The world is an astrotrurf festival. If you don’t know what astroturf is, you’re probably one of its daily victims. It’s, basically, everything that followed in mainstream media after the Astroworld Festival tragedy.
Most of the credits for the video go to Hugo @ hugotalks.com As I was investigating this, I kept falling in his footsteps. As he did it first and voiced it well, I just did a enhanced remix of his reports. Watch his stuff too, he has more to bring to the table, I brought a little something too.
UPDATE NOVEMBER 11 – POLICE ABANDONS THE INJECTED SECURITY GUARD PLOT. STILL NO REAL SURGE OR STAMPEDE IN NEWLY FOUND VIDEOS
I haven’t seen this press conference covered by any major network, maybe I just missed it…
TO PICK it UP FROM WHERE THE VIDEOS LEFT IT:
By education and work records, I’m a journalist, but more people around the world know me as a music producer / DJ / label manager. I played many of these festivals. I also like science. So I immediately knew where to look:
“Graphene oxide (GO) is one of the most frequently-used graphene-family materials, but it must often be reduced in order to restore electrical conductivity for the target applications. We have demonstrated the use of non-contact fringing field RF applicators to rapidly heat and reduce GO, both in its neat form and inside a polymer matrix such as polyvinyl alcohol (PVA). For this study, GO and GO-PVA films were prepared by the vacuum filtration method. The results demonstrate quick non-contact heating of GO and GO-PVA composite films by application of RF fields. Heating rates as high as 10.9 °C/s and 1.5 °C/s have been observed for GO and GO-PVA, respectively. RF-reduced GO and GO-PVA samples have shown conductivities of 102 S/m and 10−1 S/m, respectively. In addition, C/O ratio has increased from 2.44 to 5.22 when GO is exposed to RF waves which confirm that GO samples are reduced by the RF treatment. Unlike time-consuming or hazardous conventional reduction methods, RF waves resistively heat GO with electric fields in seconds to form reduced GO.”
Or it could be other source of frequencies at the higher spectrum where graphene is sensible and where mobile phones and other communication networks operate, or the stage equipment.
ABSTRACTWe confirm graphene oxide, a two-dimensional carbon structure at the nanoscale level can be a strong candidate for high-efficient interconnector in radio-frequency range. In this paper, we investigate high frequency characteristics of graphene oxide in range of 0.5–40 GHz. Radio-frequency transmission properties were extracted as S-parameters to determine the intrinsic ac transmission of graphene sheets, such as the impedance variation dependence on frequency. The impedance and resistance of graphene sheets drastically decrease as frequency increases. This result confirms graphene oxide has high potential for transmitting signals at gigahertz ranges.
This work was partially supported by the Priority Research Centers Program (Grant No. 2009-0093823), the Pioneer Research Center Program (Grant No. 2010-0019313), and Basic Science Research Program (Grant No. 2010-8-0874) through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (MEST) of the Korean government. We thank R. S. Ruoff and S. Stankovich for providing the GO used in this study.
Graphene Nanomaterials-Based Radio-Frequency/Microwave Biosensors for Biomaterials Detection
Recent Research Trends: RF/Microwave Biosensors Based on Graphene Nanomaterials for Wireless Biomedical Applications
Recent advances in integrated biosensing platforms associated with remote sensing via RF/microwave wireless systems have focused on design and architecture of point-of-care (POC) diagnosis, attracting considerable interest in the biomedical applications. In particular, POC has significant diagnosis possibilities for use in the continuous and real-time monitoring of human metabolites as well as cancer biomarkers [92]. In addition, flexible and stretchable-integrated biosensors can directly monitor metabolic changes on the human body and quantify the electrically fine signals generated by specific bodily fluids. As a result, from this biosensing scheme, the wearable biosensors that can be attached intimately in the skin or tissue offer new opportunities for medical diagnostics and therapy. In recent years, there has been enormous progress in graphene-integrated wireless RF/microwave systems for real-time monitoring of metabolic change [93]. For example, a wireless smart soft contact lens system composed of reconfigurable capacitive sensor interface circuitry and wirelessly powered RFID addressable system for sensor control and data communication [94,95] was developed. In particular, monitoring for glucose and other biomarkers may become more sophisticated if the sensor is coated with graphene in this system.
Conclusions and Prospective
Recent advances in graphene nanomaterials such as synthesis techniques, electrical, thermal and mechanical analysis, surface treatment and device design have accelerated the development and application of graphene nanomaterials-based nanoelectronics as well as bioelectronics. In this review, we have examined the emerging advances of graphene nanomaterials-integrated biosensors including structures and merits of graphene nanomaterials and their biological functionalization in RF/microwave biomedical applications. From the developed RF/microwave biosensors, these biosensing schemes could be classified with passive RF/microwave devices and RF/microwave systems with graphene nanomaterials. Firstly, it was used as a biosensing scheme utilizing simple RF/microwave devices such as resonators and capacitors, with graphene nanomaterials like GO or rGO. In the case of latter, it was used as a biosensing scheme utilizing RF/microwave systems with graphene nanomaterials, e.g., graphene. These RF/microwave biosensors could be detectable of biomolecules, e.g., glucose, DNA, as well as bacteria, e.g., S. aureus, E. coli and so on, via bifunctional peptide.
However, the research and development of these materials-based biosensing systems are in their infancy in the RF/microwave biomedical applications. This is because it is not only difficult to find the optimized frequency for biosensing, but devices and circuits also are dependent on the frequency. However, since there are great merits such as real-time, non-invasive, non-contact function, as a graphene nanomaterials-based RF/microwave biosensor, the biosensing scheme still needs to develop the robust biosensing platform integrated with wireless and flexible devices and circuits. In this case, there are also remains challenges how to find effective integration methods and how to secure stability for good performance of RF/microwave devices and systems with graphene nanomaterials. Before this challenge, the optimization of material fabrication and modification techniques to obtain large area, high quality, and uniform arrays will be essential for the highly sensitive and reproducible RF/microwave biosensors. Furthermore, the integration of graphene nanomaterials-based RF/microwave device needs to be optimized to minimize the entire device volume for portable, disposable and POC diagnosis and healthcare in the future.
If I’m allowed just one paragraph of semi-speculation: All living beings are natural antennas, the water molecule and the hydrogen one are antennas of sorts, this is how living beings know stuff before they consciously find out or even develop any sort of conscience. Looks like graphene oxide hyper=capacitates us.
Is this conclusive enough? I can’t give an 100% verdict on this right now, I need to revisit some physics textbooks, I need more inputs from my smartest readers, hurry up, I’m itching to make a follow up to that video! But if I were vaxxed right now, I’d stay away from powerful EMF sources and powerful anything-that-vibrates that you can hear and feel.
UPDATE NOVEMBER 14, 2021: ENTER GO-NUTS
Stacked layers of GO (clotted?) can have interesting properties. Have in mind the conversion effect described below can work both ways. It says right there “transmit and receive sound”.
Presented at IUS 2015, Taipei, Taiwan Title: Graphene Oxide Nanofabricated Ultrasonic Transducers (GO-NUTs) Abstract: Graphene Oxide Nanofabricated Ultrasonic Transducers (GO-NUTs) based on porous electrodes immersed in ionic liquid electrolyte, which use the vibration of the compressible electric double layer to transmit and receive ultrasound with signal level several order of magnitude higher than existing capacitive transducers are introduced. A simple, rapid and scalable method to reduce graphene oxide (GO) by Laser Lightscribe annealing was also demonstrated. The reduced graphene oxide (rGO) for scalable and rapid production was then fabricated to graphene-based ultrasonic transducers which exhibit supercapacitor characteristics. The vibration of ions at the electric double layer (EDL) on the interface of the multi-layer rGO electrode that immersed in liquid electrolyte can simulate the flexible vibrating membrane of capacitive micromachined ultrasonic transducers to match the acoustic impedance of the soft tissue. The amplitude and frequency response to ultrasonic source were measured by oscilloscope and analyzed by MatLab. The capacitance, potential, and frequency response measurement of the GO-NUTs had shown the functionality of the device and suggested it can be used in the high frequency range. The testing result also showed that the reduced graphene oxide had advantages over the material used in traditional piezoelectric ultrasonic transducer. The GO-NUTs could also be further fabricated to interdigitated and array patterns simply by Laser Lightscribe CD/DVD drive and software. Authors: Ka Hing Cheng, Ching-Hsiang Cheng, Kwong Chun Lo
And, to close the circle in my hypothesis: this is how GO stacks up in water, what if something similar happens in the blood, maybe just in specific conditions that were met before or at the concert?
