24 May 2012 

HOME

Natural Remedies
 

CDC Greed (won't answer the FOIA)

ELISA = arbitrary cutoff.

Disclaimer

Overview

TUSKEGEE - By Jerry Leonard

1998, CIA Oilmen & Israelis plan to overthrow Saddam for the oil.

Bush/Gore  Oil/War-(Oct,2000)  

Bush's own explainer (Oct 2000) re: Iraq Oil

 

THERE ARE TWO CRITICAL REPORTS HERE BY ALLEN STEERE that are scanned in in full text, that you can get nowhere else on the web.

   1) The Dearborn or CDC standard for IgG, which Steere invented in Europe ("Western Blotting")

   2)  Steere in Europe ("Antigens in Europe") with the bogus strains and showing that there is none of the LYMErix (from strain B31) kind of OspA in Europe.

These are both "bogus articles."  You can believe me, since I am an analytical development chemist from Pfizer.  There are FDA rules for the validation of an analytical method and the FIRST one is that your method should not miss any of the known cases.  In fact that's a given.  The crooks screw up the meanings of the terms "specific," and "sensitive" etc. to deliberately confuse MDs who have no lab experience.

 

Go to: UCONNS_ABUSE_OF_CZECH_CHILDREN    There are two links to MedLine there.  One by Allen Steere in Europe where he takes high passage strain G39/40 (illegal) with him, and recombinant OspA, to look to see if European "Lyme" comes with antibodies to strain B31 OspA or the same kind of OspA as LYMErix.

He finds they don't.  He finds 1 in 97 patients or so.

So, as shown in the second link and report, the UCONN criminal kid-abuser (Feder) gang go to Europe anyway with LYMErix (B31's OspA) and try it out on Czech children to find out how badly it will damage them (since it obviously won't prevent "Lyme").

This is technically a criminal assault. 

ERGO, you need to verify that Steere used recombinant B31's OspA (they pharm the gene into E. coli and harvest the protein- E coli's production of OspA is sloppametric and they find that the production of coli-generated OspA has variable length lipids, depending on the lipid availability in the media or the culture bath).

 

From Steere's "Antigens in Europe."  It says:

"The recombinant preparations of OspA and OspB used in this study were purified maltose-binding protein-Osp fusion proteins derived from group 1 strain B31."

 

High passage (illegal) strain B31's OspA in a recombinant form was used, since high-passage B31 will probably have dropped the OspA-B plasmid and express no OspA or B.  This was how we got the current bogus CDC IgG criteria with no band 31 (OspA) or OspB (band 34) reportable.  (OspAB in the spirochetal mash standard for Western blotting results in blot-smudging- unreadable Western blots)

That's why what Steere did in Europe is so important to the overall crime of leaving OspA and B out of the standard to set up the monopoly on testing, as Yale's Robert Schoen reports in the "Lyme is caused by Munchausen's or self-poisoning or the poisoning of one's children" book.

And presumably, LYMErix injury would also be blamed on the parents, since that's what DCF is for- blame the parent for the vaccine injuries to children.  Munchausen's is being replaced by "Shaken Baby Syndrome" as the popular thing for the DCF morons to charge parents with when the kids are vaccine injured, since vaccinations often result in intracranial hemorrhage- or the less serious "autism."

 

That Munchausen's book shows the crooks' intent to deploy the DCF morons and the superimaginators; the super-pee-pee-bators, psychiatrists, since according to the super-bators, everything bad that happens in the world is caused by their victims, because otherwise the bad things would be caused by the actual bad people who never go to psychiatrists.  Like like poles of a magnet repel or operate like two negative forces, psychopaths and/or psychiatrists stay away from each other and only prey on, well, prey.  'People not like them.

 

Schoen says in his Munchausen's book chapter that blood should be sent to a lab that uses a test that leaves OspA and B out of the standard.  Those labs would be Yale's L2 Diagnostics and probably Imugen, since Schoen was in on the development of that No-A-B in the standard method.  It comes from a strain stolen from John F. Anderson at the CT Ag Station and they stole the patent right from under his nose, like usual.

