Vaccines with Mercury & Fetal Cells ? (WTF!)

If you ever have anybody say vaccines are safe, just refer them to all this data, it shows them what the news will not show them. Then it is they have cognitive abilities… or they don’t.

Mercury is a known neurotoxin, more research should be done to ensure that mercury exposure from any source does not contribute to autism.  Anything listed such as MRC-5, RA273, HEK-293, and strain WI-38, is going to be the aborted fetal cell vaccine component.   Use of Aborted Human Cells in Vaccines are Linked to Rise in Autism.  ALso,   Glyphosate + Aluminum +Mercury + Glutamate = Autism

Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of. aluminum adjuvants through routine vaccinations.  

When I was born Jan of 1970,   Back then, there were only 7 vaccinations. It actually was 8… but they dropped Smallpox.  Today (2021) vaccinations given are somewhere between 35 and 42 vaccinations per child.  Do you think that could cause health problems for the rest of their lives?  My best friends baby cousin died in the early 1980’s.  Doctors clamed that it was 30 hours after the “Vaccinations”, so the vaccination was not the cause. (Cough, Cough)  They called it SIDS.    

Some more interesting statistics   If you want to risk it, that is your right… but you should know as much as possible before you risk your loved one’s health and life-long wellbeing.  With 35 vaccinations on the low end and up to 42 for other risk groups,  How can any doctor look at you in the face and say with 100% surity that there is nothing to worry about?

 Shot in The Dark (2020 Documentary)   

 Institutional Corruption of Pharmaceuticals and the Myth of Safe and Effective Drugs

Glyphosate + Aluminum +Mercury + Glutamate = Autism

Excerpt from Stephanie Seneff, BS, MS, EE, PhD  “I have been searching for environmental causes of autism for over a decdade, and I now believe that I have identified the key toxic environmental factors that are causal in the epidemic. The most significant factor is glyphosate, the active ingredient in the herbicide Roundup. What makes glyphosate so dangerous is that it is pervasive, cumulatively insidiously toxic, and widely believed to be nearly harmless to humans. Glyphosate collaborates with toxic components in vaccines to destroy neurons. These include primarily: aluminum, mercury and glutamate. While glyphosate contamination in the food sets up a leaky gut barrier and leaky brain barrier, glyphosate contamination in many vaccines is ominous and likely catastrophic. In this talk, I will present the hard-core scientific evidence for the complex metabolic cascade these toxic metals and chemicals induce, beginning with disruption of gut microbes, bile acids, and digestive enzymes, and ending with a devastating neurological disability.” (Statement above by Stephanie Seneff, BS, MS, EE, PhD)

There are many people that like to shoot down the pro-choice vaccine opinion, and use blanketed terms that there isn’t research to back it up. There also those keyboard warriors that like to tell parents that they aren’t doctors and that they should listen to the experts. While I would like to also point out that Bill Gates isn’t a doctor either, yet somehow he has become the voice of mandated vaccines. Since we have so much time on your hands these days, here is a laundry list of research. Both anecdotal and peer reviewed. When you have collected this much data and done this much research your opinion may change over vaccines. I bring you information media does not share…
Causal relationship between vaccine induced immunity and autism Subtle DNA changes and the overuse of vaccines in autism Vaccine and Autism- a New Scientific Review Autism and Resulting Medical Conditions: Mercury toxic encephalopathy manifesting with clinical symptoms of regressive autistic disorders. Relation of mercury to high autism rates in boys Elevated levels of measles in children with Autism Abnormal MMR antibodies in children with autism Tylenol, MMR and Autism – A parent survey study A Positive Association found between Autism Prevalence and Childhood Vaccination Peer reviewed study on fetal cell contamination with retro virus associated with autism and cancer  Epidemiologic and Molecular Relationship Between Vaccine Manufacture and Autism Spectrum Disorder Prevalence Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders Rise in autism coincides with rise in vaccines A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States

Elevated levels of measles antibodies in children with autism. – PubMed – NCBI Pediatr Neurol. 2003 Apr;28(4):292-4. Research Support, Non-U.S. Gov’t A study published in the Journal of Biomedical Sciences determined that the autoimmunity to the central nervous system may play a causal role in autism. Researchers discovered that because many autistic children harbour elevated levels of measles antibodies, they should conduct a serological study of measles-mumps-rubella (MMR) and myelin basic protein (MBP) autoantibodies. They used serum samples of 125 autistic children and 92 controlled children. Their analysis showed a significant increase in the level of MMR antibodies in autistic children. The study concludes that the autistic children had an inappropriate or abnormal antibody response to MMR. The study determined that autism could be a result from an atypical measles infection that produces neurological symptoms in some children. The source of this virus could be a variant of MV, or it could be the MMR vaccine. Doctors who explain clearly why vaccines aren’t safe or effective.

1. Dr. Nancy Banks –

2. Dr. Russell Blaylock –

3. Dr. Shiv Chopra –

4. Dr. Sherri Tenpenny –

5. Dr. Suzanne Humphries –

6. Dr. Larry Palevsky –

7. Dr. Toni Bark –

8. Dr. Andrew Wakefield –

9. Dr. Meryl Nass –

10. Dr. Raymond Obomsawin –

11. Dr. Ghislaine Lanctot –

12. Dr. Robert Rowen –

13. Dr. David Ayoub –

14. Dr. Boyd Haley PhD –

15. Dr. Rashid Buttar –

16. Dr. Roby Mitchell –

17. Dr. Ken Stoller –

18. Dr. Mayer Eisenstein –

19. Dr. Frank Engley, PhD –

20. Dr. David Davis –

21. Dr Tetyana Obukhanych –

22. Dr. Harold E Buttram –

23. Dr. Kelly Brogan –

24. Dr. RC Tent –

25. Dr. Rebecca Carley –

26. Dr. Andrew Moulden –

27. Dr. Jack Wolfson –

28. Dr. Michael Elice –

29. Dr. Terry Wahls –

30. Dr. Stephanie Seneff –

31. Dr. Paul Thomas –

32. Many doctors talking at once –

33. Dr. Richard Moskowitz – censored

34. Dr. Jane Orient –

35. Dr. Richard Deth –

36. Dr. Lucija Tomljenovic –

37. Dr Chris Shaw –

38. Dr. Susan McCreadie –

39. Dr. Mary Ann Block –

40. Dr. David Brownstein –

41. Dr. Jayne Donegan –

42. Dr. Troy Ross – censored

43. Dr. Philip Incao –

44. Dr. Joseph Mercola –

45. Dr. Jeff Bradstreet –

46. Dr. Robert Mendelson –

47. Dr Theresa Deisher

48. Dr. Sam Eggertsen- Hundreds more doctors testifying that vaccines aren’t safe or effective, in these documentaries….

1. Vaccination – The Silent Epidemic –

2. The Greater Good –

3. Shots In The Dark –

4. Vaccination The Hidden Truth –

5. Vaccine Nation –

6. Vaccination – The Truth About Vaccines –

7. Lethal Injection –

8. Bought –

9. Deadly Immunity –

10. Autism – Made in the USA –

11. Beyond Treason –

12. Trace Amounts –

13. Why We Don’t Vaccinate –

  (I woinder if this vaccination schedule has anything to do with it)

Do you want Bill Gates Vaccination with indemnity?  or NO?