Graphene nanoparticles tend to form clusters in water, due to unfavorable interfacial energy. In simple words, a graphene nanoparticle ‘prefers’ to be in contact with graphene rather than with water. This is one of the reason why it is so difficult to process graphene at a large scale.
The simulation is made using LAMMPS, the rendering using VMD. The temperature 300 K. The structure of the hexabenzocoronene molecules has been downloaded from the ATB repository https://atb.uq.edu.au/.
A script with one single hexabenzocoronene molecule is available here, and easily be adapted to study the multiple particle case: https://github.com/simongravelle
To be continued? Our work and existence, as media and people, is funded solely by our most generous supporters. But we’re not really covering our costs so far, and we’re in dire needs to upgrade our equipment, especially for video production. Help SILVIEW.media survive and grow, please donate here, anything helps. Thank you!
! Articles can always be subject of later editing as a way of perfecting them
As per usual, Reuters did not fact-check what they claimed. Almost all their smear jobs are based on this type of text-book straw-man. But you will learn more than the headline promises here.
‘I CALLED PHARMAFIA AND THEY SAID NO’ – EVERY MEDICAL FACT-CHECK EVER
The claim in the original article, the claims in the fact-check and the verdict are three separate things. Reuters manages to straw-man its own straw-man.
THIS BLOG IS NOT AN ANTI-VACCINE COMMENTARY. I WISH TO ENCOURAGE READERS TO CAREFULLY READ THE DOCUMENTATION, DO THEIR DUE DILIGENCE, AND NOT BLINDLY ACCEPT WHAT WE ARE BEING TOLD.
WOULD YOU BE SURPRISED OR CONCERNED TO LEARN THAT THE 1918 “SPANISH FLU” HAD NOTHING TO DO WITH SPAIN AND MIGHT NOT HAVE BEEN A FLU AT ALL? WELL, HANG ON TIGHT, YOU ARE IN FOR A ROUGH RIDE!
WHAT HISTORY TELLS US ABOUT THE 1918 “SPANISH FLU”
History tells us that the 1918 Spanish Flu killed between 50 – 100 million people. At the time, medical and pharmaceutical sources described it as THE MOST horrific disease process since the Black Plague of 1347, which killed an estimated 25-30 million people.
Reuters does not dispute this
VACCINATION: “THE ELEPHANT IN THE ROOM”
In the book,Vaccination Condemned, by Eleanor McBean, PhD, N.D., the author describes, in detail, personal and family experiences during the 1918 “Spanish Flu” pandemic.
McBean’s coverage of the 1918 “Spanish Flu”, as a reporter and an unvaccinated survivor, requires that the historical basis of the event needs to be revisited, not as a “conspiracy theory” but with evidence that will “set your hair on fire”.
A few years ago, I came across another book by Eleanor McBean: “Vaccination…The Silent Killer”. McBean provides evidence that not only were the historical events of the 1918 “Spanish Flu” compromised, but also those of the Polio and Swine Flu epidemics.
LET’S TALK “SPANISH FLU” FACTS:
THE SPANISH SCAPEGOAT
Spain was neutral during WW1 and did NOT censor its press, unlike the combatting countries. As a result, Spain was the first to report the 1918 Flu epidemic and the world “scapegoated” Spain as the source. Thus, the “Spanish Flu” is born.
THE FIRST CASE: MILITARY VACCINATION EXPERIMENTS IN FORT RILEY, KANSAS
In preparation for WW1, a massive military vaccination experiment involving numerous prior developed vaccines took place in Fort Riley, Kansas- where the first “Spanish Flu” case was reported.
WW1 DRAFT = HUMAN TEST SUBJECTS
The fledgling pharmaceutical industry, sponsored by the ‘Rockefeller Institute for Medical Research’, had something they never had before – a large supply of human test subjects. Supplied by the U.S. military’s first draft, the test pool of subjects ballooned to over 6 million men. CLICK HERE for more details.
BACTERIAL MENINGITIS VACCINE: THE KILLING FIELD
Autopsies after the war proved that the 1918 flu was NOT a “FLU” at all. It was caused by random dosages of an experimental ‘bacterial meningitis vaccine’, which to this day, mimics flu-like symptoms.
Reuters simply calls this main claim ‘baseless’ without providing any base for their call, then move on to flog more straw-men of their own:
So, basically, we have a Pharmafia-licensed doctor’s word vs. a Reuter presstitute’s word, and I bet my ass the Reuter NPC has no medical studies. Anyway, to settle the truth here, you have to do your own research, which I did below.
However, to settle that Reuters faked its fact-check is already adequate at this point.
The original article follows up:
The massive, multiple assaults with additional vaccines on the unprepared immune systems of soldiers and civilians created a “killing field”. Those that were not vaccinated were not affected. – Links to the article in the pic below:
Reuters claims there is a disagreement between their findings and the article’s, but they both claim the same thing: it was a flu AND a bacteria that ended the lives of those who got a flu in 1918
Undisputed
SO… HOW DID CIVILIANS DIE?
WW1 ended sooner than expected, leaving HUGE quantities of unused experimental vaccines.
Fearing that soldiers coming home would spread diseases to their families, The U.S. government pushed the largest vaccine ‘fear’ campaign in history. They used the human population as a research and development lab to field test experimental vaccines.
Tens of millions of civilians died in the same manner as did the soldiers.
Instead of stopping the vaccines, doctors intensified them, calling it the great “Spanish Flu of 1918”. As a result, ONLY THE VACCINATED DIED.
“Seven men dropped dead in a doctor’s office after being vaccinated. Letters were sent to their families that they had been killed in action.”
In the examples given in my previous blog “COVID 19: Another Chapter in the History of Deception and Secrecy”, history is replete with intentional lies told to the public to either “save face” or to deceive for nefarious purposes. The 1918 “Spanish Flu” was no exception.
So what did the autopsies really reveal?
This is the only actual dispute Reuters made to the article, and neither sides backed their claims.
Predominant Role of Bacterial Pneumonia as a Cause of Death in Pandemic Influenza: Implications for Pandemic Influenza Preparedness
Abstract
Background
Despite the availability of published data on 4 pandemics that have occurred over the past 120 years, there is little modern information on the causes of death associated with influenza pandemics.
Methods
We examined relevant information from the most recent influenza pandemic that occurred during the era prior to the use of antibiotics, the 1918–1919 “Spanish flu” pandemic. We examined lung tissue sections obtained during 58 autopsies and reviewed pathologic and bacteriologic data from 109 published autopsy series that described 8398 individual autopsy investigations.
Results
The postmortem samples we examined from people who died of influenza during 1918–1919 uniformly exhibited severe changes indicative of bacterial pneumonia. Bacteriologic and histopathologic results from published autopsy series clearly and consistently implicated secondary bacterial pneumonia caused by common upper respiratory–tract bacteria in most influenza fatalities.
