases, I began by focusing on “the gold standard” upon which all drug companies are said to rely—the placebo-controlled randomized controlled clinical trials used by Elli Lilly to gain approval for Prozac from the Food and Drug Administration (FDA).

Among many allegations in the 150 lawsuits, Lilly was charged with knowingly marketing a dangerous drug while hiding that it caused violence, suicide, and mania. When I evaluated the company’s clinical trials used for FDA approval, I added additional allegations including collusion with the FDA to conduct fraudulent clinical trials that exaggerated the drug’s effectiveness and hid the drug’s worst adverse effects. The adverse effects include a cocaine-like activation or overstimulation of the brain that leads to agitation, irritability, insomnia, mania, and even psychosis, too often resulting in violence and suicide in children and adults.

Yes, the Prozac trials were gold…a golden calf for Eli Lilly. The clinical trials were fabricated science.

A Model for Drug Company Malfeasance:

Here are just a few of the major deceptions surrounding Eli Lilly’s clinical trials, which I documented in detail Talking Back to Prozac (with Ginger Ross Breggin, 1994) and in later sources, including Brain-Disabling Treatments in Psychiatry, Second Edition (2008). I also urged the reader to look at my free Antidepressant Resource Center at www.123antidepressants.org.[14] Because documentation is needed and readily available for such strong accusations, I have indicated page numbers from the St. Martin’s Paperbacks edition of Talking Back to Prozac:

(1) Eli Lilly claimed to the public and to doctors that their approval data was based on 11,000 subjects (pp. 45-6). When I did a laborious hand count of the total number of people who actually finished their clinical trials, it was a mere 286 patients. Eli Lilly never challenged this analysis, or any of my scientific accusations, in deposition or in court.

(2) The studies were very short, lasting only 4-6 weeks, when patients end up taking antidepressants for months and years, so they were literally too short to be meaningful. But as short as they were, many patients could not finish because of adverse effects.

(3) Any improvements in patients were so marginal they were difficult to prove, even with outrageous statistical manipulations (pp.52 ff).

(4) Patients were dropping out like flies from the trials due to distressing overstimulation with agitation, anxiety, insomnia, irritability, and other amphetamine-like symptoms. Rather than let the trials fail, Eli Lilly secretly broke the rules of the studies, previously agreed upon with the FDA, by giving addictive sedatives and tranquilizers to calm the patients enough to stay in the trials (p. 55, pp. 62 ff).

(5) When the FDA later discovered the fraud, they also discovered that Prozac could not be approved without using the corrupted, illegal trials. Faced with disappointing the drug company and its political supporters, including President George Bush who had been on Lilly’s Board of Directors, the FDA agreed to use these intentionally corrupted studies to approve the antidepressant. The FDA then hid these facts, so that doctors, patients, and scientists throughout the world had no idea that it required addictive sleeping pills and tranquilizers to keep patients from dropping out of the Prozac trials.

(6) When an in-house re-evaluation of the clinical trials for adults indicated that the drug was producing a massive increase in suicidality, Eli Lilly hid the data from the FDA and from the world. I have since released their analysis, but much too late to matter.

(7) When the FDA’s chief in-house analyst for Prozac’s adverse effects found that Prozac had amphetamine-like effects that were making depressed patients agitated, causing dangerous agitated depressions, he wanted to warn about it the official FDA descriptions of the drug, but his FDA superiors rejected his recommendations (pp. 74-78).

(8) After Prozac came onto the market, my publications and those of other scientists confirmed that Prozac causes suicide and violence. The FDA responded by meeting secretly with Eli Lilly before the agency’s normal working hours to plan how to jointly fight these allegations.

(9) When data from investigators conducting new clinical trials began to show increased suicides among patients taking Prozac compared to those taking placebo, Eli Lilly order the staff to doctor the reports. They were told to change the reports to eliminate words like “completed suicide,” “attempted suicide” or “suicidal ideation” and to replace then with infinitely more innocuous terms like “no drug effect” and “emotional lability.” Some Eli Lilly employees expressed shame in memos[15] they sent up line (pages 2 and 3 of the linked document).

