Blowing the Whistle at the FDA, Jan 2001, exposing Dearborn and how OspA causes immunosuppression rather than, "was a vaccine."

01 Oct 2017


File List, RICO

1988 Steere says Lyme is like a B cell leukemia

Assoc Blogs-n-Webs:




Fungal Exosomes Inhibit Apoptosis

IDSA: "Vaccines serve the mfgs, not their victims"


BlumenthalAntiTrust Lawsuit

Exosomes, Blebs


CDC Admits Fraud, 2016
Dattwyler, 1988
Golightly, 1988
Dressler, 1994
BarbourFish, 1993
Dearborn, 1994

Pathogenic Fungi

Bush's warcrimes, Oct 2000





12071-12; Update:  Bonehead Uncle Scam will use the US Postal Service to deliver antibiotics to the leaking
CDC Bioweapons Buildings, while we assume the US Military and the DC Legislature will maintain the supply
of Trovan for a REAL dirty bomb attack ROTFL!!

Meanwhile, Boston University reports that everything Mark Klempner has said about Lyme since he reported that spirochetes are intracellular organisms and that that was the reason the antibiotics can't kill them all was FALSE:

The Role of TLR2 in Infection and Immunity:

"However, some of these methods were applied in the absence of proper ligand molecular structure analysis, leading to mistaken conclusions." - Like LYMErix, or OspA, or all the borrelial lipoproteins for that matter, leading to the "mistaken" conclusion that OspA could be a vaccine or that antibodies other than flagellin could be used for diagnosis.  And guess what, according to a conversation I had this spring (2012) with the current Lyme Program Officer (McSweegan was fired), NIAID agrees that the only valid antibody testing or all the borrelioses is band 41.

Therefore, everyone has admitted that "Lyme Disease" - redefined at Dearborn - was a lie.

This is also important because Malaria organisms bear immune-suppression ligands (TLR2-agonists) the same as the Lyme vaccine,
OspA.  Therefore Yale et al screwed up discovery in every major disease since 1995 when they knew LYMErix did not prevent Lyme, but decided to lie about it.  See more at RICO_CONPIRACY_DOCUMENTS.htm for the evidence that Yale's Robert Schoen and
Dave Persing knew in 1995 that OspA vaccination produced a Chronic-Lyme-like illness.  They reported this bad outcome 3 times.

It's been 18 years since these insane and vicious assholes associated with Yale conspired to be millionaires and falsified the testing
for Lyme in order to falsify vaccine and test kit outcomes.  It's only now that the whole scientific world - including retarded Americans - are beginning to recognize the model of fungal-viral synergy formerly known as the Great Imitator

18 years after Schoen and Persing reported inadvertently that exposure to OspA made people sick with a disease like Chronic Lyme but decided those people would be trashed - formally - as published by Schoen in 1998, in the "Lyme is Caused by Munchausen's" book...

18 years' worth of discovery in every major disease was delayed because of Yale's scientific fraud. 

Note that at the end of this article by BU, they fail to mention TLR2 ligands as the failed Tuberculosis, HIV, MRSA and Lyme vaccines:  The Role of TLR2 in Infection and Immunity

They're either trying to avoid prosecution or throw their intended bioterror victims off course.

See for yourself:

The current "Lyme Program Officer" at NIAID under Anthony Fauci advised me to look at what projects the NIH is currently funding:

Immunosuppression due to OspA-like antigens in Malaria: 

And an admission that Lyme and LYMErix cause immunosuppression (Tufts, Linden Hu-, who published that "Lyme Disease is totally imaginary" with Mark Klempner):

"A better understanding of the workings of innate immunity is important for developing therapies for diseases such as Lyme disease where either an ineffective or an over-exuberant immune response causes the symptoms of illness."

Therefore the NIAID no longer supports the notion that "Lyme is an inflammatory disease detected by the fraudulent Dearborn 2-tiered criteria."  They're admitting that Dearborn was as-yet-unprosecuted research fraud.

Apparently the likes of Anthony Fauci would not like everyone to know he owns a patented treatment for immune-suppression outcomes of fungal diseases, like MS or LYMErix-Disease.  Or maybe CDC officers Barbara Johnson and Alan Barbour would not like the public to know the contents of their patents, or in the case of Johnson, what role she played at Dearborn while owning patents in Europe with SmithKline...

"It is an indescribable experience knowing that what you are doing will have an impact on the lives… of millions of people." —Anthony Fauci, 1993


Yeah, thanks, Ton'.  It's been fabulous!!  Wonderful!!  Glad you're there, doing nothing on the Dot Gov dime, like all the rest.  "Rattling a tin-cup in front of Congress" every time one of your profit-minded associates gets his ass kicked by the USDOJ in False Claims Act cases or the various class actions against BigPharma over the years,...  

You have to try to remember, really, we're not as stupid as you government employees porking at the Dot Gov trough are.   Witnessing your decades worth of lies and failures, we can even answer:  "Which comes first, the evil or the stupidity?"  This is the paradox of "public service."


Biowarfare/Healthcare-Fraud Synergy:

This is a snippet of an advertisement that was on's website where we see Corixa/Yale/Imugen being awarded an NIH biodefense contract for lying about the outcome of LYMErix. Corixa was later purchased by SmithKline, so all that 11.5 million dollars worth of USA biodefense data is now owned by a foreign company:

More about this at the bottom of >> this page.  Scroll down for a lot more...

They were awarded this contract to specifically design a new type of OspA-Adjuvant that was a TLR4 agonist and not a TLR2 agonist because the TLR2-agonist, LYMErix, was not only toxic, but caused the same disease as "Chronic Lyme" and IDSA's "New Great Imitators."

The point I am making is that if OspA was not a vaccine, and caused the New Great Imitators (Activation of EBV/Similars), and these crooks qualified their OspA vaccines with the Dearborn standard (they claimed that they did), then the Dearborn diagnostic standard must be FALSE - and that is the FALSE CLAIM with which they should be charged, because it is a homicide charge.

The Lyme crooks know this is a homicide charge, which is why they're so vicious.

Crazy Eddie McSweegan says Europeans are dumb, and therefore good victims for a new falsified LYMErix vaccine trial.  


"Let me be clear: we will not tolerate health care fraud. And, in every instance where we uncover it, we will use all available tools to hold those responsible to account."



Lyme, MS, Fibro, Lupus, Gulf War Illness, etc., are all the same disease (reactivated EBV/similars and tolerance to fungal
infections in the blood), but the only people who are allowed to have a "disease" are those with the HLA-associations
(hypersensitivity) because the others are in the secret bioweapons class of Stealth Disablers:


If this were not true, the Anus Mundi, the, and their Porton Down cronies would not have for decades deployed
scientifically irrelevant and cowardly psychiatry to superimaginate that we're causing ourselves our own imaginary illnesses.


No more.  The cat is totally out of the bag.

email me and put "Lyme Crew" in the subject line.  This is an anti-USA-Government
group designed to destroy whatever is left of the scientific credibility of the, the FDA, the CDC, the,
all USA "universities," and will at the same time expose US Bioweapons crimes.


I am absolutely deadly serious about recruiting scientist/activist types because the USA is killing all of us.  EIGHT million
people in the USA have been diagnosed with "Fibromyalgia," while only 400,000 supposedly have Multiple Sclerosis,
when they are the same disease, one with and one without the HLA-link. 

Those Fibro/Lyme/ME victims are the new Blacks.  This is as epic a civil rights campaign as Martin Luther King's.


We have a head start because the USDOJ just recently slammed the HHS, FDA, Psychiatry-at-Large, BigPharma,
when they sued SmithKline over false claims  - finally, 8.5 years after I filed a RICO complaint against with
the USDOJ in New Haven, CT.

You can also ask me questions about the Lyme Crymes at that address, but if the subject line does not contain "Lyme Crew,"
I am deleting the mail.

You do not have to be an American to join.  I expect a dearth of qualified Americans, anyway, since most of us are cowards,
especially the "MDs."


We have already seen the CDC admit what was the cause of Vaccines-Acquired Autism.


Francis Collins (Director of the NIH) threatened to have me arrested - again, after I was arrested and charged with
"terrorism" for filing a RICO complaint against Yale - if tried to report back to him that none of the people to whom
his office referred me would tell me the structure of OspA, or Yale's LYMErix vaccine, when any REAL scientist knows
structure equals function: 120501.htm


No one was able to tell me what the structure of OspA was (which is the same answer as what it does) from among the
NIH, Sebelius' office, Collins' office, Fauci's office, NIAID's Bacteriology and Mycology Division, the CDC, Yale, Paul
Auwaerter, Adrianna Marques (the MS-Lyme Section of NINDS), or the


Therefore, none of them can claim to have any expertise in "Lyme Disease."


Officially, they have no authority and should you end up in a lawsuit over treatment or Disability, these evil creeps
cannot present an "expert" in opposition to you.  All that your lawyer would have to do when questioning the "expert
witness," is have them ask what is the structure of OspA, the LYMErix non-vaccine.


Kathleen M Dickson
FDA Whistleblower



































Lyme Cryme Talking Points:

1) Dearborn (falsified testing) 
What OspA is/does (triacyl lipopeptide TLR2-agonist, which never could have been a vaccine).
Everything the Lyme crooks have said about "Lyme" since their intent to defraud Uncle Sam Americans and Europeans with "vaccines" for relapsing fever (impossible) has been about maintaining a pretense that Dearborn was real, including issuing "guidelines."
"Lyme Borreliosis" is Relapsing Fever.  "Lyme Disease" is Steere's HLA-linked bad-knee with the high antibody response [accepted due to research fraud and a conspiracy to monopolize vector borne disease funding, grants, royalties, test kits and vaccines ( at Dearborn], the mechanism of which was never discovered by Allen Steere, but Clifford Harding.
5) Yale owns a scientifically valid antibody test for Lyme but did not use it to qualify their other patent, LYMErix, because they knew OspA did not prevent Lyme, and in fact, was toxic.

The huge
SmithKline False Claims Act fine must be why the Lyme crooks have been so hysterical, lately, with their ties to SmithKline and the healthcare fraud they committed by falsifying the testing for Lyme (see more about that below - Dearborn and Steere, and the CDC-SmithKline patents show HLA differences; CDC knows Dearborn is invalid) in order to falsify their vaccine, LYMErix.    (
Nice that they finally called Paxil and the brain-damaging of children after all these years.)

In this case, however, Yale should be sued for False Claims because they own a scientifically valid antibody test and they also own the patent for the fake vaccine, LYMErix.  Yale's valid Lyme test patent application ( USPTO # 5,618,533) preceded their fake vaccine patent, so they could have used the valid test to assess the outcome of LYMErix, but they knew LYMErix didn't prevent Lyme.  And Yale knew the adverse events to LYMErix were identical to chronic Lyme: .

