Be Strong Professor Johan Van Dongen: A Scientist’s Ordeal After Revealing Aids And Ebola Are Medical Crimes

Johan 10

“A lot has happened but I am safe for now, for no reasons I have been removed from LinkedIN social platform, losing almost all my contacts which I have build up in no time,” said Professor Johan Van Dongen, after I managed to get him in Holland.

This is the punishment meted out to the Dutch professor, Johan Van Dongen, formally at Microsurgical Educational Institute in Holland, for revealing to the world that the Ebola virus is human made and tested on black skinned people in Uganda and Zaire in Africa, in order to find vaccines against it for military defending purposes.

It will be recalled that on October 10, 2014, Diplomatic Aspects Newspaper’s journalist, Joel Savage, published the theory about the origin of Ebola in Africa, by Professor Johan Van Dongen, which research dates back as far as 1972. The professor wouldn’t like to tell me those against him for speaking the truth, but we all know. Without his knowledge I decided to publish this article. This is the kind of world we live in, world that one instantly becomes an enemy for speaking the truth.

In that publication, the Dutch Micro-Surgeon, Johan Van Dongen challenged Belgium’s professor Van der Groen’s over his claims that Ebola was invented in the 1960’s in Fort Detrick. How did he know that? Dongen asked. Was it because he knew Marburg virus experiments have been carried out in the former Belgian Congo, now Zaire, in Africa?

“ Vaccines which have been made by American, English, German and French scientists within the Yellow Fever Research Institute in Uganda, funded by the English Government and the Rockefeller Foundation, where also the with Marburg virus contaminated green monkeys came from” He added.

“I can’t live with this crime for the rest of my life. I’ve lost my job, my house and they stopped selling my book four years ago. The only thing I have strongly behind me is my wife,” says Professor Dongen. One thing people who like to cover up scandals and truth have failed to realize is, “It’s not everyone who is ready to join them in living that life of dishonesty and lies. Whatever a man sows that’s what he shall reap. I consider Professor Johan Van Dongen a hero.

I don’t think those making his life miserable for speaking the truth are genuine people. They are people far from God and truth, the reason they promote evil in the society. Good people don’t punish people for speaking the truth. That’s the same experience I am facing ever since I came to Belgium fourteen years ago, because I don’t praise their chocolate and waffles, instead, I speak about the heinous crime committed in Africa; crimes which they have praised, applauded by building statues, naming streets after the criminal King Leopold II, and the cowardly acts of most of their journalists that twist facts and cover up the truth.

For the benefit of building a healthy nation and for the sake of our children in the future, every faithful person on earth, should stand firm and support Professor Johan Van Dongen. As for me, if I die today, I will be happy to go down happily in my grave, because I’ve made them uncomfortable, by changing the landscape of journalism in Europe. They have secretly banned all my books in Belgium, but they can’t touch my soul, because that belongs to God.


Professor Johan Van Dongen’s Authentic Theory On The Origin Of The Deadly Ebola Virus

“The virus is human made and tested on black skinned people in Uganda and Zaire in Africa, in order to find vaccines against it for military defending purposes.”-Professor Johan Van Dongen.

Whenever there is epidemic or research on the origin of something, scientists come out with different theories that many aren’t accurate. We must ask ourselves, why is Darwin’s theory about human evolution now sits in a center of controversy? Today there are scientific facts proving Charles Darwin’s theory of evolution is far from the truth.

Since the outbreak of the deadly Ebola this year in Liberia, Sierra Leone and the Republic of Guinea, in West Africa, various inconsistent theories over the origin of the deadly virus are appearing in the newspaper daily. Holland’s professor Johan Van Dongen of Microsurgical Educational Institute in Holland shares his theories about the origin of Aids and Ebola, which his initial research began in 1972.

