It’s okay to have one-dimensional thinking.

I think this is the one instance we all would be better off having one-dimensional thinking: How did OspA alone cause the same “multi-system” (Persing and Schoen) disease that is “indistinguishable” from what we call “Late Neurological Lyme?” What does “Great Imitator” really mean?

Does this phenomenon of injecting fungal antigens that causes post-sepsis-like outcomes (or other conditions of immunosuppression) with reactivated viral infections, etc (“opportunistics”) occur elsewhere?

After all, Lyme is *FAMOUS* for causing MS and Lupus and those are mainly due to “dysfunctional control” of EBV, HHV-6, CMV, etc. The NIH had an “MS and Lyme” Division. Yale had a “Lyme and Lupus Clinic.”

Now they both admit MS and Lupus are really about EBV, et al. Even Steere published that Late Neuro Lyme appeared to be like a “mononucleosis” infection with the “Reed-Sternberg cells” and causing quite a lot of cellular damage (that’s post-sepsis syndrome).

When you inject fungal antigens together with live, attenuated viruses (MMR-type), you get a potentially lethal infection. That was why they invented Thimerosal. Mercury or metals apparently kill mycoplasma, et al. It is the same model. Fungal-Viral Synergy or post-sepsis syndrome. Paul Auwaerter published the exact same thing Andrew Wakefield claimed: “These are the vaccine strains, actually killing these MMR victims.”

The Pentagon published that Gulf War Illness ***was associated with vaccines,*** and we know other conditions of immunosuppression were present like DEET and nerve agent antidote (or even jet fuel). This is the same model.

The model repeats in dozens if not hundreds of other situations. Several other attempts to make LYMErix-like (lipoprotein) vaccines for Tb resulted in “immunosuppression” and a “greater susceptibility to disease.”

So, OspA alone caused the same disease we call late chronic neuro Lyme. Therefore, it’s okay to have one-dimensional thinking. Here is an instance where you can narrow the focus in trying to understand why “treatment fails in half the cases.” Baumgarth and Barthold showed your immune system is effed within the first 10 days by spirochetes destroying the B cell germinal centers. Spirochetes go directly to the lymph nodes. Most of us would not be going to a doctor with a “bad flu” until MAYBE after 2 weeks.

Dattwyler was correct to publish in 1989, that “pathological changes may occur prior to treatment.” Right, it’s sepsis and it happens within the first 2 weeks. Chiu and Aucott republished the same result in 2016. “Treatment (even early treatment) fails in half the cases.”

In 2012, the NIH Division in charge of MS-Lyme published in the New York Times that “the real culprit may be Epstein-Barr.”

Adrianna Marques (and Roland Martin) would know, wouldn’t she/they? Since she was the one who reported for the NIH that OspA as a TLR2 agonist (fungal-ish) caused global humoral immunosuppression with the opposite – chronic inflammation – in the brain?

We have all the references. Everyone KNOWS Truthcures.org is the only one talking and showing all these references and this comprehensive science with all the cross-explainers and parallel examples in the charge sheets.

Which is really one topic. This is probably the one time it’s okay to be a simpleton. OspA caused the same disease, so what is the disease they’re trying to hide with the Dearborn case definition?
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