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In collaboration with A Midwestern Doctor, we compiled all of the scientific, regulatory, and clinical evidence that mRNA vaccine recipients can cause symptoms in others via shedding of spike protein.

This version has been updated to include a “Table of Contents” which allows a direct link to the topic of interest. 

INTRODUCTION: A CALL FOR STOPPING THE MRNA VACCINE CAMPAIGN

1. REGULATORY PRECEDENT AND DEFINITIONS1a.  Shedding Via Nanoparticles
2. MECHANISMS OF MRNA VACCINE SHEDDING2a.  Evidence Supporting the Mechanisms of Shedding. 
3. PUBLISHED EVIDENCE SUPPORTING SHEDDING PHENOMENA3a.  Evidence For Shedding Via Breast Milk3b.  Evidence For Shedding Transplacentally3c.  Evidence For Person-to-Person Shedding
4. SUMMARY OBSERVATIONS OF OVER 1000 CLINICAL REPORTS OF SHEDDING4a. General Patterns Reported4b. Susceptibility to Shedding4c. Characteristics of Shedders4d. Timing of Exposure4e. Symptoms of Exposure4f. Routes of Exposure4g. Most Common Symptoms4h. Less Frequent Symptoms4i. Rarer Symptoms
5. CLINICAL GUIDANCE5a. Protection Strategies5b. Sexual Partners5c. Blood Supply
6. LEGAL CONSIDERATIONS
7. CONCLUSION
8. ACKNOWLEDGEMENTS

INTRODUCTION: A CALL FOR STOPPING THE MRNA VACCINE CAMPAIGN

This document provides evidence from regulatory documents, a review of the scientific literature of nanoparticle and gene therapy technology, published clinical studies and reports, and over 1000 compiled clinical case testimonials, many of which support the reality that clinically significant shedding of spike protein from the vaccinated to others is occurring.

We believe this knowledge — that mRNA vaccine shedding is occurring — may be the most powerful means by which the mRNA vaccine booster program is stopped, given it is clear that shedding is far more common after a booster rollout. If the mRNA vaccine program is not stopped, it is likely facilities may follow in the footsteps of the Miami private school which, in 2021, prohibited students from attending the school within 30 days of vaccination.

We believe one of the best strategies going forward is to actively petition for a federal law to be passed mandating that for a gene therapy product to enter the market it must:

1)    Have studies conducted that properly evaluate all potential routes of shedding for any gene therapy product (making it illegal to ignore current FDA guidance on gene therapy products);

2)    Have the studies be made available to the public as well as to the potential recipients, given the therapy can affect the general population and thus violates the principles of informed consent and bodily autonomy;

3)    Have clear guidance for those who receive the product so they can protect others from being shed upon (e.g., Roctavian sheds in the semen for six months, and as a result its recipients are instructed not to donate semen or impregnate someone for six months);

4)    Have the product be pulled from the market if outside investigators discover the manufacturer’s data was wrong and the product does indeed shed, or it is discovered that recipients are not following the measures necessary to mitigate the gene therapy’s shedding.

LINK TO TAKING ACTION:https://pierrekorymedicalmusings.com/i/147138060/regulatory-precedent-and-definitions