“How did the Soviets manage to get the Marburg virus only a few months after the outbreak in Marburg during the Cold War and lying behind the Iron Curtain? And how could there be an Ebola outbreak in Belgrade, also lying behind the Iron Curtain, at the same time happening in Marburg? “Asked Johan Van Dongen, the former Dutch Bio-technician, Micro/surgeon and coordinator of the National and International Experimental Course in Microsurgery and the author of ‘Pleidooi voor de Aap’-The truth behind Aids and other virus infections.

According to him, there are other strange data about the investigation of Ebola as a biological weapon in the United States. Because the American biological warfare effort was terminated only 2 years after the first Marburg outbreak which means they stopped in 1969. Since the discovery of MARV on the 22th August 1967 the virus is first identified on 20th November of the same year, three months after the outbreak had begun.

The successful isolation of the virus were first reported to the scientific community at the Fourth Congreso Latinamericano de Microbiologia in Lima, Peru on the 26th of November 1967, six days after the identification, So if Ebola came from laboratories of the US Army then, what is the connection of the presence of US Army and World Health Organization WHO and the Centers for Disease Control CDC facilities in the Philippines?

How is it possible that people from the World Health Organization examined Ebola contaminated pigs and a worker in a pig farm in Bulacan, before the outbreak in Reston in 1976? It is only the WHO and some elements of the US Army in the Philippines that have the capability to transport, spread and identify the Marburg virus in the early sixties. So who carried out the transport throughout the United States in the sixties? Asked Dongen.

The Dutch Micro-Surgeon challenges the Belgium’s professor Van der Groen’s claims that Ebola was invented in the 1960’s in Fort Detrick. How did he know that? Dongen asks. Was it because he knew Marburg virus experiments have been carried out in the former Belgian Congo, now Zaire, in Africa? Vaccines which have been made by American, English, German and French scientists within the Yellow Fever Research Institute in Uganda, funded by the English Government and the Rockefeller Foundation, where also the with Marburg virus contaminated green monkeys came from?

How is it possible that, following after the Fourth Congreso Latinamericano de Microbiologia in Lima, Peru on the 26th of November 1967, an article in German language could be published in; Deutsche Medizinische Wochenschrift on 22 December 1967? And one of the least but not the least question is: If Ebola came from laboratories of the US Army then; what is the connection of the presence of the US Army, the World Health Organization WHO and the Centers for Disease Control CDC in Ebola facilities in the Philippines in the sixties and seventies?

Firstly, as the Marburg virus before the outbreak in 1967 has not existed then, how is it possible that worldwide everybody works with the Marburg virus without Leve1-4 laboratories, and secondly how could they act without legal permission or official guidelines as I stated: It is noteworthy to remember the signing of the Geneva accord by Nixon in 1970?

According to all the aforementioned tracks, namely; involvement of national military, medical and pharmacological institutes, track of the green monkeys, the outbreak of MARV in 1967, its discovery, its detection and isolation as well as to publish about the virus at the Fourth Congreso Latinamericano de Microbiologia in Lima, Peru on the 26th of November 1967, only six days after the identification, then it is almost impossible that all those things happened within such a short notice of time.

In fact it is not possible and I think not even one single black skinned person in the most isolated part of Africa does believe that. Whatever the Marburg or Ebola virus may be it must be created long before its first outbreak in 1967. The virus is human made and tested on black skinned people in Uganda and Zaire in Africa in order to find vaccines against it for military defending purposes.


Professor Johan Van Dongen is a Dutch Micro-Surgeon at Micro-Surgical Educational Institute. From 1989 to 1997, he served at Maastrcht, Holland, writing and publishing of the “Manual of Microsurgery on the Laboratory Rat,” as a senior lecturer and co-organizer of the course of micro-surgery.

