Bio-warfare Laboratories Of German And Japanese War Criminals Under The Guidance Of USA: The Revealing Voices of AIDS/HIV Theory Dissidents

Case

By Johan van Dongen and Joel Savage

The horrific Aids pandemic, tremendously has generated scientific controversies within and outside the scientific establishment. Only a minority of scientists, like Johan van Dongen, and other engaged people have access to inside information concerning (bio-warfare) Aids and Ebola research.

As an experimental micro-surgeon in the early seventies, almost at the beginning of the multiple organ transplantation era,  Micro-Surgeon Johan van Dongen did carried out thousands of experimental organ transplantation. In order to deal with organ rejection, he administered, radiation and sera for diminishing the immunity of the organ receiver. Besides that he also administered uncountable agents to recipients of organs in order to trigger, diminish or completely wipe out the immune capacity which can be compared with Aids.

During his university and hospital appointments in the early seventies, and later undercover in the pharmaceutical industry, he discovered that animals didn’t die because of rejection of the transplanted organ but because of multiple infections which can be compared with human Aids victims. So, Johan van Dongen noticed that Aids can be induced by radiation, aflatoxins, Immuran/prednisolone combination, anti-lymphocyte sera, and many other bio-warfare agents.

Dormant HIV virus

As head of the Department of Experimental Microsurgery, and involved in all transplantation and immunological experiments, Johan also had been involved in many controversies. Especially the connection of his work and the polemic concerning the transmission of HIV.  In many ways, he discovered not only in his experiments but also in the extensive scientific literature the role of an obligatory co-factor that trans-activates the “Dormant” virus HIV in specific human cells. This obligatory co-factor which trans-activates the “Dormant” virus in specific human cells are deliberately introduced into mostly black-skinned people, collectively, Africans, governed by massive environmental factors, as you can read in our book: “Aids and Ebola the greatest crime in medical history against mankind,” in order to depopulate Africa.

Therefore we will always like to enlighten readers about the real origin of Aids and the true nature of famous international researchers as Robert Gallo. And as far as Gallo is concerned, Ricardo Veronesi, professor of the Faculty of Medicine at the University of Sao Paulo, was personally informed about the true nature of  Gallo’s research long before this controversy turned into a public scandal and as a consequence thousands of scientific Aids dissidents.

It was no less than Francoise Barré-Sinoussi of the French Pasteur Institute, who revealed the criminal intention of Gallo. And not only she became an Aids dissident but also the discovery of the HIV virus Luc Montagnier disputed Gallo, the fake discoverer of the HIV virus. In their opinion, the major bursts in the common scientific approach lie in its ignoring that the pathogenic of the HIV. Indeed it is governed by multiple deliberate environmental factors and one of these determinant factors is the PCR test (Polymerase Chain Reaction Test).

Polymerase Chain Reaction Test

This test is a technology in molecular biology used to amplify a single copy or a few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence. Especially the diagnosis of hereditary diseases; the identification of genetic fingerprints, used in forensic sciences and paternity testing; and the detection and diagnosis of infectious diseases. The PCR test can be used to investigate the connection of diseases to the specific black race. Moreover, PCR can be extensively modified to perform a wide array of genetic manipulations not only in humans but also from microorganisms which cause Aids and Ebola.

Using an extrapolation of these kinds of techniques we can conclude that almost all persons who have HIV in their bodies, were purposely infected with this virus which can lead to Aids. Bio-warfare scientists are able to make black people artificially susceptible to HIV or Ebola by using controllable diseases as a cover-up.

Most of the biowarfare research using viruses which cause Aids and Ebola was predominantly carried out in Germany and Japan until 1945 and since then mainly in the USA and France, using Nazi and Japanese (military) scientific war criminals.

The Revealing Voices of Aids/HIV Theory Dissidents

The official scientific origin of the diverse HIV-strains has been placed somewhere between 1938 and 1948 when scientist T.F. Smith et al published an article in the authoritative medical journal Nature about this period in 1988 named: “The phylogenetic history of immunodeficiency virus”.

