Vaccine Ingredients: Non-Ionic Surfactants (Tween 80, Triton X-100, Nonoxynol-9)

Vaccine inredients are known to affect the brain.

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VacTruth Comment:
Tween 80, Triton X-100, and Nonoxynol-9 are used in vaccines. Nonoxynol-9 (N-9) also is used as a spermicide in vaginal gels to prevent contraception and was used in a H1N1 Vaccine Trial.

Triton X-100 and Tween 80 were mixed with DDT to spray on crops in the 1940s and 1950s – combinations of these chemicals are still in pesticides today. Polysorbate 80, also known as Tween 80, is a surfactant in these vaccines: DTaP, DTaP-HebB-IIPV, DTaP-Hib, Gardasil, Influenza, Rotavirus, and Tdap.

Most of the following information regarding these non-ionic surfactants is taken from the National Institutes of Health web sites.

 

Specific role of polysorbate 80 coating on the targeting of nanoparticles to the brain

http://www.ncbi.nlm.nih.gov/pubmed/14967540

Being bound to nanoparticles that were overcoated by T-80 [Tween-80] later, was necessary for the loading to be delivered to brain. Partial coverage was enough for T-80 coating to play a specific role in brain targeting. It seemed that brain targeting of nanoparticles was related to the interaction between the T-80 coating and BMECs [brain micro-vessel endothelial cells]. The mechanism of endocytosis was more reasonable for nanoparticle-mediated drugs across BBB [Blood Brain Barrier]. The specific role of T-80 coating on nanoparticles in brain targeting was thus confirmed.” [Emphasis added]

 

Colloidal carriers and blood–brain barrier (BBB) translocation: A way to deliver drugs to the brain?

http://www.ncbi.nlm.nih.gov/pubmed/15896933

3.1.1. Disruption of the BBB

One of the earliest techniques to circumvent the BBB for therapeutical purpose and the first to be used in humans was developed by Neuwelt et al. (1979). The idea behind this approach was to break down the barrier temporarily by injecting a sugar solution (mannitol) into arteries in the neck. The resulting high sugar concentration in brain capillaries sucks water out of the endothelial cells, shrinking them thus opening tight junctions. In current practice, the effect lasts for 20–30 min, during which time drugs that would not normally cross the BBB diffuse freely.”

However, disrupting the BBB even for brief periods leaves the brain vulnerable to infection and damage from toxins. Even substances that circulate harmlessly through the peripheral bloodstream, such as albumin, can have deleterious effects if they enter the brain.”  [Emphasis added]

VacTruth Comment:

Neurotoxins in vaccines can enter the brain easily, which this confirms.

The “Trojan horse” mechanism postulates that infected macrophages crossactivate brain endothelial cells to take up residence in the CNS as infected microglial cells. BMEC and immune cells, activated by cytokines, overexpress adhesion molecules and their ligands, which promotes the binding of circulating immune cells to brain vasculature.Such binding could be the first step in diapedesis, the passage of immune cells across the BBB. This proximity could also facilitate the passage of viral particles between the infected immune cell and the brain endothelial cell, analogous to the transfer of virus betweeninfected immune cells.” [Emphasis added]

“After peripheral administration, these molecules themselves do not exhibit any therapeutic effect because they do not diffuse through the BBB. But, when dalargin or loperamide were absorbed onto the surface of poly(butylcyanoacrylate) (PBCA) nanoparticles further coated with the detergent, polysorbate-80 (PS-80), a pronounced analgesic effect was obtained, reaching a maximum 45 min after administration. The mechanism behind the translocation of those nanoparticles into the brain remains, however, not fully understood.”

 

 

Disclosure by triton X-100 of NMDA-sensitive [3H] glutamate binding sites in brain synaptic membranes.

http://www.ncbi.nlm.nih.gov/pubmed/2838020

Pretreatment of brain synaptic membrane homogenates with Triton X-100 resulted in a drastic disclosure of [3H]glutamate (Glu) binding activity which was sensitive to one of the central GIu receptor agonists, N-methyl-D-aspartic acid (NMDA)… These results suggest that Triton-treatment may disclose NMDA-Sensitive [3H]GIu binding sites in brain synaptic membranes.”

VacTruth Comment:

Polysorbate 80 and Tween 80 are regarded as the same chemical. For vaccines, see information under Polysorbate 80.

