January 26th 2018
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With the flu season hysteria nearing its peak, millions are being driven to vaccination as a ‘preventive’ approach. Those who abstain are often accused of being uneducated or worse, socially irresponsible “anti-vaxxers.” Nothing could be further from the truth.
As it presently stands, it is not sound medical science, but primarily economic and political motivatiosn which generate the immense pressure behind mass participation in the annual ritual of flu vaccination.
It is a heavily guarded secret within the medical establishment (especially within the corridors of the CDC) that the Cochrane Database Review (CDR), considered by many within the evidence-based medical model to be the gold standard for assessing the therapeutic value of common medical interventions, does not lend unequivocal scientific support to the belief and/or outright propaganda that flu vaccines are ‘safe and effective.’
To the contrary, these authoritative reviews reveal there is a conspicuous absence of conclusive evidence as to the effectiveness of influenza vaccines in children under 2, healthy adults, the elderly, and healthcare workers who care for the elderly. For example, here is the conclusion of the review titled, “Vaccines for preventing seasonal influenza and its complications in people aged 65 or older,”
“The available evidence is of poor quality and provides no guidance regarding the safety, efficacy or effectiveness of influenza vaccines for people aged 65 years or older. To resolve the uncertainty, an adequately powered publicly-funded randomised, placebo-controlled trial run over several seasons should be undertaken.”
Really? Why does the media and medical establishment often say “the science is settled” on vaccines? This review looked at evidence from experimental and non-experimental studies carried out over 40 years of influenza vaccination, including 75 studies. And yet still they conclude that an adequately powered and publicly-funded (read: independent, non-industry influenced study) RCT of sufficient duration has yet to be performed.
What is even more disconcerting is that only one CDR validated safety study on inactivated flu vaccines has been performed in children under 2 (the population most susceptible to adverse reactions), even though in the USA and Canada current guidelines recommend the vaccination of healthy children from six months old.
Another alarming finding following the global pandemic declared by the World Health Organization in 2009, is that receipt of the seasonal flu vaccine among Canadians actually increased the rate of medically attended pandemic H1N1 infection. Vaccines, therefore, may actually decrease resistance to viral infection via their immunosuppressive actions. View study.
Can Vaccination Replace Natural Immunity?
At the outset it should be acknowledged that there would be no medical justification for vaccination in the first place if it were not for the observation that periodic infection from wild type pathogens confers lasting, natural immunity. In a very real sense periodic infectious challenges are Nature’s immunizations, without which the very concept of vaccination would make absolutely no sense. Equating vaccination with bona fide immunity, or calling vaccines ‘immunizations,’ is highly misleading, and as you can see by the Cochrane data above, not evidence-based at all.
The vaccination process artificially simulates and co-opts a natural process, generating a broad range of adverse unintended consequences, many of which have been documented here. Vaccine proponents would have us believe that natural immunity is inferior to synthetic immunity, and should be replaced by the latter (see our article on the vaccine agenda: Transhumanism/Dehumanism). In some cases they even suggest breastfeeding should be delayed during immunizations because it “interferes” with the vaccine efficacy.
This warped perspective follows from the disingenuous standard vaccine researchers use to “prove” the “efficacy” of their vaccines. The chemical kitchen sink is thrown at the immune system in order to conserve the expensive-to-produce antigen and to generate a more intense immune response – a process, not unlike what happens when you kick a beehive. These chemicals include detergents, anti-freeze, heavy metals, xenotrophic retroviruses, DNA from aborted human fetuses (diploid cells) and other species, etc. Amazingly, vaccine researchers and manufacturers do not have to prove the antibodies actually have affinity with the antigens they are marketed to protect us against, i.e. they do not have to prove real world “effectiveness,” only a surrogate marker of “efficacy.” Yet, recent research indicates in some cases no antibodies are required for immunity against some viruses, running diametrically opposed to the orthodox tenets of classical vaccinology.
Another point that can not be understated is that the trivalent (3-strain) influenza vaccines are incapable of protecting us against the wide range of pathogens which produce influenza-like illness:
“Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only Influenza A and B, which represent about 10% of all circulating viruses.” (Source: Cochrane Summaries).
It is therefore exceedingly clear that it is a mathematical impossibility for influenza vaccines to be effective at preventing wild-circulating strains of influenza. Support of the immune system, then, becomes the most logical and reasonable solution.
Immune Status Determines Susceptibility To Infection
The fact is that our immune status determines susceptibility. If the immune system is continually challenged with environmental toxicants, nutritional deficiencies and/or incompatibilities, chronic stress, influenza is far more likely to take hold. If your immune system is strong, many infectious challenges occur, are met with an appropriate response, and often go unnoticed. In other words, it is not a lack of a vaccination that causes infection, rather, the inability of the immune system to function effectively. [Note: In some cases, we may become infected and the ultimate outcome is that we enjoy even greater immunity.]
Moreover, there is an ever-growing appreciation within the scientific community that influenza can not be defined as a completely exterior vector of morbidity and mortality, as portrayed within the mainstream, but is actually comprised of many proteins and lipids derived from the host it occupies, and may even be more accurately described as a hijacked cellular microvessicle (exosome), i.e. it’s as much us as other.
Learn more by reading our recent articles on the topic, “Why The Only Thing Influenza May Kill Is Germ Theory,” and “Profound Implications of the Virome for Human Health and Autoimmunity,”and by watching the incredibly eye-opening NIH lecture by Dr. Herbert Virgin below on the virome and the potentially indispensable role that viruses play in establishing the baseline genotype-phenotype relationship within the human immune system:
Additionally, while there are a broad spectrum of natural substances which have been studied for their anti-influenza properties, vitamin D deserves special consideration due to the fact that it is indispensable to produce antiviral peptides (e.g. cathelicidin) within the immune system, and can be supported for pennies a day.
For instance, a study published in the American Journal of Clinical Nutrition in 2010, revealed that children receiving 1200 IUs of vitamin D a day were at 59% reduced risk for contracting seasonal Influenza A infection. Moreover as a secondary outcome, only 2 children in the treatment group versus 12 for the control group, experienced an asthma attack. For more information on Vitamin D and immunity, visit the amazing research resource on the topic: VitaminDWiki.com.
Other preventive strategies that are evidence-based, and are available without prescription include:
1) Echinacea Tea: J Altern Complement Med. 2000 Aug;6(4):327-34
2) Elderberry: J Altern Complement Med. 1995 Winter;1(4):361-9.
3) American Ginseng: J Altern Complement Med. 2006 Mar;12(2):153-7.
4) Green Tea: J Nutr. 2011 Oct ;141(10):1862-70. Epub 2011 Aug 10.
5) Probiotics: Pediatrics. 2009 Aug;124(2):e172-9.
6) Vitamin D: PLoS One. 2010;5(6):e11088. Epub 2010 Jun 14.
Learn more by visiting our Anti-Influenza Research Portal.