These Guidelines below are derived from the United States Centers for Disease Control & Prevention.   Lets first look at the current VAXX schedule.  Then we can talk deeper…

Hepatitis B.  Minimum age: Birth, 3 doses.  (Dose 1 to dose 2: 4 wk,  Dose 2 to dose 3: 8 wk 16 wk after dose 1)

Rotavirus.  Minimum age: 6 wk  3 doses. (Dose 1 to dose 2: 4 wk. Dose 2 to dose 3: 4 wk

Diphtheria, tetanus, pertussis (DTaP)  Minimum age: 6 wk,   5 doses (Dose 1 to dose 2: 4 wk,  Dose 2 to dose 3: 4 wk,,Dose 3 to dose 4: 6 mo,  Dose 4 to dose 5: 6 mo)

Guidelines on Immunization from the American Academy of Pediatrics Committee on Infectious Diseases and the Advisory committee on Immunization Practices specify that if the fourth-dose DTaP vaccine was administered 4 months or more after the third dose, at an appropriate age, it can be counted as a valid dose and need not be repeated after the recommended 6-month interval between doses 3 and 4. 

Haemophilus influenza type b (Hib).  Minimum age: 6 wk,  4 doses (Dose 1 to dose 2: 4 wk (age < 12 mo), 8 wk (age 12-14 mo, final dose), none (age >15 mo) (Dose 2 to dose 3: 4 wk (age < 12 mo), 8 wk (age 12-15 mo, final dose), none (age >15 mo) (Dose 3 to dose 4: 8 wk (age 12-59 mo, final dose)

Pneumococcal.  Minimum age: 6 wk. 4 doses (Dose 1 to dose 2: 4 wk (age < 12 mo), 8 wk (age 24-59 mo, final dose), none (age >24 mo) (Dose 2 to dose 3: 4 wk (age < 12 mo), 8 wk (age >12 mo, final dose), none (age >24 mo).(Dose 3 to dose 4: 8 wk (age 12-59 mo, final dose)

Guidelines on Immunization from the American Academy of Pediatrics Committee on Infectious Diseases and the Advisory committee on Immunization Practices state to administer 1 dose of PCV13 if any incomplete schedule of 3 doses of PCV (PCV7 and/or PCV13) were received previously. Administer 2 doses of PCV13 at 8 weeks apart if unvaccinated or any incomplete schedules of fewer than 3 doses of PCV (PCV7 and/or PCV13) were received previously. [1, 2, 3]

Inactivated poliovirus  Minimum age: 6 wk  4 doses. (Dose 1 to dose 2: 4 wk) (Dose 2 to dose 3: 4 wk) (Dose 3 to dose 4: 6 mo)

Measles, mumps, rubella Minimum age: 12 mo 2 doses. (Dose 1 to dose 2: 4 wk)

Varicella.  Minimum age: 12 mo  2 doses.  (Dose 1 to dose 2: 3 mo)

Hepatitis B  Minimum age: 12 mo   2 doses.(Dose 1 to dose 2: 6 mo) 

Diphtheria, tetanus, pertussis vaccine (DTaP)  Min age: 7 years. 4 doses (Dose 1 to dose 2: 4-week interval)  (Dose 2 to dose 3: 4-week interval if dose 1 administered before first birthday; 6-month interval (as final dose) if dose 1 administered at or after first birthday (Dose 3 to dose 4) 6-month interval if dose 1 administered before first birthday

CDC recommendations for routine adolescent Tdap booster  1 dose 

Guidelines on Immunization from the American Academy of Pediatrics Committee on Infectious Diseases and the Advisory committee on Immunization Practices specify that if the fourth-dose DTaP vaccine was administered 4 months or more after the third dose, at an appropriate age, it can be counted as a valid dose and need not be repeated after the recommended 6-month interval between doses 3 and 4. 

Human papillomavirus 9-valent vaccine Minimum age: 9 yr,  Routine dosing intervals recommended Age 9 through 14 years: 2 doses 6-12 months apart Age 15 through 45 years:        3 doses at 0, 1 to 2, and 6 months

Hepatitis A vaccine.  Minimum age: 12 mo 2 doses Dose 1 to dose 2: 6 mo

Remember 1970 there was only 7 vaccinations. Why have a special court for vaccianltions ?

Worldwide Autism Epidemic & Human Fetal Manufactured Contaminated Vaccines.

Excipients Included in U.S. Vaccines, by Vaccine

Vaccine Ingredients and Manufacturer Information

(alphabetical order by vaccine)

Now read this, OMG! 

Perception….the USA population in 2019 is 328,239,523. if the Vaccines failure rate to damage a child is only at 2% then 6,564,790 people would be damaged in some way. Autism spectrum, Lifelong health issues, and even DEATH. All drugs have a failure rate. What are the Vaccines ACTUAL FAILURE RATE? If it is only 5%. The Damaged number would be 16,411,976 of USA damaged humans. If every human on EARTH (7.8 BILLION) was vaccinated the number calculates to 390,000,000. We give the same shots to a 15 Pound baby or a preemie.

” Current vaccination recommendations, schedules and vaccine design have largely neglected the growing number of risk populations that for different reasons present an impairment or modulation of immunological functions; with increased infection susceptibility and impaired vaccine responsiveness”

Rise in autism coincides with rise in vaccines…. hmmmmmm?

Subtle DNA changes and the overuse of vaccines in autism

Summary of previous Journal of Immunology…/AR-10-12-rata-AUTISM-VACCINE.pdf

Mercury toxic encephalopathy with clinical symptoms of regressive autistic disorders

Relation of mercury to high autism rates.

Abnormal MMR antibodies and autism

Tylenol, MMR and Autism

A Positive Association found between autism prevalence and childhood vaccination…/00000014/art00002…

Peer reviewed study on fetal cell contamination with retro virus associated with autism and cancer…/5402912

Study documentation, Dr. Deisher

Hypothesis: conjugate vaccines may predispose children to autism spectrum—human-diploid-cells-aborted-fetal-cell—tissue.html 

Below Is from Dirty Big Pharm Truth 

Autistic disorder change points years are coincident with introduction of vaccines manufactured using human fetal cell lines, containing fetal and retroviral contaminants, into childhood vaccine regimens. This pattern was repeated in the US, UK, Western Australia and Denmark. Thus, rising autistic disorder prevalence is directly related to vaccines manufactured utilizing human fetal cells. Increased paternal age and DSM revisions were not related to rising autistic disorder prevalence. 

Read more:

Again, this is the information that the CDC has entirely ignored. Do you really think they don’t know that this is out there? Why are there no funded follow up studies; just like there never are any serious vaccine risk issue that has been found by independent lab and researcher. Trust them, trust the CDC and FDA? I think, not.  

Impact of environmental factors on the prevalence of autistic disorder after 1979. Journal of Public Health and Epidemiology – September 2014

Title: Spontaneous Integration of Human DNA Fragments into Host Genome
K. Koyama, T. A. Deisher
Sound Choice Pharmaceutical Institute, Seattle, WA

Human Fetal DNA Fragments In Vaccines Are A Possible Cause For Autism – According To This Stanford Scientist

Functional impact of global rare copy number variation in autism spectrum disorders

Detection and characterization of copy number variation in autism spectrum disorder.

