covid is oncogenic

If I die and one of my relatives (or ex) gets on this account claiming to have loved me, please roast them mercilessly till they delete the account.

I absolutely destroyed my teeth in high school/college and its one of my deepest, life long insecurities. I have so much fear & anxiety about my teeth

I smell another lockdown coming.

Oh, and Gov UK, could you be more specific? Are we inhaling droplets or aerosols? Perhaps you missed this. Link to page in replies.

This is going to be worse than COVID. We are screwed.

A what now?! A fungal storm???

⚠️🦠The surge in meningitis and other invasive infections following the COVID-19 pandemic is increasingly understood not just as a result of "immunity gaps" from lockdowns, but as a direct biological consequence of how the SARS-CoV-2 virus interacts with the human body. Research from 2024 through early 2026 has identified several specific physiological mechanisms—ranging from the degradation of physical barriers to long-term immune remodeling—that explain why individuals may be more susceptible to bacterial and viral pathogens after a COVID-19 infection. 1. Disruption of the Blood-Brain Barrier (BBB) The most direct link to meningitis is the virus's impact on the brain's protective lining. SARS-CoV-2 doesn't just affect the lungs; it significantly compromises the integrity of the Blood-Brain Barrier. * Increased Permeability: The virus increases the expression of matrix metalloproteinase-9 (MMP-9), an enzyme that degrades type IV collagen in the basement membrane of the BBB. * Endothelial Damage: By infecting neurovascular cells, the virus triggers "mast cell activation" and restructuring of the cellular cytoskeleton. This creates "gaps" in the barrier that normally keep bacteria like Neisseria meningitidis (meningitis) out of the central nervous system. * Trojan Horse Entry: COVID-induced inflammation increases the transmigration of infected or activated leukocytes. These cells can "carry" secondary pathogens across the weakened BBB into the brain. 2. Mucosal Barrier Breakdown and "Ciliary Loss" Bacteria that cause meningitis often live harmlessly in the nasopharynx (the upper part of the throat). For these bacteria to become "invasive" and enter the bloodstream, they must bypass the mucosal immune system. * Mechanical Failure: SARS-CoV-2 causes ciliary loss—the destruction of the tiny hair-like structures that sweep bacteria and mucus out of the airways. Without this "escalator," bacteria can settle and colonize the tissue more deeply. * Epithelial "Leaking": The virus damages tight junctions (the "glue" between cells) in the respiratory lining. This allows bacteria to slip between cells and enter the bloodstream, a prerequisite for bacterial meningitis and sepsis. 3. Systematic Immune Dysregulation (T-Cell Exhaustion) While the "immunity gap" theory focuses on a lack of exposure, the "immune dysregulation" theory focuses on the damage done by the virus to the immune system's architecture. * T-Cell Exhaustion: Post-COVID patients often show signs of "T-cell exhaustion," a state where T-cells (the "generals" of the immune system) are functionally impaired and express high levels of inhibitory receptors. This limits the body's ability to mount a rapid defense against secondary viral and bacterial threats. * Lymphopenia: SARS-CoV-2 frequently causes a drop in total lymphocyte counts. Studies in 2025 have shown that even 12 months after a "mild" infection, some patients retain a signature of immunological hypofunction, making them significantly more likely (up to 46% more likely in some cohorts) to test positive for non-SARS-CoV-2 infections. * Interferon Suppression: The virus is highly effective at suppressing Type I and III interferon responses. These interferons are the body's first line of defense against both viruses and bacteria; when they are "dampened," the threshold for a secondary infection to take hold is much lower. 1/2