Conclusions
The majority of deaths in the 1918–1919 influenza pandemic likely resulted directly from secondary bacterial pneumonia caused by common upper respiratory–tract bacteria. Less substantial data from the subsequent 1957 and 1968 pandemics are consistent with these findings. If severe pandemic influenza is largely a problem of viral-bacterial copathogenesis, pandemic planning needs to go beyond addressing the viral cause alone (e.g., influenza vaccines and antiviral drugs). Prevention, diagnosis, prophylaxis, and treatment of secondary bacterial pneumonia, as well as stockpiling of antibiotics and bacterial vaccines, should also be high priorities for pandemic planning.
The 1918 to 1919 “Spanish” influenza pandemic virus killed up to 50 million people. We report here clinical, pathological, bacteriological, and virological findings in 68 fatal American influenza/pneumonia military patients dying between May and October of 1918, a period that includes ~4 mo before the 1918 pandemic was recognized, and 2 mo (September-October 1918) during which it appeared and peaked.
The lung tissues of 37 of these cases [a little over half – S.m] were positive for influenza viral antigens or viral RNA, including four from the prepandemic period (May-August). The prepandemic and pandemic peak cases were indistinguishable clinically and pathologically.
All 68 cases had histological evidence of bacterial pneumonia, and 94% showed abundant bacteria on Gram stain.
Sequence analysis of the viral hemagglutinin receptor-binding domain performed on RNA from 13 cases suggested a trend from a more “avian-like” viral receptor specificity with G222 in prepandemic cases to a more “human-like” specificity associated with D222 in pandemic peak cases. Viral antigen distribution in the respiratory tree, however, was not apparently different between prepandemic and pandemic peak cases, or between infections with viruses bearing different receptor-binding polymorphisms. The 1918 pandemic virus was circulating for at least 4 mo in the United States before it was recognized epidemiologically in September 1918.
The causes of the unusually high mortality in the 1918 pandemic were not explained by the pathological and virological parameters examined.
These findings have important implications for understanding the origins and evolution of pandemic influenza viruses.
Frederick Lamont Gates, born in Minneapolis, Hennepin County, MN, December 17, 1886, married, September 11, 1917 in Duluth, St. Louis County, MN, Dorothy Olcott, born June 20, 1891, daughter of William James and Fannie (Bailey) Olcott.
His father said he was “born for study and inquiry and disclosed this at an early age”. Ill health disqualified him from athletic activities and his life was centered wholly on activities of the mind. He was accepted at Harvard, Yale and the University of Chicago and, after a year and a half at Chicago, he chose to continue his studies at Yale. He stood at the head of his class, received the Phi Beta Kappa key, and graduated Summa Cum Laude in 1909. The same year, he entered John Hopkins Medical School, and graduated with highest honors four years later. He was recommended for research work at the Rockefeller Institute and took a position on its staff.
On the declaration of war in 1917, Mr. Gates volunteered for the U.S. Army Medical Corps, was accepted and commissioned a first lieutenant. He was assigned to duty on the Rockefeller Institute staff where he gave lectures to military groups selected to attend training there. He was also assigned to visit training camps, in the interest of preventive medicine, and traveled widely. He continued at the institute after the war and his researches, especially those on influenza, received worldwide recognition. His health failed in 1927 and he was required to undertake a less demanding schedule. He continued his research at Harvard and moved his family to Cambridge, MA where he died, June 17, 1933, at age forty-six, after suffering a concussion from a fall. – SOURCE
Frederick Lamont Gates was the son of Frederick Taylor Gates (1853-1923) was the principal business and philanthropic advisor to the major oil industrialist John D. Rockefeller, Sr., from 1891 to 1923.
In 1901, Frederick T. Gates designed the Rockefeller Institute for Medical Research (now Rockefeller University), of which he was board president.
Yale Obituary Record Frederick Lamont Gates, B.A. 1909* Born December 17, 1886, in Minneapolis, Minn. Died June 17,1933, in Boston, Main Father, Rev. Frederick Taylor Gates (B. A. University of Rochester 1877, M.A, 1879; Rochester Theological Seminary 1880$ ULD. University of Chicago 1911); a Baptist minister; business and benevolence manager for John D. Rockefeller; president of Rockefeller Institute for Medical Research; chairman of General Education Board; son of Rev. GranviUe Gates and Sarah Jane (Bowers) Gates, of Maine, N. Y. Mother, Emma Lucia (Cahoon) Gates; daughter of Lyman Hall and Cordelia Lucinda (Teague) Cahoon, of Racine, Wis. Montclair (N. J.) High School; attended University of Chicago 1905-06 as member of Class of 1909. Entered Yale as a Sophomore; Andrew D. White prize in history Sophomore year; philosophical oration appointment and honors in physical sciences Senior year; member University Orchestra, Alpha Delta Phi, Sigma Xi, and Phi Beta Kappa. M.D. Johns Hopkins 1913 (member Alpha Omega Alpha); connected with Rockefeller Institute for Medical Research, New York City, 1913-1929^ as fellow 1913-14, assistant in Department of Physiology and Pharmacology 1914-17, associate 1917-1921, and associate member 1921-29; had since been research fellow and lecturer in Department of Physiology at Harvard; member China Medical Board of Rockefeller Foundation 1916-1929 and of its commission to China 1915; commissioned First Lieutenant, Medical Reserve Corps, April 17, 1917; assigned to Base Hospital, Fort Riley, Kans., in December, 1917, and to Camp Taylor, Ky., in November, 1918; received discharge January 18,1919; contributed to Journal of Medical Research, Journal of Experimental Physiology•, and Science; member Harvey Society, Optical Society of America, Society of Experimental Physiology, and American Association for the Advancement of Science. Married September 11, 1917, in Duluth, Minn., Dorothy Olcott (B.A. Smith 1913; M.A. Columbia 1917), daughter of William James Olcott (Ph.B. University of Michigan 1883, M.S. 1884, honorary M.A. 1908) and Fanny (Bailey) Olcott. Children: Olcott, Barbara, Frederick Taylor, ad, Dorothy, and Deborah. Death due to a fractured skull and brain hemorrhage. Cremation took place. Survived by wife, five children, three brothers* Franklin H. Gates, ’12, Russell C. Gates, ’14, and Percival T. Gates (B.A. Yale College 119 University of Chicago 192a), and three sisters, Alice Gates Pudney, wife of William K. Pudney (M.D. Columbia 1917), of Montclair, N. J., Lucia Gates Hooper, wife of Leverett F, Hooper (B.A. Harvard 1915), of New York City, and Grace Gates Mitchell, wife of Morns R. Mitchell (B.A. University of Delaware 1919), of Montclair. – SOURCE (PDF) – P.118-119
Your doctor knows nothing about nutrition? Ask him confidentially and he’ll probably confess he had only one course in nutrition. And there’s a reason.
Back in the late 19th century American medicine was in a deplorable state. To the credit of the Rockefeller General Education Board and the Institute for Medical Research, funds were made available to staff teaching hospitals and to eradicate some pretty horrible diseases. On the other hand, a chemical-based medicine was introduced and the medical profession cut its ties with naturopathy. Cancer statistics tell you the rest.
For the moment we want only to note that the impetus for reorganizing medical education in the United States came from John D. Rockefeller, but the funds were channeled through a single member of The Order.”
“One day in 1912 Frederick T. Gates of Rockefeller Foundation had lunch with Abraham Flexner of Carnegie Institution. Said Gates to Flexner:
”What would you do if you had one million dollars with which to make a start in reorganizing medical education in the United States?”
“Flexner’s reply, however, to the effect that any funds — a million dollars or otherwise — could most profitably be spent in developing the Johns Hopkins Medical School, struck a responsive chord in Gates who was already a close friend and devoted admirer of Dr. William H. Welch, the dean of the institution.”
Welch was President of the Rockefeller Institute for Medical Research from 1901, and a Trustee of the Carnegie Institution from 1906.”
