US Dot Mil Talks about Trojan Horse or Time Bomb Diseases from Ticks, etc

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

01 Oct 2017

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1988 Steere says Lyme is like a B cell leukemia

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TruthCures.org
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researchfraud.com/
may12.org
meadvocacy.org/
truthbetoldx81
lymecryme
CrymeDiseaseNorway
crymedisease
theothersideofthestretcher
rjspiritualityandtuth
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CDC "SPIDER"

Fungal Exosomes Inhibit Apoptosis

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

RICO_filed_USDOJ

BlumenthalAntiTrust Lawsuit

Exosomes, Blebs

Spirochetal_Dementia

PDFs
CDC Admits Fraud, 2016
Dattwyler, 1988
Golightly, 1988
Dressler, 1994
BarbourFish, 1993
Dearborn, 1994
BarbourFishpdf.pdf

Pathogenic Fungi

Bush's warcrimes, Oct 2000

Trainer

170708

The following is from the Congressional Record on Dual-Use Bioweapons exported to Iraq:
http://www.actionlyme.org/US_SELLS_IRAQ_BIOWEAPONS.pdf

See more at BIOWEAPONS_ATTRIBUTES.htm - the ISRAELI SECTION

"Lyme" and OspA were time bombs or Trojan horses that detonate Epstein-Barr/similars and tolerize to fungal infections in the blood resulting in chronic fatigue.

Exposure to borrelial antigens (blebbing) turns off the antibody response, meaning "Lyme" could not possibly be an "autoimmune disease" - it's the reverse. It belongs in the cancer and AIDS class.

Did someone day "Lyme Disease" wasn't an accidental release from Plum Island?

1) Firstly, there is no such thing as "Lyme Disease" it's just Relapsing Fever and officially serologically so in 1990: http://www.actionlyme.org/CDC_DOCUMENTS_1990.htm

2) We have scientific evidence that "Lyme" did not naturally evolve
UNCOORDINATED PHYLOGEOGRAPHY OF BORRELIA BURGDORFERI AND ITS TICK
VECTOR, IXODES SCAPULARIS:
http://www.ncbi.nlm.nih.gov/pubmed?term=20394659[uid]&cmd=DetailsSearch
"Despite the intimate association of B. burgdorferi and I. scapularis, the population structure, evolutionary history, and historical biogeography of the pathogen are all contrary to its arthropod vector."

3) We have scientific evidence that the original outbreak area was indeed the area of Plum Island/Lyme
http://www.ncbi.nlm.nih.gov/pubmed?term=3577493 (Bosler, SUNY-SB)

4) They happen to perform that kind of vector-pathogen competence studies on Plum Island (Durland Fish)
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC109458/?tool=pubmed ,

5) Govt Goons tried to silence Willy Burgdorfer (who was recruited from Switzerland in the first place to work at the NIH Rocky Mountains Bioweapons lab specifically because he was an expert in spirochetes)
http://underourskin.com/news/lyme-discoverer-willy-burgdorfer-breaks-silence-heated-controversy ,

6) No one from the NIH, CDC, Yale or IDSA will answer the question as to what OspA is and they threatened me with jail (again) if I persisted in reporting to Francis Collins that no one to whom I was referred by Collins' office (Fauci and NIAID) could tell me what OspA was
http://www.actionlyme.org/120702.htm ,

because if anyone ever told us what OspA was, they would have to admit it could never have been a vaccine and was therefore falsely qualified (they would have to admit the Dearborn criteria was fraud). And to date, no one at MIT or Stanford or Princeton or Duke or any of the other formerly respected institutions of higher learning can tell you what OspA is either. (Because why? This is an IQ test: Why won't anyone from mit.edu or berkeley.edu or stanford.edu etcetera et al report the truth about Lyme as Relapsing Fever or what OspA is/does?)

7) The "science" of "Lyme" is about attacking the victims and calling them crazy and this has been the case since 1990 when the ALDF.com a commercial entity supported by the likes of Mort Zuckerman (CFR) and the AIG Greenbergs (CFR) was founded at New York Medical College (http://www.actionlyme.org/CONNOLLY_FISH_WEINSTEIN.htm)
Ever since the imaginary vaccine trials, the only other so-called study performed by these crooks was Klempner's bogus long term retreatment study of people 2/3 of whom never were treated according to the protocol before, and half of whom tested positive to the Dearborn protocol when no one knows what Dearborn means. The testing schema was research fraud committed by CDC officer/draft dodger Allen Steere alone in Europe.
http://www.actionlyme.org/MKLEMPNER.htm
None of the participants invited to the Dearborn conference in 1994 agreed with Allen Steere's proposal:
http://www.actionlyme.org/DEARBORN_PDF.pdf

8) The CDC deliberately falsified their mycoplasma/Chronic Fatigue Syndrome study by throwing out the red blood cells, to which the mycoplasma adhere, resulting in fatigue without the anemia:
http://www.actionlyme.org/120305_CDC_BOGUSARTICLES.htm

