Journal of Trace Elements in Medicine and Biology.

Volume 58, March 2020, 126444  – Acute Exposure and Chronic Retention of Aluminium in Three Vaccine Schedules and Effects of Genetic and environmental variation.

https://www.sciencedirect.com/science/article/pii/S0946672X19305784

Extracts: While Aluminium content in some vaccinations ‘may be necessary’ to enable these vaccinations to trigger ‘immunity’, total exposure to injected Aluminium is also an important health consideration. Aluminium Oxyhydroxide is currently allowed to be used in vaccines with per-dose limits that are body-weight independent. It may be used up to 25 μg/L in large-volume parenteral drug products, and up to 1250 μg/single dose, depending on calculation method, “provided that data demonstrating that the amount of Aluminium used is safe and necessary to produce the intended effect are submitted to and approved by the Director, Centre for Biologics Evaluation and Research or the Director, Centre for Drug Evaluation and Research.”  This regulation apparently does not, but perhaps should, apply to individual vaccine office visits to consider cumulative doses from multiple vaccines received at one time. The inexact regulatory modus operandi of employing per-dose Aluminium limits that are independent of body weight are problematic, because the CDC schedule permits many vaccines per office visit (and thus per day). Aluminium in the body has been cited as a likely contributing factor to both Autoimmune conditions and other Chronic illnesses. Person-to-person variation in whole body clearance rates due to Genetics and Environmental factors has been under-studied. Studies of human plasma or blood clearance rates offer little useful information to toxicology, for the known mechanisms of toxicity of Aluminium are intracellular and are thus intra-tissue. Thus, rapid serum or blood clearance rates can be misleadingly reassuring when considering chronic or even acute toxicity of Aluminium injected with vaccines. Aluminium in many forms has been long suspected of playing a role in Alzheimer’s disease and is supported by studies showing disease symptom reduction from ingestion of silicon-rich mineral waters. “Tagging” of Aluminium released by detoxification with compounds in Chlorella and Spirulina may be essential to allow removal by the Liver, and to prevent “detox-retox” that occurs when Aluminium is freed from cell death, redistributed and deposited via resequestration within and among tissues in the body. Medically, proper organ, cellular and body Aluminium detoxification appears to be of ever-increasing importance: Aluminium has been found in the Brains of patients with Parkinson’s Disease, Alzheimer’s Disease, Epilepsy, and Autism. Evidence is growing that a host of Chronic illnesses of unknown cause that are difficult to diagnose such as PANDAS/PANS, Chronic Fatigue Syndrome may at least in part be due to vaccine Aluminium intolerance.

Aluminium compounds occur naturally in the environment and in food, but very little ingested is absorbed through the intestines. Total Aluminium exposure is affected by the Aluminium amount in individual vaccines and the timing of repeated vaccinations in the first two years of life. Dórea and Marques compared the expected levels of Aluminium uptake into the body from intravenous and oral intake and concluded that human infants have higher exposure to Aluminium from vaccination than from food, water, and formula. Our calculations (Appendix) confirm that for the CDC schedule, infants up to six months of life receive most of their metabolically available Aluminium from vaccines. It should be expected that most Aluminium retained in the body of infants comes from vaccinations combined with the levels of exposure from other exposures to manifest health risks from total exposure, making the timing and total Aluminium content of different vaccine schedules an important consideration. In this study, we explore the effects of different dose schedules, reflecting three different vaccination schedules, on Aluminium retained fractions. We also study the effects of an important model construction assumption reflecting the effects of previous Aluminium exposures on first-day clearance, genetic variation in clearance rates, and the potential impact of Aluminium impairment on its own detoxification on the expected retained fraction in the body over time. We represent the results as the number of days a child can be expected to experience Aluminium body burdens (i.e., the entire amount of Aluminium present in the body) that exceed proposed safe levels of exposure in the first two years of life and emphasise the expected chronic toxicity in the first seven months of life. None of the individual vaccines violates the guidance of a maximum of 850 μg of Aluminium for an adult. However, because of multiple vaccines typically given together at 2, 4, and 6 months, the CDC schedule violates this limit even assuming an adult weight. Adjusting the ‘Safe Dose’ limit based on a child’s weight at these ages therefore results in doses that far exceed the estimated safe limit of acute. Even assuming infants clear at the same rate as adults, which is not based on any empirical evidence, it is reasonable to expect that not only the dosage of vaccinations but how closely they are spaced in time will impact the Aluminium level for infants in the first two years of life given their low body weight. Aluminium toxicity from vaccines can be expected to be increased from other exposures such as Aluminium in food (formula) and Aluminium used to buffer drinking water (Alum). Individual infants with incompletely closed intestinal barriers, or with Autoimmune Gastric and Intestinal Lesions may be experiencing much higher doses of Aluminium than a paediatrician may be aware. Aluminium has now been found in the Brains of individuals who have died with various diagnoses, including Multiple Sclerosis, Epilepsy, Parkinson’s Disease, Alzheimer’s Diseases and Autism Spectrum Disorder. Whole-body Aluminium toxicity is important because Aluminium affects the Brain, Bones, Parathyroid, Spleen, Kidneys, and, of course, the Immune System. Of these compartments, Brain clearance of Aluminium is the slowest; in rats, Aluminium half-life was found to be 150 days, but clearance was expedited via deferoxamine.