"Additional uncertainty may arise if the vaccines are not completely protective; vaccinated patients with multisystem complaints characteristic of later presentations of Lyme disease may be difficult to distinguish from patients with vaccine failure." - Dave Persing, USPTO # 6,045,804

Yale, et al, trashed the LYMErix victims just like they trash the chronic Lyme victims.  See what Schoen instructed MDs to do with Adverse Events victims, knowing LYMErix adverse events were the same as chronic Lyme because Schoen and Persing did the research for the above Corixa-Imugen-L2-Diagnostics RICO strain (USPTO # 6,045,804):

The Lyme criminals could not even read their Western Blots in LYMErix or ImmuLyme-vaccinated people, yet they claimed to have used the Dearborn Method to assess their vaccines outcomes:

Here are the 4 "we can't read our OspA vaccine results" reports:

1) SCHOEN and PERSING, with JOHN ANDERSON,1996 - the RICO strain report: (Schoen and Persing published this together, but Dave Persing filed the patent) where the OsPA-B plasmid is dropped:

The Dave Persing, Mayo Clinic FRAUD Patent-6,045,804 

4) Yale's ROBERT SCHOEN in the 1998 Munchausen's Book, instructing MDs to blow off LYMErix systemically injured people ("but send the post-vaccination blood to the Yale L2 Diagnostics RICO lab if you must bother to be a physician").

This ▲ is a FALSE CLAIM or a QUI TAM or FRAUD on the GOVERNMENT:



CDC officer Alan Barbour, inadvertantly admitting that Lyme is just a Relapsing Fever organism, wrote that: "An important aspect of the invention is the recognition that Borrelia VMP-like sequences recombine at the vls site, with the result that antigenic variation is virtually limitless. Multiclonal populations [or even after infection with one single spirochete] therefore can exist in an infected patient so that immunological defenses are severely tested if not totally overwhelmed."******.(compare to the "antipersonnel" criteria for bioweapons from the Congressional Record, here)


The former CDC standard to diagnose "Lyme" was to perform a series of Western Blots to look for new IgM bands because "Lyme" is actually Relapsing Fever   ▼

The New York Times never published this Lyme Cryme story.  When their writer Holc Noble tried to tell it, they refused to publish his story.  They paid off Holc to keep his mouth shut.

Jane Brody (NYT) wrote a one paragraph review of "Cure Unknown," when if either of them knew what they were talking about, the name of the book would have been "Cause Known," and the story would have been Holc's, which would have been the same one I told the FDA Jan 31, 2001

Which was the same one I told NYTimes' David Grann 4 months later.

Lawrence Altman (another NYTimes Science Tuesday writer) is a CDC officer, and of course, CDC officers Barbara Johnson, et al,  own patents with SmithKline in Europe that would have no commercial value if anyone knew what was in those patent claims ("there are 2 kinds of Lyme: the HLA-linked case definition with the lots of antibodies and the complete opposite, immunosuppression").

And especially if everyone knew Lyme was just Relapsing Fever and that the nature of the relapse was that antibodies (test kits or vaccines) are useless.   Why, it was CDC officer Alan Barbour, himself, who wrote that: "An important aspect of the invention is the recognition that Borrelia VMP-like sequences recombine at the vls site, with the result that antigenic variation is virtually limitless. Multiclonal populations therefore can exist in an infected patient so that immunological defenses are severely tested if not totally overwhelmed."******.


Yale perfected that flagellin method in 1991, but they did not use this method to qualify their other patent, LYMErix, because they knew LYMErix did not prevent Lyme.  That was the entire point of the Dearborn ruse.

The "controversy" is scientific fraud.  And that is why the Lyme crooks only conduct medicine via attack-pattern "science."  They use the invalid psychiatry to claim we're crazy instead of sick, and the psychiatrists in refuse to discuss the concept of scientific validity because it would backfire on them.

The Pope wants to make Bishop Fulton Sheen a saint specifically because he called psychiatry "BS" (not in those exact words, but close enough).  So does Malachi Martin in Hostage to the Devil, so read it.   It will help you to understand the nature of evil.  You do not want to make the mistake of hanging out anywhere near psychiatrists.

Harold Varmus trashes Yale for throwing out the LYMErix failure and immunosuppression data.  Yale and the Lyme-Crook gang at NYMC (Kaiser-Permanente's partners in cryme) effed up all sci-med research, globally, for the past 21 years:

"Dr. Harold Vamus, director of the National Cancer Institute, thinks cancer researchers should focus on these unexplained mysteries, since they may unlock cancer's secrets.

In our rush to do the things that are really obvious to do, we're forgetting
[he means falsifying the disease definition to suit the falsified OspA vaccines outcomes] to pay attention to many unexplained phenomena,'" he told the Times.

The Contents of the CDC's bogus Dearborn "consensus" conference booklet 



<< Invitation to "participate in the [Dearborn] proceedings" (implies this was a consensus conference, that ended up not to be chosen by consensus; this is when and where the testing for Lyme was falsified, as shown in the RICO complaint to the USDOJ)


<< Page 2 of the Invitation to CDC's fake Dearborn "consensus" conference

<< Page 3-5 of the Dearborn invitation:






There were 2 reports and not one- not just Desssler/Steere (the only one included in the Dearborn booklet) that were involved in falsifying the antibody panel for the current, CDC diagnostic standard. 
The most significant one was not included in the CDC's Dearborn booklet - this one:  STEERE_IN_EUROPE.htm 
Or >> (Antigens in Europe, as I call it)

Page 74 of the Dearborn booklet - Gary Wormser saying the Steere proposal sucked.  Here is the full text of that assessment:

(missed 85% of the cases)

  ◄ Page 75 (Imugen's assessment = 14% accuracy of the Steere/Dressler antibody panel proposal) of the Dearborn booklet

◄ Page 76 (Wisconsin Lutheran's submission) of the Dearborn booklet:
IgG proposal detects 22% of the cases.

◄ Page 99 of the Dearborn booklet; Ron Schell:
"Dearborn is 15% accurate in IgG, or misses
85% of the cases," which was the same result
as Imugen's and Gary Wormser's.

Nick Harris (Igenex, present at Dearborn and a participant) said Dearborn was 8% accurate.  The rest were disqualified for one reason or another, including MarDx, UConn, and the CDC (who submitted a mouse antibody result, duh).

So, of the accuracy assessments of the Dressler/Steere proposal (based on research fraud) were:
15% (Wormser),
14% (Imugen),
22% (Lutheran Hosp),
8% (Igenex)
15% (Ron Schell, State of Wisconsin)

Average, 14.8% or Dearborn misses 85% of the cases of "Lyme" and this was deliberate.

The Lyme vaccines don't work for any animals, either.  None prevent spirochetes.  But secondary to that, humans do not have a dogs' TLR2 or immune system:

Why Your Dog Can Get Vaccinated Against Lyme Disease And You Can’t
Modern science has given us a vaccine for humans against Lyme disease. But in 2002, the manufacturer pulled it off the market, citing low demand. âVaccine victimsâ

The "vaccine," LYMErix, was OspA.  The NIH, Yale, CDC, and refuse to tell us what is is.  Go ahead and ask them.  The answer is that it is a TLR2-agonist and as such could never have been a vaccine since it turns off antibody production in people without Steere's HLA.  See:

If the vaccine does not produce antibodies, it could not have been a vaccine, and therefore it must have been falsely qualified.  Of course, it was, and there lies the "controversy" over which there were all the lawsuits, including Senator Blumenthal's for AntiTrust.  They said Tobacco Science was "controversial," too, remember.

The Lyme crooks are clearly terrified.  Scroll down to the main graphics on this page to see why.   They've been caught in all their lies about what "Lyme Disease" actually is.

As for Steere being "stalked," that did not happen.  I spoke with NYTimes' David Grann in person for 30 minutes in May, 2001, at the Albany Legislative building Lyme protest.  This was 4 months after I had explained the entire crime and showed the documentation proving the testing for Lyme was falsified to the FDA Vaccine Committee.  I told Grann the exact same story I told the FDA Vaccine Committee about how the testing was falsified in person

So, we were not "stalking Steere" if we were trying to have him arrested for murder.

Soon thereafter (Feb 2002), the FDA told SmithKline and Yale to yank LYMErix or the FDA would do it for them. 

The crooks were THREATENED by the FDA in February, 2002.


And it was not Allen Steere, but Willy Burgdorfer and Polly Murray who discovered Lyme disease or the Lyme Relapsing Fever. 

And Clifford Harding explained Steere's fraudulent version of HLA-linked "only a knee," (2010)
Thus, infection with M. tuberculosis primes macrophages for the increased release of exosomes and microvesicles bearing M. tuberculosis peptide-MHC-II complexes that may generate antimicrobial T-cell responses.

while Harding with Justin Radolf explained why OspA was immunosuppressive for everyone else  - and therefore was not a vaccine - in 2001:

So, there was nothing explained by Allen Steere.  Steere falsified the testing in Europe as shown here, and of course he is famous for other imaginary stories like being stalked.  He's nothing but a lying coward, not to mention STUPID.


And these are the same crazy assholes who say Lyme is not even a disease, yet they wanted to sell a vaccine for it?


Hillary Clinton as Henry Kissinger's NWO Parrot:

“I know there are those who question whether Islamist politics can really be compatible with … democratic and universal principles and rights,” Clinton said. “Our policy is to focus less on what parties call themselves than on what they choose to do.”

Kissinger's NWO is about getting rid of nationalities and religions - ideologies opposed to the secular/financial World Order [see the interview with Charlie Rose where he admits the NWO gang causes the chaos: "looking into the abyss" (or at the chaos) so they can smash it] where the self-declared elite rape the nations for their sovereign wealth especially via debt, the fake Euro, and insisting that everyone do business with their fake petrodollar.

The main problem with the NWO ideology is that the self-declared intellectual elite isn't.  To Wit: 1) LYMErix and Lyme Disease, 2) the transparency of physical and cognitive damage caused by vaccines; A) antibodies can act as neurotransmitters and B) end up giving kids the active viruses, as has been published by the CDC and Pharma numerous times, 3) the GMO food without the natural probiotics (rendering people toxic and likely to get cancer from undigested and un-digestible food hanging around in their guts, and 4) similarly retarded and transparent stunts like the 911 Show.

To me, they're clowns.  And Clinton should be ashamed of herself, acting like a typical female who can't think for herself.  Playing a stereotype.  A dog pleasing her master...

