Vaccine Discussion Series Pt I. - Fetal Cells extracted from LIVE aborted babies and Tumorigenic Cell Lines

‘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.‘ - Dr. Theresa A. Deisher, Ph.D.

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Check out the CDC's excipient page to research the ingredients in vaccines (I recommend studying each ingredient individually using the duckduckgo.com search browser): https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

Do you see MRC-5, WI-38, DNA, MRC-5 Cellular Protein, Human Serum Albumin (all different ingredients) on the ingredients list? All of these derive from either human tissue or human blood.

*MRC-5 (Medical Research Council cell strain 5) is a diploid human cell culture line composed of fibroblasts derived from lung tissue of a 14-week gestation aborted male Caucasian fetus:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC274969/
http://www.atcc.org/products/all/CCL-171.aspx

*WI-38 is a diploid human cell culture line composed of fibroblasts derived from lung tissue of a 3-month gestation aborted female Caucasian fetus:
http://www.atcc.org/products/all/CCL-75.aspx

*Human embryonic kidney cells 293, also often referred to as HEK 293, HEK-293, 293 cells, or less precisely as HEK cells, are a specific cell line originally derived from human embryonic kidney cells grown in tissue culture.

*The newest cell line created in 2015 for vaccines: WALVAX 2 is taken from the lung tissue of a 3-month gestation female who was ultimately selected from among 9 aborted BABIES. The scientists noted how they followed specific guidelines to mimic WI-38 and MRC-5 in selecting the aborted babies, ranging from 2-4 months gestation. They further noted how they induced labor using an en caul (water bag) abortion to shorten the delivery time and PREVENT THE DEATH OF THE FETUS to ensure LIVE intact organs which were immediately sent to the labs for cell preparation.

Read more on WALVAX here:
https://www.ncbi.nlm.nih.gov/m/pubmed/25803132/

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"In some cases, the cell lines (aborted fetal cell lines) that are used might be tumorigenic, that is, they form tumors when injected into rodents. Some of these tumor-forming cell lines may contain cancer-causing viruses that are not actively reproducing. Such viruses are hard to detect using standard methods. These latent, or "quiet," viruses pose a potential threat since they might become active under vaccine manufacturing conditions.”
https://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm

"Xenotropic murine leukemia virus-related virus (XMRV) is a recently discovered human retrovirus that has been found in both chronic fatigue syndrome & prostate cancer patients. There is a potential safety concern regarding XMRV in cell substrates used in vaccines..."
https://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm

"The use of tumorigenic and tumor-derived cells is a major safety concern due to the potential presence of viruses such as retroviruses and oncogenic (CANCER) DNA viruses that could be associated with tumorigenicity, Therefore, detection of persistent, latent DNA viruses, and endogenous retroviruses in vaccine cell substrates is important for vaccine safety, particularly in the development of live viral vaccines, where there are no or minimal virus inactivation and removal steps during vaccine manufacturing."
https://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm

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The United States government has known about the dangers of human DNA from aborted fetal cell-lines since at least 2005. They set guidelines which are supposed to keep the DNA at a specific limit, which they hypothesize won't cause cancer.

There is no monitoring of vaccines by our government agencies to ensure those limits are adhered to. Vaccines (MMR, Varicella, and Hepatitis A) sent for independent analysis have consistently shown levels of human fetal DNA that are far beyond the "established safety limits."

Here is the link to the FDA PowerPoint (draft):
http://www.fda.gov/ohrms/dockets/ac/05/slides/5-4188S1_4draft.ppt

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‘Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and be integrated into the host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccines can be one of causes of autism spectrum disorder in children through vaccination.‘ - Quoted from Spontaneous Integration of Human DNA Fragments into Host by Dr. Genome K. Koyama & Dr. Theresa. A. Deisher Ph.D.

Dr. Deisher, lead scientist and SCPI founder, also noted that “Not only are the human fetal contaminated vaccines associated with autistic disorder throughout the world, but also with epidemic childhood leukemia and lymphomas.”

