From Salk Polio Vaccine to Monkey Virus Linked to HIV, AIDS and Cancer

We have a nasty cancer growing within our government and country. As far back as April 29, 1878 the U.S. government passed a Federal Quarantine Act and by 1889, mycoplasmas were identified as a transmissible agent. Within the next 100 years we had many plagues and viruses and experimenting on animals and humans.

The use of mycoplasmas in epidemics is man made because of the tell tale strains that identify them.  First it was the polio, then the mycoplasma in cattle, tobacco, horses, and birds. The cancer within the government formed the Federation of the American Society for Experimental Biology or FASEB. Then in 1918, a flu virus modified with a bird mycoplasma was created. This killed millions because there was no acquired immunity for this compound virus.

In 1935, we learned to crystallize the tobacco mycoplasma so it would remain indefinitely and not die. Then after WW II, we imported all of the scientists that Hitler was using to experiment on humans. The greatest influx of foreign scientists were welcomed into the U.S. Biological program and “Operation Paperclip” became the twisted parallel government that Bill Clinton has referred to as the “government within the government that I have no control over”.

These rather twisted war criminal scientists were hired by the Pharmaceutical fronts, one being Monsanto Corp. Aspartame, and MSG, both causing cancer then made the scene. See Dr. Russell Blaylock M.D. for information on these two silent killers. Studies by the scientific experts show all of the killer viruses in the 20th century were manipulated to some degree, including the polio (SV40), the smallpox (herpes), and so on.

The mycoplasma have become the most important transmissible agent of the makers of viruses. Instead of destroying them never to be seen again, they are saved for future epidemics. By 1954, Dr. Bjron Sigurdsson published his first paper on the Visna virus and became the inventor of AIDS along with the help of rival Dr. Carlton Gajdusek. In 1962 under the guise of cancer research, the twisted elite set up a U.S. Mycoplasma Laboratory at Sanford University and a special virus program began with a phizer contract believed to be in 1961, a year before.  Haldor Thomar publishes that viruses cause cancer

When the experimenting continuing on, the twisted people using the guise of protecting us from enemy threat, discovered that the P53 tumor gene was designed to kill cells through apoptosis so that mutated cells could not lead to cancer through multiplication and metastasis. It was necessary to manipulate the SV40 virus to cancel this effect for the highest kill ratio of the proposed enemy, which it appears we the population have become through “Big Pharma” trial and error or was it error?.

It is now known that the monkey virus given to all of us in the polio vaccine binds to and inactivates the functioning of p53, so that cells do not commit suicide even if they are damaged by chemotherapy and radiation. This suggests that cancers where SV40 is present will not respond to this treatment and about 97 ½ percent of the cancers today do not respond to Chemo or radiation effectively because of SV40.

How to test:

The test is called the PCR-DNA General Screen for Mycoplasma Species- contact·         Institute for molecular Medicine, 15162 Triton Lane, Huntington Beach, California 92649-1041  (714)-903-2900

· Immunosciences Laboratory 8730 Wilshire Blvd., Suite 305 Beverly Hills, CA 90211 (516)-434-5525
· There may be other testing facilities near you. Make sure this test is known to them or you may just be wasting your time and money.

You may have to detox  if you’ve never had an intestinal cleansing. These are Detox herbs and will not hurt you. They are readily available at most health food stores. You may have to be on them for several months according to your condition.

The natural cure

There are things that will arrest mycoplasms and slow them down.

1. One is selenium from 200 to 400 micrograms- arrests growth of mycoplasma
2. Magnesium peroxide- mycoplasms need a low oxygen environment and this inhibits growth by supplying oxygen
3. Colloidial silver in the 3 to 5 nano particle size. This will seek out the mycoplasma and kill them. About one teaspoon per day mixed in a glass of spring water.
4. Hydrogen pyroxide therapy- Consult a physician who practices this therapy

You Mean My Polio Vaccination Had a Monkey Virus in it and It’s Still There?

The polio vaccination which we all took back in the 50’s and 60’s was cultured in the monkey before the vaccine was created.  In order to do this, the monkey was given the polio virus by vaccine injection.  After recirculating the virus through the kidney and skin of the monkey, the SV40 biological evidence has been found to be a transforming cancer causing virus.

The National Academy of Science Institute of Medicine (IOM) Immunization Safety Committee in July 2002 also found that the “biological evidence is of moderate strength” that SV40 exposure could lead to cancer under natural conditions and concluded that the SV40 exposure in the polio vaccine is related to this SV40 mentioned.

Now the Swine flu, (H1N1) is a class 2 carcinogen.  It has been demonstrated that the SV40 is one of the activators of HIV-AIDS virus and causes lung and brain cancer.  Now when you combine this H1N1 (Swine flu) vaccine that is being orchestrated by the World Health Organization as being a phase 6 emergency, (legislation gets passed without it being tested properly), and add mercury, aluminum, formaldehyde and other toxins present in the vaccine,  and a possible agent for future cancers designed to decimate world population, one would have to decline this super hoax on the American people.  The Rockefeller Foundation is behind this depopulation effort.  Don’t waste your life on an unproven and known toxic cocktail.

