Evidence existed to us in the research & medical field as far back as 2,500 years ago with the Athenian Plague (PELOPONNESIAN WAR) that natural immunity was robust, life-long, bullet-proof; far super-
ior that any immunity a vaccine could confer, ever! Yet CDC, NIH, FDA, Health Canada, PHAC, Fauci, Njoo, Tam, Bourla, Bancel, Malone, Birx, Redfield, Hahn...all, LIED, misled Trump & populations
para, the same man affected was never attacked twice…that was folks, natural immunity…read the highlighted text below.
What I am showing you IS natural immunity 2,500 years ago…in the Athenian Plague…yes, 2,500 years ago…they just did not know what that was yet it was how natural immunity conferred protection…past exposure and RECOVERY conferred protection and when you read the translated account, they were describing natural immunity…akin to Edward Jenner’s rudimentary and first inoculations with cow pox pus from a blister…
Now to the Athenian Plague text, written for 2,500 years ago…para the same man was never attacked twice…that statement was all about natural immunity, see highlighted text below (2,500 years old during the plague)….:
The Project Gutenberg eBook of The History of the Peloponnesian War, by Thucydides
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Hey Doc I have some intel for you. I was tested for "immunity" to Covid 19 four times in three different labs, in two different countries in 2022 and early 2023, and my "count" was so high that the 'puzzled' family doctor sent that information off to some 'authorities' in Vancouver, B.C. We were also contacted by the La Paz County health officials and asked (because of our natural immunity) to donate blood in Phoenix, Arizona, where they were trying to save some lives in early 2022. I first had "Covid" in February 2020, a mild fever of 101F, for about six hours. Nothing worthy of calling a "pandemic". I seldom feel unwell. HOWEVER...I was denied entry to the U.S. from Canada, despite owning property and with valid visa's, in October 2022 because I was asked about my Covid "vaccination" status...a single question from the border guard...and I replied that I was not "vaccinated" but do have documents to prove I am immune to Covid, cannot receive or infect. The U.S. border guard said..."IT IS NOT ABOUT IMMUNITY....ALL CANADIANS MUST TAKE THE JAB". So we spent the winter in the Yucatan, where we were once again asked to donate blood to save another life. So.....what was all this crap about '2 weeks to achieve' "herd immunity" (a rhetorical question, of course). I thought "vaccines" were all about immunity...no one with the vax has gained immunity to infection, and they transmit infection...more so than "unvaccinated" folk. In fact, the "immunized" are sick a lot, and many are dead or sick, and dying. All of these miscreants lied repeatedly to us, and we need some justice carried out. (They are not very good at lying either.) Liars do not go to heaven. REV. {21:27}..." And there shall in no wise enter into it any thing that defileth, neither [whatsoever] worketh abomination, or [maketh] a lie: but they which are written in the Lamb’s book of life." (Jesus is our Shepherd, we are His heritage...that is why they are killing us all the day long.) So, Doc, none of those you have identified will be present in heaven...which means they will be ashes and dust, never to be remembered again for eternity. Thanks for sticking to the truth Doc. God bless you.
Immunological memory is the ability of the immune system to quickly and specifically recognize an antigen that the body has previously encountered and initiate a corresponding immune response. Generally these are secondary, tertiary and other subsequent immune responses to the same antigen. Immunological memory is responsible for the adaptive component of the immune system, special T and B cells — the so-called memory T and B cells.
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IgG antibodies are Y-shaped protein molecules that are produced by special white blood cells (B lymphocytes) in response to foreign substances (antigens) such as viruses or bacteria. Antibodies can attach to these viruses or bacteria, rendering them harmless and unable to penetrate healthy cells. They GO AWAY with time and could fall to a NEGATIVE level DOESN'T mean susceptible.
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Total immunity against viral diseases includes:
1. Local IgA and IgM
2. Humoral immunity of IgG antibodies, both those present in the blood AND those that can be produced quickly when the antigen is present
3. Cellular immunity or MEMORY
4. Other mechanisms.
When we measure antibody titers, we are ONLY documenting the IgG antibodies present in the bloodstream.
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The Immune System fires up when a pathogen, like a virus, enters the body. The pathogen releases a protein called an antigen, which calls into action the immune system’s special disease-fighting cells. "Called B and T lymphocytes", these cells NOT only destroy the virus, but they REMEMBER what it looked like so they can fend it off in the FUTURE.
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IMMUNOLOGIC MEMORY allows the immune system to REMEMBER the antigens or organisms to which it has previously been exposed. MEMORY EFFECTOR B cells (long-lived plasma cells) and MEMORY T-cells specific to a virus, give long-term immunity against these diseases.
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ADAPTIVE IMMUNITY.
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The “Adaptive Immune Response" is younger than the “Innate Immune Response" in evolutionary terms and is more specific and considerably MORE POTENT in its effects.
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The constituents of the adaptive immune response are the lymphoid cells. These include:
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The T lymphocytes and the cytokine and chemokine messenger proteins released by these cells, which direct and REGULATE the adaptive immune response.
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The B lymphocytes, which transform to the late-stage plasma cells that produce and secrete antibody.
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The lymphoid cells of the adaptive immune response reside in, and circulate between, the various lymphoid tissues of the body (e.g. the lymph nodes, spleen and mucosal lymphoid tissues). In the adaptive immune response, antigen is first transported from a site of infection by a dendritic cell to the regional lymphoid tissue. That dendritic cell in turn activates "Antigen-Specific T lymphocytes," which further activate Antigen-Specific B lymphocytes.”
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These activated, Antigen-Specific lymphocytes must then be mobilized from the regional lymphoid tissue and sent to the site of infection, a process that involves these cells moving into the lymphatic and blood circulation and interacting with the endothelial lining of blood vessels.
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Once these cells reach the site of infection, they are able to mount a full-scale ‘EFFECTOR’ response, which is considerably STRONGER than that permitted by innate immunity. As these processes take some time to occur (in the order of 4–7 days), there is a delay before adaptive immunity ‘takes over’ from the innate form of defence.
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The final component of Adaptive Immunity is the development of a “REGULATORY RESPONSE" that will "SWITCH OFF" the system when it is NO LONGER REQUIRED (i.e. when the pathogen has been ELIMINATED) so as NOT to cause DAMAGE to normal body tissue.
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HOWEVER, once this is achieved, the immune system retains the “MEMORY” of that immune response.
IMMUNOLOGICAL MEMORY is another key feature of the Adaptive Immune Response. MEMORY allows the generation of a much MORE effective SECONDARY IMMUNE RESPONSE (Anamnestic MEMORY Response) if that same antigen is EVER RE-ENCOUNTERED.
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