(10) When it came time for the first trial against Eli Lilly, I was armed with much of this information, and evidence of many other demonstrably fraudulent behaviors by the drug company. Eli Lilly did not have much of chance against so much negative information about them, so they simply fixed the trial. Eli Lilly secretly settled the case in advance in return for the plaintiff’s lawyer, with whom I was working, and he in turn faked a trial for the drug company to win. The faked trial was touted in the unwitting and witless major media as a complete exoneration of Prozac and the drug company’s value took off, while millions of Americans taking Prozac and nearly all the newer antidepressants remain in the dark about its dreadful effects. The judge later figured out that the trial had been fixed and changed the victory to a settlement. Also, the Kentucky Supreme court cited Eli Lilly for possible fraud. But the major media was now overcome with silence. My most detailed write up of these tragic and disillusioning courtroom events is in Chapter 12: “Drug Companies on Trial” in my book Medication Madness: The Role of Psychiatric Drugs in Cases of Violence, Suicide and Crime.

And on… and on…. as documented in my books and scientific articles. The placebo-controlled clinical trials for Prozac were corrupt from top to bottom and the drug should never have been approved. Then the promotion of the flawed results was equally invalid. Then the media coverage of events surrounding the trial was entirely skewed in favor of the drug company. Sound familiar? This is what Anthony Fauci has in effect been doing with Remdesivir, but so far with less success than Ely Lilly, the Master of Deception. Further, as I much earlier concluded in Talking Back to Prozac, recent studies have confirmed that Prozac and other antidepressants are no more effective than a sugar pill[16] —and of course far more dangerous.

Something I’ve Never Reported Before:

Finally, I want to write about something for the first time—what happened to me and my family while I was getting ready to testify against Eli Lilly. During the time when I was preparing to confront Eli Lilly in deposition and then in trial, my wife Ginger and then our daughter became ill with an undiagnosable disorder that involved a dry, hacking cough, shortness of breath, headache, muscle aches, and extreme fatigue. I also became ill but not quite as seriously. My home office where I spent most of my time was an add-on to the house that was above ground and separate from the old basement.

After multiple doctors could find no reason for our illnesses, our plumber was fixing something in the basement when he came upon a dismaying discovery. The exhaust chimneys to our gas hot water heater and to our oil furnace had been removed and placed out of sight in the poorly lit utility portion of the basement. We were being poisoned.

We were so demoralized by this experience that we did not report it to the police, in part because we had previously reported a serious death threat to the FBI, and when we tried to follow up, they had no record of our being visited by two agents. We never found out who was behind the life-threatening poison gas attack or the threats and since I was very much in the public eye at the time in the major media, it could have been any number of vested interests.

Placebo-Controlled Clinical Trials in the Development of Modern Vaccines:

More recently, because of COVID-19, I became interested in what kind of clinical trials are conducted for FDA approval of vaccines. I knew it would be easy to conduct placebo-controlled clinical trials, because none of the patients in typical vaccine trials are physically ill or mentally distressed. It would be relatively simple and inexpensive, for example, to test a new vaccine for measles in children by simply giving the vaccine to one group of normal children and giving the placebo to a similar group of normal children.

The children on placebo would be in little or no danger of catching measles because of herd immunity in the US. Because they were not sick, they would not be deprived of any necessary treatment. And because they were children, they could easily be followed for many years, instead of a few weeks or months, to give the trial much greater length than most involving drugs. But we’ll never know how easy it might have been to do it right.

When I started reviewing the studies for FDA approval, I was stunned by what I found out: The FDA does not require placebo-controlled clinical trials for new vaccines. The FDA gives the drug companies a pass on conducting a normal clinical trial when they are seeking approval for vaccines. Instead of comparing their new drug’s good and bad effects to a harmless placebo, the vaccine companies get away with comparing their vaccines to other vaccines.

Comparing one vaccine to another vaccine, instead of a harmless placebo, is like comparing one form of dirt to another form of dirt and finding them both dirt-free when they are alike in being dirty. Or, as perhaps an easier analogy, if you were trying to make your poisonous brand of wine look relatively safe, wouldn’t you rather compare to another poisonous wine than to a genuine placebo of flavored water or perhaps normal fresh wine?

