Archive for the ‘vaccines’ Category

The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization From Alien Human & Animal DNA Contents?

This 2012 article is as relevant today as it was then.

https://vactruth.com/2012/03/13/vaccines-human-animal-dna/

The Ultimate Gamble: Do Childhood Vaccines Result in Genetic Hybridization from Alien Human and Animal DNA Contents?

By Harold E. Buttram, M.D. / March 13, 2012

Genetic Exchanges in the World around Us

Barbara McClintock, the 1983 Nobel laureate “Corn Lady,” was the first to discover genetic mobility in the so-called jumping genes in the 1930s.   For over 50 years she pursued solitary research with corn, uncovering some of nature’s innermost secrets about life.

McClintock studied maize, a form of Indian corn where distribution of red Indian corn, where distribution of red kernels and yellow kernels is genetically determined. What she perceived  was that some of the genes were moving from one place to another on the cell’s chromosomes (the floating threads on which genes are lined up like beads on a string).  Then she saw patterns in the movements, with sharply differing results in the colored kernels, and realized that some genes, once moved into position, switched other genes on or off. It followed that, while most genes were workers, others were controllers or managers of genes. [1]

According to an article in World Medicine, 1971, (2) scientists at the University of Geneva made the startling discovery that biological substances entering directly into the blood stream may truly become a part of us and even a part of our genetic material. The article stated in part:

When Japanese bacteriologists discovered that bacteria of one species transferred their own highly specific antibiotic resistance to bacteria of an entirely different species, they seemed to hit on a unique if not startling phenomenon. Dr. Maurice Stroun and Dr. Philippe Anker, with colleagues in the Department of Plant Physiology at the University of Geneva, have now accumulated a wealth of evidence that the transfer of genetic information is not confined to bacteria but also can occur between bacteria and higher plants and animals.

“The Geneva scientists are convinced that normal animal and plant cells also shed DNA and that this DNA is also taken up by other cells in the organism. If they are right, the consequences to virtually every aspect of a cell’s metabolism would be considerable. The growth and development, diseases, and even the evolution of an organism would be affected. [2]

“Dr. Stroun and his colleagues did most of their research on plants but have now turned to animals. In their latest set of experiments they used the isolated auricles of frogs’ hearts. [3]

There is no question about the results.  They found a high percentage of RNA-DNA (ribonucleic-deoxyribonucleic) hybridization between bacterial DNA extracted from bacteria of the same species as that used in the experiment and titrated RNA extracted from auricles which has been dipped in the bacterial suspension. (DNA, the characteristic nucleic acid of the nucleus in all cells, is the fundamental substance which carries the genetic code within the cells of the body).

“Since we know that no bacteria got into the frog auricles, we can only conclude that the bacterial DNA must have been exuded from the bacteria and absorbed by the animal cells,” says Stroun.

“This transfer phenomenon, or transcession, as Dr. Anker called it, is very probably a general one, otherwise, he and Dr. Stroun would hardly have succeeded first go, in getting bacterial RNA synthesized by animal tissues…

“The implications of this work on transcession are enormous, for the Geneva work suggests that this phenomenon is going on the whole time – even in our own bodies…Could, for example, the heart damage that can follow after rheumatic fever and similar bacterial infections be the result of the body’s immunological system reacting to its own cells producing an alien RNA?” [3]

Genetic Hybridization

As purely genetic material, it would be expected that viruses are more prone to the process of “jumping genes” than other microorganisms.  The following publication tends to support this hypothesis:  In a study of 24 passages of a nuclear polyhedrosis virus through cell cultures, there were both insertions and deletions in the virus, appearing to suggest that the virus both donated genetic material to and received genetic material from the cells in which it was cultured, therefore suggesting that similar viral exchanges take place in the human system[4].

As another possible complication of viral infections (presumably also viral vaccines), similarities have been found between certain viral proteins and proteins related to myelin sheaths of the brain and nervous system.[5]  As a result of this protein mimicry between viral proteins and homologous areas of the nervous system, immunological cross reactions may take place resulting in post-infectious or post-vaccinal encephalitis, myelitis, or neuritis.  These viruses include measles, Epstein-Barr, influenza A and B, and others causing upper respiratory infections.

Following this line of thought one step further, in an article entitled, “Vaccination and autoimmunity -‘vaccinosis’: a dangerous liaison?,” the authors pointed to the potential problem of “molecular mimicry” in vaccines, in which a structural similarity existing between some viral antigen and a self-antigen could, by bringing about a slight modification of the antigenic character of tissues, cause it to appear foreign to the immune system and thus a fair target for antibody production and potential autoimmunity. [6]

The Work of Howard B Urnovitz

Urnovitz and his colleagues have been studying the implications of vaccines in cancer, Persian Gulf War Syndrome, multiple sclerosis, and AIDS.  Urnovitz, who holds doctorates in Immunology and Microbiology from the University of Michigan where he studied vaccines, has become one of the most vocal proponents for scientists to become aware of vaccine-associated genetic mutations. [7]

His work in this area has supported the concepts that:

  1. Our bodies have a “genetic memory” of foreign substances it encounters, including vaccines.
  2. There is a limit on how much foreign material our bodies can handle before genetic damage occurs and/or progresses into a chronic illness.
  3. Each person has their own unique genetic blueprint which responds to foreign substances differently.

Comment:   Although Urnovitz did not elaborate further on the subject of “genetic memory,” his reference to it can be interpreted as an inference that the genetic blueprints we inherit from our parents are influenced and potentially changed in adaptation to environmental exposures throughout our lifetimes.

Perhaps Urnovitz and colleagues are best known for the work they have published on the Gulf War Syndrome (GWS), where they found evidence of genetic alterations in human chromosome 22q11.2, a known genetic “hot spot” for mutations, which appear to have a role in the pathogenesis of GWS. [8].  Evenmore striking is that when they sequenced their findings, many enteroviral–similar segments were found suggesting that this may have played a role in causing the changes in 22q11.2.  Most Gulf War veterans received the oral polio virus vaccine, which is an enterovirus. Since the polio vaccine was originally cultured in monkey kidneys, known to be contaminated with simian (monkey) cytomegalic virus (CMV), the veterans would have also received the CMV contaminant.

Increasing Incidence of Childhood Autism and Related disorders

In a sense, modern America might be likened onto a tree on which the leaves remain green even while the roots are dying, the roots of course referring to the ominous physical and mental health trends taking place among American children, with one-in-six children being afflicted with a developmental disorder (autism, ADHD, learning disabilities, behavioral problems, allergies, and asthma. [9-10]  It is questionable whether any nation or society can long continue to thrive or even survive with the current rate of health attrition taking place among our children, unless it is reversed.

Ongoing Mass (Herd) Immunizations – Are They Necessary?

