01 Oct 2017
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File List, RICO
1988 Steere says Lyme is like a B cell leukemia
Assoc Blogs-n-Webs:
TruthCures.org
badlymeattitude.com/
immune2lies.com/
researchfraud.com/
may12.org
meadvocacy.org/
truthbetoldx81
lymecryme
CrymeDiseaseNorway
crymedisease
theothersideofthestretcher
rjspiritualityandtuth
LymeTruthSite
JC-LilnkedIn
KD-Linkedin.com
LD-LinkedIn
JC-academia.edu
KD-academia.edu
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 |
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Greetings,
This is the year the Lyme cryminals are going to get BUSTED or
we are ALL going to know why (usda.gov, Plum Island, & BigVaccines).
We're going to Occupy the USDOJ (Washington, DC) in May-July, 2015 and all
abused groups are welcome. The primary reason for the abuses of Lyme
and similar (Gulf War Illness, Chronic Fatigue, Fibromyalgia) victims is
that the CDC does not want anyone to know how the childhood vaccinations
are causing Autism,... because those mechanisms are the same in Lyme,
GWI, Fibromyalgia, ME/CFS. The children are getting the viruses
instead of the protection due to immunosuppression. And the
childrens' immune systems are being ruined by all the hypervaccination,
explaining the epidemics of allergies, asthma, ADD, and leukemia in
American children, too.
So, everyone is welcome to show up at the Occupy and stay as long as
you like. Come and in Solidarity, demand Justice. Remember,
"America" used to be short for "WE'RE NOT PUTTING UP WITH THIS
BULLSHIT!!!"
https://www.facebook.com/groups/OccupyUSDOJ
SAYS LATOV: "The similarity between the neurological sequelae observed in
the OspA-vaccinated patients and those with chronic Lyme disease suggests a
possible role for immune mechanisms in some of the manifestations of chronic
Lyme disease that are resistant to antibiotic treatment. "
http://www.ncbi.nlm.nih.gov/pubmed/15363064
Lyme Crymes Video Series (sorta like a slide show, stop
at each frame)
REVIEW:
1) You saw in video 1, 2, 3, 4 and 5 that Lyme is just another
borrelia (relapsing fever) spirochete, “Lyme disease” is just a nonsense
term;
2) all spirochetal diseases are permanent and
borrelia reliably infect the brain;
[being in the brain, a blood DNA test will not rule
out borrelial infection if they are in the brain, meaning ILADS are
morons, but so is DARPA for creating a backwards Fla test: putting Fla
antibody on nanotubes to detect free flagellin in the blood – they
should have put flagellin on the nanotubes to detect 41-antibody in the
blood, but you can’t have everything, this being the United States];
3) the cyst form is viable *is* weaponizable (says
the CDC, freeze-drying them in 1964);
4) you only need band 41 plus the triad of symptoms to detect Lyme
and/or relapsing fever, says CDC officers Alan Barbour and Allen Steere;
5) Yale validated this flagellin method in 1991 and patented it
(5,618,533);
6) OspA-disease is the same as Lyme disease, with the
fungal-antigen-induced immunosuppression leading to the reactivation of
EBV/similar (not shown, NIH thinks this could lead to us being pneumonia
carriers, which means we will be protected from pandemic Flu-monia,
since it was the hightened immune response to the secondary pneumonia
that was responsible for the 1918 flu deaths, we won’t have that); NOTE TO SELF that is “VID5_NIH_SEPSIS_PNEUMONIA.png”
7) the NIH agrees and calls this post-sepsis or chronic sepsis, implying
the reactive latent infections are still ongoing;
8) Poland, Czech Rep say OspA and Borrelia do this (activate EBV)
directly;
9) Harding and others say this TLR2/1-agonist
tolerance spreads to other TLR-agonists l-like bacteria and says
something to the affect that such cross-tolerance leads to mixed
bacterial-viral infections (‘more and more being recognized, in fact, in
the old days they used to give kids with colds antibiotics to prevent
these secondary bacterial ear infections, so that is the same dynamic as
LYMErix disease or the diseases caused by fungal contaminated live viral
vaccines run in reverse);
9) elsewhere in TLR2/1 agonist exposure we get this
immunosuppression and synergy (Brucella, Mycobacteria, Mycoplasma in
addition to Borrelia);
10) Dattwyler, Luft, and Steere know these borrelial lipids are
responsible for the immunosuppression since they wrote about it and
spoke about it at the FDA (Luft, 1998);
11) the crooks Persing (Mayo Clinic) and Robert
Schoen published that LYMErix vaccination causes the same systemic
disease as “chronic Lyme” in their RICO patent;
12) Gary Wormser published that OspA caused immunosuppression in dogs,
too (2001), but he never said anything publicly at the time, which was
when LYMErix was still on the market;
13) the crooks trashed their Lyme and LYMErix victims, using the term
Munchausen’s and other psychiatry terminology nonsense for a few
decades, such aggression towards their victims betraying their guilt;
14) Allen Steere published in the Munchausen’s book that “seronegative
Lyme in the presence of arthritis was a conflict in terms” revealing for
certain that the Dearborn stunt was meant to detect only the arthritis
cases, while throwing out the neurologic ones;
15) we know all the crooks knew there was the
non-arthritis Lyme cases and wrote about these cases numerous times;
16) Dearborn was all about throwing out these Neuro
Lyme cases as shown by what Steere did in Europe (Vid 5, What Happened
at Dearborn) –this was straight up research fraud as you saw what Steere
did with the strains and the 5 std dev ELISA cutoff, deliberately
leaving out the meningitis (neuro) cases;
17) that there was no consensus at Dearborn despite
the invited labs to the Dearborn stunt on average said the Steere/Dressler
proposal was only 15% accurate.
18) we know from Video 1 that the FDA requires your
test detect 100% of the instances of the analyte in question, meaning
you can ONLY use band 41 since that is the only one people reliably
have, not to mention is the earliest band to show up, early detection
being critical to acceptable (healthy) outcomes;
19) NOT SHOWN – In 2005 Wormser and Klempner
allegedly did a study on the HLA-related responses in his 1997 bogus
retreatment “study,” and they re-admitted that the seropositive, HLA-linked
arthritis cases were not sick, but just had arthritis (this was what
Vijay Sikand said at the 1998 FDA meeting off the record: “the arthritis
cases make enough antibodies to fight off the disease” which is why they
are not sick)
20) the strains game of Steere in Europe and also
in the 2 OspA vaccine trials, including using strain B31 which has
little to no OspC in it, the brain invasion antigen.
21) since Steere left OspA and B out of the
standard for his later monolopy on North American blood in cahoots with
Imugen, Yale’s L2 Diagnostics and Corixa, and using strain B31 in the
OspA trials, they excluded the 3 most prevalent antigens, OspA, B and C,
reducing the chances of anyone testing positive; if a person has those 3
bands plus 2 more, they will still not meet the 5 out of 10 band
arthritis criteria – that being the whole point of Dearborn,
fraudulently passing off bogus Lyme vaccines: If you can’t find Lyme, you can’t find a case of vaccine failure, right?
22) turns out, they could not even read their Western Blots in OspA
vaccinated people but both OspA vaccine experiment groups reported 76%
and 92% “safe and effective.”
23) Arthur Weinstein was both an approver of the bogus Dearborn panel
and was in charge of “data safety monitoring” for one of the OspA trials
– if the blots were unreadable, he obviously was no data-monitor.
There is not one single "doctor" in America who knows what
the hell they're talking about when it comes to Lyme or OspA-disease, and
none of them are complaining about how Dearborn was a fraud.
It was like, ever since I blew the whistle at the FDA, demonstrating how the
Dearborn "case definition" was a total fraud (was
research fraud, not to mention, was
not even a consensus), and informed the FDA that LYMErix or OspA caused
immunosuppression (produces IL-10, and regarding
Dattwyler's NK cell suppression data),
ILADS.org totally lost their minds.
That was 14 years ago and they still refuse to look at the science.
They still talk about "Biofilms," when that does not apply for 2 reasons:
spirochetes are not social animals and the
biofilms are covered in
TLR2-agonist SLYME
and the body does
not even see them. THAT is the DISEASE- the body no
longer sees the infections. These post-tick-bite-sepsis diseases are
diseases of NO-INFLAMMATION.
Not one single member of ILADS is aware of this. If their victims fail
treatment for Lyme, ILADS says it is because they needed to treat this, that
or the other "co-infection," first. They have an endless repertoire of
explanations for why their victims fail treatment until their victims go
broke... having gotten 2nd and 3rd mortgages directly upon ILADS' docs'
requests.
Now their victims are
still sick and have no house. At least
IDSA does not do that to them.
Don't you think it is about time these asshole "doctors" grew the eff up and
got OVER IT?