He wasn’t the only scientists who revealed the true nature of the HIV virus. Smith’s efforts to reveal the real origin of HIV was followed, to name a few, by Sharp et al with his article: “Understanding the origins of Aids viruses”, also in Nature, followed by Meyers et all with: “The phylogenetic analysis of the HIVs”. But the most important article is described in the top of the bill of medical journals the Lancet by scientist L.A. Evans et al who discovered the; “Simultaneous isolation of HIV-1 and HIV-2 from an Aids patient”.

All these mentioned scientists agreed that the distribution of the HIV virus was an intentional action. Their findings make it very conceivable that this distribution was intentional because sometimes both the new viruses HIV-1 and HIV-2, respectively HTLV-IV, are existing in one and the same person according to Evans. And because his publication is checked by the editing and scientific boards of the Lancet the outcome of his investigation was true. This counts also for thousands of publications in other medical journals as described in our book “Aids and Ebola the greatest crime in medical history against mankind.”

German scientist Wolff Geisler

According to the famous Aids/HIV theory dissident Wolff Geisler, further evidence of the intentional distribution, out of the mentioned simultaneous infection of the same persons, it was described as a second Aids epidemic in the same black-skinned population, by an inefficient transmission of the HIV virus. The appearance of this extremely rare retrovirus among the African Aids patients is so conspicuous that some world-famous scientists uttered a sentence about it. They alleged this to be; “Only another acquired opportunistic infection but rather an additional death sentence”. But is it?

In Africa, the probability of an early death of HIV patients is three times bigger than elsewhere when HIV patients are simultaneously infected with HTLV-1 as described in the Lancet by Page et al in his scientific publication: HTLV-I/II seropositivity and death from Aids among HIV-I seropositive intravenous drug users (Lancet, 1990; 335: 1439-41), an even more extremely important publication for the Aids/HIV theory dissidents. Because especially HTLV-I, among many other HIV viruses, was only demonstrated in Uganda, Ghana, South Africa, and Namibia.  HIV patients only in these countries appear simultaneously up till now.

According to Wolff Geisler, the concomitant existence of HTLV-I and HIV produces the observed rate of Aids patients in Uganda, Kenya and black-skinned people in Florida, USA and some Caribbean Islands, even though in general black people are by nature more resistant against HIV-infection than pale-skinned persons (see below). This means the HIV viruses are genetically engineered as described in our book.

No less than Luc Montagnier et al, the discoverer of the HIV virus stated that this virus is made out of the Nazi eugenics and genetic engineered experiments as well as the development of Aids-causing viruses in horses. In a very talked about an article he described in the authoritative Annals of Virology: “A new type of retrovirus from patients presenting with lymphadenopathy and acquired immune deficiency syndrome”: Structural and anti-genetic relatedness with Equine Infectious Anemia Virus EIAV (horse Aids), 1984; 135E: 119-31.

Equine Infectious Anemia Virus EIAV (HIV/Horse-Aids) made by Nazi Germany.

If we compare these findings to our references in “Aids the greatest crime in medical history against mankind” the book now available at Amazon, the HLA-A, B, C, DR3 and DR5 loci, is examined by the Nazi’s led by Otmar Verschuer.

In 1956 he joined the American Eugenics Society and worked under auspices of the Rockefeller-fund. He was also head of the Department of the Kaiser Wilhelm Institute in Germany.

Furthermore, we have to take into account that within people who have blood type HLA-DR3 Aids, it is much less common than in people who have the HLA-DR5 type. Under the Nazi’s research, it is important to note that precisely the HLA-DR5 type occurs mainly in Jews. The HLA-DR3 type contrast is most common in dark-colored Africans.

These two shreds of evidence or references are enough to let you know vividly what took place. In general, you can say that it is harder for blacks to get Aids than as it is for whites, but blacks have been made susceptible for a broad spectrum of brand new diseases caused by Germans, partly under the auspices of the South African Apartheid regime, and after the war under guidance of the U.S.A.