Vaccine proponents would have us believe that mass vaccine programs have been largely responsible for controlling virtually all of the former epidemics of killer childhood diseases in industrial nations. In my opinion, with the possible exception of the polio vaccine, the facts do not bear this out. According to the Metropolitan Life Insurance Company, from 1911 to 1935 the four leading causes of childhood deaths from infectious disease in the U.S.A. were diphtheria, pertussis (whooping cough), scarlet fever, and measles. Yet, by 1945 the combined death rates from these four causes had declined by 95 percent, before implementation of mass vaccine programs [11].  Other sources provide much the same information [12-14].

Furthermore, according to a report in Morbidity and Mortality Weekly Report, July 30, 1999, improvements in sanitation, water quality, hygiene, and the introduction of antibiotics have been the most important factors in control of infectious disease in the past century. Although vaccines were mentioned, they were not included among the major factors [14]

Five Autism-Free Zones in a Sea of Autism, Showing Indisputable Epidemiologic Evidence of a Vaccine-Autism Causal Relationship.

A telephone survey commissioned by the nonprofit group Generation Rescue compared vaccinated with unvaccinated boys in nine counties of Oregon and California [15]. The survey included nearly 12,000 households with children ranging in ages from 4 to 17 years, including more than 17,000 boys among whom 991 were described as completely unvaccinated. In the 4 to 11 year bracket, the survey found that, compared with unvaccinated boys, vaccinated boys were 155% more likely to have a neurological disorder, 224% more likely to have ADHD, and 61% more likely to have autism. For the older boys in the 11-17 year bracket, the results were even more pronounced with 158% more likely to have a neurological disorder, 317% more likely to have ADHD, and with 112% more likely to have autism. [15]

In addition to the Generation Rescue Survey, there are three autism-free oases in the United States. Most publicized are Amish communities, mainly studied in Ohio and Pennsylvania [16].The Amish are unique in their living styles in largely self-sustaining communities. They grow their own food. Although they have no specific prohibitions against medical care, very rarely do they vaccinate their children. In local medical centers available to the Amish, most centers reported that they had never seen an Amish autistic child. The only Amish children that were seen as a rule were those with congenital disorders such as fragile X. The one autistic Amish child that was discovered during the surveys was taken to a medical office for an ear infection where the child was incidentally vaccinated, probably without the mother’s consent.

The second is the Florida-based medical practice of Dr. Jeff Bradstreet. While treating several thousand autistic children in his practice, Bradstreet has observed that “there is virtually no autism in home-schooling families who decline to vaccinate for religious reasons” [17]

The third, the “Homefirst Health Services” located in Chicago, has a virtual absence of autism among the several thousand patients that were delivered at home by the medical practice, and remained non-vaccinated according to the wishes of the parents [18].

Clusters of autistic children have also been found among parents with occupational exposures to chemicals prior to conception [19], and in children exposed prenatally to organochlorine pesticides [20].

For those who have not already investigated vaccine contents, the following adjuvants and ingredients have been documented:

  • Acetone (solvent used in fingernail polish remover)
  • Aluminum hydroxide
  • Aluminum phosphate
  • Aluminum sulfate
  • Amphotericin B
  • Animal tissues: pig blood, horse blood, rabbit brain,
  • Dog kidney, monkey kidney
  • Chick embryo, chicken egg, duck egg
  • Calf (bovine) serum
  • Betapropiolactone
  • Fetal bovine serum
  • Formaldehyde
  • Formalin
  • Gelatin
  • Glycerol
  • Human diploid cells (originating from human aborted fetal tissue)
  • Hydrolyzed gelatin
  • Monosodium glutamate (MSG)
  • Neomycin (antibiotic)
  • Neomycin sulfate
  • Phenol red indicator
  • phenoxyethanol (antifreeze)
  • potassium diphosphate
  • potassium monophosphate
  • polymyxin B
  • polysorbate 20
  • polysorbate 80
  • porcine (pig) pancreatic hydrolysate of casein
  • residual MRC5 proteins
  • sorbitol
  • sucrose
  • streptomycin (antibiotic)
  • thimerosal (mercury)
  • tri(n)butylphosphate (neurotoxin)
  • VERO cells, a continuous line of monkey kidney cells
  • Washed sheep red blood cells

Aluminum, a neurotoxin, is associated with Alzheimer’s disease and seizures.

Formaldehyde is a known cancer-causing agent commonly used to embalm corpses.

Glycerin, a tri-atomic alcohol extracted from natural fats which are putrified and decomposed, has known toxic effects including kidney, liver, and lung damage, dieresis, pronounced local tissue damage, gastrointestinal damage, death.

Neomycin and streptomycin (antibiotics) are known to case allergic reactions.

Phenol (carbolic acid is a deadly poison, a common disinfectant and dye.)

Phenyethanol  is known to depress the central nervous system and may cause vomiting and diarrhea. (FDA)

Thimerosal (a mercury derivative) is a toxic heavy metal that is not easily eliminated from the body. Metal toxicity can result in brain injury and autoimmune disease.

Oil adjuvants are known to cause hypersensitivity reactions, cysts, and adjuvant arthritis.

In 2000, Congress strongly recommended that the pharmaceutical companies take the thimerosal out of vaccines (It was not mandated, simply recommended). The drug companies were not told to take the existing lots off the market. The recommendation only applied to new product lines…

Consumer goods are recalled, redesigned, or required to display warning danger labels when they contain toxic ingredients or cause accidents. When  cancer causing agents are found in foods, the foods are often banned and/or a warning label must be displayed on the packages. Vaccines have a different (much lower) standard for safety.

The Health Studio Newsletter (Volume 1, Oct. 1997).
Vaccine Fillers and Ingredients
Dr. Mercola Newsletter, March 7, 2001
http://www.know-vaccines.org/?page_id=301

(NOTE: Although issued in 2001, the Mercola report remains essentially valid in terms of the numbers and types of current vaccine adjuvants and additives.)

Combinations of Toxic Chemicals Bring Exponential Increases in Toxicity

It is universally recognized among toxicologists that combinations of toxic chemicals may bring exponential increases in toxicity; that is, two toxic chemicals in combination will bring a ten-fold or even a hundred-fold increase in toxicity. [21-24]

A classical example of this principle was the Schubert study [21] in which it was found that the amount of lead and the amount of mercury, when each was given separately, would be lethal for one percent of rats tested, would become lethal for one hundred percent of rats tested when combined.

In vaccines this principle would apply at least to mercury and aluminum, both of which are potent neurotoxins.

Vaccines and Subdural (Brain) Hemorrhages

The best evidence to date on this issue comes from the observations of ophthalmologist Horace Gardner who, based on an article from a Japanese neurosurgeon reporting that clusters of nontraumatic brain hemorrhages tended to occur around ages 7 to 10 months in Japan [25], Gardner astutely noted that there was a distinct age difference between nontraumatic brain hemorrhages in Japan and in the United States of America, where most nontraumatic brain hemorrhages tend to occur during the first six months of life.

