CEO and Co-founder, Neo7Bioscience https://xitter.cf/t.co/Re71BqxTXO

Hideaway, TX
Joined April 2009
BeyondBio / John Catanzaro retweeted
Post-pandemic cancer has too many mechanisms tied to mRNA vaccination--too many to ignore. @Docjohnc @NicHulscher @McCulloughFund @neo7bioscience
Tyler Cooper, Kenneth Coopers son of Cooper clinic died after a short 9 month battle with cancer, age 55. The day he died his wife was undergoing a mastectomy for breast cancer. Can't be a coincidence. Right? But it must be. 🥺🎉 #RIP
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BeyondBio / John Catanzaro retweeted
🚨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
A MAJOR scientific paper is dropping within 36 hours. The negative consequences of COVID-19 “vaccination” may not end with the person who received it. What happens inside the body may be only half the story.
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BeyondBio / John Catanzaro retweeted
Great interview with Dr. Naomi Wolf and Dr. Peter McCullough. Dr. McCullough gives detailed insight on the COVID pandemic and mRNA Vax debacle. Also, covering the latest paper on mRNA vaccine transcriptional shedding. @P_McCulloughMD @NicHulscher @Docjohnc @neo7bioscience @McCulloughFund @naomirwolf
So important. I had the honor of interviewing @P_McCulloughMD this morning (see pinned interview) and he shared life-changing information about ‘shedding’.
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BeyondBio / John Catanzaro retweeted
A tech company just put AI-created synthetic viruses into a human for the first time ever. These genetically engineered bacteriophages hijack bacterial cells, replicate their own DNA, and produce hundreds of copies of themselves. What could possibly go wrong?
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So important. I had the honor of interviewing @P_McCulloughMD this morning (see pinned interview) and he shared life-changing information about ‘shedding’.
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…
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BeyondBio / John Catanzaro retweeted
THIS is why I keep telling people defending RFK Jr. as being “pro choice” that our choice as uninjected people is completely removed from us - because of shedding.
🚨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
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BeyondBio / John Catanzaro retweeted
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…
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BeyondBio / John Catanzaro retweeted
Just more evidence of what has already been proven. Show to those who still need to see it.
🚨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
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BeyondBio / John Catanzaro retweeted
Replying to @NicHulscher
This is huge. Very important for people to know this information.
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BeyondBio / John Catanzaro retweeted
Replying to @NicHulscher
The shedding from from vaccinated to unvaccinated is happening and it is getting worse with the shear number of shots they are adding that are MRNA. This is causing the "great" poisoning the public. It is forcing a medical product on those who chose not to be injected, violating their right to consent. We must stop the use of MRNA! Our future depends on.
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BeyondBio / John Catanzaro retweeted
Leute : modRNA 💉 - Shedding
🚨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
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BeyondBio / John Catanzaro retweeted
A MAJOR scientific paper is dropping within 36 hours. The negative consequences of COVID-19 “vaccination” may not end with the person who received it. What happens inside the body may be only half the story. xitter.cf/nichulscher/status/211… [STUDY LINK] mRNA Vaccine Shedding: Internal Transcriptional Dissemination and Potential Human-to-Human Transfer: xitter.cf/nichulscher/status/211…
🚨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
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BeyondBio / John Catanzaro retweeted
Here we detect Pfizer plasmid DNA in a colon tumor biopsy 1 year after vaccination. And its not small amounts of DNA. Its so much DNA that it can only be explained by plasmid amplification post vaccination or genome integration and amplification.
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BeyondBio / John Catanzaro retweeted
Replying to @NicHulscher
Is he the Chief of Pandemics? Why is he ALLOWED to KEEP TALKING or EXISTING!!
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BeyondBio / John Catanzaro retweeted
Spike-protein thromboses forming years after vaccination. For every public figure with a COVID-19 vaccine blood clot, there are hundreds of thousands with the same complication. @RicFlairNatrBoy @McCulloughFund @JalenHurts @Eagles
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BeyondBio / John Catanzaro retweeted
🚨BREAKING: NIH-FUNDED MAD SCIENTISTS HAVE CREATED A HUMANOID ROBOT CONTROLLED BY LIVING HUMAN BRAIN TISSUE They call the monstrosity "BRAINOBOT." Mad scientists grew HUMAN BRAIN ORGANOIDS from embryonic stem cells and connected them to a humanoid robot, allowing living neurons to process information and guide its movements. The human brain cells helped the robot CHASE LASERS, GRASP OBJECTS, and LEARN from repeated tasks. The living neural networks adapted and reorganized their activity during training, with task accuracy increasing from 72% to 94%. When they chemically inhibited the neurons, the robot's decision-making performance COLLAPSED. It’s not just data centers running on human brain cells anymore. It’s now humanoid robots, too. This is EXTREMELY DISTURBING.
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BeyondBio / John Catanzaro retweeted
This is beyond DISTURBING... The Gates Foundation just developed “MARK OF THE BEAST” mRNA implants. These microneedle patches install PERMANENT quantum dot QR CODES and “vaccine” mRNA into your body. They would function as BIOLOGICAL VACCINE PASSPORTS for another plandemic.
🚨BILL GATES: The COVID pandemic “didn't work the way I expected.” “Over the next several years… you will see a lot of ATTACKS different in terms of scale than anything we've seen in the past.” That literally sounds like a threat…
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BeyondBio / John Catanzaro retweeted
🚨BILL GATES: The COVID pandemic “didn't work the way I expected.” “Over the next several years… you will see a lot of ATTACKS different in terms of scale than anything we've seen in the past.” That literally sounds like a threat…
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