For the last 12 months, Top Files - Everyone but ILADS and the LDA is paying
attention:
http://www.actionlyme.org/DEARBORN_PDF.pdf - 17,804
http://www.actionlyme.org/STEERE_OSPAB_FRAUD.jpg - 8,213
http://www.actionlyme.org/MKLEMP1.gif -- 6,454
'So damned cowardly. The whole damned country, nothing but
crooks, or cowards and ass-kissers.
What a bunch of pukes.
"Post-sepsis syndrome is a condition that affects up to 50% of sepsis
survivors. They are left with physical and/or long-term effects, such as:
"•Insomnia, difficulty getting to sleep or staying asleep
"•Nightmares, vivid hallucinations and panic attacks
"•Disabling muscle and joint pains
"•Extreme fatigue
"•Poor concentration
"•Decrease mental (cognitive) functioning
"•Loss of self-esteem and self-belief
http://www.sepsisalliance.org/sepsis/post_sepsis_syndrome/
Does that sound like you? Didn't have to
be. Some really stupid assholes somehow got ahold of Borreliosis and
ended up making a "vaccine" out of the very same thing that caused this
post-sepsis syndrome...
Too Hilarious for Words. Pat Smith is going to
straighten out the FDA and tell them
how
Method Validations are performed
(posted 141223, like a
Christmas present showing the whole world that ILADS and the LDA have no
clue what they're talking about for once and for all):
Okay, Reality Check: Go here for those FDA rules and
how you are to report your adverse events to the Dearborn case definition of
"Lyme Disease," to the FDA, per the Senators forcing the FDA to assure Lyme
testing is valid:
PRIMERSHELLGAME.htm
Both the LDA's Lorraine Johnson and Daniel Cameron (ILADS) wrote
RETARD papers on Blumenthal and the other Senators
forcing the FDA to assure testing for Lyme is valid
according to the FDA's own rules on
the validation of an analytical method,... which showed that
neither of them had a clue about this, despite all the years of me
screaming about it, making it
CHAPTER ONE of Cryme Disease, and blowing the whistle over this
very thing 14 years ago at the FDA Hearing on LYMErix in Jan, 2001:
http://www.fda.gov/ohrms/dockets/ac/01/slides/3680s2_11.pdf
That is so funny to me. Now Pat Smith makes an
announcement. like, to the whole world that "Look out! Pat
Smith is coming to famously reinstruct the entire industry on how
science is done!!"
THAT would be Pat Smith, in case you did not know
her. No one's ever met a bigger blowhard because this behavior
is straight up a cartoon in any culture.
Next BIG NEWS, Harvard says LYMErix was the very thing
responsible for extreme microbial sepsis:
"Importance of Toll-like Receptor 2 in Mitochondrial
Dysfunction during Polymicrobial Sepsis.
http://www.ncbi.nlm.nih.gov/pubmed/25272245
There is no backing away from this now. A
prosecution is the only way
to open up all treatments for Lyme-post-sepsis victims,
and as a way to assure
there are fewer cases of vaccines-acquired Autism.
And you'll notice that neither ILADS nor the LDA have any clue
what they are talking about, be it the falsified testing for Lyme
(Dearborn) or why people are so sick,...
despite the NIH
admitting to these disease mechanisms many times.
ILADS and the LDA never cared about what was true, they only
cared about themselves.
One thing we learned from
the CIA torture report is
that human experimentation
like that, and like adapting
relapsing fever from its
natural soft bodied ticks to
hard bodied ticks on
Plum
Island, and
aerosolizing them - and
deploying this aerosol, as
is supposedly what's in the
not-so-secret Willy
Burgdorfer tape ("I
didn't tell you everything,"
UOS) take by Tim (Under the
8 Ball) -, was prosecuted at
Nurenberg, making this Lyme
cryme not just against the
Human Rights Declaration,
but a straight up war crime.
Eligible for HANGING.
The original source of
Lyme borrelia was
anserina, an African
bird Borreliosis, Plum
Island is where the usda.gov
just so happens to do those
kind of vector-pathogen
competence studies with
African diseases, and
Durland
Fish participated in it.
Fish also ordered me not to
"mess
with Yale and the Fed Govt,
you loon."
Why would Yale and the
Fed Govt be the same thing?
Obvious.
Durland Fish also works for
an
international-spy-for-hire
firm, "Off the Record
Research," which is a
subdivision of Kroll
Associates, one of the
participants in the
911-Thermate stunt.
Answers a lot of questions,
right?
Like why Dodd and Kennedy
would do nothing for us,
even though they knew what
goes on on Plum Island?
Explains all this "Lyme
legislation" rather than
a prosecution by the USDOJ,
right?
With 20-30 million Americans with CFS/ME/Fibro/GWI/Lyme --
Fungal-Viral Synergy or Post-Sepsis Syndrome, with the multiple and simultaneous fungal-, viral- and bacterial- infections and no immunity (like AIDS, but no HIV T cell virus) --,
A SITUATION CREATED BY IDSA and the CDC, the cowardly asshole dick president of IDSA thinks he can make US policy on Infectious Diseases and anti-microbial use (see next note below).
What they've done is set up the mixed-microbial-cauldrons (the 20+ million of us) needed for the next super-pandemic flu soup:
H5 avian and H9 swine influenza virus haemagglutinin structures: possible origin of influenza subtypes
"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."***
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC125880/?tool=pubmed
On top of all this stupidity and bullshit, the president of IDSA works for an insurance company, literally.
Have a look at what this stupid dick has to say (president of IDSA, Steve Calderwood, an employee of Partners.org,
an insurance company):
From the Finger in the Dyke Department....
To:
scalderwood@partners.org
Cc: bowie@mail.ubc.ca, mbpfeiff@poughkeepsiejournal.com, sr393d@nih.gov, AllenM1@mail.nih.gov, francis.collins@nih.gov, ras8@cdc.gov, olib@od.nih.gov, afauci@niaid.nih.gov, joseph.breen@nih.gov, michael.greenwood@yale.edu, richard.horton@lancet.com, astrid.james@lancet.com, spinlyme@yahoogroups.com, m.zecevic@lancet.com, ideditorial@lancet.com, Lawrence.Tabak@nih.gov, pgauwaerter@gmail.com, letters@syracuse.com, tina@tidmorecommunications.com, ljason@depaul.edu, lorikroger@pandoraorg.net, sso@depaul.edu, abrown57@depaul.edu,
beatcfsfms@bellsouth.net
Subject: PATH Act re antibiotic resistance, News (Partners.org, an insurance company in cahoots with IDSA)
Date: Dec 16, 2014 12:27 PM
Hi, Mr. Calderwood, thanks for this:
http://www.healio.com/infectious-disease/.... /path-act-introduced-in-senate-to-facilitate-antibiotic-drug-approval
Question:
How well has it worked in the past to deny early diagnosis and treatment of Lyme and post-sepsis syndrome (ME/CFS) in terms of preserving antibiotic efficacy? The NIH has said there are 4 million people in the USA with ME/CFS and 8 million with Fibromyalgia,... and God only knows how many with Chronic Neurologic Lyme (post-sepsis syndrome from exposure to fungal antigens like LYMErix shed by the spirochetes). Let's just guess 8 million, to be conservative. That makes 20 million or maybe 5-10% of the adult population disabled from Yale's and the CDC's "Lyme Disease" and ME/CFS' scam?
You are aware of the new data out on chronic herpesviruses and other chronic infections being the cause of these ongoing sub-immune and also autoimmune diseases cause by these toxic, moldish - like Lyme or moldy homes or mycoplasmally contaminated vaccines exposures -, right?
Here is the NIH describing what these diseases are:
THIS IS BY THE NIH, SAYING WHAT WE ARE SAYING (READ THE RELATED ARTICLE):
"Preventing Secondary Infections "Some people who survive sepsis can develop secondary infections days or even months later. A research team that included Richard Hotchkiss, Jonathan Green and Gregory Storch of Washington University School of Medicine in St. Louis suspected that this is because sepsis might cause lasting damage to the immune system. To test this hypothesis, the scientists compared viral activation in people with sepsis, other critically ill people and healthy individuals. The researchers looked for viruses like Epstein-Barr and herpes simplex that are often dormant in healthy people but can reactivate in those with suppressed immune systems. [Sepsis Has Long-Term Impact for Older Adults, Study Finds]
"Of the three study groups, people with sepsis had much higher levels of these viruses, suggesting reactivation due to compromised immune responses. Immune suppression could make it difficult to defend against the reactivated viruses as well as new infections like pneumonia. The team now plans to test whether immune-boosting drugs can prevent deaths in sepsis survivors. "This Inside Life Science article was provided to Live Science in cooperation with the National Institute of General Medical Sciences, part of the National Institutes of Health."
http://www.livescience.com/47387-sepsis-diagnosis-treatment-research-nigms.html )
If you have been following this "post-sepsis/chronic active herpes, et al" business, you will note that the NIH is all in favor of stopping sepsis early to prevent these long term, expensive outcomes, while IDSA still refuses to admit their participation in Yale's and the CDC's crimes (particularly over the Dearborn stunt and falsifying the OspA fungal vaccines outcomes).
