Coincidentally, was Dr. Andrew Wakefield professionally eviscerated because he suggested single valent vaccines? Did Dr. Wakefield foresee what DNA vaccines could do to harm infants and children? Did his co-authored paper have to be retracted and professionally neutralized because it was a real threat to the biotech industry that was gearing up to alter humans, their DNA and the current push toward transhumanism using vaccines and their ‘magic needles’?
That somehow harks back to flashbacks of World War II era Nazi research to create the perfect Aryan race!
Furthermore, is there an aspect to the vaccine hidden agenda that may be racially or ethnically motivated? since CDC epidemiologist and whistleblower William Thompson, PhD, came forth to divulge the MMR vaccine was responsible for causing autism in young black males under three years of age, but the CDC directed Thompson and his co-researchers not to include that pertinent material in their 2004 report on autism and vaccines. Those CDC researchers physically destroyed the evidence. However, Dr. Thompson kept his files, which he turned over to U.S. Congressman Bill Posey of Florida, who has asked for an investigation several years now, but none ever has taken place. WHY? Can it be collusion to cover up the science fraud that’s pervasive at the CDC and FDA?
Well, here’s some information from the past, which possibly could point toward the future:
BALTIMORE, April 1, 2015 /PRNewswire/ — Over 750 victims have sued The Rockefeller Foundation, the Johns Hopkins Hospital, the Johns Hopkins University, The Johns Hopkins University School of Medicine, the Johns Hopkins Bloomberg School of Public Health, and the Johns Hopkins Health System Corporation, alleging that they were the driving force behind human experiments in which vulnerable populations of Guatemalans were deceived and intentionally exposed to syphilis, gonorrhea and other venereal diseases and pathogens, without giving any informed consent. [….]
[Is the same going on today regarding informed consent and vaccines?]
Researchers subjected the Guatemalans to repeated blood draws, lumbar punctures and cisternal punctures of the suboccipital portion of the brain, gynecological examinations, touching and penetration of sexual organs, and forced or coerced sexual contact.
Key Rockefeller and Johns Hopkins researchers involved in the Guatemala Experiments, were also behind the now infamous Tuskegee experiments, in which 600 impoverished African-American sharecroppers were never informed they had syphilis, and were given placebos rather than real medicine. The researchers watched while the experiment subjects wasted away and infected their wives and children with the disease. The Tuskegee experiments were halted after being exposed by a whistleblower.
[Whistleblowers NOW are condemned to prison terms!]
The case has been filed in the Circuit Court in Baltimore City, Maryland. The victims are represented by three law firms: Meridian 361 International Law Group, PLLC of Portland, Maine; Escritorio Juridico Rodriguez Fajardo y Asociados of Caracas, Republica Bolivariana de Venezuela; and Salsbury, Clements, Bekman, Marder & Adkins of Baltimore, Maryland.
READ MORE: Dr. Speaks Out: Babies Being Prepared for AI & Transhumanism Through Vaccines & Medicine
For more information:
F. R. Jenkins, Esq., Meridian 361 International Law Group, PLLC, www.meridian361.com, [email protected], Tel. + 1 866-338-7087.
Juan Pablo Rodriguez, Esq., Escritorio Juridico Rodriguez Fajardo y Asociados of Caracas, Republica Bolivariana de Venezuela, www.rodriguezfajardolaw.com, [email protected], Tel. + 58-212-720-1480, + 58-212-541-3831, + 502-227-87027
Paul Bekman, Esq., Salsbury, Clement, Bekman, Marder & Adkins, www.scbmalaw.com, [email protected], Tel.+ 1 410-215-9289.
Why such a concerted legal action, as undertaken above, has not been filed regarding the massive vaccine experiment now going on in the USA for decades, plus globally at the behest of the Gates Foundation, is beyond belief!
Pandemics will become the special means to implement the final phase of the vaccine experiment, I contend. Why? During a pandemic all will be vaccinated with chipped vaccines and become totally controllable to those who want control of the human population. There is no other reason for such a mandated push for injecting totally toxic hazmat materials into babies, infants, toddlers, teens, adults and senior citizens.
