Children of God for Life. Has anyone told you they didn’t believe we could possibly have vaccines produced right here in America from aborted fetal cell lines?
Did anyone tell you it was a hoax? Children of God for Life gives you the full truth and the resources you need to prove it! The fact that the Chickenpox, Hepatitis-A and MMR vaccines were developed using aborted fetal cell lines, MRC-5 and WI-38 has never been hidden from the public. The problem is that when parents go to their family doctors for vaccinations, who asks to see the product insert? Most parents want to know the risks and possible side effects. Click here for the Manufacturer’s package insert portion describing the fetal cell lines. But that statement alone does not mean “aborted fetal tissue”. Next, most doctors have at their disposal a book called a PDR (Physician’s Desk Reference). Aborted Fetuses in Vaccines - Stanley Plotkin Under Oath (clip) Excipient table 2. Characteristics and viral propagation properties of a new human diploid cell line, walvax-2, and its suitability as a candidate cell substrate for vaccine production. Stanley Plotkin, Godfather of vaccines, UNDER OATH! (Nine Parts). – Vaccines should be safer.
The "Godfather" of vaccines . . . Elsevier Vaccine immunology. AbortedFetalCellLines. 1-11-18-Matheson-Plotkin.pdf. CORVELVA-Study-on-the-chemical-composition-profile-of-Priorix-Tetra.pdf. Official web site of the U.S. Health Resources & Services Administration. Most Recent Data Report National Vaccine Injury Compensation Program Data Report (PDF - 297 KB) - updated March 1, 2019.
Updated monthly, and includes the number of: petitions filed,adjudications compensated and dismissed,awards paid by type and amount,claims by vaccine, andadjudication categories by vaccine. The United States has the safest, most effective vaccine supply in history. In the majority of cases, vaccines cause no side effects, however they can occur, as with any medication—but most are mild. In those instances, the National Vaccine Injury Compensation Program (VICP) allows individuals to file a petition for compensation. What does it mean to be awarded compensation?
Being awarded compensation for a petition does not necessarily mean that the vaccine caused the alleged injury. What reasons might a petition result in a negotiated settlement? Consideration of prior U.S. How many petitions have been awarded compensation? CFR - Code of Federal Regulations Title 21. (a) The aluminum content of large volume parenteral (LVP) drug products used in total parenteral nutrition (TPN) therapy must not exceed 25 micrograms per liter ([micro]g/L).
(b) The package insert of LVP's used in TPN therapy must state that the drug product contains no more than 25 [micro]g/L of aluminum. Highly delayed systemic translocation of aluminum based adjuvant in CD1 mice following intramuscular injections. Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity. - PubMed - NCBI. Al Adjuvant Causes Brain Inflammation and Behavioral Abnormalities; Low Dose Is More Harmful vaccinepapers.org. A new paper (Crepeaux et al.) by the Gherardi research group in France reports important results on the toxicity and transport of aluminum (Al) adjuvant in mice.
This study is especially valuable because it looked at many outcomes: behavioral effects, immune (microglial) activation in the brain, and Al transport into the brain. The study tested dosages of 200 , 400 and 800 mcg/Kg (mcg=micrograms, mcg/Kg = micrograms per kilogram of animal body weight), injected intramuscularly (IM). Reconsideration of the immunotherapeutic pediatric safe dose levels of aluminum. 1.
Introduction Aluminum is used as an adjuvant in vaccines licensed by the US Food and Drug Administration [[1], [2], [3], [4], [5], [6], [7]] to enhance the immunogenicity of the vaccine in various forms (e.g., aluminum oxyhydroxide and aluminum hydroxyphosphate) [9,10] (Fig. 1). The Center for Biologics Evaluation and Research (CBER) sets the amount of aluminum per dose in biological products, including vaccines, to 850 μg aluminum if measured by assay.
Two additional levels are specified by the regulations (1140 and 1250 μg respectively), depending on how the level is measured [8]. Fig. 1. PEDIARIX. Polysorbate 80 and E-Ferol toxicity. - PubMed - NCBI. Data on Campaign Finance, Super PACs, Industries, and Lobbying. Facebook. Facebook. H.R.5546 - 99th Congress (1985-1986): National Childhood Vaccine Injury Act of 1986. Dr. Palevsky's commentary on vaccine injury mechanisms, polysorbate80. Dr.
Palevsky's Comments: Interesting. They found the polio virus in waste water, and now they're going to give a polio vaccine to 200,000 children, who have previously received the polio vaccine. What they don't tell you is the polio virus was found in the waste water due to the widespread use of the oral polio vaccine, the very vaccine they will be using to vaccinate 200,000 children.
It doesn't matter that the children have already been vaccinated, they're going to be used as guinea pigs to 'protect' the adults around them from the potential of a polio illness. Polysorbate 80 risks - Vaccine Choice Canada. December, 2013 According to Wikipedia, “Polysorbate 80 (brand names include Alkest, Canarcel and Tween, which is a registered trademark of ICI Americas, Inc.) is a nonionic surfactant”, a compound which “lowers the surface tension between two liquids or between a liquid and a solid…Surfactants may act as detergents, wetting agents, emulsifiers, foaming agents, and dispersants.”
In a 2006 article, Sherri Tenpenny DO quotes from her book, Fowl! Bird Flu: It’s Not What You Think, Chapter 8 of which describes how seasonal influenza vaccines are made. Specific role of polysorbate 80 coating on the targeting of nanoparticles to the brain. Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats. - PubMed - NCBI. Recognition of microbial viability via TLR8 drives TFH cell differentiation and vaccine responses. - PubMed - NCBI. CORVELVA-Study-on-the-chemical-composition-profile-of-Infanrix-Hexa.pdf. First revision December 16, 2018 Brief presentation of the results When we started these analysis, from the metagenomics to the chemical ones, we had a lot of questions and we were only looking for answers...
After these first results, more questions have arisen and so did the concerns! The quali-quantitative analysis of organic compound is of great importance in the pharmacological field, as potential safety problems arise from the new production processes of biological drugs and from the complex structural and biological characteristics of these products. In Infanrix Hexa we found: ● chemical contamination from the manufacturing process or cross-contamination with other manufacturing lines; ● chemical toxins; ● bacterial peptide toxins; ● insoluble and indigestible macromolecule that reacts to the protein assay, but cannot be recognized by any protein databases.
We have not found: ● Formaldehyde and glutaraldehyde, phenoxyethanol, antibiotic residues indicated in the composition; Excipient table 2. Insitute for Vaccine Safety - Package Inserts and Manufacturers. Monkeys, viruses, and vaccines - The Lancet. Wild vs Artificial Exposure to Measles Are Not Equal. 157 Research Papers Supporting the Vaccine/Autism Link. Deisher article 2 FINAL1.