These are amongst the many substrates present in the huge cultivation soup tanks which are used in vaccine production. The implications may be horrendous.
DNA RESIDUE IN VACCINES
The presence in the final vaccines of residue (“adventitious agents”) including cells and fragments of DNA from foreign tissue is certainly realistic.
CDC ADMITS THE PROBLEM
“- Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines. The challenge of identifying potential adventitious agents in vaccines closely parallels the challenge of identifying the agents causing particular emerging infectious diseases.” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/pdf/11485673.pdf
The concept of unknown ingredients in vaccines is at least as frightening as the ones which are known. Some substances are unknown even to vaccine manufacturers. As analysis methods become more advanced, more substances are discovered unexpectedly in vaccines which may have been on the market for a long time.
CANCER CAUSING MONKEY VIRUS SV40 IN POLIO VACCINE
One example of many is the unexpected discovery of SV40 from monkey kidney cells which was one of several dozen viruses that contaminated the original Salk and Sabin polio vaccines administered to millions of people worldwide.
“- it has been alleged that there have been SV40- contaminated batches of oral polio vaccine administered to some children until the end of the 1990’s.” http://www.sv40foundation.org/
The tragic story of little Alexander:
SV40 VIRUS IS PASSED THROUGH GENERATIONS
“- many of the contaminant organisms can pass from generation to generation. For example, new studies have found that SV-40, a major contaminant of the polio vaccine until 1963, not only existed as a latent virus for the lifetime of those exposed to the vaccine but was being passed on to the next generation, primarily by way of sperm, something called vertical transmission. This means that every generation from now on will be infected with this known carcinogenic virus. There is also compelling evidence that some polio vaccines manufactured after 1963 may contain SV-40 virus. What makes the SV-40 contamination disaster of such concern is its association with so many cancers…” http://www.thehealthyhomeeconomist.com/if-you-are-in-support-of-vaccinations/
FDA ADMITS THAT SV40 CAUSES CANCER
“ – Millions received SV40-contaminated pRhMK-produced polio and adenovirus vaccines in the late 50s and early 60s”.
“SV40 DNA has been detected in some human malignancies…” http://www.fda.gov/ohrms/dockets/ac/01/slides/3750s1_04_krause.pdf
PIG, MONKEY AND BIRD VIRUSES
Other examples of contamination include the unexpected discovery of pig virus DNA in the rotavirus vaccine GlaxoSmithKline’s “Rotarix”, a virus similar to simian (monkey) retrovirus in Merck’s rotavirus vaccine “Rotateq” and retrovirus avian (bird) leukosis virus in a measles vaccine. http://articles.mercola.com/sites/articles/archive/2010/04/17/major-vaccine-suspended-due-to-contamination-with-pig-virus.aspx
BIOHAZARD RECOMBINANT (GENETICALLY MODIFIED) HPV DNA IN GARDASIL
The consequences of the recent discovery by an independent laboratory of the presence of recombinant HPV DNA in Gardasil, considered a biohazard, are unknown and may be horrific.
“- If recombinant HPV DNA attached to aluminum adjuvant enters a person’s blood, how long will it remain there?”
“ – What autoimmune-related disorders could result from this contamination?”
“ – Is it possible for this contamination to initiate gene mutations which may lead to cancer?”
“ – What genetic changes (mutagenesis) could occur should the residual HPV DNA enter and begin reproducing in a human cell?”
ABORTED FETAL TISSUE AND INSECT CELLS
“Human Diploid Cell Strains” (Derived from aborted fetal tissue) are associated with an increased risk of a theoretical ‘oncogenic agent’ (an agent that causes neoplasms/cancer)” http://vaccineresistancemovement.org/?p=6880
Many different vaccines are cultured on aborted tissue from fetal cell lines. http://www.catholiceducation.org/articles/medical_ethics/me0044.html
DOGS, GENETICALLY MODIFIED YEAST, RABBITS, COW HEARTS, CALF SERUM, CHICK EMBRYOS, DUCK EGGS, PIG, SHEEP AND HORSE BLOOD, GUINEA PIGS AND RABBIT BRAINS
CATERPILLAR EGGS, COCKER SPANIEL KIDNEYS, RETINAL CELLS OF ABORTED FETAL TISSUE, CANCER CELLS
In the 1960s, cells from aborted human fetal tissue, called MRC-5 and WI-38 cells, were developed and are still used for the manufacture of rubella chickenpox, hepatitis A and shingles vaccines. http://www.newswithviews.com/Tenpenny/sherri123.htm
FDA LISTS MANY CASES OF CONTAMINATED VACCINES
“-Examples include contamination of yellow fever vaccine with hepatitis B virus in the 1940s, contamination of early polio and adenovirus vaccines with simian virus 40 in the late1950s and early 1960s, contamination of blood products with hepatitis viruses and HIV, and contamination of dura mater grafts with the Creutzfeldt-Jakob disease agent. In these examples, either human or animal materials used in production usually caused the contamination.” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/pdf/11485673.pdf
MMR AND YELLOW FEVER VACCINES CONTAIN CANCER GENES
“- vaccines, especially those relying upon animal tissue to culture viruses during the manufacturing process—the influenza, the MMR, and yellow fever vaccines—are known to be highly contaminated with foreign animal viruses (including Avian Leukosis Virus and Equine Arteritis Virus), genetic fragments of such viruses, oncogenes (genes that turn normal cells cancerous), and prions (tiny proteins responsible for incurable diseases and neurological disorders in animals and humans).”