The explanation, according to Dr. Gardner, was that Japanese do not begin their childhood vaccine programs until seven months, whereas in the United States they are administered during the first six months, starting within 24 hours of birth with the Hepatitis B vaccine: [26]. In essence these observations can potentially be transformed into a gargantuan epidemiologic study involving the childhood populations of Japan and the United States that, by present indications, could prove beyond a doubt that vaccines are the primary cause of subdural hemorrhages now being misdiagnosed as SBS, NAI, and others.

Study Shows Link between Numbers of Vaccines Administered and Infant Mortality Rates (IMRs)

The study entitled Infant mortality rates regressed against number of vaccine doses routinely given.  Is there a biochemical or synergistic toxicity? was conducted by Neil Z. Miller and Gary S. Goldman and published in the reputable Human and Experimental Toxicology Journal, which is indexed by the Nat’l Library of Medicine. [27]

This shocking new study published in a prestigious medical journal has found a direct statistical link between higher vaccine doses and infant mortality rates in the developed world, suggesting that the increasing number of inoculations being forced upon children by medical authorities, particularly in the United States which administers the highest number of vaccines and also has the highest number of infant deaths is, in fact, having an over-all detrimental impact on health.

Why the MMR Vaccine-Autism Relationship?

A number of years ago at an Autism Research Institute (ARI) conference, the founding director of the institute, Dr. Bernard Rimland, announced that approximately two thirds of families bringing their autistic children to ARI referral doctors reported that the child had become autistic following the MMR vaccine. After returning home and electronically checking medical records, the writer of these lines found the same MMR-autism relationship in his own patients.

Dr. Hanan Polansky from the Center for the Biology of chronic Disease (CBCD), author of the highly acclaimed book entitled, Microcompetition with Foreign DNA and Chronic Disease, explains how foreign DNA fragments can cause many major diseases without damaging (mutating) the human DNA. Part of the explanation may also be in the fact that viruses are inherently immunosuppressive in contrast to bacterial infections, which stimulate the immune system, as reflected by the fact that viral infections tend to lower white blood cell counts in contrast to bacterial infections which raise white blood cell counts. The measles virus is especially potent in this regard, being powerfully suppressive to cellular immunity. [28-30] This powerful MMR (viral) immuno-suppression, along with toxic effects of mercury, aluminum, and formaldehyde, in effect paralyzes the body’s own immune defenses, thus allowing  genetic hybridization to take place.

Summation

It has been demonstrated that a sharp and persisting rise in childhood autism commenced following the 1978 introduction of the MMR vaccine (measles, mumps, rubella) in the U.S.A, [31] a time when mercury-laced Hepatitis B and Hemophilus influenza type b vaccines were also introduced. In a bulletin sponsored by the American Academy of Pediatrics, January, 2004 entitled AUTISM A.L.A.R.M., it was announced that 1 in 6 American children were diagnosed with a learning disability and/or significant behavioral disorder. As described and documented by Dr. Kenneth Bock, approximately one-third of America’s children are afflicted by the 4-A disorders: Autism, ADHD, Asthma, Allergies. [32] It is entirely possible or even probable, based on present knowledge, that each of these conditions is associated with underlying genetic changes.

Of all the benefits provided by God and nature for the human species, human genetics must be considered the greatest and most indispensable. Are we a nation of people incapable of recognizing imminent danger signs in the health, welfare, and genetics of our children, and in recognizing these dangers to take corrective actions in their behalf? I think we are capable of taking such actions, but time may be running out. At some unknown future time this process will reach a point-of-no-return in terms of vaccine-induced genetic hybridization that will become incompatible with human reproduction. Mass extinctions are already taking place in plant and animal species, largely due to human encroachments and interventions. [33] Are we soon to follow suit? [34-36]

References

1. Miller, Mary Beth, Geneticist and Researcher Barbara McClintock; Barbara McClintock Won Nobel 1983 Prize for Physiology and Medicine. Jan. 17, 2010.

2. World Medicine, (Scientific News Report), Mobility of genetic material between life forms, (September 22, 1971), pp 69-72; New Clareville House, Oxendon St., London.

3. Anker P, Stroun M, Transcription of spontaneously released bacterial Desoxyribonuleic acid in frog auricles, Journal of Bacteriology, 1973; 114: 114-120.

4. Kumar S, Miller LK, Effects of serial passage of Autographa Californica Nuclear polyhedrosis virus in cell culture, Virus Research, 1987; 7:335-349.

5. Jahnke U, Fischer EH, Alvord EC, Sequence homology between certain viral proteins related to encephalomyelitis and neuritis, Science, July 19, 1985; 29:242-284.

6. Shoenfeld Y, Aron-Maor A, Vaccination and autoimmunity-‘vaccinosis’: a dangerous liaison?, J Autoimmun, Feb 2000, 14(1):1-10.

7. Written testimony of Dr. Howard Urnovitz, August 3, 1999, at the Committee of government reform and oversight.

8. Urnovitz HB, Tuite JJ, Higashida JM et al, RNAs in the sera of Persian Gulf  War Veterans Have Segments Homologous to Chromosome 22q11.2, Clinical and Laboratory Diagnostic Immunology, May, 1999; 6(3):330-335.

9. AUTISM A.L.A.R.M., American Academy of Pediatrics, January, 2004

10. Bock, Kenneth. Healing the New Childhood Epidemics, Autism, ADHD. Asthma and Allergies, 2007.

11. Dublin L. Health Progress. Metropolitan Life Insurance Co., 1948:12.

12. Anderson M.  International Mortality Statistics. Facts on File. Washington D.C.,1981; 161-2, 164-5, 177-8, 216.

13. Miller NZ, Vaccine Safety Manual for Concerned Families and Health Practitioners, with forward by Russell Blaylock, Santa Fe, New Mexico, New Atlantean Press, PO Box 9638, 2008.

14. Morbidity and Mortality Weekly Report, July 30, 1999; 48:621-8.

15. On Internet: Generation Rescue Telephone Survey.

16. The Age of Autism; Mercury, Medicine, and a Man-Made Epidemic Dan Olmsted and Mark Blaxill, New York: Thomas Dunne Books, St. Martin Press. 2010: 252-253.

17 Ibid, pp. 253-254.

18. Ibid, P. 254.

19. Ibid, Pp. 214-215.

20. Roberts E.M., English P.B., Grether J.K. et al, Maternal residence near agricultural pesticide applications and autism spectrum disorders among children in the California central valley, Environmental Health Perspective, July 30, 2007.

21. Schubert J, Riley EJ, Tyler SA. Combined effects in toxicology: A rapid systematic testing procedure: cadmium, mercury and lead. Journal of Toxicology and Environmental Health, 1978; 4:763-776.

