We know that the HHS.gov Tick Borne Disease Working Group (TBDWG) created by essentially Pat Smith of the Lymediseaseassociation.org ( who should know better; see the testimony of Donald Marks, here, from Jan 2002, a year after I blew the whistle on Dearborn and the fact that LYMErix caused immunosuppression rather than, “was a vaccine”:
HOW SMITHKLINE BEECHAM (GLAXO SMITHKLINE) USED CONFUSING LANGUAGE, KEEPING FDA AND PHYSICIANS IN THE DARK:
The Company dismissed the significance of adverse events reported since marketing by stating the vaccine’s profile had not changed “except as described below…” The description referred to, rendered with numbers but given no contextual explanation, in fact implied a huge change in safety. The company’s confusing language made it sound as if the adverse events, many of them severe, had no particular significance at all.
The company has masked serious causally-related adverse events behind qualifiers, such as “…and which may have no causal relationship with the vaccine” and “…cannot be distinguished from the natural history of the underlying disease,” all the while knowing these are confusing the issues.
The company tries to shift the blame from the vaccine to the patient with statements such as “the possibility of a severe rheumatologic, neurologic, autoimmune adverse event is inherent in Lyme disease.” The company does not inform physicians that the adverse events can result from Lymerix, completely apart from the disease.
As a result of these actions, GPs in the US were kept in the dark about the life-threatening side effects of Lymerix.
) was a farce from the get-go. Everyone knew it, the “TBDWG,” would be a joke, but we played along anyway.
TruthCures.org team members attempted to contribute the conversation. It turned out none of that effort and documentation was recorded or considered as part of the record. Also, what went on – the dialog – was kept secret behind “subcommittee” status. It was a complete waste of everyone’s effort and travel expenses.
Nevertheless, this is the TruthCures/ActionLyme history – and it was ALWAYS the same complaint – , starting in 2001, and which should assure everyone, worldwide, that the US Government has no intention of correcting this crime or the others they commit (Autism vaccines work the same way – activated/reactivating viruses). This is our position:
The very same information provided to this TBDWG, to the USDOJ, to Senator Richard Blumenthal when he was CT AG and sued IDSociety.org for “antitrust”,
and to the FDA in Jan 2001 at the LYMErix hearing, has now been confirmed by Bay Area Lyme
Research Supported by Bay Area Lyme Foundation Shows Lower Immune Response Leads To Persistent Lyme Disease Symptoms
In addition to an association between plasmablasts and disease resolution, researchers also found that patients with persistent symptoms had a lower antibody response; more specifically, these patients exhibited reduced clonal expansion of B-cells.
(“this is a B cell senescence disorder;” see also, Nicole Baumgarth:
Suppression of Long-Lived Humoral Immunity Following Borrelia burgdorferi Infection )
and the new Finnish group from Nov, 2018:
Tick-borne disease is not just LymeA study recently published in Scientific Reports discovered that 65% of Lyme disease patients irrespective of their disease stage respond to several microbes. As a consequence, the authors have demonstrated that microbial infections in individuals suffering from Lyme disease do not follow the “one microbe, one disease” status-quo. Moreover, the probability that Lyme disease patients would respond to multiple microbes associated with the tick-borne disease is an astounding 85 %.
However, the research by Garg et al. argues that prolonged exposure to tick transmitted microbes weakens the human immune system increasing the host’s vulnerability to other common microbes’ labelled “non-tick-borne opportunistic microbes,” such as Chlamydia, Mycoplasma, Epstein-Barr virus and many more.
Infected ticks are global challenge
For the first time [not really, but…KMD], Garg et al. establish an astounding 85% probability for multiple microbial infections in LD patients that include tick-borne pathogens and non-tick-borne opportunistic microbes.
– that Lyme and OspA cause immunosuppression,
that Dearborn was falsified – that there was no consensus at that consensus conference (as demonstrated with the records from the Dearborn booklet – 30 pages – to the FDA Vaccine Committee on LYMErix,
Here is the Dearborn booklet if you would like to confirm that none of the labs agreed with Steere’s research fraud falsified proposal for interpreting the Western Blots: (find the file in this list in chronological order; Dearborn took place in Oct, 1994) http://www.actionlyme.org/2017_RICO_DC_File_List.htm
and that “Chronic Lyme” is about reactivated opportunistics like Epstein-Barr – exactly the same as the outcome of hospital sepsis -, but this TBDWG rejected that scientific evidence and did not record it as part of the record, EVERY TIME it was specifically delivered as part of the “record” of this work group.
We, TruthCures.org campaigners, were told in July 2015 by a Senate Judiciary Committee staffer/lawyer (in Jeff Sessions’ office) that this complaint of scientific fraud and racketeering needs to be heard in front of a Senate Hearing for referral to the USDOJ to prosecute.
If this now does not happen, with the entire Lyme community now well-aware that Lyme is really about reactivated viral infections [after all, the NIH had a “Lyme and MS group” (Martin and Marques), and Yale had a “Lyme and Lupus Clinic” (Joe Craft and Allen Steere) and those two are known to be about reactivated herpesviruses], and that is why antibiotics have always failed to cure these tick bite sepsis patients, then the people of the United States can be certain the HHS.gov is a farce and will never accept any of their recommendations, and neither will the rest of the world, especially as regards vaccines.
The references for FDA given in 2001 referred to regarding how Lyme and LYMErix cause disease via immunosuppression :
Modulation of natural killer cell activity by Borrelia burgdorferi.
Mario Philipp publishing since the 1990s that OspA alone causes the induction of the immunosuppressive cytokine Interleukin-10:
The HHS.gov does not understand the science,
IDSociety.org does not understand how science works,
and all along ILADS.org has been wrong and malpractice-treating their victims.
In January 2005 this group discovered the actual image of an analog if not the same OspA as Pam3cys on a Korean Chemistry journal (the structure was never in any patents or journal articles we could find until then).
It has been specifically that long since the TruthCures.org campaigners have tried to expose the fact that OspA and the fungal Osps or Vmps shed by Borreliae cause “Great Imitator” outcomes in the same way sepsis does, by “overwhelming” the immune system, reactivating latent opportunistics and causing tolerance and cross tolerance to other pathogens’ antigen types.