Nowadays we now know that monkeys do not get Aids when infected with the human Aids virus. The same goes for tuberculosis until the moment that monkeys in a laboratory made receptive. Therefore black-skinned people are under no circumstances contaminated with Aids by monkeys with or without eating them. That is so to speak a criminal scientific fairy tale.

Ebola Outrage: U.S. Department Of Defense “Manufactured Ebola Virus” Under Guise Of Vaccinations.

NEW EBOLA 2

Original article by Josey Wales and published in http://beforeitsnews.com/

A startling report from the Liberian Observer, Liberia’s largest newspaper, claims that the United States is directly responsible for scientifically engineering the Ebola virus in a bioterrorism lab and injecting Africans with it through the guise of vaccinations.

The wildly accusatory article, by Dr. Cyril Broderick, Titled “Ebola, AIDS Manufactured By Western Pharmaceuticals, US DoD?” Claims that the Department of Defense unwittingly used Africans to test experimental bioweapons by pretending they were vaccinating them against disease.

“Reports,” he argues, “narrate stories of the US Department of Defense (DoD) funding Ebola trials on humans, trials which started just weeks before the Ebola outbreak in Guinea and Sierra Leone.”

What’s more is that over a month ago, as reported by Jeff Rense.com, ,

The Ebola Breakout Coincided

With UN Vaccine Campaigns

By Yoichi Shimatsu

Exclusive to Rense.com

The Ebola pandemic began in late February in the former French colony of Guinea while UN agencies were conducting nationwide vaccine campaigns for three other diseases in rural districts. The simultaneous eruptions of this filovirus virus in widely separated zones strongly suggests that the virulent Zaire ebola strain (ZEBOV) was deliberately introduced to test an antidote in secret trials on unsuspecting humans.

The cross-border escape of Ebola into neighboring Sierra Leone and Liberia indicates something went terribly wrong during the illegal clinical trials by a major pharmaceutical company. Through the lens darkly, the release of Ebola may well have been an act of biowarfare in the post-colonial struggle to control mineral-rich West Africa.

 Earlier this year, rural residents eagerly stood in line to receive vaccinations from foreign-funded medical programs. Since the cover-up of the initial outbreak, however, panicked West Africans rural folk are terrified of any treatment from international aid programs for fear of a rumored genocide campaign.
 The mass hysteria is also fueled in a region traditionally targeted by Western pedophiles by the fact that filovirus survives longer in semen than in other body fluids, a point that resulted in murderous attacks on young men believed to be homosexuals. Ebola detonated fear and loathing, and perhaps that is exactly the intended objective of a destabilization strategy.
This ongoing series of investigative journalism reports on the ebola crisis exposes how West Africans are largely justified in their distrust of the Western aid agencies that unleashed, whether by mistake or deliberate intent, the most virulent virus known to man.

Guilt Without Doubt

 A pair of earlier articles by this writer examined the British and American roles in developing Ebola into a biological weapon and its antidotes into commercial products.
 This third essay examines the strange coincidence of the earliest breakout in Guinea with three major vaccine campaigns conducted by the World Health Organization (WHO) and the UN children’s agency UNICEF. At least two of the vaccination programs were implemented by Medicins Sans Frontieres (MSF, or Doctors Without Borders), while some of those vaccines were produced by Sanofi Pasteur, a French pharmaceutical whose major shareholder is the Rothschild Group.
By: Dr. Cyril Broderick, Professor of Plant Pathology

Dear World Citizens:

 I have read a number of articles from your Internet outreach as well as articles from other sources about the casualties in Liberia and other West African countries about the human devastation caused by the Ebola virus.
 About a week ago, I read an article published in the Internet news summary publication of the Friends of Liberia that said that there was an agreement that the initiation of the Ebola outbreak in West Africa was due to the contact of a two-year-old child with bats that had flown in from the Congo.
 That report made me disconcerted with the reporting about Ebola, and it stimulated a response to the “Friends of Liberia,” saying that African people are not ignorant and gullible, as is being implicated.
 A response from Dr. Verlon Stone said that the article was not theirs, and that “Friends of Liberia” was simply providing a service. He then asked if he could publish my letter in their Internet forum. I gave my permission, but I have not seen it published.
Because of the widespread loss of life, fear, physiological trauma, and despair among Liberians and other West African citizens, it is incumbent that I make a contribution to the resolution of this devastating situation, which may continue to recur if it is not properly and adequately confronted. I will address the situation in five (5) points:

1. EBOLA IS A GENETICALLY MODIFIED ORGANISM (GMO)

Horowitz (1998) was deliberate and unambiguous when he explained the threat of new diseases in his text, Emerging Viruses: AIDS and Ebola – Nature, Accident or Intentional. In his interview with Dr. Robert Strecker in Chapter 7, the discussion, in the early 1970s, made it obvious that the war was between countries that hosted the KGB and the CIA, and the ‘manufacture’ of ‘AIDS-Like Viruses’ was clearly directed at the other.
In passing during the Interview, mention was made of Fort Detrick, “the Ebola Building,” and ‘a lot of problems with strange illnesses’ in “Frederick [Maryland].” By Chapter 12 in his text, he had confirmed the existence of an American Military-Medical-Industry that conducts biological weapons tests under the guise of administering vaccinations to control diseases and improve the health of “black Africans overseas.”
The book is an excellent text, and all leaders plus anyone who has an interest in science, health, people, and intrigue should study it. I am amazed that African leaders are making no acknowledgments or reference to these documents.
2. EBOLA HAS A TERRIBLE HISTORY, AND TESTING HAS BEEN SECRETLY TAKING PLACE IN AFRICA

I am now reading The Hot Zone, a novel, by Richard Preston (copyrighted 1989 and 1994); it is heart-rending. The prolific and prominent writer, Steven King, is quoted as saying that the book is “One of the most horrifying things I have ever read. What a remarkable piece of work.”

As a New York Times bestseller, The Hot Zone is presented as “A terrifying true story.” Terrifying, yes, because the pathological description of what was found in animals killed by the Ebola virus is what the virus has been doing to citizens of Guinea, Sierra Leone, and Liberia in its most recent outbreak: Ebola virus destroys peoples’ internal organs and the body deteriorates rapidly after death.
It softens and the tissues turn into jelly, even if it is refrigerated to keep it cold. Spontaneous liquefaction is what happens to the body of people killed by the Ebola virus! The author noted in Point 1, Dr. Horowitz, chides The Hot Zone for writing to be politically correct; I understand because his book makes every effort to be very factual.
The 1976 Ebola incident in Zaire, during President Mobutu Sese Seko, was the introduction of the GMO Ebola to Africa.

3. SITES AROUND AFRICA, AND IN WEST AFRICA, HAVE OVER THE YEARS BEEN SET UP FOR TESTING EMERGING DISEASES, ESPECIALLY EBOLA

The World Health Organization (WHO) and several other UN Agencies have been implicated in selecting and enticing African countries to participate in the testing events, promoting vaccinations, but pursuing various testing regiments.
The August 2, 2014, article, West Africa: What are US Biological Warfare Researchers Doing in the Ebola Zone? by Jon Rappoport of Global Research pinpoints the problem that is facing African governments.
Obvious in this and other reports are, among others:
(a) The US Army Medical Research Institute of Infectious Diseases (USAMRIID), a well-known center for bio-war research, located at Fort Detrick, Maryland;
(b) Tulane University, in New Orleans, USA, winner of research grants, including a grant of more than $7 million the National Institute of Health (NIH) to fund research with the Lassa viral hemorrhagic fever;

(c) the US Center for Disease Control (CDC);

(d) Doctors Without Borders (also known by its French name, Medicins Sans Frontiers);

 (e) Tekmira, a Canadian pharmaceutical company;

(f) The UK’s GlaxoSmithKline; and

 (g) the Kenema Government Hospital in Kenema, Sierra Leone.

Reports narrate stories of the US Department of Defense (DoD) funding Ebola trials on humans, trials which started just weeks before the Ebola outbreak in Guinea and Sierra Leone.

