Category: Health Tips

(Just a preface from me. This is testing that was mandated to be done in the US but after a lengthy Freedom of Information request process, Robert F. Kennedy Jr got the appropriate government department to admit that the SAFETY TESTING HAS NEVER BEEN CONDUCTED!)

In December 2018, the Italian research company, Corvelva, released an explosive research paper. Vaxxter reported on their findings, exposing the ingredients in the vaccine Infanrix Hexa, the combination vaccine given to infants across Europe. Of course, the pro-vaccine machine immediately went into high gear, attacking and discrediting Corvelva’s testing methodologies. In response, Corvelva issued a technical report documenting their methods, declaring:

Protein detection is carried out using a standard approach using trypsin enzyme, a technique that has been internationally recognized for over 10 years. The peptides are then separated using chromatography and analyzed by mass spectrometry.

With this technology, there should be little doubt about the accuracy of their findings which concluded that Infanrix Hexa:

Has a molecular profile that is generally complex and largely unknown.
Contains protein contaminations with variable compositions that are not declared on the leaflet [package insert].
The entire Infanrix Hexa analysis can be found here in English.
Emboldened by these findings, researchers tested two more vaccines, Hexyon and Gardasil 9.

Hexyon – Hexacima
Hexyon is a six-in-one shot to vaccinate against diphtheria, tetanus and pertussis (DTaP), polio, hepatitis B and Haemophilus influenza b (Hib). It is called a six-in-one vaccine; however, 8 vaccine antigens are actually present because the polio vaccine has three antigens (three separate viruses). The vaccine, manufactured by a partnership between Sanofi Pasteur and MSD (Merck), was approved for use in 2013 in Western European Countries; simultaneously, it was approved for use in Eastern European countries under the brand name Hexacima. Here is the package insert.

Using the same methods used to analyze Infanrix Hexa, Hexyon was found to have 216 toxic chemicals and contaminants, of which 70% could not be identified. An additional 16 toxic residues were present and thought to be cross-contaminants from different vaccines, meaning, the machines were not thoroughly cleaned between production runs.

Researchers confirmed that all three of the DTaP toxoid antigens were present in Hexyon. However, they shockingly discovered that the antigens for hepatitis B, HiB and polioviruses 1, 2 and 3 were all missing. The entire analysis of Hexyon can be found here in English.

For those who trust that vaccines provide protection, how can Hexyon be “effective” when only 3 of the 8 stated antigens are present? Even more, how can Hexyon be called “safe” when it contains cross-contaminants and more than 150 compounds that cannot be identified in any chemical databases?

In December 2018, the FDA approved Vaxelis for use in American children from 6 weeks through 4 years of age (prior to the 5th birthday). This is the same vaccine (Hexyon) produced by the same manufacturers (Sanofi Pasteur and MSD). The FDA’s provisional approval letter to the manufacturers clearly states:

You must submit reports of biological product deviations under 21 CFR 600.14. You should identify and investigate all manufacturing deviations promptly, including those associated with processing, testing, packaging, labeling, storage, holding and distribution. If the deviation involves a distributed product, may affect the safety, purity, or potency of the product, and meets the other criteria in the regulation, you must submit a report on Form FDA 3486 to the Director, Office of Compliance and Biologics Quality.

Corvelva’s published findings regarding the contaminants and unidentifiable compounds need to be urgently submitted to the FDA and CBER so approval of Vaxelis can be reviewed and hopefully, withdrawn.

Gardasil 9
Even though Gardasil is not mandatory in Italy, the vaccine has been associated with a large number of serious injuries and even death in countries around the world, including the US. Gardasil, the vaccine promoted to prevent cervical cancer and venereal warts associated with human papillomaviruses (HPV), was approved for use in girls in 2006 and then approved for boys in 2009. The vaccine contained four antigens: HPV subtypes 6, 11, 16 and 18.

In 2014, the FDA approved Gardasil 9 for use in girls. The following year, it was approved for boys and in 2018, approval was granted to give Gardasil 9 to individuals up to 45 years of age. The new formulation added five HPV subtypes to the mix – 31, 33, 45, 52 and 58 – and increased the amount of aluminum in each injection from 250mcg to 500mcg.

