I’m type O blood and have chewed nicotine gum the past 2 years…I also take Dr. VanDeWater’s spike recovery because I’m around folks every day that have taken the gene therapy shots. When I was pregnant 2-1/2 years ago with my 3rd son I started researching to prove to my Obgyn why I wouldn’t take their shots. 2 different doctors lectured me on why it was a necessity for the health of my baby and me, but I stood strong and collected research to show them and prove why I would not be conforming. They thought I was cra-cra, but I didn’t care.
The information below is from NIH’s website, and they knew exactly what they were doing. It’s been planned for decades. One example is close to my heart and I have long suspected that there were other motives as to why I have so many half siblings. In the 1970s & 80s, UNMC had a sperm donor program through the Munroe-Meyer Institute that med students donated to. I met with Dr Warren Sanger and Dr Bruce Buehler, who headed this program up, when I was on the quest to find out my genetics and find my donor. The max offspring for each donor was 8 (unless you were type O blood type). The donor that I came from is type O and they used his sperm dozens of times. I’ve found many of my half siblings and my bio dad. He tried to find out how many times they used it and UNMC isn’t disclosing this information. My bio dad thinks there could be many more, and guess what we’re all type O.
From NIH’s website:
On the contrary, the A allele of the ABO blood group has been associated with an increased risk of developing cardiovascular diseases as reported by several studies.10 The A antigen might protect P-selectin and intercellular cell adhesion molecule 1 (ICAM1) from enzymatic cleavage by promoting stronger and longer binding of leukocytes to them on the vascular wall; more adhesion molecules attached to the endothelial cells would on one hand increase adhesion and inflammation but on the other hand decrease circulation.11 These collectively predispose type A carriers to a higher likelihood of developing cardiovascular diseases and aggregate disease situations once these individuals were exposed to redox stresses such as in the case of virus infection.
Therefore, individuals having an O blood group type are less likely to develop cardiovascular diseases and severe COVID-19 and, on the contrary, patients carrying an A blood group type, especially those already having been diagnosed with cardiovascular diseases in particular hypertension, are more likely to develop severe COVID-19 once infected (Figure 1). These individuals need to be quarantined and protected from SARS-CoV-2 infection or under special medical care to be prevented from deterioration and severe progression.
This and the comments that will be made may be the most valuable bit of knowledge we need to implement. Thank you, Walter, and those who offer comments we can use.
Thank you Walter. "For now, finding ways to reduce Spike load may be the best approach we have towards mitigation." There are companies offering Spike Support formulas -The Wellness company is one:
Mr. Chestnut, it must be very difficult and disheartening to discover and publish the facts knowing that they knew what they were doing when they created spike proteins and the vaccine. Thank you for seeking the antidote, the protection for future generations that are in peril of becoming victims of transgenic changes brought about by world totalitarian policies.
- Nattokinase 2000 FU (100) mg orally twice a day without food
- Bromelain 500 mg orally once a day without food
- Curcumin 500 mg orally twice a day (nano, liposomal, or with piperine additive suggested)
I've heard him describe the OTC supplement protocol as being effective to cleave / 'break up' the spike protein to ease the body's ability to eliminate it.
In a nutshell .. Take a noxious substance... not twice but thrice... and watch you cancer sentries disappear and get replaced by an astonishingly fast tumour... courtesy of the Gatekeeper foundation... it’s all perfectly legal once you pay off all the judges and politicians.
Interesting. Do you have any thoughts on the different periods of time that the Spike protein remains in the body? Meaning, the "natural" spike appears to clear quickly vs. the vaccine spike (created with pseudouridine, and in theory, longer lasting & reproducing?)
I am a retired (unvaxxed) RN in Canada, so I can work my way through these studies slowly, but my understanding is probably imperfect 😬
This paper https://www.mdpi.com/2077-0383/11/8/2219 found; "We did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection."
Does that not place the blame squarely with the ModRNA spike from the injections? When 40 trillion copies of ModRNA flow into every cell in a body and thse cells express not ony a cytoxic spike protein but a deliberately misshapen one the autoimmune system will attack all these poor ModRNA infected cells expresing this pathogen and the heart cells that are infected will not be precluded from attack hence heart damage.
Maybe it is time to focus on the main pathogen which is the ModRNA spike and less on the sarscov2 spike?