Dr. Fauci’s Gold Standard Turns Out to be Fools Gold

The simple truth is that every one of the hundreds of drug-company clinical trials I have evaluated has been rigged to meet the aims of the drug company—which is always to make a killing with a new drug or a variation on an old one. Worse than that, in my area of greatest experience, psychiatric drugs, all the trials are fatally rigged, and even if they turn out badly for the drug company, they are promoted as positive.

So, I wondered, “What will Fauci’s upcoming clinical trial for the antiviral drug Remdesivir look like? It’s being conducted in broad daylight, so it cannot be entirely corrupted.” Naive me…

Since I have made the details available elsewhere in a heavily documented blog and a video,[17] I will be relatively brief in describing the corruption of Fauci’s clinical trial for Remdesivir in COVID-19 patients.

First, Fauci stacked his Institute’s Covid-19 Advisory Committee with experts in the pay of Gilead, the manufacturer Remdesivir. Even before the clinical trial began, the committee recommended to America’s doctors to use Remdesivir and not to use hydroxychloroquine.

Second, Fauci knew from trials on Ebola that remdesivir did not work as an antiviral agent and was potentially life-threatening. The remdesivir arm of the Ebola trial had to be aborted because more people were dying on remdesivir faster than on other antiviral drugs in the study.

Third, as the trial got started, Lancet published an article indicating that Remdesivir was of no help and was making many patients much sicker. The remdesivir trial showed no good effect whatsoever and created a high risk with 5% of patients showing a marked worsening of their respiratory condition.

Fourth, when the trial started, its main goal was to show it could cure a significant number of Covid-19 patients and reduce the death rate. When it became obvious that the trial was not going to prove any such thing, the goal became limited to proving that the drug reduced the time to recovery. Fauci eventually claimed that the drug was shortening the average length of illness from 15 to 11 days. But to fake even this meager result, he redefined “recovery” to include patients who had not even been discharged from the hospital. Perhaps more stunning, he also included as recovered patients at home who remained on oxygen and patients at home who remained partially disabled on limited activities.

Fifth, that too must have failed to materialize, because Fauci decided to cancel the trial before it was completed, thus making it impossible to make an honest final determination that the drug was of any value whatsoever. His excuse for terminating the trial? The drug was so good he felt it had to be offered to the placebo patients. In reality, he was successfully covering up how bad his drug really was and then foisting it off on the unwitting placebo patients.

And then—in an extraordinary breach of medical and scientific ethics—Fauci and his cohort have never published a scientific analysis of the adverse effects of the drug to determine if, like the Lancet report [18] on the same drug, it was making many people worse. The only publication to date has been the Gilead press release[19] of June 1, 2020 “Gillead Announces Results From Phase 3 Trial of Remdesivir in Patients With Moderate COVID-19.”

So much for the “gold standard.”

FDA Lashes Out Against Hydroxychloroquine:

The FDA, the seemingly scientific arbiter of everything pharmacological, has recently issued a report stating that hydroxychloroquine has not been proven in any way to be safe and effective. The FDA has warned doctors to be wary of it, and to use it only in clinical trials. Doctors are not required or compelled to follow this kind of FDA warning, but the agency is acting like they must obey. Many hospitals and doctors have become intimidated, along with pharmacies. State governors have restricted[20] or suppressed the use of hydroxychloroquine.

In another report a few days ago,[21] we pointed out that the FDA has broken its own rules, and subverted established tradition and law, by telling doctors that they cannot prescribe a drug, hydroxychloroquine, off label or outside the narrow limits for which the agency has approved. We have urged President Trump to override the FDA and to declare that it cannot interfere with the off-label use of hydroxychloroquine. He should free doctors, pharmacies, and hospitals to prescribe and dispense hydroxychloroquine within the privacy of the physician-patient relationship.

