Fake Science vs Pre-Med “Nomenclature;” It never should have happened.

These Dark Ages are the result of the “Enlightenment, ‘ … which was clearly about the Vanity of Man.  Then Capitalism was the replacement for Feudalism, so we’re still enslaved by Vanity/Greed. First it was about Divine Rights and Racism.  Now it is the Tyranny of Fake Science.
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AND All this technology (you can watch TV on a hand held mobile phone), but no one in the entire HHS or among the “MDs” knows or even asked what OspA was,… while the CDC admits to 2 million cases of “Lyme” a year, reported, because it’s 10-12 times under-reported and only 15% reportable thanks to Dearborn,… and in 1989 (and in 2016), admitted half remain disabled.  One million go on to permanent disability from tick bites alone as their source of post-sepsis syndrome.
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There is no other disease that disables 1 million new people a year in America, alone. This is double the number who die from cancer, and 1/3 to 1/2 the number of TOTAL deaths in the USA from all causes:
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And the press has NEVER written a story about it, and we dont know a single MD in America who ever asked what OspA was, even though they were supposed to be trained in Organic Chemistry for a YEAR in pre-med undergraduate school where they’re taught the structure-activity relationship of molecules and learn the nomenclature of picture-talking.
[Every long chemical name you hear or see, you, as a person who studied Organic Chem, are supposed to be able to draw it- that is the whole point of it: draw it so you can predict its function.
Have a look at this…
The “Pam” in “Pam3Cys” is short for palm oil.  Grease.  Do you think it is a good idea to inject grease into your blood stream?  Oil and Water dont mix. … “MDs” are supposed to know this.  That’s what gits me the most.
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EVERYONE was supposed to have asked, “What is this shite (OspA)?”
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To this date, June 19, 2018, I have never seen an “LLMD” or anyone from ILADS.org state that OspA was Pam3Cys or a triacyl lipoprotein (tri = 3) acyl (- fatty acid added on) Cysteine (amino acid with a sulfur), much less that that was the reason spirochetes cause fungal (triacyl- /TLR2/1 agonist) endotoxin tolerance — worse than the normal “endotoxin tolerance” because it causes cross-tolerance to other pathogen types and is not reversible.  OspA and other Osps and Vmps (other Borreliae) *PARALYZE* the immune system.
See more at:
http://www.actionlyme.org/2017_All_9_Charge_Sheets.pdf
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The Osps and EBV both inhibit apoptosis, both spirochetes and EBV live in the lymph nodes, …. and EBV is dormant inside the B cells. Think about THAT for a minute.
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You have never seen it, and I have never seen it, and it has been 19.5 years since the fiasco of LYMErix — which I can *assure* you, ILADS knew about in 1999.
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Which is the bigger outrage?  That no one from ILADS ever asked and “treat” you anyway?  Or that no one at the HHS.gov, Johns Hopkins, Yale, IDSA, the CDC, NIH or NIAID knows what OspA is (this is all a fact, since I called around and was even threatened by Francis Collins) ???
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Or that no “journalist” ever asked or ever was curious as to what all the “controversy” was about?
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Or asked why ALDF/IDSA and the CDC conduct medicine by perpetual patient-bashing, but still want a vaccine against this non-disease?
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We’ll tell you why:
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The Autism (actually it’s brain damage, Autism is an undefined thing and can be genetic) Vaccines fail in the same way.  The child gets live viruses while they’re immune suppressed and you dont find out about it until after the fact,… OR, the child is vaccinated with a vaccine vial that has LYMErix in it (really, fungal antigens from mycoplasma or fungi) and became immunosuppressed by that assault.  The CDC and the MMR monographs all admit that you should not vaccinate an immunosuppression child for fear of the brain damage that could happen if the live viral vaccine viruses became reactivated as the wild type or even in their attenuated form.
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The Rubella vaccine was invented to prevent “congenital Autism” from a mother who got sick with the German Measles during pregnancy, but the likes of Paul Auwaerter also found the vaccine strain of measles virus in the brain of a child who died from MMR vaccines brain damage.
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You cant make this up (http://www.actionlyme.org/2017_All_9_Charge_Sheets.pdf  << see page 157 of these Criminal Charges Sheets):
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4) Johns Hopkins’ Paul Auwaerter says vaccines fail by becoming reactivated – by reverting to the virulent, active form; that measles itself causes immunosuppression (confirming the synergy with multiple infections); and that the virus symptoms occur “months later” (whereas none of the MMR qualifications followed these children for any of these outcomes much less more than a few weeks):
4.A) J Virol. 1999 Oct;73(10):8791-7.
Altered virulence of vaccine strains of measles virus after prolonged replication in human tissue.
Valsamakis A1, Auwaerter PG, Rima BK, Kaneshima H, Griffin DE..
“…Our data suggest that the adverse outcomes associated with immunization of patients suffering from congenital and acquired immunodeficiency syndromes are due to the emergence of an MV strain with increased virulence in a host unable to mount a sufficient immune response to clear the originally inoculated vaccine virus.
This situation is mimicked in the SCID-hu mouse. Sequence analyses of pMor-1 H and M and other isolates derived from immunodeficient patients demonstrate that these human tissue-passaged vaccine isolates are highly
related to parent vaccine strains (1, 15).
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“…However, fatal infections have been documented in immunodeficient children vaccinated with these strains (1, 12, 14, 15).  The symptoms of infection occur many months after immunization, and the viruses isolated are similar to the original LA vaccine (1, 15), 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.”
https://www.ncbi.nlm.nih.gov/pubmed/10482633

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Did you catch that?
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“The symptoms of infection occur many months after immunization, and the viruses isolated are similar to the original LA vaccine (1, 15), suggesting that in the absence of an effective host immune response, persistent infection with the vaccine strain can lead to fatal disease.
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“Viruses isolated from these children could potentially represent virulent revertants of the original LA vaccine.”
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It is the same mechanism as Lyme and LYMErix disease:  Immunosuppression and then the reactivation or activation of viruses.  There is no other outcome.  That is what happens in all immunosuppression conditions:  Activation of viruses.
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That’s why Lyme and LYMErix are “Great Imitators” because all along the “Imitator” was Epstein-Barr and Friends (other herpes, fungal diseases, etc).
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And now we know the Greatest Imitator of All is the Western Medicine Establishment, since… how easy was this to explain to you?
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What is the IS/DO?
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Fungal antigens will Eff You Up by paralyzing your immune system but you wont hear it from an “MD” because somehow they went on to medical school without learning or wanting to know how molecules work, despite that being what medicine is.
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That’s the Tyranny of Stupidity, because “ignorance” is owned by those who never went to medical school or took a college degree in a science.
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Nearly 20 years on, …. still no one from the entire HHS.gov knows what is the is-does of OspA.  You’ve never read a journalist telling the story.  You’ve never heard it from anyone with “MD” after their names, and by the CDC’s own admission, disables one million new Americans every year with tick bite sepsis.
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