Occam’s razor (or Ockham’s razor) is a principle from philosophy. Suppose there exist two explanations for an occurrence. In this case, the simpler one is usually better. Another way of saying it is that the more assumptions you have to make, the more unlikely an explanation is.
We need to understand how this disease really works. It is not about inflammation, it is about tolerance and cross-tolerance. They are polar opposites. Hope it helps 💚
Original Intro From TruthCures Edition:
“This Occam’s Razor report contains many proofs that the Health and Human Services (HHS.gov) knows what Lyme and Chronic Fatigue Syndrome are. We chose the term ”Occam’s Razor” for this section of the Cryme-ology due to all the decades-long chatter in the self-help groups that Chronic Fatigue Syndrome was due to some mysterious, unknown virus.
Eight 8 million people in the USA have Fibromyalgia (says the NIH) and 4 million have Chronic Fatigue Syndrome (CFIDS, says the NIH) and for decades the Lyme Cabal said non-Dearborn Lyme was CFIDS and Fibro, … and if OspA caused the same immunosuppression/AIDS-like outcome as Chronic Lyme, as the Cabal members themselves claimed, and if the commonest thing reactivated in immunosuppression is Epstein-Barr and its brothers, Cytomegalovirus, HHV-6, as well as Coxsackie (Foot-and-Mouth Disease), etc., … and if the NIH had a “Lyme and MS group, “ at the National Institute of Neurological Disorders and Stroke (NINDS) and who now say Lyme and LYMErix activated EBV (or whatever we’re thinking is the combination of herpes viruses that are responsible for MS) via immunosuppression,…. and who say that OspA vaccination alone causes the exact same disease as Chronic Lyme, Chronic Fatigue Syndrome and Fibromyalgia, … and if the NIH now says post-sepsis syndrome is characterized by reactivated EBV and CMV, etc., … then Chronic Lyme, Chronic Fatigue, and Fibromyalgia are probably not due to some mysterious, unknown virus.
They know what it is. It’s something common, and not extraordinary.
It’s something that happens in other cases of immunosuppression such as with Humira and Stelara, transplant victims who receive immune suppressing drugs; it happens when people have Malaria plus latent Epstein-Barr (Burkitt’s Lymphoma) it happens in experiments with other fungal antigen vaccines or vaccine-ish experiments such as Tuberculosis or with the fungal lipoproteins from Brucella, and it happens when perhaps children are injected with a live attenuated virus vaccine that is contaminated with mycoplasma or some other fungal antigens. It happens when astronauts and medical school students are stressed from strange hours and their environment, this reactivation of latent herpes viruses.
It is a well-known thing, and that is why it is ignored.
But when this immunosuppression from fungal antigens occurs via tick bites or ridiculous choices for vaccines, such as the triacyl lipoprotein “vaccine,” LYMErix or OspA, these same government employees trash and harass their victims – which is a Deprivation of Rights via Color of Law charge— because then we are barred from access to real healthcare, being labeled “psychiatric”. ”
-TruthCures Founders Kathleen Dickson and Beaux Reliosis
“When you hear hoofbeats think horses, not zebras”
The first thing we need to understand is that we are victims of a cryme. The cryme is the disease, the disease is the cryme. CDC officers committed fraud and literally changed the definition of “Lyme disease” and changed the testing so that all of the neurologic immune suppression outcomes that we know as “Chronic Lyme” would be ruled out. They did this in their pursuit to commercialize tick borne diseases and test kits. To make a long story short- if they denied that this chronic neurologic immunosuppression outcome (which accounts for 85%) of cases exists then they could say that they had an 85% effective vaccine. This is why we cannot get diagnosed or treated. “Lyme disease” today means that you just have arthritis in a knee with no other symptoms. Lyme disease in itself is a misnomer.
They changed the definition of the disease by saying you can only have “Lyme disease” if you have a robust immune response, which most of us don’t because we get the post sepsis syndrome outcome. The diagnostic standard AND the definition of the disease were both changed in their pursuit to commercialize tick borne infections by making vaccines and test kits to sell:
There are two completely separate outcomes of the disease.