The Shocking Truth about aborted human fetal cells in vaccines

Merck Has Some Explaining To Do Over Its MMR Vaccine Claims

New Study Finds A 340 Percent Increased Risk Of Autism In Boys Who Receive MMR Vaccine On Time

Translational Neurodegeneration 2014, 3:16
RESEARCH Open Access
Measles-mumps-rubella vaccination timing and autism among young african american boys: a reanalysis of CDC data

Dr Brian Hooker Presentation Exposes CDC Lies

US CDC Scientists Knew All Children At Risk of Autism from MMR Vaccine and Hid the Data – Again

Dr. Brian Hooker: Father of Vaccine-damaged Child and His Relentless Pursuit to Expose Fraud at the CDC

 (This should make all vaccine truth informed people, mad, to realize how badly they continue to lie and misrepresent the truth on the pro-vaccine, and the CDC side)

Dr. Brian Hooker: Father of Vaccine-damaged Child and His Relentless Pursuit to Expose Fraud at the CDC

Brian Hooker’s Findings Are Confirmed By CDC’s Results

The Mechanisms of Vaccine Injury and Via Cytokine Storm


Lets go to the basics of this issue. 

Autism One Preview Series – Theresa Deisher, PhD on The Robert Scott Bell Show

Theresa Deisher, PhD., from Sound Choice Pharmaceutical Institute, conducts research into the biologic and physiologic consequences of using aborted fetal material for drug, vaccine and cosmetic production. What is “decorated” DNA? How long has the FDA known about this genetic contamination?

Is it really possible to “green” a vaccine? Why do these adjuvants and  super-agonists cause autoimmunity and cancer? Dr. Deisher is an internationally renowned expert in the field of adult stem cell therapies and regenerative medicine. Her discoveries, particularly in the fields of cardiovascular biology and stem cell research, continue to be considered some of the most significant in the scientific community, including her initial discovery and identification  of adult heart stem cells.

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (1 of 4). (These are the same four videos as above, so they can easily be copied and pasted if you need them. This is some of the most important information on vaccines, to date).

Published on Dec 5, 2012
Dr. Deisher testifies at the MN House about vaccine safety. She presents research demonstrating a link between the rise in the rates of autism and the use of aborted fetal cells in the production of vaccines. Dr. Deisher is the president and founder of SoundChoice, a non-profit that works to provide safe vaccination alternatives.

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (2 of 4).

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (3 of 4).

Dr. Deisher testifies on the connection between vaccines and rising rates of autism (4 of 4).

Dr. Theresa Deisher: Moral Vaccine Development

AVM Biotechnology, LLC 
 CEO, Founder and Research and Development Director 

June 2008- Sound Choice Pharmaceutical Institute 

Dedicated to safe, effective, affordable and ethical human therapeutics, focusing initially on 
regenerative medicine and vaccinations. 

Committed to providing education, scientific research, development and resources to encourage safe 
and moral medicines and therapeutics.

AVM Biotech

August 12, 2009 – By Judie Brown
By Theresa A. Deisher, Ph.D.

Testimony Submitted by: 
Dr. Theresa A. Deisher
Sound Choice Pharmaceutical Institute 
AVM Biotechnology 
CEO and Managing Member

This is an excellent and informative read, as to the situation we are talking about here, in regard to aborted fetal cell production types of vaccines. You can easily see how strong this research is. And the CDC is doing what? Noth


Some childhood vaccines that are mandated prior to entering kindergarten are only available in the US produced using aborted fetal cells, these include MMR (mumps measles rubella) and chickenpox. Other mandated childhood vaccines are available from both animal or human sources, and yet parents and grandparents are not informed of this so that they can choose a vaccine compatible with their consciences. 

 When pharmaceutical companies switched from using animal cell lines to using aborted human fetal cells lines to produce these vaccines, in the mid to late 1970s, they assumed, without any evidence, that using aborted fetal cells would result in a more efficient production system. Brief discussions about potential adverse health consequences of using aborted human cell lines for vaccine production were captured in minutes from FDA advisory meetings about this switch. However, no studies have been done to actually measure the extent of those potential adverse consequences. 

Vaccines and biologics (engineered proteins as drugs) are too large to make in a test tube, so companies harness the normal machinery used to make these, cells. No final drug is ever completely ‘pure’ and you will find contaminating DNA and cellular debris from the production cell in your final product. When we switch from using animal cells to using human cells we now have human DNA in our vaccines and our drugs. 

Shouldn’t parents and grandparents know that when they immunize their children with a particular vaccine they are also injecting their children with DNA from an aborted fetus? Yet there are no laws that require drug manufacturers to inform the public of this. The package insert for the MMR II vaccine (mumps, measles, rubella) states : “MERUVAX* II (Rubella Virus Vaccine Live), the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung Fibroblasts”, but doesn’t tell you that contaminating DNA from the WI-38 propagation strain is found in the final product. The package insert for Varivax, a chickenpox vaccine, states that the vaccine contains “residual components of MRC-5 cells including DNA and protein”, but how many parents or grandparents, let alone pediatricians and pharmacists, would know that MRC-5, or WI-38, is a cell line derived from an aborted fetus, and that the contaminating DNA and protein listed on the package insert is the DNA and protein of an aborted fetus? If we have the legal right to know what is in our Big Macs, don’t we have the right to know what is in our vaccines and medicines? Contaminating human DNA in these vaccines has the potential to trigger auto-immune responses and also the potential to become incorporated into our own genes, a process called homologous recombination. 

Read more:

Exhibit BN. Theresa A. Deisher, Ph.D (another good informational read)

Testimony Submitted by: Dr. Theresa A. Deisher 
Sound Choice 

Pharmaceutical Institute 
President: AVM Biotechnology 
CEO and Managing Member


Aborted human DNA in our vaccines is not the end, it is only the beginning, as the creation of human-animal hybrids demonstrates.  A new aborted fetal  cell line has been developed, called PerC6, and licenses have been taken by over 50 partners, including the NIH and the Walter Reed Army Institute, to use this cell line for new vaccine and biologics production.  The goal of the company that created the PerC6 is to become the production cell line for ALL vaccines, therapeutics antibodies, biologic drugs and gene therapy.  We must know the consequences of contaminating human DNA before we wake up and discover that all newly approved recombinant drugs are produced by aborted fetal cells.

 Aborted fetal cells are also now used to discover new food additives and  flavor enhancers. Imagine that; the cells from an aborted fetus used to make your candy sweeter.  Isn’t that disgusting?  And furthermore, as the company that performs this research states, one may never know these additives will someday be in our food products due to the current labeling guidelines which would allow these new additives to be captured under the generic label of ‘artificial flavors’. 

The conscience rights of almost half of the US population are being denied by our current labeling guidelines for biologics and food additives.  A lack of information forces people to be complicit in a practice that many would find reprehensible if they only knew that aborted fetal cell lines are being used for drug discovery and production.   

