We are delighted to welcome Mr. Anthony Fulker from Canada to our Keihan Clinic! After his long flight from Canada, he is taking some time to rest and receive an IV vitamin C infusion ahead of tomorrow’s Saisei Mirai Conference 2026. We look forward to his presentation and to welcoming you all tomorrow, October 25, in Osaka! Registration is required for both in-person attendance and online viewing after the event. Please register through our website: saisei-mirai.or.jp/en/

Happy to discuss the solution. Privately or publicly. Whatever you want. We had a good discussion Jan 2024 episode 355 about kidney failure and vax deaths. I have a lot more info now that no one else in the world has discovered.

A patient tells their doctor, my arm started losing feeling two days after the vaccine, and now I’m losing feeling in my chest and I’m having trouble breathing. The doctor’s answer is that it couldn’t be the vaccine. That’s the argument happening in exam rooms right now instead of the one that should be happening. Nobody is asking which vaccine, or when, or what we should be doing to help this person’s body recover. No doctor anywhere is working on how to stop a vaccine injury once it starts, how to keep something like transverse myelitis from spreading through the whole body and paralyzing someone. There should be an entire field of science dedicated to treating adverse reactions as they unfold. Instead our doctors and scientists have spent decades looking away, and an entire group of people has been injured and had their lives destroyed in the dark. That’s not fair. It’s not right. It is not humane.

BREAKING: Absolutely outrageous. Government advisers discussed behind closed doors the potentially fatal blood-clot risks of giving AstraZeneca Covid jabs to children as young as SIX in a clinical trial. Yet the trial continued despite healthy children being at extremely low risk from Covid. How was this ethically justified? Where was the transparency and informed consent? First do no harm. There must be accountability. share.google/PodTvtMWPsAIprY…

BREAKING: New Paper Reveals How mRNA Vaccine Materials Could Spread From Vaccinated to Unvaccinated People We identified two distinct forms of mRNA vaccine shedding: internal transcriptional spread and potential human-to-human transfer. Vaccine spreads internally and potentially externally to others. @NicHulscher @Docjohnc @McCulloughFund @neo7bioscience open.substack.com/pub/peterm…

Sweden is officially ditching mRNA vaccines, and they are not hiding their reasons for doing so. artsencollectief.nl/zweden-k…

🚨BREAKING: New Paper Reveals How mRNA "Vaccine" Materials Could Spread From Vaccinated to Unvaccinated People We identified TWO distinct forms of mRNA vaccine shedding: internal transcriptional spread and potential human-to-human transfer. 1. HUMAN-TO-HUMAN SHEDDING: Studies have detected vaccine SPIKE PROTEIN and mRNA on or within circulating exosomes MULTIPLE YEARS after vaccination. Exosomes are naturally present in bodily secretions: BREAST MILK: Vaccine mRNA already DETECTED within exosomes in human breast milk, documenting its presence in a secretion naturally transferred from vaccinated mothers to their infants. SALIVA: Exosomes confirmed; vaccine materials NEVER TESTED. EXHALED BREATH: Exosomes confirmed; vaccine materials NEVER TESTED. SWEAT: Exosomes detected; vaccine materials NEVER TESTED. Exosomes can deliver genetic material into recipient cells capable of altering cellular activity. These findings establish the biological basis for potential human-to-human transfer routes. Adding to these concerns, an observational study found associations between proximity to vaccinated individuals and menstrual irregularities among unvaccinated women. Despite these findings, whether vaccine-derived materials can transfer between individuals through saliva, exhaled breath, sweat, or other bodily secretions has NEVER BEEN DIRECTLY TESTED. 2. TRANSCRIPTIONAL SHEDDING — INTERNAL SPREAD THROUGHOUT THE BODY: Following mRNA vaccination, human cells manufacture spike protein, which can be broken into fragments, released into the bloodstream, and transported throughout the body inside exosomes. Our paper identifies TWO potential mechanisms that could extend this process: CELL DIVISION (MITOSIS): When spike-producing cells divide, their daughter cells may inherit vaccine-derived proteins and other altered cellular materials, potentially extending their effects across generations of cells. CELL-TO-CELL SPREAD: Exosomes can transport spike-related materials to distant cells that NEVER received vaccine mRNA directly, disrupting their normal biological functions. Together, these mechanisms suggest a SELF-REINFORCING CYCLE of molecular dissemination: SPIKE PRODUCTION → FRAGMENTATION → EXOSOME RELEASE → CELLULAR DISRUPTION → FURTHER SPREAD As vaccine-derived materials spread between cells, they interfere with five interconnected biological systems: blood coagulation, innate immune sensing, tumor-suppressor signaling, cellular receptor regulation, and interferon signaling. The possibility of sustained cellular disruption and human-to-human exposure demands IMMEDIATE testing. In the meantime, a HALT to mRNA technology is warranted to protect innocent bystanders from potential shedding. @Docjohnc @P_McCulloughMD @neo7bioscience @McCulloughFund

We will not reverse chronic disease by waiting until Americans get sick. HHS is equipping health centers to make nutrition, physical activity, healthy sleep, and prevention part of everyday care. This commitment will help doctors and families act earlier, build healthier habits, and prevent disease before it starts.