”There is an Establishment history, an official history, which dominates history textbooks, trade publishing, the media and library shelves. The official line always assumes that events such as wars, revolutions, scandals, assassinations, are more or less random unconnected events. By definition events can NEVER be the result of a conspiracy, they can never result from premeditated planned group action. An excellent example is the Kennedy assassination when, within 9 hours of the Dallas tragedy, TV networks announced the shooting was NOT a conspiracy, regardless of the fact that a negative proposition can never be proven, and that the investigation had barely begun.
Woe betide any book or author that falls outside the official guidelines. Foundation support is not there. Publishers get cold feet. Distribution is hit and miss, or non-existent.
Just to ensure the official line dominates, in 1946 the Rockefeller Foundation allotted $139,000 for an official history of World War Two. This to avoid a repeat of debunking history books which embarrassed the Establishment after World War One. The reader will be interested to know that The Order we are about to investigate had great foresight, back in the 1880s, to create both the American Historical Association and the American Economic Association (most economists were then more historians than analysts) under their terms, with their people and their objectives. Andrew Dickson White was a member of The Order and the first President of the American Historical Association.”
It is true that in early 1918, before the first cases of Spanish flu were reported at Camp Funston at Fort Riley in Kansas in March 1918 ( here ), a trial of a vaccine made with inactivated strains of the meningococcus bacteria ( here ) was conducted on military volunteers at the same location. According to a report published in July 1918 by Frederick L. Gates, First Lieutenant of the Medical Corps, U.S. Army ( here ), the experimental vaccine created in the laboratory of The Rockefeller Institute was given to “about 3,700 volunteers” and the doses “rarely caused more than the mildest local and general reactions”, which included “headache, joint pains, and nausea” and in some cases, diarrhea.
While virology would not emerge until the 1930s, physicians could identify many of the bacteria causing the deadly pneumonias that were killing their patients, but without antibiotics they could do little to fight the infections. Thus, as the epidemic struck their camps, hospitals, ships, ports, or divisions, many medical officers documented what they saw, as if trying to define that which they could not control.
IF YOU’RE STILL NOT CONVINCED, YOU HAVEN’T FULLY READ THE REUTERS PIECE, IT DOES A GREAT JOB AT CONFIRMING EVERYTHING THEY WANT TO DEBUNK:
“Stephen Kissler, Postdoctoral Fellow of Immunology and Infectious Diseases at Harvard T.H. Chan School of Public Health ( here ) told Reuters via phone that the vaccine used at Camp Funston “was derived from existing meningitis strains” that were potentially inactivated with heat. He saw no reason to conclude a vaccine, which was made with existent, inactivated strains of meningitis bacteria from people who had previously been sick with meningitis, had “caused a major epidemic.”
As explained here the Office of Medical History of the U.S. Army Medical Department, meningococcal meningitis, which causes inflammation around the surrounding tissues of the brain ( here ), “has always been one of the most serious and important of the various communicable diseases of man” among soldiers. “It becomes more common when young people are together in closed quarters like dormitories or barracks,” so “the military had a good reason to test a vaccine against meningitis,” Burke said.
It was also not rare to research and test vaccines at this time in history given it was an “early era of microbiology,” Burke added. “The Fort Riley meningococcal vaccine experiment was not an unusual scientific undertaking” and “Many [bacterial] vaccine trials were going on all over the U.S. around 1918.”
The article “The State of Science, Microbiology, and Vaccines Circa 1918” by John M. Eyler provides more context ( here ). For example, during the 1918 flu pandemic itself, experimental bacterial vaccines for influenza were used in army camps as well as on workers, including 275,000 employees of the U.S. Steel Company ( here , here , here ). The cause of the pandemic was unknown at the time, explaining why bacterial vaccines were being tested in the hopes they might work on this new deadly disease.” – REUTERS
And this, my friends, was the kick-off for today’s Military BioTech Complex that I’ve just biographed. This was just an earlier Great Reset, like they regularly do. You have the military, the Rockefellers, the experiments, all the motives and the weapons, they assemble themselves like the Transformers. Only malfeasance or a severe cognitive-dissonance seizure could blame this on coincidence rather than conspiracy. Because if it’s not intentional, it’s coincidental, and you should know by know this is not a place for coincidence theories.
To be continued? Our work and existence, as media and people, is funded solely by our most generous supporters. But we’re not really covering our costs so far, and we’re in dire needs to upgrade our equipment, especially for video production. Help SILVIEW.media survive and grow, please donate here, anything helps. Thank you!
! Articles can always be subject of later editing as a way of perfecting them
THERE’S NO BETTER PREVENTION THAN SHARING THE KNOWLEDGE FASTER THAN THEY SHARE THEIR PROPAGANDA!
The original title of this article was URGENT! DEBUNKING THE NEXT ENGINEERED PANDEMIC: NIPAH VIRUS. I expanded the scope because in the meantime I learned they are ramping up propaganda for all three. These viruses have more things in common, as you will find out below.
You should actually begin with this earlier report:
To further develop the ChAd3 Ebola and Marburg vaccines, Sabin has entered into a Research Collaboration Agreement with the Vaccine Research Center at the National Institute of Allergy and Infectious Diseases. The Sabin Vaccine Institute, a non-profit organization founded in 1993, is a leading advocate for expanding vaccine access and uptake globally, advancing vaccine research and development, and amplifying vaccine knowledge and innovation. Sabin received more than $110 million for vaccine R&D programs from public and philanthropic funding sources, including the Bill & Melinda Gates Foundation, European Commission, Dutch Ministry of Foreign Affairs, Global Health Innovative Technology Fund and the Michelson Medical Research Foundation.
Washington DC, Oct. 21, 2021 (GLOBE NEWSWIRE) — The Sabin Vaccine Institute (Sabin) announced that the Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response within the U.S. Department of Health and Human Services, has exercised the third contract option, valued at $34.5 million, under the 2019 contract to advance the development of vaccines against Ebola Sudan and Marburg viruses through Phase 2 clinical trials.
In September 2019, BARDA awarded Sabin a development contract, valued up to $128 million, and has already provided funding of $40.5 million. This third contract option will enable continued nonclinical efficacy and safety studies, Phase 2 clinical trials in Africa, and vaccine manufacturing processes to ensure quality and safety.
In August, a case of Marburg disease was confirmed in the West African country of Guinea where the Ministry of Health officially declared an outbreak of Marburg.1 This recent case, as well as Marburg’s history of outbreaks and their potential for future devastating outbreaks, demonstrates that preventative measures are overdue to protect civilian populations, military personnel, first responders, health care workers and laboratory workers, both in the United States and abroad, against these emerging infectious diseases.
Ebola Sudan and Marburg viruses are closely related to Ebola Zaire virus, which has caused more than 2,200 deaths since 2018, leading the World Health Organization (WHO) to declare it a Public Health Emergency of International Concern. Like Ebola Zaire, Ebola Sudan and Marburg are among the world’s deadliest viruses, causing hemorrhagic fever with subsequent death in an average of 50 percent of cases.2,3
“Even as the world struggles with the COVID-19 pandemic, disease caused by Ebola Sudan and Marburg viruses continue to be a serious threat, as we have seen with the recent outbreak of Marburg in Guinea. We are grateful for BARDA’s continued support of Sabin’s efforts to advance vaccines against these deadly viruses,” said Sabin Chief Executive Officer Amy Finan. “We also thank our partners at the Vaccine Research Center of the NIH National Institute of Allergy and Infectious Diseases for their continued collaboration, and GSK for their earlier work on the candidates.”
The two candidate vaccines, based on GSK’s proprietary ChAd3 platform, were exclusively licensed to the Sabin Vaccine Institute from GSK in 2019.
This project has been funded in whole or in part with federal funds from the U.S. Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under contract number 75A50119C00055.
