Zika Virus: Factories Of Nazi Comrades Revealed

 

Bio-weapon Zika virus

A child affected with Zika Virus: The disease is a bio-weapon but World Health Organization is lying and deceiving the public

.By Micro-Surgeon and Scientist Johan Van Dongen

The scientific origin of the Zika virus is that the virus is named after the Ugandan Zikabos because it was there for the first time in 1947, isolated from the blood of a Rhesus monkey. It was only in 1968, the virus succeeded demonstrating in people.

The Zika virus is endemic in large parts of Africa. As a result of human influences, the virus also surfaced in Asia, including countries in Central Asia, South East Asia and Yap Island (Micronesia) in the Pacific.

At that specific time, the fear is that the virus will quickly spread through the different islands in the Pacific Ocean will and eventually reach the American continent. That fear has become a reality by ending up in South America and Germany today, the country of Hitler.

The Zika virus in South America, adds as a third virus disease, which can be transmitted by the Aedes aegypti mosquito, shows symptoms that match a mild form of dengue, including joint pain, headache, and fever.

On November 6, 2015, the virus also made headlines in Suriname. The laboratory of the University Hospital Paramaribo (AKKAR) has fixed may argue that some patients have sustained the Zika virus. In January 2016 first Zika test virus was developed in Germany. The researchers found out that only one in five people infected with the Zika virus will get sick.

Rockefeller Foundation in Entebbe (Uganda)

Supranational poison factories must keep running, so every day with loads of drugs out of the gate they are flooded and can be found anywhere in the world, once sold. All indications in the past century, there are science experiments in Africa with a number of manipulated infinite microorganisms in Saharan Africa and beneath. It was clear from the outset as Africa became an excellent breeding ground for those interested.

In 1936, the British Government and the Rockefeller Foundation in Entebbe (Uganda), built the Yellow Fever Research Institute. In the very isolated regions of Bwamba, West Nile Virus (1940) and a Bwamba-fever virus (1941) were discovered. In 1944, they met the Semliki Forest virus, and in 1946, two more viruses were found. They were the Mengo-encephalitis virus and the Bunyavirus (like the Crimean-Congo virus and the hantavirus which is a member of the Bunya-aviridae).

American and British scientists found out that the region of Uganda was actually swarmed with viruses. In the fifties and sixties were fifteen others, among the ‘Bwamba group. Recharged viruses found in an area mainly occupied by agricultural population. According to the Englishman Cook, in 1901, very rarely faced diseases occurred.

Within a few decades, Bwamba became a unique cluster of the most remarkable and particularly malicious virus species, which from the outset have been very willing to rely on researchers from France, England, and the United States, once one of those viruses again struck somewhere.

During the Cold War, Uganda was engaged with both military and civilian doctors. In Bwamba region, the Yellow Fever Research Institute was then very active and in Entebbe and in the Zika forest, much research was conducted by the East African Virus Research Institute. In addition, several military hospitals were scattered across the country. Hospitals were located near the city of Arua. EH Williams and Kuluva-hospitals, serving the American mission in 1941. Between 1951 and 1965, Williams’ hospital recorded more than 41,000 patients with the same disease.

For over 50 years, the region is plagued by various diseases in the city Arua. Between 1943 and 1944, there raged very deadly measles epidemic. In the early sixties, many infants had anemia and half of those children later died of malaria infection, according to official statements. The Kaposi’s sarcoma was active and in 1966, there was an epidemic of Burkitt’s lymphoma, followed by an outbreak of Hepatitis-B.

After 1970, the inhabitants of the region were particularly affected by tetanus infections and in 1978, the measles came back. In the eighties, it is known that people were suffering from AIDS and in 1989 and 1990, scientists from the Institute Pasteur were back to inject Ugandan children with 1,558,800 doses of TB vaccine. Thereafter, in Kenya and Zimbabwe, it was recorded that the vaccine had serious side effects. The diseases were then given all sorts of weird names but not the name that was right: “AIDS!”

Old Nazi institutes continue their collaboration with western institutes.
There were also three foreign delegations present namely Behringwerke AG, in Marburg, am Lahn and the Paul Ehrlich Institute, in Frankfurt am Main, both from Germany. What they did in the Second World War, we all know about it and there was also the Institute of Sera and Vaccine Immunology in Zagreb, from the former Yugoslavia.

Precisely those three institutions were closely involved in the development of the Ebola virus, which was officially born in 1967, in the German Marburg. Whereas the Wistar Institute one of the world’s leading institutes has became involved especially in the field of retroviruses and Aids in humans and animals.

Present were very smart people, but beware of the fact that they showed that ‘smartness in a form of stupidity’ because why should they use human beings to carry out experiments? They all discussed the highlights of a large number of vaccines specifically tested in Central and West Africa and innocent people were executed.

These were supposedly tested vaccines against smallpox, polio, measles, leukemia and Epstein Barr Virus. Especially the latter virus in the civilized countries just causes glandular fever, but in African countries, it leads to cancer and AIDS as a result of genetic manipulation.

The development and testing of viruses on humans and animals were mainly conducted under the auspices of the CIA and the necessary biological warfare preparations were manufactured by MSD and Litton BioNetic. The first South African who went over to ring the bell was a physician. When he published his research, what happened next: He had a motorcycle accident and was killed.

News of that accident appeared in a local newspaper in the Ugandan city of Kampala, an article that the CIA was accused of the fact that its employees disguised as scholars and journalists, spreading lies about the origin of the AIDS virus just as they did to Thabo Mbeki.

Not long after this verbal battle ended, in the house of Wilson Carswell, one of the leaders of the Ugandan AIDS research, his entire contents, including computer equipment and all files were completely destroyed. At least that was officially notified. Carswell, a soldier of the British Army, ostensibly managed to escape.

Later he dived into the complex biological warfare from the British in Porton Down. Since he became head of the AIDS Unit, at the Department of National Health, he was primarily responsible for population change in South Africa outage.

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.

Johan 2

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……

TB 3

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:

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