GlaxoSmithKline who manufactures the Swine flu vaccine has actually stated:

“Clinical trials will be limited, due to the need to provide the vaccine to governments as quickly as possible. Additional studies will therefore be required and conducted after the vaccine is made available.”   Then it will be too late!

And the World Health Organization likewise says:

“Time constraints mean that clinical data at the time when pandemic vaccines are first administered will inevitably be limited. Further testing of safety and effectiveness will need to take place after administration of the vaccine has begun.”  Again, then it will be too late!

The 1918 virus that killed millions of people, was a flu virus modified with a bird mycoplasma.  Humans had no acquired immunity.  Remember the word mycoplasmas!  These are tiny microorganisms smaller than bacteria that are commonly found in the mucous membranes of the mouth and nose. Mycoplasms can penetrate into your blood cells which travel throughout your body creating autoimmune diseases. including arthritis, chronic fatigue syndrome, AIDS, fibromyalgia and “Gulf War Syndrome”. With the mycoplasm inside the white blood cell, the body is confused and wants to attack the mycoplasm, but the mycoplasm surrounds itself with pieces of your cell membrane it takes when it travels in the blood and develops an immune response.

Mycoplasmal infections begin with flu like symptoms. Lacking a cell wall, a mycoplasma invades the synovial cells of your joints.  Once inside your cells, they cannibalize the cell using its nutrients and energy to reproduce causing the joints to be damaged. The systemic infection in slow and gradual. Symptoms include chronic fatigue, heart problems, thyroid not functioning, headaches, memory loss, eye pain, blurred vision, breathing difficulties, fever, muscle aches, and gastro intestinal disturbances.

Once inside the cells, it is difficult to test for and conventional antibody tests no longer work. If you suspect an infection of this type, test for PCR-DNA General Screen for Mycoplasma Species. Testing is available at the Institute for Molecular Medicine in Irvine California and Immunosciences Laboratory in Beverly Hills, California. There are several methods to rid yourselves of this parasite. strong antibiotic therapy, which include the use of doxycycline, levofloxacin, minocycline, and azithromycin just to name a few. Only a few are effective against mycoplasms.

If you are not interested in taking antibiotics for months or longer, the natural approach is successful with collodial silver three to five parts per million.  The particles are 2 to 5 nanometers.  The smaller size is more effective against mycoplasms than the larger size of common collodial silves of 50 to 100 parts per million. See Dr. Darryl at UC Irvine, CA.  Another successful natural is Selenium and oxygen supplements.  200 to 400 micrograms will arrest the growth of the mycoplasma and the magnesium peroxide will kill the pathogenic microbes throughout your body.

As far as putting addition toxic elements into the blood such as thimerosal which was banned in California for causing autism, proposed adjuvants are squaline (oil based) and is associated with production of auto antibodies which may be responsible for Gulf War Syndrome.

“So, what is this deadly ingredient called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern-squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected. Because squalene, the main ingredient in MF-59, can induce hyperimmune responses and induce autoimmunity, a real danger exists for prolonged activation of the brain’s immune cells, the microglia. This type of prolonged activation has been strongly associated with such diseases as multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, ALS and possibly vaccine-related encephalitis. It has been shown that activation of the systemic immune system, as occurs with vaccination, rapidly activates the brain’s microglia at the same time, and this brain inflammation can persist for long periods”. For further on this, consult Russell Blaylock MD Vaccine may be more dangerous than Swine flu

Polio Vaccines

Currently there are two polio vaccines that are in use throughout the world to fight against polio. Jonas Salk, the man who invented the first, started his work on a vaccine in 1955. The vaccine worked in two steps: first a dose of killed polio virus is injected, and then an oral polio vaccine must be taken which contains a live but much weakened form of the virus. This vaccine was first tested in 1957 on humans, and was later liscensed in 1962.

Then came along another vaccine that was developed by Sabin. This live-virus vaccine quickly became to more popular route of the two for 4 main reasons:

Due to it’s live state it has the ability to spread and to infect other individuals who have not been vaccinated. This sounds bad, but in the spread, it allows the remote body to build up some immunity to the virus.
Due to the fact that the oral vaccine performs its magic in the gut, it works on immunity there in the central system which in turn reduces the spread of the virus on the outside. If the polio vaccine is injected directly into the bloodstream it will immunize the inividual, however it does not not reduce his or her ability to spread the virus.
Everything is a matter of money these days, especially when it comes to healthcare. Sabin’s “live” vaccine was cheaper than than Salk’s “dead” vaccine.
The last reason for the increased popularity of Sabin’s vaccine is that the oral vaccine is a lot easier to widely administer to the general population than the injected vaccine. This means that patients are more likely to complete the series of vaccinations that are required to attain full immunity.

Sabin’s vaccine is the standard treatment for polio to date. The dead virus was able to bring Polio to terms, however it was the live-virus vaccine that was able to completely eliminate the wild spread of the polio virus in the United States.