“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.
Signal of Harm
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 even susceptibility to the disease intended to provide protection from, vaccines have been demonstrated to harm and several billion dollars 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 monkey’s has demonstrated injury.
Suppression of Investigation
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 for Biotechnology. 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….”