The reports continue and state that the DoD gave a contract worth $140 million dollars to Tekmira, a Canadian pharmaceutical company, to conduct Ebola research.
 This research work involved injecting and infusing healthy humans with the deadly Ebola virus.
Hence, the DoD is listed as a collaborator in a “First in Human” Ebola clinical trial (NCT02041715, which started in January 2014 shortly before an Ebola epidemic was declared in West Africa in March.
Disturbingly, many reports also conclude that the US government has a viral fever bioterrorism research laboratory in Kenema, a town at the epicenter of the Ebola outbreak in West Africa.
The only relevant positive and ethical olive-branch seen in all of my reading is that Theguardian.com reported, “The US government funding of Ebola trials on healthy humans comes amid warnings by top scientists in Harvard and Yale that such virus experiments risk triggering a worldwide pandemic.” That threat still persists.
4. THE NEED FOR LEGAL ACTION TO OBTAIN REDRESS FOR DAMAGES INCURRED DUE TO THE PERPETUATION OF INJUSTICE IN THE DEATH, INJURY, AND TRAUMA IMPOSED ON LIBERIANS AND OTHER AFRICANS BY THE EBOLA AND OTHER DISEASE AGENTS.
The U. S., Canada, France, and the U. K. are all implicated in the detestable and devilish deeds that these Ebola tests are.
 There is the need to pursue criminal and civil redress for damages, and African countries and people should secure legal representation to seek damages from these countries, some corporations, and the United Nations. Evidence seems abundant against Tulane University, and suits should start there. Yoichi Shimatsu’s article, The Ebola Breakout Coincided with UN Vaccine Campaigns, as published on August 18, 2014, in the Liberty Beacon.

5. AFRICAN LEADERS AND AFRICAN COUNTRIES NEED TO TAKE THE LEAD IN DEFENDING BABIES, CHILDREN, AFRICAN WOMEN, AFRICAN MEN, AND THE ELDERLY. THESE CITIZENS DO NOT DESERVE TO BE USED AS GUINEA PIGS!

 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.

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.

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  14. Reboli AC, Mandler HD “Encephalopathy and psychoses associated with sulfadiazine in two patients with AIDS and CNS toxoplasmosis.” Clin Infect Dis 15 (1992): 556-7
  15. Young C “Acute encephalopathy associated with sulfadiazine in a patient with AIDS-related complex.” J Infect Dis 160 (1989): 163-4
  16. Dusseault BN, Croce KJ, Pais VM Jr “Radiographic characteristics of sulfadiazine urolithiasis.” Urology 73 (2009): 928.e5-6
  17. Crespo M, Quereda C, Pascual J, Rivera M, Clemente L, Cano T “Patterns of sulfadiazine acute nephrotoxicity.” Clin Nephrol 54 (2000): 68-72
  18. Schuler AK, Talor Z “The case: 69-year-old man, with sand in the urine. N-acetyl sulfadiazine crystals.” Kidney Int 72 (2007): 769-70
  19. Perazella MA “Drug-induced renal failure: update on new medications and unique mechanisms of nephrotoxicity.” Am J Med Sci 325 (2003): 349-62
  20. Marques LPJ, Madeira EPQ, Santos OR “Renal alterations induced by sulfadiazine therapy in an AIDS patients.” Clin Nephrol 42 (1994): 68-9
  21. Anibarro B, Fontela JL “Sulfadiazine-induced sialadenitis.” Ann Pharmacother 31 (1997): 59-60

http://www.amazon.com/AIDS-EBOLA-Greatest-Medical-History-ebook/dp/B00QZCYMSS/

German Pharmaceuticals, University Vassals And The Extension Of Hitler’s Deadly Factories

Aids is a bio-weapon to depopulate Africa

Aids is a medical crime against humanity

By Johan Van Dongen and Joel Savage

“If a crime against Africa is done with impunity and crime against Europe and America is punishable, then there isn’t any true justice or media in the developed world.” – Joel Savage

In our previous articles about prohibited medicines against HIV, we described a number of successful anti-HIV agents that were suppressed by medical authorities and pharmaceutical companies in various countries. Scientist Johan van Dongen who had turned against the abuse of animal experimentation did not only suffered an unusual fate as a whistleblower, for letting the world know that Aids and Ebola are medical crimes against mankind, but also lost his profession after he was removed from all his duties as a university lecturer.