The case definition and two-teir testing method that we have right now is set up to ONLY include the 15% of cases that have the HLA-linked hypersensitivity response (think allergy) and is designed to fail detection of the other 85% of cases. The 15% are the “CDC positive” people and they make a lot of antibodies, whereas the other 85% of us have immune suppression and a very small in comparison antibody response. Here is Dattwyler talking about the difference and commenting on how rare the allergy-like response is:
DR. DATTWYLER: “I see a lot of patients, and I must say that treatment resistance lyme arthritis in our center is low, it is very rare. We see maybe one case a year. And, you know, that is using very strict criteria, saying that the person had, you know, CDC criteria for seropositivity, good history, and usually is monoarticulate knee arthritis.” http://www.fda.gov/ohrms/dockets/ac/01/transcripts/3680t2.rtf
Here is Shapiro on a TV show saying that there are two types of the disease, which we all know is the problem:
No inflammation. Spirochetes are not regular bacteria.
So, most of us have the neurologic-, sub-immune type of the disease. We are seronegative and much sicker than the HLA-linked 15%. The sickest are the OPPOSITE of what the graphic below shows. But since the Dearborn “falsification-of-the-standard-event” only the NOT-SICK, arthritis patients are allowed to have “Lyme disease,” anymore. But the TRULY sick, the 85% without the genetic predisposition to arthritis (without the HLAs), DO NOT have an immune response past the initial “cytokine storm” when bitten by the tick. Our (the 85%’s) body’s way of protecting us and surviving this is to shut down the immune response to protect us from stuff like tissue damage. This renders us immunocompromised, which means we are now susceptible to secondary infection.
If the LYMErix vaccine had no spirochetes, yet caused the same disease we know as Chronic Lyme, what does that mean for us?
The LYMErix vaccine was taken off the market because it was giving people the same chronic neurologic disease that it was intended to prevent. How could an injection of an outer surface protein (Osp) alone cause disease? Well, as it turns out, OspA is a triacylated lipoprotein, or Pam3Cys. OspA is a TLR 2/1 agonist, which means that it is fungal-ish and immunosuppressive. It’s the shed blebs that cause the disease by damaging your immune system and causing post sepsis syndrome. Humans just can’t take fungi. It effects the hosts immune system in such a way that as a preservation mechanism the immune system shuts itself down- if it didn’t you would have a cytokine storm and die. It’s a coping mechanism for the hosts survival, Borrelia Burgdorferi is not the only germ that can do this to a human.
We are not the only ones complaining about the fact that OspA alone caused the disease we know as “Chronic Lyme”. Pat Smith brought Donald Marks- a vaccine trial administrator- in a year later to the FDA to make the same claim:
“Pattern of symptoms experienced after Lymerix mimicked pattern of prior infections in many individuals.” — Donald Marks
There is yet another scientist saying the same thing that we are. OspA injection (LYMErix) caused the same neurologic immunosuppressive outcome as everyone gets from tick bites. At the time everyone thought that OspA injection was reactivating past Lyme infection, but that was before we knew the structure of OspA. Now we know exactly why these patients got sick, and this is why we are saying that this disease is NOT about spirochetes, it is NOT just a chronic bacterial infection.
You can have “Chronic Lyme disease” from just outer surface protein A. You don’t even need the whole spirochete to get this disease. OspA is an endotoxin that causes immunosuppression AKA post sepsis syndrome. OspA is Pam3Cys:
The endotoxin OspA is what is keeping patients sick, it’s about more than just persistence. You cannot kill spirochetes and expect the immune system to bounce back into functioning at normal capacity. This endotoxin causes something called immune tolerance which means that your body stops properly recognizing other pathogens, too. The result is reactivated viruses and opportunistics of all kinds flourishing unchecked and this is what makes us feel so sick. HIV/AIDS is a T cell problem, Lyme/AIDS is a B cell problem. This is called post sepsis syndrome.
All roads lead to EBV.
There is no other outcome for immune suppression- Reactivated viruses are the rule, not the exception.
Here are some reports showing us that TLR 2/1 agonists like OspA do exactly what I’m saying:
From Wormser: “…OspA interferes with the response of lymphocytes to proliferative stimuli including a blocking of cell cycle phase progression.” https://www.ncbi.nlm.nih.gov/pubmed/10865170
“This finding suggests that there is redundancy in the ability of the innate immune system to recognize B. burgdorferi and/or that these components can activate pathways that produce anti-inflammatory cytokines, … – the anti-inflammatory effects might be the more important function of TLR signaling.” http://www.actionlyme.org/Steere_Wormser_Admit_Immunosuppression.2016_Dec_15.pdf
(The full Occam’s Razor I linked at the top includes many more such reports, I encourage you all to go and read them.)