Thank you for your attention.

AVM Biotech

Human Diploid cells: MRC5 proteins:(human diploid cells, aborted fetuses)

Derived from normal lung tissue of a 14-week-old male fetus by J. P. Jacobs  in September 1966 (Nature 227: 168-170, 1970), the MRC-5 cell line was established in a growth medium consisting of Earle’s Basal Medium in Earle’s balanced salt solution supplemented with 10% calf (bovine) serum. The MRC-5 cell strain (like the WI-38 cell line) is susceptible to a wide range of human viruses. 

Viral vaccines are often cultured on aborted fetal tissue. There are several types of fetal cells in which the virus is grown: MRC5, WI-38, WI-26 VA4, RA273, PER C and HEK 293.  This has raised concerns, with reports of some individuals with religious objections to abortion refusing vaccination because they feel this makes them complicit with the original act of abortion. 

Some deem it unethical to use vaccines from fetal cell lines for the following reasons:

1) If abortion is immoral then profiting from it must also be immoral.
2) The unborn child was unable to give consent for its body
parts to be used, so it is therefore disrespectful to the dead.
3) The argument that “the fetal tissues would just go to waste if they were not used” was not accepted at the Nuremberg trials of scientists who used body parts from concentration camp victims. This abuse of the child’s body only compounds the
injustice of the original abortion, even if the vaccine producers were in no way connected to the abortion.
4) Use of this vaccine implies acceptance of the legality of abortion, and does nothing to discourage the use of fetal parts or
cell lines in vaccine manufacture or other branches of medicine.

Vaccines that use aborted fetuses in production:
Acambis 1000 (smallpox) Acambis —  MRC5
Avaxim (hepatitis A) Pateur Merieux — MRC5
Biavax (mumps, rubella) Merck — RA273, WI-38
Ervevax (rubella) Smithkilne Beecham — MRC5
Havarix  (hepatitis A) Smithkilne Beecham — MRC5
Imovax HDCV, DCO (rabies) Pasteur Merieux Connaught — MRC5
Meruvax II (rubella) Merck — RA273, WI-38
MMR II (Measles, mumps, rubella) Merck Sharp & Dohme — WI-38
MR VAX (measles, rubella) Merck — RA273, WI-38
Poliovax (polio, IPV) MRC5
Priorix (measles, mumps, rubella) Smithkline Beecham — MRC5
Proquad  (mmr, chickenpox/varicella) Merck — RA273, WI-38, MRC5
Twinrix (hepatitis A and B) GSK — MRC5
VAQTA (hepatitis A) MSD — MRC5
Varivax (chickenpox, varicella) MSD — WI-38
Zostavax (shingles) Merck — MRC5, WI-38 

Source: (for some reason this is a no longer available link)

(not available for all vaccines)

The Campaign For Ethical vaccines
Alternatives to vaccines made from aborted babies

Chickenpox Vaccine Use is Highly Statistically Related to Autism Disorder
NOVEMBER 27, 2012  

“What the graphs show you is that in almost every state in the US, the use of chickenpox vaccine is directly related to the number of children diagnosed with autism disorder in each year during which chickenpox vaccine use rose from 0% until it reached its maximum use. I’ll say that again, for emphasis: as more and more children were vaccinated with the chickenpox vaccine, more and more children were diagnosed with autism disorder. Statistical analysis on the data for the entire US yields a correlation coefficient (R2) of 0.9598. For those of you who don’t understand statistics, an R2 of 0.9598 is very significant.”

Read the entire story here.

Is Aborted Fetal DNA in Vaccines Linked to Autism?

 Fetal Tissue in Vaccine Production May be Linked to Autism in Children Claims Campaign Group

Study Confirms Autism Boom – Correlates with Aborted Fetal DNA in Vaccines

Abortion-Tainted New Flu Vaccine From Vaxin Uses Aborted Fetal Cell Lines

Spontaneous Integration of Human DNA Fragments Into Host Genomes


Spontaneous cellular and nuclear DNA uptake was evident in HFF1 and U937. Spontaneous cellular uptake was seen in NCCIT. DNA uptake in BE (2)-C, M059J, and M059K was not measurable because of high auto fluorescence of the cells. No Cy3 signal was observed in HL-60. The amount of labeled Cy3 human Cot1 DNA incorporation in U937 genomic DNA was 0.0111 +/- 0.0034pg (n=12) per cell in 24 hours, which was approximately 0.167% of total U937 genomic DNA.


This study demonstrates that primitive short DNA fragments (50-300 bp) are spontaneously taken up by HFF-1, U937 and NCCIT cells and inserted into the genome of the monocytic leukemia cell line U937. Hence, vaccines containing residual HERVK and human fetal DNA fragments may contribute to the genomic instability observed in ASD.

Autism Research

The scientific community now knows that children with regressive autism have hundreds of de novo and diverse gene mutations. That means that regressive autism is not genetic. It must be triggered by an external event that can create
hundreds of different DNA breaks and mutations. That has been obvious to us at SCPI since we were founded.

Since 2008, SCPI has been ahead of the field, doing the cutting edge biology, molecular modeling, computational informatics, and ecology to figure out what is causing so many DNA breaks and mutations in our children, long before the 2011 and 2012 publications put the hundreds of de novo mutations together. That’s because we knew that a condition associated with hundreds of different genes could not possibly be genetic. We knew that DNA and retroviral contaminants are present in some childhood vaccines and that these types of contaminants are known to cause DNA breaks and mutations.

Have we created the perfect storm for DNA breaks, mutations, and regressive autism in our children? In 1979 we started injecting our children with vaccines that are contaminated with aborted fetal DNA fragments and a retrovirus, and autism began to rise. Then we added more jabs with aborted fetal vaccines and thimerosal, which can also cause DNA breaks, to vaccines in 1988, and autism rose more. Then in 1995, we added much more aborted fetal DNA contaminants to the chickenpox vaccine, and autism really rose. And now we have children born to older dads who have sperm with very breakable DNA. Aborted fetal contaminated vaccines plus thimerosal plus older dads result in more DNA breaks, thus more de novo mutations, in our children.

Drugs and vaccines are too large to produce in a test tube, and therefore, they must be manufactured using cell lines. The final products contain contaminants from the cell line used to manufacture the drug or vaccine. When animal cell lines are utilized, these contaminants are recognized by our immune systems as ‘foreign’ and are eliminated from our bodies. However, when primitive human cell lines (such as an aborted fetal cell line) are used, these contaminants have the potential to trigger autoimmune diseases or genomic instability. When we use aborted fetal produced vaccines or cosmetics, we are
also injecting or transferring DNA and viruses from the aborted fetus used to create the cell line into our own bodies.


The contaminants found in vaccines and drugs that are manufactured using aborted fetal cell lines present the perfect storm of contaminants to cause genomic instability. Some childhood vaccines contain very high levels of short human fetal DNA fragments, which gene therapy studies have taught us are the perfect size to insert into our genes. Some childhood vaccines also contain a retroviral contaminant called HERVK, which is in the same family of retroviruses as the one that caused cancer in 4 of 9 boys.

