Human Experimentation Without Consent. The History Of Vaccinations.

California vaccine bill SB 277 signed into law by Jerry Brown-Jun 30, 2015 Changed Public Trust And Overstepped Authority Under The Constitution. We Are Not Human Experiments For The Pleasure Of Profits.

Galatians 5:19 Now the deeds of the flesh are evident, which are: immorality, impurity, sensuality, 20 idolatry, sorcery (pharmakeia), enmities, strife, jealousy, outbursts of anger, disputes, dissensions, factions, 21 envying, drunkenness, carousing, and things like these, of which I forewarn you, just as I have forewarned you, that those who practice such things will not inherit the kingdom of God.

Sen. Richard Pan, D-Sacramento, is thanked by Leah Russin, holding her son Leo, 21 months, after Pan’s measure.


This is human experimentation without consent.

WHAT IS WRONG WITH THIS PICTURE? Bill Gates weird business practices.

A small but growing number of parents who object to vaccinating their children on religious grounds say they do so because many common vaccines are the product of cells that once belonged to aborted fetuses.

There is a grain of truth to this statement. But even religious leaders, including a future pope, have said that shouldn’t deter parents from vaccinating their children.

Vaccine and Cell Line Science

Some childhood vaccines, including the one against rubella — which is part of the MMR vaccine given to millions of children worldwide for measles, mumps and rubella — is cultured in “WI-38 human diploid lung fibroblasts,” according to the U.S. Food and Drug Administration’s fact sheet on the vaccine’s ingredients.How to Tell If Winter Blues Are Seasonal Affective DisorderWhat to Know About the Apple That Doesn’t Turn BrownThis Couple Might Be Dead If They Hadn’t Met

Merck, the vaccine’s manufacturer, acknowledged that those cells were originally obtained from an electively aborted fetus. They were used to start a cell line, which is a cell multiplied over and over again to produce cells that are of a consistent genetic makeup. The WI-38 cell line is used as a culture to grow live viruses that are used in vaccines.

Vaccines Developed Using Human Cell Strains

“Merck, as well as other vaccine manufacturers, uses two well-established human cell lines to grow the virus for selected vaccines,” Merck said in a statement to ABC News. “The FDA has approved the use of these cell lines for the production of these Merck vaccines.”

Other common vaccines, including those for chicken pox, hepatitis and rabies, are also propagated in cells originating from legally aborted human fetuses, according to the FDA.

“These abortions, which occurred decades ago, were not undertaken with the intent of producing vaccines,” said a spokeswoman for the U.S. Centers Disease Control and Prevention.

The original cells were obtained more than 50 years ago and have been maintained under strict federal guidelines by the American Type Culture Collection, according to Merck.

“These cell lines are now more than three generations removed from their origin, and we have not used any new tissue to produce these vaccines,” the company added in its statement.

To say that the vaccines contain a significant amount of human fetal tissue, as some objectors to the vaccines claim, is misleading, stressed Dr. Paul Offit, the director of the vaccine education center at the Children’s Hospital of Philadelphia.

“There are perhaps nanograms of DNA fragments still found in the vaccine, perhaps billionths of a gram,” he said. “You would find as much if you analyzed the fruits and vegetables you eat.”

And to remove human fibroblast cells entirely from vaccines is out of the question, Offit explained, noting they are necessary because human viruses don’t grow well in animal cells.

“They have also been tested for safety and the fetal cells can go through many more divisions than most other cells before dying,” he said.

Ethical Considerations

Religious organizations have sided in favor of vaccines as well, even those generally opposed to abortion.

“We should always ask our physician whether the product he proposes for our use has an historical association with abortion,” the National Catholic Bioethics Center states on its website, but then goes on to say “one is morally free to use the vaccine regardless of its historical association with abortion.”

“The reason is that the risk to public health, if one chooses not to vaccinate, outweighs the legitimate concern about the origins of the vaccine,” the center’s position statement continued. “This is especially important for parents, who have a moral obligation to protect the life and health of their children and those around them.”

Offit said he was glad the Catholic Church supports vaccination.

He noted it is particularly ironic to object to the rubella vaccine using fetal cells because Cardinal Joseph Ratzinger, who later became Pope Benedict XVI, commented on the subject in 2003, saying: “Universal vaccination has resulted in a considerable fall in the incidence of congenital rubella, with a general incidence reduced to less than 5 cases per 100,000 livebirths.”

In other words, Offit explained, the rubella virus increases the risk of spontaneous abortion.

In the U.S., vaccination prevents up to 5,000 miscarriages each year in the U.S. alone, he said.

n 1941, Australian ophthalmologist Norman Gregg first realized that congenital cataracts in babies were the result of their mothers being infected with rubella during pregnancy. Along with cataracts, it was eventually determined that congenital rubella syndrome (CRS) could also cause deafness, heart disease, encephalitis, mental retardation, and pneumonia, among many other conditions. At the height of a rubella epidemic that began in Europe and spread to the United States in the mid-1960s, Plotkin calculated that 1% of all births at Philadelphia General Hospital were affected by congenital rubella syndrome. In some cases, women who were infected with rubella while pregnant terminated their pregnancies due to the serious risks from CRS.

Following one such abortion, the fetus was sent to Plotkin at the laboratory he had devoted to rubella research. Testing the kidney of the fetus, Plotkin found and isolated the rubella virus. Separately, Leonard Hayflick (also working at the Wistar Institute at that time) developed a cell strain using lung cells from an aborted fetus. Many viruses, including rubella, grew well in the resulting cell strain, and it proved to be free of contaminants. The strain was eventually called WI-38.

Descendant cells are the medium in which these vaccines are prepared. The cell lines under consideration were begun using cells taken from one or more fetuses aborted almost 40 years ago. Since that time the cell lines have grown independently. It is important to note that descendant cells are not the cells of the aborted child. They never, themselves, formed a part of the victim’s body.\

Due to dwindling capacity for existing aborted fetal cell lines to self-replicate, scientists in China have developed a new aborted fetal cell line, WALVAX 2 that will be used for viral vaccine production.  The existing cell lines, MRC-5 and WI-38 are currently used in MMR, Varicella, Hepatitis-A, Shingles, some rabies and some polio 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 a “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.

According to the studies published earlier this year in the NIH Pub Med, scientists noted that Walvax-2 cells replicated more rapidly than MRC-5 cells, attained greater population doubling and performed better or equal to the existing cell lines for culturing viruses.

In 1964 Leonard Hayflick introduced what is known as the “Hayflick limit” – how all normal cells have a finite lifespan and limited capacity to replicate before going into senescence and eventually, become unstable and form tumors. (L. Hayflick, The Limited In Vitro Lifetime of Human Diploid Cell Strains, Experimental Cell Research, Vol 37, 1964)  Attempts to immortalize these cells to extend their lifespan have likewise introduced problems with tumor formations, as in aborted fetal cell line PER C6, introduced into the US in 2001.

HeLa cells are the world’s most commonly used human cell lines, and have served as a standard for understanding many fundamental biological processes.

Hela cells

Lacks was born in Roanoke, Virginia, in 1920 and grew up poor and with little education on a tobacco farm. She was married at the young age of 15 and later moved her family to Baltimore, where her husband sought employment as a steelworker. In 1951, after the birth of her fifth child, she was treated at Johns Hopkins Hospital for an aggressive form of cervical cancer. During her treatment, doctors removed a piece of her tumor without her knowledge and used her cancer cells without her permission. Just eight months after undergoing agonizing radiation-tube inserts, Lacks died at the age of 31. However, millions of her cells, known as “HeLa,” are still alive today. The cells from that tissue sample were mass-produced and have become priceless pieces of medical research. HeLa cells are shipped around the world and have even been sent into space to study the effect of zero gravity on human cells.