Besides this function he worked especially on the development of Alternatives in Animal Surgery in order to diminish the use of animals. Therefore he developed the “Anastomosis Simulator” and the “Artificial Rat” (Kunstrat) For these inventions in the field of Alternatives in Animal Experiments he received the “Price Alternatives for Animal Experiments” from the “Ministry of Health” of the Dutch Government at the Annual Congress of Animal Technicians

Under his administration at the Departments of General Surgery and Immunology, Johan Van Dongen at the Maastricht University As an all round experimental microsurgeon Johan van Dongen carried out thousands of heart-, kidney-, liver-, small bowell and Islets of Langerhans transplantation, as well as vessel-, nerves-, testes-, stomach- and spleen transplantation for immunological investigation of rejection. Furthermore he developed tissue suspensions and vaccines in order to manipulate the immunity of animals.

In 1977 He presented a new cardiac transplantation model, the so called “Extra Corporeal Cardiac Transplantation Technique”, in order to manipulate the graft extensively because of the subcutaneous position, at the Transplantation Society Meeting Helsinsinki Finland. At the same congress he also presented a new Cardiac Transplant Technique with Portal Venous Outlet and Local Per-fusion.

From October 1981 till May 1983 he organizes a National Courses in Microsurgery at the Department of Experimental Microsurgery at the Bio-medical Center Medical Faculty Maastricht the Netherlands. During the above mentioned period he also organizes Courses in Microsurgery at the Universities of: Stuttgart, Heidelberg and Mannheim Germany, University of Aarhus Denmark as well as the University of Mexico City Mexico.

Furthermore, Johan van Dongen gives technical assistance in the completion of sixty three Theses in the field of Immunology, Anatomy,Surgery,Biochemistry, Microbiology, Pathology, Physiology and Animal Technology. Professor Johan Van Dongen is the author of “Aids de grootste misdaad in de medische geschiedenis”. (Aids the Greatest Crime in Medical History) “Pleidooi voor de aap”. (Pleaded for the Ape) and Manual of Microsurgery on the Laboratory Rat.

Photo: Johan Van Dongen, the Dutch Micro/surgeon and coordinator of the National and International Experimental Course in Microsurgery.

The development Of Ebola Laboratory By Hitler’s Vassals In USA, Russia, Germany, Belgium And The Philippines.

Marburg 2

By Johan Van Dongen and Joel Savage

Western journalists, soldiers, politicians, as well as scientists, now over more than a decade after the second millennium, should realize what exactly took place in the last two hundred years on the African continent. Africa is used as a dumping ground for drugs, testing of drugs, exposing people to bio-warfare products and deliveries of war material to the wrong regimes, which have adversely affected the continent as well.

Actually you could say that the rest of the world have seriously abused Africa and degraded its people, as if they are creatures walking around on earth without brains, yet Africans are in the same products of Quantum Physics and Quantum Mechanics realized as whites, so I don’t understand why the many white leaders have taken advantage to treat blacks unfairly?

The aforementioned establishments should know what actually took place on the continent of Africa and therefore should also be aware of the fact that the United States Of  America, that claim ‘In God We Trust’  turned against God and became a land which supported Hitler’s evil and Nazi war criminals.

The shocking story of how America became one of the world’s safest postwar havens for Nazis, has revealed in Eric Lichtblau’s remarkable book: “The Nazis Next door. How America becomes a safe haven for Hitler’s men.”

Thousands of Nazis from concentration camps, guards to high-level officers in the Third Reich and other Nazi criminals, came to the United States after World War II and settled quietly to begin a new life. They had little trouble getting in, with scant scrutiny, many gained entry on their own as self-styled war “refugees,” avoiding the detection of their criminal history and their war crimes soon forgotten. But some had help and protection from the U.S. government.

The CIA, FBI, and the military, gave support to Hitler’s minions to work as spies, intelligence assets, and leading scientists and engineers, whitewashing their histories.

In the United States of America, the Nazi war criminals collaborated with top American scientists, to manufacture viruses of deadly diseases, financed by the CIA, the Rockefeller Foundation and their counterparts the Rothschilds, thus; Ebola and Aids viruses were some of the engineered diseases and spread by the Germans and Americans.

