12 Comments

Location, location, location - good advice in real estate but even better when applied logically to viral pathology, vaccinology , & immunology . But true logic was sold out to the highest bidder a while back & the vaccinees were all left holding the empty bag .

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They wanted the needle in every arm. That was the purpose. The virus was just a tool to get there. They want money, compliance, power, treating people well could only complicate that, pamper them, make them more aware of suffering, less available to experiments, manipulation and power grab.

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The jab/s are the bioweapon not the virus.

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Simple: Covid was never the depopulation weapon, but an excuse for the bioweapon, depopulating "vaccine".

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The reason the “vaccine” failed is because it is designed to fail.

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I’m looking forward to reading your book. Is it possible to get a signed copy?

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"vaccines that are injected into the muscle—i.e., the interior of the body—will only induce IgG and circulating IgA, but not secretory IgA"

I am not pro-vax at all (never took it) and think it's dangerous; Vit.D + Vit.C + zinc are actually safe & effective in comparison. But I told someone else there's no secretory IgA in mucous membranes from injections to the arm and they showed me some studies claiming to have found it post-vax

I didn't save them but I searched and found these:

https://www.nature.com/articles/s41385-022-00511-0

https://www.nejm.org/doi/full/10.1056/NEJMc2213153

for example. so the shots are alleged to result in secretory IgA, but of course only for the spike protein, not the whole virus

But there's also this:

https://www.aacc.org/science-and-research/scientific-shorts/2022/covid-breakthrough-infections-may-be-due-to-failure-of-systemic-vaccine-to-induce-nasal-iga-immunity

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This was a planned bioweapon to use against humanity. The whole COVID-19 AND ‘vaccine’ are a huge experimental psyop and attack on the people of the world to reduce the population planned by eugeinicists for many years, using the military industrial medical complex and public funds.

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I had a patient with secretory immunoglobulin A, sIgA, immunodeficiency, lack of ability to produce it, apparently a genetic mutation, presumably from birth. This was dramatically different from another patient(s) with other Ig deficiency (IgG, IgM, ...), although all had some bronchiectasis.

The patient with sIgA deficiency had chronic sinusitis, and only mild bronchiectasis, which was found on an immunoglobulin screening assay for bronchiectasis. He had been mostly healthy to retirement age, but I first met him in extremis, low SpO2, with chest x-ray white-out, pulmonary edema versus pneumonitis or likely both, unlikely to be fibrosis, as it cleared shortly after starting Prednisone & Azithromycin. Need for supplemental O2 declined over weeks, to complete recovery. He had occasional repeat bouts, with years between attacks, although chronic sinusitis was a continuing complaint. The impressive point though was his relatively mild disease, doing quite well without sIgA, which was in contrast to other patients with other immunodeficiency. Maybe that's why an IgA, mucosal vaccine was not considered earlier? IgA seems to have less importance to protecting the lung, though just conjecture. I understand though sIgA can be very important to mucosal infection and spread of disease. Just another viewpoint...

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It failed for the same reasons all vaccines fail. The body does not need or want them. If you read "Turtles All The Way Down", you will discover the entire vaccine empire is built on quicksand, a total lack of science and mystique. There is no proof anywhere that supports vaccines or mRNA gene altering injections saving lives, making people healthier or preventing anything...except maybe a healthier life.

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The win was in our capture.

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I can see how this course could help prophylacticly, but once in your blood stream don't see it.

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