Saturday, February 19, 2011

Unthinkable FDA Corruption

It is true that FDA Michael Taylor has a long history of a FDA revolving door.... pleasing health-destructive Monsanto, of which may explain why the FDA will not publicly report their acknowledgment of numerous published study reports that conclude a multitude of developmental (physiological, neurological and reproductive) adverse soy-poisoning effects.

The FDA lists "soybean, genistein, daidzein" (soy phyto-estrogens) on their "Poisonous Plant Database"....... without public disclosure.

The FDA confirms soy toxicity as having "endocrine disruptor properties," and acknowledges that soy is also loaded with; "phytic acid, heavy metals, and soy inhibits several essential developmental enzymes" of which each and all are known by the FDA as especially contaminating to the most vulnerable fetus, infants, and children..... a developmental poison! The FDA confirms that soy phyto(plant)- toxins are not proven as safe .....while without public disclosure!

2004 NIH CRISP Database concludes, "Proper functioning of the endocrine system especially during developmental time-frames must not be jeopardized."

Soy's several toxic components and especially soy's estrogenic endocrine disruptors are confirmed to jeopardize the entire endocrine system of which increases the risk of adverse health effects.....throughout the body and brain, especially during developmental exposure.

As confirmed in the1999 FDA Federal Register; "GRAS status of soy did not include a thorough evaluation of the safety of potentially harmful components, e.g. lysioalanine, nitrites and nitrosamines, trypsin inhibitors, phytates, and isoflaovnes. Trypsin inhibitors (have) potential effects on pancreatic function....deleterious effects in the pancreas....responsible for hyperplasia and formation of nodules seen in animal studies."

Each and all of these natural soy components: estrogenic isoflavones (endocrine disruptors) phytic acid, heavy metals, and inhibition of essential enzymes are repeatedly proven with potential to especially damage the physiological, reproductive and neurological health of fetus, infants and children .....while simply remaining FDA withheld from public disclosure.

At this time prior Monsanto attorney Michael Taylor found his way back into the position of Senior Advisor to FDA Commissioner Hamburg. In 1976 Michael Taylor was FDA staff attorney, but later left to work as an attorney representing Monsanto, the profiteer of a host of horrific massive destruction of health products; Agent Orange, PCB's, Aspartame, DDT, Pesticides including Roundup, Bovine Growth Hormones, and Genetically Modified (GM) Roundup Ready soyseed for human consumption. Taylor conveniently returned to the FDA in 1991 as Deputy Commissioner for Policy becoming part of a team working on industry-friendly policy on food biotechnology while approving Monsanto's genetically engineered bovine growth hormone, while successfully helping to confirm FDA's decision NOT to label "rBGH" milk for public disclosure. Then in 1994 Taylor landed a job with the U.S. Department of Agriculture as administrator of its Food-Safety and Inspection Service, while Monsanto enormously profits from Genetically Modified (GM) seed such as; soybean, corn, beets, etc., .....without public disclosure, without GM,"Frankenfood" labeling.

After successfully satisfying Monsanto's wishes, Taylor leaves the USDA and is again hired by Monsanto as Vice President of Public Policy as a chief lobbyist ensuring that USDA, and FDA, and Congress continue to approve Round-up Ready GM,(RRGM) seed, (including soybeans) again helping Monsanto rake in billions in profits without confirming evidence of health safety.

It is 2009 when Michael Taylor returns to the FDA, this time hired as Senior Advisor to the Commissioner, resulting in the most probable explanation as to why GM foods are increasingly marketed without truthful labeling..... without public disclosure. Chances of the FDA to legitimately reveal overwhelming study evidence proving developmental soy toxicity is also sorely diminished because Monsanto's profits from the marketing of RRGM soybean seed will likely nose dive if the truth prevails, protecting industry profits over the protection of health, developmental health.

To this date FDA Hamburg, Schneeman, Silverman, as well as HHS Sebelius refuse to reply to a 2009 Child Health Advocates' Petition request for appropriate developmental WARNING Labels on soy products, and a second request for the WITHDRAWAL of soy formulas. FDA acknowledges several hundred scientific studies that overwhelmingly concluding soy high risk for soy phyto-toxic causation of fetal, infant, and child developmental (physiological, reproductive, and neurological) adverse effects.

Massive numbers of scientific studies conclude that developmental exposure to soy-toxicity can cause; premature birth, allergies, asthma, gastrointestinal distress, thymus damage, hypothyroidism, immune deficiency disorders, liver, kidney and pancreas damage, diabetes, reproductive disorders, infertility, gender chaos, homosexuality, leukemia, multiple cancers, and cancer metastasis. Toxic components of soy have also been study reported to encourage the cause of autism, seizures, mental retardation, behavioral disorders and more.

In truth, the FDA has no evidence that any particular healthy fetus, infant, or child can survive soy-poisoning-causation of neurological, reproductive, or physiological disorders and diseases of which the FDA continues to withhold from public disclosure.

During pregnancy women transfer soy toxicity to her fetus, and then to her child while breast feeding. Male soy consumption can contaminate the sperm that fertilizes the egg.

It is no quesiton that fetus, infants, and children exposed to soy contamination continue to participate in an undisclosed, undocumented experiment. No follow-up, no physician reports. However, several parents have themselves reported to FDA MedWatch, multiple soy damaging effects caused to their soy exposed child. However, these reports silently accumulate in a dusty FDA MedWatch file...... without public disclosure.

That boys are especially sensitive to soy's estrogenic endocrine disruptors may explain why boys are at greater risk for autism. That several children in a family are diagnosed with autism may also be explained by FDA withholding of developmental soy toxicity as families are unable to know the importance to exclude soy from their child's dietary intake.

First 3 ingredients of soy infant formulas are : Corn syrup, Soy, Sugar..... of which each and all are FDA known as developmental toxins! Often soy formula may be 100% of an infant's dietary intake for several months or longer! No FDA Warning labels, no FDA soy formula Withdrawal....no FDA disclosure!

2010 NTP Soy Formula Brief, the expert panel concluded "Clear evidence of (soy formula) adverse effects" while deciding to withhold this information from public disclosure! 12 of 14 panel members are directly and/or indirectly funded by a very powerful soy industry, with soy lobbyists dancing with joy (as I was witness to).

FDA allowed: Marketed soy foods and beverages increasingly target infants and children. Soy cereals, crackers, snack bars, packaged foods, bread, on and on and on! Most difficult is to avoid soy consumption, or avoid soy toxicity!

Alarmingly, infant milk formulas are also becoming increasingly contaminated with soy, without any rhyme or reason! There are also a few listed vaccinations stated to contain soy fillers; Hib/HepB (comvax) and Pneumococcal (Prevnar, Prevnar13), a direct injection of soy endocrine disruptors, phytic acid, heavy metals, and essential enzyme inhibitors.

As days fold into weeks, and weeks into months, and into years....it is clear that the FDA intends to continue to conceal massive evidence proving developmental soy poisoning from public disclosure. If you will care to protect children's health please review this urgently important health safety measure:

http://www.petition2congress.com/4607/petition-to-protect-childrens-health

If we, the American public do not pressure Congress into investigating such extensive and horrific FDA failure to protect developmental health, then the FDA will clearly continue to conceal their acknowldegment of massive evidence proving soy phyto-toxic causation of developmental destruction of health from public disclosure! This is a matter of fact!

Thank you for caring!!!!