In neonates, the GFR at birth is even worse and increases more slowly compared to infants (3,761,090). While the Kidney is structurally mature at 36 weeks, the GFR does not reach adult levels until 2 years of age. Common emergent conditions in the NICU include Respiratory Distress Syndrome, Seizures, and Arrhythmias and Cardiac arrest. To maximise ‘efficiency,’  infants in the NICU are often vaccinated simultaneously with crash teams on stand-by. Studies in the 2000′s of DTP vaccines showed an incredible 46 % Cardiac Event Rate in infants in the NICU following vaccination.

Hepatitis B vaccination studies in the 1990s are not relevant to concerns over Aluminium-induced adverse events because the HepB vaccine did not contain Aluminium Oxyhydroxide (although it did contain ethylmercury); however, studies from passive surveillance systems routinely oddly attribute the majority of deaths to coincidence. A Chinese study found 795 deaths, with >95 % of them occurring following Hepatitis B vaccination in children <5 years old, but the majority were attributed to “coincidence.” This is an odd conclusion, given that passive surveillance systems cannot attribute causality. Of the 795 deaths, 594 (74 %) were classified as ‘coincidental’ events, but SIDS was found to be a main cause of death in infants. SIDS, a condition of otherwise unknown cause, is not considered an expected adverse event. The studies from the 1990s in the US similarly attributed, without independent evidence, the majority of serious adverse events from HepB vaccination to coincidence. Since passive surveillance systems cannot attribute causality, they also cannot rule out causality, and thus attribution to coincidence seems opportunistic at worst and optimistic at best. The authors of the Chinese study lauded the ‘sensitivity’ of their passive surveillance system after ruling out unexpected deaths as ‘coincidence.’ In reality, this reflects a serious flaw in the use of passive surveillance systems to monitor vaccine safety, which routinely underreport adverse events by a factor of 100 misses to each report. We cannot stress how important it is that infants avoid Aluminium from all sources, at all doses, due to the realities of cumulative risk from cumulative exposure. Selecting brands of vaccines that contain lower amounts of Aluminium and avoiding the combination vaccines that have the greatest amounts of Aluminium would be advisable for reducing toxicity. Recalling that Aluminium adjuvants induce a Th2-biased immunological state, the use of other adjuvants known to induce both Th1- and Th2- reactions may prove to be medically beneficial and economical shift in the focus of developing ‘safer vaccines.’ Requiring lower doses of adjuvants, longer periods of immunoefficacy, and safer vaccine schedules for vaccine approval by FDA so that neonates and infants have lowered exposures to neurotoxic metals during development may be more acceptable to an increasingly vaccine-risk aware public due to lowered exposures to Neurotoxic and Immunotoxic metals during development.  References:  58 articles included.

COMMENT: Claims that Mercury has been removed from some ‘vaccines’ is not always true – many times it has been reduced (because its harm was becoming obvious) below a ‘threshold’ that does not ‘need’ to be shown by the manufacturer. It is still in the Influenza ‘vaccines’ in high amounts. Toxic Synergy of these two metals is then concealed. The very fact that Mercury and Aluminium were ever allowed in ‘vaccines’ then injected into people is Proof Positive that ‘vaccines’ were always Agents of Deliberate Harm. The whole filthy business of ‘vaccines’ is Criminal, and the oft-convicted Pharma Felons are still committing this Crime Against Humanity without hindrance. Their Mind Numbing Propaganda worked then and is further working now with their ‘Depopulate With Profit’ bogus Covid ‘vaccine’ Dogma mandates. Pharmaceuticals are Synthetic Biological Incompatible Imposts against our once natural Immune Systems.