Do you ever stop to wonder what is in those seemingly harmless vaccines that doctors routinely shoot up your children with within their first years of life? Have you ever stopped to wonder what that clear liquid contains or how it could possibly contribute to your child’s future health problems? Do you ever wonder why the government is making it increasingly mandatory for your children to get vaccinated? Now is the time to get informed about the truth behind these vaccinations.
One of the most disturbing things about today’s vaccinations is that they are often made from human fetal tissue! The government is allowing these companies to inject our children with aborted fetal tissue. Have you ever wondered why abortion is so widely accepted and often encouraged? The abortion industry gets paid by vaccine companies and the government for the exchange of deceased human beings! If you are pro-life, but choose to vaccinate, you would be a hypocrite after now knowing this information!
Here is a breakdown of the Cell Lines from the above chart:
MRC-5- First derived from normal lung tissue of a 14-week-old male fetus by J. P. Jacobs in September 1966.The MRC-5 cell strain (like the WI-38 cell line) is susceptible to a wide range of human viruses. This cell line supports the growth of a broad range of viruses, including Adenoviruses; Coxsackie A; Cytomegalovirus; Echovirus; Herpes simplex Virus; Poliovirus; Rhinovirus; Respiratory Syncytial Virus; and Varicella Zoster Virus. Also used for in vitro cytotoxicity testing.
RA 273- Cell line RA273 is commonly called Rubella, which was developed during the 1964 Rubella epidemic. Women were told to abort their children to avoid passing the disease on to the child. The first 26 aborted babies were healthy until the 27th baby they found the living virus, Rubella. Rubella is clinically named: RA273 (R=Rubella, A=Abortus, 27=27th fetus, 3=3rd tissue explants) cultivated on WI-38 cell line. Rubella was developed from the lung, skin, and kidney of aborted fetuses.
WI-38- The WI-38 human diploid cell line was derived by L. Hayflick from normal embryonic (3-month gestation) lung tissue of a female. The cell line has been shown to have one of the broadest human virus spectra of any cell population that has been tested and is especially useful for isolation of rhinoviruses. This cell line supports the growth of a broad range of viruses, including Adenoviruses; Coxsackie A; Cytomegalovirus; Echovirus; Herpes simplex Virus; Poliovirus; Respiratory Syncytial Virus; Rhinovirus; and Varicella Zoster Virus. Also used for in vitro cytotoxicity testing.
PER C6- Created from retinal tissue of 18 week gestation aborted fetus. Developed in 1985, PER C6 is the growth medium for a wide variety of human disease-causing viruses that can be processed into inactivated whole virus, live-attenuated, live-vector, split, subunit and recombinant vaccines. Crucell’s PER.C6® cell line is derived from a single, human retina-derived cell, which was purposely immortalized using recombinant DNA technology. As a result, PER.C6® cells can replicate indefinitely, allowing them to be cultured in single cell suspension under serum-free conditions in quantities appropriate for large-scale manufacturing. PER.C6® cells support growth production of many viral vaccines.
HEK 293- The 293 cell line was derived by transformation of primary cultures of human embryonic kidney(HEK) cells with sheared adenovirus (Ad)5 DNA. HEK 293 cells were generated by transformation of cultures of normal human embryonic kidney cells with sheared adenovirus 5 DNA in the laboratory of Alex Van der Eb in Leiden, Holland in the early 70s. The human embryonic kidney cells were obtained from a healthy aborted fetus and originally cultured by Van der Eb himself.
ViroMed obtains these primary cells from 7- to 15-day old New Zealand white rabbit kidneys that have been treated with enzymes. Commonly used for the isolation of the Herpes Simplex Virus.
(Kidney, African green monkey, Cercopithecus aethiops)
Monkey kidneys are obtained from healthy animals with documented clinical and reproductive histories. The resulting cultures of epithelial-like cells are susceptible to and used as a standard cell substrate for isolation of a broad range of viruses. Supports the growth of a broad range of viruses, including Coxsackie A; Coxsackie B; Echovirus; Influenza A, B; Measles; Mumps; Parainfluenza; Poliovirus; and Rubella.
