Ingestion vs. Injection… what’s the difference?
Ingestion substances flow through the body’s biological detox pathway, which includes the mucosal cells, stomach, intestines, kidneys and liver. The gastrointestinal (GI) tract, which digests it to extract and absorb energy and nutrients, expelling the remaining waste as feces.
Injection skips the body’s entire detox pathway, including the GI tract, and slowly leaks into the bloodstream from the muscle tissue. From there, these toxins have access to major organs (heart, brain, Central Nervous System, kidney, lungs, etc) as well as other important body tissues (thyroid, intestines, etc) through the lymphatic pathway. Numerous scientific studies have reported the serious health issues that can result from injected toxins (see below).
Biologically, they’re very different… and so are the risks.
Injected aluminum = around 95% absorbed into body tissues
Ingested aluminum = around 95% excreted through the body’s detox pathway
We all can handle different levels of synthetic chemicals — determined by our genetics — before inflammation takes hold and cause a health issue, most often chronic. You NEVER know when you will be pushed past the tipping point of what your body can handle and you develop a neurological or autoimmune issue, cancer, heart disease or even death.
Anything injected is far more damaging than anything ingested
All exposure adds to the toxic mix, but when it’s injected, the aluminum bypasses the body’s natural detox pathway. Around 95% of injected toxins, including aluminum, pass from muscle tissue and go straight into the circulatory system (aka bloodstream). From there, the aluminum and other toxins can reach vital organs like the brain, heart, kidney, liver, and others. One study shows that most aluminum remains in the body for months, possibly years, after the injection. This can cause chronic health issues as the toxins raise inflammation levels in the body.
When aluminum is ingested (via food, water or air), only about 5% is absorbed into the body, whereas most if filtered through the body’s natural detox pathway. So the toxic chemicals in vaccines are FAR MORE POTENT than those that come into the body in other ways. The toxic ingredients in vaccines include aluminum, but also mercury, barium, monosodium glutamate (MSG) formaldehyde (known to cause cancer in humans).
THE DIFFERENCE BETWEEN NANOPARTICULATE ADJUVANT ALUMINUM (VACCINE) AND IONIC ALUMINUM (FOOD)
The biggest problem of all: injected aluminum cannot be removed by the kidneys, whereas ingested aluminum can. This is because injected aluminum is in the form of nanoparticles, which dissolve very slowly into ionic form. These nanoparticles are too large to be removed, especially when they have absorbed antigen. On the other hand, aluminum absorbed from ingestion if already in ionic form, which is rapidly removed by the kidneys.
Injection vs Ingestion — Brandy Vaughan founder of Learn The Risk
Did you know formaldehyde is far more toxic when injected than when ingested?!!
INJECTING ALUMINUM VS. INGESTING ALUMINUM
THERE IS MUCH LESS DANGER BY EATING THEN INJECTING!
When you inject something into the muscle, it goes through your lymphatic system and is processed through lymph nodes before being dumped into your bloodstream to be filtered by your liver. When you eat, it is only partially absorbed by your intestines and the rest leaves with your feces. Eating is much less dangerous than injecting.
The vast majority of infections enter the body through the nasal passages (mucosal membrane) and the gastrointestinal tract, also known as the guts. Accordingly, 80% of the body’s natural defenses are aligned at these junctures. This represents the body ‘s primary guard against incoming viral, bacterial & fungal pathogens. Vaccines are injected subcutaneously, or intramuscularly, a route which literally bypasses your natural defenses altogether. The contents of these vials go directly into the bloodstream, which is 90% water & 10% colloidal blood product – thereby getting direct access to the innermost reaches of the body
TOXIC INGREDIENTS IN MOST VACCINES
- Mercury – one of the most toxic elements in humans. Tiny doses cause damage to the brain, gut, liver, bone marrow, nervous system and/or kidneys. Also linked to neurological and autoimmune disorders.
- Aluminum – a proven neurotoxin. Linked to Alzheimers disease, dementia, seizures, autoimmune issues, SIDS and cancer.
- Formaldehyde – known to cause cancer in humans. Probable gastrointestinal, liver, respiratory, immune, nerve and reproductive system.
- Polysorbate 80 – known to cause cancer in animals. Also linked to infertility and allows other unfiltered chemicals to enter the brain
- MSG – a toxic chemical, linked to birth defects, developmental delays and infertility.
- Beta-Propiolactone – known to cause cancer, such as gastrointestinal, liver, nerve and respiratory, skin and sense organ poison.