HeLa cells are considered the first “immortal” human cell line because they reproduce infinitely in a laboratory setting. Before the discovery of HeLa, scientists were challenged in their research due to the difficulty of keeping cells alive outside of the body. HeLa cells irrevocably changed the medical landscape. They were used by Jonas Salk to test the first polio vaccine, which protected millions of people around the world. HeLa cells also led to breakthroughs in the study of herpes, leukemia, influenza, hemophilia, Parkinson’s disease, certain types of genetic diagnoses, cancer, AIDS, cloning, the effects of radiation and toxic substances, and in vitro fertilization. They were also the first cells used to determine that humans have 23 pairs of chromosomes.

Despite her amazing contributions to science and medicine, it wasn’t until the 1970s that Lacks’ identity was revealed. While breakthroughs and advances were occurring using HeLa cells, her family had no idea what a vital role their mother was playing in medicine and biomedical research. They didn’t know that part of their mother was still alive. When her family found out, they wondered if she had gone to heaven or if she had been cloned. Skloot reveals that the injustice continued with Lacks’ relatives — scientists at Hopkins conducted research on her descendants 25 years after her death without their full understanding of the research’s purpose.

That HeLa cells helped launch the multibillion dollar biomedical industry is undisputed, yet that aspect of Skloot’s story remains surrounded by controversy. Despite the tremendous value of their mother’s legacy, her children have led a life of poverty, and they tragically suffer chronic health problems without the benefit of health insurance. Skloot established a fund for Lacks’ descendants and others to assist them with health and educational expenses.

This is forced medical procedures.

This violates The Nuremberg code

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California, West Virginia, and Mississippi only allow Non-Medical Exemptions from School Immunization Requirements 2015

50. ALASKA 3.57 (LOWEST)
The great idea of immunizing began around 1000 in China. They had discovered that inhaling ground powder of smallpox scabs, they could inoculate, or gain immunity, to the disease. Clearly though, inoculation wasn’t enough to stop the breakout.

The History Of Vaccinations:

Vaccination milestones from ancient Greece to the 21st century

Vaccination is a miracle of modern medicine. In the past 50 years, it’s saved more lives worldwide than any other medical product or procedure. However, the fascinating story of vaccination goes back all the way to ancient Greece.

429 BC: Thucydides notices that people who survive smallpox do not get re-infected

As long ago as 429 BC, the Greek historian Thucydides observed that those who survived the smallpox plague in Athens did not become re-infected with the disease.

900 AD: Chinese discover variolation

The Chinese were the first to discover and use a primitive form of vaccination, called variolation. It was carried out as early as the 10th century, and particularly between the 14th and 17th centuries.
The aim was to prevent smallpox by exposing healthy people to tissue from the scabs caused by the disease. They did this by either putting it under the skin or, more often, inserting powdered scabs from smallpox pustules up the nose.

1700s: Variolation spreads around the world

Variolation eventually spread to Turkey, and arrived in England in the early 18th century. At this time, smallpox was the most infectious disease in Europe. It struck rich and poor alike, and killed up to one-fifth of those infected in numerous epidemics. Variolation caused mild illness but, although it occasionally caused death, smallpox rates were lower in populations that tried it.

1796: Edward Jenner discovers vaccination

British physician, Dr Edward Jenner (pictured), discovered vaccination in its modern form and proved to the scientific community that it worked.

1803: Royal Jennerian Institute founded

Support for vaccination grew. Jenner was awarded government funding, and in 1803 the Royal Jennerian Institute was founded. Vaccination became popular throughout Europe and, soon after, the US.

1870s: Violent opposition to vaccination

Although vaccination was taken up enthusiastically by many, there was some violent opposition as it became more widespread. People found it hard to believe that it really worked. They also felt that it took away people’s civil liberties, particularly when it was compulsory.

1880s: A vaccine against rabies

Louis Pasteur improved vaccination even more, and developed arabies vaccine. As the science of immunology developed and scientists began to understand more about how diseases worked, other vaccines were created.

1890: Emil von Behring discovers the basis of diphtheria and tetanus vaccines

German scientist Emil von Behring was awarded the first Nobel Prize in Physiology or Medicine. Japanese physician and bacteriologist Shibasaburo Kitasato discovered the antitoxins of diphtheria andtetanus. He demonstrated that animals injected with small amounts of the tetanus toxin became immune to the disease.

1920s: Vaccines become widely available

By the end of the 1920s, vaccines for diphtheria, tetanus, whooping cough and tuberculosis (TB) were all available. Vaccination spread across the globe and although these early vaccines were crude, they worked. The first vaccination programmes dramatically reduced the number of deaths from disease, and they were crucial in establishing the concept of preventive public health measures.

1955: Polio vaccination begins

Polio vaccination was introduced in the UK and it dramatically reduced the number of cases. Nowadays, polio is extremely rare and is close to being completely eliminated from the planet.

1956: WHO fights to eradicate smallpox

The first attempt to use the smallpox vaccine on a global scale began when the World Health Organization (WHO) decided to try and eradicate smallpox across the world.

1980: Smallpox eradicated from the world

Smallpox was declared as being eradicated in 1980. It was one of the most remarkable achievements in the history of medicine.

2008: Cervical cancer scientist awarded Nobel Prize

Professor Harald zur Hausen discovered that cervical cancer was caused by a virus, making it possible to develop a vaccine for the disease. The scientist proved that a group of viruses called human papillomaviruses (HPV) caused cervical cancer. This discovery led to the development of the HPV vaccine, which protects against cervical cancer, and is now widely available.

2008: NHS vaccinates girls against cancer

In England, the NHS cervical cancer vaccination programme began, whereby all 12-13 year-old girls are offered HPV vaccination to protect them against cervical cancer. It is the first time that a routine universal vaccine has been given to prevent a type of cancer.

2013: NHS vaccinates against shingles and rotavirus and children’s flu

The NHS vaccination programme saw the introduction of rotavirus vaccination for babies and a shingles vaccine for over-70s. A children’s flu vaccine was launched. This is given as a nasal spray rather than an injection.

2015: NHS vaccinates babies against meningitis B

The NHS vaccination programme saw the introduction of Men B vaccination for babies. The program is the first national, routine, universal and publicly funded Men B vaccination program in the world.

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Small-Pox Epidemics, Cost, and Fatality Rates Compared

Vaccinal ConditionSmall-Pox CasesSmall-Pox DeathsFatality-rate Per CentCost of Epidemic
London 1900-02Well Vaccinated9,6591,59416.50£492,000
Glasgow 1900-02Well Vaccinated3,41737711.03£ 150,000
Sheffield 1887-88Well Vaccinated7,0666889.73£32,257
Leicester 1892-94Practically Unvaccinated393215.34£2,888
Leicester 1902-04Practically Unvaccinated731304.10£1,60
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What is Humira?

Humira (adalimumab) reduces the effects of a substance in the body that can cause inflammation.

Two hundred Harvard Medical School students are confronting the school’s administration, demanding an end to pharmaceutical industry influence in the classroom
Since about the mid-1980s, research funding by pharmaceutical firms has exceeded what the National Institutes of Health spends. Last year, the industry spent $39 billion on research in the United States while NIH spent $31 billion.

The billions that the drug companies invest in such experiments help fund the world’s quest for cures. But their aim is not just public health. That money is also part of a high-risk quest for profits

They also own the legislature, the media, the unions and those that ostensibly exist to protect us.