 

 

Interference of the Detergent Tween 80 in Protein Assays

http://www.ncbi.nlm.nih.gov/pubmed/1481978

Detergents are often used to dissociate cell membrane components in biological systems. The nonionic detergent, polyoxyethylene sorbitan monooleate (Tween 80) has been widely used at concentrations of 0.051.0% to increase secretion of enzymes or other exoproteins in both bacteria and fungi.”

Tween 80 is one of the polyoxyethylene family of nonionic detergents which includes, among others, the Tritons (X-100 and X-114) and the Genapols (X-080, X-100, and X-150). These detergents are gentle in their action, and most enzymes retain their activity after exposure to levels of l-3% w/v (26). Because of their mild action and their compatibility with most chromatographic systems, these detergents have found widespread application as extractive agents for proteins which are structurally associated with organelles such as mitochondria, chloroplasts, plasmalemma, endoplasmic reticulum, and nuclear membrane.[Emphasis added]

 

 

Tween 80 Immunosuppression

Food and Chemical Toxicology, Vol 20. No. 6 pp. 983.

Tween 80 (polyoxyethylene sorbitan monooleate), an emulsifier, is yet another example or a commonly used chemical being implicated in the suppression of the immunological response. Barnett reports that recent work in his laboratory has suggested that the primary IgE and IgG, MS suppressed in mice pretreated with Tween 80 followed by an immunizing dose of ovalbumin adsorbed to aluminium hydroxide (an antigenadjuvant combination known to produce high levels of IgE and IgG,)… The authors conclude from these findings that the immunosuppression caused by Tween 80 is restricted to the primary humoral response.” [Emphasis added]

VacTruth Comment:

The adjuvant aluminium hydroxide is in the following vaccines: Anthrax, DTaP, DTaP-HepB-IPV, Td, Hepatitis A, Hepatitis A-Hepatitis B, Hepatitis B, Tdap.

 

 

Tween 80 and Epileptic Seizures

Some solvents for antiepileptics have proepileptic potencies in the WAG/Rij rat model for absence epilepsy

http://www.ncbi.nlm.nih.gov/pubmed/1393624

To suppress these symptoms [of epilepsy], anticonvulsants or antiepileptics have been developed…that can be used in experimental studies as a solvent, emulsifier, or dispersing agent for these difficult to dissolve drugs. Tween-80 is used to dissolve benzodiazepines and P-carbolines. Carbamazepine and trimethadione are dissolved in a mixture of saline, ethanol, and propylene glycol.

These solvents, however, are also known to disrupt the bloodbrain barrier, change receptor affinity, and manipulate membrane structure…It is not clear why the used solvents are proepileptic but their usage in experimental absence epilepsy research should be avoided.” [Emphasis added]

 

 

Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats

http://www.ncbi.nlm.nih.gov/pubmed/8473002

Tween 80 is a classical non-ionic surface-active detergent. It is widely used as an additive in pharmaceuticals and in the food industry. Some of the Tweens are considered to be carcinogens or cocarcinogens. Several of the stimulating properties of tweens are already known.” [Emphasis added]

and …

In our study, we found that 4-day administration of Tween 80 to female rats during the period crucial for the development and function of reproductive organs accelerates the maturation of these organs. We found significant prolongation of the oestrous cycle and induction of persistent vaginal oestrus. The persistence of vaginal oestrus after the perinatal exposure of female rats to oestrogens used to be ascribed to oestrogens.” [Emphasis added]

VacTruth Question:

Could Tween 80, being a carcinogen or co-carcinogen, also be one of the reasons vaccines are not tested for causing cancer? Please research the vaccine inserts (http://vactruth.com/vaccine-inserts) to confirm.

 

 

Treatment of Cells with Detergent Activates Caspases and Induces Apoptotic Cell Death

http://www.ncbi.nlm.nih.gov/pubmed/10833528

The biochemical properties of detergents and biomembranes suggest that the initial event of apoptosis induction may occur at the cell membrane. Although the Triton concentration required for apoptosis induction did not immediately disrupt the cell membrane, detergent molecules may be incorporated into the lipid bilayer. This may result in subtle alterations of the physical properties of the membrane including an increased permeability for small charged and neutral solutes… In conclusion, treatment of human and nonhuman cells with detergent at concentrations below the level that causes cytolysis induced apoptotic death.”

