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“If you want to know whether or not something is harmful in children, test it in children.”

~Paul Offit, vaccine profiteer

Alternatively, pretend that you don't really want to know whether that thing is harmful; after all, "the science is settled." Then conduct worldwide, decades-long experiments, anyway, and lie about the results.

If you want to know whether or not something is harmful in children, open your eyes. Take a look around. Our kids are the sickest of any generation. Is it any surprise that "healthcare" costs in the U.S. are higher than anywhere else in the world? We have an epidemic of chronically ill children who need constant care.

The truth, for those who wish to see it, is that vaccines have created chronic health problems (lifetime pharmaceutical customers) as a trade-off for common childhood illnesses.

This is not acceptable. 


Self-professed Lyme & EBV expert Paul Auwaerter of Johns Hopkins says, 

"…However, fatal infections have been documented in immunodeficient children vaccinated with these strains (1121415). The symptoms of infection occur many months after immunization, and the viruses isolated are similar to the original LA vaccine (115), suggesting that in the absence of an effective host immune response, persistent infection with the vaccine strain can lead to fatal disease. Viruses isolated from these children could potentially represent virulent revertants of the original LA vaccine.”

Go ahead and read it for yourself, here.



You don't need to read a whole lot of research to know that kids are getting the very diseases that the vaccines are meant to prevent, especially when it comes to live virus vaccines that are neurotropic. 

Just read the MMR package insert.


Hypersensitivity to any component of the vaccine, including gelatin.{40}


Do not give M-M-R II to pregnant females; the possible effects of the vaccine on fetal development are unknown at this time. If vaccination of postpubertal females is undertaken, pregnancy should be avoided for three months following vaccination (see INDICATIONS AND USAGE, Non-Pregnant Adolescent and Adult Females and PRECAUTIONS, Pregnancy).

Anaphylactic or anaphylactoid reactions to neomycin (each dose of reconstituted vaccine contains approximately 25 mcg of neomycin). 3

Febrile respiratory illness or other active febrile infection. However, the ACIP has recommended that all vaccines can be administered to persons with minor illnesses such as diarrhea, mild upper respiratory infection with or without low-grade fever, or other low-grade febrile illness.{41}

Patients receiving immunosuppressive therapy. This contraindication does not apply to patients who are receiving corticosteroids as replacement therapy, e.g., for Addison's disease.

Individuals with blood dyscrasias, leukemia, lymphomas of any type, or other malignant neoplasms affecting the bone marrow or lymphatic systems.

Primary and acquired immunodeficiency states, including patients who are immunosuppressed in association with AIDS or other clinical manifestations of infection with human immunodeficiency viruses;{41-43} cellular immune deficiencies; and hypogammaglobulinemic and dysgammaglobulinemic states. Measles inclusion body encephalitis{44} (MIBE), pneumonitis{45} and death as a direct consequence of disseminated measles vaccine virus infection have been reported in immunocompromised individuals inadvertently vaccinated with measles-containing vaccine.

Individuals with a family history of congenital or hereditary immunodeficiency, until the immune competence of the potential vaccine recipient is demonstrated. 

What they are saying is, don’t vaccinate someone who is immunosuppressed. But whose pediatrician ever pre-screens for immune incompetence prior to vaccination?  You see clearly they write in the contraindications the same warnings we are proving to you – don’t vaccinate someone who is immunosuppressed and be sure the vaccine vials are not contaminated with fungal mycoplasma and the like, but how does anyone know what’re the states of the vaccine vial or the children?

Even the Infectious Diseases Society of America (IDSA) has said that babies are over-vaccinated at too young an age, and that "a forced schedule that suits the manufacturer as opposed to the patient" could be not-such-a-great-idea. See the "Common Mechanisms" charge sheet, since IDSA had that article removed from the Internet, but we grabbed a screen shot.


We have shown elsewhere that what fungi do is cause immunosuppression. As you've seen above, immunosuppression is a contraindication for live virus vaccines. Well, what if a "vaccine" *is* a fungus (a TLR2/1 agonist, such as LYMErix), or contains a fungal type of contaminant, such as mycoplasma? 

December 2012:  New York Times; Doctors admit Thimerosal is put in vaccines to prevent fungi:

Vaccine Rule Is Said to Hurt Health Efforts 
"But a proposal that the ban include thimerosal, which has been used since the 1930s to prevent bacterial and fungal contamination in multidose vials of vaccines, has drawn strong criticism from pediatricians…. They say that the ethyl-mercury compound is critical for vaccine use in the developing world, where multidose vials are a mainstay…Banning it would require switching to single-dose vials for vaccines, which would cost far more and require new networks of cold storage facilities and additional capacity for waste disposal, the authors of the articles said.'"


LYMErix, a fungal-type endotoxin, caused the acquired immune deficiency outcome of "chronic Lyme," which features reactivated viruses (mainly the herpesviruses, such as EBV and CMV), plus increased susceptibility to other infections of all kinds. Fungal toxins in vaccine vials do the same thing, and when injected along with live, attenuated viruses, produce catastrophic results. These results are obvious, if we only open our eyes and have a look around. Are we ready to protect our children, their future, and the very future of our country by acknowledging the obvious and holding our federal health agencies accountable?




Of the more than 20 Institutes that make up the National Institutes of Health, none acknowledge this entire class of immunosuppression diseases. None. There is no National Institute of Immunodeficiency and Infectious Diseases; only the opposite: the National Institute of Autoimmune and Infectious Diseases.


The only people who are allowed to have an immunosuppression disease are those with HIV/AIDS. According to the NIH, CDC, Pharma, BigInsurance, and all the clueless doctors, you can't have a disease without the classic signs of inflammation. Their agenda is clear: as long as they pretend this category (Lyme, ME/CFS, fibromyalgia, Gulf War Illness immunosuppression diseases) does not exist, the longer they can maintain the lie that #vaccineswork.