SACRAMENTO – California State PTA, the state’s largest children’s advocacy organization, has taken a support position on Senate Bill 277 (Pan).


California School Nurses Organization

Health Officers Association of California

American Academy of Pediatrics California

County Health Executives Association of California

Pasadena Public Health Department

California Hospital Association

Children’s Hospital of Oakland

Kaiser Permanente

Providence Health and Services Southern California

American Nurses Association

California Academy of Family Physicians

California Pharmacists Association

California Primary Care Association

California Children’s Hospital Association

California Healthcare Institute & BioCom

American Lung Association

California Association of Nurse Practitioners

California Chapter of the American College of Emergency Physicians

California Coverage and Health Initiatives

California Optometric Association

March of Dimes

First 5 Association of California

Children Now, Here and Strong

California Immunization Coalition

California Black Health Network

Aids Healthcare Foundation

Children’s Specialty Care Coalition

California Association of Physician Groups

California Academy of Physician Assistants

California Society of Health System Pharmacists

American College of Emergency Physicians California

Children’s Healthcare Is a Legal Duty (CHILD)

Monterey Bay Independent Physician Association


California School Boards Association

California School Employees Association

California Parent Teacher Association


UAW Local 5810-Union for Post-Doctoral Researchers at University of California


AFSMCE American Federation of State Municipal County Employees

Secular Coalition for California

Cafe de California

National Coalition of 100 Black Women Sacramento

Childcare Law Center

Silicon Valley Leadership Group

The Children’s Partnership

Children’s Defense Fund California

National Council of Jewish Women California

Alameda City Firefighters IAFF Local 689


California Young Democrats

Orange County Democratic Party

Santa Cruz County Democratic Party

San Francisco Democratic County Central Committee

Peninsula Young Democrats

Diablo Valley Democratic Club

Silicon Valley Young Democrats

Peninsula Democratic Coalition

Contra Costa Central Committee Democrats

Miracle Mile Democratic Club

Cesar Chavez Democratic Club


San Francisco Chronicle

Santa Cruz Sentinel

L.A. Times

Sacramento Bee

Fresno Bee

George Skelton, Journalist-L.A. Times

The Monterey County Herald

San Jose Mercury News

The Sun San Bernadino

Oakland Tribune

The Press Democrat

Los Angeles Daily News

Contra Costa Times

San Gabriel Valley Tribune

Pasadena Star News

Inland Valley Bulletin

Whittier Daily News

Daily Breeze


The Vacaville Reporter

Enterprise Record

Merced Sun-Star

Sacramento News and Review

Times Standard

They even own the controlled opposition that threw the capitol hearings at every juncture, controlled the debates and the rallies.

Two vaccines are specifically recommended for pregnant women: the flu(influenza) vaccine, which should be given during the first or second trimester of pregnancy; and the Tdap (tetanus-diphtheria-acellularpertussis) vaccine, given when you’re 27 to 36 weeks pregnant to guard against whooping cough (aka pertussis).

The problem with vitamin K is not only the aluminum but the fact that the dosage is 20,000 times greater than what should be given to a newborn.

Hepatitis B Vaccine: Refuse This Routine Procedure – Or Expose Your Baby’s Brain to Severe Danger For most children, the risk of a serious vaccine reaction may be 100 times greater than the risk of hepatitis B.”

SB 277


Parents must show their child’s Immunization Record as proof of immunization. These immunization requirements also apply to students entering transitional kindergarten.

Students Admitted at Ages 7-17 Years Need These Immunizations:

  • Diphtheria,Tetanus, and Pertussis (DTaP, DTP, DT, Tdap, or Td)—4 doses
    (3 doses OK if last dose was given on or after 2nd birthday)
  • Polio (OPV or IPV)—4 doses
    (3 doses OK if one was given on or after 2nd birthday)
  • MeaslesMumps, and Rubella (MMR)—1 dose
    (2 doses required at 7th grade)
  • Varicella (chickenpox)
    (Admission at ages 7-12 years need 1 dose; ages 13-17 years need 2 doses)
  • TetanusDiphtheria,and Pertussis (Tdap) —1 dose at  7th grade or out-of-state transfer admission at 8th–12thgrades
    (1 dose on or after the 7th birthday)

California schools are required to check immunization records for all new student admissions at Kindergarten/TKthrough 12th grade and all students advancing to 7th grade before enttry. Parents must show their child’s Immunization Record as proof of immunization.

39 shots by the time they are six


POLIO : was it a fraud caused by toxic overload? DDT SPRAYING AND NUCLEAR FALLOUT CAUSE PARALYSIS

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The Years of Atmospheric Testing: 1945-1963





“Bernard was right; the pathogen is nothing; the terrain is everything.” — Louis Pasteur’s deathbed words

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If our bodies are relatively free of toxic wastes, serious disease bacteria cannot develop within us. No harmful bacteria, parasite, or virus can proliferate in a body that does not have a build-up of toxic waste. A body that has healthy levels of cellular oxygen and a strong immune system will remain a healthy body.

The body has a built-in natural intelligence. It knows how to fight germs and viruses.When it comes to disease, there are three principles that must be understood:

1 All forms of disease are caused by accumulations of acid and toxic waste in the body’s systems, the first and foremost of which is the colon. Disease starts in the colon.
2 The body initiates all acute diseases like colds, flu, fever, skin eruptions, diarrhea, scarlet fever, and measles, in attempts to reduce the accumulation of stored waste material. Chronic diseases, such as diabetes, arthritis, bronchitis, heart disease, and cancer, are caused by the continued build-up of waste in the system, and the suppression of acute disease cleansing attempts by wrong treatment.
3 The body has the ability to return to health provided it is given the proper nutrition and conditions to do so.

We don’t “catch” diseases.We cause them! We create them by the way we live.We don’t “catch” a cold or flu.We actually “earn” it by fostering toxic waste conditions in our bodies, as a result of our lifestyles.

When we continue to suppress illnesses with drugs and antibiotics, the body eventually develops degenerative disease conditions because it has not been allowed adequate opportunity to detoxify and heal naturally.



1900 nyc


Measles Mortality 1900-1984 - NonLog Scale


vaccines contain excipient-table-2Adenovirus sucrose, D-mannose, D-fructose, dextrose, potassium phosphate, plasdone C, anhydrous lactose, micro crystalline cellulose, polacrilin potassium, magnesium stearate, cellulose acetate phthalate, alcohol, acetone, castor oil, FD&C Yellow #6 aluminum lake dye, human serum albumin, fetal bovine serum, sodium bicarbonate, human-diploid fibroblast cell cultures (WI-38), Dulbecco’s Modified Eagle’s Medium, monosodium glutamate

March 2011 Anthrax (Biothrax) aluminum hydroxide, benzethonium chloride, formaldehyde, amino acids, vitamins, inorganic salts and sugars May 2012 BCG (Tice) glycerin, asparagine, citric acid, potassium phosphate, magnesium sulfate, Iron ammonium citrate, lactose February 2009 DT (Sanofi) aluminum potassium sulfate, peptone, bovine extract, formaldehyde, thimerosal (trace), modified Mueller and Miller medium, ammonium sulfate December 2005 DTaP (Daptacel) aluminum phosphate, formaldehyde, glutaraldehyde, 2-Phenoxyethanol, Stainer-Scholte medium, modified Mueller’s growth medium, modified Mueller-Miller casamino acid medium (without beef heart infusion), dimethyl 1-beta-cyclodextrin, ammonium sulfate