 

UCONN tests this strain B31's OspA as a recombinant vaccine on Czech children, when they all know goddamned well that there is none of that kind of OspA in Europe.  So, the Czech kids were "adverse event" guinea pigs.  They were technically, "assaulted." 

SmithKline is a British company so they could be taken before The Hague (the International Criminal Court, or ICC) by the Czech Republic and charged with multiple counts of assault.  If UCONN does not render their criminals to The Hague, perhaps they could be kidnapped by a Europeans' CIA-like entity,  like the US does to anyone they like, all over the world.

 

---------------------------------------

 

STEERE IN EUROPE

The CDC's old standard, performing serial Western Blots to look for changing and expanding IgM and IgG antibodies, was Steere's old standard.   This is the 1990 CDC standard criteria for Lyme.  This all changed in 1994 at the CDC's Dearborn Conference, where, actually no one has any idea why we still got stuck with Steere's new bogus method, since no one agreed with Steere at the conference, as I told the FDA Vaccine Committee in Jan 2001.

 

Steere's original observations published in 1986:

http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=423723&blobtype=pdf

Steere said OspA and B were prominent antibody bands, originally, but later he said they weren't.  How did that happen? 

Steere illegally used high-passage strains since Yale, Imugen and L2 Diagnostics wanted a monopoly on vaccines and testing:

 

The downloadable Lyme RICO movies are here. 

No one is allowed to have "Lyme disease," unless they have the genes for the arthritis or inflammatory presentation, due to the scientific fraud committed by Yale and Allen Steere. 

How did Allen Steere end up leaving OspA and B out of the CDC's diagnostic standard?  He used a high-passage strain of borrelia that he knew would have dropped the OspA and B plasmid- which is a crime.  Steere originally said "Lyme disease is a genetically linked condition of a high antibody response to OspA !!!"  And then suddenly OspA and B are left out of the CDC's standard testing for Lyme???

 

"ANTIGENS IN EUROPE," bringing "high passage" G39/40 plus recombinant OspA from B31:

 

 

 

 

 

This is the CDC's Dearborn method:

http://www.cdc.gov/mmwR/preview/mmwrhtml/00038469.htm

Notice there is no band 31 (OspA) or 34 (OspB)

After saying Lyme was a condition of a high antibody response to OspA and B, Steere deliberately invented a standard where OspA and B were not present as diagnostic antigens so Yale could pass off a bogus Lyme vaccine and also have a monopoly on all the national testing for Lyme, by being the only labs (Imugen and L2 Diagnostics) licensed to use Dave Persing's test with the Borrelia burgdorferi bug that had dropped the OspA-B plasmid.

That was the scientific fraud and RICO part of the scientific fraud and racketeering in Lyme disease.  That was the monopoly on testing.  It all happened as a result of Steere fraudulently using high-passage strains of borrelia to determine that OspA and B should be left out of the standard testing for Lyme- yet OspA is the vaccine?

The following is the CDC's IgG method developed by Steere in Germany with Frank Dressler (and you cannot obtain this online):

 

Here is the bogus part about high concentration (ROC area) equaling greater accuracy.  It does not.  This is where Steere claims that high antibody concentration associated with Lyme arthritis is a validation of the method, when we know the specificity of each antibody is the accuracy of the test in a human.  If a person has OspA antibody, they have a 100% chance of having Lyme, and the goal in Methods Development and Validations is to validate a method that detects the LOWEST concentration of something, reliably.

These idiots say this Lyme test is "sensitive" when obviously is does not detect LOW concentrations of antibody, if the area of the darkened (absorbance) means MORE AREA EQUALS MORE (higher) CONCENTRATION OF ANTIBODY.  This Dressler/Steere article is the exact opposite of the truth!  This is a bogus validation and "a bogus article."