VLA COMMENT: AWESOME/BRILLANT
COMPLETE GRAPHIC EVIDENCE PRESENTATION THAT VACCINES DID NOT SAVE US …by Raymond Obomsawin pHD. 2009 (32 graphic pages evidencing disease decline PRIOR to the introduction of the vaccine)
VLA COMMENT: AWESOME/BRILLANT
VLA Comment: Really worth watching. It is interesting to note…all the evidence of malfeasance, corruption and strategy to sell Round Up to Bayer, at the end there is a few minutes injected that “Round Up is not THAT BAD as we evidenced” Wonder Why????
Despite that strange injection, it is really worth watching the details of Round Up’s history
Here is why: Cytochrome P450 (CYP450) refers to a superfamily of enzymes primarily located in the liver, but also present in the intestines, lungs, kidneys, mitochondria and other tissues. These enzymes play a central role in the phase I metabolism of endogenous compounds (e.g., hormones, fatty acids) and exogenous substances (e.g., drugs, environmental toxins, vaccine excipients and xenobiotics).
VACCINE EXCIPIENTS: It is the inability of the child under 3 years old to metabolize accumulating multiple excipient toxins as Cyp 450 system is needed to remove toxins from the body. Dr. Gary Goldman’s recent study (The Immature Infant Liver: Cytochrome P450 Enzymes and their Relevance to Vaccine Safety and SIDS Research)
PolySorbate 80 is an emulsifier in Vaccines. Emulsifiers are also in baby formulas.
Emulsifiers need Cyp 450 to metabolize. Infants and children under 3 do not have mature cyp 450 enzymes resulting in life altering toxicity. Another poison in vaccines that cannot be metabolized by infants. (see Dr. Gary Goldman’s recent study and interview on Highwire
In a discovery with profound implications for public health, a team of scientists from France’s prestigious Institut Pasteur and the National Institute of Health and Medical Research (Inserm) has uncovered a disturbing transgenerational link. Their research, published in the journal Nature Communications, reveals that a mother’s consumption of common food emulsifiers can permanently alter the gut bacteria of her children, significantly increasing their risk of developing chronic inflammatory diseases and obesity later in life. This finding suggests that the health consequences of processed foods may not be confined to the individual who eats them but could be passed down, programming the next generation for metabolic disorder.
The culprits in this study are dietary emulsifiers, detergent-like molecules ubiquitous in the modern food supply. They are added to thousands of processed productsfrom ice cream and baked goods to creamy salad dressings and even some powdered infant formulasto create a smooth texture, prevent separation and extend shelf life. For decades, their safety was assumed, but a growing body of evidence is now challenging that long-held belief, pointing to a potential role in the global rise of inflammatory and metabolic diseases. (Related: STUDY: Pregnant women who consume garbage “reprogram” their unborn children’s brains to become junk food addicts.)
The new research, led by microbiologist Benoit Chassaing, builds upon previous studies that showed emulsifiers can directly harm the gut health of the individual consuming them. These additives can damage the protective mucus layer lining the intestines and disrupt the tight seals between intestinal cells. This allows gut bacteria to get dangerously close to the sensitive gut lining, potentially triggering inflammation, metabolic toxemia and weight gain. The critical question this study answered was whether a mother’s exposure could negatively affect her offspring who never directly consume the additives themselves.
To investigate this, Chassaing’s team exposed female mice to low concentrations of two widely used emulsifiers, carboxymethylcellulose (E466) and polysorbate 80 (E433), for ten weeks before they became pregnant and then throughout gestation and nursing. The offspring were never fed the emulsifiers directly. The scientists then meticulously compared these pups to those born from mothers who had not been exposed to the additives, focusing on the development and composition of their gut microbiomes.
Altered from the start
The results were striking. From their earliest weeks of life, the offspring of emulsifier-exposed mothers showed significant and detrimental alterations to their gut microbiota. This period is critical, as a mother naturally transfers a foundational set of bacteria to her newborn through close contact and nursing. The study suggests that the emulsifiers consumed by the mother somehow distort this initial microbial gift, setting the child on a path toward poor health before it ever eats solid food.
“In the food industry, emulsifiers are commonly used to create smooth textures and prevent separation in products like mayonnaise, sauces and baked goods,” said Brighteon.AI‘s Enoch. “However, many emulsifiers are synthetic and can have adverse health effects, making it beneficial to opt for natural alternatives or homemade versions of these foods.”
The path forward
Benoit Chassaing and his team emphasize that their work in mice must now be followed by rigorous clinical research in humans. The critical next steps are to study mother-infant pairs to understand how maternal diet with and without food additives influences the transmission of microbiota and to assess the direct impact of additives in infant formula on a child’s developing immune system. This research is essential to inform public health policy and regulatory decisions.