22. Abou-Donia MB, Wilmarth KR, Ochme F, Jensen KF, Kurt, TI. Neurotoxicity resulting from coexposure to pyridostigmine bromide, DEET, and permithrin: Implications of Gulf War chemical exposures. Journal of Toxicology and Environmental Health, 1996; 48:35-56.

23. Arnold SF, Koltz DM, Collins B, Vonier PM, Guilette LJ, McLachlan JA. Synergistic activation of estrogen receptor with combinations of environmental chemicals. Science, 1996; 272: 1489-1492.

24..Chester AC and Levine PH. Concurrent Sick Building Syndrome and Chronic Fatigue Syndrome: Epidemic Neuromyalgia Revisited. Clinical Infectious Disease, 1994; 18(Suppl1): S43-8.

25. Aoki N, Massuzawa H. Infantile acute hematoma. Clinical analysis of 26 cases.  J of Neurosurg. 1984:61:273-280.

26. Gardner, H.B. Retinal and subdural hemorrhages – Aoki revisited.  Brit J Opththal.2003: 87:919-920.

27. Miller NZ and Goldman GS, Infant mortality rates regressed against the number of vaccine doses routinely given: Is there a biochemical or synergistic toxicity? Human and Experimental Toxicology, May 4, 2011,  http://www.prisonplanet.com/new-study-finds-direct-link-between-vaccines-and-infant-mortality.html

28. Miller, NZ, Vaccine Safety Manual, for Concerned Families and Health Practitioners, New Atlantean Press, 2008; p. 202.

29. Bock, Kenneth, Healing the New Childhood Epidemics, Autism, ADHD, Asthma, and Allergies, Ballantine Books, New York: 2007.

30 Mass (plant and animal) Extinctions Underway, Majority of Biologists Say, Washington Post, Tuesday, April 21, 1998.

31. Deisher, Theresa, Is Aborted Fetal DNA Linked to Autism? July 21, 2009..

32. Ratajczak, HV, (Review Article) Theoretical aspects of autism: Causes – A review. Journal of Immunotoxicology, 2011; 8(1): 68-79.

33. Lunoe, Sandy, Excuse Me Waiter – There’s a Fly in My Soup! http://vactruth.com/2012/01/21/fly-in-my-vaccine-soup/

Photo Credit: MJ/TR

 

Category:

Activism, vaccines

Cancer Expert Dies After Vaccination – Total Organ Failure

https://www.dailymail.co.uk/news/article-6579561/Leading-cancer-expert-dies-suddenly-routine-yellow-fever-jab.html

Leading cancer expert, 67, described by the Duke of Cambridge as an ‘inspiration’ dies suddenly after a routine yellow fever jab

  • Martin Gore, 67, suffered total organ failure shortly after having the vaccination 
  • Vaccine is recommended for visiting Africa and South and Central America 
  • Serious side effects are rare, but are more common in those who are over 60 

By Dianne Apen-sadler For Mailonline

Published: 10 January 2019

A leading cancer expert once described by the Duke of Cambridge as an ‘inspiration’ has died suddenly after a routine yellow fever jab.

Martin Gore, 67, passed away after suffering total organ failure shortly after having the injection, which is recommended to anyone visiting Sub-Saharan Africa, South and Central America and the Caribbean, reports The Times.

Serious side effects from the vaccine are very rare, but are more common in those over the age of 60, or in anyone with HIV/AIDS.

Professor Gore, who worked as an oncologist for more than 35 years, focused on ovarian cancer, melanoma and renal cell carcinoma.

In 2015, he was given The Royal Marsden’s Lifetime Achievement Award, presented by Prince William.

Leading cancer expert Martin Gore, 67, (pictured) has died suddenly after a routine yellow fever jab

Leading cancer expert Martin Gore, 67, (pictured) has died suddenly after a routine yellow fever jab

The Duke of Cambridge said at the time: ‘I’ve found Martin a source of inspiration – his infectious enthusiasm and passion for his work, and his obvious compassion and kindness for his patients, their family and friends, reinforces my knowledge that The Royal Marsden is a truly special place.

‘He’s one of the pioneers of 20th century cancer care, and a friend, colleague and trusted doctor to many.’

Just a year later he was an awarded a CBE in the Queen’s Birthday Honours for his work in these areas.

Martin Gore, pictured left while meeting the Duke of Cambridge, has died suddenly after a routine yellow fever jab

Martin Gore, pictured left while meeting the Duke of Cambridge, has died suddenly after a routine yellow fever jab

Serious side effects from the vaccine are very rare, but are more common in those over the age of 60 (file photo)

Serious side effects from the vaccine are very rare, but are more common in those over the age of 60 (file photo)

Serious adverse effects recorded in the study included hospitalization, life-threatening illness, permanent disability and death. Five people died from the jab in this period. 

Peter Openshaw, an ex-president of the British Society for Immunology, told the Times that there has been a four-fold increase in the risk of side-effects for those 60 and above.

But he emphasised that the jab was much safer than exposure to yellow fever, which killed around 78,000 people in Africa in 2013.

 

The Royal Marsden Cancer charity shared the news on Facebook, saying: ‘It is with deep sadness that The Royal Marsden announces the sudden death of Professor Martin Gore CBE who died this morning.

‘Martin was at the heart of The Royal Marsden’s life and work in research, treatment and the training of our next generation of oncologists.

‘His contribution as Medical Director for 10 years, a Trustee of The Royal Marsden Cancer Charity, and as a clinician is unparalleled.

‘He has been a friend, colleague and mentor to so many people and his loss will be immense.

________________

For more:  https://madisonarealymesupportgroup.com/2018/09/24/more-deaths-after-hpv-vaccination/

https://madisonarealymesupportgroup.com/2018/12/11/ny-senator-passes-away-at-47-after-linking-illness-to-flu-shot-symptoms/

https://madisonarealymesupportgroup.com/2018/12/14/man-blames-flu-shot-for-blindness-partial-paralysis/

https://madisonarealymesupportgroup.com/2018/12/07/nevada-man-diagnosed-with-guillain-barre-syndrome-after-getting-flu-shot/

https://madisonarealymesupportgroup.com/2018/10/21/woman-undergoes-extensive-arm-surgery-after-flu-shot/

https://madisonarealymesupportgroup.com/2016/07/19/motor-and-sensory-findings-in-girls-who-received-gardasil/

 

 

Category:

Activism, mosquitoes, vaccines

IPAK Model of Autism Spectrum Causality

http://ipaknowledge.org/ASD-Causality-Model.php

“Personal Communication, Dr. J. Lyons-Weiler, The Institute for Pure and Applied Knowledge”

The IPAK Model of ASD Causality (aka “The IPAK Model”)

After reviewing thousands of studies over two years, a more complete picture of the causality of ASD has now emerged.

We are working on an interactive web resource to allow the public and researchers to access the scientific literature in support of each component of this ASD causality model.