And if you had a brain in your head, you would wonder if we, the walking cesspools of disease as described in this, finally, post-sepsis admission (NIH reported that it was LYMErix that was responsible for the chronic immunosuppression in chronic Lyme/ME/CFS with the chronic inflammation in the brain:
http://www.ncbi.nlm.nih.gov/pubmed/16783164 )....
... you would wonder if we, the walking cesspools of disease as described so well by the NIH, could possibly contract that next swine flu, for instance, and having no immunity-but-tons-of-viruses-and-otherbacteria/fungi... could be the next, say,
mixed-microbial cauldron, producing the next pandemic flu?
http://www.ncbi.nlm.nih.gov/pubmed/?term=china+swine+influenza+H9
When I called and emailed IDSA about 2 years ago asking if anyone at IDSA new what OspA was, no one replied. The CDC said they did not know. Yale said no one knew (LYMErix was Yale's patented OspA). The NIH said they did not. Francis Collins said he did not know. Anthony Fauci did not know. Paul Auwaerter did not know.
And such people as yourself, criminals or covering for criminals, and people who know ZERO about infectious diseases want to write policy?
Seriously?
Ain't that a bit like the 911 perps saying they'd like to donate a bag of cement to patch the holes in the World Trade Center?
Kathleen M. Dickson
http://www.actionlyme.org
These people make me completely crazy. Like Dick Cheney defending torture and destroying whole countries, ... for what? So Israel could have pipelines and an oil exporting/refining port on the Mediterranean?
It's the same delusion Hitler suffered: "My Will Makes It Fact."
That's America. "Our Will Be Done. Nevermind what happens to peoples in the past who try to rule the world but don't have the mental or physical capacity. Nevermind any details, facts, science, truth, or the mental disturbances that come with delusions of grandiosity.
WE are a new species. Homo sapiens amerisraelis."
"And with the hopes and powers will come dangers out of all proportion to the growth of man's intellect, to the strength of his character and to the
efficacy of his institutions. Once more the choice is offered between Blessings and Cursings. Never was the answer that will be given harder to foretell." - Winston Churchill, 1932,
Popular Mechanics
And we're not putting up with this bullshit any more from the CDC. So, join us at the Occupy Justice in Washington May 30- 4 July, 2015: ME/CFS, Gulf War Illness, Parents' Rights, Psych Rights,
Vaccines-Autism Parents, Racial Injustice Victims, etc. The CDC is going to be prosecuted over their relationship with BigPharma and Big Insurance. You heard about the CDC shredding documents in Maine, right? 'Pretty sure these documents revealed the CDC's liaison with insurance companies.
https://www.facebook.com/groups/OccupyUSDOJ/
And something's always being brought to my attention, right? Lately it is the ME/CFS people who don't understand the connection between Lyme-and-EBV(similars) and ME/CFS-and-EBV (similars) and "Post Sepsis Syndrome" -and-chronic-active-EBV(similars) and I have written at least 10 reports covering that in the last 5 weeks, including
the main ones. It's just something people are going to have to put the time into. After all, all along Lyme was called the New Great Imitator because it produced Lupus, MS, Cancer, ME/CFS... and now they've found it was EBV all along that was the Great Imitator, so read that report. It seems to be about fungal-viral synergy. I'll write another report, soon...
But the latest thing brought to my attention is how exactly Lyme Cryme is a
RICO & false claims act case. The essence of it was how Allen Steere falsified the testing, leaving OspA and B out of the diagnostic standard through pure research fraud. Why did he do this? Because of what was to happen after LYMErix came on the market. It was for a monopoly on testing and the Mayo Clinic stood to gain royalties for that RICO monopoly patent. Second to that, no one agreed with Steere's proposal at Dearborn that "Lyme was only the arthritis, HLA-linked hypersensitivity case." The consensus at the Dearborn consensus conference was that
Steere's proposal was only 15% accurate. That is why you are going to report your adverse events to the FDA due to the falsified case definition. The third thing is you have to have to prove a RICO case is intent to cause harm. Part of that aspect of
this RICO case
is that these criminals knew LYMErix caused a "multisystem disease" just like Chronic Lyme before they held the Dearborn event. We know for sure because the vaccine trials were underway by 1993 when
Barbour and Fish started trashing us. Use the Navigation bar at the left for the sequence of events in the crime.
No one at IDSociety.org understands any of this actual science. No one there explains any of this to you in a way you can fact check and verify independently. Talent and insight in science has a lot to do with intent.
Go here for more on this topic (with all the scientific references)
http://www.actionlyme.org/141212_MECFS_REVEALS_AUTISMVACCINES.htm
See how fungal antigen tolerance is not reversible, which means LYMErix Disease is not curable, here:
http://www.ncbi.nlm.nih.gov/pubmed/?term=TLR2+and+lipoprotein+and+tolerance
4 Dec 2014:
Greetings, again, Hi,...
This report is more for the "journalists" and the "lawyers" who just don't seem to get it, reminiscent of the people with CFIDS-brains (see the 3 Dec report below in the yellow box).
Originally posted in WaPo in Sept, 2014
"Lingering Effects of Lyme Disease"
http://www.thestarphoenix.com/health/lingering+effects+Lyme+disease/10210998/story.html
It should be entitled, the
"Lingering Effects of LYMErix, spoken- and written- about by the very same perps, is the reason the CDC vaccine patent-owning pimps and their whorey ALDF/IDSA perps falsified the case definition at Dearborn, Michigan in 1994"
It should be, "What is LYMErix? Why did it cause a disease identical to late Chronic Lyme Disease? What are they hiding?"
It's very clear that the CDC/ALDF crooks (leave IDSA out, we've just learned from an insider that IDSA are total morons, much like the State Health Departments) can't admit what chronic Lyme is because they know the vaccine caused it too. So what is the disease? It's post-sepsis syndrome (chronic active herpesviruses and other opportunistics), or like AIDS, caused by shed fungal OspA-like toxins.
The CDC also does not want to admit to the mechanisms of disease caused by Lyme and LYMErix because that same
fungal-induced immunosuppression data/mechanism reveals the cause of the Autism pandemic.
The criteria for a
bioweapon is also identical to post-sepsis syndrome - "overwhelm the immune system." Everyone is either
playing dumb or is dumb. Never was there such complete perfection in perpetrating the total absence of knowledge or even of questioning. Key to it was the inability of "doctors" to either read, or be trained in basic sciences like chemistry, taxonomy, biology, ... like asking what is this molecule, OspA? Why does it suppress antibody production? Why is it a "vaccine" because it is 100% specific to Lyme, but if you have this 100% specific marker, you can't have that disease?
On LYMErix-Disease, 1998, at the FDA, BEN LUFT:
"The point that I wanted to make in regard to the study is that there is very heavy dependence on serologic confirmation. And when we start thinking about the adverse events, ***
it was stated originally when we got the overview of the disease that the disease is really quite protean [means not limited to "bad knees- KMD].
And actually the adverse events are very similar to what the disease manifestations are.**** And if you start to, as I think Dr. Hall was eluding to -- if you start to kind of say well how often do you actually become sero positive, you can start to have a different take on when someone has an adverse event of whether it is disease specific or infection specific versus vaccine specific. And I think that that is an important issue that we have to deal with. I can only say from my own..."
http://www.fda.gov/ohrms/dockets/ac/98/transcpt/3422t1.rtf
Persing and Schoen's RICO strain and intended monopoly on post-LYMErix blood patent:
"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....
http://patft1.uspto.gov... 6045804
(?? Wait, what? You can’t tell the difference between late chronic Lyme and LYMErix Disease ???)
Dave Persing discussing why you should not use the native or original Osps as vaccines (and Robert Schoen would know this too):
"Accordingly, the methods of the invention provide a powerful and selective approach for modulating the innate immune response pathways in animals
without giving rise to the toxicities often associated with the native bacterial components that normally stimulate those pathways."
http://patft.uspto.gov/....6800613
1988, Raymond Dattwyler & immune-suppressing, seronegative Lyme; supernatant (lipid layer) of borrelia mash causes NK cell anergy or a blunted immune response.
Later Dattwyler tells the FDA Vaccine committee that the seronegative patients are the sickest (now we know why, as shown above where Lyme and LYMErix are the Great Detonators of the latent herpesviruses and expanded or cross tolerance to other than TLR2/1-agonist bearing antigens; in short, they’re double-fatigued and neurologically damaged):
http://actionlyme.org/DATTWYLER_NK_SUPPRESSION.htm
http://actionlyme.org/1988DATT_SUPRNATNT_FUNGAL2.gif
Transcript of June 1994 FDA Meeting Minutes, Dattwyler
http://actionlyme.org/141113_1994_DATTWYLERMINUTES.jpg
“So, individuals with a poor immune response tend to have worse disease.”