(Connective tissue, mouse)
The L-929 cell line (also referred to as NCTC-clone 929) was derived in March 1948 by K.K. Sanford, W. R. Earle, and G. D. Likely. Strain L, one of the first cell strains to be established in continuous culture and one of the most widely studied cell strains, was derived from the normal subcutaneous areola and adipose tissue of a 100-day-old male C3H/An mouse. Clone 929, the first cloned strain developed, was established from the 95th subculture generation of the parent strain. Commonly used for immunologic, radiation and toxicological studies. Also used for in vitro cytotoxicity testing.
(Kidney, Rhesus monkey, Macaca mulatta)
The LLC-MK2 line was derived from a pooled cell suspension prepared from kidneys removed from six adult Rhesus monkeys by R. N. Hull, W. R. Cherry and I. S. Johnson. The LLC-MK2 cells have been reported to be susceptible to a broad range of viruses that includes members of the enterovirus, rhinovirus, myxovirus, and poxvirus groups. Susceptible to Poliovirus type 1; as well as Coxsackie A; Coxsackie B; Echovirus; Influenza A, B; Mumps; and Parainfluenza.
The flu vaccine is grown in chicken eggs and thus has the genetic material of the nervous system of chickens as an antigen in the vaccine, which is attracted into the human nervous system and capable of producing an undesirable inflammatory immune response.
Chinese Hamster Ovary
Chinese Hamster Ovary (CHO) cells are being increasingly used in industry to manufacture complex proteins for both therapeutic and diagnostic purposes. Suggested to indirectly suppresses tumor growth of certain tumors by inhibiting infiltration of macrophages which may provide tumor growth promoting activity.
Yeast is a single-celled (unicellular) fungi used to grow vaccine antigens. There has been evidence that the ingestion of genetically modified (GMO) yeast may be detrimental to human health. It is not well studied what effects direct injection into the bloodstream may have. But yeast has been implicated to cause anaphylactic reactions, asthma, allergies, death.
From a fall armyworm (caterpillar). Used to grow flu vaccine instead of usual method using chicken eggs. Findings suggest a possible short-cut to making flu vaccines, focusing on a single protein in the flu virus.
As shown on the above chart, vaccines can cause mild to fatal reactions. Vaccine risk may be a difficult thing to precisely assess, but undeniably each vaccine includes a significant risk worth considering and investigating. The following excerpt outlines a few major problems concerning the monitoring and risks of vaccinations.
Many doctors, understandably, are not willing to admit causation, blame or potential liability and have little incentive to report. Although the federal government’s adverse reactions data are already alarming, even the FDA has confesses that serious reactions to vaccines go unreported by doctors nearly 90% of the time. Some experts estimate that underreporting may be far worse than these figures.
Questionable criteria are too often used in evaluating vaccine “safety.” The practice of biased, skewed science has become commonplace in pharmaceutical risk assessment.
a. Death or weight gain/loss in mice is used to determine human risk — even though animal tests have consistently proven to be inappropriate for human safety assessment.
b. Often, one vaccine is evaluated for adverse effects and compared to another vaccine’s adverse effects, not placebo.
c. The EPA uses Methyl mercury to evaluate the mercury in vaccines, even though ethymercury goes into thimerosol (preservative in vaccines).
d. Many “safety studies” only report adverse effect within a limited time frame. Six, seven or fourteen days after injection is often the cut off criteria for causation.
Risk Assessment is Elusive
Chronic auto-immune, neurological disorders, and other effects of vaccines are difficult to establish by their very nature. Ask yourself this: if you drank something moderately poisonous and ten days later came down with symptoms, could you prove, definitively, a causal link between the two? This could be more difficult than you might think, especially if there were influential counterforce with every incentive in the world to prove that it was coincidental or untrue. In the past thirty years, rates of asthma and AD have doubled, diabetes and learning disabilities have tripled.