Note that this model includes an important component of genetic susceptibility, never addressed in whole-population ecological correlational association studies.

Again, the hypothesis of genetic susceptibility has not been addressed.

USAGE: Please use with citation and reference

Also available for download as .tiff, .ppt

Vaccine Metals and ER Stress

Aremu DA, Ezomo OF, Meshitsuka S. Gene expression in primary cultured astrocytes affected by aluminum: alteration of chaperons involved in protein folding. Environ Health Prev Med. 2011;16:16-24.

Franchi L, Núñez G. The Nlrp3 inflammasome is critical for aluminium hydroxide-mediated IL-1beta secretion but dispensable for adjuvant activity. Eur J Immunol. 38(8):2085-9.

Rizvi SH, Parveen A, Ahmad I, Ahmad I, Verma AK, Arshad M, Mahdi AA. Aluminum Activates PERK-EIF2α Signaling and Inflammatory Proteins in Human Neuroblastoma SH-SY5Y Cells. Biol Trace Elem Res. 2016;172(1):108-19.

Rizvi MSH, Parveen A, Verma AK, Ahmad I, Arshad M, Mahdi AA. Aluminium induced endoplasmic reticulum stress mediated cell death in SH-SY5Y neuroblastoma cell line is independent of p53. PLoS One. 2014;30;9(5):e98409.

Stamogiannos A, Papakyriakou A, Mauvais FX, van Endert P, Stratikos E. Screening Identifies Thimerosal as a Selective Inhibitor of Endoplasmic Reticulum Aminopeptidase 1. ACS Med Chem Lett. 2016;7:681-5.

Direct Mitotoxicity

Kahrizi F 2016. Repeated Administration of Mercury Intensifies Brain Damage in Multiple Sclerosis through Mitochondrial Dysfunction. Iran J Pharm Res. 15:834-841.

Lemire et al., 2009. Aluminum-induced defective mitochondrial metabolism perturbs cytoskeletal dynamics in human astrocytoma cells. J. Neurosci Res 87:1474-83

Sharpe, MA et al., 2012. Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes: Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA Journal of Toxicology Volume 2012 Article ID 373678, 12 pages.

Vaccine ER Stress + Unfolded Protein ER Stress = ER Hyperstress

Lyons-Weiler, J. 2018. Autism is an Acquired Cellular Detoxification Deficiency Syndrome with Hetergeneous Genetic Predisposition. Autism Open Access, (Publisher’s “editing version” online: https://www.omicsonline.org/open-access/autism-is-an-acquired-cellular-detoxification-deficiency-syndrome-with-heterogeneous-genetic-predisposition-2165-7890-1000224.pdf

ER Hyperstress -> Impaired Cellular Detoxification

ER/Mito/Golgi Citations in: Lyons-Weiler, J. 2018. Autism is an Acquired Cellular Detoxification Deficiency Syndrome with Hetergeneous Genetic Predisposition. Autism Open Access, (Publisher’s “editing version” online: https://www.omicsonline.org/open-access/autism-is-an-acquired-cellular-detoxification-deficiency-syndrome-with-heterogeneous-genetic-predisposition-2165-7890-1000224.pdf

Leaky Gut -> Absorption of Toxins

De Chambrun G.P., Body-Malapel M., Frey-Wagner I., Djouina M., Deknuydt F., Atrott K., Vignal C. Aluminum enhances inflammation and decreases mucosal healing in experimental colitis in mice. Mucosal Immunol. 2014;7:589–601.

Kirschbaum, BB and C Schoolwerth. 1989. Acute Aluminum Toxicity Associated with Oral Citrate and Aluminum-Containing Antacids. The American Journal of the Medical Science 297:9-11.

Tian F. 2017. The therapeutic protection of a living and dead Lactobacillus strain against aluminum-induced brain and liver injuries in C57BL/6 mice. PLoS One. 12:e0175398. doi: 10.1371/journal.pone.0175398

Yu L 2016. Potential of Lactobacillus plantarum CCFM639 in Protecting against Aluminum Toxicity Mediated by Intestinal Barrier Function and Oxidative Stress. Nutrients. 8:pii: E783.

Yu, L 2017. Lactobacillus plantarum CCFM639 can prevent aluminium-induced neural injuries and abnormal behaviour in mice. Journal of Functional Foods 30:142-150.

Yu, L. 2017. Dietary Lactobacillus plantarum supplementation enhances growth performance and alleviates aluminum toxicity in tilapia Ecotoxicology and Environmental Safety 143:307-314.

Chronic Microglial Activation -> Leaky Gut

Grubišić V and Parpura V. 2015. The second brain in autism spectrum disorder: could connexin 43 expressed in enteric glial cells play a role? Front Cell Neurosci. 9:242. doi: 10.3389/fncel.2015.00242.

Kirchgessner AL et al., 1997. Excitotoxicity in the enteric nervous system. J Neurosci. 17(22):8804-16.

Unfolded Proteins -> Autoimmunity

Garaud JC, Schickel JN, Blaison G et al. B cell signature during inactive systemic lupus is heterogeneous: toward a biological dissection of lupus. PLoS One 2011;6:e23900.

Clavarino G, Adriouach S, Quesada JL, Clay M et al. Unfolded protein response gene GADD34 is overexpressed in rheumatoid arthritis and related to the presence of circulating anti-citrullinated protein antibodies. 2016;49(3):172-8.

Immunoneuroexcitotoxicity -> Aberrant Pruning

Cunningham CL et al., 2013. Microglia regulate the number of neural precursor cells in the developing cerebral cortex. J Neurosci. 33(10):4216-33. doi: 10.1523/JNEUROSCI.3441-12.2013. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711552/

Fiorentino et al., 2016. Blood–brain barrier and intestinal epithelial barrier alterations in autism spectrum disorders. Molecular Autism 4:49

Strunecka A., et al. 2018. Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: A possible role of fluoride and aluminum. Surg Neurol Int. 2018; 9:74.

Aberrant Pruning -> Altered Development

Thomas MS. The over-pruning hypothesis of autism. Dev Sci. 2016 19(2):284-305.

Kim HJ et al. Deficient autophagy in microglia impairs synaptic pruning and causes social behavioral defects. Mol Psychiatry. 2017 22(11):1576-1584.

Vaccine Metals Release -> Autoimmunity

Tomljenovic L, Shaw CA Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations. Lupus. 2012 21(2):223-30.

Autoimmunity -> Altered Development

Braunschweig D et al., 2008. Autism: maternally derived antibodies specific for fetal brain proteins. Neurotoxicology. 29(2):226-31.

Cabanlit M et al., 2007. Brain-specific autoantibodies in the plasma of subjects with autistic spectrum disorder. Ann N Y Acad Sci. 1107:92-103.

