Monday, October 2, 2017

Prophecies, conspiracies, and endtimes stuff: Fw: Idaho Toxicologist Reveals Censorship of Vaccine Science in CBS Interview that Never Aired...

Prophecies, conspiracies, and endtimes stuff: Fw: Idaho Toxicologist Reveals Censorship of Vaccine Science in CBS Interview that Never Aired - Watch it Here...: Show original message Vaccine Impact Idaho Toxicologist Reveals Censorship of Vaccine Science in CBS Interview that Never Aired - Watch it Here...


Information about The Vitamin K shot being linked to leukemia

Another one that the overzealous bastards want to jab into newborns as soon as they exit the womb.


Information about The Vitamin K shot being linked to leukemia.




"The Vitamin K shot has been linked to leukaemia, including acute lymphoblastic leukaemia, which is characterized by an increased number of white corpuscles in the blood, and accounts for about 85 percent of childhood leukaemia. Research carried out by Dr. Louise Parker, of the Sir James Spence Institute of Child Health in Newcastle upon Tyne, produced the most startling results. Dr. Louise
Parker was quoted in the British Medical Journal in 1998 as stating, "It is not possible, on the basis of currently published evidence, to refute the suggestion that neonatal IM vitamin K
administration increases the risk of early childhood leukemia.".
The British Journal of Cancer published "Factors associated with childhood cancer" by J. Golding, et al, in 1990. The report indicated that universally administered IM vitamin K injections significantly increase our children's chances of developing childhood cancer.

A follow-up study published two years later in the British Medical Journal (Golding J, Paterson K, Greenwood R, Mott M. Intramuscular vitamin K and childhood cancer. BMJ 1992; 305:341-346.) reinforced the findings of the previous study. The authors' comments, in keeping with scientific style, are conservatively stated, but parents who are concerned about the health of their babies will read "danger" between the following lines: "The only two studies so far to have examined
the relation between childhood cancer and intramuscular vitamin K have shown similar results and the relation is biologically plausible. The prophylactic benefits against haemorrhagic disease are unlikely to exceed the potential adverse effects from intramuscular
vitamin K..."

The chance of your child developing leukaemia from the Vitamin K shot
is estimated to be about one in 500 (MIDIRS Midwifery Digest, Vol 2 #3, September 1992)

Animal studies have linked large doses of vitamin K to a variety of conditions that include anaemia, liver damage, kidney damage and death.

Interestingly the common problem that occurs these days of jaundice in newborns has only been reported since the introduction of Vitamin K administration.

According to the product insert, adverse reactions include haemolysis (or hemolysis - American spelling) (meaning breakdown of red blood cells), haemolytic anaemia (a disorder characterised by chronic premature destruction of red blood cells), hyperbilirubinemia (too much bilirubin in blood) and jaundice (yellow skin and eyes resulting from hyperbilirubinemia), and allergic reactions include face flushing, gastrointestinal upset, rash, redness, pain or swelling at injection site and itching skin. It also warns that large enough doses can cause brain damage in infants and/or impairment to liver function. Hypoxia has also been published as having occurred in infants after Vitamin K administration.


Vitamin K Shot Black Box Warning:


https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/012223Orig1s039Lbl.pdf




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Senor Citizens Targeted by the Vaccine Mafia

A Dear Friend of mine, who shall remain nameless shared this with me about her work. So PLEASE SAVE THIS AND SHARE WITH YOUR LOVED ONES. PROTECT THEM. Often Immunity in our loved ones is weak, and Pharma is CLUELESS on what builds a STRONG IMMUNE SYSTEM. ~ Deniece Young




Five seniors die in Georgia care center after receiving flu shot - report
https://www.naturalnews.com/047746_flu_shots_senior_citizens_vaccine_deaths.html

Not the same story but...
23 Seniors Died After Receiving Flu Shot Sold by Pharmacies

Package insert for Fluzone flu vaccine marketed to seniors reveals 23 seniors died during drug trial
http://healthimpactnews.com/2013/23-seniors-died-after-receiving-this-years-flu-shot-sold-by-pharmacies/


The Mental Wellness Summit 2 Day 6: It’s Encore Day at Mental Wellness Summit!

DAY 8 (Oct 2, after 10am US eastern)

It’s Encore Day at The Mental Wellness Summit 2! Missed some of the life-changing expert talks this past week? They’re all unlocked for free today! And, with mental health struggles as slow, silent killers sapping us of energy and happiness, it’s important for us to learn more about achieving mental wellness!

Registration Link:  http://healthaffiliate.center/13197-18.html


It’s Encore Day at #MentalWellnessSummit! All expert talks available for free TODAY ONLY!
http://healthaffiliate.center/13197-18.html

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Thoughts and Commentary:

There was no spare time to post notes and comments due to time constraints and other summit events going on at the same time. When there are two or more events happening at one time or one after another, it's harder to keep up. I can go grab notes from Katerina's posts, as she loves to outline some of the snippets.


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Breakdown of Individual Vaccine Ingredients

Breaking down the vaccine ingredients even more. I am breaking the ingredients down, per ingredient in the Vaccine Excipient and Media Summary from the CDC website.