In 2004, scientists reported in the Journal of Virology the emergence of a new virus due to the amalgamation of a flavivirus called “Modoc” with the yellow fever vaccine virus. The risk of creating an emerging, pathogenic virus during recombination between vaccine viruses and other viruses is very real, and cannot be ignored.
Perhaps the gravest of concerns is how neurotoxin and carcinogenic (cancer-causing) substances within vaccines are having long-term health effects on our children. As more and more vaccines are added to the “recommended” and “mandatory” lists, young parents are being told that their children must be injected with thirty-seven doses of eleven different vaccines before the age of five.
Autism is a disease involving the brain, the immune system, and the gastrointestinal tract. Once an uncommon disorder in the United States, the incidence of autism is now occurring at epidemic rates. Whereas during the 1970’s one in 10,000 children developed autism, it now affects as many as one in 150. During the 1970’s and 80’s, the federal government established goals for improving vaccination rates. To achieve high vaccination rates (97%), the government implemented nationwide vaccine initiatives, which included offering federal grants to states and encouraging strict enforcement (state mandates for forced vaccination). During this time period, the number of mandated vaccines gradually increased (from 8 in 1980 to 22 in 2000) as vaccination became a requirement for a much younger population (the majority of all 30 childhood vaccines are administered before the age of 18 months). Only after these developments did autism cross class lines. Today autism is widespread in all socioeconomic groups. While it is certain that genetics predisposes individuals to certain diseases, as with all pathology the triggers for disease involve immune system dysfunction brought about by dietary deficiencies and/or environmental stress. In the case of autism, research shows that a high percentage of those affected are victims of massive chemical toxicity. The neurological damage that is characteristic with autism is strikingly similar to the well-established side effects of mercury, aluminum and formaldehyde toxicity. These neurotoxins are common vaccine ingredients. During the 1940’s and 50’s when only some of the population was exposed to only a few vaccines, autism was primarily confined to the upper and upper-middle socioeconomic classes, those who could afford good health care and the cost of vaccination. Strong correlation between autism and vaccine history becomes even more credible when the disease characteristics for both autism and mercury poisoning are compared:
Be Safe! Don’t Vaccinate!
“In conclusion, vaccines are a perfect manifestation of everything that is satanic. They represent an adulterous and arrogant tampering with divine creation, based on the intellectual conceit of “perfecting” creation. They are poisonous, containing derivatives from metals such as mercury and aluminum, and from formaldehyde. They are made from the cell lines and viruses of biblically unclean animals such as monkeys, cats, etc. Worst of all, they are made from the cell lines of premeditatedly murdered children. When such abortion-derived vaccines are injected into other living human beings, a subtle form of cannibalism has occurred, a satanic sacrament has been partaken of, straight from the “table of demons” (1 Cor. 10:21).” -Bob Sperlazzo
References and Beneficial Links:
Abortion Industry Exposed (http://www.jesus-is savior.com/Evils%20in%20America/Abortion%20is%20Murder/aborted_fetus_vaccines.htm)
Future Vaccination Concerns (http://blog.novaccine.com/blogvax/2008/03/index.html)
Sample Religious Exemption Form (http://www.know-vaccines.org/exemption2.html) (http://www.know-vaccines.org/images/DH-681_sample_web.pdf)
Vaccine Laws (http://www.nvic.org/vaccine-laws.aspx)
Vaccine Exemption Forms By State (http://www.unhinderedliving.com/statevaccexemp.html)
Vaccine Law Firm Directory (http://www.nvic.org/lawfirmdirectory.aspx)
Vaccine Reactions and Conditions List (http://www.novaccine.com/reactions-conditions/)
Vaccine List (http://www.novaccine.com/specific-vaccines/)
Vaccine Ingredients (http://www.novaccine.com/vaccine-ingredients/)