October 2013 DTaP (Infanrix) formaldehyde, glutaraldehyde, aluminum hydroxide, polysorbate 80, Fenton medium (containing bovine extract), modified Latham medium (derived from bovine casein), modified Stainer-Scholte liquid medium November 2013 DTaP-IPV (Kinrix) formaldehyde, glutaraldehyde, aluminum hydroxide, Vero (monkey kidney) cells, calf serum, lactalbumin hydrolysate, polysorbate 80, neomycin sulfate, polymyxin B, Fenton medium (containing bovine extract), modified Latham medium (derived from bovine casein), modified Stainer-Scholte liquid medium November 2013 DTaP-HepB-IPV (Pediarix) formaldehyde, gluteraldehyde, aluminum hydroxide, aluminum phosphate, lactalbumin hydrolysate, polysorbate 80, neomycin sulfate, polymyxin B, yeast protein, calf serum, Fenton medium (containing bovine extract), modified Latham medium (derived from bovine casein), modified Stainer-Scholte liquid medium, Vero (monkey kidney) cells

November 2013 DTaP-IPV/Hib (Pentacel) aluminum phosphate, polysorbate 80, formaldehyde, sucrose, gutaraldehyde, bovine serum albumin, 2-phenoxethanol, neomycin, polymyxin B sulfate, Mueller’s Growth Medium, Mueller-Miller casamino acid medium (without beef heart infusion), Stainer-Scholte medium (modified by the addition of casamino acids and dimethyl-betacyclodextrin), MRC-5 (human diploid) cells, CMRL 1969 medium (supplemented with calf serum), ammonium sulfate, and medium 199 October 2013 Hib (ActHIB) ammonium sulfate, formalin, sucrose, Modified Mueller and Miller medium January 2014

Hib (Hiberix) formaldehyde, lactose, semi-synthetic medium March 2012 Hib (PedvaxHIB) aluminum hydroxphosphate sulfate, ethanol, enzymes, phenol, detergent, complex fermentation medium December 2010 B Appendix B-7 Centers for Disease Control and Prevention Epidemiology and Prevention of Vaccine-Preventable Diseases, 13th Edition April, 2015 Appendix B B Vaccine Contains Source: Manufacturer’s P.I. Dated Hib/Hep B (Comvax) yeast (vaccine contains no detectable yeast DNA), nicotinamide adenine dinucleotide, hemin chloride, soy peptone, dextrose, mineral salts, amino acids, formaldehyde, potassium aluminum sulfate, amorphous aluminum hydroxyphosphate sulfate, sodium borate, phenol, ethanol, enzymes, detergent December 2010 Hib/Mening. CY (MenHibrix) tris (trometamol)-HCl, sucrose, formaldehyde, synthetic medium, semisynthetic medium 2012 Hep A (Havrix) aluminum hydroxide, amino acid supplement, polysorbate 20, formalin, neomycin sulfate, MRC-5 cellular proteins December 2013

Hep A (Vaqta) amorphous aluminum hydroxyphosphate sulfate, bovine albumin, formaldehyde, neomycin, sodium borate, MRC-5 (human diploid) cells February 2014 Hep B (Engerix-B) aluminum hydroxide, yeast protein, phosphate buffers, sodium dihydrogen phosphate dihydrate December 2013 Hep B (Recombivax) yeast protein, soy peptone, dextrose, amino acids, mineral salts, potassium aluminum sulfate, amorphous aluminum hydroxyphosphate sulfate, formaldehyde, phosphate buffer May 2014 Hep A/Hep B (Twinrix) formalin, yeast protein, aluminum phosphate, aluminum hydroxide, amino acids, phosphate buffer, polysorbate 20, neomycin sulfate, MRC-5 human diploid cells August 2012

Human Papillomavirus (HPV) (Cerverix) vitamins, amino acids, lipids, mineral salts, aluminum hydroxide, sodium dihydrogen phosphate dehydrate, 3-O-desacyl-4’ Monophosphoryl lipid A, insect cell, bacterial, and viral protein November 2013 Human Papillomavirus (HPV) (Gardasil) yeast protein, vitamins, amino acids, mineral salts, carbohydrates, amorphous aluminum hydroxyphosphate sulfate, L-histidine, polysorbate 80, sodium borate June 2014 Human Papillomavirus (HPV) (Gardasil 9) yeast protein, vitamins, amino acids, mineral salts, carbohydrates, amorphous aluminum hydroxyphosphate sulfate, L-histidine, polysorbate 80, sodium borate December 2014 Influenza

(Afluria) beta-propiolactone, thimerosol (multi-dose vials only), monobasic sodium phosphate, dibasic sodium phosphate, monobasic potassium phosphate, potassium chloride, calcium chloride, sodium taurodeoxycholate, neomycin sulfate, polymyxin B, egg protein, sucrose December 2013 Influenza (Agriflu) egg proteins, formaldehyde, polysorbate 80, cetyltrimethylammonium bromide, neomycin sulfate, kanamycin, barium 2013 Influenza (Fluarix) Trivalent and Quadrivalent octoxynol-10 (Triton X-Į-tocopheryl hydrogen succinate, polysorbate 80 (Tween 80), hydrocortisone, gentamicin sulfate, ovalbumin, formaldehyde, sodium deoxycholate, sucrose, phosphate buffer June 2014 Influenza (Flublok) monobasic sodium phosphate, dibasic sodium phosphate, polysorbate 20, baculovirus and host cell proteins, baculovirus and cellular DNA, Triton X-100, lipids, vitamins, amino acids, mineral salts March 2014

Influenza (Flucelvax) Madin Darby Canine Kidney (MDCK) cell protein, MDCK cell DNA, SRO\VRUEDWHFHW\OWULPHWKO\DPPRQLXPEURPLGHȕ-propiolactone, phosphate buffer March 2014 Influenza (Fluvirin) nonylphenol ethoxylate, thimerosal (multidose vial–trace only in prefilled syringe), polymyxin, neomycin, beta-propiolactone, egg proteins, phosphate buffer February 2014 Influenza (Flulaval) Trivalent and Quadrivalent thimerosal, formaldehyde, sodium deoxycholate, egg proteins, phosphate buffer February 2013

Influenza (Fluzone: Standard (Trivalent and Quadrivalent), High-Dose, & Intradermal) formaldehyde, octylphenol ethoxylate (Triton X-100), gelatin (standard trivalent formulation only), thimerosal (multi-dose vial only) , egg protein, phosphate buffers, sucrose 2014 Appendix B-8 Centers for Disease Control and Prevention Epidemiology and Prevention of Vaccine-Preventable Diseases, 13th Edition April, 2015 Appendix B Vaccine Contains Source: Manufacturer’s P.I. Dated Influenza (FluMist) Quadrivalent ethylene diamine tetraacetic acid (EDTA), monosodium glutamate, hydrolyzed porcine gelatin, arginine, sucrose, dibasic potassium phosphate, monobasic potassium phosphate, gentamicin sulfate, egg protein July 2013

Japanese Encephalitis (Ixiaro) aluminum hydroxide, Vero cells, protamine sulfate, formaldehyde, bovine serum albumin, sodium metabisulphite, sucrose May 2013 Meningococcal (MCV4- Menactra) formaldehyde, phosphate buffers, Mueller Hinton agar, Watson Scherp media, Modified Mueller and Miller medium, detergent, alcohol, ammonium sulfate April 2013 Meningococcal (MCV4- Menveo) formaldehyde, amino acids, yeast extract, Franz complete medium, CY medium August 2013 Meningococcal (MPSV4- Menomune) thimerosal (multi-dose vial only), lactose, Mueller Hinton casein agar, Watson Scherp media, detergent, alcohol April 2013 Meningococcal (MenB – Bexsero) aluminum hydroxide, E. coli, histidine, sucrose, deoxycholate, kanomycin 2015 Meningococcal (MenB – Trumenba) polysorbate 80, histodine, E. coli, fermentation growth media October 2015