Malkki H. Neurodevelopmental disorders: Maternal antibodies induce autism-like phenotype in mice. Nat Rev Neurol. 2016 12:678-679. doi: 10.1038/nrneurol.2016.165.

 

Category:

Activism, Autism, research, vaccines

The Vaccine Debate – Top Government Expert States Vaccines CAN Cause Autism in Some Children

UPDATE Nov. 2024:

Over 300 pages of evidence from the CDC shows that ‘vaccines’ cause autism. Investigative reporter Sharyl Attkisson exposes that the “bulk of credible science finds ‘vaccines’ ‘can and do’ cause autism.” See 76 Studies and Comprehensive Resource on vaccines.  Dr. Andrew Wakefield was right all along despite his seminole paper being retracted 12 years after the fact without any violations of guidelines.  The Cabal systematically destroyed his reputation for reporting his findings.  He later produced Protocol 7 which details Merck’s MMR fraud.  This is what they do to dissenters – merciless, ad hominem attacks.

http://fullmeasure.news/news/full-episodes/full-measure-january-6-2019    Video in Link.  Approx. 23 Min.

Full Measure With Sharyl Attkisson

Sunday, Jan. 6, 2019

By Full Measure Staff

Transcript of Video:

Today we investigate one of the biggest medical controversies of our time: vaccines. There’s little dispute about this much– vaccines save many lives, and rarely, they injure or kill. A special federal vaccine court has paid out billions for injuries from brain damage to death. But not for the form of brain injury we call autism. Now—we have remarkable new information: a respected pro-vaccine medical expert used by the federal government to debunk the vaccine-autism link, says vaccines can cause autism after all. He claims he told that to government officials long ago, but they kept it secret.

Yates Hazlehurst was born February 11, 2000. Everything was normal, according to his medical records, until he suffered a severe reaction to vaccinations.

Rolf Hazlehurst: And at first, I didn’t believe it. I did not think that, I did not believe that vaccines could cause autism. I didn’t believe it.

But there’s a hard reality for Yates. The trademark brain disease, pain and inability to communicate that’s common with severe autism.

In 2007, Yates’ father sued over his son’s injuries in the little known Federal Vaccine court. It was one of more than 5000 vaccine autism claims.

Congress created vaccine court in 1988, in consultation with the pharmaceutical industry. In the special court, vaccine makers don’t defend their products—the federal government does it for them, using lawyers from the Justice Department. Money for victims comes from us, not the pharmaceutical industry, through patient fees added onto every vaccine given.

Denise Vowell: Our hearings are all closed to the public. And that’s statutory.

In 2007, Yates’ case and nearly all the other vaccine autism claims lost. The decision was based largely on the expert opinion of this man, Dr. Andrew Zimmerman, a world-renowned pediatric neurologist shown here at a lecture.

Dr. Zimmerman was the government’s top expert witness and had testified that vaccines didn’t cause autism. The debate was declared over.

But now Dr. Zimmerman has provided remarkable new information. He claims that during the vaccine hearings all those years ago, he privately told government lawyers that vaccines can, and did cause autism in some children. That turnabout from the government’s own chief medical expert stood to change everything about the vaccine-autism debate.

If the public were to find out.

Hazlehurst: And he has come forward and explained how he told the United States government vaccines can cause autism in a certain subset of children and United States government, the Department of Justice suppressed his true opinions.

Hazlehurst discovered that later when Dr. Zimmerman evaluated Yates as a teenager. That’s when he partnered with vaccine safety advocate Robert F. Kennedy, Junior—who has a voice condition.

Kennedy: This was one of the most consequential frauds, arguably in human history.

Kennedy was instrumental in convincing Dr. Zimmerman to document his remarkable claim of the government covering up his true expert opinion on vaccines and autism.

Dr. Zimmerman declined our interview request and referred us to his sworn affidavit. It says: On June 15, 2007, he took aside the Department of Justice—or DOJ lawyers he worked for defending vaccines in vaccine court. He told them that he’d discovered

“exceptions in which vaccinations could cause autism.” “I explained that in a subset of children, vaccine induced fever and immune stimulation did cause regressive brain disease with features of autism spectrum disorder.”

Kennedy: This panicked the two DOJ attorneys and they immediately fired Zimmerman. That was on a Friday and over the weekend they called Zimmerman and said his services would no longer be needed. They wanted to silence him.

Days after the Department of Justice lawyers fired Dr. Zimmerman as their expert witness, he alleges, they went on to misrepresent his opinion to continue to debunk autism claims. Records show that on June 18, 2007, a DOJ attorney Dr. Zimmerman spoke to told vaccine court,

“We know [Dr. Zimmerman’s] views on the issue…There is no scientific basis for a connection” between vaccines and autism.

Dr. Zimmerman now calls that “highly misleading.”

The former DOJ lawyer didn’t return our calls and emails. Kennedy has filed a fraud complaint with the Justice Department Inspector General, who told us they don’t “comment on investigations or potential investigations.”

Meantime, CDC—which promotes vaccines and monitors vaccine safety– never disclosed that the government’s own one-time medical expert concluded vaccines can cause autism – and to this day public health officials deny that’s the case.

Dr. Anne Schuchat: “Based on dozens of studies and everything I know as a physician and a scientist, there’s no link between autism and vaccines.”

CDC declined our interview request. In addition to filing a fraud complaint, Kennedy has delivered Dr. Zimmerman’s affidavit to leaders on Capitol Hill. But there he claims, is another key part of this story: roadblocks set up by the pharmaceutical industry—or PhRMA.

Kennedy: But everybody takes money from PhRMA so they’ve all been corrupted. And it’s almost impossible to get anything done on Capitol Hill.

Kennedy, a Democrat, isn’t the only one claiming vaccine industry money rules the day. We spoke to 11 current and former members of Congress and staff who claim they faced pressure, bullying or threats when they raised vaccine safety questions. Several of them agreed to appear on camera.

Burton: There’s no question in my mind whatsoever that the pharmaceutical industry had a great influence with people over at the CDC and FDA. There’s no question in my mind.

Republican Dan Burton—former Chairman of the House Oversight Committee—has an autistic grandson.

Burton: I am not against vaccinations.

He pursued vaccine investigations in the early 2000s. Beth Clay was one of his staffers.

Clay: There was a lot of pressure from people on the Hill.

When you say people on the hill were exerting pressure, what kind of people? Colleagues?

Clay: Colleagues, there were pharmaceutical lobbyists. The pharmaceutical lobbyists had, you know, they are the same people that have been entrenched. They can walk into any office in Capitol Hill, and they’ll talk to staff, they’ll talk to members and they’ll encourage them to discourage, our investigation.

Sharyl: At the risk of stating the obvious why did they have that kind of access to members?

Clay: It’s money. And if you look at the donations over the last 20 years, the pharmaceutical industry, and Republican and Democrat, they’re nonpartisan. They put money everywhere.

