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

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“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.

NB. BELOW IS THE ORIGINAL ARTICLE WHICH HAS BEEN TAKEN AWAY FROM THE WEB WITHOUT ANY TRACE; AFTER PUBLICATION AT DIPLOMATIC ASPECTS NEWSPAPER.

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?

Conclusion:
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.

Biography

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.

http://www.shout-africa.com/bottom-story/opinion-origins-of-aids-a-new-view-on-the-origin-of-the-world-wide-aids-problem

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

http://www.amazon.com/Greatest-Medical-History-Against-Mankind-ebook/dp/B016W89W1G

Pharmaceutical Disease Producing Factories Administered Dangerous Isoniazide And Sulfadiazide To Spread Tuberculosis

“Pharmaceuticals Companies Make Business With Intentionally Created Diseases In Africa”- Professor Johan Van Dongen.

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Professor Johan Van Dongen, the former Micro-Surgeon.

According to the German scientist Wolff Geisler, thousands of Aids patients affected with tuberculosis in Africa, are not caused by the HIV virus. In my opinion he is right, because the increase of the number of tuberculosis patients in Africa, is a result of intended spread of the disease through dangerous medicines like Isoniazid and Sulfadianozide , given to Africans in tuberculosis clinics in African countries, such as Burundi, the former Belgian Congo, Uganda and Zambia. Instead of curing, the two mentioned medicines rather cause a tremendous acceleration of HIV infections amongst African people.

The WHO/IUATLD Working Group And Wolff Geisler

In 1989, the WHO/IUATLD working group declared in the “Bulletin International Union Tuberculosis Lung Disease” that HIV in TB-hospitals could have been spread as a result of unhygienic anti-tuberculosis injections, but as a former micro-surgeon, I, Johan van Dongen challenge them to prove that statement.

Again according to Wolff Geisler, remarkably horrendous numbers of HIV-infections originate only from US American or British financed and managed hospitals in the respectively mentioned countries. For instance in hospitals in Kitgum and Kagando in Uganda (where there was no recognizable USA or British finance), 10% of the TB patients, normally an average of 15% of the total population were HIV infected.

Aids Causing Factories

According to the World Health Organization, in Africa 17-55% of TB patients have HIV-antibodies. The WHO expert Slutkin mentioned 30-60% in some of the developing countries, a clear sign of intentional infection of tuberculosis patients in Zambia with HIV. The same evidence was provided by the same expert in the Chinkala Hospital, TB patients Mazubuku. 23% of the TB patients in the middle of 1987 were also infected with HIV.

Six months later, the virus was located in 50% of patients within the same hospital, after administering Isoniazid and Sulfadiazide. The same figures slightly increased in 58% of TB patients in Ndola, and in 60% of TB patients in the University Teaching Hospital in Lusaka, Zambia.

In the Makalala Sanatorium in Kinshasa, Zaire, 33% of TB patients had HIV antibodies (among the staff: 4-8%), and in Chinkankata 36%. In Malawi, 50-66% of TB patients also had HIV antibodies. In the TB clinic, Centre Anti Tuberculeux de Bujumbura in Burundi, 55% of TB patients were HIV-infected in 1986, and in the Mwanza region of Tanzania, 25% of TB patients had HIV-antibodies. Moreover, the patients were treated with forbidden drugs, because in New York, 1972, about 21 people who were taking intravenous agents had succumbed to inexplicable tuberculosis before 1972.

Already written in a previous article, in contrast, patient with a cellular deficiency hypersensitivity following the polio- and cowpox vaccinations, are particularly prone to certain bacterial, viral and protozoal infections caused by Mycobacterium tuberculosis TB. And then the pharmaceutical disease producing factories appear by using deadly toxic agents such as Isoniazid, produced by Teva Netherlands BV (Holland, and Sulfadiazide, produced by Pfizer in Germany.

What Is Tuberculosis?

Tuberculosis is a chronically infectious disease which generally affects the lungs. The causing agent, tubercle bacilli, is mostly passed on from person to person through coughing of droplets from the respiratory tract (lungs), and can also be transmitted onto the skin, eyes of persons in the immediate vicinity. Tubercles also can penetrate the body through drinking.