But then again, all lawyers and psychiatrists are like that.  Cynical and unable to think outside the box.  A darkening spirit who loses any creative ability with which they were ever born, with each deception they perform:

"15 All things are clean to the clean: but to them that are defiled, and to unbelievers, nothing is clean: but both their mind and their conscience are defiled.  

16 They profess that they know God: but in their works they deny him; being abominable, and incredulous, and to every good work reprobate."

The same will happen to the  Everything they touch or encounter will henceforth turn to crap.  They've had plenty of direct opportunity to fix this Relapsing Fever thing.



120624; Lawyers and psychiatrists are the Pharisees of our time.  Read Hostage to the Devil by Malachi Martin, read/watch the audiofile of the exorcism of Annaliese Michel, study what was revealed at Fatima, and read other exorcism transcripts (what the demons are forced to reveal under the command of heaven).

These will answer your question as to why "Lyme Disease" (a cryme because it was redefined) is not prosecuted.  We have the means to discover what is scientifically true, but lawyers want none of it because it exists outside their left-liars' brain.  Psychiatrists, also left-liar-brain dominant and tending to behave like women, don't want anyone to know that there is nothing true or valid about anything they do or say.

Note that I could not have been clearer in the cryme's description to the US Attorney's office in New Haven, to which I was referred by Richard Blumenthal's 3 staff lawyers once they saw, with the documentation, that there were 2 definitions of Lyme:  1) the pre-Dearborn, "Lyme is Relapsing Fever" definition and 2) the later, false Dearborn "Lyme is just an auto-immune bad-knee" definition.

Data has only added to the model of Dearborn as a fraud and that LYMErix caused the systemic disease about which the other participants complained at that Jan, 2001, FDA Vaccine Meeting on LYMErix.


Notice also that the Lyme crooks associated with Yale never say what LYMErix or Lyme is.  

Instead, they perpetuate only a full-blown, hilarious, inverted, perverted, circuitous, self-contradictory doctrine based on their intention for OspA a vaccine to be the launchpad for their tick borne diseases enterprise called the "American Lyme Disease Foundation."  The vaccine for Lyme was to be the first product in a 30 year roll-out plan of vector-borne diseases test kits and vaccines.  Next was Ehrlichia or Babesia. etc.  All of it depended on the royalties, grants, and goodies to be found in the blood of post-LYMErix victims as described by Imugen's Dave Persing and Yale's Robert Schoen in their RICO patent where the OspA and B plasmid was missing from the Borrelia strain that determined was burgdorferi by 23S RNA testing:

See what Schoen and Persing said about this strain in their RICO (No OspA/B, just like the Dearborn panel) patent associated with this report

"Additional uncertainty may arise if the vaccines are not completely protective; vaccinated patients with multisystem complaints characteristic of later presentations of Lyme disease may be difficult to distinguish from patients with vaccine failure."

"The present invention provides a method useful to detect a B. burgdorferi infection in a subject. The method provided by the invention is particularly useful to discriminate B. burgdorferi infection from OspA vaccination, although it is sufficiently sensitive and specific to use in any general Lyme disease screening or diagnostic application. Thus, the method of the invention is particularly appropriate for large scale screening [THE MONOPOLY] or diagnostic applications where only part of the subject population has been vaccinated or where the vaccination status of the population is unknown. "

The crux of the Lyme crimes was the falsified test used to qualify OspA as vaccines

But they won't tell you what OspA is.  (Go ahead and ask.)  And in all these years since Willy Burgdorfer tried and tried to explain to Allen Steere how to dissect a tick (prior to 1982 when Willy Burgdorfer in total fed-up exhaustion with the stupidity of Allen Steere, had some ticks sent to him), Yale still says Lyme is not a disease:

See Govt Goon Tries to Silence Willy Burgdorfer ►:

Lyme is nothing, they say.  But Yale intended to make 5 million dollars a year in royalties from LYMErix.  Said Vijay Sikand at the 1998 FDA Vaccine Meeting [click here for that FDA transcript]:

"It is well known that Borrelia burgdorferi indeed after asymptomatic infection can lurk or secrete itself in certain areas of the body, perhaps the central nervous system or perhaps the joint spaces, only to reappear months or maybe years later in the form of late stages of illness which are harder to diagnosis and treat."


What Lyme is, is Relapsing Fever.  The name itself, "Lyme Disease" is a ruse that few people understand:  The former official name of the disease according to the CDC was Lyme Borreliosis or Lyme Relapsing Fever

The former serological definition was to perform serial or sequential Western Blots to look for new IgM bands.  New IgM bands meant the spirochete was still alive, that Lyme is a relapsing fever spirochete and that the nature of the relapse was new IgM bands:  See CDC_DOCUMENTS_1990.htm for the proof that this was the previous standard.

After that former standard was falsified by CDC and associated Yale crooks (Dearborn and Steere in Europe) - today "Lyme Disease"  ONLY refers to the HLA-linked (see the RICO complaint for what the difference in bloodwork looks like) autoimmune arthritis in a knee that is characterized by too-many-antibodies - the crooks have done nothing but try to perpetuate the lie that the new Dearborn definition was real.

The reason this crime is not prosecuted is because everyone associated with Yale and the Federal Government is an asshole.


CHAPTER 5, the RNA and DNA Primers Shell Game-

Where the crooks use one set of primers to indentify spirochetes to patent, but another to find "NOT-LYME" in humans :)))


A) The Klempner - No-DNA/RNA-primers-listed-in-the-Method - report;  Mass Medical Society never noticed that Klempner did not report what primers he used to exclude people who were DNA positive in spinal fluid (yes, there were some, we know of one person who was excluded).

B) CDC officer Alan Barbour (owner of the ImmuLyme OspA vaccine) reports in 1992 that like all other antigens in Relapsing Fever spirochetes, OspA undergoes antigenic variation or "selection pressure" (means vaccines and antibody testing based on variable surface anitgens are useless):  BARBOUR_MUTANTS_1992.htm  (Note that this is GENETIC variation of the OspA gene, meaning an OspA primer is useless.)

C) Yale's Erol Fikrig (owner of Yale's OspA/LYMErix vaccine) reported that due to antigenic variation and selection pressure, OspA, one of the variable surface antigens in Lyme Relapsing Fever would be useless as a vaccine.

Note:  The antigens vary in ticks and in mammals.  Therefore, you have to use non-variable antigens if you are to perform an antibody test, and guess what, Yale developed such an accurate and specific test in 1991:  CRYMEDISEASE_CHP1.htm

Please see the PowerPoint Explainer on Scientific Validity:

It shows that Yale and others are completely aware and certain that the only scientifically valid antibody test for Lyme is flagellin, and the current NIH Lyme Program Office not only agreed with me, but said we should be using all the reombinant  flagellin from all the borreliae to detect "Lyme" (real name of the disease is Relapsing Fever).

"Lyme Disease" is a ruse.  When the crooks use that phrase, they are talking about their own, Dearborn, re-definition of "autoimmune arthritis in a knee." does not give you this information for 2 reasons:  1) the concept of scientific validition would backfire on a bunch of psychiatrists, and 2) they simply aren't trained scientists (which is the same as the first reason).


1) [GARY WORMSER] Genetic diversity of Borrelia burgdorferi in lyme disease patients as determined by culture versus direct PCR with clinical specimens:

Departments of Biochemistry and Molecular Biology, New York Medical College, Valhalla, New York 10595, USA.

Two hundred seventeen isolates of Borrelia burgdorferi originally cultured from skin biopsy samples or blood of early Lyme disease patients were genetically characterized by PCR-restriction fragment length polymorphism (RFLP) typing of the 16S-23S ribosomal DNA intergenic spacer. Three major RFLP types were observed. Of the cultured isolates, 63 of 217 (29.0%) were type 1, 85 of 217 (39.2%) were type 2, and 58 of 217 (26.7%) were type 3; mixtures of two RFLP types were obtained in 6.0% (13 of 217) of the cultures. Comparison of typing of B. burgdorferi performed directly on 51 patient skin specimens with typing of cultures originally isolated from the same tissue revealed that a much larger proportion of direct tissue samples had mixtures of RFLP types (43.1% by direct typing versus 5.9% by culture [P < 0.001). In addition, identical RFLP types were observed in only 35.5% (11 of 31) of the paired samples. RFLP type 3 organisms were recovered from blood at a significantly lower rate than were either type 1 or type 2 strains. These studies demonstrate that the genetic diversity of B. burgdorferi patient isolates as determined by cultivation differs from that assessed by PCR performed directly on patient tissue.


2) Yale's Robert Schoen discussing how the species determinant is not the OspA gene, but RNA:


3) When CDC officer Alan Barbour patented Masters' Disease, he went straight for the flagellin DNA, since he knows that is the species determinant, and not the OspA gene:

1996 B. theileri
patent (Master's Disease is Cow Relapsing Fever Alan Barbour patent application for Masters' Disease 5,932,220


4)  Here GARY WORMSER uses the correct RNA to determine that 2/9 people with Lyme rashes still had spirochetes in their skin after treatment for tick attachment:



5) Here Durland Fish uses the correct RNA to determine that spirochetes were present (he did not use the OspA gene, which is used by the crooks on humans to determine "NO LYME"):


"To identify the Borrelia genospecies and to detect Borrelia double infections within the produced tick batches, ticks were analysed by PCR using Borrelia genus-specific amplification of 16S rDNA and subsequent dot-blot hybridization.


These crooks did not think they would get caught.   And they had very good reason to think so because the vast majority of American MDS have no science training and the rest are cowards.


KMDickson 120623-24


SLU Program seeks to Reform Crooked Scientists  ◄  Awesome.  Maybe you could have a look at CDC officer Alan Barbour's patent for the Pasteur-Connaught OspA vaccine and see that he makes a claim about flagellin as the earliest and best test for Lyme:


Note that in the Taxonomy database, Borrelia are characterized by differences in their flagellin:

Note that when Alan Barbour patented Masters' Disease, he only went for the flagellin DNA, since he knew that was the species determinant, and NOT the presence of the OspA gene (main element of the crooks' DNA/RNA shell game):

1996 B. theileri patent (Master's Disease is Cow Relapsing Fever Alan Barbour patent application for Masters' Disease 5,932,220"

And CDC officer Alan Barbour also makes the claim in that World Patent Database (WO1990004411) OspA patent that Lyme goes for the brain and can be mistaken for Multiple Sclerosis. 

Because that's not what Allen Steere, Robert Schoen and his little RICO cabal with Dave Persing (now works at Imugen, Norwood, MA) have said when they falsified the testing for Lyme in Europe to set up a monopoly on testing for vector-borne diseases once Yale's OspA vaccine product was on the market.

Good Luck "reforming" these genocidal maniacs associated with Yale.