The same Nazi war criminals became normal American citizens, while years after the Second World War, the Jews captured in war concentration camps, were still going through the cruelties of life.  In America, the Nazi criminals taught students and they found out the way of making deadly viruses in animals. Financed by Bill Gates, vaccines were contaminated with the deadly viruses to be inflicted on Africans.

All the manufactured viruses, such as the Ebola virus got their names according to how they were prepared in the concerned laboratory or how it originated. But can someone for a moment think of and ask the reason Aids and Ebola have killed thousands of Africans.

*In 1989, the CDC reports, Ebola-Reston virus was introduced into quarantine facilities in Virginia and Pennsylvania by monkeys imported from the Philippines. No humans were infected.

*In 1990, Ebola-Reston virus was introduced once again into quarantine facilities in Virginia and Texas by monkeys imported from the Philippines. Four humans developed antibodies but did not get sick.

*In 1996, Ebola-Reston virus was introduced into a quarantine facility in Texas by monkeys imported from the Philippines. No human infections were identified.

*In May of 2004, a Russian scientist died of Ebola after accidentally pricking herself with a syringe while conducting research on infected guinea pigs in Siberia.

*A similar accident with Ebola had reportedly occurred several months earlier at the US Army’s biodefense laboratory at Fort Detrick in Frederick, Md., but the researcher involved didn’t acquire the disease. This incident is not listed on the CDC’s list of confirmed outbreaks, perhaps because the researcher didn’t develop antibodies.

In 2009, a scientist in Berlin, Germany accidentally pricked herself and was infected with Ebola. She was given an experimental vaccine as part of her treatment and did not become ill.

And only accidentally somebody dies because of a stupid accident. And what about all those students who are writing scientific papers and abstracts, as three of them are depicted, published in top medical journals in the last seventy years! Because Aids and Ebola viruses were man-made long before their outbreaks in black communities in Africa.

Lethal experimental infections of rhesus monkeys by aerosolized Ebola virus

Johnson E1, Jaax N, White J, Jahrling P,

Int J Exp Pathol. 1995 Aug;76(4):227-36.


The potential of aerogenic infection by Ebola virus was established by using a head-only exposure aerosol system. Virus-containing droplets of 0.8-1.2 microns were generated and administered into the respiratory tract of rhesus monkeys via inhalation. Inhalation of viral doses as low as 400 plaque-forming units of virus caused a rapidly fatal disease in 4-5 days.

The illness was clinically identical to that reported for parenteral virus inoculation, except for the occurrence of subcutaneous and venipuncture site bleeding and serosanguineous nasal discharge. Immunocytochemistry revealed cell-associated Ebola virus antigens present in airway epithelium, alveolar pneumocytes, and macrophages in the lung and pulmonary lymph nodes; extracellular antigen was present on mucosal surfaces of the nose, oropharynx, and airways.

Aggregates of the characteristic filamentous virus were present within the type I pneumocytes, macrophages, and air spaces of the lung by electron microscopy. Demonstration of fatal aerosol transmission of this virus in monkeys reinforces the importance of taking appropriate precautions to prevent its potential aerosol transmission to humans.

Transmission of Ebola virus (Zaire strain) to uninfected control monkeys in a biocontainment laboratory

Jaax N1, Jahrling P, Geisbert T, Geisbert J, teele K, McKee K, Nagley D, Johnson E, Jaax G, Peters C.

Lancet. 1995 Dec 23-30;346(8991-8992):1669-71.


Secondary transmission of Ebola virus infection in humans is known to be caused by direct contact with infected patients or body fluids. We report transmission of Ebola virus (Zaire strain) to two of three control rhesus monkeys (Macaca mulatta) that did not have direct contact with experimentally inoculated monkeys held in the same room.