The study from the Institut Pasteur and Inserm serves as a stark warning. It suggests that the choices we make about the food we eat today may echo through generations, influencing the health of our children in ways we are only beginning to understand. It underscores an urgent need to re-evaluate the pervasive use of these chemicals in the food supply, particularly in products designed for the most vulnerable among us. The pursuit of longer shelf life and perfect texture may be coming at a hidden and far too high a cost.
Watch and learn about the impact of processed foods and emulsifiers on gut health. 3min
This video is from the Daily Videos channel on Brighteon.com.
See also:
MOTHERS BEWARE: Consuming these common food additives may program babies for lifelong illness, study finds
https://www.naturalnews.com/2025-09-30-common-food-additives-program-babies-lifelong-illness.html
What is Cytochrome P450? How does it cause SIDS, Autism, Suicides and Homicides?
OTC
1. Tylenol: The most well-known brand for acetaminophen.
2. Excedrin: Often used for headaches, it combines acetaminophen with aspirin and caffeine.
3. NyQuil: A cold and flu medication that includes acetaminophen for pain relief.
4. DayQuil: Similar to NyQuil but formulated for daytime use.
5. Advil Dual Action: Combines ibuprofen and acetaminophen for enhanced pain relief.
6. Alka-Seltzer Plus: Some formulations include acetaminophen for cold and flu relief.
7. Midol: Often used for menstrual pain, some versions contain acetaminophen.
8. Aspirin-Free Excedrin: Contains acetaminophen, caffeine, and other ingredients for headache relief.
9. Bayer Back & Body: Combines acetaminophen with aspirin for back pain relief.
10. Aleve-D: Some formulations may include acetaminophen for added pain relief.
11. Tylenol Extra Strength: A higher dose formulation of acetaminophen for more severe pain.
12. Advil PM: Some formulations may include acetaminophen along with diphenhydramine.
Cold and Allergy Medications
1. Zyrtec-D: Some formulations may include acetaminophen for allergy relief.
2. Sudafed PE: Certain combinations may contain acetaminophen for cold symptoms.
3. Robitussin Cough + Chest Congestion DM: Some versions include acetaminophen for pain relief.
4. Vicks DayQuil: A daytime cold and flu relief option that contains acetaminophen.
5. Benadryl Allergy Plus Congestion: Certain formulations may contain acetaminophen for added relief.
6. Claritin-D: Some versions may include acetaminophen for allergy relief.
RX
1. Percocet: A combination of oxycodone and acetaminophen used for pain relief.
2. Tylenol with Codeine: Combines acetaminophen with codeine for more severe pain.
3. Fioricet: Contains acetaminophen, butalbital, and caffeine, often prescribed for migraines.
4. Vicodin: A combination of hydrocodone and acetaminophen, used for moderate to severe pain.
5. Lortab: Another combination of hydrocodone and acetaminophen.
6. Norco: Similar to Vicodin, it combines hydrocodone with acetaminophen.
7. Roxicet: A combination of oxycodone and acetaminophen, used for pain management.
8. Cocet: Combines acetaminophen with oxycodone for pain relief.
9. Fentanyl Combination Products: Some formulations may combine fentanyl with acetaminophen for pain management.
10. Lorcet: A combination of hydrocodone and acetaminophen.
11. Percodan: Combines oxycodone with acetaminophen for pain management.
12. Tylenol with Tramadol: A combination of acetaminophen and tramadol for moderate to severe pain.
Combination Products
1. Cold and Flu Formulations: Many products for cold and flu symptoms contain acetaminophen, such as Theraflu and Robitussin.
2. Pain Relievers: Some multi-symptom pain relievers may include acetaminophen along with other active ingredients.
3. Robitussin Multi-Symptom: Contains acetaminophen along with other ingredients for cough and cold relief.
4. Theraflu: Various formulations include acetaminophen for symptom relief.
5. Excedrin Tension Headache: Specifically formulated for tension headaches, containing acetaminophen.
6. Mucinex: Some formulations include acetaminophen for cold and flu symptom relief.
7. Coricidin HBP: Certain versions contain acetaminophen for cold symptoms, designed for those with high blood pressure.
8. Sominex: Some formulations may include acetaminophen for sleep aid with pain relief.
Pediatric
1. Children’s Tylenol: Liquid formulations specifically designed for children.
2. Infants’ Tylenol: Liquid acetaminophen specifically designed for infants.
3. Children’s Motrin: Some formulations may include acetaminophen alongside ibuprofen.
4. Children’s Advil: Some formulations may include acetaminophen alongside ibuprofen.
5. Pediatric Fever Reducers: Various brands offer liquid acetaminophen specifically for children.
Predictive Programming
A theory that claims governments or powerful groups use fiction (movies, TV, books) to subtly condition or desensitize the public to future events — such as disasters, false flags, pandemics, or major political shifts — so that when the real event happens, the public is more likely to accept it without resistance.
