Against The Wind with Dr. Paul - Episode 035

​ In this week’s From the Heart segment, Dr. Paul addresses the FDA’s recent decision to halt distribution of monoclonal antibodies, calling out the government’s refusal to apply this same logic to the C19 jab when it produces a similar lack of response to Omicron. He reminds us to think for ourselves, pay attention, and remember that our best defense against any variant will always be a strong immune system supported by good, healthy living! 
 
This week Dr. Paul interviews Dr. Janci Lindsay, PhD, Director of Toxicology and Molecular Biology for Toxicology Support Services, who dives deep into the C19 shot science. Starting with a detailed explanation of what was not studied in the clinical trials, Dr. Lindsay brings to light the alarming safety signals that carry significant implications for women’s reproductive systems and our children. To learn more, visit toxicologysupport.com.
 
Next, Dr. Paul talks with Janet, a nurse and mother of four from Texas who shares her experience with getting Covid. She stresses the importance of being prepared, especially if you have loved ones who are at high risk. Her advice is to have a doctor lined up with a proven treatment protocol who is willing to prescribe off-label medication. Janet encourages us to do our own research and always follow what is in our hearts.
 
Finally, Bernadette Pajer, Public Policy Director of Informed Choice Washington, shares with us a preview of a soon-to-be released film that focuses on the indoctrination and trafficking of our children. This film calls us to end the tyranny that’s threatening our freedoms and future and is a must see!

The CDC’s vaccine adverse event reporting system is the mechanism by which the CDC tracks the relative numbers of adverse events and deaths relating to various vaccines in the US. In 2007, a Harvard Grant Study aimed at improving the system’s data collection, noted the following:
 
“Adverse events from drugs and vaccines are common but underreported. Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA). Likewise, fewer than 1% of vaccine adverse events are reported. Low reporting rates preclude or slow the identification of “problem” drugs and vaccines that endanger public health. New surveillance methods for drug and vaccine adverse effects are needed.” [1]
 
Some of the reasons for this gross underestimation were a widespread lack of awareness of the database as well as poor reporting practices by healthcare practitioners into the passive database. Despite its poor track record, the numbers for deaths which have been reported as attributable to the Covid genetic vaccines indicates case numbers hundreds, if not thousands, of times above the number of deaths reported as attributable to past vaccines cumulatively, for all years (see below).[2] As of January 7, 2022 there have been 185 deaths in the 12-24 age group as related to the Covid genetic vaccines reported into the VAERS system and in excess of 22,000 deaths overall across the age groups.

[1] Grant Final Report. Grant ID: R18 HS 017045. Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS)https://digital.ahrq.gov/sites/default/files/docs/publication/r18hs017045-lazarus-final-report-2011.pdf
[1] www.openvaers.co