This above is the official Sabin Inst. press release, this below isn’t:
November 4, 2021 – The U.S. CDC published a Level Three Travel Advisory for the recent Ebola outbreak in the Beni Health Zone of the Democratic Republic of the Congo.
November 3, 2021 – The U.S. CDC vaccine advisory committee reviewed previous recommendation preexposure vaccination with Ervebo for adults aged ≥18 years in the U.S. population who are at highest risk for potential occupational exposure to Ebola virus species Zaire ebolavirus because they are: responding to an outbreak of Ebola Virus Disease (EVD), or work as health care personnel at federally designated Ebola treatment centers in the U.S., or work as laboratorians or other staff at biosafety level 4 facilities in the U.S.
November 2, 2021 – The WHO reported additional cases and deaths confirmed in the Ebola virus disease outbreak in the Democratic Republic of the Congo with two new health areas affected. A total of 394 people (67 primary care providers including nine high-risk contacts, nine contacts of contacts, and 49 probable contacts) have been vaccinated including 182 contacts of contacts, 125 probable contacts, and 87 high-risk contacts.
October 29, 2021 – A Research Article – Safety and immunogenicity of 2-dose heterologous Ad26.ZEBOV, MVA-BN-Filo Ebola vaccination in healthy and HIV-infected adults: A randomized, placebo-controlled Phase II clinical trial in Africa – was published by the journal PLOS Medicine. Conclusion – The Ad26.ZEBOV and MVA-BN-Filo combo vaccination were well tolerated and immunogenic in healthy and HIV-infected African adults. Increasing the interval between vaccinations from 28 to 56 days improved the magnitude of humoral immune responses. Antibody levels persisted to at least 1 year, and an Ad26.ZEBOV booster vaccination demonstrated the presence of vaccination-induced immune memory. These data supported the approval by the European Union for prophylaxis against EBOV disease in adults and children ≥1 year of age.
October 27, 2021 – IAVI announced an award of up to US$126 million from the Biomedical Advanced Research and Development Authority to develop two recombinant vesicular stomatitis virus (rVSV)-vectored filovirus vaccine candidates. This award supports preclinical activities and includes options for clinical development up to and inclusive of a Phase II clinical trial of IAVI’s rVSV Sudan ebolavirus vaccine candidate (rVSVΔG-SUDV-GP). Optional work that would continue the development of IAVI’s Marburg virus vaccine candidate (rVSVΔG-MARV-GP) that is currently supported by the Defense Threat Reduction Agency of the U.S. Department of Defense could be funded at a later date.
“Vectored” means, most likely, mRNA or some other genetic / nanotech targeting technology.
October 20, 2021 – The WHO African Region reported 5 Ebola cases, and over 27,000 travelers have been screened in the DRC. Furthermore, over 116 people have been vaccinated.
October 17, 2021 – Africa News reported Ebola vaccinations started in Beni, DRC, after at least two people died due to the virus in October 2021. The WHO African Region Tweeted DRC Situation Report (17/10/21) 5 confirmed cases, three deaths, 369 contacts identified, and 308 contacts monitored.
October 13, 2021 – Democratic Republic of the Congo (DRC) health officials confirmed an Ebola vaccination campaign had launched in the North Kivu province where one confirmed Ebola case, plus three related suspected deaths, were recently reported. About 1,000 doses of the rVSV-ZEBOV Ebola vaccine and other medical supplies were delivered from the capital Kinshasa to Goma city in North Kivu. The DRC has more than 12,000 vaccine doses in Kinshasa that can be deployed if necessary.
October 10, 2021 – The WHO reported additional Ebola cases related to the recent DRC case of a 3-year-old boy. A cluster of three deaths (two children and their father) who were neighbors of the case. These three patients died on 14, 19, and 29 September 2021 after developing symptoms consistent with Ebola. However, none were tested for the virus. As of October 9th, a total of 148 contacts have been identified and are under follow-up by the local response team.
October 8, 2021 – A case of Ebola has been confirmed in the eastern Democratic Republic of the Congo, five months after the end of the most recent Ebola outbreak there. The child died on October 6th. It was not immediately known if the Ebola case was related to the 2018-20 outbreak that killed more than 2,200 people in eastern Congo or the flare-up that killed six people in 2021.
September 13, 2021 – A new study based in Sierra Leone concluded the Ebola vaccine regimen from Janssen – J&J. It was found well tolerated with no safety concerns in children aged 1–17 years and induced robust humoral immune responses, suggesting the suitability of this regimen for Ebola virus disease prevention in children.
August 31, 2021 – The government of Cote d’Ivoire has informed the WHO that a second laboratory has tested samples from a patient suspected of having Ebola and has found no evidence of the virus. Around a dozen WHO experts were mobilized to support the country’s efforts, and 5,000 Ebola vaccine doses which WHO had helped Guinea procure were sent from Guinea to Cote d’Ivoire.
August 23, 2021 – The WHO African region reported Ebola booster dose vaccinations in Sierra Leone following administration of the prime dose of the Johnson & Johnson Ebola vaccine in May 2021. Frontline health workers, practitioners of traditional medicines or traditional healers, and commercial motorbike riders who received the first dose are now given their second jab to maximize their protection against the disease.
August 17, 2021 – The WHO confirmed Cote d’Ivoire deployed 2,000 vaccine doses from Merck and around 3,000 vaccine doses manufactured by Johnson & Johnson – Janssen.
August 14, 2021 – The WHO Africa reported the Ministry of Health of Cote d’Ivoire today confirmed the country’s first case of Ebola since 1994. This came after the Institut Pasteur in Cote d’Ivoire confirmed the Ebola Virus Disease in samples collected from a patient hospitalized in Abidjan’s commercial capital after arriving from Guinea.
August 9, 2021 – The WHO confirmed ‘Marburg virus disease (MVD) is a highly virulent, epidemic-prone disease associated with high case fatality rates (CFR 24-90%). In the early course of the disease, the clinical diagnosis of MVD is difficult to distinguish from other tropical febrile illnesses because of the similarities in the clinical symptoms. Differential diagnoses to be excluded include Ebola virus disease, as well as malaria, typhoid fever, leptospirosis, rickettsial infection, and plague.’
June 15, 2021 – The Southwest National Primate Research Center at Texas Biomedical Research Institute (Texas Biomed) has been awarded more than $37 million from the U.S. National Institutes of Health to continue operations into 2026. The P51 grant, given by the NIH Office of Research Infrastructure Programs, provides essential funding to house and care for nearly 2,500 non-human primates that are part of life-science research programs at Texas Biomed and partners around the globe.
June 4, 2021 – Johnson & Johnson welcomed a new recommendation by the Strategic Advisory Group of Experts on Immunization for the WHO that supports the use of the Johnson & Johnson Ebola vaccine regimen both during outbreaks for individuals at some risk of Ebola exposure and preventively, in the absence of an outbreak, for national and international first responders in neighboring areas or countries where an outbreak might spread.
April 10, 2021 – The government of Sierra Leone and the WHO announced Johnson & Johnson had donated about 4,500 Zabdeno and Mvabea Ebola vaccines to Sierra Leone to help prevent any Ebola outbreak. The last Ebola outbreak in Sierra Leone was in 2016.
March 25, 2021 – Ohio Gov. Mike DeWine revealed health officials are monitoring 44 people who have returned from areas of Africa with active outbreaks of Ebola.
March 25, 2021 – Oregon public health officials announced they are monitoring four people who recently visited the West African countries of Guinea and the Democratic Republic of the Congo. Regions in each of these countries are currently experiencing outbreaks of Ebola virus disease. The Oregon Health Authority and local public health departments have been in contact with these individuals, considered “persons under monitoring” since they arrived in the state earlier in March 2021.
March 23, 2021 – The WHO African Region Tweeted Guinea Ebola outbreak Situation Report (22/03/21) 18 cases, nine deaths, 78 contacts, 82% monitored. And 3,905 people have been vaccinated.