Snake Eyes synopsis: Charles Kirkland is shot in the neck in a stadium setting One of the players in a boxer named Tyler.
occurs from an overdose of acetaminophen (APAP), which is a common occurrence in pregnancy. While NAPQI does not cross the placenta, the parent compound, APAP, does, posing a risk of liver damage to both the mother and the fetus. Fetal risk increases after 14 weeks gestation when the fetal liver begins metabolizing APAP into NAPQI
• Normal APAP metabolism: At therapeutic doses, acetaminophen is metabolized in the liver and detoxified by glutathione.
• Overdose: In an overdose, the glutathione supply is exhausted, and the APAP is shunted to the cytochrome P450 (CYP450) system, which produces the toxic metabolite NAPQI.
• Cellular damage: In the absence of sufficient glutathione, NAPQI binds to and damages liver cells, leading to severe hepatotoxicity, acute liver failure, and potentially death.
o The fetus can produce its own NAPQI starting around 14 weeks gestation and has a limited supply of glutathione, making it vulnerable to APAP’s effects.
o The fetal liver’s CYP450 activity increases with gestational age, peaking in the third trimester.
• Hepatic: Liver injury, fulminant hepatic failure, liver transplant, and death.
• Other organs: Renal failure and pancreatitis.
• Gastrointestinal: Nausea, vomiting, anorexia, and abdominal pain.
• Neurological: Hepatic encephalopathy and confusion.
• Fetal hepatotoxicity: The fetus’s developing liver can suffer direct damage, especially in the third trimester.
• Fetal death: Overdose can lead to spontaneous abortion and fetal demise in all trimesters, with late presentation of maternal toxicity being a significant risk factor.
• Premature birth: Acetaminophen overdose can induce premature labor.
• Neurodevelopmental: Some studies suggest an association between prenatal APAP exposure at therapeutic doses and an increased risk of ADHD and other neurodevelopmental disorders, but data remains observational.
When acetaminophen is taken at therapeutic doses, most of it is processed differently, but high doses can overwhelm these pathways, leading to increased NAPQI production and potential liver damage.
How CYP Enzymes are involved:
Key CYP Enzymes:
Implications:
@drjoshreddTylenol breaks down into a toxic byproduct (NAPQI). Normally, glutathione—the body’s master antioxidant—neutralizes it. But in pregnancy, Tylenol use can cross into the placenta, and stresses the baby’s immature liver and brain. 💡 Safer support options: hydration, rest, lukewarm baths, arnica, chamomile, vitamin C, glutathione-supporting foods, and when needed, talk to your doctor for alternatives. Here are 3 human studies from Johns Hopkins, Yale & Harvard: Yale (Liew et al., 2022): Observational studies link frequent prenatal acetaminophen use with ↑ risk of asthma, neurodevelopmental issues, and genital malformations. • Harvard (Baccarelli et al., 2025, BMC Environ Health): Systematic review of 46 studies found prenatal exposure associated with higher risk of autism & ADHD. • Johns Hopkins (Ji et al., 2019, JAMA Psychiatry): Cord blood biomarkers of acetaminophen linked to ~2–3× higher risk of autism/ADHD in children. Here are 10 more. This isn’t new news: References (Human Studies on Acetaminophen Toxicity): • Mitchell JR et al. J Pharmacol Exp Ther. 1973 — First evidence that acetaminophen depletes glutathione and forms toxic metabolites. • Prescott LF et al. Lancet. 1977 — NAC rescues patients by replenishing glutathione. • Rumack BH & Matthew H. Pediatrics. 1975 — Classic clinical description, origin of the APAP nomogram. • Heubi JE et al. J Pediatr. 1998 — Pediatric hepatotoxicity after repeated dosing. • Davern TJ et al. Gastroenterology. 2006 — Serum protein adducts confirm NAPQI formation in humans with acute liver failure. • James LP et al. Clin Pharmacol Ther. 2009 — Adducts track with severity of overdose in adults. • James LP et al. J Pediatr. 2001 — Adducts also confirmed in children with toxicity. • Larson AM et al. Hepatology. 2005 — U.S. multicenter study: APAP is the leading cause of acute liver failure. • Hinson JA et al. Handb Exp Pharmacol. 2010 — Comprehensive human/mechanistic review.♬ original sound – Dr. Josh Redd
@dailymail President Trump claimed Tylenol taken during pregnancy is linked to autism, urging people not to take it. Read more at DailyMail. #news #breakingnews #trump #politics #autism ♬ original sound – Daily Mail