One problem all of us abused groups have is that we all tend to focus on our own personal narrative, rather than look at what we have in common. As a victim of chronic Lyme abuse, if I say anything about Myalgic Encephalomyelitis (M.E.) I am immediately perceived as attacking the M.E. crowd. Fingers shoot into the ears and the “la la la la las” shoot out of the mouths. I have news for you: the same thing happens in my Lyme groups, Lymie on Lymie! Very few people want to hear what I (along with ActionLyme, Ohio ActionLyme and CrymeDisease.com) am saying. I dare you, right now, to remove fingers from ears and listen up, because the science tells us that what unites us all is Chronic Sepsis or Post-sepsis Syndrome.
Take a look at this graphic. What it illustrates is that TLR2/1 agonists, at the center of all medically abused groups, provide the mechanism for nearly all chronic illnesses for which cures are denied by the government and medical establishment.
Scroll down here to the list of TLR2 agonists. There’s your OspA, your mycoplasma, your CMV (a herpesvirus), your candida, among many others. Now, remember what I’ve said before about OspA, how it causes immunosuppression and reactivation of those nasty herpesviruses In Lyme disease. All of those TLR2-agonists function in the same way. Yes, mycoplasma, candida and OspA do the same thing. This model of immunosuppression has been known since the 1950s, and has been repeatedly validated in the years since.
See here for Lyme Cryminal Dattwyler talking about a “blunted” immune response, AKA immunosuppression.
The NIH agrees with this model. We are talking about TLR-2 agonists–fungal antigens–which turn off the immune system to prevent death from sepsis and reactivate herpesviruses, whose chronicity have been widely proven as leading to cancers and neurological diseases.
NIH: profound immunosuppression is one of the chronic consequences of severe sepsis
Washington University in St. Louis: Reactivation of multiple viruses in patients with sepsis
NIH: Chronic active EBV disease (CAEBV) is a lymphoproliferative disorder
University of Michigan: The chronic consequences of severe sepsis
NIH saying medical students are *allowed* to have chronic fatigue/reactivated herpesviruses but the rest of us suckers are useless wastes of healthcare, social services and air.
Now can you see what they have done to divide us? They take our varied symptoms and use them to dump us into these different buckets, even though we all are suffering from a trashed immune system, chronic viruses, that toxic fungal-viral-bacterial soup, and all of the cancerous and neurological consequences.
As long as we are divided, money will continue to be thrown at non-curative, symptom-hiding and “psychological” treatments that do not address the root cause of all our suffering: the trashed immune system, or chronic sepsis, or post-sepsis syndrome. (And by the way, there is nothing “post” about it, really, because this immune system damage is permanent and ongoing.)
Now, if you have M.E./CFS or some variation, and you’re still with me, here is how you nail the government crooks who deny your disease and bash you as a mental case or malingerer:
“Blood was collected in sodium citrate Vacutainer tubes (Beckton Dickinson) and shipped by overnight courier to the Centers for Disease Control (CDC), where plasma was collected by separation on lymphocyte separation medium (LSM; ICN Biomedicals). Plasma (1 ml) was concentrated to approximately 250 μl in a Centricon centrifugal filter unit YM-100 (Millipore). Cell-free plasma DNA was extracted by using a QIAamp DNA Mini kit (Qiagen) according to the manufacturer’s instructions and quantified by using a DyNA Quant 200 fluorometer (Amersham Biosciences).”
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