In vivo absorption of aluminium-containing vaccine adjuvants using 26Al
This Flarend study shows that even after a month, only about 6% (of Al hydroxide) or 22% (of Al phosphate) is eliminated in urine. Most aluminum adjuvant is retained in the body 1 month after injection. The Flarend study also shows that the aluminum spreads to numerous organs, including the brain.
https://www.ncbi.nlm.nih.gov/pubmed/9302736/
Effect of Routine Vaccination on Aluminum and Essential Element Levels in Preterm Infants
The Movsas study (published in 2013) used human infants and obtained the similar results. Movsas looked for aluminum in urine and blood before and after routine vaccination with 1200mcg aluminum at the 2-month date. No change in urine or blood levels was observed. Movsas states: “No significant change in levels of urinary or serum aluminum were seen after vaccination.“ (http://vaccinepapers.org/wp-content/uploads/Effect-of-Routine-Vaccination-on-Aluminum-and-Essential-Element-Levels-in-Preterm-Infants.pdf)
Nanomolar aluminum induces expression of the inflammatory systemic biomarker C-reactive protein (CRP) in human brain microvessel endothelial cells (hBMECs)
10 nano-molar Al causes inflammation in human blood vessel cells (https://www.ncbi.nlm.nih.gov/pubmed/26265215)
Nanomolar aluminum induces pro-inflammatory and pro-apoptotic gene expression in human brain cells in primary culture
100 nano-molar Al causes inflammation in human neurons
(https://www.ncbi.nlm.nih.gov/pubmed/15961160)
HUMAN HEALTH RISK ASSESSMENT FOR ALUMINIUM, ALUMINIUM OXIDE, AND ALUMINIUM HYDROXIDE
We concluded that there is strong evidence that aluminium can cause irritation following exposure via either inhalation or injection. Modest evidence of an effect exists for reproductive toxicity following oral exposure, for neurological toxicity following either oral or injection exposure, and for bone toxicity following injection exposure.
https://www.ncbi.nlm.nih.gov/pubmed/18085482
Total allowable concentrations of monomeric inorganic aluminum and hydrated aluminum silicates in drinking water
Signs of Al toxicity in the central nervous system (speech difficulty to total mutism to facial grimacing to multifacial seizures and dyspraxia) are related to Al accumulation in the brain and these symptoms can progress to frank encephalopathy.
https://www.ncbi.nlm.nih.gov/pubmed/22512666
Biopersistence and brain translocation of aluminum adjuvants of vaccines.
This Gherardi study shows that poorly biodegradable aluminum-coated particles injected into muscle are promptly phagocytosed in muscle and the draining lymph nodes, and can disseminate within phagocytic cells throughout the body and slowly accumulate in the brain. This strongly suggests that long-term adjuvant biopersistence within phagocytic cells is a prerequisite for slow brain translocation and delayed neurotoxicity.
https://www.ncbi.nlm.nih.gov/pubmed/25699008
Kinetics of the inflammatory response following intramuscular injection of aluminum adjuvant.
Recent evidence suggests an important role for inflammation in the immune response to aluminum-adjuvanted vaccines. To better understand them, vaccines with aluminum adjuvant were injected into naïve or previously immunized mice and the injection sites were characterized for the corresponding primary and secondary inflammatory response at different time points after immunization.
https://www.ncbi.nlm.nih.gov/pubmed/23770306
Chronic fatigue syndrome and subsequent risk of cancer among elderly US adults.
This study concludes that chronic immune activation or an infection associated with chronic fatigue syndrome (CFS) may play a role in explaining the increased risk of blood cancers – non-Hodgkin’s lymphoma (NHL).
https://www.ncbi.nlm.nih.gov/pubmed/22648858
Aluminum adjuvants of vaccines injected into the muscle: Normal fate, pathology and associated disease.
“In healthy subjects, only 0.3% of orally administered aluminum is absorbed via the GI tract, and the kidneys effectively eliminate aluminum from the human body. Only when the GI barrier is bypassed, such as by intravenous infusion or in the presence of advanced renal dysfunction, does aluminum have the potential to accumulate. As an example, with intravenously infused aluminum, 40% is retained in adults and up to 75% is retained in neonates.”
“If a significant aluminum load exceeds the body’s excretory capacity, the excess is deposited in various tissues, including bone, brain, liver, heart, spleen, and muscle. This accumulation causes morbidity and mortality through various mechanisms.”
https://www.ncbi.nlm.nih.gov/pubmed/26948677
Systematic review of potential health risks posed by pharmaceutical, occupational and consumer exposures to metallic and nanoscale aluminum, aluminum oxides, aluminum hydroxide and its soluble salts
Aluminum exposures during neonatal and pediatric parenteral nutrition (PN) can impair bone mineralization and delay neurological development.
https://www.ncbi.nlm.nih.gov/pubmed/25233067