How Gender Ideology Escaped the Lab to Become a Treatment Protocol

How did such a flimsy theory become an on-the-ground preferred treatment for so many health care providers? How did it come to be that so many highly trained doctors will surgically remove healthy body tissue of teenagers or inject them with cross-sex hormones, thus making them infertile? Dr. Stephen Levine, a clinical professor of psychiatry at Case Western Reserve University, explains at Public:

[A] vast chasm that exists between affirmative care doctors who believe that medical interventions should be the first line of treatment for people suffering from gender dysphoria and those like Levine who remain committed to the Hippocratic Oath to first do no harm.

“It’s been for over 2,500 years that we in medicine, we have said we do not remove healthy tissues, and we do not alter the physiology of the body,” he explains, adding that there is no data to suggest that a child who undergoes medical transition can grow up to have a full, happy, accomplished life. “It’s a belief system…and beliefs are not what parents want from doctors. They want to know what the facts are, and part of the facts is the uncertainty of outcome.”

Given that existing long-term data indicate that the “suicide rates of adult transsexuals are much higher than the suicide rate of the general population, not slightly higher, much higher,” Dr. Levine is horrified by doctors who perpetuate the transition-or-suicide narrative as a way to coerce parents into consenting to their child’s transition... A principle of medical ethics is that interventions need to be based on science, and Dr. Levine argues that the evidence for pediatric medical transition is “pretty lousy.”

The entire child sex change experiment is based on a single “innovative experiment” conducted in a Dutch gender clinic. Dr. Levine explains that innovative experiments are how medicine advances. Someone has an idea, tests it out on a tiny patient group, and if the results are promising, that justifies a more controlled study.

“The innovative experiment with patients demands that we repeat and we refine the method to establish the facts,” he said, explaining that this didn’t happen with the puberty blockers experiment.

The original Dutch study began with 197 children, but 86 were ruled out for reasons of mental disturbance. Of the remaining 111, 41 parents refused to allow their children to take part. Of the remaining 70, only 55 were entered into the final reports, and the researchers only had psychological data on 32 of the 55. There was no control group, and no long-term follow-up, as well as other serious methodological flaws. There was one attempt at replication, conducted at the Tavistock gender clinic in London, and it failed to produce the same supposedly positive result.

But Dr. Levine says the Dutch experiment “escaped the lab,” and rapidly spread into general medical practice via a process called “runaway diffusion,” which is when the medical world mistakes a small innovative experiment for proven practice and a potentially harmful treatment becomes widespread medical practice...

When asked what advice he would give to a teenager seeking medical transition, Dr. Levine replied that he says to the young person, “I know that the most important thing about you is that you’re a human being, and you think the most important thing about you is that you’re a trans person.” He seeks to help his young patients understand that anything that is true about human beings is also going to be true about them, including uncertainty, ambivalence, and the influence of the past on their current identity. And above all, he tells them, “Don’t make your parents the enemy.”

Continue ReadingHow Gender Ideology Escaped the Lab to Become a Treatment Protocol

About Captured Medical Organizations

Many left-leaning people are currently insisting that we should trust medical organizations to lead the way on public health issues. I disagree. Many of these organizations have been captured by activists and have lost their scientific moorings. An example the AAP's position on transgender issues, as reported by Helen Joyce: "The American Academy of Pediatrics sidelines formal proposal to revise Pediatric Medical Transition policy for the 4th consecutive year: Unfortunately, it seems that U.S. medical organizations have allowed politics to overshadow their commitment to evidence-based medicine." Here an excerpt:

The American Academy of Pediatrics (AAP) has, once again, overlooked a formal proposal—its fifth iteration for the fourth year running—intended to amend its stance on pediatric medical transitions. This proposal, known as Resolution #37, was co-authored by 24 pediatricians who are also AAP members. It called for the AAP to align its policy with findings from systematic evidence reviews, universally considered the gold standard of evidence-based medicine.

Resolution #37, titled "Align the AAP Treatment Recommendations for Gender Incongruence and Gender Dysphoria with Findings from Systematic Reviews of Evidence," was submitted on April 1, 2023. The resolution sought a comprehensive review and update of the AAP's current policy on gender-affirming care for trans-identified youth, as stated in the 2018 AAP position paper titled "Ensuring Comprehensive Care and Support for Transgender and Gender Diverse Children and Adolescents." The existing policy endorses the view that immediate affirmation through psychosocial and medical interventions is the only appropriate approach for youth experiencing gender dysphoria, a stance that Resolution #37 argues requires reevaluation.

Despite assurances from the AAP in February 2023 that policy statements undergo a review every five years, and thus an update of the 2018 statement is already underway, Resolution #37 states that the AAP is proceeding with the update without conducting a systematic review of the evidence. No AAP committees working on these policy updates plan to perform such a review, and there's no indication that a systematic review related to treatments for gender dysphoria is even being considered.

Continue ReadingAbout Captured Medical Organizations

Dr. Peter McCullough Discusses COVID-19 Vaccine Injury Syndromes

Why have I (and many other Americans) lost so much faith in American public health officials and institutions? Well, there was the official narrative that we heard from government officials, something like, "The vaccine is safe. Take it. Or else you will be socially ostracized, perhaps fired from your job." Matt Orfalea's mashup illustrates that official narrative:

On the other hand, consider the testimony of Dr. Peter McCullough in the Pennsylvania Senate. You will learn about massive conflicts of interest among public health institutions, including the CDC and the FDA. You will hear that there was no independent organization dedicated to patient safety of the vaccines, which is ghastly.  McCullough discusses the VAERS risk signal associated with the vaccines, which has been corroborated by subsequent studies.

McCullough testifies that 5% of Americans have suffered permanent disability, primarily stroke and neurologic disability as a result of taking the mRNA vaccine (min 27). He discusses the use of therapeutics for those detrimentally affected by the mRNA vaccine, including the use of the supplement called Nattokinase and other natural substances that seem to dissolve the spike protein that is already in the human body (discussed at min 27). Throughout this video you will hear his descriptions of a hubristic network of government "experts" and pharmaceutical manufacturers who are withholding data and refusing to enter into wide-open no-limits discussions regarding potential adverse affects of the COVID vaccines.

Why are some Americans having adverse affects regarding the vaccines while others are not? McCullough cites to a new R-Squared analysis study tracing problems to certain batches of the vaccines (and not others) (min 22). About 1/3 of people who received Batch 1 and report no side effects. Almost 2/3 of of people took Batch 2 and had side effects, but very few serious side-effects. About 4.2% of Americans received Batch 3, the bad batches and about 75% of those people receiving the bad batch have health issues related to the vaccine. Why? McCullough suggests that there was a "product manufacturing problem."  Either hyper-concentrated lipid nano-particles with an excessive amount of messenger RNA or CDNA contamination or other types of contamination.

I am not an expert, so I have no ability to evaluate McCullough's claims, but I listened closely as he cited to recent studies. What he is saying very much concerns me. At a minimum, how was it that experimental vaccines that never received standard testing labeling (with package inserts) were foisted (often under duress) on Americans via the Emergency Use Authorization?

And again, why are we not seeing wide discussion of these issues?  Why, instead, are we seeing suspicious activities by public health officials, things like this?

Continue ReadingDr. Peter McCullough Discusses COVID-19 Vaccine Injury Syndromes