The Aids Hypothesis is a Lie – AZT Causes Aids

From Rethinking Aids:

This open letter to scientists worldwide asking them to look at the AIDS hypothesis that HIV causes AIDS now has over 5,000 signatures from doctors and scientists worldwide. There is no evidence that HIV causes AIDS. It is only a hypothesis.

READ BEFORE ENTERING; This website is for information purposes only; This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of Top-life coach or its staff.

Rethinking Aids Mission Statement

It is widely believed by the general public that a retrovirus called HIV causes the group diseases called AIDS. Many biochemical scientists now question this hypothesis. We propose that a thorough reappraisal of the existing evidence for and against this hypothesis be conducted by a suitable independent group. We further propose that critical epidemiological studies be devised and undertaken.

Signatories: From six hundred reputable scientists and doctors. If you do not believe six hundred reputable doctors and scientists who say we need to question the hypothesis, two of which are Nobel prize winners, then the manipulation of the masses is beyond repair.

So why in the eighties were we all terrified of getting the disease, and we were not gay and did not do IV drugs? Because mainstream media made us believe we were all severely at risk of getting AIDS and dying. The propaganda machine was hard at work using a fear factor to promote the money-making big pharma machine. We looked back, and we were all terrified. Now ask, what does .0007% look like? It is similar to your chances of dying while playing soccer.

“If there is evidence that HIV causes AIDS, there should be scientific documents which either singly or collectively demonstrate that fact, at least with a high probability. There is no such document.” -Dr. Kary Mullis, Biochemist, 1993 Nobel Prize for Chemistry.

It was all about fear to promote the disease to sell the drugs. The chance of an HIV Infected male transmitting HIV to a female is 0.0007%

The Multi-billion Dollar AIDS Hypothesis is Crumbling

Aids has terrorized Americans for many years. We are told there is no cure. The U.S. government mobilized a war against AIDS to fight a microscopic enemy when, in fact, there is no ultimate proof that the virus is the cause of AIDS. The media bombardment with propaganda was and is a big part of this money-making business. We have heard about AIDS so much and so often that almost all of us believe the hypothesis even though it has never been proven at all. Many scientists and doctors Do Not Believe the Hypothesis.

There is no evidence on this unproven hypothesis that HIV causes AIDS. HIV is not the cause of aids. The drugs such as AZT can cause AIDS.

Millions have died from drugs that treat AIDS. It has all been a scam. A government-funded multi-billion dollar scam. Peter Duesberg, in 1987 he started questioning HIV. He states that there is no virological nor epidemiological evidence to back up the HIV-AIDS hypothesis.

HIV does not cause AIDS. Treatment with drugs like AZT cause AIDS. This has been one of the largest, most horrifying medicine for-profit scams in the history of pharmaceutical companies globally. The scare tactics used for the promotion of the drugs are horrendous. All anti-retroviral medicines are highly toxic to humans and cause symptoms of AIDS.

In 1981 an alarm was set off when there was an illness in the gay and drug communities. We were told that this new immune disease could also be obtained by sexual contact. AIDS was then born. They speculated that the lack of T-cells in the blood was responsible for AIDS. T-cells identify invading viruses. The normal CD4 t-cells identify invading viruses and send signals for the immune system to attack the infection. In a normal person, there are 612 t-cell in one microliter of blood plasma. HIV patients have 200 or lower of these T-cells. This is what is thought to be the direct cause of AIDS. What is contradictory is that people with a 200 or lower count can and do remain perfectly healthy.

So if we stop what is killing the t-cells, you find the cure. What kills t-cells? Heroin, cocaine, barbiturates, and amphetamine use along with malnutrition, stress, repeated infections, and overuse of antibiotics. But the pharmaceutical vaccine industry wanted to get involved. They transformed a drug problem into a disease, and the money supply began. Grants and support from the government began. Big pharma gave hundreds of thousands of dollars to AIDS organizations to promote seminars promoting AIDS drugs.

Even Martin Delaney reversed the opinion about AIDS drugs. What we call local lipodystrophy began to show up. This is a large redistribution of the body area. People would start to develop huge lumps in their abdomen, back, and or neck. Women developed enormous breast growth to the point where they needed surgery sometimes to correct it. Other people had the opposite, which is called lipoatrophy, where they would lose fat. You would see all the fat disappear in the face and the limbs, even though their body weight didn’t change. It was called “the look” back in the eighties.

Nobel Prize Winners Dr. Walter Gilber and Dr. Karry Mullis also questioned the HIV hypothesis.