FDA: ONLY NONBINDING RECOMMENDATIONS FOR TESTING
There is no incentive for vaccine promoters to find substances which are detrimental to health. FDA only presents nonbinding recommendations:
“If an adventitious agent is known to be present in your cell substrate or viral seed, then you should demonstrate that your production process is sufficiently robust to eliminate or inactivate the agent with an appropriate margin of safety.” http://www.fda.gov/downloads/biologicsbloodvaccines/guidancecomplianceregulatoryinformation/guidances/vaccines/ucm202439.pdf
VAGUE OFFICIAL SPECIFICATIONS FOR TESTING
Here are some illustrations of how vaguely the testing for detection of adventitious agents is specified by the authorities:
FDA: “-Several promising areas of research suggest that experimental assays to detect unknown adventitious agents could soon become more generally available. As such assays become available, they could be considered for use in qualifying novel cell substrates, including neoplastic cell substrates.” http://www.fda.gov/ohrms/dockets/ac/01/briefing/3750b1_01.htm
FDA: “- Thus, ensuring that vaccine products that are administered to the public do not contain adventitious agents is a regulatory goal.”
“Of course, the potential for the presence of adventitious agents in any vaccine must also be evaluated in terms of the overall benefit of the product.” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631857/pdf/11485673.pdf
FDA: “ -These factors underscore the need for developing a regulatory framework in which the relative benefits and risks in using tumorigenic (cancer) cell lines for vaccine production can be carefully and cautiously revisited.” http://www.fda.gov/ohrms/dockets/ac/01/briefing/3750b1_01.htm
TESTING OF BATCHES – NO TWO ARE THE SAME
In pharmaceutical production there are never two batches which are the same with respect to test results, be they physical, chemical or microbiological etc. This applies to all injections including vaccines.
One operates in regions, for example: the amount of an ingredient must be within +10% to – 10% of the stated amount.
A certain (small) percentage from each batch is tested and it is deduced from these results whether or not the whole batch should be approved.
POSSIBLE CONSEQUENCES OF INJECTING FOREIGN DNA
“ – DNA is used from such organisms as animals, animal viruses, fungi, and bacteria. It has been documented that injecting foreign DNA in a human may cause it, or a portion of it, to be incorporated into the recipient’s DNA. The horrendous implications for the unborn defy the imagination.” http://healthwyze.org/index.php/vaccine-secrets.html
“- most vaccines are contaminated with a number of known and yet-to-be discovered viruses, bacteria, viral fragments, and DNA/RNA fragments. And, further, our science demonstrates that these contaminants could lead to a number of slowly-developing degenerative diseases, including degenerative diseases of the brain.” http://www.thehealthyhomeeconomist.com/if-you-are-in-support-of-vaccinations/
“- The risks of residual retinal DNA and stray viral contaminants from the animal tissues getting into flu shots are real. DNA snips are classified as either “infectious” or “oncogenic” (tumour causing) by researchers who worry that the stray DNA is being incorporated into the recipient’s DNA …” http://www.newswithviews.com/Tenpenny/sherri123.htm
Interview with Dr. Suzanne Humphries. (Regarding contaminants from 33 minutes):
“- DNA particles from disease matter can get into our DNA and alter us and in my opinion these vaccines are turning us into genetically modified organisms.” http://naturalnews.tv/v.asp?v=BAE7F6323813CFAFB8338173FB11D429
IMPOSSIBLE TO REMOVE DNA CONTAMINANTS
“Manufacturers have been instructed to ensure the final vaccine contains less than 1 million residual animal cells and the amount of stray DNA is less than 10 ng. per vaccine. These regulations admit that animal DNA is injected into human babies and adults with every shot.” http://www.newswithviews.com/Tenpenny/sherri123.htm
“ – FDA also admits concerns about cancer-causing possibility from all types of cell lines. The question begging to be answered is, knowing the potential risks of using cell lines to create vaccines, why is research using cell line technologies allowed to be used at all?”
“ – It is impossible to remove DNA contaminants from vaccines. Although weight limits for contaminating DNA were set by the FDA as far back as 1986, vaccine makers have never been able to reach that goal. The CDC decided to limit their weight recommendation to cancerous cell lines and then increase the other DNA contamination allowance one hundred-fold. However, these limits are only “recommendations” and, therefore, the FDA is unable to enforce them. Vaccine manufacturers continue to have the freedom to take scientific measures to reduce contaminants only if they wish. http://www.opednews.com/populum/diarypage.php?did=14455
This level of contamination (10 nanograms) only applies to a single vaccine. Children today are inoculated with many vaccines before entering school, each with unique DNA and viral contaminants due to the specific cell substrates used for a given vaccine.
This toxic genetic soup is what then flows through a vaccinated person’s body.”
SO WHAT ABOUT THE FLY IN OUR SOUP?
It may not do any harm at all, especially if it has been well heated in the soup!
However, all injected substances including insect fragments bypass the body’s intricate defense mechanism. The same substances which are harmless when ingested are shown to be extremely detrimental to health when injected. This is learned by medical students and others, but many doctors, health authorities and other vaccine promoters appear to ignore this basic fact.
WHERE’S THE LOGIC?
It is thought provoking that doctors and nurses swab the skin with disinfectant to remove some microbes, then jab and force into our children a contaminated, poisonous, genotoxic, disease and cancer causing vaccine soup!