Corvelva’s analysis of Gardasil 9 found:

Only 7 of 9 HPV antigens were present; subtypes 11 and 58 were not detected.
338 signals of chemical contaminants were detected, of which 78% were unknown.
10 chemical toxins, thought to be cross-contaminants from manufacturing of other vaccine production lines.
These findings again open questions about product compliance and clean manufacturing processes. The evidence should quickly be corroborated by other laboratories and if confirmed, reported immediately to the FDA, the European Commission on Vaccine Safety, the WHO, UNICEF, GAVI and corresponding bodies in all countries of the world.

If there is any doubt that vaccines may contain unknown, untested chemical contaminants, there can be no doubt that children must be protected from what is coming through that needle. A worldwide moratorium of the entire vaccination program must be implemented immediately until this investigation is concluded.

Exposing Vaccine Contamination – More Results from Corvelva

Specific respiratory microbiome communities may be linked to influenza susceptibility, according to a study published January 9, 2019 by Betsy Foxman from the University of Michigan, USA, and colleagues. Influenza virus, the causative agent of flu, primarily targets and infects the epithelial cells in the respiratory tract. The epithelial cells of the nose and throat are enveloped by complex bacterial communities, leading Foxman and colleagues to hypothesize that this respiratory microbiome might interact with the virus — and could play a role in the body’s defences against flu. In this study, 144 Nicaraguan households with a member identified as having influenza were enrolled between 2012 and 2014 and all household adults and children monitored for up to two weeks. Study staff visited each household five times, sampling the respiratory microbiomes of all household members as well as testing for influenza infection; participants also kept symptom diaries. Using statistical modeling, the authors were able to categorize each participant’s respiratory microbiome into one of five distinct community types at every visit, though approximately half of participants underwent changes in microbiome type between study visits. The authors could then compare participants’ microbiome types to the likelihood of their contracting flu. One of the five respiratory microbiome community types across age groups clearly demonstrated decreased susceptibility to the flu. This microbiome type was significantly less common in infants and young children, and when present also appeared less stable in these age groups compared to older children and adults. While the link between microbiome and influenza susceptibility was not shown to be causal in this study, the authors suggest that these microbiome differences might contribute to the increased influenza risk observed among young children. The authors note that the further work could examine whether the high degree of change to microbiome types seen in many participants represents normal variation among healthy individuals or a response to influenza exposure. Nonetheless, the authors believe this is the first human population study to indicate that your respiratory microbiome may affect your susceptibility to flu. https://www.nexusnewsfeed.com/article/climate-ecology/respiratory-microbiome-may-influence-your-susceptibility-to-flu/

After my post last week on dental floss one of my readers did some homework and found this he was kind enough to share.

Silk dental floss with NO chemical on it.

Just bought some.

But after examining it, will get some silk thread from somewhere, and some real bees wax.

Good to know silk can be used

https://au.iherb.com/pr/RADIUS-Natural-Silk-Floss-33-yds-30-m/43959

“If you inject thimerosal into an animal, it’s brain will sicken. If you apply it to living tissue, the cells die. If you put it in a petri dish the culture dies. Knowing these things, it would be shocking if one could inject it into an infant without causing damage.” Boyd Haley PhD, Professor and Chair, Department of Chemistry, University of Kentucky.

Something to consider.. Text version can be viewed here: http://mdbad.com/forum/topic/a-list-of-psychiatric-drugs-and-the-nutrients-they-deplete-from-the-body/

We are all being “slowly poisoned to death” by glyphosate, warns Erin Brockovich, who has vowed to topple agriculture giant Monsanto in order to improve the health of the world. Strikingly tall, with blonde hair coiffed, Brockovich doesn’t mince her words. A single mother and beauty pageant winner with no legal training, Brockovich once destroyed a billion-dollar corporation in one of the largest environmental pollution lawsuits in American history. Now she has set her sights on Monsanto. https://nworeport.me/2018/12/09/erin-brockovich-we-are-being-slowly-poisoned-to-death-by-monsanto

You know those hot cross buns you buy at the supermarket? Have a read of the poison warning on the label of the spice ingredient. The REALLY disturbing nature of this ingredient is bad enough but then you are not given this data on the packet of the final product.