Dr. Charles Thomas and The Group for Scientific Reappraisal of the HIV/AIDS Hypothesis are reputable scientists questioning the hypothesis. They wrote a letter and JAMA, and The Lancet refused to publish the letter. By 1994, 600 people signed the letter. Its content is highlighted above in green. It now has over 5,000 signatures. Don’t let the trolls fool you. They are all reputable doctors and scientists who have an abundance of experience in the field. Pharma has no defense to this, so they create stories and spew propaganda to discredit them.

In 1987 they knew the disease did not spread through male to female sexual contact. There was a 0.0009% chance of it spreading male to female and less from female to male. Aids needed to become a disease; everyone could raise billions of dollars by using a fear factor.

“I do not believe there is an AIDS epidemic in Africa or Asia. People, there are still dying from the combined effects of chronic infectious diseases plus malnutrition, poverty, and other factors, just as they always have.”

Virusmyth.net — Dr. James Hudson, Ph.D., Professor of Pathology and Medicine, University of British Columbia, Canada.

“Evidence is rapidly accumulating that the original theory of HIV is not correct.”

Sunday Times (London) 3 April 1994

“…The point that everybody is missing is that all those original papers Gallo wrote on HIV have been found fraudulent. Well, then, that throws into question the entire HIV hypothesis, doesn’t it? The HIV hypothesis was based on those papers.”

Spin June 1992

Antiretroviral Side Effects

Antiretroviral drug toxicity is extremely broad. Side effects include renal toxicity, gastro, and cardiovascular effects, insomnia and the list goes on. You can read the list below rather than repeat it.

Mitochondrial toxicity caused by (NRTIs)Nucleoside Reverse Transcriptase Inhibitors

They produce a wide range of adverse effects, such as lactic acidosis, hepatic steatosis (fatty liver disease) myopathy, cardiomyopathy,(affects the heart muscle) peripheral neuropathy (pain from nerve damage, weakness, and numbness) pancreatitis, and possibly lipodystrophy syndrome. Lipodystrophy is the loss of fat we discussed earlier. Peripheral neuropathy and lipodystrophy syndrome are most familiar with long term use. They both only partially reverse and sometimes do not reverse at all when discontinuing the medication.

There have been multiple reports of fatalities connected with NRTI use. NRTI-related lactic acidosis is the build-up of lactate in the body and also low pH levels in the blood. It is a life-threatening condition.

Abacavir – A hypersensitivity reaction is a potentially life-threatening reaction to abacavir that occurs in up to 5% of patients.

Didanosine – Didanosine is rarely ever used due to the potential for multiple adverse effects and serious complications, such as pancreatitis, lactic acidosis, and peripheral neuropathy.

Emtricitabine and Lamivudine – Approved for children starting at birth.

Dr. Stolbach owns stock in Gilead Pharmaceuticals, and he reports in the conclusion of his study that: “Adverse effects are inevitably seen with all medications.” But he states mitochondrial toxicity is the most consequential of the side effects. Mitochondrial toxicity can manifest as myopathy, neuropathy, or potentially life-threatening lactic acidosis.

Neutropenia Lactic acidosis, along with severe hepatomegaly (enlarged liver) with steatosis (build-up of fat in the liver), Fatalities have been reported.

Non-Nucleoside Reverse Transcriptase Inhibitors

Stavudine – Stavudine is no longer recommended in the United States due to an abundance of adverse side effects, including peripheral neuropathy, lactic acidosis, and facial and body lipoatrophy.

Zidovudine -Bone Marrow Suppression: Zidovudine is a well-established cause of reversible anemia and leucopenia. It is also associated with myopathy in up to 17% of patients.

Efavirenz – Efavirenz is a highly potent NNRTI, but it is no longer recommended as a part of preferred antiretroviral regimens, mostly due to neuropsychiatric adverse effects. Rare severe rash cases, including Stevens-Johnson syndrome (very serious disorder), toxic epidermal necrosis, erythema multiform, and DRESS (drug rash with eosinophilia and systemic symptoms) syndrome, have been reported.

Author

James Heilman, MD

Steven-Johnson Syndrome Image From Wikimedia Commons

Immune reconstitution syndrome: Patients may develop immune reconstitution syndrome resulting in the occurrence of an inflammatory response to an indolent or residual opportunistic infection during initial HIV treatment or activation of autoimmune disorders (e.g., Graves’ disease, polymyositis, Guillain-Barré syndrome) later in therapy; further evaluation and treatment may be required.