MMR (MMR-II) Medium 199 (vitamins, amino acids, fetal bovine serum, sucrose, glutamate) , Minimum Essential Medium, phosphate, recombinant human albumin, neomycin, sorbitol, hydrolyzed gelatin, chick embryo cell culture, WI-38 human diploid lung fibroblasts June 2014 MMRV (ProQuad) sucrose, hydrolyzed gelatin, sorbitol, monosodium L-glutamate, sodium phosphate dibasic, human albumin, sodium bicarbonate, potassium phosphate monobasic, potassium chloride, potassium phosphate dibasic, neomycin, bovine calf serum, chick embryo cell culture, WI-38 human diploid lung fibroblasts, MRC-5 cells March 2014 Pneumococcal (PCV13 – Prevnar 13) casamino acids, yeast, ammonium sulfate, Polysorbate 80, succinate buffer, aluminum phosphate, soy peptone broth January 2014

Pneumococcal (PPSV-23 – Pneumovax) phenol May 2014 Polio (IPV – Ipol) 2-phenoxyethanol, formaldehyde, neomycin, streptomycin, polymyxin B, monkey kidney cells, Eagle MEM modified medium, calf serum protein, Medium 199 May 2013 Rabies (Imovax) Human albumin, neomycin sulfate, phenol red indicator, MRC-5 human diploid cells, beta-propriolactone April 2013 Rabies (RabAvert) ȕ-propiolactone, potassium glutamate, chicken protein, egg protein, neomycin, chlortetracycline, amphotericin B, human serum albumin, polygeline (processed bovine gelatin), sodium EDTA, bovine serum March 2012 Rotavirus (RotaTeq) sucrose, sodium citrate, sodium phosphate monobasic monohydrate, sodium hydroxide, polysorbate 80, cell culture media, fetal bovine serum, vero cells [DNA from porcine circoviruses (PCV) 1 and 2 has been detected in RotaTeq. PCV-1 and PCV-2 are not known to cause disease in humans.] June 2013

Rotavirus (Rotarix) amino acids, dextran, sorbitol, sucrose, calcium carbonate, xanthan, Dulbecco’s Modified Eagle Medium (potassium chloride, magnesium sulfate, ferric (III) nitrate, sodium phosphate, sodium pyruvate, Dglucose, concentrated vitamin solution, L-cystine, L-tyrosine, amino acids solution, L-glutamine, calcium chloride, sodium hydrogenocarbonate, and phenol red) [Porcine circovirus type 1 (PCV-1) is present in Rotarix. PCV-1 is not known to cause disease in humans.] May 2014 Smallpox (Vaccinia – ACAM2000) human serum albumin, mannitol, neomycin, glycerin, polymyxin B, phenol, Vero cells, HEPES September 2009 B Appendix B-9 Centers for Disease Control and Prevention Epidemiology and Prevention of Vaccine-Preventable Diseases, 13th Edition April, 2015 Appendix B Vaccine Contains Source: Manufacturer’s P.I. Dated Td (Decavac) aluminum potassium sulfate, peptone, formaldehyde, thimerosal, bovine muscle tissue (US sourced), Mueller and Miller medium, ammonium sulfate March 2011

Td (Tenivac) aluminum phosphate, formaldehyde, modified Mueller-Miller casamino acid medium without beef heart infusion, ammonium sulfate April 2013 Td (Mass Biologics) aluminum phosphate, formaldehyde, thimerosal (trace), ammonium phosphate, modified Mueller’s media (containing bovine extracts) February 2011 Tdap (Adacel) aluminum phosphate, formaldehyde, glutaraldehyde, 2-phenoxyethanol, ammonium sulfate, Stainer-Scholte medium, dimethyl-beta-cyclodextrin, modified Mueller’s growth medium, Mueller-Miller casamino acid medium (without beef heart infusion) March 2014 Tdap (Boostrix) formaldehyde, glutaraldehyde, aluminum hydroxide, polysorbate 80 (Tween 80), Latham medium derived from bovine casein, Fenton medium containing a bovine extract, Stainer-Scholte liquid medium February 2013 Typhoid (inactivated – Typhim Vi) hexadecyltrimethylammonium bromide, formaldehyde, phenol, polydimethylsiloxane, disodium phosphate, monosodium phosphate, semi-synthetic medium March 2014

Typhoid (oral – Ty21a) yeast extract, casein, dextrose, galactose, sucrose, ascorbic acid, amino acids, lactose, magnesium stearate. gelatin September 2013 Varicella (Varivax) sucrose, phosphate, glutamate, gelatin, monosodium L-glutamate, sodium phosphate dibasic, potassium phosphate monobasic, potassium chloride, sodium phosphate monobasic, potassium chloride, EDTA, residual components of MRC-5 cells including DNA and protein, neomycin, fetal bovine serum, human diploid cell cultures (WI-38), embryonic guinea pig cell cultures, human embryonic lung cultures March 2014 Yellow Fever (YF-Vax) sorbitol, gelatin, egg protein May 2013 Zoster (Shingles – Zostavax) sucrose, hydrolyzed porcine gelatin, monosodium L-glutamate, sodium phosphate dibasic, potassium phosphate monobasic, neomycin, potassium chloride, residual components of MRC-5 cells including DNA and protein, bovine calf serum February 2014 A table listing vaccine excipients and media by excipient can be found in: Grabenstein JD. ImmunoFacts: Vaccines and Immunologic Drugs – 2013 (38th revision). St Louis, MO: Wolters Kluwer Health, 2012.

The immune system is made up of the skin, mucous membranes in the nose and throat, ears and eyes, nasal hairs, saliva, the spleen, intestines, tonsils, the thymus gland and even the brain. All of these parts work together in a holistic way to bring about a whole body immunity, which is only in part to do with antibodies.

• The skin acts as a barrier to prevent bacteria entering the body. It also filters out toxins through fever, which is the purpose of a fever when your child is ill

.• The nasal hairs prevent foreign particles from travelling up the nose, and the mucous membranes excrete a substance which is anti-bacterial.

• Tonsils help prevent respiratory diseases and illnesses such as Polio, and saliva contains substances which destroy and neutralize microbes.

• The spleen and intestines, among other organs, deposit fats and vitamins around the body and protect against viral and bacterial invasion.

• The thymus gland produces thymus cells, known as ‘T’ cells, which are antibodies to infection.

• There are various glands (nodes) in the body that drain it of toxins and useless material. For instance, the cervical nodes drain the head, neck and chest.

• The pituitary gland in the brain directs all of the systems above, so if the brain goes wrong, so does the immune system. It sends electrical impulses to all areas of the body, stimulating cell re-generation and muscle growth. These electrical impulses also stimulate the thymus gland – the centre of immune function.

Factors That Influence the Immune Response to Vaccinations.

What effect does vaccination have on this immune function?

Vaccination – the act of artificially acquiring a disease so as to become immune to it – is flawed in a number of ways. Firstly, a vaccine contains many hazardous chemicals and not just the viruses to immunise against. These each have their own toxic affect on the body. Secondly, the route of entry is different to a naturally occurring disease. Most natural diseases would enter through the mouth or the nasal cavity, not the skin.Vaccination breaks the skin with a needle and injects foreign matter into the blood supply.

