Madison Area Lyme Support Group

Welcome to the Substack of the Biosecurity Ethics and Immune Tolerance Awareness Initiative. The Biosecurity Ethics & Immune Tolerance Awareness Initiative exists to educating the public about the role of immune tolerance in chronic diseases, neurological and neuropsychiatric disorders, and cancers. We further educate and advocate for ethical biosecurity practices and informed policy decisions made in full transparency, through ethical guidelines, working to close critical vulnerabilities, and defend actual national security from foreign influence in public health and biodefense strategies, rather than using National Security as guise to hide scandals and evade accountability.

The Truth of Chronic Disease in America Shall be Unveiled. The Health of All Depends on it.

In 1960, the science of slow, chronic disease and persistent infections, once baptized “immune tolerance” was obscured and marginalized to the realm of organ transplantation and its recipients, as the 1960 Nobel Prize was given in error to Frances MacFarland Burnet and Peter Medawar for immune tolerance through organ transplantation even though the two never worked together nor were they nominated together by anyone. However, it was Erich Traub, who had discovered it in 1935 through his discovery of Lymphocytic Choriomeningitis Virus (LCM) in white mice.

Immune tolerance is a term applied to the state of chronic suppression of the immune system, where the immune system is too overwhelmed to adequately fight back. It is specifically defined as :

A state of unresponsiveness to a specific antigen or group of antigens to which a person is normally responsive. Immune tolerance is achieved under conditions that suppress the immune reaction and is not just the absence of an immune response.

This same condition correlated to another phenomenon alternatively coined “immune paralysis” following injection of large doses of pneumococcal polysaccharide antigens. In short, immune tolerance is immune paralysis. This was a major finding that would have vastly changed our understanding of chronic disease and immunology, yet the scientific establishment ignored it and marginalized it to organ transplantation, because the same condition is also seen in organ transplant recipients, and this is also thought to be the result of antigenic stimuli. Attributing it to organ transplantation only totally ignores something so immensely important about immunology and the disease process that it might as well be considered one of the pillars of chronic disease showing that unlike acute diseases measured by heavy inflammation and immune response, there is a polar opposite side of disease, measured by immunosuppression, lack of visible inflammation, and chronic disease.

However, the Nobel Prize “given in error” appears more likely to have been a deliberate choice as it would have devastated Western immunology and the science of infectious disease determined by antibodies and observable inflammation. Equally so, it would have flipped vaccine science on its head and exposed the true nature of vaccine-induced “immunity” as a slow destruction of the immune system rather than building it up as strong and healthy.

Erich Traub first elucidated the condition during vaccine research at the Rockefeller Institute in 1935 when he injected the brains of mice with foreign proteins, reactivating dormant LCM virus from within the mice, causing an epidemic from scratch. The result was a slow chronic disease via immunosuppression and persistent viral infection that could be passed congenitally from mother to newborn, maintaining itself through generations, while silently degenerating the genetic integrity of subsequent generations, plaguing them with chronic disease, neurological syndromes/wasting disease, and cancer.

In short, antigenic stimuli were behind this condition which produced chronic immunodeficiency and reactivated dormant viruses from within the body, invited additional opportunistic infections to create a highly complex and complicated chronic disease accompanied by neurological/neuropsychiatric disorders, wasting disease, and cancer. It would present in the absence of detectable antibodies and little to no outward inflammation. Likewise, Traub’s experiments demonstrate how a vaccine antigen too toxic for the body can cause new outbreaks with other diseases already dormant in the vaccine recipient.

Since the 1960s when the infectious origins of immune tolerance were buried and obscured, the science of chronic disease and neurological/neuropsychiatric disorders began working in reverse. Public Health has been ignoring the underlying condition at the root of these diseases for decades by using tests and diagnostics that evade the evidence of the condition by using the wrong biomarkers of disease and calling it “evidence-based medicine.” This so-called Evidence-based medicine only uses antibody response and inflammation as its criteria for diagnosis but immune tolerance is the polar opposite. There are ways to detect and diagnose immune tolerance using other biomarkers, but these are very different than biomarkers used to study acute diseases marked by robust antibody response and heavy inflammation. By using inadequate biomarkers like antibodies and acute inflammation as criteria for diagnosis, this will invariably show nothing of value for diagnosing a disease that is marked by immune tolerance outcomes and as a result, no disease will be recorded.   (See link for article)

_______________

**Comment**

Important quote:

Nowhere is this more apparent than the recent wave of sick people injured by the COVID-19 vaccine.

Mandatory reading for each and every Lyme/MSIDS patient and every person who still believes in ‘vaccines.’

This, right here, is the pearl that has been trampled on by public health and mainstream medicine.

Yale scientists have found T-cell exhaustion and prolonged spike protein production in some COVID shot recipients with spike levels increasing over time leading to post-vaccine brain fog and immune dysfunction. Finally, someone is connecting the dots between ‘long COVID’ and post vaccination syndrome.  Findings Suggest Immune Imbalances and Viral Reactivation May Contribute to Chronic Symptoms After COVID-19 Vaccination.

But mainstream medical journals won’t publish it.

The variety of symptoms include:

• Excessive fatigue (85%)

• Tingling/numbness (80%)

• Exercise intolerance (80%)

• Brain fog (77.5%)

• Difficulty concentrating (72.5%)

• Sleep disturbances (70%)

• Neuropathy (70%)

• Muscle aches (70%)

• Anxiety (65%)

• Tinnitus (60%)

• Burning sensations (57.5%)​

Immunosuppression can be caused by vaccinations of all kinds as well as unethical biodefense practices using simulants in open-air tests since the 50’s.  Finnegan states:

Lyme disease had been one such simulant spread through ticks on shorebirds in the early 1950s under the supervision of Erich Traub on Plum Island, using strains of Borrelia anserina that he had acquired from Rockefeller-funded psychiatrist Franz Jahnel through his student Werner Schäfer in 1939.

Finnegan goes on with the sordid history of immune tolerance and how public health officials understand it fully and are deliberately using it as a defense strategy, while misleading the public.

Certain antigens responsible for immune tolerance are also potent mitogens which are responsible for cancer through the upregulation of telomerase.

MAHA will fail if the origins of immune tolerance via toxic antigen is not addressed.