Fauci’s Inevitable Career on Behalf of the Pharmaceutical Empire:

Now we will look at Fauci’s career and how it led him to betray America. Thirty-six years ago, Dr. Anthony Fauci was appointed director of NIH’s National Institute of Allergy and Infectious Diseases (NIAID). According to his Institute profile,[22] “He oversees an extensive portfolio of basic and applied research to prevent, diagnose, and treat established infectious diseases” and he “has advised six presidents on HIV/AIDS and many other domestic and global health issues.” He is the “author, coauthor, or editor of more than 1,300 scientific publications, including several textbooks.” Dr. Fauci is probably the most influential American in respect to anything that has to do with epidemic diseases, including our current struggle with COVID-19.

Nothing important or controversial happens at NIAID without Director Fauci knowing or learning about it. He determines, oversees, and guides the activities of the Institute, including setting its research priorities. That is his job description.

Unfortunately, we have discovered that Dr. Fauci has enormous responsibility for the pandemic ever beginning in China. Against the advice of others, and perhaps against the law, he continued funding collaborative research between American scientists and Wuhan scientists in developing more deadly coronaviruses. We blew the whistle[23]on this unholy, dangerous alliance, and within days President Trump stopped Fauci from funding it any longer.

It is highly likely that China would not have developed the expertise to work with coronaviruses, eventually setting one free by accident, if it were not for Fauci’s support of the collaborative research and the Wuhan Institute itself. Because Wuhan is a military facility, Fauci is also responsible for enabling China to create biological weaponry that constitutes one of the greatest military threats that America and the free world now faces and will continue to face for the foreseeable future.

In evaluating Dr. Fauci’s motives, keep in mind that it is impossible to remain Director of the NIH Institute of Allergy and Infectious Diseases for 36 years and a consultant to six presidents without being deeply beholden and obedient to pharmaceutical companies who manufacture and sell antibiotics, antiviral agents, and vaccines. I had a brief two-year career as a Full-time Consultant to the National Institute of Mental Health (NIMH) with the rank of Commander in the US Public Health Service. It was clear from the beginning that government health officials work as if industry, powerful lobbying groups, and politicians are sitting on their shoulders, pulling strings to make their heads nod.

Fauci’s longevity is a testimonial to his responsiveness to the enormous power wielded by the pharmacological industry. Their influence and control over him explains Fauci’s suppression of a tried-and-true treatment while promoting remdesivir, a very expensive and experimental alternative with known severe adverse effects and no evidence of effectiveness. It accounts for the egregious support he gave to research in collaboration with China that created deadly viruses, which gave the pharmaceutical industry more information about developing vaccines. Most sinister of all, Fauci’s funding and support eventually gave China the SARS-CoV-2 virus that turned into a pandemic. In a bitter irony, that pandemic has already become a multi-billion dollar boondoggle as Fauci pumps huge bundles of money into the coffers of his friends and partners in industry.

A Warning for the Future:

When evaluating a “scientific” claim, always consider the source. Science is no better than the people and institutions who conduct it, and the people who interpret it to the public. The new “partnership” between big industry and big government, led by Anthony Fauci, will produce “science” that favors their power and their wealth. It will not be genuine science in pursuit of the objective truth or better theories, it will inevitably be science in the interest of accruing wealth. We already have compelling evidence[24] that hydroxychloroquine in combination with zinc and azithromycin is a very helpful treatment for COVID-19 and that it saves lives.

President Donald Trump, as leader of the Executive Branch, can override the FDA and remind the agency that it has no legal right to forbid doctors from prescribing hydroxychloroquine off label, alone or in combination with zinc or azithromycin. He can override the FDA’s warnings that have vastly reduced the use of the best treatment we have for COVID-19, resulting in considerable loss of life. In doing so, he will save thousands of American lives; and as we suggested in our earlier report, he can liberate America to save itself and to save the world as well by strengthening supply lines and ramping up production of hydroxychloroquine, azithromycin, and zinc.

