Katie: They got the "surgery" because they were poisoned with Bisphenol A! (See link) 2-22-2024#2

Katie: They got the "surgery" because they were poisoned with Bisphenol A! (See link) 2-22-2024 #2

Ask Nik & Jimbo WHY they didn't mention this to "X Factor 444" aka "Karen" 2-22-2024
https://www.bitchute.com/video/HLXhacU58LG7/

Investigate Bisphenol A (B-P-A) regarding sexually dimorphic phenotypes, sex-specific effects on social and anxiety-like behavior

https://www.returnofkings.com/169359/gender-altering-chemical-bisphenol-a-bpa-is-turning-more-than-just-frogs-gay
https://www.sciencemag.org/news/2015/10/homosexuality-may-be-caused-chemical-modifications-dna
http://www.hormonesmatter.com/endocrine-disruptors-mens-health/
https://archive.jsonline.com/watchdog/watchdogreports/54195292.html/

Abstract
Bisphenol A (BPA) is an estrogenic endocrine disruptor widely used in the production of plastics. Increasing evidence indicates that in utero BPA exposure affects sexual differentiation and behavior; however, the mechanisms underlying these effects are unknown. We hypothesized that BPA may disrupt epigenetic programming of gene expression in the brain. Here, we provide evidence that maternal exposure during pregnancy to environmentally relevant doses of BPA (2, 20, and 200 µg/kg/d) in mice induces sex-specific, dose-dependent (linear and curvilinear), and brain region-specific changes in expression of genes encoding estrogen receptors (ERs; ERa and ERß) and estrogen-related receptor-? in juvenile offspring. Concomitantly, BPA altered mRNA levels of epigenetic regulators DNA methyltransferase (DNMT) 1 and DNMT3A in the juvenile cortex and hypothalamus, paralleling changes in estrogen-related receptors. Importantly, changes in ERa and DNMT expression in the cortex (males) and hypothalamus (females) were associated with DNA methylation changes in the ERa gene. BPA exposure induced persistent, largely sex-specific effects on social and anxiety-like behavior, leading to disruption of sexually dimorphic behaviors. Although postnatal maternal care was altered in mothers treated with BPA during pregnancy, the effects of in utero BPA were not found to be mediated by maternal care. However, our data suggest that increased maternal care may partially attenuate the effects of in utero BPA on DNA methylation. Overall, we demonstrate that low-dose prenatal BPA exposure induces lasting epigenetic disruption in the brain that possibly underlie enduring effects of BPA on brain function and behavior, especially regarding sexually dimorphic phenotypes.