Diseases and Pathogens Associated With IRIS

Castleman disease
Cryptococcus neoformans
Cytomegalovirus (CMV)
Eosinophilic folliculitis
Graves’ disease
Hansen’s disease (leprosy)
Hepatitis B virus (HBV)
Hepatitis C virus (HCV)
Herpes simplex virus (HSV)
Herpes zoster (shingles)
Histoplasma capsulatum
Human papillomavirus (HPV)
Kaposi’s sarcoma (KS)
Mycobacterium avium complex (MAC)
Myopathy
Non-Hodgkin’s lymphoma (NHL)
Pneumocystis carinii (P. jiroveci) pneumonia (PCP)
Progressive multifocal leukoencephalopathy
Sarcoidosis
Systemic lupus erythematosus
tuberculosis

Diseases that Define AIDS

- Bacterial infections, multiple or recurrent
- Candidiasis of bronchi, trachea, or lungs
- Candidiasis of the esophagus
- Cervical cancer (invasive)
- Coccidioidomycosis, disseminated
- Cryptococcosis, presenting outside of the lung
- Cryptosporidiosis, chronic intestinal for longer than one month
- Cytomegalovirus (CMV) with loss of vision
- Cytomegalovirus disease (other than in the liver, spleen, or lymph nodes)
- Encephalopathy (HIV-related, also knows as AIDS dementia complex)
- Herpes simplex virus (HSV), lasting longer than a month or appearing in an area other than the skin (such as the esophagus or lungs)
- Histoplasmosis, disseminated
- Kaposi’s sarcoma (KS)
- Lymphoid interstitial pneumonia or pulmonary lymphoid hyperplasia complex
- Burkitt lymphoma (or equivalent term)
- Immunoblastic lymphoma (or equivalent term)
- Primary lymphoma of the brain
- Mycobacterium avium complex or Mycobacterium kansasii, disseminated
- Mycobacterium tuberculosis of any site in or out of the lungs
- Mycobacterium or similar species, disseminated beyond the lung

Pneumocystis pneumonia caused by the fungus Pneumocystis jiroveci
Pneumonia, recurrent
Progressive multifocal leukoencephalopathy (PML)
Salmonella septicemia, recurrent
Toxoplasmosis of the brain
Tuberculosis
Wasting syndrome

Integrase Strand Transfer Inhibitors

Bictegravir – Bictegravir is an INSTI that is available only in the single-tablet regimens bictegravir-tenofovir alafenamide-emtricitabine.

In clinical trials, the most common adverse effects associated with bictegravir-tenofovir alafenamide-emtricitabine were diarrhea, nausea, and headache. There have been reports of Steven Johnson Syndrome with use. See the image above. They say it is rare but do not give statistics.

Dolutegravir

Potential Neural Tube Defects: On May 18, 2018, an FDA Safety Alert was posted that warned of potential serious neural tube birth defects in infants born to mothers who received Dolutegravir at the time of becoming pregnant or early in the first trimester. Elevated Serum Creatinine, Insomnia, Myopathy, and Elevated Creatinine Phosphokinase: Rhabdomyolysis, myopathy, and myositis have been reported.

Raltegravir

Elevated Creatine Kinase, Proximal Myopathy, Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis.

Protease Inhibitors

There are currently 10 FDA-approved protease inhibitors. None are designated in the category of Recommended Initial Regimens for the majority of people with HIV. Here are a few of them.

Gastrointestinal Adverse Effects have been associated with dyslipidemia, insulin resistance, premature atherosclerosis, and myocardial infarction. Some people taking protease inhibitors have developed asymptomatic atrioventricular (AV) block. Lipoaccumulation – abnormal central fat accumulation, sometimes referred to as buffalo hump.

Indinavir – It is rarely used in clinical practice due to an increased risk of nephrotoxicity. Indinavir is associated with many different urologic and renal abnormalities. These include dysuria (pain while urinating) flank pain, (discomfort to agony below the rib) renal colic, (pain when urinary stones block urinary tract), hematuria, crystalluria, nephrolithiasis (calculi in the kidneys), acute renal failure, chronic renal failure, and papillary necrosis, (a disorder of the kidneys where part of the renal papillae die),

Lopinavir-Ritonavir – Approved for infants. It is not used often due to greater toxicity than with many other currently available antiretroviral medication options. Side effects include hyperlipidemia, especially hypertriglyceridemia, elevated transaminases, hyperglycemia, PR interval prolongation, QT interval prolongation and torsades de pointes, risk of toxicity—including life-threatening cardiotoxicity—is increased in premature infants (see Major Toxicities below)

Less common (more severe): Fat maldistribution.
Rare: New-onset diabetes mellitus, hyperglycemia, ketoacidosis, exacerbation of preexisting diabetes mellitus, hemolytic anemia, spontaneous and increased bleeding in hemophiliacs, pancreatitis, elevation in serum transaminases, and hepatitis (life-threatening in rare cases). PR interval prolongation, QT interval prolongation, and Torsades de Pointes may occur.