I mean, this is a SIMPLE crime.  A "vaccine" for relapsing fever?  When the nature of the relapse is antigenic variation, meaning vaccines absolutely will not work?

When Alan Barbour clearly states in that patent above that flagellin is the earliest and most accurate (greatest % of Lyme victims have this specific antibody, band 41, and Alan Barbour says it is good enough to detect ALL borrelioses) test?

The first false claim was Steere in Europe, falsifying the antibody panel with high-passage strains that drop plasmids and with recombinant OspA and B without the lipids attached.  This is research fraud.

The second false claim was that there was a consensus at the CDC's Dearborn consensus conference, which was a claim I made and PROVED to the FDA Vaccine Committee with 30 pages of documentation from the Dearborn Meeting Booklet on Jan 31, 2001.

The third false claim was all the claims Yale made about LYMErix, and especially that they used the Dearborn method to qualify it because the Western Blots were unreadable due to the fact that OspA is Pam3Cys and it sticks to itself, as Alan Barbour once said, and as is revealed by the Koreans when they blew up the HIV gp120 LYMErix vaccine.  You can't do HPLC on it, they said.

The fourth false claim was that LYMErix victims did not have an illness (Schoen).  And that autoimmune arthritis in a knee - the Dearborn definition of the very disease (autoimmunity against OspA in a knee), and as shown in the RICO complaint to the Justice Department - was not caused by OspA.

Yale said: "Autoimmune arthritis caused by OspA (the current definition of 'Lyme Disease,' since the former definition was Lyme Borreliosis or Lyme Relapsing Fever) is not caused by OspA when the OspA is our vaccine."

But worse still was what OspA actually is, which Yale did not investigate.  Yale did not investigate the brain and multiple sclerosis outcomes of Lyme Borreliosis and their vaccine.  They literally - and to this day,- throw those cases out.  How do we know for sure?  The falsified Klempner report based on the DNA/RNA shell game and the bogus Dearborn definition of Lyme.

The fifth false claim was this Klempner "Long Term Repeat Treatment Study," which was actually a standard of care study (since 2/3 of his victims of repeat ceftriaxone had never had ceftriaxone before), was based on the "bad knee autoimmunity to OspA" definition.  Therefore, since that definition is false, the Klempner study has to be thrown out.

And with it, IDSA's "guidelines."

I will tell you why this isn't prosecuted, and let me quote from Assange's mother:

"I hope the third world can stand up for what’s morally right when the first world can’t and won’t because they’ve got their snouts in the trough, rolling over for U.S. greed and big business."

The USDOJ is comprised solely of pigs, sluts and morons, and so is the and the  There is no other kind of Uncle Sam employee or this crime would have been prosecuted in Feb., 2002, when I first contacted the New Haven, CT FBI about it.

"For a June 27 story, Attkisson interviewed Sen. Charles Grassley (D-Iowa) about Edward McSweegan's predicament. McSweegan was a National Institutes of Health scientist who blew the whistle against mismanagement at the agency only to have all his duties revoked while he drew a $100,000 annual salary..."


120621; KMDickson


120620: Several people in the State of CT, Tufts, Yale, and the US Navy and Army freaked out over all of these reports.  

So, take another, closer look at what makes such extreme assholes nervous:

1911, on the Incurability of Lyme/Relapsing Fever:


Spheroplasts are either reproductive forms or they are regeneration forms, there are reports discussing both:


1992, Formation of CDC officer Alan Barbour's replication form called "gemma" in oral spirochetes.


NEXT:  1983, "Proposed Life Cycle for the Reiter Treponeme"  (validity of "cysts", or spheroplasts. or regeneration forms):


And here we have in the same CDC officer's (Alan Barbour) 1986 report that there are, gasp, "gemma"
(a replication form)













-- 1963:



   US scientists discussing spheroplast forms (click to enlarge)



But the disease is more than persistent - permanent, un-eradicable - spirochetes.  It's reactivated viruses because of OspA-induced immunosuppression, just like AIDS.

Coincidentally or not, HIV and SIV gp120 appears to be OspA in triplicate and people with HIV have antibodies against LYMErix.

And that is stuff you just can't make up.

This "stealth-bomber" flak about which CDC officer and multi-patent holder Alan Barbour speaks (see the graphic, below), which I call flak, and which is technically "blebbing" (analogous to shedding), Willy Burgdorfer and Friends at the NIH seem to think is a reproductive form (blebs contain DNA, cysts or "gemma" seem to be a reproductive form).

So did the dude who wrote that 1911 report above.  So did some other scientists.

A "stealth bomber" within a stealth, seronegative spirochete,... which deploys antigens that inhibit antibody production, ... which seem to reactivate viruses like the opportunistic-friendly HIV, ... which deploys intracellular spheroplast reproductive forms, ... within a microscopic tick, ... surrounded by an enormous set of lies, starting with its very name, ... and managed by complete and total morons associated with Yale and Plum Island, ... because there are no other kind of Yale associates.

The ultimate question is whether or not we can show that it is known that the free, dessicated cyst or spheroplast forms are viable, and it appears that the US Army thinks so, because they warned soldiers not to inhale dried animal urine.  It's been taken off the web, but here is a snippet:  CRYMEDISEASE_CHP3_B.htm







Invasion [a la Mark Klempner, 1992] of human neuronal and glial cells by an infectious strain of Borrelia burgdorferi.

Centers for Disease Control and Prevention, Division of Vector-borne Infectious Diseases, 3150 Rampart Road, CSU Foothills Campus, Fort Collins, CO 80522, USA.

Human infection by Borrelia burgdorferi, the etiological agent for Lyme disease, can result in serious acute and late-term disorders including neuroborreliosis, a degenerative condition of the peripheral and central nervous systems. To examine the mechanisms involved in the cellular pathogenesis of neuroborreliosis, we investigated the ability of B. burgdorferi to attach to and/or invade a panel of human neuroglial and cortical neuronal cells. In all neural cells tested, we observed B. burgdorferi in association with the cell by confocal microscopy. Further analysis by differential immunofluorescent staining of external and internal organisms, and a gentamicin protection assay demonstrated an intracellular localization of B. burgdorferi. A non-infectious strain of B. burgdorferi was attenuated in its ability to associate with these neural cells, suggesting that a specific borrelial factor related to cellular infectivity was responsible for the association. Cytopathic effects were not observed following infection of these cell lines with B. burgdorferi, and internalized spirochetes were found to be viable. Invasion of neural cells by B. burgdorferi provides a putative mechanism for the organism to avoid the host's immune response while potentially causing functional damage to neural cells during infection of the CNS.

PMID: 17045505 [PubMed - indexed for MEDLINE


I don't really understand why there's really any debate.  The IDSA and Yale Lyme crooks - including several CDC "officers" - who were sued by AG Blumenthal, simply don't want to go to jail for fraud and homicide.   OspA wasn't a vaccine, Dearborn and what Allen Steere did in Europe to falsify the test is classic research fraud, and CDC officers own worthless patents because Lyme is Relapsing Fever...

The United States, by its denial of the crime, merely reveals and reveals and reveals... to its adversaries - and there are many, now - that they have committed more than the Iraq and 911 stunt war crimes, that they tried to stifle Willy Burgdorfer - who calls Allen Steere a moron, too, if you notice -

See Govt Goon Tries to Silence Willy Burgdorfer ►:

, ...  We know all about "Lyme;" it happened in Europe with a stains-game and lame recombinant, lipid-less antigens at the hands of Allen Steere (which is hard to believe because everyone knows he has a low IQ), ... Relapsing Fever, what happens on Plum Island, ... we know spheroplasts are viable outside an animal, we know what OspA is, we know why the entire tries to pretend they don't know what OspA is,

we know this hypervaccination business renders kids retards, messes up natural immunity, puts people into an immunofugue (VaccinoZombies) state both medically and cognitively, ... we know these GMO foods are the reason probiotics are so popular these days....  We know the Bigs are interested in depopulation for the simple reason that they don't like to see all these indigenous "people" clogging up the beautiful beaches and what-not, ... We know the NWO gang does not really care if they, themselves, can produce no highly intelligent offspring and simply expect to hire, threaten or bribe real scientists just like Hitler did.  But the problem is that there really aren't any brilliant scientists available.

Look at the flop this "Lyme" fiasco was.  Look how transparent were all of their lies.  Look at the Lyme crooks' personalities.  You just can't hire evil and expect it to have any creative abilities.  LOGIC dictates the NWO depopulation plan is not going to work because they will not and do not have the tools to deploy it successfully, nevermind prophecy or the influence of the real intelligences in the other dimensions. 

In the end, the greatest insult to-, and the eventual failure of-, this evil will be its abundantly clear - to all - lack of intelligence.



A Yalie Lawyer Op-Eds for the NYTimes on the issue of illegality of leaking "government" crimes?   

What happens when we leak Yale's crimes to the USDOJ and regarding their subsequent threats to human health?  Is it OK to call that whistleblower a "terrorist?"   It's complete and total cowardice, and no one at Yale is qualified to discuss any health, moral, legal or scientific matters.  They have no standing whatsoever. 

We learned from the mysterious LYMErix vaccine owned by Yale what were the causes of vaccines-acquired autism (now considered real and in the news- scroll down), and we learned the basic causes of nearly every disease: Lupus, ALS, Multiple Sclerosis, Cancer, Childhood Leukemia, Arthritis, and most diseases of "autoimmunity."

We turned the world upside down when we demonstrated (via OspA and the resultant reactivation of EBV) that no disease or infection could be diagnosed based on antibodies.   And no one in the entire, not the CDC, not NIH, not Anthony Fauci, not NIAID, not Yale, not, and not Francis Collins - NO ONE ASSOCIATED WITH UNCLE SAM - would answer the question of what was OspA (see it below on this homepage), because it is the key to every disease, it is the key to vaccines-acquire autism, and it is the key to all (stealth) bioweapons

There is no National Institute of Immune-Suppression Diseases because that would betray the nature of USA's illegal bioweapons and the fact that the NIH and CDC know about the brain damage outcomes of mycoplasmally contaminated vaccines..

Everyone associated with "Yale and the Federal Government" is useless, spineless, brainless scum.  There is no middle ground.  You can't be associated with either Yale or Dot Gov and not be scum.  There are no other outcomes.  The NAZIs tortured and killed sick people.  So does Uncle Sam.

See Govt Goon Tries to Silence Willy Burgdorfer ►:


NIH Crook Phil Baker Refuses to Answer Why He is a Crook►:

We already know Lyme/Spirochetes are permanent infections from NIH/CDC/Yale's own publications, and because "Lyme" is actually simply Relapsing Fever.  The nature of the relapse is antigenic variation, and that means no vaccines or antibody test kits based on anything other than flagellin will be useful.