Former Congressman, Dr. Dave Weldon, a Republican, says he got the message loud and clear.

Sharyl: If you would want to hold a hearing on an issue like vaccines and autism, your own leadership might fight you on that because of the financial influence, the pharmaceutical industry

Dave Weldon: They wouldn’t fight you. They’d kill it. It’s dead. They don’t even want to discuss it. It’s dead on arrival. If you, if you as an individual member want to take on the pharmaceutical industries. It’s forget it.

Sharyl: Can you describe an incident or just how it, how that would go?

Weldon: It would typically be in a hallway or the street and people would come up to you and say, “You know, you really need to, you know, back off on this. It could be, it could be bad for the community or bad for the country or bad for you.”

Weldon says he’s generally pro-vaccine, depending on the patient and the shot—and gives flu shots to adults. We asked him to review Dr. Zimmerman’s new affidavit.

Weldon: I found his affidavit and testimony through that affidavit to be consistent with my opinions. That some children can get an autism spectrum disorder from a vaccine.

Republican Bill Posey is a current member of Congress.

Rep. Bill Posey: I don’t have to tell you that industry is a very, very powerful industry. Matter of fact, I don’t know of anyone more powerful than that industry.

Posey says his own party leaders twice promised to hold hearings on the topic, only to scuttle them in the end.

Hazlehurst – who happens to be a criminal prosecutor– was scheduled to be a witness at one such Congressional hearing. Two weeks before the hearing in 2013, he briefed Congressional staff.

Hazlehurst: I presented at that Congressional briefing and I explained in that hearing, if I did to a criminal in a court of law what the United States Department of Justice did to vaccine injured children, I would be disbarred and I would be facing criminal charges. I think that scared the hell out of them.

The hearing was abruptly cancelled. Meantime, Dr. Zimmerman – the one-time expert used to debunk vaccine autism claims—now says several of his own patients got autism from vaccines. They include Yates Hazlehurst.

Today, with intensive treatment, Yates is doing better. His dad hopes the new testimony from a most unlikely source will get new attention.

Hazlehurst: A child that was unnecessarily sacrificed and hopefully some good, will come from his suffering.

The lobby group representing the pharmaceutical industry wouldn’t agree to an interview but told us they’re working with Congress and other stakeholders on the importance and safety of vaccines to support the health and safety of individuals and communities.

_________________

**Comment**

The plot against vaccines just keeps thickening.

Here you can see the ACIP vote “yes” for a new vaccine despite the lack of safety studies on the cumulative effects: https://madisonarealymesupportgroup.com/2018/09/08/acip-vote-yes-for-new-vaccine-despite-no-safety-studies-on-cumulative-effect-with-other-vaccines/  It’s all right here in bright purple crayon.

This is how brand new vaccines are approved to the pediatric immunization schedule. Basic dialogue before they voted:
Q: Is it dangerous to use this vaccine with other vaccines?
A: We have no data on that. Once approved, it will be given along with other vaccines but we have no clue whether that’s safe or not.

Somehow approving a new vaccine with no data on the accumulated cocktail effect is OK to them IF you put them in different limbs……scientifically, this is quite a head scratcher.

By nature, vaccines are systemic.

Q: Do we at least have any data from other countries that used this vaccine in combination with other vaccines?
A: Not to my knowledge.

Sounds good to me. Lets vote yes!

Only after they vote, one guy voices concern over 16 heart attack deaths in the safety trials.

Illogic at it’s best.

Perhaps it has something to do with money & power? https://thevaccinereaction.org/2018/09/global-vaccine-market-expected-to-reach-50-52-billion-by-2023/   The value of the vaccine market will reach $50.42 billion by 2023 from $36.45 billion in 2018, at a Compound Annual Growth Rate (CAGR) of 6.7 percent, according to recently published report by private research firm MarketsandMarkets of India.1

https://madisonarealymesupportgroup.com/2018/08/24/financial-kickbacks-for-vaccinations-abusive-illegal-fraudulent/ “This brings us to the financial incentives to pediatricians offered by insurance companies for vaccinating our children. The Blue Cross Blue Shield health insurance document explaining these financial incentives can be found here: https://jeffreydachmd.com/wp-content/uploads/2018/08/Pediatricians-Receive-Financial-Incentives-Kickbacks-to-Vaccinate-Children-BCBS-2016-Booklet.pdf Pediatricians are raking in 40-80 thousand dollars a year from these kickback schemes.”

https://madisonarealymesupportgroup.com/2018/10/05/drug-companies-pay-fda-nih-to-fast-track-market-vaccines/

https://madisonarealymesupportgroup.com/2018/10/19/fda-official-uses-revolving-door-to-join-biotech-company-developing-mrna-vaccines/

Category:

Activism, Autism, vaccines

FDA Approves 6 in 1 Combo Vaccine for Babies

https://thevaccinereaction.org/2019/01/fda-approves-6-in-1-combo-vaccine-for-babies/

FDA Approves 6 in 1 Combo Vaccine for Babies

by Kate Raines
Published January 3, 2019

FDA Approves 6 in 1 Combo Vaccine for Babies

Story Highlights

  • On Dec. 21, 2018, the U.S. Food and Drug Administration (FDA) approved a new combination hexavalent vaccine (Vaxelis) that includes antigens for six diseases to be given in three doses to infants and children between six weeks and four years of age.
  • Manufacturers Sanofi Pasteur and Merck jointly developed Vaxelis, which combines diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenza type B vaccines into one shot, and the new combination vaccine is expected to be commercially available in the U.S. in 2020.
  • The FDA has only approved Vaxelis to be given to infants for the first three doses, usually given at two, four and six months, and children will have to get a separate dose of DTaP vaccine to complete the primary pertussis vaccine before age four.

On Dec. 21, 2018, the U.S. Food and Drug Administration (FDA) approved a new combination hexavalent vaccine (Vaxelis) that includes antigens for six different diseases: diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and invasive haemophilus influenza type B.1   Vaccine manufacturers Sanofi Pasteur and Merck jointly developed Vaxelis, which is approved to be given in three doses to children between six weeks and four years of age but children will have to get a separate dose of DTaP vaccine to complete the primary pertussis vaccine series before age four. The new combination vaccine is expected to be commercially available in the U.S. in 2020.2

Sanofi provided the antigens for diphtheria, tetanus, pertussis, and poliomyelitis for Vaxelis production and Merck provided antigens for H. influenzae type b and hepatitis B.3 Vaxelis has been approved by government regulators in the European Union since 2016.4

Monovalent vaccines include only one antigen, while multivalent or polyvalent vaccines like Vaxelis include either more than one strain of a microorganism or more than one type of microorganism. Widely used multivalent vaccines include the live attenuated measles, mumps and rubella vaccine (MMR) and the inactivated diphtheria, tetanus and acellular pertussis vaccines (DTaP for children under age seven and Tdap for older children and adults). Separate vaccines for measles, mumps, rubella and pertussis are not available in the U.S., while tetanus and diphtheria vaccines are only available as a combination (DT or Td) vaccine.