Why?

Because no one else has bothered to do so.  This is a work in progress and will probably take several months to get it completed.

And I'm still on the first one listed (Adenovirus), and this is what I have, so far.  All of this is being injected into the human body.


Vaccine Excipient and Media Summary 

- - - -

Adenovirus:

human-diploid fibroblast cell cultures (strain WI-38),  -  
Aborted fetal tissue cells.

WI-38 is a diploid human cell culture line composed of fibroblasts derived from lung tissue of an aborted white (caucasian) female fetus. ... One article published in the 1970s suggested that half of the WI-38 cells stocked by Hayflick at the passage 8th would be used up in 66 years from that time.
Source:  WI-38 - Wikipedia -  https://en.wikipedia.org/wiki/WI-38 

WI-38 cells were derived from human fetal lungs obtained through a legal abortion in Sweden; the fetal lung tissue was shipped from Stockholm to Philadelphia for Dr. Hayflick’s research, which at the time was looking for normal cells—not cancerous like those of the HeLa line—in order to determine whether some forms of cancers in humans could be caused by viruses. The cervical cancer line HeLa was not much use to Dr. Hayflick, so he established this new line, WI-38, which became one of the most important cells lines in history.
Source:  The Story of WI-38, the Other Famous Cell Line - http://www.ascb.org/activation-energy/the-story-of-wi-38-the-other-famous-cell-line/  
  
The WI-38 cell line was developed in July 1962 from lung tissue taken from a therapeutically aborted fetus of about 3 months gestational age. Cells released by trypsin digestion of the lung tissue were used for the primary culture. The cell morphology is fibroblast-like. The karyotype is 46,XX; normal diploid female. A maximum lifespan of 50 population doublings for this culture was obtained at the Repository. A thymidine labelling index of 86% was obtained after recovery. G6PD is isoenzyme type B. This culture of WI-38 is an expansion from passage 9 frozen cells obtained from the submitter.

Religious Conscience & Aborted Fetal Vaccines


- - - -

Dulbecco’s Modified Eagle’s Medium, - 
What is Dulbecco's modified Eagle's medium?
DMEM is a modification of Basal Medium Eagle (BME) that contains a four-fold higher concentration of amino acids and vitamins, as well as additional supplementary components. The original DMEM formula contains 1000 mg/L of glucose and was first reported for culturing embryonic mouse cells.

Eagle's minimal essential medium (EMEM) is a cell culture medium developed by Harry Eagle that can be used to maintain cells in tissue culture.
It contains:
glucose
A variation of this medium, called Dulbecco’s modiļ¬ed Eagle's medium (DMEM), (Dulbecco/Vogt modified Eagle's minimal essential medium), contains approximately four times as much of the vitamins and amino acids present in the original formula and two to four times as much glucose. Additionally, it contains iron and phenol red. DMEM is suitable for most types of cells, including humanmonkeyhamsterratmousechicken and fish[1] cells.
Other Sites:

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microcrystalline cellulose, - 

A DNA Disrupter.
Source:  Tony Pantalleresco (HerbsPlusBeadWorks on Youtube)

good article but you have to remember that this is not just the microcrystaline all the celluose today being used in nutreceuticals as well as pharmaceuticals are all nano~ the methods are going to a “nanodelivery” and this is also being utilized in vaccines and in alot of health supplements which when consumed aggragate and agglomerate and morph and get activated with almost any form of frequency and it begins it’s assmblying and as a result it densifies even more
augmentinforce.com has several links on the topic and yes you can get this out but with great difficulty
Source:  Comment on another article - http://augmentinforce.com/

Nearly all supplements found online come along with many fillers, other ingredients like: Cellulose, Microcrystalline cellulose, silica, silicon dioxide, sodium carboxymethylcellulose, magnesium stearate. 

Microcrystalline cellulose is a term for refined wood pulp and is used as a texturizer, an anti-caking agent, a fat substitute, an emulsifier, an extender, and a bulking agent in food production. The most common form is used in vitamin supplements or tablets.

DANGERS OF MICROCRYSTALLINE CELLULOSE, FILLER IN PHARMACEUTICALS

Posted on January 10, 2014 by Emi Miller

DANGERS OF MICROCRYSTALLINE CELLULOSE

I have some NEW concerns for us to think about as far as using MICROCRYSTALLINE CELLULOSE as a filler in Nature Throid, Westhroid and ArmourThyroid tablets.

I am a Registered Nurse, with an extensive background in physiology. It occurred to me that just as the cells cannot keep out artificial sweeteners, but absorb them as if they were ordinary glucose, and that this wreaks havoc in our cells ability to function, leading to many forms of physical discomfort and illness, that the same thing would apply if we use MICROCRYSTALLINE CELLULOSE as a filler in our Thyroid products. I remembered reading on this forum about why Armour stopped working well for many people, even when they adjusted their dosage correctly. The reason stated was that they had started using artificial fillers.

