OspA, how we make em pay!

Click on the link below to view video titled “Chronic Lyme” What is the Illness to get an explanation of OspA by whistler blower Kathleen Dickson.

Kathleen Dickson explaining OspA

In the Lyme world OspA is the beginning of wisdom.

There is nothing the (CDC/ALDF) would like more than for us to continue believing that Lyme is just a bacterial infection that can be cured with antibiotics. In fact they would love it if we continued arguing over the false dichotomy, the fabricated battle between acute IDSA vs. chronic ILADS. The truth is neither of them have it right and we are wasting time fighting the wrong battles, spinning our wheels and getting nowhere. I don’t know about you but I get pretty mad when someone tries to pull the wool like this.

Lyme causes Post Sepsis Syndrome, it’s a B cell AIDS and just like HIV AIDS the initial infection isn’t what ends up doing the most damage its the immune suppression which leads to reactivations of latent viruses primarily the herpes viruses EBV, CMV etc and opportunistic infections that are the real culprits. The up side to this information is it matches our reality so well that you will likely see yourself very clearly in the following explanation and hopefully get relief from the chasing your tail game of treating infections ad infinitum and in vain. The other motivating factor is that there is no way any of us should allow the CDC/ALDF to get away with a medical genocide that has caused the suffering and deaths of millions of people – Selah (Pause and think on this).

By changing the case definition to exclude that vast majority of us with Neuro lyme and immune suppression and fraudulently removing OspA and B from testing they have deliberately left us on the side of the road to suffer and die. They committed this crime for the sole purpose of selling fake vaccine and test kits; kids dying so they can make a buck SMH. This is not some victimless crime this is a Medical Holocaust. I know OspA and permanent immune suppression isn’t a popular truth – I get that, it can be hard to come to terms with a piece of information like this, especially when many of us have believed if we treated long enough all would be well. However it IS the truth and denying it doesn’t change that so the best thing to do is learn the science as best you can, share the information and advocate for change that is based on the reality we live.

There is no celebrity waiting in the wings to save us, its just regular Joe’s like you and me and I for one do not want another generation of people completely guttered from this hideous disease.  So pony up!


OspA is an outter surface protein of the Spirochete that literally detonates and permanantly shuts down the immune system causing Post Sepsis Syndrome. The NIH agrees that 50% of people have immune suppression following a septic event.

TruthCures Justice in Healthcare

Carolyn Beans (NIH) on Live Science:

Surviving Sepsis: Detection and Treatment Advances

Some people who survive sepsis can develop secondary infections days or even months later. A research team that included Richard Hotchkiss, Jonathan Green and Gregory Storch of Washington University School of Medicine in St. Louis suspected that this is because sepsis might cause lasting damage to the immune system. To test this hypothesis, the scientists compared viral activation in people with sepsis, other critically ill people and healthy individuals. The researchers looked for viruses like Epstein-Barr and herpes simplex that are often dormant in healthy people but can reactivate in those with suppressed immune systems. [Sepsis Has Long-Term Impact for Older Adults, Study Finds]

Of the three study groups, people with sepsis had much higher levels of these viruses, suggesting reactivation due to compromised immune responses. Immune suppression could make it difficult to defend against the reactivated viruses as well as new infections like pneumonia. The team now plans to test whether immune-boosting drugs can prevent deaths in sepsis survivors.”  Taken from Truthcures.org


  • Lethargy/excessive tiredness
  • Poor mobility / muscle weakness
  • Breathlessness / chest pains
  • Swollen limbs (excessive fluid in the tissues)
  • Joint and muscle pains
  • Insomnia
  • Hair loss
  • Dry / flaking skin and nails
  • Taste changes
  • Poor appetite
  • Changes in vision
  • Changes in sensation in limbs
  • Repeated infections from the original site or a new infection
  • Reduced kidney function
  • Feeling cold
  • Excessive sweating


  • Anxiety / fear of sepsis recurring
  • Depression
  • Flashbacks
  • Nightmares
  • Insomnia (due to stress or anxiety)
  • PTSD (Post Traumatic Stress Disorder)
  • Poor concentration
  • Short term memory loss
  • Mood swings

OspA is the mechanism and Post Sepsis Syndrome/ B cell AIDS is the outcome. Blebs or Osps that the Spirochete sheds are triacylated lipoproteins that are TLR 2/1 agonists. Anything that is a TLR 2/1 agonist sends the message to the immune system to shut down in order to prevent a deadly cytokine storm. Prior to this shut down the Septic event is in process and is causing a range of damage in the person depending on many factors such as virulence of the infection and the size and health of the person at the time of the event. A serious septic event can cause organ, vascular and cellular damage that can be permanent. These triacylated lipoproteins are so toxic that the body has no other option but to shut down in order to preserve life. While this is an adaptive response of the host it also causes many negative downstream effects such as immune suppression, tolerance and cross tolerance.

1-These results demonstrate that B. burgdorferi can stimulate the production of an antiinflammatory, immunosuppressive cytokine in naive cells and suggest that IL-10 may play a role both in avoidance by the spirochete of deleterious immune responses and in limiting the inflammation that the spirochete is able to induce.

Tolerance means that the immune system is no longer mounting a response to the pathogen, in this case borrelia burgdorferi (Bb) so in essence it has learned to ignore it, but that doesn’t mean it doesn’t continue to do damage because it certainly does. Cross tolerance is when the immune system also ignores other pathogens that bind to different TLR’s. For example OspA causes the immune system to ignore your common bacteria’s that normally bind to TLR 4 as well as viruses that bind to TLR 7 and 9 along with Borrelia itself (this is why if you get lyme a second or third time the immune system does nothing to combat it, it has not created memory cells from the previous exposure as the immune system normally would).

OspA is the main mechanism of the disease, we know this because you don’t actually need spirochetes to get all the symptoms of Neurological lyme all your need is OspA. Additionally, the first Lyme vaccine which was an OspA vaccine gave many people all the symptoms we associate with chronic Lyme disease.

Within 10 days of infection the germinal centres where B cells are assigned an immune duty have been shut down. B cells normally mature into antibody secreting cells, however in the presence of lyme they do not mature properly and therefore are functionally unable to produce antibodies needed to flag the immune system to respond causing B cell AIDS.  A permanently paralyzed immune system is a big deal that deserves real research attention and dollars and WE DESERVE JUSTICE!!! 

Post Sepsis Syndrome -Non HIV B Cell AIDS


#OccupyJustice # JoinUs

For more info check us out at TruthCures.org


1. Infect Immun. 1998 Jun;66(6):2691-7. Borrelia burgdorferi stimulates the production of interleukin-10 in peripheral blood mononuclear cells from uninfected humans and rhesus monkey

2. Sepsis Alliance Webpage.

3. TruthCures Justice In Healthcare

4.Borrelia burgdorferi Induces TLR1 and TLR2 in human microglia and peripheral blood monocytes but differentially regulates HLA-class II expression.

5. Circulating bacterial membrane vesicles cause sepsis in rats


Author: flipside908602935

Post Sepsis Syndrome patient and citizen scientist.

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