Saquinavir
Saquinavir is infrequently used in current clinical practice due to the high pill burden, poor tolerability, and the potential for serious adverse effects. The combination of saquinavir and ritonavir may cause prolongation of the cardiac QT and PR intervals, which increases the risk for serious.
Cardiac arrhythmias, including heart block and polymorphic ventricular tachycardia (torsades de pointes).

Tipranavir
Tipranavir is rarely used now because of the high pill burden and the potential for serious complications, including intracranial hemorrhage and hepatotoxicity. The drug carries a black box warning for both conditions. In June 2006, the U.S. Food and Drug Administration (FDA) reported
that 14 patients taking tipranavir in combination with ritonavir developed intracranial hemorrhage; among them were 8 fatalities.

Entry Inhibitors

Enfuvirtide is a fusion inhibitor medication and administered twice daily by subcutaneous injection. Injection site reactions are common (occurring in up to 98% of patients in some studies) and include erythema, induration, cysts, nodules, and rarely more severe reactions.[149,150] The acute injection site reactions appear within hours after the injection and some patients have persistent sclerotic lesions that can persist for
months after discontinuation of enfuvirtide.

Ibalizumab requires intravenous infusion. In clinical trials, the most common adverse effects associated with ibalizumab have been diarrhea, dizziness, nausea, and rash.[151]

Maraviroc is an entry inhibitor that exerts its action by directly binding to a host protein—the CCR5 co-receptor. Because maraviroc binds to a human protein, there have been concerns it could have unique toxicity. Rash: Maraviroc has been linked to at least one case of severe rash with systemic symptoms, although most cases of severe reactions (i.e. Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms) in patients taking maraviroc have involved patients who were also taking other drugs associated with these conditions. Hepatotoxicity: The FDA labeling now includes a black box warning for hepatotoxicity.
Impact of Host Immune Function: Maraviroc is the only antiretroviral drug that acts directly on a host (human) protein—the CCR5 coreceptor. The binding and impairment of the human CCR5 coreceptor by maraviroc has raised concerns for potential maraviroc-induced problems with host immune function or cancer surveillance, but trial data does not show an excess of infections or malignancies, with the exception that blockade of CCR5 receptor may increase the risk of developing symptomatic West Nile virus infection.[153,157,158]

The Journal of American Retrovirals

All four classes of ARV and the nineteen FDA-approved antiretrovirals are directly or indirectly associated with life-threatening events.

Hemophiliacs – foreign proteins in clotting factor 8 have an immunosuppressant effect and can cause AIDS. The date indicated the HIV only start to die after they were told they were infected and begin taking antiviral medications.

HIV causes AIDS is a failed hypothesis that terrorized people into taking a deadly medication AZT.

AZT, a toxic chemotherapy drug, proved too deadly to be given to cancer patients, but it was approved for AIDS. It was banned for being too toxic but now was approved for AIDS. AZT causes cancer in rodents. It destroys cells that are most important to immunity. AZT directly causes immunodeficiency. It was designed to kill human cells. The manufacturer says it can cause AIDS-like diseases. It is impossible to know the difference.

The book “Poison by Description” states the AZT studies were fraudulent. The long term toxic effects were impossible since the placebo group was eventually given AZT. One in 1000 t-cells are infected; therefore, 999 healthy t-cells are killed to kill the one infect t-cell.

AZT costs approximately $8,000 to 12,000 per year, and it is paid mostly by the taxpayer. It is a one billion dollar per year industry. It can cost $5.00 to make and can be sold for $500.00. An immediate increase in t-cells is a short term effect. All toxic substances exhibit a positive response before higher doses kill them. Low doses of AZT kills off bone marrow. Within a year or two, most die from AZT, depending on their sensitivity to the drug.

AZT drug promoters Margaret Thistle call for pregnant women to be tested for the virus and treated with AZT like medicines. This can kill the baby and the mother; they are calling it retroactive abortion. Many who know facts, not propaganda, think it is an absolute atrocity and cannot believe this is allowed.

