Stuff to know about the perceptions of aggressor/incompetent "MDs."

III. Antibody testing for infectious diseases-associations with the likes of cancer/leukemia should be thrown out:

We now know that fungal antigen-related immunosuppression and Epstein-Barr virus agonism of the same TLRs, TLR2, will render sufferers of fungal diseases and Epstein-Barr seronegative.

Because of Yale's lies about LYMErix, much previously published research is going to have to be discarded.

Eg., Throw the following study out- there aren't going to be any antibodies against these TLR2 agonists.

It is clear now why there would be a NEGATIVE CORRELATION between antibodies against TLR2 agonists
such as Epstein-Barr in childhood leukemia.

These activated viruses and fungi have defeated the antibody response thru TLR2 agonism and the resultant
downregulation of antigen-presenting (HLA molecules) and therefore antibodies.

Cancer Causes Control. 2001 Sep;12(7):645-52.
http://www.ncbi.nlm.nih.gov/pubmed/11552712

Evidence on the infectious etiology of childhood leukemia: the role of low herd immunity (Greece).

Petridou E, Dalamaga M, Mentis A, Skalkidou A, Moustaki M, Karpathios T, Trichopoulos D; Childhood Haematologists-Oncologists Group.

Department of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA.

Abstract

OBJECTIVE: Acute lymphoblastic leukemia (ALL) among children may be a rare outcome of a delayed non-specific infection in situations of overall low herd immunity. We evaluated the hypothesis as to whether newly diagnosed ALL cases, compared to their controls, are characterized by lower herd immunity, as reflected in a more seronegative spectrum to several agents, with the exception of a strongly positive response to a single infectious agent, assumed to trigger ALL. METHODS: The study included 94 incident cases of ALL, from all pediatric hematology-oncology units of Greece, and 94, matched for age and gender, controls hospitalized with minor non-infectious conditions. The past exposure to common infections was assessed using 10 serological markers. RESULTS: There was little evidence for an association of ALL with the serology of any of the studied infectious agents among the very young children. In contrast, among children aged 5 years or older, leukemia was inversely associated with seropositivity to Epstein-Barr virus, human herpes virus-6, Mycoplasma pneumoniae and parvovirus B19. CONCLUSIONS: Among children aged 5 years or older the risk of leukemia may be higher when the low herd immunity for several agents is challenged by late infection from an agent that, as a rule, would attack children at a younger age.

PMID: 11552712 [PubMed - indexed for MEDLINE]

IV: The New Disease Paradigm was revealed via the revelation of the 1) bogus testing for Lyme [this had the PsyOsps (Freudian slip) effect and was the intent of Kaiser-in-cahoots-with-the-CDC of spinning diseases for non-treatment and the non-revelation that indeed, Plum Island was the original accidental release outbreak area] and that 2) Not All Diseases Are Inflammatory- most of them, in fact, are secondary-immune dysregulation, like AIDS. The result of opportunistics (which later may cause chronic inflammation or the chronic production of the likes of antiphospholipid antibodies/Lupus).

In the New Disease Paradigm, through which you, the Patient-Acting-In-Your-Own-Defense-Against the "Vast-Majority"-of-Medical-Moronicals, are in charge:

You will state that "Lyme is simply Relapsing fever with the HIV gp120 vaccine hoax (Dearborn)" and that you're "not interested in their fairy-ass politics, one way or the other."

And you "want to know what kind of research is applicable for the condition" that you have, which is "badly cloned B cells and the activation of latents, in addition to CHRONIC SPIROCHETES, since they're all chronic and always have been."

This was how NINDS' Roland Martin treated his Lyme-and-MS patients. They got treatment for spirochetes in addition to the MS treatment.

And say, "And can this be done without Stem Cells?"

And, "Can we do this with recombinant DNA transfection of cloned new B cells?"

"If Craig Ventnor can invent 'life' by stealing it from another organism, can we transform, say rat brain cells or discarded McSweegan-brain cells, with the DNA of new B cells before they differentiate?"

You confront these morons and let them know you're not paying them unless they have some novel medical expertise to sell.