The two control monkeys died from Ebola virus infections at 10 and 11 days after the last experimentally inoculated monkey had died. The most likely route of infection of the control monkeys was aerosol, oral or conjunctival exposure to virus-laden droplets secreted or excreted from the experimentally inoculated monkeys. These observations suggest approaches to the study of routes of transmission to and among humans.

Lethal experimental infection of rhesus monkeys with Ebola-Zaire (Mayinga) virus by the oral and conjunctival route of exposure

Davis K.J, Geisbert TJ, Vogel P, Jaax GP, Topper M, Jahrling PB.

Arch Pathol Lab Med. 1996 Feb;120(2):140-55.



The source of infection or mode of transmission of Ebola virus to human index cases of Ebola fever has not been established. Field observations in outbreaks of Ebola fever indicate that secondary transmission of Ebola virus is linked to improper needle hygiene, direct contact with infected tissue or fluid samples, and close contact with infected patients.

While it is presumed that the virus infects through either break in the skin or contact with mucous membranes, the only two routes of exposure that have been experimentally validated are parenteral inoculation and aerosol inhalation. Epidemiologic evidence suggests that aerosol exposure is not an important means of virus transmission in natural outbreaks of human Ebola fever; this study was designed to verify that Ebola virus could be effectively transmitted by oral or conjunctival exposure in nonhuman primates.


Adult rhesus monkeys (Macaca mulatta) were exposed to Ebola-Zaire (Mayinga) virus orally (N=4), conjunctively (N=4), or by intramuscular inoculation (N=1, virus-positive control).


Four of seven monkeys exposed by the conjunctival route, three of four monkeys exposed by the oral route, and the intramuscularly inoculated positive control monkey were successfully infected with Ebola-Zaire (Mayinga). Seven monkeys died of Ebola fever between days 7 and 8 post-exposure, but one of the monkeys given aggressive supportive therapy and a platelet transfusion; lived until day 12 post-exposure.


Belgian scientist and discoverer of Ebola, Peter Piot, knew everything about the virus but wouldn’t say publicly was a medical crime against Africa, because his country was involved.


Findings from the experiment study confirm that Ebola virus can be effectively transmitted via the oral or conjunctival route of exposure in nonhuman primates.

Well, Nazi students prepared many dangerous viruses, thus; everyone blames them for the crimes they committed, but the real question is: Who discovered officially those devilish and deadly viruses? It was a Belgian scientist named Peter Piot!

Peter Piot

Nearly 40 years ago, a young Belgian scientist traveled to a remote part of the Congolese rainforest – his task was to help find out why so many people were dying from an unknown and terrifying disease. In September 1976, a package containing a shiny blue thermos flask arrived at the Institute of Tropical Medicine in Antwerp, Belgium.

Working in the lab that day was Peter Piot, a 27-year-old scientist and medical school graduate training as a clinical microbiologist. “It was just a normal flask like any other you would use to keep coffee warm,” recalls Piot, now Director of the London School of Hygiene and Tropical Medicine. But this thermos wasn’t carrying coffee – altogether inside was a different cargo.

Nestled among a few melting ice cubes were vials of blood along with a note. It was a Belgian doctor based in what was then Zaire, now the Democratic Republic of Congo – his handwritten message explained that the blood was that of a nun, also from Belgium, who had fallen ill with a mysterious illness which he couldn’t identify.

The samples were treated like others, lab tested, but when the scientists placed some of the cells under an electron microscope they saw something they didn’t expect. “We saw a gigantic worm-like structure – gigantic by viral standards,” says Piot. It was a very unusual shape for a virus, only one other virus looked like that of the Marburg virus.” The Marburg virus was first discovered in 1967 when 31 people became ill with hemorrhagic fever in the cities of Marburg and Frankfurt in Germany and in Belgrade, the capital of Yugoslavia.

This Marburg outbreak was associated with laboratory staffs who were working with infected monkeys imported from Uganda – seven people died. Piot knew how serious Marburg could be – but after consulting experts around the world, he got confirmation that what he was seeing under the microscope wasn’t Marburg, but different which hasn’t been seen before. After that what’s next?Marburg

Aids And Ebola: Why So Much Military Personnel Involved In The Fight Against The Diseases In Africa?