Read more:

DNA Fragments Research
 •Vaqta Hepatitis A Vaccine is contaminated with MRC5 aborted fetal DNA and proteins (see page 1)
•MMR II is manufactured in WI 38 aborted fetal cell line
•Hepatitis A vaccine contaminated with MRC5 aborted fetal debris (see page 8)
•Chickenpox Contaminated with Human Fetal DNA (see page 3)
•Chickenpox and MMR II vaccines are contaminated with a retrovirus


The dangers of using aborted fetal cell lines for vaccine manufacture have been debated by the FDA for over 50 years, and yet they have not done sufficient safety studies.  The active component of a vaccine is a virus. Viruses are too large to manufacture in test tubes. Therefore, vaccine manufacturers exploit the natural method of producing virus– they inoculate
cells and the cells produce the virus for them.  Each vial of vaccine contains contaminants from the cells used to make the virus.  When we use animal cells to make viruses, the residual material is not human and so we mount an immune response to it and eliminate it.  However, in the case of vaccines produced using aborted human fetal cell lines, we have the dangers of triggering an autoimmune response and insertion of the contaminating DNA to disrupt the child’s own genes.

In the US, autism has spiked up in 3 distinct years, called changepoints.  The first changepoint occurred in 1981, the second in 19881, and the third in 1996.  These spikes coincide with the introduction of vaccines that are produced in aborted fetal cells.  In 1979, aborted fetal cell produced MMR II was approved in the US. Compliance campaigns brought MMR II  use up from as low as 49% for children born before 1987 to over 82% for children born in 1989 and later. A second dose of MMR II was also introduced to the vaccination schedule for children born in 1988 and later. The third changepoint corresponds to the approval of aborted fetal cell produced Varivax (chickenpox) in 1995 (See figure below).

Read more:

Did you know that some vaccines are made using aborted fetal cells?
Read the June 2013 Newsletter

1) Did you know that some vaccines are made using aborted fetal cells?

 On June 24, we sent a survey to 3,738 people on our email list asking this question. Of the 1,138 people who have taken the survey so far, 23% (298) did not know that some childhood vaccines, as well as the shingles vaccine and a rabies vaccines, are manufactured using aborted fetal cell lines. Once people know how vaccines are manufactured, 94% of them do not feel comfortable using vaccines made in aborted fetal cell lines. The information is difficult to obtain because many pediatricians and other doctors do not know that the vaccines are manufactured using aborted fetal cells. This survey shows that we must do a better job of keeping people informed!

2) Did you know that those vaccines are contaminated with DNA, cellular debris, and in some cases, a retrovirus from the aborted fetus?

Surprisingly, only 50% of respondents said they were aware that some vaccines are contaminated with aborted fetal DNA and cellular debris. This response has let us know that we must do a better job explaining to people where the contaminants come from!

3) Our newsletters can keep you informed and up-to-date. Please read the whole newsletter so you don’t miss anything that you might want to know.

Aborted Fetal Vaccines

Vaccines, Abortion, & Fetal Tissue

Vaccines using aborted fetal cell lines

This study is as well another big strike against several of the currently made vaccines that are made by used of aborted fetal cells. Although the study article doesn’t makes reference per say to human diploid cells, it rather uses terminology referring to human DNA residuals. That to me would be the same thing, or derived from the same thing. Human diploid cells of course can only come from and typically one thing, aborted fetal tissue.

The MMR vaccine is made by use of aborted fetal tissue; more specifically, MRC-5 and WI-38. For a list of other vaccines that are as well made with and by the use of human diploid tissue, a list of those vaccines is in the link below. 

Computational Detection of Homologous Recombination Hotspots in X-Chromosome  Autism Associated Genes
Friday, May 21, 2010
Franklin Hall B Level 4 (Philadelphia Marriott Downtown)
A. Ard , University of Portland, Portland, OR M. LaMadrid , Sound Choice Pharmaceutical Institute, Seattle, WA
S. Bwabye , Sound Choice Pharmaceutical Institute, Seattle, WA
K. Koyama , Sound Choice Pharmaceutical Institute, Seattle, WA
T. Deisher , Sound Choice Pharmaceutical Institute, Seattle, WA

Background: Autism prevalence rates in the US and UK began increasing temporally close to the time that the MMR vaccine was switched from the type manufactured using animal cells to a type manufactured using human cells. A yet unstudied possible environmental cause for autism is residual human DNA contaminant in the vaccines produced using human
cells.    Debate about the dangers of residual human DNA in vaccines has been going on for 50 years, mainly related to cancer initiation. Clinical gene therapy (1996) of male infants has induced childhood leukemia due to improper  DNA insertion. To minimize the possibility of oncogenic DNA integrating into a vaccine recipient’s genome, the WHO and FDA have recommended DNAse treatments to reduce the size of contaminant DNA fragments to less than genic lengths, ~200-1000bp.   

These recommendations were developed before the sequencing of the human genome. DNA cellular diffusion studies have shown that short DNA fragments (<250bp) have higher probability of entering the nucleus than longer lengths. Gene therapy studies have also demonstrated that naked DNA, injected intramuscularly, can remain  intact and be transported
to the brain via retrograde axonal transport in motor neurons. Once inside the nucleus, exogenous DNA can  integrate via homologous recombination, potentially in genomic regions called ‘recombination hotspots’. Intra-species DNA integration, e.g., by homologous recombination, occurs with a probability a billion times greater than inter-species homologous recombination.   Integration of short human DNA fragments has the potential to contribute to various human diseases,
including autism.

Objectives: To verify the lengths of residual human DNA in vaccines and to determine if recombination hotspots occur near or in X-chromosome genes known to be associated with autism.

Methods: Human DNA from inactivated vaccines was isolated and characterized using standard procedures. A list of recombination hotspots, computationally derived by using Hapmap Phase II data, was downloaded.   A list of 238 genes associated with autism (AAGs) was downloaded from the ACGMAP website. Gene coordinates, including transcription start and end sites, were downloaded from the UCSC Human Genome website. Software was written to automate the location of overlaps between autism associated genes and recombination hotspots.

Results: The average human DNA fragment length in rubella vaccine was 220 base pairs.  Out of 1145 hotspots in the X-chromosome, 25 hotspots are located in 5 of 15 X-chromosome AAGs, between the transcription start and end
sites.   These genes are NLGN3 and NLGN4X (neuroligins involved in synapse formation), AFF2 and  IL1RAPL1 (involved in X-linked mental retardation), and GRPR (gastrin releasing peptide receptor).

Conclusions: Autism-associated genes in the X-chromosome contain multiple regions where potential insertion of short, non-host homologous DNA can occur. With new knowledge due to the human genome project, particularly in regards to
SNPs and epigenetics, further work must be done to understand the implications of integrated residual human DNA to the etiology of autism.

Computational Detection of Homologous Recombination Hotspots in X

Excerpt from the abstract:

June 3, 2010
SCPI Study on Aborted Fetal DNA in Vaccines Presented at International Meeting for Autism Research

For Scientific Data: Homologous Recombination Study

There is also shown in the study itself, what they call a Changepoint analysis for US(DOE) and CA(DDS) Autistic Disorder, Fig. 1. You can see the what appear to be direct increases in ASD after the use of vaccines containing human DNA residuals.