You can believe "Lyme" was an accidental release of a bioweapon for three reasons:

1) Lyme, CT, USA was the original outbreak area,

2) B. burgdorferi (Lyme spirochete) did not evolve and adapt to the Ixodid tick naturally, and

3) the obvious cover-up and persecution of sick people, especially scientists with Lyme who blew the whistle to the FDA about the falsified testing standard (Dearborn) and about how OspA (LYMErix, Yale's non-vaccine) was actually immunosuppressive (and therefore, hardly a vaccine), specifically mentioning to the FDA the A) production of the immunosuppressive cytokine, IL-10 in response to exposure to OspA (a triacyl lipopeptide), and B) inhibition of NK cell activity (Ray Dattwyler's 1988 reports) upon exposure to Borrelial antigens (on the FDA's website).

When American bioweaponeers created a whole new "species" of Relapsing Fever organism to be adapted to the smallest of ticks, making it the stealthiest, it appears that bacteriophage-vectored DNA helped deliver something like OspA from another organism in the tick, presumably from mycoplasma or some other fungal-antigen-bearing organism. OspA helped the African avian borreliosis (anserina) to "take" to these hard-bodied ticks, apparently.

The experiments conducted on Plum Island were absolutely about trying to add African diseases to North American vectors (ticks and insects).


The U.S. Blood Supply is in Danger. 

And if something isn't done about this now, it is going to boomerang on HomeLame Stupidity in a very big way. 
(Some other natural condition will emerge in the United States that will be bigger than the drought, the dead bats, the dead bees, and the incurable Chagas...)

Here is why:

Yale's (L2 Diagnostics, Inc) Lyme Cryme Introduction and Background [120612]:

The falsified Dearborn (MI; CDC's 1994 "Consensus on Standardization of Testing for Lyme" "Conference") diagnostic standard,  where OspA and B antibody bands are left out of the positive case panel, and only the hypersensitivity or arthritis cases are detectable (see the actual RICO complaint to the USDOJ because that complaint is so simple, even a lawyer could understand it) - gave IMUGEN, Yale and CORIXA a monopoly, because they were the only ones licensed to use this (RICO) patented test with OspA and B left out of the Western Blot.

The fraud committed by Allen Steere (CDC officer, believed to be partners in Imugen) in Europe, falsifying the Lyme test (1992), leaving all but the arthritis cases (do not need intravenous ceftriaxone) detectable, and fraudulently leaving OspA and B (encoded on the same plasmid) out of the diagnostic panel, allowed for the CorixaRICO to be the only labs licensed to test for Tick Borne Diseases once LYMErix (OspA) was approved for the market by the FDA.

This fraud also benefitted other CDC officers like Alan Barbour and Barbara Johnson who owned patents for Lyme in Europe, Johnson's specifically with SmithKline.  The patented antigens would be worthless if it were known that all borrelia are relapsing fever organisms, that the nature of the relapse is antigenic variation and that vaccines and test kits are useless.

When the LYMErix trial was being conducted, the criminals learned that LYMErix produced a chronic Lyme-like response.  Their answer to that was to publish a book the same year (1998) wherein Robert Schoen instructed MDs to simply blow these people off and not perform any testing on them - the same way chronic Lyme victims have been treated for the last 22 years, since the cabal was formed (1990) and was part of the original plan of capitalizing on new and emerging vector borne disease, and will happen again, should Imugen retain this contract with the Red Cross.

These criminals have no problem being vicious liars, harassers, and stalkers of sick people. This aggression and Color of Law Abuses meet the USDOJ's definition of RICO (coercion, etc).

Meanwhile, Yale owned the only scientifically valid antibody test for Lyme - band 41 - but they did not deploy it to qualify their other patent, LYMErix, because it does not support all their other lies:  LYMErix, the L2-Diagnostics' RICO, and Dearborn.

You don't think these crooks wouldn't pull the same stunt with this new contract with the Red Cross?

'Falsify the definition of the diseases they find in the Red Cross' blood supply to suit their own commercial products?

American Red Cross Participating in an Investigational Study to Test [with the Lyme Criminals]...


‎About Corrupticut and the Warning I Gave the HomeLames in 2005:

2nd Circuit Chief Justice John M. Walker - a George H. W(alker). Bush cousin who lives near Jonathan "Riggs-Bank/CIA Spook Bank/Money-Launderer" Bush (brother of GHWBush) in Killingworth, CT - ran over a cop in New Haven, CT. Of course, he got away with the homicide.
  This incident happened after I filed this complaint with Homelame Stupidity about all the crime and related crime originating out of Corrupticut and among CT's associated New World Orderite Whores, like David and William Weld ("build jails in rock quarries," again), especially about Yale's RICO enterprise, which now (June 2012)  has been given to the same Yale Lyme Cryme RICO gang gang through a new contract with the Red Cross:

120612; See Aaron Russo and his conversation with Nick Rockefeller re The 9/11 Stunt, how we're all to be microchipped but that associates of the NWO gang will be allowed to get away with crime, and how and why the Rocky's funded the Women's Sluttification Movement, supported, of course, by the Chief Sluts of Corrupticut, Yale and duh DCF, who I call the Whorey-Glories.


American Red Cross Participating in an Investigational Study to Test ...

MarketWatch (press release) - May 30, 2012
For more information, please visit or join our blog at . About IMUGEN, Inc.Incorporated in May 1989, ...

This, this new contract with the Red Cross, is with the same Yale-Corixa-Imugen criminal enterprise: they're after all the patentable goodies in the national blood supply, human DNA and infections DNA- that is the "gold mine" about which the Lyme criminals have spoken.

It's Dave Persing, Allen Steere and Yale, at it again.  The first time they attempted this monopoly of course was over the very - the Steere/Dearborn definition - of "Lyme Disease," where the Corixa RICO of Yale, Imugen and Corixa were to be the only companies licensed to test for Lyme after LYMErix was on the market.  (see the patent, 3 paragraphs down...):

The entire Lyme RICO scam was about the fortune the Lyme crooks (racket started in 1990 at NYMC) were going to make AFTER LYMErix was on the market, because Borrelia burgdorferi was only the first phase of their 50 year roll-out plan for a monopoly on all Vector Borne Diseases, worldwide.  See what's in the Corixa, Persing, RICO patent claim, next...


(Repeating:) Why sue Yale to recover personal damages?

 It was their "vaccine," and Corixa, Imugen and Yale's L2 Diagnostics were the central RICO scammers: Robert Schoen, Dave Persing, Allen Steere.  Schoen and Persing's RICO patent (No OspA-B plasmid) set up a monopoly (with LYMErix) on all future TBDs, test kits, "vaccines" and goodies in the national post-LYMErix blood:

6)  The RICO Monopoly on testing and LYMErix  The Dave Persing, Imugen Mayo Clinic FRAUD Patent-6,045,804  Note the date on the patent.  May, 1996.

"Additional uncertainty may arise if the vaccines [sic] are not completely protective; vaccinated patients with multisystem complaints characteristic of later presentations of Lyme disease may be difficult to distinguish from patients with vaccine [sic] failure."

"The present invention provides a method useful to detect a B. burgdorferi infection in a subject. The method provided by the invention is particularly useful to discriminate B. burgdorferi infection from OspA vaccination, although it is sufficiently sensitive and specific to use in any general Lyme disease screening or diagnostic application. Thus, the method of the invention is particularly appropriate for large scale screening or diagnostic applications where only part of the subject population has been vaccinated or where the vaccination status of the population is unknown. "




WASHINGTON (Reuters) - Free vaccines [sic] meant for children as part of a U.S. government program may have been stored at the wrong temperature, which could make them less effective, according to a report released on Wednesday.

Deadly Mycoplasma in Vaccines - Garth Nicolson_ microbiologist ... 8, 2011 - 11 min - Uploaded by Conflagration2100
This is an excerpt from the Snowshoe Documentary film: Mycoplasma - Dr. Garth Nicolson-microbiologist, this ...

You can't say the epidemic of Autism isn't greater than the so-called mortality of the viruses against which we're forced-vaccinated.  There is a negative "benefit" overall, to "vaccinations."

When Garth Nicolson talks about mycoplasmally-contaminated vaccines, he refers to the OspA-like, TLR2-agonist antigens in the mycoplasma.  So, the Lyme crymes really did reveal the problem with the Autism pandemic.  This is undeniable science - so undeniable that Mark Klempner's partner, Linden Hu, now has a grant to study the immune suppression outcomes of Lyme and LYMErix.

Garth Nicolson talks about the damage to the membranes from the immune response to the toxins like OspA, but there is more to it - the fungal antigens help activate the viruses by inhibiting apoptosis of the infected cells and by turning off the immune response.  Keep reading....

Update 1; In Parallel, The Honeybee Virus carried by mites (mini-ticks), and no doubt aided by new fungi, since fungal/toxic immunosuppression helps viruses very much, thanks.
In other words, if the bees had any immune competence towards these mite-viruses, the fungi/toxins would turn the immunity off.  (UNDISCLAIMER: I know very little about insect immunity, other than toll-like-receptors were first discovered in insects.)


Update 2: "Rockefeller Anti-Fertility Vaccines Exposed"

It's interesting that the murdered Iraqi scientist (bumped off while changing a flat tire, just like Don "It's Swine H9N5" Wiley) who worked on Plum Island, worked on ***mycoplasma and infertility in cows/bulls,"*** while at the same time, the Genetic *and* Acquired "Autism" (see above) have the same "inhibition of apoptosis and that mechanism's effect on immunity" mechanism either from a reversed duplication of BCL2-type genes or mycoplasma contamination, respectively.  When the likes of mycoplasmal or mycobacterial TLR2-agonists or OspA (see below) get into a cells, they gum up the natural immune response. 

Additionally, Epstein-Barr (associated with all kinds of cancer, including childhood leukemia) is both activated by exposure to fungi and the viruses themselves have BCL-2 gene homologs.  See, that is two (dependent and independent) mechanisms of inhibition of apoptosis.

So, unless the brain damage we call autism is meant to be the infertility-inducer, the only connection I can make between infertility and "vaccines" at the present time is this B-cell linked dysimmunity.  It's junk.  Fungus is junk and should not be injected into the bloodstream.

I have no other data on female or male outcomes of "vaccines"-induced dysimmunity and infertility, but I have not really looked because promiscuity, alone, does the job of making people infertile.  Most notably, chlamydia and its resultant endometriosis.

