I know I no longer should, but it turns out, some stories are so outrageous that I still find myself thinking, no, the CDC wouldn't do that, would it?

Of course, when you read that Pfizer fought to keep this data secret, and the governing body for obstetricians imposed a gag order forbidding doctors from even discussing it, you might think, as I do, “well, maybe”. If it is true, there will be nothing left, not even a shred, of our public health system’s credibility.

On the other hand, and from the full cellar of salt department, these claims are coming from Naomi Wolf, who has had her problems with conspiracy theories in the past. Another misinterpretation of data, or a case of “even paranoids have enemies”? I guess what I’m saying is that I’m not so quick to slap tinfoil hats on people these days. It’ll be interesting to see how this develops.

More than 40 percent of pregnant women who participated in Pfizer’s mRNA COVID vaccine trial suffered miscarriages, according internal Pfizer documents, recently released under court order. Despite this, Pfizer, and the Biden administration insisted that the vaccines were safe for pregnant women. Out of 50 pregnant women, 22 of them lost their babies, according to an analysis of the documents.

In a January court ruling, U.S. District Judge Mark Pittman of the Northern District of Texas, ordered the Food and Drug Administration (FDA) to release around 12,000 documents immediately, and then 55,000 pages a month until all documents were released, totaling more than 300,000 pages.

The nonprofit group, Public Health and Medical Professionals for Transparency, sued the FDA last September, after the agency denied its Freedom of Information Act (FOIA) request to expedite the release of mRNA vaccine review documents. In a November 2021 joint status report, the FDA proposed releasing only 500 pages of the documents a month, which would have taken up to 75 years.

Trial documents released in April revealed that Pfizer had to hire 1,800 additional full-time employees in the first half of 2021 to deal with “the large increase” of adverse reactions to its COVID vaccine.

The Pfizer-BioNTech COVID-19 Vaccine was made available under the Emergency Use Authorization (EUA) on Dec. 11, 2020. By February of 2021, the company was seeing so many safety signals, including in pregnant and breastfeeding mothers, it had to immediately hire 600 employees to process the data.

A batch of documents released in late July showed that 44 percent of women who were pregnant during the trial suffered miscarriages, feminist author and journalist Dr. Naomi Wolf revealed on Steve Bannon’s War Room podcast. Wolf has been spearheading research and analysis of the Pfizer documents through her website Daily Clout.

In the past, only 10 to 15 percent of known pregnancies ended in miscarriage.

“Pfizer took those deaths of babies—those spontaneous abortions and miscarriages—and recategorized them as recovered/resolved adverse effects,” Wolf told Bannon. “In other words, if you lost your baby, it was categorized by Pfizer as resolved adverse event, like a headache that got better,” she added.

Wolf said adverse event cutoff report showing the miscarriages was March 13, 2021, and the FDA received the report on April 1, 2021.

Therefore, the FDA had this data nearly a year and a half ago, and instead raising an alarm, they, along with the CDC, went ahead and recommended the experimental injections for expectant mothers anyway.

…. In September of 2021, the American Board of Obstetrics and Gynecology (ABOG) put out a statement in support of the Federation of State Medical Boards’ (FSMB) contention that “providing misinformation about the COVID-19 vaccine contradicts physicians’ ethical and professional responsibilities.” The ABOG said physicians disseminating “misinformation” would be subject to “disciplinary actions, including suspension or revocation of their medical license.”