The Ebola scandal

Instead of sending medical staff to Ebola-struck countries, Obama sent the military force, raising a lot of suspicions that Ebola is indeed a medical crime

By Johan van Dongen and Joel Savage

Following the first article, ‘Message to all African leaders,’ over Aids and Ebola as medical against Africans, which was published in, Reverend P.A. Wilson made a comment over the article on December 16, 2014. Below is his comment.

“This is gross wickedness to humanity. What have Africans done to deserved this? The eyes of The Lord moves to and fro throughout the whole earth , to make himself strong to those whose heart are perfect towards Him. My prayer is “Let God arise and let His enemies be scattered.” May The good Lord who gives life to humanity (Africans) take vengeance and bring the West to exposure and bring them to justice for He (GOD) vengeance is mine I will repay. To you all writers to expose such malicious and wicked device of those haters of Africans, God will guide and guard you all in standing for truth. God bless you.”


Open letter to reverend Wilson

Honourable Reverend Wilson we will like to thank you for the inspirational words of God , which have encouraged us to continue with our efforts to bring those who are responsible for these medical and other crimes committed in Africa to justice.

You may have noticed that few weeks after your statement, we have published an indictment about these committed crimes onto the websites of Sprout-Africa and the blog of Joel Savage in order to activate African lawyers to pick up our discussion published onto websites and within our book: “Aids and Ebola the greatest crime in medical history against mankind.”

We are not mere revealing the truth about the origin of these diseases without facts, the truth is guided by 25.000 scientific papers, published in the most important scientific journals. The truth can be read in scientists and medical journals like the Lancet and Immunology do also.

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US military personnel in Africa to fight against Ebola.

Together with our findings, we will use these publications as a reference for bringing governments, pharmaceutical plants, investment groups and specific persons to the International court of Justice in The Hague, the Netherlands.

As we said, Reverend Wilson, they are probably continuing their crimes because of what we have written below, in our publications, onto the social media, in our indictment and within our books.  If you want to look for yourself, how they act, the only thing you have to do is to follow the way the respective establishments discuss their application of experimental Ebola and Aids vaccines and their dangerous medicines to cope with these criminal diseases.

The World Health Organization WHO

When you read our book “Aids and Ebola the greatest crime in medical history against mankind” on this very website “Spout-Africa”, our “indictment” and second message to all African leaders, you will notice again the appearance of all those institutes and pharmaceutical plants who collaborated to vaccinate millions with experimental vaccines in Africa.

It gives us goosebumps and the feeling as we turned back to the period during the “First, Second and Cold War” when pharmaceutical plants were raised in Germany and after the wars committed those crimes in the jungles of Central Africa.

WHO and non-approved vaccines and Dr. Marie-Paule Kieny

Immediately after a World Health Organization panel was installed they advised that it was ethical to use experimental, non-approved drugs to combat the ongoing Ebola virus epidemic in West Africa. There was unanimous agreement among the experts that in the special circumstances of this Ebola outbreak, “it is ethical,” said Dr. Marie-Paule Kieny, Assistant Director-General of the United Nations Health Agency.

“This is typically a disease of poor people in poor countries where there is no market,” Kieny said. “If it hadn’t been for the investment of a few governments in the development of a vaccine, we would have been nowhere.”

Have you heard something like that before? Is it really ethical to use unregistered interventions that have shown promising results in the laboratory and in animal models? What is the consequence of unknown adverse effects in humans for possible treatment of people who are infected? Did they know of the scrupulous actions of Hillary Koprowski?

Have they read our book “Aids and Ebola the greatest crimes in medical history against mankind published on Although for some vaccines it looks like they are working in the short term, but what about the long term effects and exposure to such experimental Ebola vaccines and what about these previous symptoms of volunteers?

