“ALL TRUTH passes through three stages. First, it is ridiculed. Second, it is violently opposed. Third, it is accepted as being self-evident”.
~~~Arthur Schopenhauer (1788-1860)
Are you tired all the time and can’t function like you used too? Tired like you just finished a triathalon – are your MUSCLES tired? Do have chronic flu-like symptoms? Do you have a hard time remembering things, and have a headache and stiff neck?
Do you have radiating twitching, tingling and pain in your extremities? Do you have a hard time walking or holding on to things with your hands? Do you have air hunger? Do you have heart issues? Do you have arthritic pain? Are you bedridden?
Have you been diagnosed with any auto-immune diseases, like Lupus, Fibromyalgia, or MS? Do your symptoms keep changing causing your doctor or team of doctor’s to become perplexed? Have you been told that you need to see a psychologist because your long list of symptoms must be in your head?
Well, your doctor or team of doctors are sort of right by saying your symptoms are caused by something in your head. Yes, you have issues in your head….you have a permanent brain infection(s) AND post-sepsis syndrome which is a form of AIDS.
You are NOT crazy, your doctors are just ignorant and are not educated properly as to what Lyme or other immunosuppression diseases like Chronic Fatigue Syndrome or Fibromyalgia are or what to look for.
Why aren’t medical doctors being educated about Lyme disease and their co-infections? The truth is not easy to swallow and you may become upset or shocked when you hear it. Or, if you have God-like faith in your Doctor’s and who trains them, this may piss you off! Regardless, you need to hear the truth!
“Lyme disease gets its name from a small coastal town in Connecticut called Lyme. In 1975, a woman brought an unusual cluster of pediatric arthritis [and chronic fatigue cases] to the attention of Yale researchers. In 1977, the Yale researchers identified and named the clusters “Lyme arthritis” [essentially ignoring the chronic fatigue part of it]. In 1979, the name was changed to “Lyme disease,” when additional symptoms such as neurological problems and severe fatigue were linked to the disease. In 1982 the cause of the disease was discovered by Dr. Willy Burgdorfer. Dr. Burgdorfer published a paper on the infectious agent of Lyme disease and earned the right to have his name placed on the Lyme disease spirochete now known as Borrelia burgdorferi.”
Notice, the influx of additional symptoms that followed, ‘neurological problems and severe fatigue’. Most importantly, the infectious agent was identified, the spirochete called Borrelia. The problem is, this infectious agent (bug) is not a normal bacteria. It is actually a parasitic spirochete that sheds fungal antigens. And while spirochetes shed off blebs with DNA in them and outer surface proteins on them, it also creates new antigens variations (shows up on Western Blot test as a new IgM), to dodge any immune system response. This is why spirochetes from arthropods were called borrelioses or why they are known as Relapsing Fever organisms. Once a cluster or antibodies are made against a population of them, new spirochetes emerge with different antigen profiles. Yale staff has said antibodies “select for” new “mutants.”
These fungal antigens shut down the immune system such as to allow for the re-emergence of latent viruses like Epstein-barr virus (EBV) or other herpes viruses, can run wild, causing chronic neurological Lyme or Post-Sepis Syndrome:
It is well-known that in immunosuppression cases, “lymphoma” or the reactivation of Epstein-Barr occurs. It happens in cases where immunosuppression therapy is called for (you hear it in the TV commercial warnings for the likes of Humira and Stelara, and the risk of lymphoma happens in transplant recipients who have to take immunosuppressive drugs).
What was causing the children in Lyme Connecticut to fall ill with Lyme disease? After WWII, the US government brought over Erich Traub (a German veterinarian, scientist and virologist, who specialized in Hand-Foot-and-Mouth and other animal diseases) to gain insight on the Nazi’s biological germ weapons and run top secret research on Plum Island. Theoreticall, they couldn’t contain these ‘weaponized’ (spirochete mixed with animal viruses or the likes of Brucella) ticks or other ‘weaponize’ vectors (biting insects) from escaping the island via birds or deer into the small town of Lyme Connecticut, near Plum Island. After all, B. burgdorferi’s phylogenetic parent strain is B. anserina, an African bird borreliosis.
Fast forward to 1990, certain CDC officers saw a huge market in these new tick-borne or vector-borne diseases, so they started a fake non-profit (ALDF .com) to spin the disease. This occurred one year after the Infectious Disease Society of America (IDSA or
These officers knew that this so called, “bacteria,” that causes Lyme disease, was not a regular “bacteria.” They also knew from their previous research that the majority of people do not have an antibody or hypersensitivity response to this “bacteria,” which hypothetically makes it the “perfect stealth” biological weapon.
The CDC says you don’t have a disease if you don’t have antibodies to that disease and an inflammation response. American Lyme Disease Foundation’s (ALDF’s) main objective was to deceive the world into thinking Lyme was not a disease that causes immune suppression, but one that causes inflammation or arthritis only. By spinning the disease, they were able to call anyone experiencing neurological Lyme, crazy.
In 1992-1993, we think it appears that CDC officer Barbara Johnson sent CDC officer, Alan Steere (who were also both members of the ALDF) to Germany to change the case definition as to what Lyme disease is. Instead of it being called “Relapsing Fever” Lyme, the case definition was changed to a “bad knee” (arthritis only) that required a hypersensitivity antibody response.