A striking phenomenon! Side Effects Of Isoniazid And Sulfadiozanide.

Hospitals, including Mbare Hospital in Harare, were suddenly full of tuberculosis patients and the people were suffering from venereal diseases at the same time, as a side effect consequence, because Isoniazid and Sulfadiazide made them susceptible for these. It is obvious that Isoniazid and Sulfadiazide are the cause of these venereal diseases because it appears in almost all infected children under the age of ten.

As described before, in Africa tuberculosis and HIV go hand in hand, but the mass spread of tuberculosis infections in Africans with Aids is not caused by HIV-infection at all. The increase in the number of African TB patients is the result of intended spread of special tuberculosis agents, and patients treated with Sulfadiozanide and Isoniazid at the end caught Aids!

Disease Factories Using Isoniazid And Sulfadiozanide

The two medicines, Isoniazid and Sulfadiazide, shouldn’t have been used as medications against TB and most certainly not in Aids patients. Only the long list of side effects gives you the shivers. Therefore we will describe a list with side effects causing a huge amount of invented new diseases in order to sell more medicines against these side effects……

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Tuberculosis patients in a hospital.

Side Effects Caused By Isoniazid And Sulfadiazide There we go! And We Are starting With:

“Anxiety, blurred vision, changes in menstrual periods, chills, cold sweats, coma, confusion, cool, pale skin, decreased sexual ability in males, depression, dizziness, ‘dry’ puffy skin, fast heartbeat, feeling cold, headache, increased hunger, nausea, nervousness, nightmares, seizures, shakiness, slurred speech, swelling of front part of the neck, unusual tiredness or weakness and last but not least: weight gain.”

There You Have It. And If You Think This List Of Side Effects Is Completed, Not at all! There Is More: Let’s continue:

“Abdominal or stomach pain, back- leg- or stomach pains, ‘black’ tarry stools, bleeding gums, bleeding under the skin, blindness or vision changes, “blistering, peeling, or loosening” of the skin, bloating, blood in the urine or stools, “bluish-colored lips, fingernails or palms”, burning of the face or mouth, –burning, crawling, itching, numbness, painful, prickling, “pins and needles”, or tingling feelings–, chest pain, cloudy urine, clumsiness or unsteadiness.

Constipation, continuing ringing or buzzing or other unexplained noise in the ears, cough or hoarseness, cracks in the skin, darkened urine, decrease in the amount of urine, diarrhea, difficulty with breathing, difficulty with moving, dizziness or lightheadedness, feeling of discomfort, fever with or without chills, general body swelling, general feeling of tiredness or weakness, headache, hearing loss.

Indigestion, itching- joint or muscle pain, light-colored stools, loss of appetite and weight, loss of heat from the body, lower back or side pain, muscle pain or stiffness, nosebleeds, not able to pass urine, pain or burning while urinating, painful or difficult urination, “pains in the stomach side or abdomen and possibly radiating to the back”, pale skin, pinpoint red or purple spots on the skin, rapid heart rate, rash, “red skin lesions often with a purple center.”

Red irritated eyes, red swollen skin, redness of the white part of the eyes, scaly skin, “seeing, hearing, or feeling things that are not there”, seizures, shakiness and unsteady walk, shortness of breath, sore throat, soreness of the muscles, sores, ulcers, or white spots on the lips or in the mouth, sudden decrease in amount of urine, swelling around the eyes.

“Swelling of the face, hands, legs, and feet”, swelling or inflammation of the mouth, swollen lymph glands, swollen or painful glands, tightness in the chest, “unsteadiness, trembling, or other problems with muscle control or coordination”, unusual bleeding or bruising, upper right abdominal pain, vision changes, vomiting, weakness in the hands or feet, wheezing, yellow eyes or skin.”

“Some side effects do not need medication, because of fear, you will pay a visit to a doctor, you have to pay consultation fee, you also have to pay for the prescription and medicines and together we pay billions of dollars to the pharmaceutical industry, and  in turn they pay scientists, pharmacists and everybody else who wants to be paid in order to sell medicines for causing the above-mentioned side effects for the production of diseases.”