The study is said to be only a hypothesis, but none the less comes up with some very significant findings, not only in relation to autism, but as well in what would be clear resulting in potential adverse effects on health, irregardless of if actual ASD has resulted.  

Is There a Link Between Aborted Fetal DNA in Vaccines and Autism?

Do you see how close it comes in use of aborted fetal cells in the use of vaccines, to changing the makeup of human genetics? This is man replacing the creator. Literally so, and thinking that man can improve on and make what was created, better. You can see how entirely misguided and oblivious to what potentially can happen, this is. Triggers for autism? They clearly do not have a clue, nor care to at pharma, FDA, and nor the CDC.

Using Homologous Recombination to Manipulate the Genome of Human Somatic

Non-homologous DNA end joining – Acta Biochimica Polonica—Acta-Biochimica-Polonica-download-w4566.html

Mechanism of Eukaryotic Homologous Recombination

Genomic disorders: A window into human gene and genome evolution

Claudia M. B. Carvalhoa, Feng Zhanga, and James R. Lupskia,b,c,1
Author Affiliations
Edited by Diddahally R. Govindaraju, Boston University School of Medicine, Boston, MA, and accepted by the Editorial Board November 5, 2009 (received for review July 22, 2009)


Gene duplications alter the genetic constitution of organisms and can be a driving force of molecular evolution in humans and the great apes. In this context, the study of genomic disorders has uncovered the essential role played by the genomic architecture, especially low copy repeats (LCRs) or segmental duplications (SDs). In fact, regardless of the mechanism, LCRs can mediate or stimulate rearrangements, inciting genomic instability and generating dynamic and unstable regions prone to rapid molecular evolution. In humans, copy-number variation (CNV) has been implicated in common traits such as
neuropathy, hypertension, color blindness, infertility, and behavioral traits including autism and schizophrenia, as well as disease susceptibility to HIV, lupus nephritis, and psoriasis among many other clinical phenotypes. The same mechanisms implicated in the origin of genomic disorders may also play a role in the emergence of segmental duplications and the evolution of new genes by means of genomic and gene duplication and triplication, exon shuffling, exon accretion, and fusion/fission events.

Aborted Fetuses Used in Vaccines!


Here is a little more information; if you are unaware of this. An informational expose and a list of vaccines that have been made with human diploid cells, (shocking).

Children of God for Life:

U.S. Vaccines Derived From Abortion

MRC-5 (Lung, diploid, human)

Derived from normal lung tissue of a 14-week-old male fetus by J. P. Jacobs  in September 1966 (Nature 227: 168-170, 1970), the MRC-5 cell line was established in a growth medium consisting of Earle’s Basal Medium in Earle’s balanced salt solution supplemented with 10% calf serum. Following initial  cultivation, subcultures were prepared twice weekly at a 1:2 ratio. When the cells reached approximately the 7th population doubling, the majority of the cultures were harvested to prepare a frozen cell stock. Subsequent observations revealed that the MRC-5 cells are capable of attaining 42-46 population doublings before onset of the decline in proliferation usually experienced with human fibroblast lines. The MRC-5 cell strain (like the WI-38 cell). 

Culture Medium
Minimum essential medium (Eagle), with 10% heat inactivated fetal bovine serum. 

Growth Characteristics
Cells seeded at a concentration of 4×104 cells/cm2 in the above culture medium will be 100% confluent in 7 days. 

Plating Efficiency Less than 1%. Morphology Fibroblast-like. Karyology

Chromosome Frequency Distribution is 46 Cells: 2n = 46. 

Species: Confirmed as human by cytotoxic-antibody dye exclusion test.

Common Utilization 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 Culture Medium


Look healthy, in regard to injecting a vaccine made from these cells? Not at all.

Just to show you a bit about what unresolved vaccine contamination is, and what it can do!

The CDC and FDA would have us believe that vaccines go through an adequate step process of purification. 

With what we have more recently seen since the days that SV- 40 was known of  as a contaminant in the polio vaccine, there has been as well ongoing issues since with such as so called pig virus DNA in Rotarix, and HPV DNA found in such as Gardasil, that DNA is said to be or have been firmly locked onto the aluminum adjuvent. 

Then we can add this information below as well and piece it together as a conclusion in fact that vaccine makers hav NOT been able to purify these vaccines anywhere nearly as well as they would have us believe they are.

The whole picture leaves remaining as to these kinds of vaccines, a showing as to the facts in reality of there being something far less remaining than a picture of proven and unquestioned safety. 

The CDC and FDA know of the past problems with contamination, and they essentially admit they have not a solution to it, and they do know that such contamination can cause chronic disorders and disease in the human body.

“Designer” Cells as Substrates for the Manufacture of Viral Vaccines

Excuse Me Waiter – There’s a Fly in My Vaccine Soup! DNA RESIDUE IN VACCINES

The below gives a basic outline of what they have the ability to find in vaccines in regard to contamination; but what assurance is that these vaccines are ever actually tested. And they can not find what they do not know to look for and in most cases of vaccine contamination they new knew what they needed to be looking for. In all cases the vaccine contamination was found the details of that, by an independent lab. The FDA did not find it, and the CDC did not find it and make that public; and nor did big pharma.

Viral Nucleic Acids in Live-Attenuated Vaccines: Detection of Minority Variants and an Adventitious Virus

J Virol. 2010 Jun;84(12):6033-40. doi: 10.1128/JVI.02690-09. Epub 2010 Apr 7.
Viral nucleic acids in live-attenuated vaccines: detection of minority variants and an adventitious virus.

The presence in the final vaccines of residue (“adventitious agents”) including cells and fragments of DNA from foreign tissue is certainly realistic.

The Genomic Instability Associated with Integrated Simian Virus 40 DNA Is Dependent on the Origin of Replication and Early Control Region

E. DNA tumor viruses. A variety of DNA viruses cause cancer in humans and other animals (Table 15.2). Viruses like SV40 (simian virus40) and polyoma, and adenovirus (Figs. 15.13, 14, and 16) generally grow in a lytic mode and kill their host cells rather than causing cancer. However, in cells that do not support lytic growth (usually from species related to, but outside of, the normal host range), all or part of the viral DNA is integrated into the host genome (at random) which can lead to transformation of the cell to a cancerous state (Fig. 15.13). Cancer is caused by viral proteins (T-antigen in SV40 and E1A and E1B in adenovirus) which bind to and inactivate the host tumor suppressor gene products Rb and p53 which normally suppress the cell cycle and thereby regulate cell growth. (Many animal viruses can only replicate when the cell is in S phase, so they express gene products which shift the host cells out of a resting state into the cell cycle.) Papillomaviruses (Fig. 15.15) usually induce benign cell proliferation, again by blocking Rb and p53, but they can also cause cancer directly or in combination with additional mutations in the host genome. The mechanisms by which hepatitis B virus and herpesviruses (e.g., Epstein Barr virus) cause cancer are not yet well understood.