During this time, the Lyme vaccine trials had already begun. The victims in the vaccine trials started reporting neurological and multiple symptoms problems, but these were literally not allowed to be considered “adverse events,” in the trials. They also could not tell the difference in the blood tests between people with Lyme or the ones in the vaccine trials. Perfect time to hold a conference to change the testing for the disease.
In 1994, CDC/ALDF officers held the, “Second National Conference on Serologic Diagnosis of Lyme Disease”, in Dearborn, Michigan. This is where they didn’t listen to the consensus of their peers on the new, “Steere in Europe,” falsified the testing for Lyme disease. They added the ELISA test, a screening test for highy antibodies, only, because they knew that 85% of the public don’t have an arthritis-type, or hypersensitivity-type antibody response to Borrelia. They also used high-passaged strains to test against, making it harder to test positive on the Western Blot since the primary Osps, OspA and B could be dropped in multiple passages. They added the requirements of at least 5 specific IgG (post infection bands) and 3 specific IgM (current infection bands).
Originally you only needed to show 41 kD (IgG or IgM band) on the Western Blot test to prove you had Lyme, along with a clinical diagnoses (multiple symptoms and not just a ‘bad knee’). This was according to Allen Steere himself in 1986:
They tested you for new IgM bands to see if you still had an ongoing infection.
This ALDF RICO (organized crime) fraudulently changed the case definition and falsified the testing for Lyme to make it look like their vaccines were working. Steere, in Europe used OspA and OspB (Outer surface proteins of Borrelia) without the lipids attached as a vaccine to falsely claim there are no antibodies to OspA and B early in the disease, but actually they wanted OspA and B out of the positive test antibody panel for a later monopoly they had planned:
Here was that later intended monopoly (involved Yale, Mayo Clinic, Corixa and Imugen labs):
US Patent # 6,045,804
This patent reveals they knew LYMErix causes a systemic disease like chronic Lyme, and in this patent they reveal their intended monopoly on post-LYMErix testing for the USA and Canada as they claimed in their advertising:
“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. “
”Large scale screening where whether or not the person has been vaccinated is unknown?”
You can see that they planned to leave OspA and B out of the diagnostic standard, so they would have a standard in place once the/an OspA vaccine was on the market, such that everyone in North America would have to send their tick borne diseases bloodwork to their labs, alone, because they were the only ones licensed to test for Lyme, once LYMErix was on the market. You never test for a disease with the same antigen as the vaccine because you would not be able to tell if that antibody came from the vaccine or the infection.
They used OspA and B without lipids to make sure they didn’t have an antibody response. The protein ends of OspA or B alone are not “immunogenic” or likely to produce antibodies.
In the end, they were injecting fungal antigens into their victims in the human trials and didn’t report anyone that had symptoms of more than a “bad knee,” and they did this for a monopoly not only one lab fees for testing, but in order to patent any future new tick borne diseases in that monopoly/RICO blood, so they could run to the patent office again, with NEW test kits and vaccines!!
Again, once their fake LYMErix vaccine was on the market, they said you can only send blood samples to their 3 ‘specialty’ labs; Corixa, Yale’s L2 Diagnostics, and Imugen.
Yale owns the patent on the fake LYMErix vaccine and they own the only FDA validation test, US patent #5,618,533 (a specific recombinant fragment of Borrelia burgdorferi flagellin, an improvement of the band 41-only antibody test). This test is not being used to test for Lyme, instead their bogus ‘Dearborn’ two tier testing is. That alone is a crime. They knew the Dearborn method would not detect Lyme, but their own Flagellin patent would. Yale never said anything; they never objected to the Dearborn scam.
So the question is why would they do this? These CDC officers and the Cabal (ALDF) wanted to have a monopoly on all new tick or vector-borne diseases. They wanted everyone to send their blood to their labs so they could patent new tick or vector-borne diseases, testing kits, and vaccines. Bottom line, it was all about the money at the expense of millions of victims. This my friends, is the greatest Crime against Humanity!
So, the bottom line, your doctor or doctors are ignorant because they are not being properly informed by the CDC and IDSA (ALDF front).
There is a lot more to this Lyme crime, I just wanted to show you why people are not being diagnosed with this deadly and debilitating disease. You can read the full crime and criminal charge sheets @ https://www.truthcures.org
Googles Patent for Tracking: Methods of measuring human body frequencies or harmonics and treating conditions based on the resonance phenomenon between a product and a human body’s frequencies or harmonics: https://patents.google.com/patent/WO2010039465A2/en
A61B5/411 – Detecting or monitoring allergy or intolerance reactions to an allergenic agent or substance
Evaluation of allergies or intolerances, with or without sensors of physiological quantities:
Search Add to query
from Cooperative Patent Classification
A – HUMAN NECESSITIES
A61 – MEDICAL OR VETERINARY SCIENCE; HYGIENE
A61B – DIAGNOSIS; SURGERY; IDENTIFICATION
A61B5/00 – Measuring for diagnostic purposes; Identification of persons
A61B5/41 – Detecting, measuring or recording for evaluating the immune or lymphatic systems
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