Abstract
Myocarditis and pericarditis are potential post-acute cardiac sequelae of COVID-19 infection, arising from adaptive immune responses. We aimed to study the incidence of post-acute COVID-19 myocarditis and pericarditis. Retrospective cohort study of 196,992 adults after COVID-19 infection in Clalit Health Services members in Israel between March 2020 and January 2021. Inpatient myocarditis and pericarditis diagnoses were retrieved from day 10 after positive PCR. Follow-up was censored on 28 February 2021, with minimum observation of 18 days. The control cohort of 590,976 adults with at least one negative PCR and no positive PCR were age- and sex-matched. Since the Israeli vaccination program was initiated on 20 December 2020, the time-period matching of the control cohort was calculated backward from 15 December 2020. Nine post-COVID-19 patients developed myocarditis (0.0046%), and eleven patients were diagnosed with pericarditis (0.0056%). In the control cohort, 27 patients had myocarditis (0.0046%) and 52 had pericarditis (0.0088%). Age (adjusted hazard ratio [aHR] 0.96, 95% confidence interval [CI]; 0.93 to 1.00) and male sex (aHR 4.42; 95% CI, 1.64 to 11.96) were associated with myocarditis. Male sex (aHR 1.93; 95% CI 1.09 to 3.41) and peripheral vascular disease (aHR 4.20; 95% CI 1.50 to 11.72) were associated with pericarditis. Post COVID-19 infection was not associated with either myocarditis (aHR 1.08; 95% CI 0.45 to 2.56) or pericarditis (aHR 0.53; 95% CI 0.25 to 1.13). We did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection.
I’m type O blood and have chewed nicotine gum the past 2 years…I also take Dr. VanDeWater’s spike recovery because I’m around folks every day that have taken the gene therapy shots. When I was pregnant 2-1/2 years ago with my 3rd son I started researching to prove to my Obgyn why I wouldn’t take their shots. 2 different doctors lectured me on why it was a necessity for the health of my baby and me, but I stood strong and collected research to show them and prove why I would not be conforming. They thought I was cra-cra, but I didn’t care.
The information below is from NIH’s website, and they knew exactly what they were doing. It’s been planned for decades. One example is close to my heart and I have long suspected that there were other motives as to why I have so many half siblings. In the 1970s & 80s, UNMC had a sperm donor program through the Munroe-Meyer Institute that med students donated to. I met with Dr Warren Sanger and Dr Bruce Buehler, who headed this program up, when I was on the quest to find out my genetics and find my donor. The max offspring for each donor was 8 (unless you were type O blood type). The donor that I came from is type O and they used his sperm dozens of times. I’ve found many of my half siblings and my bio dad. He tried to find out how many times they used it and UNMC isn’t disclosing this information. My bio dad thinks there could be many more, and guess what we’re all type O.
From NIH’s website:
On the contrary, the A allele of the ABO blood group has been associated with an increased risk of developing cardiovascular diseases as reported by several studies.10 The A antigen might protect P-selectin and intercellular cell adhesion molecule 1 (ICAM1) from enzymatic cleavage by promoting stronger and longer binding of leukocytes to them on the vascular wall; more adhesion molecules attached to the endothelial cells would on one hand increase adhesion and inflammation but on the other hand decrease circulation.11 These collectively predispose type A carriers to a higher likelihood of developing cardiovascular diseases and aggregate disease situations once these individuals were exposed to redox stresses such as in the case of virus infection.
Therefore, individuals having an O blood group type are less likely to develop cardiovascular diseases and severe COVID-19 and, on the contrary, patients carrying an A blood group type, especially those already having been diagnosed with cardiovascular diseases in particular hypertension, are more likely to develop severe COVID-19 once infected (Figure 1). These individuals need to be quarantined and protected from SARS-CoV-2 infection or under special medical care to be prevented from deterioration and severe progression.
These Bioweapon designers play to win.
This and the comments that will be made may be the most valuable bit of knowledge we need to implement. Thank you, Walter, and those who offer comments we can use.
Thank you Walter. "For now, finding ways to reduce Spike load may be the best approach we have towards mitigation." There are companies offering Spike Support formulas -The Wellness company is one:
https://www.twc.health/collections/top-pick-3-products/products/long-haul-formula
Jennifer DePew has written extensively about the benefits of pomegranate:
https://denutrients.substack.com/p/spike-protein-risks-aids-summary-page
Thanks for all your hard work and for always telling the truth. May God bless you and continue to guide you in your work. Peace.
I don't think they created a bioweapon that can be dangerous for themselves via shedding. Maybe there is a drug protecting them
Is there any way for folks to supplement the ACE 2 to keep their heart health strong?