1990, Allen Steere reports that "NeuroLyme won't test positive;" uses Dattwyler and Volkman’s Seronegative Lyme T Cell Assay
http://www.actionlyme.org/STEERES_SERONEG_LYME_ASSAY.htm
Hence,
the RICO complaint filed with the USDOJ in July 2003, explains the crime very simply - so simply even a lawyer can follow it :
http://www.actionlyme.org/USDOJ_COMPLAINT_RICO.htm
The crooks changed the disease definition at Dearborn (1994, Michigan, as CDC conference) to suit the about-to-be-falsified vaccines outcomes, as I told the FDA in Jan 2001:
http://www.fda.gov/ohrms/dockets/ac/01/slides/3680s2_11.pdf
They threw out all the neurologic cases. You can see how Steere did this in Europe when he came up with the Dearborn proposal:
http://www.actionlyme.org/STEERE_IN_EUROPE.htm
Here is a fully referenced report on what the crooks did, especially on how Allen Steere left OspA and B out of the diagnostic standard for his later monopoly on blood, testing, vaccine candidates and HLA-bioweapons datapharming. You don't give people a bioweapon when too many or the residents or people will have the HLA-linked hypersensitivity response that identifies the initial Trojan Horse infection or antigen. In the case of Lyme, it was OspA that made these organisms more invasive (OspA hijacks plasminogen allowing greater tissue penetration) and detonators of EBV/similar herpesviruses. OspA was the Greatest Detonator.
http://www.actionlyme.org/PLUMSTUPID.htm
CDC's lies at Dearborn, and Steere traveling to Europe and Russia, were meant to fool people wprldwide into thinking "Lyme Disease" was a different disease than Relapsing Fever. They were counting on ignorance of spirochetal diseases. It was a competency test for all American "doctors," essentially testing their ability to you know, go on the internet or the original MedLine (now PubMed) and read the literature.
For non-Americans reading this, you can see that the entire USA has dementia. "Doctors," "journalists," the "lawyers," at the USDOJ, State "Health Departments," the FDA, ... One should wonder more about
that, really, than OspA-Disease.
How is it that no one says anything true, and so few even know true things are
available to be said?
141113
The Lyme Vaccine Scam, Facebook "All
Abused Groups Occupy
the USDOJ" Group version
You need to study this information in order to file your Adverse Event (AE) to the Dearborn Lyme case definition to the Food and Drug Administration. Hopefully, when this cryme is prosecuted you can be compensated by the USDOJ in a similar manner to the other Vaccine Injury Compensation cases the USDOJ handles.
THAT is our ultimate goal.
Here is the FDA's AE reporting form re bogus medical testing:
https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=consumer.reporting1
You need to study this report (in this yellow box) as well as the
Primers Shell Game in order to see why you only ever needed antibody band 41 and the triad of Neurological, Cognitive, and Musculoskeletal signs after ruling out cancer, etc. for a diagnosis of borreliosis.
And if you already know about this cryme and are still wondering why the US "government" is so friggin stupid and incompetent, don't. They just are. It goes with the territory of government-employee-cults and government-employee union-cults. Read about cults - they just protect themselves, their retirement funds and investments, and each other, you know, like cops.
First let’s examine the following 7
compelling reports from the “20
Reports that show the
Lyme-and-LYMErix-Post-Sepsis Cover-up
has to do with Hiding Autism Brain
Damage from Vaccines (http://www.actionlyme.org/POST_LYME_SEPSIS_2014_SUMMER.htm
);”
These next 7 reports are basically by
the NIH, especially the NINDS’s
Lyme-And-MS group (Martin and Marques)
which confirm and endorse the idea that
the Lyme vaccine (OspA, which is a basic
Pam3Cys molecule type and a
TLR2/1-agonist) gave people the same New
Great Imitator and especially Multiple
Sclerosis outcomes as “Chronic Lyme” or
Late Neurologic Lyme;
These reports are from the NIH, IDSA,
the US ARMY, Ft. Detrick, the National
Cancer Institute (NCI), and Washington
University, St. Louis, MO (wustl.edu)
about post-sepsis and the reactivation
of the herpesviruses, et al (like AIDS)
from exposure to Lyme. [This is how it
appears anyway. If it is some other
virus like a mouse herpesvirus from a
tick bite, we don’t have that data yet.
It’s something like that, that obviously
no one at the Uncle Sam “government”
seems too worried about, therefore, it
must be a common thing like from the
herpes family. There are easily 20
million of us with a CFIDS, Lyme, or
Fibromyalgia etc junk-science diagnosis
in America alone (NIH’s own published
stats) and no one’s panicking like we
got a new, slow Marburg, or contagious
scrapie, or a new HIV or whatever going
on.]
==================== The 7 Reports, 6 of
NIH’s plus wustl.edu’s =================
1989 (this is in IDSA's own
journal): NCI and US Army Ft Detrick Pathologist
Paul Duray on the CSF cells looking like
"Epstein-Barr-like transformed cells" in
IDSA's 1989 Reviews Supplement on
Spirochetal Diseases: Rev Infect Dis. 1989 Sep-Oct;11 Suppl
6:S1487-93. Clinical pathologic correlations
of Lyme disease.
"Immature B cells can also be seen in
the spinal fluid. These cells can appear
quite atypical- not unlike those of
transformed or neoplastic lymphocytes."
--
http://www.ncbi.nlm.nih.gov/pubmed/2814170
Full Text:
http://www.actionlyme.org/IDSA_CLINIPATH_DURAY.htm
=====
1992:
Duray again in 1992, in Steve Schutzer's
review of the 1992 Cold Spring Harbor
Conference on Lyme:
"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. - book.
=====
2006:
The NIH (NINDS’s MS-Lyme Group) group
that discovered that *** OspA *** was
the cause of the MS/New Great Imitator
outcome of Lyme reporting in the New
York Times in the summer of 2013 (Martin
and Marques, 2006); this article says these OspA like
antigens constantly shed by Borreliae
cause immunosuppression in the humoral
immune system, but apparently a chronic
inflammatory state in the central
nervous system:
"Borrelia burgdorferi Induces TLR1
and TLR2 in human microglia and
peripheral blood monocytes but
differentially regulates HLA-class II
expression."
http://www.ncbi.nlm.nih.gov/pubmed/16783164
and this report means you might not even
have anti-flagellar antibodies
(flagellin is a TLR5-agonist) after
being exposed to shed fungal OspA like
antigens (TLR2/1-agonists):
"Borrelia burgdorferi
lipoprotein-mediated TLR2 stimulation
causes the down-regulation of TLR5 in
human monocytes.
http://www.ncbi.nlm.nih.gov/pubmed/16479520
2013 - Same NIH MS-Lyme Group as
above, Martin and Marques:
"When Lyme Disease Lasts and
Lasts" – Jane Brody
"Complicating the picture is the fact
that some people with PTLDS symptoms
apparently never had Lyme disease in the
first place, Dr. Marques said in an
interview. There are other infectious
organisms — Epstein-Barr virus, for
example — that can produce similar
symptoms and may be the real culprits."
http://well.blogs.nytimes.com/2013/07/08/when-lyme-disease-lasts-and-lasts/
=====
2014:
Wustl.edu discovers that sepsis is like
Lyme, in that the survivors of it are
likely to have survived via the
immunosuppression (TLR2-agonist
tolerance/Endotoxin tolerance), but the
result is the reactivation of latent
viruses:
"Dormant viruses re-emerge in patients
with lingering sepsis, signaling immune
suppression"
"Patients with lingering sepsis had
markedly higher levels of viruses
detectable in the blood, compared with
the healthy controls and critically ill
patients without sepsis. Among the
sepsis patients, for example, the
researchers found that 53 percent had
Epstein-Barr virus, 24 percent had
cytomegalovirus, 14 percent had
herpes-simplex virus, and 10 percent had
human herpes simplex virus-7.
"These viruses generally don’t lead to
significant illness in people who are
healthy but can cause problems in
patients who are immune-suppressed. "
http://news.wustl.edu/news/Pages/27015.aspx
FULL JOURNAL REPORT, snippet…
Reactivation of Multiple Viruses in
Patients with Sepsis
“Sepsis is the host's non-resolving
inflammatory response to infection that
leads to organ dysfunction [1], [2]. A
current controversial hypothesis
postulates that if sepsis pursues a
protracted course, it progresses from an
initial primarily hyper-inflammatory
phase to a predominantly
immunosuppressive state [3]–[7].
Experimental therapeutic approaches in
sepsis have almost exclusively focused
on blocking early inflammation or
host-pathogen interaction and failed
[8]–[10]. Recently, immuno-adjuvant
therapies that boost host immunity,
e.g., GM-CSF and interferon-γ, have been
successful in small clinical trials
thereby supporting the concept that
reversing immunosuppression in sepsis is
a plausible strategy to improve outcome
[11], [12]. However, several issues have
limited this approach including lack of
consensus that immunosuppression is a
clinically important phenomenon [5],
[6], [13]. Also, difficulty in
identifying patients with impaired
immunity as well as determining optimal
timing for administration pose
significant challenges to pursuing this
approach [14]. While immuno-adjuvant
therapies might improve sepsis survival
if administered during the later
immunosuppressive phase, these agents
might worsen outcome if given during the
early hyper-inflammatory phase [4],
[14]. Thus, a means to distinguish these
two contrasting phases of sepsis is
needed not only to verify the hypothesis
that sepsis progresses to an
immunosuppressive state but also to
guide use of potential agents which
boost immunity.
