CEO and Co-founder, Neo7Bioscience https://xitter.cf/t.co/Re71BqxTXO
Hideaway, TX
Joined April 2009
- Tweets8.3K
- Following575
- Followers5.3K
- Likes4.8K
Pinned Tweet
If you’re facing cancer, an active illness, or an injury connected to the COVID vaccine, we’re here to help. Please reach out to us through our website:
neo7bioscience.com/contactus
BeyondBio / John Catanzaro retweeted
A new paper by John Catanzaro, Nicolas Hulscher, and Peter McCullough proposes that mRNA COVID vaccines may produce persistent biological effects and potentially transfer vaccine-derived material between people.
The accompanying article goes further, calling for an immediate halt to mRNA technology.
Those are extraordinary claims. But the paper also cites several genuine scientific observations that deserve to be understood rather than dismissed.
So what does the evidence actually establish?
And where does a plausible biological mechanism become an unsupported conclusion?
Let’s examine the science.
🤖 Made with AI
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
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…
BeyondBio / John Catanzaro retweeted
Shedding within the body from cell to cell and with close contacts from person to person--a "spreading vaccine."
🚨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
BeyondBio / John Catanzaro retweeted
And Blood banks? Apparently they don’t distinguish between vaccinated and unvaccinated blood.
BeyondBio / John Catanzaro retweeted
I have explained this more times than I care to count!
I suffered from a spike protein infection that nearly took my life 17 times over the last six years because inmates were forcibly vaccinated through coercion by the State of Arizona.
I turned the State of Arizona in to the United States Department of Justice for the deaths of these inmates because they were not informed that what they were receiving was a biological weapon aimed at taking their lives!
BeyondBio / John Catanzaro retweeted
数年前に拙著でも提唱した「ワクチンシェディング」相談が、いま増えています。
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…
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
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’.
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?
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’.
BeyondBio / John Catanzaro retweeted
"Dr Peter McCullough: Could Pharma Shortages Leave us Vulnerable?" xitter.cf/i/broadcasts/1nJOLQlwV…
BeyondBio / John Catanzaro retweeted
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…
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
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
BeyondBio / John Catanzaro retweeted
[STUDY LINK] mRNA Vaccine Shedding: Internal Transcriptional Dissemination and Potential Human-to-Human Transfer: zenodo.org/records/23666330
BeyondBio / John Catanzaro retweeted
This is huge. Very important for people to know this information.
BeyondBio / John Catanzaro retweeted
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.
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