Of course, the use of unregistered vaccines could cause some problems, they say, taking poor African people into consideration. Why is it necessary to talk about this? Doesn’t poor African know how important these criminal medical experiments are for stakeholders of the pharmaceutical industry as discussed in our indictment?

A Tulane professor working at the Emerging Infections Department of Naval Medical Research Unit 6

Why is it that so much western military personnel are involved in the fight against Ebola? Many countries such as Cuba, China and several other countries send healthcare workers, doctors and technical personnel but the United States of America and the United Kingdom respectively sent 7000 and 3000 troops. What are they doing there exactly?

Why is the U.S. Department of Emerging Infections of Naval Medical Research Unit 6 involved with experimental vaccines again? But if you have read the indictment article, then you will notice why again the appearance of all those institutes and pharmaceutical plants wants to vaccinate millions with experimental vaccines.

Ebola vaccines trials

Due to the recent Ebola virus outbreak in 2014, the National Institutes of Health (NIH) announced that initial treatment testing of  investigational vaccines to prevent Ebola virus disease will begin early 2015 in Africa.

This phase 1 clinical trial will help investigators at the NIH and Glaxo Smith Kline (GSK) determine the safety and efficacy of a new vaccine against Ebola. In another major trial, a vaccine has been carried out within the fall of 2014; this vaccine is being developed by the Public Health Agency of Canada and NewLink Genetics Corp. In addition, the NIH has partnered with the British consortium to test the National Institutes of Allergy and Infectious Diseases/GSK vaccine in the United Kingdom and in the West African countries of Gambia and Mali. Again in Africa onto ignorant people with a different genetic pattern!

Therefore we would like to warn all African leaders to take notice for what has happened in the past and what we have described in our books, social media, and websites!!!

It is said by many scientists that these vaccines do not contain live Ebola viruses, only antigens or parts of the virus that can stimulate a protective immune response. The vaccines can’t cause Ebola infections, they say, but if so, then why are antigens against Ebola were found in Africans after smallpox and polio vaccinations?

The pharmaceutical industry considers and accesses the ethical implications for clinical decision-making of use of unregistered interventions that it have shown promising results in the laboratory and in animal models but that have not yet been evaluated for safety and efficacy in humans. But African Leaders, laboratory circumstances and animal models and primates are not African natives but ‘Human Rats’…!!!…

Daniel Bausch a Tulane professor

Daniel Bausch at the end of 2014 stated: “If it’s easier to do the trial, by using an active control rather than a placebo, then fine, do the trial that way,” Smith says. “But to believe one is more ethical than the other is not the issue.” He stressed that the main benefit of joining a vaccine trial, especially in resource-strained countries like these, is that people who do develop the disease “are generally looked after better than people not in trials.”

This is, therefore, a message to all African leaders in West Africa, especially Gambia and Mali, because there they come again to do what they know best,to infest. The pharmaceutical industry always will act the way as they did in the past because of the fact that they couldn’t compare the laboratory outcome of experimental vaccines with human beings. Especially Africans and who will stop them?

African leaders and governments are too much dependant of the Western Countries, China, Russia, and Japan. Therefore experimental vaccines will be given to ignorant Africans as they did in the past with dramatic consequences such as Aids, Ebola, Burkitt’s Lymphoma and many other brand new diseases!

There have been some significant developments in both vaccines and treatments for Ebola and its sister virus, Marburg virus scientists say. What about this last mentioned virus? The Marburg virus is a virus which has been made in biochemical warfare laboratories in Reston, Marburg, Frankfurt, Belgrade and Russian laboratories in the fifties and sixties as we have described in our book.

We hope all African leaders will listen to us because Bausch most suddenly will not! Why not? Because of the fact that he stated: “That the obstacle to developing an Ebola vaccine isn’t the science; researchers have actually made really great strides in figuring out how to fight back against Ebola and the Marburg virus. We now have a couple of different vaccine platforms that have shown to be protective with non-human primates,” Bausch says. As a naval officer, he received awards for his work containing disease outbreaks in Uganda. He is currently stationed in Lima, Peru, as the director of the military: “Emerging Infections Department of Naval Medical Research Unit 6.