“Latent viruses such as cytomegalovirus
are normally held in abeyance by
cellular and immune surveillance
mechanisms which if impaired, for
example by immunosuppressive
medications, often result in viral
reactivation, replication, and
virally-mediated tissue injury
[15]–[20]. Sepsis impairs innate and
adaptive immunity by multiple mechanisms
including apoptosis-induced depletion of
immune effector cells and induction of
T-cell exhaustion thereby possibly
predisposing to viral reactivation and
dissemination [21]–[23]. …”
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0098819
=====
2014, Here the NIH confirms that
they agree that post-sepsis, like wustl
above describes, matches their own
observations of what happens as a result
of Chronic Lyme (EBV reactivated; ie,
that being generally accepted as the
main driver of MS and Lupus):
NEW, by the NIH: "Surviving
Sepsis: Detection and Treatment
Advances"
By Carolyn Beans for the National
Institutes of Health | August 18, 2014
08:43am ET
http://www.livescience.com/47387-sepsis-diagnosis-treatment-research-nigms.html
"Preventing Secondary Infections
"Some people who survive sepsis can
develop secondary infections days or
even months later. A research team that
included Richard Hotchkiss, Jonathan
Green and Gregory Storch of Washington
University School of Medicine in St.
Louis suspected that this is because
sepsis might cause lasting damage to the
immune system. To test this hypothesis,
the scientists compared viral activation
in people with sepsis, other critically
ill people and healthy individuals. The
researchers looked for viruses like
Epstein-Barr and herpes simplex that are
often dormant in healthy people but can
reactivate in those with suppressed
immune systems. [Sepsis Has Long-Term
Impact for Older Adults, Study Finds]"
======================== End 7
Reports =================
So, that data, those 7 reports are hard
to argue with, and they also point to someone else
potentially
hypothesizing on what the treatment is
for post-Lyme-post-sepsis, like wustl or
the NIH and not me ☺
Importantly, everyone should go to
PubMed and look at the data on medical
school students and astronauts and see
how the stress hormone cortisol is
well-known to be activating mono or
Epstein-Barr. If you are an astronaut or
a medical school student or overworked
resident, your chronic fatiguing disease
is allowed to be real and not
somatoformically produced with your
magical brain ☺
Let's side step to show that LYMErix or OspA and OspA-like antigens constantly shed by borrelia in an immune-evasion-come-antigenic variation mechanism that can leave the immune system "completely overwhelmed," even if a mammal was infected with just one spirochete (see the
Primers Shell Game). We all
have to know what these fungal OspA etc antigens
are, that are shed by borreliae such that we know the pathology it causes. OspA is or Pam3Cys or tripalmitoyl cysteine molecular type (see that this is confirmed by Ray Dattwyler in the "20 Reports that show the link between Lyme Cryme and Autism"). We have to know what these antigens
are in order to know what they do (structure predicts function). So, if you can't determine the structure, you can go by their function or biochemical properties and in this case, Pam3Cys type antigens are managed by TLR2/1 and that means they are fungal. So what happens when the body is hyperexposed to fungal antigens? In most cases, immunosuppression as shown by Justin Radolf and Clifford V. Harding,
here, in the Plum Island chapter of Cryme Disease. They cause the HLA molecules to fail to present antigen and thus, no more antibodies are made. This is called tolerance. Use PubMed to examine further what people like Medvedev and Harding have to say about what happens to the immune system after chronic exposure to fungal antigens. Note in parallel, the data on the
NO-TB-VACCINES, duh. The Lyme criminals were too stupid to even try to discover if there had been any successful lipoprotein vaccines in the past.
http://www3.interscience.wiley.com/cgi-bin/fulltext/120763430/PDFSTART
Use
141114_FUNGAL_FAILED_VACCINES.htm for about 12 reports that show you can't use this molecule type for a vaccine and that the Lyme criminals never gave a shit what it was or if it had been tried before as a vaccine.
Returning
to what happened with LYMErix - the
vaccine that gave people the very
disease the ALDF-come-IDSA now deny
exists and wrote out of the Dearborn
serodiagnostic criteria specifically
because of that ☺
[Repeat: The definitions of Lyme
borreliosis excluded from the Dearborn
case definition (falsified by Allen
Steere in Europe in 1992) are the very
ones caused by OspA vaccination. You
just saw how in the above 7 reports, and
there is much more data on that
available on PubMed about the
pathologies caused by chronic exposure
to fungal antigens including cancer, and
the similar outcomes of worse disease
and immunosuppression from other
experiments with fungal vaccines of this
same TLR2/1 agonist type such as all the
failed Tuberculosis vaccines ☺ ]
We back up to what was the original case
definition serology the CDC published in
1990 such that we know it was falsified
at Dearborn, and this data jives with
what we know from the 7 reports by the
NIH above:
1986, Allen Steere says:
“Antigens of Borrelia burgdorferi
recognized during Lyme disease.
Appearance of a new immunoglobulin M
response and expansion of the
immunoglobulin G response late in the
illness.
“Using immunoblots, we identified
proteins of Borrelia burgdorferi bound
by IgM and IgG antibodies during Lyme
disease. In 12 patients with early
disease alone, both the IgM and IgG
responses were restricted primarily to a
41-kD antigen. This limited response
disappeared within several months. In
contrast, among six patients with
prolonged illness, the IgM response to
the 41-kD protein sometimes persisted
for months to years, and late in the
illness during arthritis, a new IgM
response sometimes developed to a 34-kD
component of the organism. The IgG
response in these patients appeared in a
characteristic sequential pattern over
months to years to as many as 11
spirochetal antigens. The appearance of
a new IgM response and the expansion of
the IgG response late in the illness,
and the lack of such responses in
patients with early disease alone,
suggest that B. burgdorferi remains
alive throughout the illness.”
http://www.ncbi.nlm.nih.gov/pubmed/3531237
1990, CDC publishes this case
definition:
http://www.actionlyme.org/CDC_DOCUMENTS_1990.htm
The 1990 case definition standard
(above) was basically based on the 1986
report (above that) by Allen Steere,
which was that you have to merely show a
person has a Relapsing Fever infection,
with the “new IgM and changing bands
emerging over time seen in repeat or
serial Western Blots.” That meant,
according to Allen Steere, “the bug is
still alive.” New, IgM type bands meant
the bug was still alive and you have not
killed it with antibiotics. Steere also
wrote in that same report that really
all you need is band 41 to diagnose
Lyme, just rule out Syphilis. That is
important to remember. You only need
band 41or the anti-flagellar antibody
and the triad of symptoms to diagnose
Lyme. The US patent 5,618,533 specific
recombinant fragment of Borrelia
burgdorferi flagellin of Yale’s is a
better test and is an actual
FDA-validation according to their
criteria (as
shown in the Primers Shell Game chapter
of Cryme Disease).
I personally – and I am not a doctor –
recommend everyone rule out all blood
cancers since the symptoms of Chronic
Lymphocytic Leukemia for example are
identical to Chronic Lyme or MS, not to
mention the fact that Lyme and LYMErix
both are known to cause cancer as are
the mycoplasma to which chronic late
neurologic Lyme victims now are
tolerized to (fungal).
And what is the current, 1994 CDC
Dearborn case definition?
http://www.cdc.gov/mmwr/preview/mmwrhtml/00038469.htm
“It was recommended that an IgM
immunoblot be considered positive if two
of the following three bands are
present: 24 kDa (OspC) * , 39 kDa
(BmpA), and 41 kDa (Fla) (1). “It was further recommended that an that
IgG immunoblot be considered positive if
five of the following 10 bands are
present: 18 kDa, 21 kDa (OspC) *, 28
kDa, 30 kDa, 39 kDa (BmpA), 41 kDa
(Fla), 45 kDa, 58 kDa (not GroEL), 66
kDa, and 93 kDa (2).”
That is very different criteria from the
first criteria. First you only needed
band 41, or test using repeat Western
Blots to look for new IgM bands since
Lyme is a relapsing fever organism, and
the nature of the relapse is antigenic
variation (producing new antigen and
thus new IgM bands will be produced in a
human), … and now all of a sudden you
have to have all these bands showing up
at once (indicative only of the
hypersensitivity, HLA-linked response)
and just ignore IgM bands, basically.