Mr. Chestnut, it must be very difficult and disheartening to discover and publish the facts knowing that they knew what they were doing when they created spike proteins and the vaccine. Thank you for seeking the antidote, the protection for future generations that are in peril of becoming victims of transgenic changes brought about by world totalitarian policies.
One of the best strategies to attenuate SP and more importantly SP 2 damage is with IVM: https://www.virex.health/index.php?route=product/product&product_id=53
If the vaccines worked
It would mean that those who have
Died Suddenly
Would be dying from something else (Covid)
Everyone would NEED the vaccine.
And the pharmaceutical companies
Would be shouting from the rooftops
About those who are dying suddenly.
.
Pomegranate peel
any thoughts on Dr Peter McCullough's spike detox protocol?
from his website: https://www.petermcculloughmd.com/
- Nattokinase 2000 FU (100) mg orally twice a day without food
- Bromelain 500 mg orally once a day without food
- Curcumin 500 mg orally twice a day (nano, liposomal, or with piperine additive suggested)
I've heard him describe the OTC supplement protocol as being effective to cleave / 'break up' the spike protein to ease the body's ability to eliminate it.
In a nutshell .. Take a noxious substance... not twice but thrice... and watch you cancer sentries disappear and get replaced by an astonishingly fast tumour... courtesy of the Gatekeeper foundation... it’s all perfectly legal once you pay off all the judges and politicians.
Interesting. Do you have any thoughts on the different periods of time that the Spike protein remains in the body? Meaning, the "natural" spike appears to clear quickly vs. the vaccine spike (created with pseudouridine, and in theory, longer lasting & reproducing?)
I am a retired (unvaxxed) RN in Canada, so I can work my way through these studies slowly, but my understanding is probably imperfect 😬
What are the symptoms of ACE2 depletion? Do we know?
Hi Walter
This paper https://www.mdpi.com/2077-0383/11/8/2219 found; "We did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection."
Does that not place the blame squarely with the ModRNA spike from the injections? When 40 trillion copies of ModRNA flow into every cell in a body and thse cells express not ony a cytoxic spike protein but a deliberately misshapen one the autoimmune system will attack all these poor ModRNA infected cells expresing this pathogen and the heart cells that are infected will not be precluded from attack hence heart damage.
Maybe it is time to focus on the main pathogen which is the ModRNA spike and less on the sarscov2 spike?
Abstract
Myocarditis and pericarditis are potential post-acute cardiac sequelae of COVID-19 infection, arising from adaptive immune responses. We aimed to study the incidence of post-acute COVID-19 myocarditis and pericarditis. Retrospective cohort study of 196,992 adults after COVID-19 infection in Clalit Health Services members in Israel between March 2020 and January 2021. Inpatient myocarditis and pericarditis diagnoses were retrieved from day 10 after positive PCR. Follow-up was censored on 28 February 2021, with minimum observation of 18 days. The control cohort of 590,976 adults with at least one negative PCR and no positive PCR were age- and sex-matched. Since the Israeli vaccination program was initiated on 20 December 2020, the time-period matching of the control cohort was calculated backward from 15 December 2020. Nine post-COVID-19 patients developed myocarditis (0.0046%), and eleven patients were diagnosed with pericarditis (0.0056%). In the control cohort, 27 patients had myocarditis (0.0046%) and 52 had pericarditis (0.0088%). Age (adjusted hazard ratio [aHR] 0.96, 95% confidence interval [CI]; 0.93 to 1.00) and male sex (aHR 4.42; 95% CI, 1.64 to 11.96) were associated with myocarditis. Male sex (aHR 1.93; 95% CI 1.09 to 3.41) and peripheral vascular disease (aHR 4.20; 95% CI 1.50 to 11.72) were associated with pericarditis. Post COVID-19 infection was not associated with either myocarditis (aHR 1.08; 95% CI 0.45 to 2.56) or pericarditis (aHR 0.53; 95% CI 0.25 to 1.13). We did not observe an increased incidence of neither pericarditis nor myocarditis in adult patients recovering from COVID-19 infection.
"Herbs that upregulate ACE-2, increasing its levels in the body, are
Pueria spp (kudzu), Salvia miltiorrhiza (Dan shen), and Ginkgo biloba]. ACE
inhibitors (in contrast to ACE-2 upregulators) will actually increase the presence
of ACE-2 and help protect the lungs from injury [ Some herbs that do that are
Crataegus spp (hawthorn) and Pueraria spp (kudzu"
https://www.stephenharrodbuhner.com/wp-content/uploads/2020/03/coronavirus.txt.pdf