Dr. Paul Offit is a pediatrician who co-invented/patented a rotavirus vaccine (trade name RotaTeq), and once stated in interview that a child can be administered 100,000 vaccines safely at once (later revised to 10,000). A professor of Pediatrics at the University of Pennsylvania, he is the darling of the lamestream media and a widely cited self-appointed ‘vaccine safety expert,’ despite the glaring conflict of interest implied by such a designation.
Unfortunately for Dr. Offit (not so affectionately named Dr. Profit), a 2010 study published in Journal of Virology revealed that his multi-million dollar grossing patent on the RotaTeq vaccine contains a live simian retrovirus (with a 96% match of certainty) that has likely infected millions of children over the past few years with a virus that causes great harm. Retrovirus infections are permanent, and can carry on indefinitely into future generations. In other words, once they are inserted into the human genome they cannot be removed.
Moreover, a 2014 study published in Advances in Virology found Dr. Offit’s vaccine contains “a baboon endogenous virus strain M7… likely due to the monkey cell line in which RotaTeq was produced from.”
In order to grasp the dire significance of these findings, you might want to familiarize yourself with the history of adventitious viruses in so-called attenuated or live vaccines.
These contain the actual disease vector they are supposed to prevent. While considered “weakened,” their process of manufacture often make them more adaptable to the host within which they are injected. Many rounds of passage through human and animal cells often makes these vaccines far more dangerous than the natural ‘wild-type’ infections that we encounter naturally. You only have to look to oral polio vaccine to understand the dangers of the vaccine model. In 2011, the Indian Journal of Medical Ethics published a study revealing that vaccine strain polio is twice as lethal as wild-type, and has been identified to cause over 47,000 cases of polio-associated paralysis in 2011 alone.
The theory is that by infecting healthy bodies with them you generate an immune response – validated by elevated antibody titers, regardless of their affinity to the pathogen – that results (in theory) in increased protection. Regardless of the justification for using monkey cells for vaccine production, monkey retroviruses contaminate the vaccines nonetheless. By infecting healthy infants with these viruses you are making them sick. Retroviruses use reverse transcriptase – a viral enzyme – to insert pathogenic genetic information into healthy cells, effectively converting them into virus-manufacturing factories. And no matter what your medical philosophy is, monkey viruses have no place in a human body.
For context, consider the deleterious role of a previous monkey virus – simian virus 40 (SV40) – in the polio vaccination campaigns. This ‘hidden’ cancer-causing virus infected millions of unsuspecting polio vaccine recipients during the initial polio eradication campaigns. Not only is it cancer-causing, but it is passed down transgenerationally. Merck’s senior vaccine scientist confessed in interview as to the damage these SV-40 contaminated vaccines did to millions of unsuspecting victims, including causing cancer. These vaccines did untold damage to the following infected generations, leaving a legacy of untold pain and suffering in millions of offspring whose parents unwittingly succumbed to one of the most dangerous biological experiments in human history.
Retroviruses are just as serious. HIV for instance, is a retrovirus whose phylogenetic lineage also comes from a monkey virus: simian immunodeficiency virus (SIV). Offit’s RotaTeq vaccine should be pulled from the market, considering it contains live viruses that are capable of infecting the bodies of those within which they are injected. For information on the exploding epidemic caused by hidden viruses in vaccines, read Judy Mikovits’ incredible new book Plague: One Scientist’s Intrepid Search for the Truth About Human Retroviruses and Chronic Fatigue Syndrome, Autism and Other Diseases. It’s a must read!
The significance of these findings cannot be underestimated. Childhood infections are a natural rite of passage for the developing immune system. In developed nations, where nutrition, hygiene and sanitation are up to par, infection from childhood pathogens normally proceed without morbidity or mortality – lest the infant/child is already immuno-compromised. In fact, rotavirus challenges result in lasting immunity and provide the justification ultimately for the vaccinology model, which draws from the normal (arguably millions of years old ) experience of overcoming infection, constructing a model of vaccine-induced immunity upon this natural fact.
Paul Offit, the patent holder of the RotaTeq vaccine is morally obligated to call for an immediate halt of the use of his vaccine in infants and children. Failing to do so makes him culpable in the harm of millions of children that he personally profits from infecting with retroviruses.
Enough is enough. The facts are clearly available for anyone with an ‘evidence-based’ bent to ascertain.
The credibility of the entire vaccination schedule is on the line.
This article first appeared at GreenMedInfo.