Doing some research I came upon this article, and want to share it here. It says exactly that: Our cells cannot stop the micro-nano particles from entering them, and once there they are not able to be useful, but float in and out of the cell membranes, and basically clog up tiny places in our bodies, bioaccumulating as we take more, and causing background inflammation to rise.


A couple of excerpts from the article follow:

Nanotechnology: benefits vs toxic risks,

Feb. 1, 2007 George Burdock |Functional Ingredients

“”Once in the body, some particles have changed the shape or conformation of proteins, creating a protein similar to that produced in Alzheimer’s disease. Changing protein conformation can potentially create new allergenic proteins in organs to which the body could mount an immune response.

While easy entry into the cells of the intestine and target organs can be beneficial, the other side of the coin is that because these particles are so ‘slippery,’ how can they ever be excreted by the body? Because much of our excretory system at the cellular level is based on a cell successfully excreting a substance (as in the kidney) to be flushed away, how can the particle be made to remain in the waste stream if it can so easily gain re-entry into other cells downstream?

While some of the more dramatic examples of actual physical damage are described above, the damage most often seen in response to nano-materials is the generation of reactive oxygen species, resulting in oxidative stress to the biological system.

In oxidative stress, the universal antioxidant chemical in the body, glutathione or GSH, is converted to the oxidized inactive form, GSSH. As reserves of GSH are depleted and the GSH:GSSH ratio lowers, the body mounts a progressively more assertive reaction. The first stage of oxidative stress is to produce special enzymes to detoxify the new invading chemical; if, however, there is no enzyme for this purpose or the human does not have the capability to produce the enzyme, the body progresses into the next stage, inflammation.””

Microcrystalline cellulose
Microcrystalline cellulose is a purified, partially depolymerized cellulose prepared by treating alpha-cellulose, obtained as a pulp from fibrous plant material, with mineral acids. The degree of polymerization is typically less than 400.


- - - - -

A Work in Progress...


DANGERS OF MICROCRYSTALLINE CELLULOSE, FILLER IN PHARMACEUTICALS

DANGERS OF MICROCRYSTALLINE CELLULOSE, FILLER IN PHARMACEUTICALS

http://www.integrativeholistichealth.org/information/dangers-of-microcrystalline-cellulose-filler-in-pharmaceuticals/

Posted on January 10, 2014 by Emi Miller

DANGERS OF MICROCRYSTALLINE CELLULOSE

I have some NEW concerns for us to think about as far as using MICROCRYSTALLINE CELLULOSE as a filler in Nature Throid, Westhroid and ArmourThyroid tablets.

I am a Registered Nurse, with an extensive background in physiology. It occurred to me that just as the cells cannot keep out artificial sweeteners, but absorb them as if they were ordinary glucose, and that this wreaks havoc in our cells ability to function, leading to many forms of physical discomfort and illness, that the same thing would apply if we use MICROCRYSTALLINE CELLULOSE as a filler in our Thyroid products. I remembered reading on this forum about why Armour stopped working well for many people, even when they adjusted their dosage correctly. The reason stated was that they had started using artificial fillers.

Doing some research I came upon this article, and want to share it here. It says exactly that: Our cells cannot stop the micro-nano particles from entering them, and once there they are not able to be useful, but float in and out of the cell membranes, and basically clog up tiny places in our bodies, bioaccumulating as we take more, and causing background inflammation to rise.

A couple of excerpts from the article follow:

Nanotechnology: benefits vs toxic risks,

Feb. 1, 2007 George Burdock |Functional Ingredients

“”Once in the body, some particles have changed the shape or conformation of proteins, creating a protein similar to that produced in Alzheimer’s disease. Changing protein conformation can potentially create new allergenic proteins in organs to which the body could mount an immune response.

While easy entry into the cells of the intestine and target organs can be beneficial, the other side of the coin is that because these particles are so ‘slippery,’ how can they ever be excreted by the body? Because much of our excretory system at the cellular level is based on a cell successfully excreting a substance (as in the kidney) to be flushed away, how can the particle be made to remain in the waste stream if it can so easily gain re-entry into other cells downstream?

While some of the more dramatic examples of actual physical damage are described above, the damage most often seen in response to nano-materials is the generation of reactive oxygen species, resulting in oxidative stress to the biological system.

In oxidative stress, the universal antioxidant chemical in the body, glutathione or GSH, is converted to the oxidized inactive form, GSSH. As reserves of GSH are depleted and the GSH:GSSH ratio lowers, the body mounts a progressively more assertive reaction. The first stage of oxidative stress is to produce special enzymes to detoxify the new invading chemical; if, however, there is no enzyme for this purpose or the human does not have the capability to produce the enzyme, the body progresses into the next stage, inflammation.””

http://newhope360.com/nanotechnology-benefits-vs-toxic-risks

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Microcrystalline cellulose
www.fao.org/docrep/w6355e/w6355e0l.htm
Microcrystalline cellulose is a purified, partially depolymerized cellulose prepared by treating alpha-cellulose, obtained as a pulp from fibrous plant material, with mineral acids. The degree of polymerization is typically less than 400.