ABORTED HUMAN FETUSES BEING USED FOR "FLAVOR ENHANCER" RESEARCH -- ENDING UP IN THE FOOD YOU CONSUME

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Comment by truth on November 15, 2012 at 8:44am

this is so creepy

Comment by Farida Magdalena Gillot on May 22, 2012 at 9:01am

Senomyx and Partners – All the Proof You Need

UPDATE:  Proof No. 1:  PepsiCo attorneys plead with the SEC to exclude the shareholder resolution filed in October 2011.  Were it not true that they are funding the use of aborted fetal cell lines in the research, development and discovery of new flavor enhancers, they would have answered in one brief paragraph asking for dismissal.  They did not do this.  Read PepsiCo attorneys letter here.

Since issuing our first press release on March 29, 2011 regarding the work of Senomyx using aborted fetal cell lines to produce artificial flavor enhancers for several major food giants, the public has responded to these companies with letters and phone calls expressing their concern, shock and utter disgust.  Unfortunately, both Senomyx and their partners have been less than honest in their responses to the public, causing even further confusion to the public, even to the point of convincing some that its simply not true.  We have compiled the following information to help you in your boycott and letter writing efforts in order to ensure this undeniable truth is no longer kept hidden from the public. 

So let's start right out with the undisputable fact that aborted fetal cell lines are indeed being used by Senomyx in the research and development of artificial flavor enhancers.

READ MUCH MORE !!.......


Comment by Farida Magdalena Gillot on May 22, 2012 at 4:44am

Comment by Farida Magdalena Gillot on May 22, 2012 at 4:27am

http://vaccinequestions.wordpress.com/2012/04/08/cell-lines-from-ab...

Cell lines from aborted human fetus in vaccineproduction

Some of today’s vaccines are cultivated on cell lines from aborted human fetuses. This itself promotes ethical questions, which is further reinforced by the fact that mostly no one have knowledge of these facts. Few parents are aware of this when they vaccinate their children, and it is unlikely that the topic is well-known among health professionals. It is reasonable to think that some people based on ethical education and religious reasons will be uncomfortable about these facts. One can question whether this issue is controversial to such a degree that it would be prudent to disclose the circumstances to the patients – in this respect their parents.

Cell lines and virus strains from aborted fetuses:

Among the cell lines that have been used we find WI-38 derived from the lung tissue of a three-month-old girl fetus. Another cell line, MRC-5 derived from lung tissue of a 14 week old male fetus. These cell lines was derived in the 1960s and 70s, but came in use in vaccines at a later date. The vaccines that have been cultivated on these lines is rubella (German measles), varicella (chickenpox), hepatitis A and rabies.

Virus strain used in MMR vaccine rubella-component are also taken from aborted fetal tissue. This strain is called RA 27/3 and was obtained from a fetus whose mother had rubella during pregnancy and performed an abortion because of risk of fetal damage. RA 27/3 is also grown in cell line WI-38.

(Ph. D. John D. Graben Stein 1999)

http://www.immunizationinfo.org/files/nnii/files/Moral_Consideratio...

Further information about fetal cellines with links:

MRC-5: “The MRC-5 cell line was developed in September 1966 from lung tissue taken from a 14 week fetus aborted for psychiatric reason from a 27 year old physically healthy woman. The cell morphology is fibroblast-like. The karyotype is 46,XY; normal diploid male. Cumulative population doublings to senescence is 42-48. G6PD isoenzyme is type B.”

http://ccr.coriell.org/Sections/Search/Sample_Detail.aspx?Ref=AG059...

http://www.viromed.com/services/product/mrc5.htm

WI-38: “The WI-38 cell line was developed in July 1962 from lung tissue taken from a therapeutically aborted fetus of about 3 months gestational age. Cells released by trypsin digestion of the lung tissue were used for the primary culture. The cell morphology is fibroblast-like. The karyotype is 46,XX; normal diploid female. A maximum lifespan of 50 population doublings for this culture was obtained at the Repository. A thymidine labelling index of 86% was obtained after recovery. G6PD is isoenzyme type B. This culture of WI-38 is an expansion from passage 9 frozen cells obtained from the submitter.”

http://ccr.coriell.org/Sections/Search/Sample_Detail.aspx?Ref=AG068...

http://www.viromed.com/services/product/wi38.htm

IMR-90: ”The human diploid fibroblast strain IMR-90 was derived by W.W. Nichols and associates from the lungs of a 16-week female fetus. 
The division potential, viral susceptibilities and other properties have been thoroughly studied such that the line may be considered as an alternate for WI-38 and other standard human lung cell strains. 
The cells have been reported to be capable of attaining 58 population doublings before the onset of senescence.”

http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/...

http://ccr.coriell.org/Sections/Search/Sample_Detail.aspx?Ref=I90-1...