You can assume that the reason the IDSA/ALDF/CDC/Yale Lyme criminals do not want anyone treated for Lyme is because late in the disease it’s really about fungal antigen tolerance and cross tolerance, as well as reactivated herpesviruses. They don’t want Lyme victims being treated with antibiotics because that might help transfer antibiotic resistance genes between all the
OTHER infections we have, like fungal, like Tuberculosis, Chlamydia, Candida, and whatever else … for which we are now carriers, … and you don’t treat the herpesviruses and subsequent B cell mutations with antibiotics.
IDSociety.org likes to say what diseases are not, but they never say what diseases are. It’s pretty strange but we got no Einsteins in that bunch. IDSA be like… an incomplete sentence. They’d be good screenwriters for American soap operas. The rest of MD-America does not even notice that IDSA’s is one funny script, even after these crooks lost their “vaccine,”
Senator Richard Blumenthal (a former USDOJ prosecutor) sued them for Anti-Trust, and Edward McSweegan became America’s infamous NIH employee and America’s one and only
“Man With No Work.”
So, Follow: First, Lyme was a regular
old Relapsing Fever organism and a “New
Great Imitator!” Later, it at the same
time the crooks had a vaccine candidate
in early phase trials, become nothing
and a non-disease. We were then about to
get “a vaccine for a disease that causes
no illness.” That is still the current
position of Yale, CDC, IDSA, and the
ALDF/EUCALB. “Lyme patients are not
sick, and OspA was a vaccine.” IDSA
still makes that claim today. No one in
the AMA or Mass Medical Society or NEJM
or any other association or society of
“doctors” even blinks at these
contradictory notions. To me it looks
like a case of Kraepelinian split-brain.
We should wonder what other evidence
there might be that medical school is a
cult that produces schizophrenia.
Here is basically of
the series of events that occurred in
the process of redefining Lyme as a
non-disease to pass off a bogus vaccine:
1986, Edward McSweegan trashes
U.S. Navy for $$$ for his psycho buddies
at the ALDF.com cabal in a letter to
Senator Barry Goldwater. See the Navy’s
furious response. Sweeg thinks there can
be a vaccine for Relapsing Fever,
confirming the paraphysical theory that
arrogance is the seed corn or germinal
element in true, genuine stupidity
and/or the development of a criminal
mind.
http://www.actionlyme.org/GOLDWATER_LETTER.htm
1988, Raymond Dattwyler &
immune-suppressing, seronegative Lyme;
supernatant (lipid layer) of borrelia
mash causes NK cell anergy or a blunted
immune response. Later Dattwyler tells
the FDA Vaccine committee that the
seronegative patients are the sickest
(now we know why, as shown above where
Lyme and LYMErix are the Great
Detonators of the latent herpesviruses
and expanded or cross tolerance to other
than TLR2/1-agonist bearing antigens; in
short, they’re double-fatigued and
neurologically damaged):
http://actionlyme.org/DATTWYLER_NK_SUPPRESSION.htm
1990, CDC: "Diagnose Lyme as if
it was Relapsing Fever."
http://www.actionlyme.org/CDC_DOCUMENTS_1990.htm
1990, Allen Steere reports that "NeuroLyme
won't test positive," uses Dattwyler and
Volkman’s Seronegative Lyme T Cell Assay
http://www.actionlyme.org/STEERES_SERONEG_LYME_ASSAY.htm
http://www.actionlyme.org/DATTWYLER_NK_SUPPRESSION.htm
CHRONIC NEUROLOGIC MANIFESTATIONS
OF LYME DISEASE (NEJM, Nov 1990)
http://www.nejm.org/doi/pdf/10.1056/NEJM199011223232102
Says Steere:
“If the patient was seronegative
according to these methods, the serum
was further tested by immunoblotting
(25) and peripheral blood mononuclear
cells were tested for reactivity with
borrelial antigens by proliferative
assay.(26)"
And what was reference number 26?
Pretty amazing, huh?
1990, ALDF.com founded, self-
proclaimed “entrepreneurial quartet” is
McSweegan, Fish, Wormser and Connolly.
(You will want to look at who are their
sponsors and on their board, seriously.)
http://www.actionlyme.org/CONNOLLY_FISH_WEINSTEIN.htm
http://www.actionlyme.org/ALDF_BOARD.htm
1992, CDC officer Allen Steere
falsifies testing in Europe:
http://www.actionlyme.org/STEERE_IN_EUROPE.htm
The PubMed links to those 2 reports – no
full text available, that is why I got
them out of the Yale Medical Library in
2002 and scanned them in are: “Antibody responses to the three
genomic groups of Borrelia burgdorferi
in European Lyme borreliosis.”
http://www.ncbi.nlm.nih.gov/pubmed/8106763
“Western blotting in the
serodiagnosis of Lyme disease.”
http://www.ncbi.nlm.nih.gov/pubmed/8380611
Of those 2 reports of Steere’s
shenanigans in Europe, only the second
one is made a part of CDC’s Dearborn
booklet but the first one is where you
can see how he falsified the testing.
Steere in Europe used bogus high passage
strains that drop plasmids helping leave
OspA and B out of the diagnostic
standard (by using the recombinant
protein end only- you need the lipids to
be immune stimulatory) for his later
monopoly on post-LYMErix-approval North
America, with Corixa, Yale’s L2
Diagnostics and Imugen, officially
listed on the Securities and Exchange
Commission (SEC) as “partners” in
sharing licensing of the RICO Monopoly
patent with the strain of Borrelia that
had dropped an OspA-B plasmid US Patent
6,045,804 (we will come to this later,
it is critical to the whole scam and
shows the intent of their entire
enterprise);
Here is a transcript of what is in the
first report on exactly how Steere
defrauded Uncle Sam:
“The group 1 strain of B. burgdorferi,
G39/40, used in this study and in the
previous study of US patients was
isolated from an Ixodes damini tick in
Guilford, Connecticut [21]. The group 2
strain, FRG [Federal Republic of
Germany], was isolated from Ixodes
ricinus near Cologne [22]. The group 3
strain, IP3, was isolated from Ixodes
persulcatus near Leningrad [23]. All
three strains used in this study were
high passage isolates, which were
classified by Richard Marconi (Rocky
Mountain Laboratory, Hamilton, MT) using
16S ribosomal RNA sequence determination
as described [11, 24]. The recombinant
preparations of OspA and OspB used in
this study were purified maltose-
binding protein-Osp fusion proteins
derived from group 1 strain B31 [25].
The fusion proteins contained the
full-length OspA or OspB sequence
without the lipid moiety or the signal
sequence -"
Here is what it says in the
Persing/Schoen/Steere or Imugen RICO
Monopoly patent, that shows the
intended monopoly:
“Method for detecting B.
burgdorferi infection”
"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
or diagnostic applications where only
part of the subject population has been
vaccinated or where the vaccination
status of the population is unknown. "
http://patft1.uspto.gov/...6045804
The monopoly on
post-LYMErix-FDA-approval testing for
all vector borne diseases in America and
Canada was their stated intention.
Once LYMErix was on the market, you had
to use a strain of borrelia that did not
have the vaccine antigens in them,
because you never test for vaccine
efficacy with the very same antigen as
the vaccine antigen (you would not know
if the person has the actual virus or
whatever, or that antibody came from the
vaccine). So, their monopoly depended on
LYMErix being on the market. That
way, Corixa, L2 Diagnostics and Imugen
would be the only labs in the country
licensed to use this RICO strain.
They, at the same time would have access
to all the human blood to pharm all
sorts of DNA data from humans as well as
any new and emerging infectious
diseases... meaning even more vaccine
patents.
So, they falsified the case definition
to leave out neurologic Lyme cases, and
they left OspA and B out for a later
monopoly on testing and future patents.
And there, you just read that in a
patent developed by Schoen and Persing
in 1995.
1992, CDC staff, Barbara Johnson
and Joe Piesman, own patents with
SmithKline that show 2 kinds of Lyme,
HLA-linked and non-HLA-linked antigens:
http://www.google.com/patents/CA2135800A1?cl=en
“Summary of the Invention
“In one aspect, the invention provides isolated --B. burgdorferi antigens which are regulated and differentiated by growth of the B. burdorferi in a tick vector. Novel antigens of the invention are listed below in Table I.
“Certain of these antigens are characterized as being B. burgdorferi B31 strain specific and major histocompatibility complex (MHC) nonrestricted. Certain other of these antigens are characterized as being MHC-restricted.”
So, what the hell is the CDC talking
about ”MHC-restricted and MHC
non-restricted?” What we know that to
mean is for instance, classic autoimmune
diseases tend to be MHC-restricted, or
the antigens, due to intermolecular
forces, bind in the HLA groove too
strongly causing a hypersensitivity
response. That is the new definition
Steere claimed in these 1992 reports and
at the CDC’s 1994 Dearborn conference. The very re-definition of “Lyme Disease”
at Dearborn became “HLA-restricted,”
“just the arthritis,”
“too-many-antibodies-HLA-associated
response.” In short, Steere and the CDC
claim Lyme Disease is just an
HLA-restricted disease. Here in their 5
1992 patents with SmithKline, the CDC
mentions the other outcome? The no- or
fewer antibody result?