1992; [The effect of Eperythrozoon suis infection on the osmotic fragility of erythrocytes]

Osmotic fragility of erythrocytes was tested in weaned pigs experimentally infected with Eperythrozoon (E.) suis. Acute eperythrozoonosis of splenectomized pigs led to an increase of osmotic fragility. It is supposed that E. suis infection causes a structural change in erythrocyte membrane. Possible mechanisms of this cell membrane injury are discussed.
http://www.ncbi.nlm.nih.gov/pubmed/1471973

And you can see more images of mycoplasma adhering to erythrocytes here:
http://www.actionlyme.org/PAM3CYS_IMMUNE_SUPPRESSION.htm
http://www.actionlyme.org/BIOMARKERS.htm

The process by which people become tolerized to mycoplasma (bearing TLR2-agonists) is due to the chronic exposure of persons with Lyme Relapsing Fever to shed antigen (blebbing) as demonstrated by UConn's Justin Radolf, here:
http://www.actionlyme.org/PIIB.htm
Blebbing, by Alan Barbour
http://www.actionlyme.org/BARBOURS_STEALTH_BOMBERS.htm

9) Durland Fish admitted he writes "bogus articles" when planning to stalk, wiretap, and harass Karen Forschner of the Lyme Disease Foundation
http://www.actionlyme.org/TICK_BITE_CONSPIRACY.htm

10) IDSA fellas have referenced the "cysts are viable" study performed at URI in 2000, shown next

        URI's Dave Nelson "Reversion of cyst form to intact spirochetes within one minute of addition of rabbit blood:"
        http://mic.sgmjournals.org/cgi/reprint/146/1/119 (This was published in the United States in recent time so the CDC
        can't reject it which is what they always do with data they don't like from Europe.)

See who referenced the above "cysts are viable" report (Steere, Wormser, Radolf, etc):
http://www.ncbi.nlm.nih.gov/pubmed?db=pubmed&cmd=link&linkname=pubmed_pubmed_citedin&uid=10658658

Therefore, although we have plenty of evidence from history since 1911 that the cysts were known to be either a regeneration form or a reproductive form or a survival form, the crooks who referenced the above article about the viability of the spheroplast form, now say these cysts or spheroplasts are dead. They lied about everything else, so why not?

The biggest problem for these Lyme crooks is that they're stupid.

1911, on the Incurability of Lyme/Relapsing Fever and the formation of viable cysts or spheroplasts:

See much, much more older data on the incurability of Relapsing Fever here:
http://www.actionlyme.org/RICOCHRON.htm

And see much, much more from the crooks themselves, when they report treatment failure, here:
http://www.actionlyme.org/BRAIN_PERMANENT.htm

And here is evidence that OspA and HIV are basically the same thing (HIV gp120 appears to be OspA in triplicate).

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.
http://www.sciencedirect.com/science/article/pii/S0006349511054075

Go to http://www.actionlyme.org/101016.htm for the following full text pdf (performed by the Koreans, 1996):

and see...

People with HIV have antibodies to LYMErix (next report), 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).

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.”
http://www.ncbi.nlm.nih.gov/pubmed/2464607

('Must have been early cases of HIV.)

and see...

Fauci the Fumbler on the outcomes of the HIV/LYMErix Vaccine (?) which are identical (both the vaccines and the outcomes):

‎"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"

An HIV Vaccine — Challenges and Prospects — NEJM
www.nejm.org

Again from the Congressional Record:

"Methods of using antipersonnel agents undoubtedly wary so that no uniform pattern of employment or operation is evident [make sure it does not produce antibodies, is the short version- KMD]. It is likely that agents will be used in combinations so that disease symptoms will confuse diagnosis and interfere with proper treatment. It is also probable that biological agents would be used in heavy concentrations to insure a high percentage of infection [or just use the OspA vaccine- KMD] in the target area. The use of such concentrations [or the multiple infections it causes, due to the immunosuppression like HIV, Lyme, or LYMErix as acquried immune deficiencies - KMD] could result in the breakdown of individual immunity because the large number of micro-organisms entering the body could overwhelm the natural body defenses [or just infect or inject people with an immune suppressor like OspA from a tick or a syringe, and the reverse will happen: people will acquire multiple infections because their immunity is trashed by OspA- KMD].

This snippet can also be compared to CDC officer (bioweaponeer) Alan Barbour's explainer on how after being infected with even one spirochete, the immune system can be overwhelmed by exposure to a nearly infinite number of antigen variants, rendering the immune system "overwhelmed":

CDC officer Alan Barbour 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."******

So, we have no real proof that Lyme was an accidental release from Plum Island, but we have circumstantial evidence that certainly would be upheld in a former US court of law (there are none anymore, but if...), and certainly enough evidence for a RICO case, due to the harassment of Lyme victims and their treaters.

Color of Law abuses

Deprivation of Rights

Perjury committed by the crooks

Discrimination

You name it

"Lyme disease" was a phenomenon that exposed the substance - the essence, the nature - of American males.

What a laugh.

kmdickson 120701, 19:00 EST, USA