This bypasses the skin’s role in immune function, as well as the tonsils, the mucous membranes, and so on.Normally, the body produces extra antibodies after being primed by the tonsils that there is impending infection. Therefore, if the infection takes hold, there will be an army of white blood cells, ready to neutralise the infection.In the case of vaccination, this infection goes straight to the blood, with no prior build up for the body, and there are no extra immune cells to deal with it.

Also, with vaccination there is more than one disease present (e.g. measles, mumps, rubella all in one), whereas naturally a child would never contract 3 diseases at the same time. This puts additional strain on the immune system.

What problems can this cause?Injection of vaccine via this unnatural route can use up 70% of the immune system’s resources, instead of the usual 3 to 4% with a wild occurring disease (according to Cynthia Cournoyer, ‘What About Immunizations?’, Dennis Nelson Publishers, 1991).

Because the body has no extra antibodies waiting to counter the vaccine, it can go into overdrive in an attempt to deal with the situation, taking much needed vitamins away from bones and other organs, to use for the production of more antibodies. This means that the other vital systems go short on vitamins, in extreme cases leading to bone fractures caused by the immune response leaching vitamins to cope with the vaccine. This lack of vitamins can also cause bruising and retinal bleeding and hemorrhaging, which is why some vaccine damaged babies have been falsely labelled as ‘shaken baby syndrome’ cases. These type of vaccine injuries are similar to those caused by trauma.

The massive surge of antibodies created by the vaccine can also cause the body to become hypersensitive and this is responsible for the increase in allergies and auto-immune diseases. Allergies are an over-exposure to toxic elements which the body is unable to cleanse itself of.If the adrenals, which include the pancreas, the pituitary gland and the spleen, become over-stimulated, for instance, by vaccination, this can cause the body to become toxic and unable to regulate itself. This has been linked to heart disease, diabetes, asthma and bronchitis, to name a few. Over-stimulating the adrenals also causes a decrease in circulation of blood round the body, and atrophying of vascular vessels.

It is in this state of dysfunction and chemical overload, from vaccines, pollution, junk food, pharmaceutical drugs and so on, that our bodies become less able to stay healthy.

‘When the body is in its ideal state of harmony, there is no need for “immunity.” In such a state of harmony and balance, the thymus functions properly as the central regulator for the proper digestion of elements and all that is taken into the body is digested and excreted.’ – (Stonebridge Associated Colleges, 2005).

In the time immediately following vaccination, when extra vitamins are being used up to fight the vaccine, this may actually make the person more susceptible to the disease. For instance, in the Merck, Sharp and Dohme LTD product information for HIB vaccine, it states: ‘Cases of Haemophilus B disease may occur in the weeks after vaccination’, and in Lederle Hibtiter information sheet, ‘Cases of HIB disease, although rare, may occur after vaccination.’ This is known as ‘PROVOCATION disease’, i.e. disease caused by vaccine.Live vaccines are more likely to pass on the disease to their recipient or his close contacts, as the viruses are excreted in urine, faeces and saliva for upto 3 weeks after each shot.

The polio vaccine was changed from the live oral vaccine to part of the injectable, killed 5 in 1, because the only cases of polio in western countries were caused by the vaccine.Vaccine caused diseases are often more severe than the naturally occurring disease. For instance, ATYPICAL measles, only got by vaccinated children, is much more serious because the vaccine suppresses the child’s rash, which is his means of excreting the toxins, and this leads to the toxins being pushed deeper into the body and affecting the major organs and sometimes the brain, as atypical measles encephalitis.Vaccine viruses can also attach themselves to cells, organs and brain tissue and cause cancers, disabilities and brain injury, as in the case of a boy who became autistic and had a seizure disorder after his MMR jab at 15 months. Great Ormand Street Children’s Hospital tested him at 13 years of age and found remains of vaccine viruses in the injured parts of his brain. (The Sunday Express, 6 October 2002).

Antibodies to brain tissue have also been found in blood tests of autistic children.

Disease Mutations

Even with inactivated vaccines, it is possible for the killed virus or bacteria to mutate into a different form of the disease. For instance, a 16 year old Canadian girl died of Meningitis B after her boyfriend had been given the Meningitis C vaccine. Lab tests confirmed that the vaccine can mutate into B form and infect both the recipient and his or her close contacts. (Pulse, doctor’s magazine, 20th November 1999).

Large numbers of chronic diseases have evolved in the place of infectious disease, since the introduction of mass vaccination, including ME, Lupus, Guillain-Barre Syndrome, Autism (previously known as Kanner Syndrome, discovered by Dr. Kanner in the 1940’s), MS, Ebola virus, AIDS, Lichen Planus, Vulvodynia and other hypersensitivity conditions, not to mention the rife and uncontrollable rates of cancer, heart disease, asthma, eczema and other allergies. Even meningitis was extremely rare before the 20th century.We are killing ourselves in our quest to ‘prevent’ childhood illness, as mother nature is stronger than man, so tampering with immune function can have disastrous consequences for all.

Henrietta Lacks was a poor black tobacco farmer-THE SOURCE OF VACCINE CELL LINES.



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CDC Admits as Many as 98 Million Americans Could be at Risk for Cancer Due to Polio Vaccine


Several vaccines currently available in the United States were developed using animal cell lines, primarily using cells from African green monkeys. These include vaccines against Japanese encephalitis, rotavirus, polio, and smallpox. Of these, only rotavirus and polio vaccines are routinely given.

Dr. Mary’s Monkey: How the Unsolved Murder of a Doctor, a Secret Laboratory in New Orleans and Cancer-Causing Monkey Viruses are Linked to Lee Harvey Oswald, the JFK Assassination and Emerging Global Epidemics.

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Human Diploid Cells (aborted fetal tissue) provide the “Cell culture” in which vaccine formulas are often grown or nurtured. Current vaccines in circulation which contain aborted fetal tissue include:

1. Polio vaccine (inactivated/IPV) & Oral Polio (live virus) drops
2. Measles, Mumps, Rubella vaccine/MMR (Rubella component)
3. Diphtheria, Tetanus, Pertussis, Poliomyelitis vaccine (DTaP/TdP) 
4. Varicella (Chickenpox) vaccine & Shingles (zoster) vaccine
5. Hepatitis A vaccine
6. Rabies vaccine


Vaccines Cause Immune Suppression

Immunostimulation Versus Immunosuppression after Multiple Vaccinations: the Woes of Therapeutic Vaccine Development

Three articles in this issue of Clinical Cancer Research show how multiple vaccinations can lead to immunosuppression. Moreover, two studies in patients show that granulocyte macrophage colony-stimulating factor (GM-CSF) as an adjuvant immunostimulant to different kind of vaccines can lead to adverse outcome in terms of relapse-free and overall survival. Modulation of regulatory T-cell activity may be required to overcome this outcome and may be crucial for the successful development of therapeutic vaccines.

Source: (Clin Cancer Res 2009;15(22):6745–7)

Cancer Patients Injected With Cancer Vaccine Caused ‘Early Melanoma Deaths’

Ninety-seven patients with resected melanoma (stage II-IV) were enrolled, stratified by stage, and randomized to receive a cellular melanoma vaccine with or without GM-CSF. The primary endpoint was delayed-type hypersensitivity (DTH) response to melanoma cells. Antibody responses, peripheral leukocyte counts, and survival were also examined.