1993, Barbour and Fish slam
Neurologic Lyme victims: The SOCIAL Phenomenon of Lyme
Disease or what the hell ever…
where they admit Phase I and Phase II
trials of OspA vaccines are underway.
Therefore, as is shown in the Persing
RICO Monopoly patent from 1995 shown and
linked above (US 6,045,804), they
already knew the OspA vaccines were
causing a disease indistinguishable from
vaccine failure, or CHRONIC LYME:
http://actionlyme.org/BarbourFishpdf.pdf
Compare the 2 kinds of Lyme in the RICO
complaint filed with the USDOJ in July
2003– compare the blots. On the left is
neurological Lyme (the sickest,
according to Ray Dattwyler) and on the
right is the HLA-linked outcomes of
arthritis and acrodermatitis:
http://www.actionlyme.org/USDOJ_COMPLAINT_RICO.htm
So, these assholes left out the
left-sided, neurological outcomes in
their Dearborn scam. The whole point of
the redefinition of Lyme at Dearborn was
to narrow it to just the HLA-linked
hypersensitivity cases. This is how and
why they get away with perjury. When the
IDSA/Yale Lyme crooks say “Lyme Disease”
that means HLA-linked arthritis AND NO
OTHER SYMPTOMS.
Here next, in 2005, Klempner and Wormser
re-revealed that “Lyme Disease” is just
one thing. There are 2 things, and the
controversial thing really does not have
a name right now, but “Lyme Disease” is
JUST a bad knee and no other illness
signs. THAT is the definition. It’s a
legal one and a criminal one, and based
on bullshit and no consensus, but here
is what it is again (2005):
“A Case-Control Study to Examine
HLA Haplotype Associations in Patients
with Posttreatment Chronic Lyme Disease”
People with ONLY the HLA-linked
arthritis (the falsified Dearborn case
definition)…“Patients generally feel
well aside from their arthritis
symptoms,” Say Wormser and Klempner.
Pretty amazing right? That the people
with the falsified Dearborn case
definition of “only an HLA-linked
arthritis in a knee” have only an
HLA-linked arthritis in a knee and no
other symptoms?
http://jid.oxfordjournals.org/content/192/6/1010.full
I love it when that happens ☺ You falsify the case definition and say
“ONLY the HLA-linked hypersensitivity
response can be a ‘case’ of ‘Lyme
Disease,’" and then 11 years later say,
“Oh, how amazing for us to find only the
HLA-linked case definition is HLA-linked
and is only a bad knee. Maybe someone
can promote me to the head of a CDC
bioweapons lab in Boston on accountta my
astuteness.”
1994, June FDA LYMErix Meeting
(note that June precedes October, so the
FDA never approved of the Dearborn
method, not to mention it was research
fraud and not a consensus):
http://www.actionlyme.org/1994_FDA_MEETING_LYMERIX.htm
Transcript of June 1994 FDA Meeting
Minutes:
“So, individuals with a poor immune
response tend to have worse disease.”
We know why now ☺ Borrelial fungal
antigens cause immunosuppression and… a
classic “post-sepsis” like result with
chronic active EBV, et al.
The CDC recently made a big ta-do over
the Blumenthal et al letter to the
Office of Policy and Management, where
the Senators are forcing the FDA to do
their jobs and assure that the testing
for Lyme is validated according to their
own FDA rules (See the Primers Shell
Game for more on that). The CDC is
trying to say the Dearborn method was
FDA validated.
False. The FDA had nothing to do with
the Dearborn stunt.
1994, CDC's invitation to
participate in Dearborn .pdf
Labs were invited, they said the Steere
proposal sucked, CDC blew off these labs
recommendations:
http://www.actionlyme.org/DEARBORNINVITATION.pdf
1994, October CDC's Dearborn
Booklet .pdf
http://www.actionlyme.org/DEARBORN_PDF.pdf
Dearborn, Who Said What?
http://www.actionlyme.org/DEARBORN_WHO_SAID_WHAT.htm
1) Gary Wormser at New York Medical
College reports that Steere’s Dearborn
proposal method detected 9/59 of IgG
cases (which, most very sick people
being detected too late are obviously
not going to have this Early Lyme
profile, especially considering Steere’s
Late Lyme Arthritis Dearborn falsified
definition was intended to be for early
Lyme, regardless of his lab shenanigans
with the strains and the phony
recombinant OspA and B in Europe): Serodiagnosis in Early Lyme Disease
So, Wormser says only 9 of the 59 meet
Steere’s Late Lyme Arthritis case
definition. That’s 15% accurate.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC266355/pdf/jcm00024-0026.pdf
2) Igenex- Steere’s IgG detected 8% of
the cases
3) Imugen – Steere’s method detected 14%
of the cases:
4) Wisconsin - Steere’s method was 15%
accurate
5) UCONN- Larry Zemel was referring to
Lyme as comparable to juvenile
rheumatoid arthritis. Recommended adding
band 50 for children’s blots.
6) Roche—28% were positive for 5 of 10
Steere IgG bands.
7) Wadsworth – had some different
scoring system. Did not report on
accuracy of Steere
8) Ontario Ministry of Health
9) Lutheran Hospital— 22 % were accurate
by Steere’s IgG
10) MarDx Labs – recommended adding
bands 31 and 34, but were given CDC
positive arthritis positive blood to
falsely qualify their test strips.
Theirs were used in both vaccine trials.
MarDx was later sold to an Irish
company, Trinity Biotech, Dublin, so
presumably all they know about the crime
was taken out of the country.
11) CDC Atlanta – talked about mice, not
humans. The mouse criteria was 2 out of
three from OspC, 16 kD, 17.9 kD, for the
mice. Wonderful. Everyone is concerned
about Western Blotting the poor little
mice. Such a tragedy that they have to
run around sick. We read about this
tragedy at least once a week in the
New York Times. People say
each other all the time, “Oh, what
wonderful weather we’re having, too bad
the mice are too sick with Lyme Disease
to enjoy it. “ You see those little
collection tins at all the supermarket
check-outs: “Please Donate One Dollar
for the Poor Mice with Lyme Disease!”
So, we got this standard anyway, even
though none of the invited participants
agreed - not by a long shot. See
the Primers Shell Game reports here or
at this link:
http://www.actionlyme.org/PRIMERSHELLGAME.htm
for an explanation of how VALID testing
is performed according to the FDA rules
and how Yale knows all about how to
validate a method, validated one (Bb
specific flagellar antigen) and patented
it (US 5,618,533). So that's all
obvious criminal fraud.
Who was involved with approving the
bogus Dearborn method at Dearborn when
all the invited labs said it sucked??
Why, none other than the CDC vaccine
patent owners and all the scammers
you see here:
http://www.actionlyme.org/Dearborn_Who_Approved.htm
Alan Barbour, Edward McSweegan, Allen
Steere. Arthur Weinstein, "The CDC Lyme
Disease Group" (Barbara Johnson)
Kind of amazing. The same people
involved in the OspA vaccines scam were
involved in falsifying the testing.
==================
Igenex, Harris’ view of the Dearborn
event .pdf published in the Lyme Disease
Foundation’s journal:
http://www.actionlyme.org/HARRIS_IGENEX_DEARBORN.pdf
1998 FDA Meeting where Luft says
LYMErix produces a multi-system disease
just like chronic Lyme:
http://www.fda.gov/ohrms/dockets/ac/98/transcpt/3422t1.rtf
BEN LUFT: "The point that I wanted to
make in regard to the study is that
there is very heavy dependence on
serologic confirmation. And when we
start thinking about the adverse events,
*** it was stated originally when we got
the overview of the disease that the
disease is really quite protean [means
not limited to "bad knees”- KMD]. And
actually the adverse events are very
similar to what the disease
manifestations are.**** And if you start
to, as I think Dr. Hall was eluding to
-- if you start to kind of say well how
often do you actually become sero
positive, you can start to have a
different take on when someone has an
adverse event of whether it is disease
specific or infection specific versus
vaccine specific. And I think that that
is an important issue that we have to
deal with. I can only say from my own
..."
Evidence
Lyme criminals knew LYMErix produced the
same "multisystem disease" as "Chronic
Lyme"
1) Ben Luft said it at the 1998
FDA meeting (above), 2) Dave Persing
said it in his RICO patent (above),
3) Fish and Barbour started
trashing us with their “Social Aspects”
bullshit in 1993 (above) paving the way,
claiming we’re all nuts and hysterics
for when the vaccine produced the same
result so they’d have a ready made
derogatory slander/libel answer and
propaganda,…
... 4) Dave Persing and his company
Corixa wanted to sell vaccine
adjuvants but they had to drop OspA as a
candidate adjuvant because, he said… in
another patent (applied for May, 2001
while LYMErix was still on the market,
harming people and he never said
anything to the FDA about it)… “Prophylactic and therapeutic treatment
of infectious and other diseases with
mono- and disaccharide-based compounds” "Accordingly, the methods of the
invention provide a powerful and
selective approach for modulating the
innate immune response pathways in
animals without giving rise to the
toxicities often associated with the
native bacterial components that
normally stimulate those pathways."
http://patft.uspto.gov/...