WI-26 VA4: An SV40 transformed derivative of WI-26, a human diploid cell line derived from embryonic lung tissue of a male Caucasian. The cells have SV40 T-Ag but infectious virus has not been rescued.

http://www.cellbankaustralia.com/estore/ProductDetail.aspx?ProductI...

HEK-293: cells were generated in the early 70s by transformation of cultures of normal human embryonic kidney cells with sheared adenovirus 5 DNA in Alex Van der Eb’s laboratory in Leiden, The Netherlands. The human embryonic kidney cells were obtained from previously healthy aborted fetus.

http://en.wikipedia.org/wiki/HEK_cell#Origins_of_HEK_293_Cells

PER.C6: Cell line from retinal tissue of a 18 month old fetus aborted in 1985, further developed and prepared as cell line in 1995.

http://www.fda.gov/ohrms/dockets/ac/01/transcripts/3750t1_01.pdf (Page 91)

http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=DetailsS...

RA 27/3: ”Various strains of rubella virus were used. RA 27/3 was isolated previously in this labratory from an aborted fetus.” 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC375746/?pageindex=1 (Page 157)

RA 27/3Note the RA27/3 strain of rubella virus was observed to induce brain cell death in rats: The induction of cell death by the Therien strain of rubella virus (RVT), and the vaccine RA27/3 strain, was investigated in mixed glial cell cultures derived from the rat CNS. Cell death induction in Vero and rat glial cells by RVT and RA27/3 was dependent on virus replication. In both cell types and for both virus strains, cell death induction had the hallmarks of apoptosis,”

http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed...

http://www.sailhome.org/Concerns/Vaccines.html

Study finds time related association between the introduction of fetal cell lines in vaccines and autism:

In 2010 a published survey claims to have found an association between the use of vaccines made from aborted fetal cells and autism. McDonald and Paul found that the increase of autism holds correlation to the introduction of these types of vaccines, respectively, in the years 1981, 1988 and 1995.

http://www.lifenews.com/2010/04/21/nat-6272/

http://www.all.org/pdf/McDonaldPaul2010.pdf

HV Ratajczak (2011) studied the correlation of autism and the introduction of these vaccines and also supports a possible connection. According to Dr. J Mercola (07/10/2011) this was reported by New CBS:

“That Ratajczak reports that at the same time Vaccine makers took most thimerosal out of most Vaccines (with the exception of flu shots still Widely Which Contain Thimerosal), They Began making some Vaccines Using human tissue. 

Ratajczak says human tissue is currently used in 23 Vaccines. She discuss the Increase in autism incidences corresponding with the introduction of human DNA MMR Vaccine two, and suggest the two could be linked. “

http://www.rescuepost.com/files/theoretical-aspects-of-autism-cause...

The number of 23 vaccines contaminated with aborted human fetus is also confirmed by other medical sources:

“Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law that requires that consumers be informed that some vaccines are made using aborted fetal cells and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells do inform consumers, in their package inserts, that the vaccines contain contaminating DNA from the cell used to produce the vaccine, they do not identify the cells as being derived from electively aborted human fetuses.”

The same group og physicians claims that there could be relations between this type of vaccines and diseases like diabetes, lupus, MS and autism:

“How could the contaminating aborted fetal DNA create problems? It creates the potential for autoimmune responses and/or inappropriate insertion into our own genomes through a process called recombination. There are groups researching the potential link between this DNA and autoimmune diseases such as juvenile (type I) diabetes, multiple sclerosis and lupus. Our organization, [3] Sound Choice Pharmaceutical Institute (SCPI), is focused on studying the quantity, characteristics and genomic recombination of the aborted fetal DNA found in many of our vaccines.”

http://www.physiciansforlife.org/content/view/1758/2/

Cancer virus contamination in vaccines:

About the medical issues it should also be taken note of the aspect of viral contamination. In the 60`s a cancer virus was spread with contaminated polio vaccines. The story starts like this:

“In 1961, SV40 was discovered by Dr. Bernice Eddy of the National Institute of Health, Division of Biologics when she took the material used to grow polio vaccines and injected it into hamsters. Tumors grew in the hamsters. Her discovery was subsequently validated by Drs. Maurice Hilliman and Benjamin Sweet of Merck.”

http://www.sv40foundation.org/

As we can see from the cell lines mention above – one of the lines has antibodies against SV-40 virus although the virus was not traced:

WI-26 VA4: An SV40 transformed derivative of WI-26, a human diploid cell line derived from embryonic lung tissue of a male Caucasian. The cells have SV40 T-Ag but infectious virus has not been rescued.

http://www.cellbankaustralia.com/estore/ProductDetail.aspx?ProductI...