Instead of conducting safety studies they regulated the amount of human DNA that could be present in a vaccine to no greater than 10ng.

Unfortunately, Dr. Deisher’s team discovered that the fetal DNA levels ranged anywhere from 142ng – 2000ng per dose, way beyond the so-called “safe” level.

Dr. Deisher’s study is available on the Academic Journals website at:

http://soundchoice.org/wp-content/uploads/2012/08/DNA_Contaminants_in_Vaccines_Can_Integrate_Into_Childrens_Genes.pdf

Dr. Theresa Deisher is a Ph.D. in Molecular and Cellular Physiology from Stanford University with over 20 years in commercial biotechnology, prior to founding AVM Biotechnology and Sound Choice Pharmaceutical Institute. As an inventor of 23 issued US patents, she is world-renowned for her work in adult stem cell research and the first to discover adult cardiac-derived stem cells. Dr. Deisher was a plaintiff in the US federal lawsuit to prohibit the use of taxpayer dollars for embryo-destructive research, which resulted in steering science towards adult stem cell research and 14 US FDA approved adult stem cell products.

More on Deisher’s studies: www.ms.academicjournals.org/article/article1409245960_Deisher%20et%20al.pdf
or on their website at www.soundchoice.org/scpiJournalPubHealthEpidem092014.pdf

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Vaccines that have been cultured on or manufactured using the WI-38 fetal cell line such as MeruvaxII®, MMRII®, Varivax®, Havrix® and Pentacel® are additionally contaminated with fragments of human endogenous retrovirus HERVK (Victoria et al., 2010). Recent evidence has shown that human endogenous retroviral transcripts are elevated in the brains of patients with schizophrenia or bipolar disorder (Frank et al., 2005), in peripheral blood mononuclear leucocytes of patients with autism spectrum (Freimanis et al., 2010) as well as associated with several autoimmune diseases (Tai et al., 2008). The strong ecological association between human fetal cell line-manufactured vaccines and autistic disorder change points calls for further investigation of these childhood vaccine contaminants.

http://academicjournals.org/article/article1411048618_Deisher%20et%20al.pdf

If the link above doesn’t work, try this one: http://soundchoice.org/scpiJournalPubHealthEpidem092014.pdf

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Vaccines manufactured in human fetal cell lines contain unacceptably high levels of fetal DNA fragment contaminants: https://www.ncbi.nlm.nih.gov/m/pubmed/26103708/?i=2&from=vaccine%20contaminants

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More info on cell lines from the manufacturer: https://www.quidel.com/cultures-fluorescent-tests/cell-cultures

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Lastly (for today), I'd like to leave you with the deposition of Stanley Plotkin - commonly known as the "Godfather of Vaccines" - giving his testimony, under Oath, on the aborted fetal cell lines used in vaccines:

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Future articles in this vaccine series will include:

• Peer-reviewed studies/journals
• Infant mortality rates and their correlation to vaccines
• The connection to autoimmune disease (it's in the inserts, in addition to numerous peer-reviewed studies)
• Other serious life-long adverse reactions and risks of vaccination, including death
• Low risk of complications from contraction of "preventable" diseases in a healthy body
• Vaccine failures, short immunity duration, and no guarantee of immunity
• Live vaccine shedding and spreading disease
• The impossibility of herd immunity
• Lack of clinical and safety studies
• The toxicity of aluminum, polysorbate 80, cell strains, and other adjuvants
• Usage of animal components and DNA in vaccines (Fetal Bovine Serum/Calf Serum Protein, Embryonic Guinea Pig Cell Cultures, Monkey Kidney Cells, and more)
• How we are destroying our natural immunity through vaccines
• Exemptions - including religious, philosophical, etc
• Cell-mediated and humoral immunity - how vaccines trigger the immune system in an unnatural way
• The benefits of contracting diseases naturally (cancer reduction, etc)

If you'd like to hear more about this, please comment and let me know which topic above interests you the most. I encourage you to research both sides of this topic and make an informed choice for yourself and your family. Please feel free to share!