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|    Message 31,903 of 32,593    |
|    Carlos E.R. to Retirednoguilt    |
|    Re: Higher Cancer Rates Found After Rece    |
|    06 Nov 25 21:21:50    |
      From: robin_listas@es.invalid              On 2025-11-06 16:26, Retirednoguilt wrote:       > On 11/5/2025 6:58 PM, T wrote:       >> On 11/5/25 7:39 AM, Retirednoguilt wrote:       >>> On 11/4/2025 8:23 PM, Ketanji Kornrows wrote:       >>>>       >>>> A new, peer-reviewed study by researchers in South Korea has found that       people who received COVID-19 shots showed significantly higher rates of       >>>> developing several cancers—including thyroid, stomach, colon, lung,       breast, and prostate—compared to unvaccinated individuals. The research,       >>>> published on Sept. 26, 2025 in the journal Biomarker Research, was       authored by South Korean medics in orthopedic surgery and critical care and       >>>> evaluated data from over eight million adults in the Korean National       Health Insurance database to identify a potential link between COVID mRNA       >>>> shots and cancer risk within one year after receipt of different types of       vaccines.1       >>>>       >>>> The data indicate that vaccinated individuals had roughly a 35 percent       greater increased risk of thyroid cancer and 34 percent greater risk of       >>>> gastric cancer, with lung and prostate cancers showing even higher       relative risks—53 percent and 68 percent respectively. Breast and colorectal       >>>> cancers showed increases of 20 percent and 28 percent. The authors of the       study noted that vaccinated men were more likely to develop gastric       >>>> and lung cancers, while vaccinated women were more likely to develop       thyroid and colorectal cancers.1       >>>>       >>>> https://thevaccinereaction.org/2025/11/higher-cancer-rates-       ound-after-receipt-of-covid-19-shots/       >>>>       >>>> The clot-shots don't sound safe and effective to me. Glad I'm an       anti-vaxxer.       >>>       >>> I'll provide a different explanation for the apparent finding of       >>> increased cancer incidence. People who are intelligent enough to       >>> understand the importance of quality information and advice provided by       >>> experts in virology, immunology, infectious diseases etc., are much more       >>> likely to get recommended vaccinations and are also more likely to have       >>> regular visits with medical personnel.       >>       >> Your reference?       >>       >>> Those people will experience a       >>> much greater incidence of early detection of many diseases, including       >>> cancers. People with no training in any of those fields, and who don't       >>> trust things they don't understand and therefore feel suspicious of       >>> those things and prefer to believe conspiracy theories are less likely       >>> to get recommended vaccinations and less likely to interact regularly       >>> with medical professionals.       >>       >> Your reference?       >>       >>> Their cancers remain non-existent and       >>> untallied when considering the methodology of the reference cited by the       >>> OP. Faulty study design inevitably leads to faulty data, which leads to       >>> faulty conclusions.       >>       >> The study was not faulty. But your analysis was. You       >> are pulling things out your ears based on your "beliefs".       >>       >> You are presenting your beliefs as "axiom" and challenging       >> others to disprove them. That is not how the scientific       >> method works.       >>       >> https://biomarkerres.biomedcentral.com/articles/10.1186/s4036       -025-00831-w?utm_source=chatgpt.com#citeas       >>       >>       >> Was a painstakingly well documented. But you did not       >> read it as it challenged your "axioms".       >>       >>       > Can you demonstrate where the experimental design of the study you cite       > precludes what I stated? No you can't, because the reference web page       > you cite only provides the abstract, not the nitty-gritty details of the       > experimental design. A good study protocol contains a discussion of how       > the design of the study attempts to eliminate or at least minimize the       > type of faulty conclusions you have accepted as valid.       >       > Also, your selective quotation from the abstract failed to include the       > following direct quotes from the abstract:       >       > "However, the researchers cautioned that the findings represent a       > statistical association, not proof of causation, emphasizing the need       > for further research to determine whether the increases reflect a       > biological effect or are influenced by other factors such as healthcare       > access, screening frequency, or population demographics."       >       > and       >       > "Some medical professionals caution, however, that these patterns may       > also reflect non-vaccine factors, including pandemic-related health care       > disruptions, delayed diagnoses, expanded screening programs, or an aging       > population—all of which can elevate reported incidence rates. Yale       > Medicine reports that rates of early-onset breast, colorectal, stomach,       > thyroid, and prostate cancers have been rising for years across multiple       > countries."       >       > How convenient for you not to have included those portions of the abstract!              Ah!              >       > If you try to go head to head with me I strongly suspect that you will       > lose. I spent more than a decade working full time in the management of       > human subjects medical research in a huge federal organization. For       > much of that time, I was the sole individual personally responsible for       > the safe and ethical treatment of human subjects in a huge program (over       > $100M/year) of world-wide clinical investigations. My personal       > signature was required before any human subjects medical research funded       > by the organization I worked for was authorized to recruit a single       > subject. I also had full authority to grant or retract permission to       > perform any human subjects clinical research whatever at the facilities       > where funding for these projects included funds from my organization's       > budget. I was second level review after local institutional review       > board approval of each study and commonly sent IRB approved protocols       > back for revision because of flaws in experimental design. Junk       > protocols yield junk data which reach unsupportable conclusions. It is       > unethical to subject human subjects to any risk if the outcome of the       > study is predetermined to be junk science. My background includes a       > M.D. degree and more than 5 years of post-graduate training at a       > nationally recognized ivy-league medical school. Why don't I still work       > at that organization? I'm happily retired after many decades of hard work.              Thank you.              --       Cheers, Carlos.       ES🇪🇸, EU🇪🇺;              --- SoupGate-Win32 v1.05        * Origin: you cannot sedate... all the things you hate (1:229/2)    |
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