If I were to win the Qui Tam award  (that is, if USDOJ was forced to undergo testosterone treatments) - and I was thinking of this just yesterday - the name I would pick for the institute would be B-Cell Technologies.  Obviously my  lab would investigate the mechanisms of dysimmunity from exposure to fungi like OspA/Lyme, as well as contaminated childhood injectable "vaccines." 

USA supported "T cell autoimmunity" for years, knowing they were throwing research off-track, since the truth has bioweapons value.  To Wit: Roland Martin studying MS-Lyme at NINDS and his all foreign students ??

And my new lab, B Cell Technologies would get real lab equipment.  No more ancient-history "blots."

Failure to phosphorylate.  Stuck on the lysosomes.  TLR2-agonist blobs stuck to the mitochondrial membranes...  Production of IL-10.  Inhibition of CD4+ managing EBV.  Inhibition of nf-kappa.  Inhibition of HLA-molecule migration and expression/presentation...  fungi are wonderful stuff and their best friends are herpesviruses.  :))

LYMErix Disease/Autism are an anti-toxic-shock-stop-fugue (TLR2-agonism), for both the immune system and the brain.

Doesn't kill you, just turns you into Zombees and Zombats.  Autism.  Special-Ed drones.  Rx-Stoner kids.  White-people sluts infertile.  "Child-Protective Services" sluts and slut-mongers servicing all of it...  (LMAO)

The NIH, CDC, Yale, Paul Auwaerter, NIAID, Anthony Fauci, Francis Collins, Kathleen Sebelius, and all refuse to answer, "What is OspA," ...

... because what OspA is, is the disease, stuff doing what it is, at the molecular level.  (Chemists speak in structures for this reason.)

4-10 June 2012: Four Five Six separate groups of Lyme/CFS people have suggested lawsuits over the Lyme crymes in the past week, most without an understanding of what actually was criminal about the crime. Lyme is a False Claims Act case, and the false claim was the Dearborn [Michigan, the place where took place a bogus CDC consensus conference - there was no consensus - and where Steere's research fraud proposal (Steere in Europe), with bogus high-passage strains and recombinant OspA/B with no lipid attached, which will result in no antibodies being produced] diagnostic standard

Almost *** 20 BILLION DOLLARS *** Is Available for Payment of Damages to "Lyme" Victims from Yale's Endowment Fund.  And Yale's properties, antiques, fossils, and rare books are worth even more:
Yale’s endowment earned a 21.9% investment return for the year ending June 30, 2011, Chief Investment Officer David Swensen announced today. The endowment value rose to $19.4 billion based on investme

Why Yale?  It was their "vaccine," and Corixa, Imugen and Yale's L2 Diagnostics were the central RICO scammers: Robert Schoen, Dave Persing, Allen Steere.  Schoen and Persing's RICO patent set up a monopoly on all future TBDs, test kits, "vaccines" and goodies in the national post-LYMErix blood:

6)  The RICO Monopoly on testing and LYMErix  The Dave Persing, Mayo Clinic FRAUD Patent-6,045,804  Note the date on the patent.  May, 1996.

"Additional uncertainty may arise if the vaccines [sic] are not completely protective; vaccinated patients with multisystem complaints characteristic of later presentations of Lyme disease may be difficult to distinguish from patients with vaccine [sic] failure."

"The present invention provides a method useful to detect a B. burgdorferi infection in a subject. The method provided by the invention is particularly useful to discriminate B. burgdorferi infection from OspA vaccination, although it is sufficiently sensitive and specific to use in any general Lyme disease screening or diagnostic application. Thus, the method of the invention is particularly appropriate for large scale screening or diagnostic applications where only part of the subject population has been vaccinated or where the vaccination status of the population is unknown. "

Yale also owned the only scientifically valid antibody test for Lyme - band 41 - but they did not deploy it because it does not support all their other lies.  Like LYMErix, the L2-Diagnostics' RICO, and Dearborn.


All aspects of the crime, including 1) Klempner's bogus retreatment study of patients (66% of whom had never had ceftriaxone before; it wasn't a "retreatment" "study"), 2) the IDSA "guidelines," 3) the fake OspA "vaccines", and 4) perjury cases where the crooks claimed under oath that a person did not have Lyme because they did not have the HLA-linked, hypersensitivity response (the "Steere in Europe"/Dearborn falsified case definition) are based on/dependent upon the bogus Dearborn "case definition."

If the Dearborn case definition is shown to be false and bogus, all the rest of Yale's/IDSA's Baloney can be thrown out as well.  There will be no limitations on testing and treating.  All the crap and nonsense out of Yale and IDSA will have no reference point.  Their crap will not hold up in court. 

Everyone can win their own private lawsuit.  Yale's Endowment Fund - the fund that established Schoen's L2 Diagnostics - is today worth nearly 20 Billion Dollars

And Yale's properties, antiques and rare books are worth even more.

Lyme Disease is not Lyme Disease.  It is Relapsing Fever with an OspA-twist
 The name implies chronicity.  OspA implies invasiveness (binds plasminogen, tolerizes to other fungal antigens in the blood and brain) and the lack of blood-borne, antibody- evidence of infection.

The reason the Justice Department refuses to prosecute is because several CDC staff members own patents in Europe that would be worthless to their partner, SmithKline, if it is known that Lyme is Relapsing Fever, that the nature of the relapse is antigenic variation ("vaccines" and test kits would be worthless).   Something like OspA could never be a "vaccine" because it is a TLR2-agonist.  And Lyme is an accidental release of a bioweapon from Plum Island, where they happened to do this kind of vector-pathogen tolerance testing and development.  (Lyme, CT, USA, is the original outbreak area, and the Ixodid is not a natural vector for Borrelia, says the published science.) 

USA could be under blackmail threat by the Israelis because Durland Fish for years stalked, harassed and made such a fuss about us Lyme activists, calling us "NAZIs."   Whereupon, we looked into the matter of the predominance of Israelis among the Lyme criminals.  Crazy Eddie McSweegan, the "Blaster" to Fish's "Master," also posted about his trip to an Israeli Bioweapons plant on one of his several, private, Crazy-Eddie-the-Famous-Bioweaponeer-Wannabee blogs. 

The best option for a treater ("Lyme-Literate"/"LLMD" - which is also a joke, since none of them discuss/sue over Dearborn or OspA) of this new, scientifically unlikely, Ixodid Relapsing Fever is to use the Brazilian definition (see 101016.htm and search for Brazil in the page),

if the "LLMD" or treater wanted to treat Lyme as if it is just spirochetes.  But we know from other similar "vaccines" trials (Tb and HIV), and we know from the failed childhood vaccinations (and this is CDC's own data as well as Pharma's), that OspA-like antigens suppress the immune system (produce IL-10) and appear to reactivate latent viruses.  

Note how many people specialize in Lyme and Epstein-Barr, only - all of them belonging to the Lying Lyme Crook Class.

There is some evidence (Martin, Marques/NINDS' MS-Lyme Group) that exposure to OspA-like antigens in the brain make that compartment more susceptible to reactivated seronegative herpesviruses.

I emphasize finding out what this disease actually is that produces the likes of arthritis or MS or Lupus in those HLA-linked hypersensitivity cases and the likes of Chronic Lyme/ Fibromyalgia, ME, etc, in all the non-HLA-linked cases before considering treatment protocols.  But the problem with this proposal is that the MDs/Similars who take advantage of these desperate people are not even remotely qualified as scientists.  (Who could I talk to?  These "LLMD"/treaters are not readers.)

Note that all similar "vaccines" to OspA failed in the same way OspA failed (Tb, HIV, MRSA)- they all made existing infections worse and did not produce antibodies.   The prosecution of the Lyme criminals should include damages for these failed Tb, HIV, MRSA outcomes as well.  Imagine if Yale had told the truth in 1995, when they knew they did not have a "vaccine," but amazingly, OspA caused all the same "New Great Imitator" neurological outcomes. 

The failed LYMErix "vaccine" was also the key to the "vaccines"-induced brain damage called AUTISM pandemic.  ◄ This is the criteria upon which parents of vaccines-brain-damaged children should sue for damages.  It's winnable because it includes CDC's own data as well as BigPharma's

It is quite literally the truth that the USDOJ and NIH have no brains or balls.  For one thing, a person who had a natural tendency to be a scientist would never be a lawyer.  For another, whoever is hired by the CDC is never a high-level, high-caliber scientist.  They're usually just "MDs," like Allen Steere.  They're usually PR (bullshit) type people.  They're usually Masters of Kool-Aid (trained by BigInsurance and BigPharma) otherwise known as Masters in "Public Health."  (Think about it. A "Masters in Public Health" only appeals to social climbers and authoritarian cowards.)

US Medicine is a complete failure for the simple reason of a lack of courage.  Really.  And it will remain stagnated until this crime is prosecuted.

The persistence of this unprosecuted "Lyme" crime really is about nobody in America having any balls.  And I wonder to myself, is that no-balls fact finer than having a resolution of that crime?  Could a fact about cowardly American humankind be more exquisite than a resolution, a prosecution, retraction of bogus articles, and a final declaration of TRUTH for once from the NIH about the crime?

Sometimes it really is.  Sometimes it seems that there really is no other fact worth knowing.  The males in this country are not men.

When Pfizer fired all 1104 of their scientists from Groton, CT, Central Research and said they would hire 400 new ones from Cambridge, the reason given was that their science sucked.  That, too, was exquisite, because Central Research was located right exactly in global Lyme Central yet Pfizer did nothing for us, except train yours truly in Scientific Validity and the FDA's rules for the validation of an analytical method.

Now, where is Pfizer?  Sucking up to the NIH for any actual science anybody can today produce.  And that is really, really, funny.

The essence of every major disease (cancers of all kinds, MS, Lupus, arthritis, ALS, strokes, dyslipid-metabolism, etc) was sitting right in Pfizer's lap for 37 years (1975-2010), and all they did was sell the accidental venous dilator, Viagra, and buy up other companies in order to own and sell the other companies' drugs.


120604 KMDickson


June 1st, 8 PM, This just in...

"Philip Wang, M.D., deputy director of the National Institute of Mental Health (NIMH), reported that many pharmaceutical companies are abandoning efforts to find new and efficacious treatments for mental disorders because of clinical-trial failures and a sense that not enough is known about the underlying mechanisms of the disorders (Psychiatric News, April 6)."
Since funding from the National Institutes of Health is tight, a new private-funding institute in Washington, D.C., might prove of value to psychiatric researchers looking for funding sources.

‎TRANSLATION:  "Due to the fact that psychiatric disorders are not scientifically real or medical,... and due to the fact that no one can trust a 'publishing' psychiatrist (Nemeroff and Grassley in the news again) not to be a whore beholden to phake pharma, no one can get a grant to study them."