Results: The GM-CSF arm showed enhanced antibody responses with an increase in IgM titer against the TA90 antigen and increased TA90 immune complexes. This arm also had diminished antimelanoma cell delayed-type hypersensitivity response. Peripheral blood leukocyte profiles showed increases in eosinophils and basophils with decreased monocytes in the GM-CSF arm. These immune changes were accompanied by an increase in early melanoma deaths and a trend toward worse survival with GM-CSF.

Conclusion: These data suggest that GM-CSF is not helpful as an immune adjuvant in this dose and schedule and raise concern that it may be harmful. Based on the discordant findings of an immune endpoint and clinical outcome, the use of such surrogate endpoints in selecting treatments for further evaluation must be done with a great deal of caution.

Source: (Clin Cancer Res 2009;15(22):7029–35)

Partial CD4 Depletion Reduces Regulatory T Cells Induced by Multiple Vaccinations

Results: Multiple vaccinations, rather than boosting the immune response, significantly reduced therapeutic efficacy of adoptive immunotherapy and were associated with an increased frequency and absolute number of CD3+CD4+Foxp3+ T regulatory (Treg) cells. Anti-CD4 administration reduced the absolute number of Treg cells 9-fold. Effector T-cells generated from anti-CD4–treated mice were significantly (P < 0.0001) more therapeutic in adoptive transfer studies than T cells from multiply vaccinated animals with a full complement of CD4+ cells.

Conclusion: These results suggest that CD4+ Treg cells limit the efficacy of multiple vaccinations and that timed partial depletion of CD4+ T cells may reduce suppression and “tip-the-balance” in favor of therapeutic antitumor immunity. The recent failure of large phase III cancer vaccine clinical trials, wherein patients received multiple vaccines, underscores the potential clinical relevance of these findings.

Source: (Clin Cancer Res 2009;15(22):6881–90)

1 in 5 Americans Suffer From Allergies

If springtime breezes bring you sniffles, you can take comfort in the knowledge that you are not alone.

For reasons that researchers do not fully understand, allergies to pollen, dust, pet dander and food have become more prevalent among Americans in recent decades. Today, one out of every five Americans suffers from allergies, according to the Asthma and Allergy Foundation of America.

“We don’t know why the incidence of allergies is on the rise,” said Maya Jerath, M.D., Ph.D., an assistant professor in the University of North Carolina at Chapel Hill School of Medicine and director of the UNC Allergy and Immunology Clinic.

Nor do researchers understand why an allergy develops in the first place. “That has baffled people and continues to baffle people in this field a lot,” she said.

An allergy is an immune reaction to a harmless substance, such as a pollen grain or peanut protein. Instead of ignoring the substance, the body produces antibodies to mount a fight against it. Allergy symptoms can range from itchy eyes and sneezing to life-threatening anaphylactic reactions.

The causes of allergies remain elusive in part because the immune system’s role is complex, Jerath said. The system must defend the body from countless foreign invaders in food, water and the air around you.

Significantly for allergy sufferers, the immune system must also learn to distinguish particles that are dangerous from those that are not. For most people, this learning occurs during early childhood.

“If it doesn’t get adequate exposure to certain things, those regulatory mechanisms don’t get set up,” Jerath said.

For that reason, some researchers believe that a lack of exposure to microorganisms early in life may precondition a person to allergies. This explanation, called the “hygiene hypothesis,” suggests that growing up surrounded by many other children, dirt or livestock helps the immune system develop a tolerance to harmless irritants.

Source:, by Sara Peach, 24 February 2010.


The spectrum of post-vaccination inflammatory CNS demyelinating syndromes

A wide variety of inflammatory diseases temporally associated with the administration of various vaccines, has been reported in the literature. A PubMed search from 1979 to 2013 revealed seventy one (71) documented cases. The most commonly reported vaccinations that were associated with CNS demyelinating diseases included influenza (21 cases), human papilloma virus (HPV) (9 cases), hepatitis A or B (8 cases), rabies (5 cases), measles (5 cases), rubella (5 cases), yellow fever (3 cases), anthrax (2 cases), meningococcus (2 cases) and tetanus (2 cases). The vast majority of post-vaccination CNS demyelinating syndromes, are related to influenza vaccination and this could be attributed to the high percentage of the population that received the vaccine during the HI1N1 epidemia from 2009 to 2012. Usually the symptoms of the CNS demyelinating syndrome appear few days following the immunization (mean: 14.2 days) but there are cases where the clinical presentation was delayed (more than 3 weeks or even up to 5 months post-vaccination) (approximately a third of all the reported cases).

In terms of the clinical presentation and the affected CNS areas, there is a great diversity among the reported cases of post-vaccination acute demyelinating syndromes. Optic neuritis was the prominent clinical presentation in 38 cases, multifocal disseminated demyelination in 30, myelitis in 24 and encephalitis in 17. Interestingly in a rather high proportion of the patients (and especially following influenza and human papiloma virus vaccination-HPV) the dominant localizations of demyelination were the optic nerves and the myelon, presenting as optic neuritis and myelitis (with or without additional manifestations of ADEM), reminiscent to neuromyelitic optica (or, more generally, the NMO-spectrum of diseases). Seven patients suffered an NMO-like disease following HPV and we had two similar cases in our Center. One patient with post-vaccination ADEM, subsequently developed NMO.

Overal, the risk of a demyelinating CNS disease following vaccination, although non-negligible, is relatively low. The risk of onset or relapse of CNS demyelination following infections against which the vaccines are aimed to protect, is substantially higher and the benefits of vaccinations surpass the potential risks of CNS inflammation. This does not in any way exempt us from “learning” the lessons taught by the reported cases and searching new and safer ways to improve vaccination techniques and increase their safety profile.

Source: Autoimmunity Reviews, Volume 13, issue 3, March 2014.


Lie # 1 “Thimerosal, 49.55% mercury by weight, is safe when used as a preservative in vaccines and other drugs.”

Lie #2   “Mercury was removed from all childhood vaccines in (pick any year between 1999 and the present).”

Lie #3 “Thimerosal is well-tested, having been used for 70 years with no problems.”

Lie #4 “No published peer-reviewed studies have shown any harm from Thimerosal.”

Lie #5 “No federal statements indicate any cause for concern regarding the continuing use of Thimerosal.”

Lie #6 “Individuals who oppose the use of mercury in medicine are anti-vaccine.”

Lie #7 “Autism is genetic.”


Wireless radiation-microwaves? AUTISM-


Ferritin and iron levels in children with autistic disorder

Carbonyl Iron Powder (CIP) Radar and microwave absorbing materials




Timing of Umbilical Cord Clamping After Birth IS A CAUSE OF AUTISM


The following are established facts regarding umbilical cord clamping before pulmonary oxygenation is established:

1. Placental oxygenation is arrested and the brain is deprived of oxygen until the lungs
2. Placental transfusion is arrested and the child is hypovolemic.
3. Blood flow through the lungs and other organs is not optimal and pulmonary oxygenation
is not optimal.
4. The child’s life support systems are not optimal for survival or for optimum health.

 The immediately clamped newborn may be missing one third to one half of its normal blood volume and is very prone to develop infant anemia, [13] and as shown previously, it is also at risk for hypoxic, ischemic brain damage at birth. While some studies on treatment of the anemia in infancy have shown some behavioral improvement, most studies show no improvement or prevention of the brain dysfunction following correction of anemia, [16] making it difficult to establish a cause and effect relationship between anemia and brain dysfunction.

The Potential Dark Side of the Routine Newborn Vitamin K Shot


 There are thousands upon thousands of declassified and publicly produced medical citations in the GWU archives indicating all manner of conceivable experiments with radiation and radioactive chemicals on human beings. Paralysis, cancer, birth defects, psychological disorders.