March 13, 2021 – After a request from the Guinean authorities, Russia is considering supplying a domestic vaccine against the Ebola virus to the African country, reported TASS.
May 13, 2020 – BARDA Provides the Sabin Vaccine Institute with an Additional $20 Million for Further Development of Ebola Sudan and Marburg Vaccines
The Sabin Vaccine Institute (Sabin) and its partner ReiThera Srl today announced that the Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response within the U.S. Department of Health and Human Services, has exercised the first two options, valued at $20 million, under the 2019 contract to advance the development of vaccines against Ebola Sudan and Marburg viruses through Phase 2 clinical trials. In September 2019, BARDA awarded Sabin a development contract, valued at $128 million, and provided the initial funding award of $20.5 million. This second $20 million award will enable the manufacture and release of clinical vaccine material developed by ReiThera, a specialist in the development and cGMP manufacture of adenoviral vector vaccines. The funding will also support non-clinical studies to evaluate efficacy and immune response.
UPDATE 5: NOVEMBER 7, 2021: MARBURG GOES VIRAL ON INTERNET ONLY, YET. I’m happy awareness increases, it’s crucial. I’ve addressed this virus below, but not many had the patience to go through all text, and I kind of understand them, but there’s no easier way than reading. Here’s another angle to keep in sight when computing all this info:
UPDATE 4: OCTOBER 19 2021: THE FEARPORN CAMPAIGN TAKES SPEED AS IF THEY ARE TO RELEASE THIS SOON. IF YOU FALL FOR THEIR BRAINWASH, THEY HAVE NO REASON TO STOP.
And they’re still not running out of stupid ideas we can see through:
Oh, look who pushes the fear! Exactly who I would’ve expected:
Later update: In the meantime I’ve learned that Marburg (an Ebola relative) and Xinjiang fever, a Chinese relative of the Yellow Fever virus, are also top candidates, and that goes in line with the Fauci e-mails I highlighted below. I will be back with more details shortly. Almost certainly it will be some form of hemorrhagic fever, most likely to cover for injections side-effects on the blood stream.
UPDATE 2:
One month later, they’re starting to catch up and it’s still not too late to un-play it if this goes BOOM NOW!
By the end of last century, The Military has abandoned you and has joined Pharmafia and the super-rich elites in a plan to govern you with bioweapons and psy-ops. As I’ve said many times, Big Pharma and Big Tech are long gone, The Military BioTech Complex has been running the show for quite a while. This is just a chapter from that book, more to come if we get some love.
Canadian lab’s shipment of Ebola, Henipah viruses to China raises questions
Henipah and Nipah are interchangeable
Scientists at the National Microbiology Lab sent live Ebola and Henipah viruses to Beijing on an Air Canada flight March 31, and while the Public Health Agency of Canada says all federal policies were followed, there are questions about whether that shipment is part of an ongoing RCMP investigation.
Ebola and Henipah are Level 4 pathogens, meaning they’re some of the deadliest viruses in the world. They must be contained in a lab with the highest level of biosafety control, such as the one in Winnipeg.
Two months after that shipment, on May 24, the Public Health Agency of Canada (PHAC) referred an “administrative matter” to RCMP that resulted in the removal of two Chinese research scientists — Xiangguo Qiu and Keding Cheng — and several international students on July 5.
Both agencies have said repeatedly that public safety has not been at risk.
PHAC will not confirm if the March 31 shipment is part of the RCMP investigation.
Strict protocols
Several sources, who have asked to remain anonymous because they fear for their jobs, say the pathogens may have been shipped to the Chinese Academy of Sciences in a way that circumvented the lab’s operating procedures, and without a document protecting Canada’s intellectual property rights.
Researchers working at the National Microbiology Lab on cutting-edge, high-containment research are not allowed to send anything to other countries or labs without the intellectual property office negotiating and having a material transfer agreement in place, in case the material sent leads to a notable discovery.
A PHAC spokesperson did not confirm if this shipment included such an agreement.
However, Eric Morrissette said it’s “routine” for the lab to share samples of pathogens and toxins with partners in other countries to advance scientific work worldwide.
“All transfers of Risk Group 4 samples follow strict transportation requirements and are authorized by senior officials at the lab and the NML tracks and keeps electronic records of all shipments of samples in accordance with the HPTA. Agreements for the transfer of materials are determined on a case-by-case basis,” Morrisette wrote in an email statement.
“On the specific shipments to China earlier this year, we can confirm that we have all records pertaining to the shipment, and that all protocols were followed as directed by the above Acts and Standards.”
Sources say Xiangguo Qiu and her husband, Keding Cheng, were escorted from the National Microbiology Lab in Winnipeg on July 5. (Governor General’s Innovation Awards)
Xiangguo Qiu is head of the National Microbiology Lab’s Vaccine Development and Antiviral Therapies section in the Special Pathogens Program. She is responsible for the lab that works with Ebola. Her husband, Keding Cheng, is also a PHAC biologist.
After their security clearance was revoked and they were escorted from the lab, the University of Manitoba also cut ties with them and re-assigned Qiu’s graduate students, pending the RCMP investigation. No charges have been laid.
Neither scientist has responded to requests for comment, although some of their former colleagues say Qiu is not just a world-renowned scientist who helped develop a treatment for Ebola, but also a researcher with ethics and integrity.
Case raises questions
One question raised by this case is that of intellectual property protection, says Leah West, who practises, studies and publishes in the field of national security law and lectures at the Norman Paterson School of International Affairs.
“If China was leveraging these scientists in Canada to gain access to a potentially valuable pathogen or to elements of a virus without having to license the patent … it makes sense with the idea of China trying to gain access to valuable IP without paying for it,” she said.
Leah West says she hopes the lab and Health Canada are doing an investigation in addition to the one the RCMP is conducting. (Submitted by Leah West)
West accepts PHAC’s assertion that public safety is not an issue, even though the viruses were transported on a commercial Air Canada flight.
However, she says the fact the RCMP is involved means there’s a legitimate concern.
“You don’t send a policy breach, a bureaucratic policy breach, to the RCMP to investigate unless you believe that that policy breach has resulted in a criminal offence or could have resulted in a criminal offence. So what is the criminal offence potentially here?” West said.
She said she hopes the lab and Health Canada are also doing an internal investigation.
“I think there will need to be an inquiry into the scientists to potentially see whether or not they were compromised or any elements of their work were compromised and that China gained illegal or improper access to Canadian intellectual property … to see what China may have gained access to without knowledge, prior to this incident,” West says.
Don’t ‘jump into any conclusions too quickly’
However, the deputy director of the University of Alberta’s China Institute is urging caution when it comes to making assumptions.
Jia Wang doesn’t dispute China has been involved in the past in espionage and intellectual property theft, but she says that country is making big investments in developing STEM (science, technology, engineering and mathematics) scholars and then putting that into innovation.
China has its own reasons to protect intellectual property because many new ideas are coming from there, Wang says.
She’s waiting to see what comes of the RCMP investigation of the lab in Winnipeg.
“As China observers, we’d like to perhaps gently remind people not to jump into any conclusions too quickly,” she said.
“It will be good to get to the bottom of this and see what might have gone wrong and what was the oversight and how can the procedures be improved or people involved can be reminded of how to adhere to the policies better.”
Jia Wang, deputy director of the University of Alberta’s China Institute, is advising caution about making assumptions concerning the case. (Submitted by Jia Wang)
The shipment of the viruses took place at a time when relations between Canada and China have been strained over the arrest of a Huawei executive, at the request of the United States.
In retaliation, China has detained two Canadians and is boycotting Canadian canola and pork.
Because of the strained relationship between the two countries, and this case at the lab, Chinese-Canadian researchers and academics are starting to worry they may be singled out and targeted, Wang said.
