….Continuing on to Part 2 – Click here for Part 1
The LYMErix vaccine caused the same disease that us tick bite sepsis victims know as “Chronic Lyme disease”. It was not taken off the market due to low sales. The manufacturer SmithKline Beecham was given an ultimatum in 2002 by the FDA to take it off the market or they would. This whole LYMErix fiasco is the reason that no one can get diagnosed or treated today. I am shocked and astounded that anyone would even try to put out another vaccine for a disease caused by an organism capable of antigenic variation. The French company Valneva is starting their phase 1 trials here in the United States and in Belgium this year.
OspA vaccination caused the same disease from a syringe as it does when you get Lyme disease from a tick bite. LYMErix victims immune systems were destroyed by the vaccine because OspA is an endotoxin that causes immunosuppression and subsequent severe neurologic multi-system disease.
“A wide range of neurological complications have been reported via the medical literature and the VAERS system after vaccination with recombinant outer surface protein A (OspA) of Borrelia. To explore this issue, 24 patients reporting neurological adverse events (AE) after vaccination with Lymerix, out of a group of 94 patients reporting adverse events after Lymerix vaccination, were examined for causation. Five reports of cerebral ischemia, two transient Ischemic attacks, five demyelinating events, two optic neuritis, two reports of transverse myelitis, and one non-specific demyelinating condition are evaluated in this paper.” https://www.ncbi.nlm.nih.gov/pubmed/21673416
LUFT: “The point that I wanted to make in regard to the study is that there is very heavy dependence on serologic confirmation. “And when we start thinking about the adverse events, it was stated originally when we got the overview of the disease that the disease is really quite protean. And actually the adverse events are very similar to what the disease manifestations are.” http://www.fda.gov/ohrms/dockets/ac/98/transcpt/3422t1.rtf
DR. PARENTI (SMITHKLINE): “Basically the two groups had the same suspect symptoms. We didn’t put it through statistical rigor, but when you looked at what it is that people came into the office with, what complaints, there was basically the same complaints in both groups. So both groups were being evaluated for the same things.” http://www.fda.gov/ohrms/dockets/ac/98/transcpt/3422t1.rtf
“Additional uncertainty may arise if the vaccines are not completely protective; vaccinated patients with multisystem complaints characteristic of later presentations of Lyme disease may be difficult to distinguish from patients with vaccine failure.” http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6045804.PN.&OS=PN%2F6045804&RS=PN%2F6045804
OspA is Pam3Cys, a TLR 2/1 agonist which makes it an endotoxin. What that means is that it causes permanent immune suppression. This is referred to as “immune tolerance”, or “immune paralysis”, or when you read about the immune system becoming “overwhelmed”. It creates a state of chronic sepsis, or post sepsis syndrome. Once this happens viruses (that everyone has but can usually keep under control) like EBV and herpes reactivate and these are drivers of the “Great Imitator” outcomes we are all so familiar with. Your body loses the ability to fight off other pathogens as well as the reactivation of latent viruses. Injecting someone with an endotoxin like OspA and calling it a vaccine is criminal, plain and simple. The reason the vaccine failed and caused these severe adverse reactions is because of what OspA is and does, being a TLR 2/1 agonist.
“The similarity between the neurological sequelae observed in the OspA-vaccinated patients and those with chronic Lyme disease suggests a possible role for immune mechanisms in some of the manifestations of chronic Lyme disease that are resistant to antibiotic treatment.“ https://www.ncbi.nlm.nih.gov/pubmed/15363064
The criminals produced all of this data to market the vaccine saying how bad Lyme was to create a demand for their product. We all needed to get this vaccine because the disease was so devastating and damaging to the brain. The victims themselves said that this was the reason they got the vaccine in the first place, so it’s a little ironic that now it’s “anti-vaxxers” fault that people are contracting Lyme because there is no vaccine.