But it reminds me, too, of Simon Wessely on CFS and Gulf War Illness:

"One way of doing that is through neuro-imaging, but we didn’t get the money to do that, so instead we have used sophisticated neuro-psychological testing,"  [TRANS: scientifically bogus "checklists"]

"Those tablets, the NAPS tablets, it’s just not possible to study. Pesticides, we don’t find evidence. [The antidotes to nerve agents given to veterans are a problem- KMD]  Chemical weapons, well, we don’t think that for the British armed forces that was a big issue. But we do think there is a relationship between a particular pattern of protection and what happened later."-- Simon Wessely on Gulf War Veterans and how they're actually cowards and therefore faking illness.

SYNOPSIS: Don't perform any valid scientific analyses.  Throw out variables that could present a problem to a "study"  designed around the intended non-results.

See more at:

"Science for Everyone
"Sound simple? It is.
"Once, when the secrets of science were the jealously guarded property of a small priesthood, the common man had no hope of mastering their arcane complexities. Years of study in musty classrooms were prerequisite to obtaining even a dim, incoherent knowledge of science.

"Today, all that has changed: a dim, incoherent knowledge of science is available to an
yone. Popular science books, magazines and computer programs - with their simple, fatuous and misleading prose, their garish illustrations, their flimsy modern production values - have brought science within the reach of anyone who can afford their inflated prices or who can mooch off someone else.
"Indeed, today a myriad of sources are available to explain science facts that science itself has never dreamed of."

Inductive, Deductive and the Ever-likely Excretive (Lyme and Psychiatry)



"Cause Known"

Japanese identify the structure of OspA; It appears to be Pam3Cys:

A delicate interplay of structure, dynamics, and thermodynamics for function: a high pressure NMR study of outer surface protein A.


But the CDC says they do not recognize foreign research.  The CDC only apparently only recognizes their own foreign research, such as what's in their European patents with SmithKline regarding the 2 outcomes of Lyme:  1) The HLA-linked Bad Knees and the 2) Chronic Neurologic,  and when the CDC sent Allen Steere to Germany to falsify the diagnostic standard for Lyme, such that only the "Bad Knees" outcome is considered a "case."


1996; KOREANS identify the structure of the OspA and HIV gp120:

 : Characterization of Extremely Hydrophobic Immunostimulatory Lipoidal Peptides by Matrix Assisted Laser Desorption Ionization Mass Spectrometry

Synthetic lipoidal peptides based on viral protein sequences have been prepared. These peptides contain an N-palmitoyl group at the N-terminal residue, which is a modified cysteine, containing a S-[2,3-bis(acyloxy)-(2-R,S)-propyl] moiety. When this residue (Pam3Cys) is at the N-terminus of a synthetic peptide, it acts as potent immunoadjuvant to enhance both IgM and IgG antibody responses to the attached peptide. Conventional analytical procedures (e.g., Edman degradation and amino acid analysis) are either not applicable due to the N-terminal modification, or do not provide confirmation of the intact structure. Chromatographic analysis is also hindered by the tendency of these lipoidal Pam3Cys peptides to form large aggregates, and in some cases to be permanently adsorbed on reversed phase columns. We have applied several mass spectrometric techniques, including fast atom bombardment (FAB), electrospray ionization (ESI) and matrix assisted laser desorption ionization (MALDI) to characterize the intact structures of a number of different Pam3Cys synthetic peptides. The MALDI-MS has been found to be the most sensitive for the analysis of the structure of Pam3Cys peptides. PDF


Fauci the Fumbler on the outcomes of the HIV/LYMErix Vaccine:

‎"The initial empirical approach of immunizing with VaxGen's AIDSVax, a recombinant form of the outer glycoprotein-120 (gp120) portion of the HIV envelope, which was based on a strategy that was successful with hepatitis B, failed to protect volunteers from infection, apparently because the vaccine did not induce broadly neutralizing antibodies.3"  



Tolerance induced by the lipopeptide Pam3Cys is due to ablation of IL-1R-associated kinase-1.

"Preculture of the cells with Pam(3)Cys [LYMErix or OspA Blebs, as shown below- KMD] at 1 microg/ml leads to a reduced response after subsequent stimulation with Pam(3)Cys at 10 microg/ml, indicating that the cells have become tolerant to Pam(3)Cys. The CD14 and TLR2 expression is not decreased on the surface of the tolerant cells, but rather up-regulated. Analysis of the NF-kappaB binding in Pam(3)Cys-tolerant cells shows a failure to mobilize NF-kappaB-p50p65 heterodimers, while NF-kappaB-p50p50 homodimers remain unchanged. Pam(3)Cys-tolerant cells showed neither IkappaBalpha-Ser(32) phosphorylation nor IkappaBalpha degradation but MyD88 protein was unaltered." 

More here


LYMErix-Disease helps us understand the epidemic of "Autism" from vaccines [1) vaccination of immunosuppressed kids causes the kids to suffer reactivated viruses from the vaccines, or 2) via immunosuppression by mycoplasmal (OspA-like) contamination of vaccines and subsequently reactivated viruses];

That is why what Lyme, OspA, and LYMErix disease is, is such a big secret that NIH Director Francis Collins threatened to have me arrested if I kept asking what OspA was (LOL).

OspA-like Blebs (see arrows in the below micrograph) are shed lipoproteins, so everyone with "Lyme disease," also has LYMErix Disease, because that is actually the disease - the chronic exposure to Borrelial OspA-like blebs resulting in immunosuppression, tolerance to mycoplasma in the blood (causes fatigue), results in no antibodies being produced, and the activation of Epstein-Barr/Similars.

Or, as CDC officer and owner of the ImmuLyme OspA patent Alan Barbour says, we're exposed to/autovaccinated with OspA-like fungal blebs like flak:

"Or, using another diversionary tactic called blebbing, the spirochete can pinch off bits of its membrane in order to release its surface proteins. Explains Barbour: "It's like a bacterial Star Wars defense program," in which released surface proteins might intercept incoming host antibodies, keeping the spirochete safe from immunological attack. --



An Admission that Lyme and LYMErix cause immunosuppression (Tufts, Linden Hu-, who published that "Lyme Disease is totally imaginary" with Mark Klempner):

"A better understanding of the workings of innate immunity is important for developing therapies for diseases such as Lyme disease where either an ineffective or an over-exuberant immune response causes the symptoms of illness."



Lyme/LYMErix Cryme Reveals New Paradigm in Health/Disease:
"Bacterial/Viral Coinfections";

TLR2 [fungi, like OspA vaccination or blebbing] Signaling Depletes IRAK1 and Inhibits Induction of Type 1 by TLR7/9  [manages viruses, like latent EBV]--  -CV Harding, 2012

Vaccines' Brain Damage - these are the scientific reports which demonstrate that the CDC knows what "autism" is.

Epstein-OspA-Borreliosis - these are these scientific reports (most of which are by the Lyme bad-guys, themselves) that demonstrate that Lyme/OspA cause immunosuppression, tolerance to mycoplasma in the blood, and apparently the reactivation of Epstein-Barr/Similars.

A few years ago Roland Martin who headed the NIH's MS-Lyme research group wanted to try Leukophoresis to get rid of the badly cloned B cells in the MS version of "Lyme Disease."  Later came Rituximab.  Clue.

Soon after Roland Martin discovered that LYMErix or OspA vaccination produced the antibody-negative, MS-version of Chronic, Incurable Lyme that he was hired to study for the NIH, he went back home to Germany. 









1989, Paul Duray (in IDSA's journal), Clinical pathologic correlations of Lyme disease.

“Frank signs of meningeal irritation herald stage II illness, reflected by an increase of CSF lymphocytes and plasma cells and moderate increases in total protein in CSF [9,16,17].  Immature B cells can also be seen in the spinal fluid.  These cells can appear quite atypical- not unlike transformed or neoplastic lymphocytes."
IDSA_CLINIPATH_DURAY.htm ("Epstein-Barr-like transformed B cells")

1992 Duray:
"On occasion, these atypical-appearing large lymphocytes have been misinterpreted in biopsy by several laboratories as cells of a malignant lymphoma or leukemia.  Bb antigens, then, may stimulate growth of immature lymphocytic suibsets in some target organs, as well as in the cerebrospinal fluid (Szyfelbein and Ross 1988).  Usual bacterial infections do not produce such lymphocytic infiltrates in tissue.  These immunoblastoid cells in Bb infections at times resemble those found in Epstein-Barr virus infections.  Does Bb reactivate latent virus infections in tissues?  Do some tick inocula harbor simultaneous infectious agents (ixodid ticks can harbor Rickettsiae, Babesia microti, and Ehrlichia bacteria, in addition to Bb), producing multi-agent infections in some hosts?  Further studies can clarify these issues by mans of tissue-based molecular probe analysis." - 
 Paul Duray, NCI, NIH, Ft. Detrick, at the 1992 Cold Spring Harbor Crooks' Conference, published in Steve Schutzer's
Lyme Disease: Molecular and Immunologic Approaches

This table is working.  We see the hijacking of the Life of a Cell ...  Or as Gary Wormser declared in 2000 (while OspA was still on the market), "OspA interferes with the response of lymphocytes to proliferative stimuli including a blocking of cell cycle phase progression."   It's like immunological paralysis.  To go with the NIH's intellectual paralysis.  Additionally, it seems flagellin and other bacterial antigens (besides TLR2 agonists) activate mouse EBV.

Herpes Mouse Herpes/ XMRV Fungal/Viral Spirochetes Myco/OspA EBV/HERVs Tuberculosis Q Fever
Interleuken-10 (caused by Lyme &  LYMErix) inhibits the management of EBV (1991)
This article was cited over 100 times.

The latent membrane protein 1 (LMP1) oncogene of Epstein-Barr virus can simultaneously induce and inhibit apoptosis in B cells.


