SHORT VERSION of “the disease is caused by the vaccine.” Lyme and LYMErix disease = same post-sepsis syndrome.

Circled in red = 3 fatty acids of essentially pam3cys. Humans cant tolerate having little fat blobs of a fierce endotoxin (3-fatty acids) injected or into their blood stream. It’s the same as scraping off some bathtub scum and injecting it.
.
This is also how spirochetes (not “bacteria”) cause a chronic disabling AIDS-like disease. They, spirochetes, go to the lymph nodes, shed these fatty acid covered blebs, thereby wreck the immune cell (B cell) maturation process, and *tolerize* against all kinds of infections.
.

UPDATE:
https://www.prnewswire.com/news-releases/research-supported-by-bay-area-lyme-foundation-shows-lower-immune-response-leads-to-persistent-lyme-disease-symptoms-300701693.html

These data confirm previous findings in some animal models showing demonstrable immune system suppression after infection and wide variability in the immune response among different animals after infection.

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.

It CAUSES “post-sepsis syndrome” without the classic sepsis process. Happens within a month after a tick bite (Baumgarth).
.
SOME PEOPLE will have an HLA-linked autoimmune response to the herpesviruses that are reactivated. THOSE people will end up with like MS or Lupus as a result. See Yale (who had a “Lyme and Lupus” clinic) for that…
https://www.ncbi.nlm.nih.gov/pubmed/14707107

Most of us dont have the HLAs for anything. That is why you see far more people with Fibromyalgia or Chronic Fatigue Syndrome than with any classic “autoimmune” disease.
.

Here are several articles that basically show that, observed, empirically, and then the mechanism (tolerance and cross tolerance):

Lyme Crooks *All* Admit OspA Was the OPPOSITE of a Vaccine

https://www.youtube.com/watch?v=zOKYtN6Labc

. Go ahead and acquire ^^ all those references for yourselves. Everything is referenced in that movie.

Allen Steere showing you end up with reactivated EBV, much tissue and organ damage, and especially messed up lymph nodes and B cells.
Go ahead and read this thoroughly, you will see it is like post-sepsis syndrome:

http://www.actionlyme.org/clinical-pathologic-correlations-of-lyme-disease-by-stage-Steere-Duray.pdf

Nicole Baumgarth showing the process (targeting B cell maturation centers in the lymph nodes, showing you cant then fight off viral infections):
https://www.ncbi.nlm.nih.gov/pubmed/26136236

Linden Hu (responsible for the IDSA “Guidelines”) saying this model that TruthCures describes is correct:
https://crymedisease.wordpress.com/2018/03/16/linden-hu-tufts-claims-truthcures-org-is-right-about-everything-lyme-is-like-aids/

The NIH (the former “Lyme and MS” group) saying Chronic Lyme is really about reactivated latent viral infections like EBV, after the same NIH employee published that OspA alone causes this too (or the fungal – TRIACYL or “3-fatty acid” groups of the Borrelial lipoproteins cause this), in the scientific journals:
“There are other infectious organisms — Epstein-Barr virus, for example — that can produce similar symptoms and may be the real culprits”
https://well.blogs.nytimes.com/2013/07/08/when-lyme-disease-lasts-and-lasts/

Adrianna Marques would know. It was her job to find out (for the NIH) how Lyme causes MS. She said it was via immunosuppression from the shed Osps and Vmps of Borreliae:
https://www.ncbi.nlm.nih.gov/pubmed/?term=Martin+and+Marques+and+tlr2

So, everyone MUST understand that the issue is that the Osps or the Vmps are triacyl lipoproteins. More toxic than classic endotoxins. They turn off the immune system against “Bacteria (LPS),” viruses, and of course, other fungal diseases via TOLERANCE – look up that word.

You end up with essentially chronic mono on steroids. And no antibodies will show up, so it looks like you dont have anything. And you cant treat this with antibiotics or “immune boosters;” immune science does not work like that. You cant take anything oral for “immature, neoplastic-looking B cells.”
.

“Doctors” dont know any of this science because they were trained in Organic Chemistry too and are supposed to be asking the same questions we ask (“What is it?”). They have the acquired dementia of arrogance. They either forgot or never learned this basic science.

But this is really how the essential human life science (chemistry) is done. After all, Pharma is based on it. Ask what the fekker is, before you go making a vaccine out of it.

Go ahead and google what is the meaning of “Organic Chemistry.” “Doctors” are supposed to have taken 2 semesters of it in a pre-med Bachelors program. You’ll see. They’re supposed to be telling you what we are telling you. There is no excuse for their incompetence – on a massive, global scale. No “doctor” is telling you the obvious. Medical schools really flopped, big time. They ignore basic science, on a scale no one can even capture if there are 2 million tick bites in the USA alone.

Now go research for yourselves what are the outcomes/clinical/poor health outcomes in post-sepsis syndrome. It is the same for Lyme and CFIDS/ME/Fibro:

You have chronic active infections of all kinds – and especially the herpes -, tissue, immune system, organ and nerve damage. And it’s not actually post-anything since these infections are still active and ongoing:

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/

Think about it. There really isn’t any “post” anything, medically. Have a look at Paul Auwaerter talking about how vaccine viruses hang around, damaging forever…