“How do our shorts taste?” — TruthCures vindicated by the science.

You heard it here first, folks:
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“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.”

https://www.news-medical.net/news/20181101/Tick-borne-disease-is-multiple-microbial-in-nature.aspx
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Lyme is not about spirochetes and “co-infections” as ILADS.org has been saying for 2 decades;
It, a post-sepsis syndrome outcome, is not cured by antibiotics;
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OspA injections alone cause this immunosuppression/post-sepsis syndrome outcome as a fungal endotoxin with tolerance and cross tolerance to other TLR agonists besides the 1/2 which handle triacyl lipoproteins (see the TruthCures.org or ActionLyme.org “Criminal Charges Sheets” – which are criminal charges since this, the Lyme crimes, all revolve around tossing out this very immunosuppression disease at Dearborn to pass off  this bogus OspA Lyme vaccines by the CDC staff who owned patents and their co-corrupt-cronies at Yale.edu and NYMC.edu – the ALDF.com);
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ILADS.org and all the other fake non-profits except, lately, Bay Area Lyme
https://markets.businessinsider.com/news/stocks/research-supported-by-bay-area-lyme-foundation-shows-lower-immune-response-leads-to-persistent-lyme-disease-symptoms-1027481288 
(we’ve been saying for 14 years that that this was a B cell senescence disease due to the shed fungal Osps, and that they cause antigen to not be presented or the downregulation of HLA molecules, .. which means no antibodies will be produced)
fought against TruthCures.org and ActionLyme.org and booted us from all their online groups – the WHOLE TIME…;
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Trashed us repeatedly, called us “conspiracy theorists” (when not a one of the ones who said this had any scientific background or standing to address the science of fungal endotoxin induced tolerance and cross tolerance, and in fact NEVER addressed what OspA actually was such that it alone could cause such a disease) and every other name in the book;
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And we are the ONLY ones who went straight to the USDOJ after blowing the whistle on the fraudulent Dearborn case definition which excluded these immunosuppression outcomes with research fraud performed by Allen Steere in 1992-1993 at the FDA in Jan, 2001…
https://web.archive.org/web/20040203184937/http://www.fda.gov/ohrms/dockets/ac/01/slides/3680s2_11.pdf
and over the fact that OspA caused immunosuppresssion, referencing Raymond Dattwyler and Mario Philipp, to have this prosecuted, while ILADS did not participate in that at all, or in the 2006 Senator Blumenthal lawsuit against IDSA.
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Nobody else can claim they consistently explained what this was about, ever since the beginning – since we saw that LYMErix caused the same chronic neurological disease in 1999 when it first came on the market -, that the CDC denied existed (they own patents for worthless Osps), and we were trashed the whole time for staying on this exact course, by our own side (not to mention being treated pretty viciously by the Yale/UConn Lyme criminals, too, obviously, for these EXACT same claims), and since ActionLyme was founded in August, 1999.

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Nevertheless, with this new news, ILADS and the non-non-profits who trashed us still have no record of going to the USDOJ over these crimes and have never presented anyone with any authoritative standing (neither the FDA or the DOJ) with any scientific evidence of anything to claim fraud or some other injustice such as “Deprivation of Rights Under Color of Law” for all the slander, libel and other abuse by the CDC over this for the last 28 years since the founding of the ALDF (1990).

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“Heroes” and “Saviors,” they called ILADS.
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Yikes.
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It was none of them – no ILADS “doctor” or “LLMD” – who participated in any of these new revelations, yet they charge people the likes of $3,000 to walk in their doors, and never run the right tests to help these people get disability, since there is no cure for post-sepsis syndrome…

Dormant viruses re-emerge in patients with lingering sepsis, signaling immune suppression

https://source.wustl.edu/2014/06/dormant-viruses-reemerge-in-patients-with-lingering-sepsis-signaling-immune-suppression/

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There is no cure for that, post-sepsis syndrome, at the moment.  Look that up, and even look it up officially because even the CDC admits this is a permanent disability.  ILADS all along falsely claimed they could cure it.  They should be prosecuted, too, for that, in addition to the ALDF.com cabal which is the RICO organization (and not IDSA) named in the first USDOJ complaint filed by ActionLyme.org in July 2003.

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And finally this (below), after they bashed and booted us (and in public – at the CDC rally this year, 2018), somehow we knew when it all came out they would take credit and *never* say, “You were right and we were wrong, thank you.”
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Jenna Luche Thayer on LinkedIn:

“FRIENDS, YOU ARE NOT ALONE! Many hundreds of medical professionals & scientists are assembled in Chicago at the ILADS conference.

“These persons defend our human rights to health and dignity. Because of corruption, many provide the Lyme/TBD community care at the risk of their medical licences and livelihoods.

“They are in the process of learning about the latest findings on this complex illness and how to better serve our community.

“The broad focus of this conference is on immunity and ***many of the presentations focus on immunosuppression and dysregulation, opportunistic infections, the resurgence of latent infection*** and how to strengthen the immune system.

“It is wonderful to be among many hundreds of persons who are trying to help the Lyme/TBD community!

#lymeborreliosis #humanrights #tickbornediseasesworkinggroup
#ILADS #SLyme

 

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Cheers.  When you’re right you’re right and the first thing any true scientist would have asked was WHAT IS THIS OSPA?  HOW COULD HAVE CAUSED THE SAME DISEASE AS LYME, ALONE?  And then showed how the model repeated independently with other triacyl lipoproteins from the multiply-published literature regarding these types of antigens.  That’s the requirement of the Scientific Method.  Not a single “MD” in America, no one from IDSA, no “LLMD” or any of the Lyme non-profits have ever acknowledged this to this day (Nov 4, 2018).
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Still waiting to hear it….

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Still waiting to hear how OspA alone causes this post-sepsis syndrome from any “treater” allegedly on the patients’ side.  They’ve never asked because they knew all along.  I was a member of the group that became ILADS in 1999 (called MMI), so they knew what I blew the whistle over and what it was all about.  They ignored it because they knew antibiotics were not going to cure this immunosuppression.  Still true, 19 years later.

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Still true and still waiting for someone from ILADS to grow a pair, not to mention the CDC, FDA or NIH.  We can understand the FDA and NIH not giving a shit.  Welfare Queens on the dot guv dole never give a shit about anything other than their retirement funds and what goodies they can get from the government, free, at the used government property auctions and stuff.   At this point, we know they are too scared shitless to say anything for having sat on their hands for all this time while the patients – we, the sick people -, did their jobs for them.

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And now the whole world outside America can watch what America does.  Then they’ll know.  The “Great” paper tiger has no balls.

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But for the last 19 years, ILADS.org did nothing but take people’s money and claimed to be “curing Lyme” with antibiotics.  And of course they never proved it.  They never even attempted to.  They never even attempted to EXPLAIN how spirochetal illnesses cause disease.  And NOW they’re claiming they can help your immune system without, once again, explaining scientifically how you can reverse poly-antigen tolerance and the tissue damage from sepsis, as explained by Allen Steere and Paul Duray in 1988:
http://www.actionlyme.org/clinical-pathologic-correlations-of-lyme-disease-by-stage-Steere-Duray.pdf

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Maybe at the thought of getting their money back from ILADS charlatans will other Lyme victims start participating in the effort to get this crime prosecuted.  Even a class action against just one “LLMD” would probably work, easily.  Several law firms could be involved.  Imagine 3 million dollars divided 100 ways. …  Some of ILADS’ victims might be able to get the houses back they had to lose with multiple mortgages to cover an “LLMD’s” charges, where these “LLMDs” literally told them to do that (get second and even third mortgages) to pay for “treatment.”

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