“Certain assumptions are made or their loyalty to Canada is questioned in any way. And as multicultural as we are in Canada, we don’t want to see that.” – CBC, 2019
On December 19, 2019, the U.S. Food and Drug Administration announced the approval of Ervebo to prevent EVD caused by Zaire ebolavirus in individuals 18 years of age and older. This report, published by the U.S. CDC on January 8, 2021, summarizes the Advisory Committee on Immunization Practices (ACIP) recommendations for using the rVSVΔG-ZEBOV-GP Ebola vaccine (Ervebo) in the USA.
On July 1, 2020, the European Medicines Agency granted Johnson & Johnson Janssen’s Zabdeno and Mvabea Ebola vaccine therapy, a prime-boost vaccination approach for preventing infectious diseases. Janssen’s Ebola vaccine regimen is specifically designed to induce long-term immunity against the Ebola virus in adults and children aged one year and above.
CanSino Biologics’s Ad5-EBOV Ebola vaccine received approval in China in October 2017. Ad5-EBOV is an adenovirus type 5 vector-based Ebola virus disease vaccine that protects against Ebola by relying on the recombinant replication-defective human adenovirus type-5 vector immune response. In addition, Ad5-EBOV is manufactured as a lyophilized powder, highly stable, and does not require storage at ultra-low temperatures. This feature renders it viable for use in resource-limited tropical areas.
The WHO published the revised Ebola Vaccine FAQ on January 11, 2020.
Henipaviruses belong to the family of paramyxoviruses. Two species have been identified to be zoonotic, causing disease in animals. These are the Hendra virus (HeV) and the Nipah virus (NiV). They produce severe and often fatal illness in humans and horses.
Samples from early Wuhan COVID-19 patients show the presence of genetically modified Henipah virus, an American scientist has found.
Henipah was one of the two types of viruses sent to China by Chinese-born scientists from a Canadian laboratory at the centre of a controversy over the firing of the scientists and collaboration with Chinese military researchers. It is not clear whether the virus found in the Chinese samples is related to the samples sent by the Canadian lab, which were shipped in late March 2019.
The finding was confirmed for The Epoch Times by another qualified scientist.
The evidence was first found by Dr. Steven Quay, a Seattle-based physician-scientist and former faculty member at the Stanford University School of Medicine, who looked at early COVID-19 samples uploaded by scientists at the Wuhan Institute of Virology (WIV) shortly after China informed the World Health Organization about the SARS-CoV-2 outbreak.
Chinese virologist Shi Zhengli is seen inside the P4 laboratory in Wuhan, China, on Feb. 23, 2017. (Johannes Eisele/AFP via Getty Images)
The samples from the patients, who reportedly were found to have the “unknown pneumonia” in December 2019, were uploaded to the genetic sequence database, GenBank, on the website of the U.S. National Institute of Health (NIH).
Quay says that while other scientists around the world were mostly interested in examining the genome of SARS-CoV-2 in the samples uploaded by the WIV scientists, he wanted to see what else was in the samples collected from the patients.
So he collaborated with a few other scientists to analyze sequences from the samples.
“We started fishing inside for weird things,” Quay told The Epoch Times.
What they found, he says, are the results of what could likely be contamination from different experiments in the lab making their way into the samples, as well as evidence of Henipah virus.
“We found genetic manipulation of the Nipah virus, which is more lethal than Ebola.” Nipah is a type of Henipah virus.
The Epoch Times asked Joe Wang, PhD, who formerly spearheaded a vaccine development program for SARS in Canada with one of the world’s leading pharmaceutical companies, to verify the finding. Wang is currently the president of NTD Television Canada, the sister company of The Epoch Times in Canada.
After examining the evidence, Wang said he was able to replicate Quay’s findings on the Henipah virus. He explains that the genetic manipulation of the virus was likely for the purposes of vaccine development.
Winnipeg Lab
The firing of Chinese-born scientist Xiangguo Qiu and her husband, Keding Cheng, from the National Microbiology laboratory (NML) in Winnipeg has been the subject of much controversy in Canada, with opposition parties pressing the government for more details on the case, and the government refusing to release information citing national security and privacy concerns.
Qiu and Cheng along with several Chinese students were escorted out of NML, Canada’s only Level 4 lab, in July 2019, amid a police investigation. The two scientists were formally fired in January 2021.
The Public Health Agency of Canada (PHAC), which is in charge of NML, said the termination was the result of an “administrative matter” and “possible breaches of security protocols,” but has declined to provide further details, citing security and privacy concerns.
House Speaker Anthony Rota admonishes Public Health Agency of Canada President Iain Stewart in the House of Commons on June 21, 2021, for failing to provide documents related to the firing of two scientists from the National Microbiology Laboratory in Winnipeg. (The Canadian Press/Sean Kilpatrick)
During her time at NML, Qiu travelled several times in an official capacity to WIV, helping train personnel on Level 4 safety. The Globe and Mail later reported that scientists at NML have been collaborating with Chinese military researchers on deadly pathogens, and that one of the Chinese military researchers worked at the high-security Winnipeg lab for a period of time.
Documents and emails released by PHAC show that the shipment of Henipah and Ebola samples was done with the permission of NML authorities.
In one of the emails sent in September 2018, David Safronetz, chief of special pathogens at PHAC, informs then-head of NML Matthew Gilmour and other lab administrators about the request from WIV for the shipment of the samples, saying “I trust the lab.”
In response, Gilmour asks about the nature of the work that will be done at the Wuhan lab, and why the lab doesn’t get the material from “other, more local labs.” He also tells Safronetz that it’s “good to know that you trust this group,” asking how NML was connected with them.
In his reply, Safronetz doesn’t specifically say what the samples will be used for in China, but notes they will only be sent once all paperwork and certification is completed. He also says the WIV is requesting the material from NML “due to collaboration” with Qiu.
He adds, “Historically, it’s also been easier to obtain material from us as opposed to US labs. I don’t think other, closer labs have the ability to ship these materials.”
Gilmour resigned from his position at NML in May 2020 and joined a UK-based bioresearch company.
MPs have asked NML management why shipment of the samples was allowed and whether they knew if China performs any Gain of Function (GoF) research at WIV. GoF research involves increasing the lethal level (virulence) or transmissibility of pathogens.
NML’s acting scientific director general Guillaume Poliquin told MPs during a parliamentary committee meeting on March 22 that the lab only sent the samples to WIV after receiving assurance that no GoF research would take place.
Conservative MP John Williamson pressed for more answers, saying the word of the state-run Chinese lab can’t be trusted as the Chinese regime “has a history of theft and lies.”
The issue of GoF research at WIV has been a point of contention in the United States between lawmakers and Dr. Anthony Fauci, NIH’s head of the National Institute of Allergy and Infectious Diseases, whose organization has funded research (through EcoHealth Alliance) on coronaviruses at the Wuhan lab. U.S. Sen. Rand Paul says published work from WIV on coronaviruses shows the lab is conducting GoF research, a charge Fauci denies.
The P4 laboratory on the campus of the Wuhan Institute of Virology in Wuhan, China, on May 13, 2020. (Hector Retamal/AFP via Getty Images)
The Epoch Times sought comment from PHAC, including as to how the agency addressed issues of intellectual property and the development of any products such as vaccines with WIV, but didn’t hear back by time of publication.
Despite repeated requests by opposition parties for more details related to the firing of the two NML scientists, the Liberal government has refused to provide records, saying there are national security and privacy concerns.
After the House of Commons issued an order for the government to disclose the information, the government took the Speaker of the House to court to obtain confirmation from a judge that it can withhold the documents. The government later dropped its court case once Prime Minister Justin Trudeau called an election and Parliament was dissolved. – Epoch Times
UPDATE 3: I FOUND CREDIBLE SOURCES FOR MOST OF DR. ARYANA LOVE’S EXPLOSIVE CLAIMS BELOW:
I didn’t have an in depth look at all her sources, I can’t have a final 100% verdict, but I did more than a glance and no lies detected. You can review her blog post yourself HERE. This might be the closure to this report and the start for another.