H. pylori works with EBV (stomach cancer)

Flagellin activates Mouse Gammaherpes TLR2 Signaling Depletes IRAK1 and Inhibits Induction of Type 1 by TLR7/9  (viruses)--

-Clifford Harding, 2012 "Bacterial/Viral Coinfections"

Justin Radolf report on Plum Island page re spirochetes and mycos (no antibodies) NIH: says "OspA suppresses & reprograms immunity" (wins Nobel; means Dearborn is a lie as are "Lyme" "guidelines" EBV transformed cells help present fungal antigens    
Stevil Straus: Characterization & treatment of chronic active EBV disease: 28yrs, USA (CFIDS is Chronic EBV)

CFIDS = EBV Seronegative (4 reports)

Down-regulation of MHC class II expression through... [J Immunol. 2009] - PubMed - NCBI


Mouse Herpes 68 hijacks MAVS and IKKbeta TLR2 agonists synergistically increase the proliferation of EBV


Duray at Ft. Detrick in 1992 and reporting to IDSA about EBV- transformed lymphocytes in 1989


Formation of cysts within cells results in the release of flagellin (See H. pylori & EBV

Flagellin (and other antigens) activates Mouse Gammaherpes


Chronic Lyme is seronegative because Lyme is chronic
(downregulation of MHC-II; Justin Radolf) due to (blebbing)
H. Pylori/EBV affect NF-kappa-B

Harold Varmus, Denise Huber
Huber says there is 2 kinds of Lyme: the EBV evoking kind and Steere's "knees"

101016.htm Q-Fever/Chronic Lyme (activation of viruses) TLR agonism becomes seronegative.
Update, Mayo Clinic on RA and Cytomegalovirus (120202)

A profile of immune response to herpesvirus... [Arthritis Res Ther. 2012] - PubMed - NCBI

NCI/XMRV  and NF-kB Interleukin-10 [produced by exposure to OspA] inhibits apoptotic cell death in infectious mononucleosis T cells.(1994) "Pam3Cys keeps the precursors in a more immature stage"  (IL-17)

Borrelia & IL-17


Tolerance induced  Pam3Cys (Yale's LYMErix "vaccine") is due to ablation of IL-1R-associated kinase-1. 15294992   EBV transformed cells help present fungal antigens Coxiella agonizes TLR2 (would be seronegative)

"Conclusions: EBV DNA was often found together with other microbial findings in CSF of immunocompromised [LYMErix- or Lyme-Disease]  patients." 


  "Conclusions: EBV DNA was often found together with other microbial findings in CSF of immunocompromised [LYMErix- or Lyme-Disease]  patients."   

101016.htm Epstein-Borreliosis datapage; Note: Harding explains Steere's Knees (HLA-antigen complex is shed)

OspA induces IL-10

IL10>>CD4- = EBV

EBV & IL-10  

OspA delays apoptosis through inhibition f caspase-3 activity:  CD14&TLR-2.  (Ireland,  BLP (OspA) inhibits neutrophil mitochondrial membrane depolarization"

"It has been demonstrated that LPS inhibits PMN apoptosis preferentially through stabilization of the mitochondrial membrane and subsequent inhibition of caspase-3 (33)."



Gulf War Illness Q Fever

No one can be diagnosed with anything that's  a bioweapon.

Stress steroid hormones literally activates EBV Which means is trashed, once again   Interaction of Borrelia burgdorferi sensu lato with Epstein-Barr virus in lymphoblastoid cells Structure of Leptospira TLR2 agonists  They say not to use mice TLR2. TLR2 and nf-kappa     Q Fever &  inhibition of apoptosis Could be missed.  Crooks  playing RNA/DNA ShellGame is trashed (NYT)   "Internal"  Lyme spirochetes increase EBV  replication. Lyme causes CLL Leukemia

(Look up the symptoms of that)

IL-10 (induced by OspA)

IL10>>CD4- = EBV


    RML:  Sustained of Akt and Erk1/2 is required for Q Fever anti-apoptotic activity
15950179  - EBV alters mitochondrial membrane (as do mycoplasma)       TLR2 activation inhibits embryonic neural progenitor cell proliferation     C. burnetii inhibits activation  apoptosis through a mechanism that involves preventing cytochrome c release from mitochondria
EBV transformed cells help present fungal antigens       Systemic stimulation of TLR2 (such as in vaccination with OspA) impairs neonatal mouse brain development      
EBV LMP1 reduces p53 protein levels independent of the PI3K-Akt pathway. Dec 21, 2011

111222: HSV-1 Infection Activates the Epstein-Barr Virus Replicative Cycle via a CREB-Dependent Mechanism

  H. pylori works with EBV

H. Pylori/EBV affect NF-kappa-B



Treatment of Throat Cancer Caused by Epstein-Barr is to Reverse Dattwyler's NK-Cell Suppression:        
Despite the NIH anti-CD20 datapage      


Seronegative EBV (downregulation of MHC-II)

BCL-2 Homolog BHRF1


PubMed: "Endotoxin Tolerance and TLR2" [means LYMErix (OspA) was not a vaccine, Dearborn is a lie, and Borrelial antigens are immunosuppressive as TLR2 agonists.]

EBV & LMP1              
Oncogene BCL2-like in EBV              
EBV &  mycoplasma              
EBV inhibits p53 auto-kill kinase              
NF-Kappa B and Herpes (PubMed, General search)      


Herpes Simplex Immunosuppression (NF-kappa)              
Epstein-Barr and anti-CD20 (Rituximab)
(PubMed, 500+)(and CFIDS)
IL10>>CD4- = EBV              
EBV & IL-10              

Lipoteichoic acid (LTA) of Streptococcus pneumoniae and Staphylococcus aureus activates immune cells via Toll-like receptor (TLR)-2, lipopolysaccharide-binding protein (LBP), and CD14, whereas TLR-4 and MD-2 are not involved.

PubMed: Chlamydia and TLR2

PubMed: Chlamydia and Epstein-Barr

Here is what we know about what is the requirement for a pandemic flu human strain to take off:

Chinese: Characterization of H9 subtype influenza viruses from the ducks of southern China: a candidate for the next influenza pandemic in humans? 

Don Wiley, 2001, before he was murdered "changing a flat tire":    

"α2,6-Linked sialosides bind in a cis conformation, exposing the glycosidic oxygen to solution and nonpolar atoms of the receptor to Leu-226, a human-specific residue. ...

..."Evidently, the “closed” geometry of the avian H5 HA, which prefers α2,3 linkages, results from the Gln-226/Gly-228 pair. This geometry appears optimal for positioning Gln-226 to hydrogen-bond to the α2,3 trans motif composed of the 4-OH of Gal-2 and the glycosidic oxygen (Fig. ​(Fig.22c). The human H3 HA with the Leu-226/Ser-228 pair is at the opposite extreme, more “open” at both 228 and 226, which may be optimal for Leu-226 to make nonpolar contacts to α2,6 cis linkages. Swine H9 HA (Leu-226/Gly-228) and the L226Q variant of human H3 HA (Gln-226/Ser-228) appear to be intermediate, with partial avian and partial human character and the nonstandard Leu/Gly and Gln/Ser pairs
(Fig. ​(Fig.22f)."


CDC, Jan 2012In vitro evolution of H5N1 avian influenza virus toward human-type receptor specificity.

"Acquisition of α2-6 sialoside receptor specificity
by α2-3 specific highly-pathogenic avian influenza viruses (H5N1) is thought to be a prerequisite for efficient transmission in humans. By in vitro selection for binding α2-6 sialosides, we identified four variant viruses with amino acid substitutions in the hemagglutinin (S227N, D187G, E190G, and Q196R) that revealed modestly increased α2-6 and minimally decreased α2-3 binding by glycan array analysis. However, a mutant virus combining Q196R with mutations from previous pandemic viruses (Q226L and G228S) revealed predominantly α2-6 binding. Unlike the wild type H5N1, this mutant virus was transmitted by direct contact in the ferret model although not by airborne respiratory droplets. However, a reassortant virus with the mutant hemagglutinin, a human N2 neuraminidase and internal genes from an H5N1 virus was partially transmitted via respiratory droplets. The complex changes required for airborne transmissibility in ferrets suggest that extensive evolution is needed for H5N1 transmissibility in humans."

Pandemic flu and the "Unknown Intermediate" host being a pig:  "Reassortant viruses appear to have caused the pandemics of 1957 and 1968; the 1957 H2 virus differed by three genes, those for HA, NA and the RNA polymerase subunit PB1, from the H1 virus that infected humans between 1918 and 1957; the 1968 H3 virus differed by two genes, those for HA and PB1, from the H2 virus that infected humans between 1957 and 1968 (Kawaoka et al., 1989). In both cases, the genes for the H2 and H3 HAs are proposed to have been contributed by avian viruses, ***during infection of an unknown host that was infected simultaneously by the prevalent human virus."***


"Also in "Emerging Viruses: AIDS & Ebola," you will learn exactly what was done with the $10 million Congress gave the DOD for the development of AIDS-like viruses, because I published the relevant contracts. You will learn that Dr. Robert Gallo, the famous NCI molecular biologist, pardoned by President Clinton last year for scientific fraud and misconduct, and credited with the discovery of the AIDS virus, set about to develop immune system ravaging, AIDS-like viruses, along with other Litton Bionetics researchers. You will learn that they took monkey viruses that were humanly benign, recombined them with DNA, RNA, and enzymes from other animal viruses that caused leukemias, lymphomas, and sarcomas, and then to get them to jump species, they cultured these new mutant viruses in human white blood cells in some studies, and human fetal tissue cells in other studies, to produce immune-system-destroying, cancer-causing viruses that could enter humans and produce virtually identical effects to what the AIDS virus is currently doing in people around the world."



Howard Storm:  "There is NO sitting on the fence"  (@8:40 mins)  "There is no middle ground."

That goes for everyone, especially alleged "government" "employees."



Go to for the following full text pdf


and see...

1988, Distinction between HIV-1 and HIV-2 infection using novel synthetic lipopeptide conjugates as antigens in enzyme immunoassays.

“A novel immunoassay technique using synthetic lipopeptide (Pam3Cys-Ser) linked to immunodominant peptide domains of HIV-1 and HIV-2 envelope proteins as an antigen adsorbent has been developed. Attachment of peptides to microtiter plates can be considerably improved with this method by employing the hydrophobic properties of lipopeptide. From the sera of 121 HIV-1 infected patients 117 reacted with Pam3Cys-Ser-[HIV-1(598-609)cyclic disulfide]. Five of 5 HIV-2 positive sera were positive with Pam3Cys-Ser-[HIV-2(593-603)cyclic disulfide]. Control sera failed to react with these conjugates.”


People with HIV have antibodies to LYMErix, and as we will see later, apparently it was put into a vaccine for HIV and failed in the same way LYMErix failed - it did not produce antibodies and it made existing infections worse (Fauci).


The Japanese identify the structure of OspA; It appears to be Pam3Cys:

A delicate interplay of structure, dynamics, and thermodynamics for function: a high pressure NMR study of outer surface protein A.


Fauci the Fumbler on the outcomes of the HIV/LYMErix Vaccine which are identical:

‎"The initial empirical approach of immunizing with VaxGen's AIDSVax, a recombinant form of the outer glycoprotein-120 (gp120) portion of the HIV envelope, which was based on a strategy that was successful with hepatitis B, failed to protect volunteers from infection, apparently because the vaccine did not induce broadly neutralizing antibodies.3"