“THE ANTI-INFLAMMATORY EFFECTS MIGHT BE THE MORE IMPORTANT FUNCTION OF TLR SIGNALING” <<<<<<<!!!!!!!!!!!! This is exactly what we all need to understand. This is what the disease is about. It is not autoimmune, it is the opposite. Post sepsis is much more serious than autoimmune. You are literally the walking dead. Your B cells have turned into zombies and killing bugs will NOT undo that. Your immune system is already calmed down, so is the inflammation. It’s the VIRUSES like EBV, Herpes and CMV that are the true drivers of disease and the true culprits of autoimmune type responses. Not everyone gets the autoimmune stuff, some of us don’t have the HLAs for that type of response to stuff like EBV. Everyone keeps insisting that they have inflammation from Lyme disease and that isn’t true at all. The patients with MS or Lupus have an HLA that makes them create lots and lots of antibodies to VIRUSES and that is the true reason for the autoimmune response. It is the SECONDARY opportunistics, not LYME. Not everyone with this disease gets an autoimmune disease from it, in fact most of us don’t. Please let me know if this isn’t making sense to you and I will try and explain it in a different way perhaps. We need to look at this without our own experiences blinding us. You won’t see the big picture if you are trying to relate yourself to it. Once you learn what it actually does then you will naturally see where you fall. But for the sake of millions of us suffering and only a handful of us trying to get this prosecuted, let’s try to take ourselves out of the equation. We need to come together and stand up for each other.
“It is a well known thing, and that is why it is ignored”. The frustration is due to the medical community NOT getting that, or giving it the attention that it really deserves.
They use OspA to induce experimental sepsis. But they called it a vaccine for “Lyme disease”. OspA is worse than lipopolysaccharide (LPS), the more highly acylated the worse it is. OspA is a very potent endotoxin. TLR 2/1 agonists are known to do this. Doctors seem to be lacking the scientific knowledge or reading ability (PubMed is there for them after all) to learn about how their patients can be sick WITHOUT INFLAMMATION.
(Now they are trying to come out with another OspA vaccine for Lyme disease, trials are set to start very soon in Nebraska. I recently did a series about LYMErix and OspA vaccines that you can check out.)
Something like 90% of the population is infected with EBV. EBV is known as the cancer virus and has been the suspect of causing all kinds of illnesses from MS to Lupus to cancer etcetera. So the take home point here is:
- We can’t get diagnosed or treated because we are victims of a cryme
- Lyme causes immunosuppression because OspA is Pam3Cys, we know this because of the downfall of LYMErix causing the same multi-system neurologic disease as “Chronic Lyme”
- The type of immunosuppression from the shed blebs from spirochetes is irreversible, it is a problem of tolerance and cross tolerance in the immune system.
- That means NO INFLAMMATION which is all doctors are trained to look for.
- Viruses reactivate in the presence of immune suppression (EBV, CMV, Herpes..) and these are the true drivers of the Great Imitator outcomes (CFS, Fibro, even ALS, MS, Lupus) that we are seeing
- Killing spirochetes is not going to fix this
We all really need to understand what this means. The crux of this whole issue lies in understanding what OspA is and what it does. OspA is the reason we don’t have inflammation that can be measured in tests and what gives doctors the idea that we are not physically sick. It’s the reason we stay sick and the reason that none of the available treatments actually help us in the long run. You may feel better temporarily killing off the mycoplasma, but it will grow back and you will likely relapse and it’s because of this tolerance and cross-tolerance in the immune system. There is no cure, we all know this. What most of us don’t seem to know is what the disease actually is and that is the fault not only of the CDC but of ILADS as well.
If OspA caused the same disease, then what are they all treating? We can all see in the groups that a lot of people don’t improve by killing bugs.
How are antibiotics supposed to fix this?
Please visit TruthCures.org and check out the Charge Sheets, it’s a free book telling us everything we need to know about this disease from why we can’t get diagnosed, what it does to our bodies, and what the solution to get out of this mess is.
I wrote another blog post recently about tolerance and cross-tolerance, click HERE to read it.