https://petermcculloughmd.substack.com/p/concerns-over-cumulative-cardiotoxicity?
Concerns over Cumulative Cardiotoxicity with mRNA Injection
Troponin Measurements Before and After 4th Shot Give Clues
The field of pharmacovigilance and drug safety is loaded with regulatory structure and milestones. One of the exercises a new drug must go through is “cumulative toxicity” testing. If a drug is harmful, one dose may not be enough to bring out a side effect. However after 5 or more does, many times problems will emerge. It is usual and customary to count all adverse events for 30 days after a drug is stopped because it may have accumulated in the body or have induced lingering effects.
We have learned COVID-19 vaccines are very long lasting in the body, and since the start of the worldwide mass vaccination campaign, our public health agency sponsors have never mentioned cumulative toxicity as a concern.
Levi et al published an analysis in the European Journal of Heart Failure that appeared to make the COVID-19 vaccines look “safe.” But on the surface there are problems. 324 healthcare workers had cardiac troponin (test for cardiac damage) blood testing before and after the 4th injection. The authors focus on one unfortunate soul who had chest pain, a pathologic rise in troponin, and had to undergo more blood testing, ECG’s, echocardiography, and cardiac MRI. One out of 324 is far to many to have this problem with a routine vaccination!
What authors may have revealed in the cohort is cumulative cardiotoxicity. These patients were ~147 days after the last shot. Among healthy persons, we should be concerned over troponin elevated BEFORE the fourth shot. (See link for article)
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Important points:
- as many as 14.81% cumulatively sustained damage from shots 3 and 4
- all small prospective cohort studies have found one or more cases indicating cardiac damage: Mansanguan, Beurgin, and now Levi
- 75% of people in the U.S. took one or more shots
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Nearly 1 in 3 COVID-19 Vaccine Recipients Suffered Neurological Side Effects: Study
The study analyzed 19,096 people who received COVID-19 vaccines in Italy in July 2021, out of which 15,368 had taken the Pfizer vaccine, 2,077 had taken the Moderna version, and 1,651 took the AstraZeneca version.
While both Pfizer and Moderna are mRNA vaccines, AstraZeneca, being an adenovirus vaccine, uses a different mechanism to trigger the immune response.
The study found that about 31.2 percent of vaccinated individuals developed post-vaccination neurological complications, particularly among those injected with the AstraZeneca jab. Different vaccines had a different “neurological risk profile.” (See link for article)
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Important points:
- females faced an “increased risk of developing neurological complications”
- a primary female sex steroid called estradiol triggers a specific immunity process to produce “antibodies against infections.”
- “Caution should be used when administering COVID-19 vaccines to vulnerable people, such as to those who suffer from allergies,” the study stated. “We strongly believe that our findings are relevant for public health regarding the safety of vaccines in a large cohort.”
If you are a Lyme/MSIDS patient YOU ARE VULNERABLE.
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https://childrenshealthdefense.org/defender/pfizer-vaccine-dna-pregnant-mother-fetus/?
DNA Contamination in Pfizer Shots Could Transfer From Pregnant Mom to Fetus, Experts Suggest
According to a panel of experts, led by Steve Kirsch, regulators are ignoring proof that Pfizer intentionally concealed the presence of contaminants in its COVID-19 vaccines. Those contaminants could threaten unborn babies whose mothers receive the vaccine, the experts said in a recent video.
Madison Area Lyme Support Group 