One such pandemic possibly could be a ‘rare’ strain of a flu virus that was genetically modified to make it more virulent, something that happens in government research labs as part of “biological warfare” research. Ft. Detrick, Maryland, is the home of such clandestine research. Another place used to be Plum Island out in the Atlantic Ocean about two miles off the NE shore of Long Island, New York. Plum Island, as I understand, will be closed and moved inland to Manhattan, Kansas—“Tornado Alley.”
The U.S. military has played a role in vaccines[1] and works closely with the CDC, which owns dozens of vaccine patents. According to the Ginger Taylor article published at GreenMed Info:
When I contacted Blaxill to ask how to run a patent search, he was kind enough to do it for me. He found 57 granted US patents with the CDC listed as an assignee. You can see the search results here.
Upon cursory review of the patents, I found that one did not seem applicable to vaccination, but merely referenced an article on vaccination. That leaves us with 56 CDC patents to scrutinize.
Here is what I found.
There are CDC patents applicable to vaccines for Flu, Rotavirus, Hepatitis A, HIV, Anthrax, Rabies, Dengue fever, West Nile virus, Group A Strep, Pneumococcal disease, Meningococcal disease, RSV, Gastroenteritis, Japanese encephalitis, SARS, Rift Valley Fever, and chlamydophila pneumoniae.
There is a CDC patent for “Nucleic acid vaccines for prevention of flavivirus infection,” which has applications in vaccines for Zika, West Nile virus, Dengue fever, tick-borne encephalitis virus, yellow fever, Palm Creek virus, and Parramatta River virus.
CDC also has several patents for administering various “shots” via aerosol delivery systems for vaccines.
There’s a CDC patent on a process for vaccine quality control by “quantifying proteins in a complex preparation of uni- or multivalent commercial or research vaccine preparations.”
There’s a CDC patent on a method “for producing a model for evaluating the antiretroviral effects of drugs and vaccines.”
CDC has a patent for companies who want to test their respiratory system applicable vaccine on an artificial lung system.
If a vaccine maker is concerned that their vaccine might contain a human rhinovirus, CDC has a patent on a process for determining if such contamination exists.
CDC has a patent on an assay to assist vaccine makers in finding antigen-specific antibodies in a biological sample.
CDC holds a patent that provides vaccine makers with a method of “reducing the replicative fitness of a pathogen by deoptimizing codons.” Asserting that, “pathogens with deoptimized codons can be used to increase the phenotypic stability of attenuated vaccines.”
The agency also holds a patent on adjuvants for a vaccine used on premature infants and young babies.
There is a CDC patent to cover a vaccine for an infection induced by a tape worm found in pork.
They even have patents that cover vaccines for animal illnesses including Canarypox virus, Fowlpox virus, Sealpox virus, dog fluand monkey cancer.
Does this seem like a public health agency making “independent” vaccine recommendations, or a private company with an impressive portfolio to which one might look for investment opportunities?
One of the more egregious ‘ingredients’ in vaccines is the “adjuvant,” usually some form of aluminum to induce a vaccinee’s system to produce an unnatural response, which vaccine makers consider “immunity,” or what’s referred to as an “adaptive response.”
Back in November of 2015 the “FDA approves first seasonal influenza vaccine containing an adjuvant”[4] MF59 containing squalene.
The U.S. Food and Drug Administration today approved Fluad, the first seasonal influenza vaccine containing an adjuvant. Fluad, a trivalent vaccine produced from three influenza virus strains (two subtype A and one type B), is approved for the prevention of seasonal influenza in people 65 years of age and older.
Fluad, which is manufactured using an egg-based process, is formulated with the adjuvant MF59, an oil-in-water emulsion of squalene oil.[5]
I can’t tell you how many stories I’ve heard from nurses about senior citizens given flu shots in nursing homes and other managed care facilities, only to die shortly thereafter!
Peter Doshi, PhD, a former researcher at Johns Hopkins Baltimore, released the paper “Influenza: marketing vaccine by marketing disease”[6] published in the British Medical Journal [BMJ 2013;346:f3037].
I find it ironic that Dr. Doshi says, “The vaccine may be less beneficial and less safe than has been claimed, and the threat of influenza seems to be overstated.” Another reason to question the incessant push to receive influenza vaccines is it’s been known and proven they really don’t work as promoted. According to a study, the flu vaccine was about 9 percent effective in protecting seniors against the 2012-2013 most virulent influenza strain!
There has to be another reason for pushing aluminum-containing vaccines!