Drawbacks of Combination Vaccines

Combination vaccines have been created by manufacturers to purportedly reduce the number of shots a child must receive to be in compliance with government recommended childhood vaccine schedules and to simplify ordering, transport and storage of vaccines.5

Drawbacks to the multivalent vaccines include a higher risk of pain and swelling at the injection site and, and for Merck’s MMRV (mumps, measles, rubella, varicella) vaccine in particular, a higher incidence of febrile seizures in children under age four.7   The product manufacturer package insert for the new hexavalent vaccine states that,

“Vaxelis is contraindicated in children with a history of severe allergic reaction to any of the ingredients of the vaccine, or to any “other diphtheria toxoid, tetanus toxoid, pertussis-containing vaccine, inactivated poliovirus vaccine, hepatitis B vaccine, or H. influenzae type b vaccine.”

According to the Vaxelis product insert, contraindications include

“a history of encephalopathy (coma, decreased levels of consciousness, prolonged seizures) within 7 days of a previous dose of pertussis-containing vaccine, that is not attributable to another cause” and “a history of progressive neurologic disorder, including infantile spasms, uncontrolled epilepsy, or progressive encephalopathy until a treatment regimen has been established and the conditions has stabilized.”

Warnings and Precautions include temperature over 105F within 48 hours not attributable to another identifiable cause; collapse or shock-like state (hypotonic-hyporesponsive episode (HHS) within 48 hours; persistent, inconsolable crying lasting more than three hours within 48 hours; and seizures with or without fever within three days.

The product insert reports high rates of adverse reactions among children receiving the experimental hexavalent vaccine in clinical trials:

“Rates of adverse reactions varied by number of doses of Vaxelis received. The solicited adverse reactions 0-5 days following any dose were irritability (≥55 percent), crying (≥45 percent), injection site pain (≥44 percent), somnolence (≥40 percent), injection site erythema (≥25 percent), decreased appetite (≥23 percent), fever ≥38.0°C (≥19 percent), injection site swelling (≥18 percent), and vomiting (≥9 percent).”1

References:

1 Sanofi Pasteur. FDA Approves VAXELIS™, Sanofi and MSD’s Pediatric Hexavalent Combination Vaccine. Press Release Dec. 6, 2018.
2 Sheinin AG. FDA Approves New Children’s Vaccine. WebMD Dec. 28, 2018.
3 Hackett DW. Hexavalent Vaccine for Children Less Than 5 Years of Age Approved. Precision Vaccinations Dec. 27, 2018.
4 Vaxelis®, New Fully-liquid Paediatric Hexavalent Vaccine Approved in the European Union. Ciston PR Newswire Feb. 19, 2016.
5 Lee BY. How About 6 Vaccines In One? FDA Approves New Vaccine From Sanofi, Merck. Forbes Dec. 28, 2018.

__________________

**Comment**

http://www.greenmedinfo.com/blog/vaccine-bombshell-leaked-confidential-document-exposes-36-infants-dead-after-vacc?

In the above link, a confidential GlaxoSmithKline document revealed 36 infants died after another 6 in 1 shot called Infanrix Hexa.  It also caused 1,742 adverse reactions, including 503 which were serious.

Another drawback not mentioned is the inability to track adverse reactions to any one particular vaccine since they are all thrown together. Secondly, when you consider that each of these vaccines has their own set of adverse reactions, one can only imagine the combined effect upon immature immune systems.  

It’s sad that manufacturers are more concerned with convenience (ordering, transporting, and storage of vaccines) than with public health.  This is a problem.

With increasing rates of childhood autism, neurological issues, and the polio-like condition known as acute flaccid myelitis (AFM), you’d think there would be extra caution taken regarding childhood vaccines not less.  Yet, vaccine manufacturers and our government bullishly move forward despite increasing evidence of lack of vaccine safety studies and even proof of vaccine effectiveness.

Regarding AFM, the CDC has confirmed 158 cases in 36 states, and they’ve only been recording cases since 2014:  https://thevaccinereaction.org/2019/01/cdc-reports-182-confirmed-cases-of-afm/  AFM causes inflammation of the spinal cord.  As to cause, authorities bounce from a pathogen to an autoimmune syndrome (similarly to chronic Lyme).  It’s been compared to Guillain-Barré Syndrome (GBS), in which the immune system attacks healthy nerve cells.  Some believe AFM is caused by a virus.

Again, since there is an upsurge in AFM with cause unknown, prudence would err on the side of caution regarding vaccinations since retroviral contamination in vaccines has been discovered:  https://madisonarealymesupportgroup.com/2017/10/15/vaccines-and-retroviruses-a-whistleblower-reveals-what-the-government-is-hiding/

https://madisonarealymesupportgroup.com/2018/03/01/vaccines-could-contribute-to-disease-epidemics-due-to-retrovirus-contamination/

https://madisonarealymesupportgroup.com/2018/12/09/vaccines-likely-infected-with-retroviruses-linked-to-chronic-disease/

https://madisonarealymesupportgroup.com/2018/06/23/the-role-of-retroviruses-in-chronic-illness-a-clinicians-perspective/  Retroviruses can be acquired (inhalation, blood-based products, physical contact) or the viruses already present in our DNA can be activated through influences such as a viral infection or chronic inflammation (Manghera and Douville, 2013).

For example, the Epstein Barr virus induces expression of the HERV-K envelope gene and the transactivation of MSRV, the Multiple Sclerosis retrovirus (Mameli et al, 2007; Sutkowski et al, 2001). Herpes simplex type-2 activates members of the HERV-W family. These and other mechanisms are likely responsible for the activation of HERVs seen in rheumatoid arthritis, SLE, Sjorgens disease, schizophrenia, autism, MS and cancer. Cell phone radiation has disabled many of our protective proteins (Fragopoulou et al, 2012) and so have many of the food-based toxins such as glyphosate (Seneff et al, 2017) and air-based inhalants (aluminium etc). An unintended source of retroviruses are some vaccines as reported in Frontiers in Microbiology in January 2011).

It’s all here in purple crayon yet isn’t making any mainstream news.

It is estimated that 6% of the U.S. population is harboring a retrovirus in their bodies that can develop into an acquired immune deficiency. This is not the well-known AIDS caused by HIV, but Acquired Immune Deficiency Syndrome (AIDS) associated with other retroviruses.

That’s 20 million Americans with a retrovirus that can be spread through inhalation, blood-based products, and physical contact.

Many are also including vaccines.  

A simple tick bite could be one trigger that ignites the sleeping retrovirus giant.

 

 

 

 

 

 

 

 

Category:

Activism, vaccines