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𝐂𝐚𝐧 𝐚𝐧 𝐢𝐧𝐣𝐞𝐜𝐭𝐞𝐝 𝐯𝐚𝐜𝐜𝐢𝐧𝐞 𝐩𝐫𝐞𝐯𝐞𝐧𝐭 𝐭𝐫𝐚𝐧𝐬𝐦𝐢𝐬𝐬𝐢𝐨𝐧 𝐨𝐟 𝐚 𝐫𝐞𝐬𝐩𝐢𝐫𝐚𝐭𝐨𝐫𝐲 𝐯𝐢𝐫𝐮𝐬 ❓ In the last episode of the The Darkhorse Podcast , Bret Weinstein explains the difference between Mucosal Immunity and Blood Immunity, and how that relates to injected vaccines. Open 🧵- Thread - #MedicalFreedom ⇒

Uriel Cohen

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20,116 görüntüleme • 1 yıl önce •via X (Twitter)

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“Hundreds of millions of people who already had Covid did not need to take any risk whatsoever from a novel vaccine.” Bret Weinstein is calling out doctors who pushed COVID-19 vaccines and are now reversing course on effectiveness. “All of the major players gathered together and privately understood the very same thing that they were gaslighting us over.” “They understood that natural immunity was the best immunity that you were going to come by and that a vaccine wasn't going to augment it.” “And they decided to keep that to themselves in spite of the fact that these vaccines are built on a novel technology they didn't know the hazards of at best.” “They were not just disagreeing with us.” “They were gaslighting us and telling people like you that people like me were crazy.” Bret Weinstein The DarkHorse Podcast Michael Shermer

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I asked Grok to explain why intramuscular vaccines don't work against respiratory viruses. The answer may surprise you; The explanation for why intramuscular (IM) vaccines might not be as effective against respiratory viruses involves understanding both the nature of the immune response and how vaccines work: 1. Site of Action and Immune Response Location: 👉Respiratory Viruses: These viruses primarily infect and replicate in the respiratory tract, including the nasal passages, throat, and lungs. The immune system's response needed here involves mucosal immunity, particularly in the upper respiratory tract where viruses first encounter human tissues. 👉Intramuscular Vaccines: These are injected into the muscle, which stimulates systemic immunity. This type of immunity primarily involves circulating antibodies in the blood and systemic T-cells. While this can offer protection against infection by mobilizing an immune response throughout the body, it is less effective at directly combating pathogens at mucosal surfaces like the respiratory tract. 2. Type of Immune Response: 👉Mucosal Immunity: For respiratory viruses, an effective defense includes IgA antibodies on mucosal surfaces, which can neutralize viruses before they enter cells. IM vaccines do not primarily induce this type of local, mucosal immune response. 👉Systemic Immunity: IM vaccines excel at producing IgG antibodies in the blood, which are effective against systemic infections but might not reach sufficient concentrations or be in the right form (like secretory IgA) in the respiratory tract to prevent infection at the point of entry. 3. Antibody Distribution: 👉Antibodies produced from an IM vaccine primarily circulate in the blood, with limited direct transport to the respiratory mucosa. The antibodies that do reach these areas might not be in the same concentration or form as those produced by a local (mucosal) immune response. 4. Memory and Rapid Response: 👉While IM vaccines can create systemic memory B and T cells, the speed at which these cells can migrate to and act in the respiratory tract might not be fast enough to prevent viral replication in the initial stages of infection. Mucosal vaccines can create a more rapid, localized response. 5. Viral Replication Sites: 👉Respiratory viruses often replicate in the epithelial cells lining the respiratory tract. An IM vaccine's immune response might not be as targeted to these specific sites compared to a vaccine administered via a route that directly stimulates mucosal immunity. 6. Durability and Cross-Protection: 👉There's also the issue of how long immunity lasts at the site of infection. Mucosal immunity might provide a more durable barrier at the entry point for respiratory pathogens, potentially offering broader or longer-lasting protection against various strains or mutations of viruses. Conclusion: While intramuscular vaccines can still provide some level of protection against respiratory viruses by reducing disease severity or preventing systemic spread, they are less ideal for preventing the initial infection at the mucosal surfaces. This is why alternative vaccine strategies, like nasal sprays or other forms of mucosal vaccination, are often considered for better efficacy against respiratory pathogens. However, IM vaccines remain crucial due to their ease of administration, stability, and effectiveness in inducing systemic immunity, which can be vital for reducing severe outcomes even if initial infection occurs. My remarks: 1. Most infectious diseases are mucosal in nature, so most IM vaccines don't work as intended, be it the flu vaccine, HIV, or RSV. 2. At best, they can reduce severe outcomes, but the opposite can also be true. Doctors have many alternative ways og reducing severe outcomes. 3. There are many alternative ways of treating and preventing severe outcomes and by doing so, inducing natural immunity. 4. So yes, vaccines are mostly just fraud.