50-90% of all babies develop natural immunity and no longer show signs of HIV. They are born HIV positive, and they become HIV negative. AZT damages the brain, bones, lungs, kidneys. Mothers who resist are sometimes losing custody of their children.

Smith Klien Laxo HIV test produces many false positives.

HIV “DNA chain-terminators and protease inhibitors” that affect healthy cells as well as the virus.

The new drug protease inhibitors – was approved in 42 days. Valid clinical benefits are scares – 0 people showed improvement in one study.

They have stopped the virus but not AIDS. HIV proponents ignore science. Now you have to explain why annihilating HIV does not stop AIDS.

It has been proven that HIV does not cause AIDS. Aids patients have died due to AZT. It is a myth that HIV is responsible for AIDS. The fear has driven this propaganda fear campaign, and it has all been based on lies.

HIV cannot be proven to cause aids 9 times out of 10 – World Health Organization

False-positive is caused by malaria, flu, infections, and hormone changes during pregnancy. The HIV blood test can be wrong 71% of the time for people not in a high-risk group.

There is no specific HIV disease anywhere.

97% of people with HIV are healthy and do not have AIDS in Africa.

In 100,00o studies on HIV and AIDS and there is no proof that HIV causes AIDS.

NO HIV test has ever been approved by the FDA.

There has never been a group of people that were HIV positive who were proven to have active HIV in the blood(not just antibodies).

There has been a group of people that were HIV negative who were proven not to have HIV in the blood.

60% of all AIDS patients are gay.

Nitric-oxide (poppers) is extremely immunosuppressant. Drugs, Heroin, cocaine amphetamines are immunosuppressants. This can be a culprit.

HIV Tests Are Not Accurate

American Journal of clinical pathology. One sample was tested 525 times. It was identified as positive for HIV 59% of the time. There are 10 different ways of interpreting these results. A positive test result in one country does not mean it is positive in another.

HIV Viral Load – Viral tests have never been validated. The results have a high amount of false positives – According to JAMA

Disclaimer on Package Inserts for HIV testing – some say

CDC t0pcells can fluctuate from day to day. WHO below 350 indicated HIV infections yet, 3-5% of HIV negative people had t-cells below 350.

Male to female infection is 0.0007 per contact. Female to male is even lower. JAMA

Rethinking Aids Mission Statement.

HIV FACTS DO NOT ADD UP TO AIDS

HIV reproduces rapidly in the body. The antibodies in our body kill HIV. Ironically the HIV tests for the antibodies, not the virus. When they test positive for HIV, they have produced their own antibodies and are now immune to the virus. The vaccine already exists.
HIV does not kill the T-cells it infects. Retroviruses do not kill the host.
HIV does not affect enough cells to cause AIDS. HIV infects as few as one out of 1000 or as few as one cell out of 100,000 T-cells reproduce 5% a day. This low amount of t-cell cannot cause AIDS. You need half of all t-cells to die for the disease to kill you.
There is no such thing as a slow virus. They state the virus takes 10-12 years to cause AIDS. Ten years later, 30 diseases are caused? Someone is buying time. 35 billion dollars, and there is not any idea why it would take ten years. That is because it is not possible.
They say this is a new virus. It has to be, or the epidemic would have happened a long time ago. No one in the government-funded research program has addressed this question. Experts say it has been around for centuries and spread through mother-child and have lived healthily for years.
10-20% of AIDS patients do not have any HIV at all. When it is found, most of the time, there are only tiny dormant amounts present.
HIV injection does not cause AIDS in monkey test animals.
All efforts to find an infectious cause have failed.
97% of AIDS is locked into the risk groups. If it were a virus, it would be spreading. 9 out of 10 people with AIDS are male. Suppose AIDS was caused by a virus, just as many women would be diagnosed as men. In Africa, is it evenly spread between men and women? An estimated 14 million have AIDS in Africa. The disease is very different in Africa.
The USA developed AIDS ten times faster than in Africa, where hard drugs are used.
Most people who test positive for HIV never develop AIDS

President Mbeki might have a case on rethinking AIDS

ATRIPLA is a three-drug combination of efavirenz(EFV), a non-nucleoside reverse transcriptase inhibitor,and emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF), both HIV-1nucleoside analog reverse transcriptase inhibitors,and is indicated as a complete regimen or in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patients weighing at least 40 kg.

Package Insert

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