There are concerns, for example, about Ebola being used as bioterrorism, and that drives a lot of the funding for this. The U.S. Department of Defense might be interested in a vaccine if they thought the disease could be used as a weapon.

They think there could be a case for limited widespread use if that doesn’t sound too contradictory.

Bausch: “I wouldn’t anticipate it would be cost-effective or really practical to take the approach of widespread vaccination. It would work more like how we currently handle Yellow Fever: when you have an outbreak, you go in and really rapidly vaccinate the 100,000 or so people who are in the area that is at risk. I would see it more like that, but with an Ebola vaccine. We would go in right away and say, the next day, we have 100,000 doses with our teams and start protecting people.

So far it’s been more tossed around but not really acted on yet. There is one exception, but it wasn’t an outbreak. There was a needle-stick injury in a lab, and that person was able to get a post-exposure Ebola vaccine. The person didn’t get sick, but we don’t know if the vaccine was what protected him. We can’t even be sure the accident infected him. The only conclusion we can make is that, with this sample size of one, is that person did not have severe side effects from taking it.”

To investigative, journalist Joel Savage and scientist Johan van Dongen seem something between ‘shotgun’ experiments in African countries and walking on the edge of a volcano, as they did in the past as described in “Aids and Ebola the greatest crime in medical history against mankind.”

Reverend Wilson? Are you there?

Friday, December 12, 2014

The clinical trial of an Ebola vaccine has faced a problem in Switzerland

Some white volunteer patients have complained of joint pains in their hands and feet after a clinical trial in Switzerland at the University of Geneva Hospital, said on Thursday in a statement that: “scientists decided to stop the trial one week early in all 59 volunteers as a measure of precaution.”

But why are they continuing their trials in Africa then??!!**

It is noted that four volunteers complained of the side-effects of the vaccine, which is developed by pharmaceutical company NewLink and recently bought by Merck.

Doctors and Scientists of the Geneva Hospital stated: “They are all fine and being monitored regularly by the medical team leading the study.”

The hospital said also that it would resume human safety trials on January 5, 2015, with the participation of 15 volunteers after checks take place to ensure the joint pain symptoms were “benign and temporary.”

Spread of Ebola

Ebola spreads through contact with infected bodily fluids such as blood, saliva, sperm and sweat. It has killed around two-thirds of those it has infected over the last four decades. At this very moment, the virus has killed more than 7.500 people in West Africa, most of them in Guinea, Liberia, and Sierra Leone. This figures were raised by the U.S. Centers for Disease Control CDC and the WHO, but are these figures accurate? We don’t believe the figure is real because Ebola victims are rotting in the streets mounted up in remote areas and hide in slums of big cities.

The epidemic has slowed down in Liberia and Guinea the authorities say, but: “Transmission still continues across large parts of Sierra Leone,” the World Health Organization, the United Nations Public Health Body, have also stated that.

Military 5

American soldiers destined to Africa to fight Ebola.

Scientific Statements

Knoxville lab to test potential Ebola vaccine

Merck told  NBC News the volunteers with symptoms similar to rubella are okay, adding this is a measure of caution.

In the study in Switzerland, it was more than 10 times the dose that would be our highest dose of our study here, Dr. Smith added.

Dr. Smith said there are no signs of any problems with testing or volunteers on the same vaccine at Walter Reed Army Medical Center in Washington D.C.

The 70 local people who qualified for the test were told to wait a few weeks. The study here at home is to see if smaller doses of the vaccination would still fight off Ebola in larger quantities.

I’m sure that with the change in schedule, some people will be unable to participate or lose interest, Dr. Smith said.

He expects to test in Knoxville to begin in January 2015


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