Molecular Basis of Cancer (Chapter 15)

Research links 29 genome regions with common form of inflammatory bowel disease

Its not only what is listed as vaccine ingredients, it is as well what is unlisted, and that they do not even know is in there. (below)

Adventitious Agents and Vaccines
Philip R. Krause
Food and Drug Administration, Bethesda, Maryland, US

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.”

Guidance for Industry

Characterization and Qualification of Cell Substrates and Other Biological Materials Used in the Production of Viral Vaccines for Infectious Disease Indications

VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity

The advent of cloned DNA vaccines & Synthetic Genomics, backed by proponents of the Trans-humanist & Bioethics movements (post-Darwinian view, in which the species has the power to direct its own evolution), has opened a
Pandora’s Box spelling the inevitable death of natural immunity.

VRM: The Rise of Mutagenic Viruses

Vaccine Contamination

Biologicals. 2010 May;38(3):371-6. Epub 2010 Apr 8. Endogenous retroviruses as potential hazards for vaccines.

The true story of SV40, the cancer-causing virus hidden in polio vaccines

How SV40 Causes Cancer, (again denied by the CDC and other so called authorities)


Who Knew What, When.

Current Literature, (the CDC and FDA clearly do not care about the science, and only what little from and connected to the pharma industry, that they can cherry pick).



Oral Presentation to the subcommittee on human rights and wellness of the committee on government reform: “The SV40 Virus: Has tainted polio vaccine  caused an increase in cancer?

The Paper Trail

Here is an eye opening document as well.

The polio vaccine: a critical assessment of its arcane history, efficacy, and long-term health-related consequences

Vaccine Contamination: Pig Virus DNA Found in Rotarix

Detection of DNA from PCV1 in Rotarix

Gardasil Vaccine rDNA Introduced at Coroner’s Inquest

Bombshell Interview Reveals DNA Fragments Discovered 6 Months After Vaccination, (Gardasil)

Vaccine Contamination Pig Virus DNA Found in Rotarix April 7, 2010

Corrupted Rotavirus Vaccine Contains Pig Virus (Part 1 of 6)

Science 14 February 1975: 
Vol. 187 no. 4176 pp. 522-523 
DOI: 10.1126/science.187.4176.522

Phage in Live Virus Vaccines: Are They Harmful to People?

And since 1975, do you think anything has changed to correct that situation? The answer is clearly, no.

Autism Epidemic, Is Foreign DNA in MMR II Vaccine Responsible? CBCD Suggests CDC Study Microcompetition Theory. The Center for the Biology of Chronic Disease (CBCD) believes that the cause of the epidemic is the foreign DNA in the MMR II vaccine.

Foreign DNA Fragments Cause Major Diseases

Toxic Vaccines? CBCD Sends Letter to FDA & CDC on Foreign DNA Fragments in Gardasil and MMR

The CBCD sent a letter this past week to the offices of the FDA Commissioner, Dr. Margaret Hamburg,and to the offices of the CDC’s director, Dr. Thomas R. Frieden.

Proof of Childhood Vaccinations’ Lack of Effectiveness and Dangers
Anyone who sees this information and refuses to admit that vaccines are questionable simply doesn’t want to know the truth.

Gardasil Vaccine Found to be Contaminated, HPV DNA, (stated firmly attached to the vaccine aluminum adjuvant)

SANE Vax to FDA: Recombinant HPV DNA found in multiple samples of

Related Video – Sane Vax – Gardasil Contamination

So, again quite obviously you can see that those so called purification steps used to so called purify vaccines, are NOT working. The FDA already knows what should not and can not be in the vaccines, and that in relation to causation of
chronic disorders and illness. What amazes me is how they can and have admitted to what they know, and have known; yet in the public light they return and resent with a complete denial of all, and with complete denial of that there is any issue nor evidence of any problem, anywhere.

Officially they have told us as well that even though aborted fetal tissue are used to make vaccines, that no cells remain in the vaccine after the manufacturing process. Yet as well, how then and do they list diploid cells, and human albumin on the vaccine ingredient list; but yet they still state there are none in the vaccines.


You can very clearly right here again, see that the FDA is covering up the truth and the facts, and all while with no ability to scientifically defend their claims and statements.

Read the response from the FDA here; regarding the Gardasil contamination issue.

SANE Vax Inc. issued the following rebuttal to the FDA response:

Merck Sponsored Study Returns Dubious Gardasil Autoimmune Safety Results,
 (The wolves guarding the chickens again, all is good, trust us).

Merck and the FDA, no cover-up at all, right? 
SANE Vax, Inc. Reports Human Papillomavirus (HPV) DNA Contamination in Gardasil™ To FDA: Requests Public Safety Investigation

Big Pharma + Big Gov’t = Big Trouble  (More on Gardasil)!

S.A.N.E. Vax, Inc. and Sin Hang Lee, MD offers American consumers reliable HPV genotyping, but gets turned down by the FDA.

Lets take another look at the contamination in Gardasil, and the potential harm that can come from that, which the FDA of course, still denies. 

Gardasil Contamination: EMA Steps Up to the Plate, FDA drops the Ball


Sutton I, Lahoria R, Tan I, Clouston P, Barnett M. CNS demyelination and quadrivalent HPV vaccination. Mult Scler. 2009; 15:116-9.

 Wildemann B, Jarius S, Hartmann M, Regula JU, Hametner C. Acute disseminated encephalomyelitis following vaccination against human papilloma virus. Neurology. 2009;72:2132-3.

Mendoza Plasencia Z, González López M, Fernández Sanfiel ML, Muñiz Montes JR.
Acute disseminated encephalomyelitis with tumefactive lesions after vaccination against human papillomavirus. Neurologia. 2010; 25:58-9.

Chang J, Campagnolo D, Vollmer TL, Bomprezzi R. Demyelinating disease and polyvalent human papilloma virus vaccination. J Neurol Neurosurg Psychiatry. 2010 Oct 9. doi:10.1136/jnnp.2010.214924

DiMario FJ Jr, Hajjar M, Ciesielski T. A 16-year-old girl with bilateral visual loss and left hemiparesis following an immunization against human papilloma virus. J Child Neurol. 2010; 25:321-7.

Balamoutsos G, Bouktsi M, Paschalidou M, Tascos N, Milonas I.  A report of five cases of CNS demyelination after quadrivalent human papilloma virus vaccination: could there be any relationship?  (Abstract No. P297) Poster
Access :

Rossi M, Bettini C, Pagano C. Bilateral papilledema following human
papillomavirus vaccination. J Med Cases. 2011; 2:222-4.

van der Aa MA, Huth US, Häfele SY, Schubert R, Oosting RS, Mastrobattista E,
Hennink WE, Peschka-Süss R, Koning GA, Crommelin DJ. Cellular uptake of cationic
polymer-DNA complexes via caveolae plays a pivotal role in gene transfection in
COS-7 cells. Pharm Res. 2007 Aug;24(8):1590-8. Epub 2007 Mar 24.

Lechardeur D, Verkman AS, Lukacs GL. Intracellular routing of plasmid DNA
during non-viral gene transfer. Adv Drug Deliv Rev. 2005 Apr 5;57(5):755-67.