“I am unable to attend the January 31 FDA Vaccine Advisory Committee meeting due to a restrictive condition, Transverse Myelitis, resulting from the Lymerix vaccine. In the spring of 1999, I decided to get the series of Lymerix shots, after, viewing a very convincing TV commercial touting the importance of protecting oneself from Lyme Disease. I felt this would be a good thing to take advantage of since I had had numerous bites from the ticks which cause Lyme Disease.” https://www.fda.gov/ohrms/dockets/ac/01/slides/3680s2_11.pdf
The reason that this fraud was committed was solely to qualify the LYMErix vaccine, they knew as early as the phase 1 trials that OspA was causing the same disease. The plan the entire time was to make Lyme disease only 15% detectable, and to do that they needed to change the testing and the case definition. If they said that the 85% of immunosuppression neurologic outcomes didn’t exist then they could say that they vaccine was 85% effective. It’s really that simple. They realized that there were two types of the disease, so they cut one of them out effectively ruining millions of lives. They saw an opportunity to corner the market by patenting all of the different tick borne diseases and only allow certain labs to test the blood. (They wanted all of the blood to go only to them so they could find other diseases to patent for vaccines and test kits, but thats another story for another post.)
Before this master plan was put into motion Allen Steere wrote all about deformed B cells with Paul Duray. Lyme Borreliosis went from being a severe multi-system neurologic disease largely driven by immune suppression/dysfunction to being Lyme disease with just an arthritic knee and robust antibody production.
“The plasma cell precursors are large, appear tumor-like, and can resemble Reed-Sternberg cells. Others look like typical immunoblasts (FIG. 1). In one example, cervical lymph nodes show cell degeneration with karyorrhexis and nuclear debris of lymphoid elements. This patient had repeated high fevers and marked discomfort of neck nodes. Large atypical immunoblasts can also be seen in the spleen and bone marrow. The red pulp of the spleen is congested, not unlike that seen in infectious mononucleosis. Spirochetes can be demonstrated in the lymph nodes, spleen and bone marrow and liver.” https://www.ncbi.nlm.nih.gov/pubmed/2847622
That certainly doesn’t sound like an easy to cure illness with 21 days of doxy to me..
”…when lymphocytes are cultured in the presence of growing Bb there is a marked inhibition ( p < . 0005 ) of NK activity on days 3, 5, and 7 when compared to lymphocytes cultured in BSKII media in the absence of spirochetes. This effect is not due to a selective depletion or toxicity to endogenous NK since viability studies and monoclonal antibodies demonstrate no significant changes after culture with the organism. The inhibition is directly attributable to the organism or its supernatants [lipid layer] (data not shown).” http://www.ncbi.nlm.nih.gov/pubmed/3056196
“OspA interferes with the response of lymphocytes to proliferative stimuli including a blocking of cell cycle phase progression.”
Immune suppression. Dattwyler says that the lower the antibody production (seronegativity) the sicker the patient is.
Dr.O’BRIEN: “I was concerned about your last slide where you said there was a poor correlation between serologic response and clinical disease. And as I heard you to say, some people who mount better immune responses get worse disease. Did I hear you say that?”
DR. DATTWYLER: “No, no, I said the reverse. The better responses tended to have better response. And I should clarify where this is from. This is from antibiotic trials. These are treatment trials of erythema migrans, in which individuals given an antibiotic regimen which was not optimal – we did not know that it was not optimal at the time – the ones that failed to mount a vigorous response tended to do worse, clinically. So, there was an inverse correlation between the degree of serologic response and the outcome.” “So, individuals with a poor immune response tend to have worse disease.“
There you have it. Everyone is saying that tick bite Lyme disease and LYMErix cause immune suppression and severe debilitating illness. This is just a tiny snapshot of the data compared to what is in the Charge Sheets on TruthCures website. As always, I encourage you all to go there and check them out in their entirety.
Stay tuned, we still have more to talk about 😉