I asked Grok to explain why intramuscular vaccines don't work against respiratory viruses. The answer may surprise you; The explanation for why intramuscular (IM) vaccines might not be as effective against respiratory viruses involves understanding both the nature of the immune response and how vaccines work: 1. Site of Action and Immune Response Location: 👉Respiratory Viruses: These viruses primarily infect and replicate in the respiratory tract, including the nasal passages, throat, and lungs. The immune system's response needed here involves mucosal immunity, particularly in the upper respiratory tract where viruses first encounter human tissues. 👉Intramuscular Vaccines: These are injected into the muscle, which stimulates systemic immunity. This type of immunity primarily involves circulating antibodies in the blood and systemic T-cells. While this can offer protection against infection by mobilizing an immune response throughout the body, it is less effective at directly combating pathogens at mucosal surfaces like the respiratory tract. 2. Type of Immune Response: 👉Mucosal Immunity: For respiratory viruses, an effective defense includes IgA antibodies on mucosal surfaces, which can neutralize viruses before they enter cells. IM vaccines do not primarily induce this type of local, mucosal immune response. 👉Systemic Immunity: IM vaccines excel at producing IgG antibodies in the blood, which are effective against systemic infections but might not reach sufficient concentrations or be in the right form (like secretory IgA) in the respiratory tract to prevent infection at the point of entry. 3. Antibody Distribution: 👉Antibodies produced from an IM vaccine primarily circulate in the blood, with limited direct transport to the respiratory mucosa. The antibodies that do reach these areas might not be in the same concentration or form as those produced by a local (mucosal) immune response. 4. Memory and Rapid Response: 👉While IM vaccines can create systemic memory B and T cells, the speed at which these cells can migrate to and act in the respiratory tract might not be fast enough to prevent viral replication in the initial stages of infection. Mucosal vaccines can create a more rapid, localized response. 5. Viral Replication Sites: 👉Respiratory viruses often replicate in the epithelial cells lining the respiratory tract. An IM vaccine's immune response might not be as targeted to these specific sites compared to a vaccine administered via a route that directly stimulates mucosal immunity. 6. Durability and Cross-Protection: 👉There's also the issue of how long immunity lasts at the site of infection. Mucosal immunity might provide a more durable barrier at the entry point for respiratory pathogens, potentially offering broader or longer-lasting protection against various strains or mutations of viruses. Conclusion: While intramuscular vaccines can still provide some level of protection against respiratory viruses by reducing disease severity or preventing systemic spread, they are less ideal for preventing the initial infection at the mucosal surfaces. This is why alternative vaccine strategies, like nasal sprays or other forms of mucosal vaccination, are often considered for better efficacy against respiratory pathogens. However, IM vaccines remain crucial due to their ease of administration, stability, and effectiveness in inducing systemic immunity, which can be vital for reducing severe outcomes even if initial infection occurs. My remarks: 1. Most infectious diseases are mucosal in nature, so most IM vaccines don't work as intended, be it the flu vaccine, HIV, or RSV. 2. At best, they can reduce severe outcomes, but the opposite can also be true. Doctors have many alternative ways og reducing severe outcomes. 3. There are many alternative ways of treating and preventing severe outcomes and by doing so, inducing natural immunity. 4. So yes, vaccines are mostly just fraud.

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