Matzuzawa Y, Emi N, Kanbe T. Calcium phosphate and aluminum hydroxide as non-virus gene carrier: the morphology of DNA-salt complex and the effects it has on DNA transfection. Kagaku Kogaku Ronbunshu. 2003; 29:680-684. In Japanese
(English Abstract)

 Bergen JM, Park IK, Horner PJ, Pun SH. Nonviral approaches for neuronal delivery of nucleic acids. Pharm Res. 2008 May;25(5):983-98. Epub 2007 Oct 12.

Berg P, Baltimore D, Boyer HW, Cohen SN, Davis RW, Hogness DS, Nathans D, Roblin R, Watson JD, Weissman S, Zinder ND. Potential biohazards of recombinant DNA molecules. Proc Natl Acad Sci U S A. 1974; 71: 2593–4.

Würtele H, Little KC, Chartrand P. Illegitimate DNA integration in mammalian cells. Gene Ther. 2003 Oct;10(21):1791-9. Review.

Milot E, Belmaaza A, Wallenburg JC, Gusew N, Bradley WE, Chartrand P.
Chromosomal illegitimate recombination in mammalian cells is associated with intrinsically bent DNA elements. EMBO J. 1992 Dec;11(13):5063-70.

 Doerfler W, Schubbert R, Heller H, Kämmer C, Hilger-Eversheim K, Knoblauch M,
Remus R. Integration of foreign DNA and its consequences in mammalian systems. Trends Biotechnol. 1997 Aug;15(8):297-301.

Hilleman MR. History, precedent, and progress in the development of mammalian cell culture systems for preparing vaccines: safety considerations revisited. J Med Virol 1990 May;31(1):5-12.

Testimony on Cervical Cancer by Nancy C. Lee, M.D. Before the House Committee on Commerce, Subcommittee on Health and Environment  March 16, 1999

Merck & Co., Inc. 2006. Gardasil [Quadrivalent Human Papillomavirus Types 6,11,16,18) Recombinant Vaccine] product insert. Table 9.  Merck 9883616

Leadbetter EA, Rifkin IR, Hohlbaum AM, Beaudette BC, Shlomchik MJ,
Marshak-Rothstein A. Chromatin-IgG complexes activate B cells by dual engagement of IgM and Toll-like receptors. Nature. 2002;416(6881):603-7.

Zhong XY, von Mühlenen I, Li Y, Kang A, Gupta AK, Tyndall A, Holzgreve W, Hahn S, Hasler P. Increased concentrations of antibody-bound circulatory cell-free DNA in rheumatoid arthritis. Clin Chem. 2007;53:1609-14.

Marichal T, Ohata K, Bedoret D, Mesnil C, Sabatel C, Kobiyama K, Lekeux P,
Coban C, Akira S, Ishii KJ, Bureau F, Desmet CJ. DNA released from dying host ells mediates aluminum adjuvant activity. Nat Med. 2011;17:996-1002.

The truth about the HPV vaccines or what they do not want you to know (Part 5), article by, Cynthia Janak.

Gardasil HPV Vaccine Related Death Rate Rising Among Women and Sterilization of young girls and boys

Pictures, (Jessica), when will country demand that this dangerous vaccine be removed from the shelves of the medical community, this is long over due, and all they do is pushed harder for this vaccines promotion. The power of money and
control by one pharmaceutical giant Merck

Jessica – Memorial Page


Merck employees had “hit list” of doctors they sought to “neutralize”, court documents reveal (it gets dirty)

Are Vaccines REALLY Safe? – Mary Tocco

Vaccine References and Research Citations, (long list)


Vaccines Contaminated with Mycoplasma’s – by Garth Nicolson microbiologist

Chronic Diseases: Who’s killing us, and how? – by Garth Nicholson

Dr. Nicolson is the President, Chief Scientific Officer and Research Professor at the Institute for Molecular Medicine in Huntington Beach, California. Born in 1943 in Los Angeles, Dr. Nicolson received his B.S. in Chemistry from University of California at Los Angeles in 1965 and his Ph.D. in Biochemistry and Cell Biology from the University of California at San Diego in 1970. He is currently Professor of Integrative Medicine at Capitol University of Integrative Medicine and a Conjoint Professor at the University of Newcastle (Australia). He was formally the David Bruton Jr. Chair in Cancer Research and
Professor and Chairman of the Department of Tumor Biology at the University of Texas M. D. Anderson Cancer Center in Houston, and he was Professor of Internal Medicine and Professor of Pathology and Laboratory Medicine at the University of
Texas Medical School at Houston. He was also Professor of Comparative Pathology at Texas A & M University. Among the most cited scientists in the world, Professor Nicolson has published over 550 medical and scientific papers (including 3 Current Contents Citation Classics), edited 14 books, served on the Editorial Boards of 20 medical and scientific journals and is currently serving as Editor of two (Clinical & Experimental Metastasis and the Journal of Cellular Biochemistry). Professor Nicolson has received peer-reviewed research grants from the U. S. Army, National Cancer Institute, National Institutes of
Health, American Cancer Society and the National Foundation for Cancer Research. Dr. Garth Nicolson has won many awards, such as the Burroughs Wellcome Medal of the Royal Society of Medicine (United Kingdom), Stephen Paget Award of the Metastasis Research Society, the U. S. National Cancer Institute Outstanding Investigator Award, and the Innovative Medicine Award of Canada. He is also a Colonel (Honorary) of the U. S. Army Special Forces and a U. S. Navy SEAL
(Honorary) for his work on Armed Forces and veterans illnesses.

Institute for Molecular Medicine

That’s right, as a fact were were ALL mislead and lied to!!!

CDC Vaccine Schedule: 49 doses of 14 vaccines before the age of 6. 69 doses of 16 vaccines by the age 18. That is recklessly insane

Aborted Fetuses Used in Vaccines!

The Costs of Vaccine Damage: The Payout Figures
Catherine J. Frompovich

Vaccines are supposed to be safe according to the U.S. CDC/FDA, so how come the HRSA division of the U.S. Department of Health and Human Services published Statistics Reports [1] for the period ending September 3, 2013 providing data verifying that vaccines cause damage and even kill?

The period covers fiscal years (FY) 1989 to FY 2013. There were 3,387 compensable claims—meaning those claims that received compensation or money, and 9,651 claims that were dismissed, an awful miscarriage of the original intent of the National Vaccine Injury Compensation Program created by Congress and Public Law 99-660, in this writer’s opinion. 

The U.S. Court of Federal Claims (aka the vaccine court) paid out $2,569,336,538.59 for compensable claims and $104,202,681.85 for attorneys’ fees representing those claims. The court paid another round of attorneys’ fees for dismissed claims totaling $56,375,431.34, plus $15,190,454.29 for interim attorneys’ fees. Judging by attorneys’ fees paid out, it looks like attorneys do pretty well, instead of injured claimants, i.e., those the court decides to dismiss. 

Here is the nitty-gritty of the reports filed: Injuries, Deaths, Compensated, and Dismissed claims.

Read more:



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 host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through vaccination. Vaccine must be safe without any human DNA contaminations or reactivated viruses, and must be produced in ethically approved manufacturing processes.

Thanks for stopping by and making it this far. Sick amount of links and hours of easy to understand information here. Glad you made it.


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