vaccine
With so much information being given out regarding the Covid-19 vax I felt it was my responsibility to share the knowledge I have learned from Dr. Aimee Tramm.  I believe God put Dr. Tramm in my path for a reason.  My listeners should know that I believe each American should be given free choice when it comes to their body and their healthcare.  This episode is not meant to persuade anyone in one direction or another.  It is simply to share information that is out there in the medical field so that each individual can educate herself and then come to the decision that she feels is best for her.

REFERENCES REFERRED TO IN THIS EPISODE:

 

Informed consent cannot occur unless a person is informed.  I respect and support a patient’s right to decide their own medical treatment and will support whichever decision a person makes.  With the knowledge I have, I try to inform my patients of all risks and alternatives specific to their individual cases.  Using words like “always, never, impossible, 100%” should raise an alarm bell, because each person’s genetic makeup and health conditions are different.  Medications and vaccines should not be viewed with a “one size fit all” approach.

 

  • FDA EUA application – Page 6 (FDA uses investigational and experimental interchangeably)

https://www.fda.gov/media/144416/download

 

  • Re: No animal trials

-Preclinical (animal) trials are normally done over 1-5 years to assess the safety and long-term risk. Pfizer and Moderna injected animals and checked for “efficacy” (meaning if the injection would cause the immune system to respond). None were tested for safety and there has been no peer review of the data. Only 1-2 months later were Phase 1 trials begun for both.  See the timeline in the attached article.

https://www.biopharma-reporter.com/Article/2021/03/03/Inside-the-Pfizer-BioNTech-COVID-19-vaccine-trial-Insights-on-speed-agility-and-digital-development

 

  • See also FDA explanation of Preclinical Trials

https://www.fda.gov/patients/drug-development-process/step-2-preclinical-research

 

 

Before testing a drug in people, researchers must find out whether it has the potential to cause serious harm, also called toxicity… these studies must provide detailed information on dosing and toxicity levels. After preclinical testing, researchers review their findings and decide whether the drug should be tested in people.”

 

  • American Medical Association’s explanation of informed consent

https://www.ama-assn.org/delivering-care/ethics/informed-consent

 

  • True Animal studies of SARS-CoV-1, all showed “efficacy” like the 73-79% similar SARS-CoV-2(COVID) vaccine, but when exposed to the virus after injection there was inflammation found in the lungs caused by a hypersensitivity caused by the injection.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335060/

 

“These SARS-CoV vaccines all induced antibody and protection against infection with SARS-CoV. However, challenge of mice given any of the vaccines led to the occurrence of Th2-type immunopathology suggesting hypersensitivity to SARS-CoV components was induced. Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated.

  • Possible correlation between antigens against COVID spike protein and placental development (syncytin, HERV-W)

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810191/ see 4.1.2

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092852/

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC111833/


About Dr. Aimee Trammell

Dr. Aimmee Trammell is currently a pharmacy manager in California.  She received her undergraduate in Biochemistry (graduated Summa Cum Laude) and her  Doctorate in Pharmacy both from the University of Illinois at Chicago.


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* If you enjoyed this episode you may also enjoy Episode 62.

 

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