OBAMA: EBOLA RESPONSE A TRIAL RUN FOR A POTENTIAL AIRBORNE VIRUS THAT MIGHT HIT SOON (2014)
BONUS
This is from 2014, but the story goes a way long back. And forward. Let’s not forget Putin is a Davos regular since before he became such a literal czar.
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If you’re the kind of people who read this kind of websites, you should be aware of the fact that the US government has branded both of us as ‘terror threats’. They have also branded skepticism and dissidence as ‘mental illnesses’ or ‘psychological disorders’ before. Complying with their standards and wanting to show a collaborative side I’ve just discovered in myself, I’d like to rat on some organization that has caused tremendous damage and setbacks to ‘covid measures’.
Now, if anyone knows where I should file my report officially, please fax me the contacts!
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So, is this the world you guys plan to live in? Nazis are babies next to covidiots and you might be next in line. Not to have my fate, but to have this poor man’s fate…
Poor people get ‘terminated’ by medical assassins, then their partners in crime terminate any witnesses and whistleblowers. This seems to be the new business and social model. Our site is crippled again because YouTube terminated our second channel, without any possibility of appeal or anything. Ten minutes after the upload it was down. Just please watch the 100 seconds that triggered the Googlag mass-murderers so much and think for yourself!
Sorry for the site being incomplete again, we’re too poor to afford enough server space and our host, WordPress, only embeds censored platforms, but most articles should hold even without the video support. Most videos are already backed up on Odysee, Brighteon and Bitchute, I just can’t embed them here. We’re not done, just a bit hurt, but we’re exhausted of energy and resources, a lot is going out, very little coming in. Most exhausting is, though, watching people still feeding and collaborating with their Nemesis.
I still have some scattered back-ups and I’m going to make more and keep red-pilling YouTubers. Help, if you will, preaching only to the choir is not that efficient.
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We gave up on our profit shares from masks, if you want to help us, please use the donation button! We think frequent mask use, even short term use can be bad for you, but if you have no way around them, at least send a message of consciousness. Get it here!
No, I’m not going tabloid, bare this knuckle-head with me for a minute!
I’m guilty of fermenting well-founded indignation against some celebritard and professional tough guy who last year was begging “the powers that be” (exact quote) to save his tough ass from the Macarenavirus by locking his people down and ruining their lives, with military intervention, if needed. You may have heard of this clown that goes around unsupervised, yet heavily guarded, under the name of Conor McGregor. He beats people for money and he’s very good at it, apparently, and that’s the least annoying thing about him. And thing is he has just addressed his stupidity, proving he has taken his vitamins and has grown half a testicle since. So I have the professional obligation (no, I don’t, but it’s a good lesson) to reflect his latest brain-fart accurately. Point being: if we don’t take our daily dose of intellectual vitamins, we end up like this nitwit. I sweat hard to make it easier, I provide, free of charge, donations welcome, and my monthly earnings from this probably can’t pay a ticked to this door-knob’s 5-minute performances. But l retain immensely more human dignity and tight sleep from my position. I wish you what you wish yourself after watching this:
This was early 2020 when people where “collapsing in the streets” I was scared for my family. I urged everyone to sit tight for a few weeks to see where we land. My opinion on this situation now is night and day to then. I actually feel I was lied to originally. As where we all.
No, dipshit, we weren’t all lied! As a matter of fact, many of us sounded the alarm long before you vomited that abomination, and you social parasites slandered us, some still do. You learned your lesson 20 years too late to be an useful member of your society. See about catching up before your tiny brain falls out through your big mouth! There’s no scientific evidence for a novel coronavirus, it all points at your novel species of remote-controlled brainless NPCs being the cause for the current societal collapse.
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Not the writer, the first man to undertake the Covid gene therapy.
I closed the case in this post’s cover gif animation. All I have to add is a few references:
We're sorry to hear of the death of Coventry Labour stalwart Bill Shakespeare. Bill made global headlines as 1st first man to have Covid vaccine. His decades of service to the party were recently recognised by @Keir_Starmer. Our thoughts are with Joy and Bill's family & friends. pic.twitter.com/ANCTeGFYEs
“Experimental” means we are not done finding out what relates to it, how and when.
SILVIEW.media
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I survived many tough times focusing on the humor in them. And I find this highly amusing. But even more disturbing, when I look around and I see most people don’t flinch hearing such a claim.
As for insurances and vaccines, the topic of that Forbes article… oh boy, oh boy… Check this out! And then THIS!
Follow up:
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Sometimes my memes are 3D. And you can own them. Or send them to someone. You can even eat some of them. CLICK HERE
Facts speak a million times louder than the NPC noise around. And they say that, after the Unholy Trinity: Gates – Fauci -Schwab, this Biden clown is the most unpopular thing on TV and Internet. And it’s so easy to prove it.
I can’t stomach either, but Biden’s presidential foe gets a thousand times more thumbs up if he bats an eyelash alone in an elevator.
US is under a hostile takeover by illegitimate external powers, but most of it is too dumb to get it and all of them are too numb to protect themselves, forget about the country. The concept that this hairy sniffy babbly joke is a legitimate POTUS is utterly hilarious, not based on this evidence alone. But he is still on that chair because he is a legit mirror of US now: an old senile impotent Zionist slave being retired and replaced with a more vigorous an masculine China. If things aren’t even spoken as they are, how can they be bettered?
We spotted this new video getting destroyed and we seized the opportunity.
With your help, we are going to put them in a lose-lose-lose situation: – they let the video listed = they get destroyed – they unlist it and don’t delete the dislikes = a ton of people still have the link and can follow the developments, proving the point – they unlist it and delete the dislikes just as we predict = 200% ownage from all of us
How we accomplish that? Very simple: 1. Hit the video page, leave your love and take screenshots regularly 2. Spread this post and/or our video below, to get more people aboard
buh bye evidence!
It doesn’t get any more simple and fun.
UPDATE: Comments are already off, Biden is at 4000 dislikes, which is more than 10x the likes 😀
UPDATE 2: I THINK WE REACHED OUR FIRST TARGET: YOUTUBE KNOWS WE’RE WATCHING AND WHATEVER THEY DECIDE FROM HERE IT’S GONNA GO OUR WAY, OUTING THEM AS HACKS. JUST KEEP AT IT AND SPREAD THE WORD MUCH MUCH WIDER, PLS!
Notice that the views have more than doubled, reactions went up less than 50%, which is another tampering evidence
UPDATE MARCH 9TH: LMAO!
And yet another one!
How are you the most voted and popular with 500 likes / 80k views and YouTube has to pick up after every of your videos?
I rest my case but not my action. So our video is one of the few that actually hasn’t been unlisted yet because YouTube knows very well at this point we’re watching. But the reacts are still frozen, while views kept going up by about 50% again. Soon it’s gonna become most under-reacted video on Youtube, relatively to its views.
Took a while, instant gratification zombies didn’t bet on us much, but we made them crack!
Few people got involved, but those who did did a great job! Gateway Pundit kept following the subject, eventually RT and other bigger media sharks got in and the fraud is about to become mainstream.
As a result, YouTube is experimenting with removing the dislike button! BWAHAHAHA!
That’s no loss to people, just to zombies.
People should keep at it until BigTech removes itself from the planet, piece by piece!
I made this in January 2021. Let’s see when it hits everyone “by surprise”
THIS IS FAR FROM OVER! STAY TUNED!
UPDATE NOVEMBER 11, 2021: I THINK WE WON THIS ROUND
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! Articles can always be subject of later editing as a way of perfecting them
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