This is just a taste. X-ray abuse was an essential component in paving the way for nuclear proliferation and high-energy weapons. Chemical giant Monsanto, wartime operator of the Oak Ridge nuclear facility along with Union Carbide, began pumping out reactor-made radioisotopes for medical ‘study’ in 1946 under the direction of the Atomic Energy Commission and its chief, David Lilienthal. The imperative of covering up the radiation cause of polio, and “racing for a vaccine” after 1945, is obvious in retrospect. The military-medical establishment put its top guns on the task. The anomalous propaganda and distortion of polio takes on a meaningful light with the knowledge that Operation Polio was integral to maintaining and advancing nuclear weapons. TheSalkvaccinewasamassiveradiationexperiment. See the Atomic Weapons page for the timing of this event


The truth is Polio like all viruses follows a bell curve and was 90% gone when the Salk vaccine was introduced. Polio reportedly died off after the vaccine was mandated.  

The CDC has quickly removed a page from their website, which is now cached here, admitting that more than 98 million Americans received one or more doses of polio vaccine within an 8-year span when a proportion of the vaccine was contaminated with a cancer causing polyomavirus called SV40. It has been estimated that 10-30 million Americans could have received an SV40 contaminated dose of the vaccine.


Dr. Mary’s Monkey: How the Unsolved Murder of a Doctor, a Secret Laboratory in New Orleans and Cancer-Causing Monkey Viruses are Linked to Lee Harvey Oswald, the JFK Assassination and Emerging Global Epidemics

The Exploding Autoimmune Epidemic – Dr. Tent – It’s Not Autoimmune, you have Viruses




The US Government Has Paid out $3 Billion

Claims Filed and Compensated or Dismissed by Vaccine 1 September 3, 2013Vaccines Listed in Claims as Reported by Petitioners

Census Bureau: 94.6 Percent of U.S. Is Rural Open Space


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 Schematic diagram showing formation of the fertilization envelope.
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The progress and current status of vaccines which induce antibodies against human chorionic gonadotrophin (HCG) and luteinizing hormone-releasing hormone (LHRH) are reviewed. Three vaccines devised against HCG have undergone phase I clinical trials documenting their safety, and reversibility. One of these, the heterospecies dimer (HSD)–HCG vaccine has also completed phase II efficacy trials in sexually active women of proven fertility. Immunization with the vaccine prevents pregnancy, as long as the antibody titres remain ≥50 ng/ml HCG bioneutralization capacity. There is no disturbance of menstrual regularity and women continue to ovulate normally. The antibody response is predominantly againsy an epitope in the core part of β-HCG. Fertility is regained at titres <35 ng. These observations have laid the scientific foundations of a birth control vaccine. Research suggests the feasibility of making a cost-effective recombinant vaccine. The carriers tetanus toxoid (TT) and diptheria toxoid (DT) can be advantageously replaced by peptide determinants recognizing T, not B cells. l,

Human Reproduction Update 1997, Vol. 3, No. 4 pp. 301–310 European Society for Human Reproduction and Embryology Fertility regulating and immunotherapeutic vaccines reaching human trials stage


Vaccines for Children LIST OF PACKAGE INSERTS (click here for INFLUENZA VACCINES)

VaccineBrandname(click for package insert)CorporateManufacturer
DTaPDaptacel®Sanofi Pasteur
DTaP-Hep B-IPVPediarix®GlaxoSmithKline
DTaP-IP-HIPentacel®Sanofi Pasteur
e-IPVIPOL®Sanofi Pasteur
Hepatitis B-HibComvax®Merck
Hepatitis A PediatricVaqta®Merck
Hepatitis A PediatricHavrix®GlaxoSmithKline
Hepatitis A-Hepatitis B 18 onlyTwinrix®GlaxoSmithKline
Hepatitis BPediatric/AdolescentEngerix B®GlaxoSmithKline
Hepatitis BPediatric/AdolescentRecombivaxHB®Merck
HibActHIB®Sanofi Pasteur
HPV – Quadrivalent Human Papillomavirus Types 6, 11, 16 and 18 RecombinantGardasil®Merck
HPV -Bivalent Human Papillomavirus Types 16 and 18Cervarix®GlaxoSmithKline
Meningococcal Conjugate (Groups A, C, Y and W-135)Menactra®Sanofi Pasteur
Meningococcal Conjugate (Groups A, C, Y and W-135)Menveo®Novartis
Measles, Mumps and Rubella (MMR)MMRII®Merck
13-valent (Pediatric)Prevnar 13 TMPfizer
Pneumococcal Polysaccharide (23 Valent)Pneumovax®Merck
Rotavirus, Live, Oral, PentavalentRotaTeq®Merck
Rotavirus, Live, Oral, OralRotarix®GlaxoSmithKline
Tetanus & Diphtheria ToxoidsTTOX®Sanofi Pasteur
Tetanus & Diphtheria ToxoidsTdMerck
Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular PertussisBoostrix®GlaxoSmithKline
Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular PertussisAdacel®Sanofi Pasteur

Cannot find a brandname?  See inserts.htm

Fertility Not A Concern?

CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY  IPOL Long-term studies in animals to evaluate carcinogenic potential or impairment of fertility have not been conducted.

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility HAVRIX has not been evaluated for its carcinogenic potential, mutagenic potential, or potential for impairment of fertility.
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility RECOMBIVAX HB has not been evaluated for its carcinogenic or mutagenic potential, or its potential to impair fertility.
Carcinogenesis, Mutagenesis, Impairment of Fertility Liquid PedvaxHIB has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.
GARDASIL has not been evaluated for the potential to cause carcinogenicity or genotoxicity. GARDASIL administered to female rats at a dose of 120 mcg total protein, which is equivalent to the recommended human dose, had no effects on mating performance, fertility, or embryonic/fetal survival. The effect of GARDASIL on male fertility has been studied in male rats at an intramuscular dose of 0.5 mL/rat/occasion (120 mcg total protein which is equivalent to the recommended human dose). One group of male rats was administered GARDASIL once, 3 days prior to cohabitation, and a second group of male rats was administered GARDASIL three times, at 6 weeks, 3 weeks, and 3 days prior to cohabitation.
13 Menactra vaccine has not been evaluated for carcinogenic or mutagenic potential, or for 2 impairment of fertility.
Carcinogenesis, Mutagenesis, Impairment of Fertility M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.
A developmental and reproductive toxicity study has been performed in female rabbits at a dose approximately 20 times the human dose (on mg/kg basis) and revealed no evidence of impaired female fertility or harm to the fetus due to Prevnar 13.
CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY No studies have been performed with Tetanus Toxoid Adsorbed manufactured by Sanofi Pasteur Inc. to evaluate carcinogenicity, mutagenic potential, or impact on fertility.
Animal reproduction studies have not been conducted with Tetanus Toxoid Adsorbed manufactured by Sanofi Pasteur Inc. It is also not known whether Tetanus Toxoid Adsorbed manufactured by Sanofi Pasteur Inc. can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Tetanus Toxoid Adsorbed manufactured by Sanofi Pasteur Inc. should be given to a pregnant woman only if clearly needed.

Animal fertility studies have not been conducted with BOOSTRIX.

pathogenesis of, or immunity to, pertussis has not been clearly defined. 13 NON-CLINICAL TOXICOLOGY 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Adacel vaccine has not been evaluated for carcinogenic or mutagenic potential, or impairment of fertility.





QAnon WWG1WGA Inc 2020

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