This happened in a country they claim follows justice, thus; in The Hague, Holland, is the International Court of Justice, bringing people who commit atrocity against mankind to face justice, but since Africans are not ‘human beings,’ they don’t have any privilege to enjoy any justice, in regard to crime committed by Europe and America against them. Hypocritically, they brought Africans, for example, perpetrators of the Rwanda genocide (Excluding the Belgians that ignited the flame) and Charles Taylor of Liberia to answer charges of crime against them. What a mockery of the judiciary system in Europe and America?

Several years later Scientist Johan Van Dongen wrote his first book  about the truth behind Aids and other virus infections; “Pleading for the ape;” in 1997. In his second book entitled: “AIDS, the greatest medical crime in history,” published in 2003(both in Dutch) Scientist Johan Van Dongen devotes eighteen pages to a cure for Aids and describes many medical substances that are effective against the Aids virus.

Together with the Ghanaian investigative journalist and writer Joel Savage, Scientist Johan van Dongen published his third book:“Aids the greatest crime in medical history against mankind” available at amazon.com (English version), in which are all the evidence about the criminal activities of the political, pharmaceutical, medical and military establishments against Africans.

The previous articles described the therapeutical use of several important substances, one called DHEA, dehydroepiandrosterone, and the other substance, being a combination of sugar and sulphate, called dextran-sulphate. Other highlights are the mentioning of Suramin and Kemron, which are also effective medicinal substances but blacklisted by medical authorities and pharmaceutical companies.

Hoechst, Bayer, Dupont, Merk Sharp and Dome are Mafioso Institutions!

A great number of those effective medicinal substances were blacklisted by medical authorities and pharmaceutical companies, such as Hoechst, Bayer, Dupont, Merk Sharp and Dome MSD, without any public explanation. Especially German pharmaceutical plants were involved in the prohibition of effective medicines against Aids. Do they want the slow death of Africans? It’s hard to understand, but the way Aids has taken thousands of Africans into their untimely grave means, it was done on purpose.

AL-721 A Prohibited Protein By Hoechst and Bayer

Another medicinal substance that suffered suppression is the substance called AL-721. It contains lecithin, an extract of the American pokeweed (Phytolacea American). It proved to be highly effective against the Aids virus. It was researched by J.M. Zarling, a well known Aids-researcher. Publications about this finding appeared in 1989 in the Deutsches Aerzteblatt and in 1990 in Nature. The USA government tried to prevent the sale of AL-721, an egg-nut mixture, which requires no authorization.

Hoechst and Bayers’ Prohibition of HB 946, L661, RU/486, Imreg-1, and Hyperacin.

Also in Germany; many substances with a strong working against the Aids virus were put on the blacklist for reasons not specified by the companies. This happened to the following polysaccharides produced by the German pharmaceutical companies Hoechst and Bayers’ HB 946, L661, RU/486, Imreg-1 and AL -721, also known under the names Arteparon and Arumalon. Scientist Johan Van Dongen further noticed the unexplained halting of the production of the successful Bayolin for unknown reasons.

The Imreg-1, a very effective drug against Aids, was twice rejected  by the USA government on account of alleged inefficiency.

For a study of Hyperacin, the University of Düsseldorf, Germany, refuses more participants to the tests as described by CB Pert called: “A pent peptide sequence in the Aids virus envelope, which blocks ineffective essentially conserved across nine isolates. In: Clin Neuropharmacol 1986; 9 (Suppl 4): 482-4.”

Also about Octapeptides Pert describes the same effective working pattern against HIV.

Dupont, MSD, and Hoechst

The substance Ampligen was stopped from being produced by the pharmaceutical company Dupont, thus; MSD halted their production of  L661. Methadone, which also shown effective against the Aids virus, was also prohibited in Germany. This well-known substitute for heroin, prescribed for intravenous drug users, was even denied to those very users by the Hoechst company, a state of Northern Westfalen in Germany. In addition to this also the following list of substances was prohibited in Germany : Diethylcarbamate; iosinpranobex, ribavirin, pentamidine, dehydroandrosterone and hypericine.

