By Anna Hunt | Activist Post | November 24, 2013
Have you ever considered the similarities between vaccinations and genetically modified foods (also referred to as GMOs)?
Both of these ‘innovations’ illustrate clearly our human desire to fix what doesn’t necessarily need fixing, manipulate what doesn’t suit us, and take control over what is mysterious and seems uncontrollable. They also show how easily we take something that could be beneficial and quickly we get carried away with our desire to control what may not be intended by nature and God to be under our power.
1. Blind Disregard to Nature’s Infinite Sophistication
Corporations that are pushing vaccines, and GMOs are escalating the war with Nature. No matter how hard we try, our collective intelligence will never outsmart the natural forces of the universe.
Nature has a sense to it, cultivated over billions of years of evolution. The complexity of botanical systems, the relationship to pests, soil, and the elements sustains optimal diversity and reproduction. It was only when we began to industrialize the process, hijack growth with an eye toward yield, and allow chemical companies to attempt to regulate variables of perceived adversity that we ended up in the mess that GMO crops are in today. Now we have randomly spliced animal DNA with bacterial vectors inserting into plant genomes, disrupting the natural functioning of the plant, and allowing for supersaturation with the toxic, endocrine-disrupting and gut bug slaughtering herbicide, Roundup.
Pharmaceutical companies and doctors think they can outsmart immune systems that have evolved to coexist with microbes, to be primed and educated by them. We are at war with infectious disease, and as a consequence, our fear and malice toward bacteria and viruses have lead us to compromise and alter our immune systems with pathogens entering our bodies through our muscles, accompanied by toxic additives that cripple our natural immune function and cause chronic inflammation. The notion of improving upon our human capacities, as we understand them is discussed by Sayer Ji of GreenMedInfo as “transhumanism.”
2. Lack of Safety Research Prior to Mass Distribution
Most vaccine and GMO products often lack the extensive clinical trials on humans, which are typically required to be conducted on other inventions that are marketed and distributed to the mass population. Why the exception?
Monsanto claims that GMOs are simultaneously equivalent to existing foods (relieving them of any real duty to demonstrate safety), and novel enough that they can be patented. Despite the Frankensteinian effects of genetic manipulation on proteins and gene expression, these foods have never been studied in a human population, let alone assessing for long-term effects. What happens as a result of this fast-track-to-market process is that slow-emerging trends of harm at the population level begin to emerge. Differing patterns of chronic disease in Europe and America at this point may have some relation to limitations of GMO products in Europe. There is inherent difficulty in associating cause to effect in chronic disease; however, arguing for the importance of long-term premarketing trials.
Vaccines have similarly, never been studied against an unvaccinated control group, allegedly because they are assumed to be so vital to our health that it would be unethical to withhold them even though basic epidemiology demonstrates that hygiene and nutrition have played the most significant role in elimination of infectious disease. They have never been studied in their current schedule, nor have the additives (adjuvants) which include known body toxins, aluminum, mercury, formaldehyde, and polysorbate 80.
3. Evasion of Evidence that Points to Potential Harm
Vaccines and GMOs continue to be linked to a plethora of illnesses and ailments through a variety of third-party scientific institutions and independent researchers, many contradicting studies funded by Big Pharma and Biotech that seem to find no reason for concern.
Despite this lack of effort and incentive to support safety data in these two arenas, both have suffered a signal of harm that should have activated the precautionary principal. Monsanto monitored GM and non-GM fed rats for 90 days, and declared that changes in liver and kidney function were not clinically significant. Seralini et al, copied this design, but extended the observation period to years. Take a gander at what happened to these animals. The first tumor sprouted at the 4 month mark. Multiple animal studies have emerged mirroring this study’s provocative findings. Glyphosate, the herbicide that has been sprayed in escalating quantities, is an endocrine-disruptor that has been linked to obesity, liver disease, birth defects, autism, and cancer. This is the most enlightening exploration of its toxic mechanisms. Bt-toxin in GMO corn has been found to puncture intestinal cells and circulate into fetal tissue.
Whether in the realm of neurodevelopment, death, autoimmunity, or evensusceptibility to the disease intended to provide protection from, vaccines have been demonstrated to harm and several billion dollars of taxpayer money have been paid out to victims through the National Vaccine Injury Compensation Program. Patterns of chronic illness such as atopy and autism have been demonstrated to correlate with vaccine uptake and prospective study of neurodevelopment in monkeys has demonstrated injury.
4. Suppression of Conflicting Information in the Mainstream
It is difficult for independent researchers to make their voices heard when going against multi-billion dollar companies entrenched in existing regulatory and industry organizations. Anyone going against the status quo adapted by the medical and biotech industries are often shunned and belittled.
Seralini was silenced. His work was roundly attacked, censored from the media, and demands from industry ties for the paper to be retracted from its journal of publication. Several months after Seralini’s paper, Richard Goodman, a former Monsanto employee was fast-tracked to the position of Associate Editor forBiotechnology. With Monsanto now at the helm of influential medical journals, the prospects for publication of independent research are diminishing.
The now infamous Andrew Wakefield, who published a paper on the presence of vaccine-strain measles in the guts of autistic children was stripped of his license and maligned for fraud in a witch-hunt intended to suppress any further investigation into this connection. Fortunately, at least 28 independent studies from around the world have confirmed his findings.
5. Government Support of Rich, Corporate Fat-cats
Companies that make billions each year are heavily involved in affecting regulatory and government policies through extensive support of political parties, lawmakers and regulatory initiatives, unlike non-profit activist and consumer groups who do not have the funds to help sway policy-makers in their favor.
The “Monsanto Protection Act” was designed to provide legal immunity to GM technology so that citizens could never litigate on the grounds of harm secondary to GM food exposure. In this way, corporations would be protected above farmers and citizens.
The National Vaccine Injury Compensation Program was established in 1986 to assume liability from corporations so that any incentive to police the safety of their product was roundly eliminated and civilians could only engage in a non-jury-mediated “trial” of red-tape and rejection as a means of seeking justice for injury.
6. Conflict of Interest At Its Best
Industry experts that preside over regulatory agencies such as the FDA and the CDC have often come from the corporations that they later regulate. Many still own stock or hold patents for certain GMO and vaccine innovations and have a vested interest in the success of these products.
This is where the rubber meets the road on these issues, and, truly the source of all corruption. When those regulating a system in need of checks and balances are the same people who have profited or are profiting from its protection and success, we have a critical breakdown in protection of the interests of consumers and patients. The revolving door of Monsanto and government ranges from Michael Taylor, FDA Deputy Commissioner for Foods and former Monsanto Vice President of Public Policy to Supreme Court Justice Clarence Thomas, former Monsanto attorney. Enjoy this pictoral.
The list of interchangeable figures between the CDC, pharmaceutical industry and Vaccine Advisory Committee features more conflicts than exceptions. Notably, in January 2010, Julie Gerberding, former director of the CDC, became the President of Merck’s vaccine unit. In January 2011, Elias Zerhouni, former director of the NIH became President of Sanofi-Aventis’ research labs. These relationships are known to be kindled far in advance of the job acceptance. The most outspoken mouthpiece of today’s vaccine schedule is Paul Offit MD, Merck employee and Rotavirus vaccine patent holder. This paper details the many layers of profit-motivation that cloud regulators’ judgment. Here’s a little video if you’d rather not read.