6,800,613
5) In 1998 Robert Schoen
(involved in developing the RICO
monopoly patent - US 6,045,804 - with
Dave Persing, 1995) wrote this, once
again, paving the way for when the
vaccine came on the market and caused
the same systemic, seronegative disease
damage…
says in 1998 not to test LYMErix victims and minimizes their symptoms knowing chronic Lyme is identical to what Schoen says is "nonspecific" because the exact reverse statement is in the Corixa-RICO patent "multisystem complaints characteristic of late Lyme", This is that textbook:
http://www.amazon.com/Lyme-Disease-Key-Diseases-Series/dp/0943126584....
http://www.actionlyme.org/SCHOEN_INSTRUCTING_DOCS_TO_BLOW_OFF_LYMERIX_INJUREES.htm
========
Next, how
these crooks lied about their vaccine
results, and what happened after LYMErix
was approved and on the market.
The 1998 Vaccines Reports (ImmuLyme and LYMErix):
LYMErix results (76% "safe and effective"):
http://content.nejm.org/cgi/content/abstract/339/4/209
ImmuLyme results (92% "safe and effective"):
http://content.nejm.org/cgi/content/abstract/339/4/216
From the LYMErix trial, "categories of
outcomes:"
http://content.nejm.org/cgi/content-nw/full/339/4/209/T1
Here the crooks
claim
"we can't read our OspA vaccine results" reports,
which means the lied in their OspA vaccine safety and
efficacy reports, since they both claimed to be using the
Dearborn method and MarDx's Western Blot test strips:
1)
SCHOEN and PERSING, with JOHN ANDERSON,1996
- the RICO report:
http://jcm.asm.org/cgi/reprint/35/1/233?view=long&pmid=8968914
2) SCHOEN AND PERSING IN THEIR 1996
RICO METHOD PATENT:
The Dave Persing, Mayo Clinic FRAUD Patent-6,045,804
3) PERSING WITH SIGAL EXPLAINING THAT THE WESTERN BLOTS WERE
UNREADABLE, 2000:
http://www.journals.uchicago.edu/doi/pdf/10.1086/313920
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
obviously a FALSE CLAIM or a QUI TAM or FRAUD on the
GOVERNMENT since they're declaring to the FDA, in the
LYMErix case, saying they had a vaccine.
http://www.usdoj.gov/usao/eousa/foia_reading_room/usam/title9/crm00921.htm
I'll just plagiarize myself here and just use the text from the reports below on "Lyme Facts" and "Borreliosis Basics":
So in the Fall of 1998,
the LYMErix vaccine was approved,
anyway, by the FDA (the FDA panel being loaded with people like Allen Steere, Robert Schoen, and Vijay Sikand – the very people who ran the OspA trials) and came on to the market in late 1998 despite numerous “provisos.” More than 1,000 systemic adverse events were reported through the VAERS from September 1999 to November 2000, whereupon the FDA granted a public hearing, January 31, 2001:
http://www.fda.gov/ohrms/dockets/ac/01/slides/3680s2.htm
Whereupon I blew the whistle on
Dearborn and how LYMErix actually caused
immunosuppression (the FDA did not scan
in the last 19 pages of this booklet,
which were 19 pages out of the Dearborn
booklet, proving no one agreed with
Steere's proposal for an antibody panel
for a "case definition":
http://www.fda.gov/ohrms/dockets/ac/01/slides/3680s2_11.pdf
Several months later, in the fall of 2001,
Karen Forschner of the Hartford, CT based Lyme Disease Foundation
(Lyme.org) delivered to the FDA – in person -, a patent owned by Bridgitte Huber at Tufts where it was declared that OspA was technically a “toxin,” right in the abstract (US Patent 6,689,384). The FDA then gave SmithKline and Yale (the assignee of the LYMErix patent), an ultimatum: “Either you remove LYMErix voluntarily or we will order it off the market.” SmithKline chose to avoid the embarrassment and pulled their own non-vaccine.
We’re still stuck with this bogus Dearborn case definition, despite numerous attempts at lawsuits against IDSA, SmithKline, and
filing complaints to the U. S. Department of Justice. It is still very dangerous for the public to be unaware that the average person, or 85% of us – who are the “seronegative patients are the sickest ,“ according to Raymond Dattwyler at the 1994 FDA meeting on Lyme and LYMErix (which preceded Dearborn) - have no chance of testing positive to this criminal CDC’-Dearborn standard, because the actual disease is one of immunosuppression, or
is an Acquired Immune Deficiency,… or is similar to AIDS with all the opportunistic infections that the Lyme and LYMErix victims cannot control.
It was said at the time LYMErix was still on the market that this vaccine, via its claimed mechanism of disinfecting ticks with human antibodies (yes, if you can believe it),
that LYMErix would turn humans into walking cannisters of tick disinfectant, when in fact,
LYMErix turned people into walking “cesspools of disease.” The same is true for Chronic Lyme. Chronic Lyme victims’ immune systems are “overwhelmed”- a term used by CDC officer Alan Barbour, when describing what antigenic variation in spirochetes does to humans (US Patent
6,719,983). This is a term you want to remember in case you hear it again: “overwhelmed” immune system means: “turned off.” “Turned off” is the complete opposite of an “inflammatory” or “autoimmune disease.”
That's all for now, folks.... KMD
Nancy captures the Zeitgeist
By our friend Nancy Rubenstein
Delgiudice (recently married to Jim Gottstein of psychrights.org)
"Torture is a doctor blaming your mother for asking for a second
opinion, and taking custody as retribution. Torture is a suffering child
being told it is all in her head."
Dear
Vice President Dick Cheney,
Thank you for
explaining your definition of torture (falling
from the twin towers on 9/11)
I'd like to share my
own current working
definition.
Torture is when a
government violates your rights as a human
being to give your children the kind of
childhood that prepares them to be engaged
in society. To pursue their rights to be an
American Citizen. To feel safe. Loved. to
define for themselves whom they want to be.
Torture is being drugged out of your
fragile, tender, developing mind/brain when
you are three years old. Torture is
suffering in the hospital and having doctors
forbid you from being with the people you
love most; your parents. Torture is a doctor
blaming your mother for asking for a second
opinion, and taking custody as retribution.
Torture is a suffering child being told it
is all in her head.
************************************************************************************************* I wanted to write a Christmas message of
peace, but I could not find that peace in my
heart. Many of my friends believe in seeing
what they want, and "manifesting" it into
reality. Some people want to pray it
away.Maybe our differences are semantic in
the end, but I don't want to feel peace when
others are suffering. I can feel that kind
of peace when my life ends.I believe in
making it happen.
You would think that in the 20th and 21st centuries we
in the English speaking world would have some sort of a
collective idea on how to prevent all but a couple' percent of our
populations from falling through the cracks into poverty, near-starvation,
homelessness, chronic illness, drug addiction, getting nothing but
assholes-and-morons for politicians, our childish "foreign policy," having
to suffer the cognitive-deficits-in-journalism, etc. But when you
consider who are the characters who have self-assigned themselves the
Authority, or are the planners, or are the people who originally thunk up
the idea that post-WWII, America was going to rule the Earth (Rockefellers,
Israelis, Banksters, the Petro-fellas), you would think they would have come
up with some sort of a moral theme or motif or humanness concept that ties
together the plight of Earth itself, with harmonious cooperation between
needs and resources. But that never enters the Capitalists' minds.
No. They were convinced by some diabolical influence that humans are
mere animals, competing as animals to be the fittest.
Now consider the word "fit." When you think of "fit," does some bankster or
lawyer or salesman come to mind? When someone like Mr. Kahn of Kahn Academy
comes along and blows the entire Education industry out of the water - from
out of nowhere - what does that say about the Establishment? What are
we doing wrong? Who comes up with the idea that a formal education on
education makes you a teacher? They consumed this education on
education but by what criteria are the planning and the protocols weighted?
Why do we have the entire CDC, NIH, AMA, FDA, DHHS, and all of medical
mainstream America not aware of the fact that there is no Tuberculosis
vaccine for the same reason there is no Lyme vaccine, ... and is the same
reason we put Thimerosal in vaccines (fungi = bad)? How dare the NIH
and CDC (not to mention Yale) tell me they don't know what the Lyme vaccine
was?
Where does anyone get off saying they should be paid for being an expert,
when they admit they do not know the basic things about human illness and
disease ("doctor," or HMO CEO)?
The world now dominated by the USA has no cohesive plan or idea. No
reputable intent. The United States Government are a bunch of animals
who think their job is to control the other animals. Fear is their essential
theme and motif.
The world is ruled by a bunch of cowards.
And that's funny to me because COWARD was the thing I was
always taught was the LAST thing you'd ever want to be.
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