Ethical dilemma:

Ethical dilemmas of this kind, can be discussed in light of many factors. That the abortions where provoked is one aspect to some people, whether there was any intention of using a tissue is a different theme, and of course a wide range of issues related to information components and consent aspects of the various parties and stakeholders. Some will want to see the benefits in terms of prevention of disease and death. Others choose to emphasize the fundamental ethical principles that prevent a life of having to be regarded as a vehicle for another life. Regardless of how one views these matters – the fundamental ethical issue rest on whether one is aware that these conditions exist. If people do not know the facts – there is no requirement to make an ethically based choice. For that reason, the lack of information is to be regarded as the most fundamental ethical dilemma for patients in a practical context.

Legal aspects of patient and donor information:

Patients, in this case – their parents have a legally fundamental right to receive information about drugs and treatment their children receive. Given that vaccination is a planned medical intervention there should be room for the patients receiving more complete information than they do today. Health professionals are also obliged to provide information as well as possessing a working knowledge of drugs they administer. Based on the theme: “the use of fetal human diploid cells in medicine” has repeatedly been up to political and legal debate. It must be assumed that this subject holds such controversial aspects that it in no way should be withheld from general patient information. It may also be advisable to question aspects of consent of the patients as a supplementary matters of legal nature based on the fact that some of the abortions were performed on psychiatric ill patients.

Other intricate questions may be raised on the basis that we still in 2012 possesses legislation that fails to define and review human cell lines explicitly. One should also take into account that the use of such cell lines both in vaccines as well as general research made its entrance already in the 1950s, then in the form of the HPV virus infected Hela cell line. From a donor who never consented that her cervical cancer cells were immortalized in medical laboratories worldwide. It is assumed that the use of aborted human fetal cell promotes just as many controversies – both medical and ethical.

http://en.wikipedia.org/wiki/HeLa

© 2012



Comment by Farida Magdalena Gillot on May 22, 2012 at 4:17am

Obama agency rules Pepsi's use of aborted fetal cells in soft drinks constitutes 'ordinary business operations'

(NaturalNews) The Obama Administration has given its blessing to PepsiCo to continue utilizing the services of a company that produces flavor chemicals for the beverage giant using aborted human fetal tissue. LifeSiteNews.com reports that the Obama Security and Exchange Commission (SEC) has decided that PepsiCo's arrangement with San Diego, Cal.-based Senomyx, which produces flavor enhancing chemicals for Pepsi using human embryonic kidney tissue, simply constitutes "ordinary business operations."

The issue began in 2011 when the non-profit group Children of God for Life (CGL) first broke the news about Pepsi's alliance with Senomyx, which led to massive outcry and a worldwide boycott of Pepsi products. At that time, it was revealed that Pepsi had many other options at its disposal to produce flavor chemicals, which is what its competitors do, but had instead chosen to continue using aborted fetal cells -- or as Senomyx deceptively puts it, "isolated human taste receptors" (http://www.naturalnews.com).

A few months later, Pepsi' shareholders filed a resolution petitioning the company to "adopt a corporate policy that recognizes human rights and employs ethical standards which do not involve using the remains of aborted human beings in both private and collaborative research and development agreements." But the Obama Administration shut down this 36-page proposal, deciding instead that Pepsi's used of aborted babies to flavor its beverage products is just business as usual, and not a significant concern.

"We're not talking about what kind of pencils PepsiCo wants to use -- we are talking about exploiting the remains of an aborted child for profit," said Debi Vinnedge, Executive Director of CGL, concerning the SEC decision. "Using human embryonic kidney (HEK-293) to produce flavor enhancers for their beverages is a far cry from routine operations!"

To be clear, the aborted fetal tissue used to make Pepsi's flavor chemicals does not end up in the final product sold to customers, according to reports -- it is used, instead, to evaluate how actual human taste receptors respond to these chemical flavorings. But the fact that Pepsi uses them at all when viable, non-human alternatives are available illustrates the company's blatant disregard for ethical and moral concerns in the matter.

Back in January, Oklahoma Senator Ralph Shortey proposed legislation to ban the production of aborted fetal cell-derived flavor chemicals in his home state. If passed, S.B. 1418 would also reportedly ban the sale of any products that contain flavor chemicals derived from human fetal tissue, which includes Pepsi products as well as products produced by Kraft and Nestle (http://www.naturalnews.com).

Comment by Cryptocurrency on May 20, 2012 at 8:51pm

Soo, not only are we killing unborn children, but now we're eating them? Why does this NOT surprise me?

Comment by honeygirl on May 20, 2012 at 4:05pm

Comment by honeygirl on May 20, 2012 at 4:03pm

Comment by honeygirl on May 20, 2012 at 2:06pm

Comment by Maria De Wind on May 20, 2012 at 11:43am

THIS IS A MUST WATCH AND FURTHER RESEARCHED!

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