Heteropolyanion-23 (HPA-23)

HPA 23, according to Professor  Johan Van Dongen, is another substance capable of tackling HIV and stopping its growth. The workings of Heteropolyanion-23 have been described in 1954 and 1969, as a substance which is extraordinarily effective against the retrovirus that causes the Creuzfeld-Jacob disease (BSE and Kuru). Also the substances polyvinylsulphate sulphate powder, extracts of alges and dextran-sulphates are helpful against the HIV virus.

Prostatin

A medicinal substance developed by etno-botanics, who gather medicinal herbs and plants in the tropical rainforests, is called Prostatin. It is taken from a tree in the rainforests of the isle Samoa in the Pacific Ocean. Traditionally an extract of this tree was used as a remedy against yellow fever. When researched more closely in the United States. however, strong activity also against HIV was registered. Prostatin belongs to a category of chemicals called Forboles, which usually are carcinogenic substances.

It turned out however Prostatin was the only Forbole that was an exception to this rule, so it would not obstruct the possibility of Prostratin to become a helpful substance in fighting the Aids virus. Prostatin, according to van Dongen never appeared on the market as an anti-Aids agent, because the research conducted in the American laboratories never went public. As a result of all these prohibitions, false reports and panic measures and responsible respective establishments have prevented the cure for Aids infections and Aids diseases which affected millions, mostly Africans. All mentioned remedies still can be produced throughout the world.

Luc Montagnier, discoverer of the HIV/Aids virus

Very spectacular we may also call the recent stand taken by the French 2008 Nobel laureate Dr. Luc Montagnier, discoverer of the HIV/Aids virus. He now also advocates a completely natural cure for HIV/Aids! In an interview for the HIV/Aids-documentary; “House of Numbers,” he recommends the application of nutrition and micronutrients in the fight against HIV.

In the interview he states that there are many ways to decrease the transmission of HIV/Aids, just by making use of simple measures such as nutrition, providing antioxidants, taking hygienic measures and fighting at the same time the other infections that are present in the patients. He also states that if one has a good immune system the body can get rid of HIV naturally, this statement confirms that HIV/Aids is not at all an incurable disease.

 

World Health Organization and the Centers For Disease Control in America have many questions to answer.

Poor African Aids Patients Partially Cured With Proper Food

As mentioned before, the emphasis, especially for poor African patients, should be the building up of the immune system, making it possible to get rid of HIV by proper functioning of the natural defense system of the body itself. And therefore no antiretrovirals and/or vaccines should be used and proper food must be applied. Montagnier declares that all the above-mentioned measures constitute very important knowledge. But according to Johan van Dongen, unfortunately, this mentioned measures has been willingly completely neglected by the pharmaceutical, medical and political establishments up till now.

If Montagnier says  a good immune system can get rid of HIV naturally, then was is needed is the pushing for combinations of measures, such as antioxidants; nutrition advice; nutrition; fighting the other infections that are present in patients such as malaria, tuberculosis, parasitosis and worms; education and promoting genital hygiene. People always think of drugs and vaccines because there is no profit in nutrition. If you take a poor African patient who has been infected with HIV and you build up their immune system it should also be possible for them to get rid of HIV naturally. All of the above constitutes important knowledge which has been completely neglected.

A lot of other scientists including Johan van Dongen, who have been warning the world about the pharmaceutical business with the Aids epidemic for years, have received support from the discoverer of HIV, Luc Montagnier. A discoverer of an HIV virus who also stated: “The HIV is completely identical to the horse flu virus, Equine Infectious Anemia Virus EIAV,” a virus nowadays known as Hitler’s horse-aids. Because of the prohibition of very effective medicines against deadly diseases, causing millions of unnecessary death, Hoechst, Bayer, MSD, Dupont and the University of Dusseldorf, among many others, can be called “The Vassals Of The Extension Of Hitler’s Deadly Factories.”