Pharmacists, Doctors And Scientist Paid By The Pharmaceutical Industry

Some Sulfadiazine side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects but do check with them if any of the following side effects continue, or if you are concerned about them.

And for each and every one of these checks, because of side effects you will pay a visit to a doctor, you have to pay for the consultation fee, you also will have to pay for the prescription and medicines and together we pay billions of dollars to the pharmaceutical industry and the pharmaceutical industry pay scientists, pharmacists and everybody else, who wants to be paid in order to sell medicines for causing the above-mentioned side effects for the production of diseases.

Incidence Side Effects Not known

Feeling of constant movement of self or the surroundings, hives or welts, the sensation of spinning, restlessness, and trouble with sleeping.

Healthcare Professionals Applies To Sulfadiazine: Compounding Powder, Oral Tablet Causing Hypersensitivity

Hypersensitivity side effects include urticarial rash (most common), allergic myocarditis, anaphylactoid reactions, anaphylaxis, arthralgia, conjunctival and scleral injection, drug fever and chills, epidermal necrolysis, erythema multiforme, exfoliative dermatitis, generalized skin eruptions, periorbital edema, photosensitization, serum sickness, Stevens-Johnson syndrome, and urticaria.

The use of sulfonamide antibiotics, including sulfadiazine, is associated with large increases in the risk of Stevens-Johnson syndrome and toxic epidermal necrolysis, although these phenomena are rare as a whole.

Hematologic

Hematologic side effects include agranulocytosis (0.1%), aplastic anemia, hemolytic anemia (0.05%), hypoprothrombinemia, leukopenia, methemoglobinemia, and purpura. Hemolytic anemia occurs less often with sulfadiazine than with other sulfonamides. Aplastic anemia may be more likely in patients with poor bone marrow reserves.

Gastrointestinal Side Effects

Gastrointestinal side effects include nausea, vomiting, abdominal pain, diarrhea, anorexia, pancreatitis, and stomatitis.

Hepatic Side Effects

Hepatic side effects are rare but can be serious. Isolated cases of hepatitis and jaundice due to cholestasis have been associated with sulfadiazine. Elevated liver function tests (with a negative hepatitis panel) have been reported in at least one case associated with psychosis.

Psychiatric Side Effects

Psychosis associated with Sulfadiazine and Pyrimethamine therapy in patients with AIDS and CNS toxoplasmosis has been described in two separate case reports. In each case, tremulousness and disorientation developed within three days to two weeks after starting therapy, despite partial resolution of the size of the intracranial T Gondii lesions. No other obvious cause for mental status changes was found.

The delirium resolved upon discontinuation of therapy in each case and was reproducible upon re-challenged. In one case, the patient had elevated liver function tests (hepatitis panel was negative), which were reversible upon discontinuation of therapy. Psychiatric side effects include frank psychosis in patients with AIDS and CNS toxoplasmosis. Tremulousness, disorientation, and delirium have been reported.

Nervous System Side Effects

Nervous system side effects include ataxia, convulsions, hallucinations, headache, insomnia, mental depression, peripheral neuritis, tinnitus, and vertigo.

Renal Side Effects

Renal side effects include crystalluria, lupus erythematosus, periarteritis nodosa, toxic nephrosis with oliguria and anuria, and acute renal failure secondary to crystalluria or tubulointerstitial nephritis.

Genitourinary Side Effects

In one case, analysis of the stone fragments showed a composition of 100% acetylated 2-sulfanilamidopyrimidine, a metabolite of sulfadiazine.

Genitourinary side effects include urolithiasis.

Metabolic Side Effects

Metabolic side effects have included hypoglycemia.

Endocrine side effects

Endocrine side effects associated with sulfonamides have rarely included diuresis, goiter production, and sialadenitis.

If you swallow Isoniazid and Sulfadianozide or AZT as mentioned in one of our previous articles, then you are a lunatic.

References:

  1. Tenant-Flowers M, Boyle M, Carey D, et al “Sulphadiazine desensitization in patients with AIDS and cerebral toxoplasmosis.” AIDS 5 (1991): 311-5
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