[1] https://www.nih.gov/news-events/news-releases/nih-clinical-trial-remdesivir-treat-covid-19-begins

[2] https://breggin.com/faucis-remdesivir-inadequate-to-treat-covid-19-and-potentially-lethal/

[3] https://breggin.com/america-time-to-save-the-world-again/

[4] https://breggin.com/stunning-news-about-hydroxychloroquine-to-treat-covid-19/

[5] https://breggin.com/coronavirus-resource-center/

[6] https://files.internetprotocol.co/ebook-covid-19.pdf

[7] https://breggin.com/america-time-to-save-the-world-again/

[8] https://clinicaltrials.gov/ct2/results?cond=Covid19&term=hydroxychloroquine2C+zinc+&cntry=&state=&city=&dist=

[9] https://www.dailymail.co.uk/news/article-8337773/Fox-News-host-Neil-Cavuto-renews-attack-Donald-Trump-recommending-hydroxychloroquine.html

[10] https://breggin.com/negative-study-of-trump-miracle-drug-actually-shows-it-works/

[11] https://www.click2houston.com/news/local/2020/07/31/full-interview-houston-doctor-in-viral-video-touting-hydroxychloroquine-as-virus-cure-doubles-down-on-claims/

[12] https://www.click2houston.com/news/local/2020/07/31/full-interview-houston-doctor-in-viral-video-touting-hydroxychloroquine-as-virus-cure-doubles-down-on-claims/

[13] https://www.politico.com/news/2020/05/06/remdesivir-helps-coronavirus-patients-but-at-what-cost-240230

[14] https://breggin.com/antidepressant-drugs-resource-center/

[15] http://breggin.com/wp-content/uploads/1997/01/elilillydocspart4.pdf

[16] http://breggin.com/antidepressant-drugs-resources/Kirsch2014.pdf

[17] https://breggin.com/faucis-remdesivir-inadequate-to-treat-covid-19-and-potentially-lethal/

[18] http://breggin.com/coronavirus/remdesivir/RemdesivirChinadoubleblind-WangApr-29-20.pdf

[19] http://archive.is/NKM0X

[20] https://www.nashp.org/wp-content/uploads/2020/03/State-covid-drug-chart-3-27-2020.pdf

[21] https://breggin.com/america-time-to-save-the-world-again/

[22] http://archive.is/iBf1T

[23] https://breggin.com/us-chinese-scientists-collaborate-on-coronavirus/

[24] https://breggin.com/america-time-to-save-the-world-again/

If Bill Gates Was President… [easily the most urgent video on the internet]:

https://www.brighteon.com/e468c1ea-7fcd-41af-b84d-4c877fe7d14f

Incredibly important, highly intelligent, credible and enlightening discussion between two of the best independent investigative journalists of our time, James Corbett and Spiro Skouras

The content of this discussion goes WAY beyond the question of Bill Gates. There is an urgency to this message everyone needs wake up to, pay attention to and take seriously.

Fauci Recommends Goggles for Protection From COVID-19:

https://articles.mercola.com/sites/articles/archive/2020/08/12/do-you-need-goggles-for-coronavirus.aspx

Poignant article and video footage – everyone needs to see this:

https://childrenshealthdefense.org/news/rally-in-berlin/

Germany…possibly more than most any other country on earth, recognizes the all-too familiar implications of what is happening and knows all too well what is at stake.

Charlene Bollinger Interviews Sheriff Richard Mack plus more info:

I believe it is this man, Richard Mack (and his CSPOA Organization) more than any other, that has the key to our liberation from this nightmare. This dedicated and brilliant officer took on the entire Supreme Court and won on matters of our Constitution and Bill of Rights on OUR behalf a few years ago. No small accomplishment. Right now he heads the CSPOA (Constitutional Sheriffs and Peace Officers Association).

What he is doing is key to our personal protection in these times.

I have written back and forth with him, and incredulously received a wonderful, genuine and thoughtful replies.  I spent about 30 minutes on the phone with his wife, Dawn (who was simply lovely) the other day.

https://cspoa.org/

I am a proud, contributing member to this organization.  Everyone should be supporting them.  Here is a general description of their mission:

https://cspoa.org/about/join/

Here is what they stand for:

https://cspoa.org/2014-resolution/

ALSO:  Richard Mack offers a training course on understanding the Constitution and Bill of Rights, which he offers both to law-enforcement and anyone else that would like a strong education in this area. It has never been more needed than it is now, and training like this can prepare you to deal with would be despotic dictocrats and others seeking to erode your inalienable human rights.

~ Nora

PS. Please consider donating to support my work and research. Thank you!