 

 

Cancer and Tween-80 Injections

Effects of repeated subcutaneous injection of Tween-80 in rats 
http://www.ncbi.nlm.nih.gov/pubmed/5914564

In the rats injected with Tween-80, 1 subcutaneous sarcoma was found at the site of injection, and 2 similar sarcomas were also found in the rats injected with Tween-80 and small amounts of 3′-me-DAB. In mice 2 subcutaneous sarcomas were induced by injections of Tween-80 alone. These results raise the possibility that Tween-80 may be directly involved in carcinogenesis.” [Emphasis added]

 

 

Triton X-100 and Tween 80 Damage the Gut (Ciba-Geigy Corporation)

Evaluation of mucosal damage of surfactants in rat jejunum and colon

http://www.ncbi.nlm.nih.gov/pubmed/7766919

In particular, surfactants, which are commonly used adjuvants in oral pharmaceutical preparations to improve wetting and solubilization for insoluble drugs, have come under investigation as absorption enhancers. The goal of an enhancer is to improve membrane permeability without unwanted side effects. However, this is a formidable task because absorption is often increased due to intestinal damage.”

Tween 80 is an orally approved surfactant routinely used in drug formulations and food products (FDA Inactive Ingredient Guide, 1991). In contrast, Triton X-100 is not approved for oral use and is regarded as toxic.”

Denudation of villous tips, desquamation of the epithelial surface, and intervillous adhesion by LM and SEM were noted with Triton X-100 exposure, while minimal changes were noted with Tween 80 and controls. These results are consistent with the known systemic toxicity of Tween 80 and Triton X-100 and suggest that this method is valuable for the early assessment of intestinal damage and irritation.”

VacTruth Comment:

Triton X-100 is a nonionic surfactant used in influenza vaccines.

 

 

Encyclopedia of Pharmaceutical Technology Vol. 11
Authors James Swarbrick & James C. Boylan
1995 New York: Marcel Dekker, Inc.

“The addition of surfactants to ophthalmic solutions is permitted, even though their use is greatly restricted. The toxicity of surfactants is on the order anionic > cationic > nonionic. Nonionics are used in low concentrations to increase the dispersion of suspended drugs, such as steroids, and thereby improve solution clarity. The ability of these compounds to bind and thereby inactivate certain preservatives, coupled with their irritation potential, limits their use to low concentrations. For example, the FDA limits the concentrations of Tween 20 and Tween 80 to 1%.”
 (page 61)


“In the early 1980s, reports appeared in the literature about deaths in neonates associated with the administration of IV E-Ferol, a product that contained Vitamin E (dl-a-tocopherol) and the emulsifiers polysorbate 80 (9%) and polysorbate 20 (1%).
 Some infants who received this vitamin E product developed coagulopathy, renal failure, hepatic failure, and death. On autopsy, the infants who died from hepatic failure demonstrated cholestasis similar to that associated with parenteral nutrition. Toxic reactions may have occurred because of the high doses of vitamin E, the presence of polysorbate(s), a contaminant in the pharmaceutical preparation, or a combination of all three.” (page 345) [Emphasis added]

VacTruth Comment: 

Medical personnel often ignore the potential side effects of the chemicals in vaccines because of the ‘trace’ amounts in vaccines, or because an ingredient is labeled inactive. The same text referenced above notes,

“Pharmaceutical products may contain, in addition to the active or therapeutic agent(s), a variety of other ingredients, termed inactive or inert, which are categorized as excipients or additives (flavorings, sweeteners, preservatives, stabilizers, diluents, lubricants, etc.). The words inert or inactive may be misnomers for some excipients because some have been shown to cause adverse effects. Neonates and young children are at risk for such effects because they may not be able to metabolize or eliminate an ingredient in a pharmaceutical product in the same manner as an adult.” (pp. 344) [Emphasis added]

 

 

Nonoxynol-9 Induces Apoptosis of Endometrial Explants by Both Caspase-Dependent and -Independent Apoptotic Pathways

http://www.biolreprod.org/content/73/2/382.full.pdf

This study demonstrates for the first time that N-9 induces apoptosis in human endometrial explants. As a membrane- active surfactant spermicide, N-9 induces membrane permeability and membrane fusion. It is well known that cell membrane integrity is essential to maintain intracellular homeostasis, viability, and function. It was recently reported that detergents such as Triton X-100, Nonidet P-40 (NP-40), n-octylglucoside, and the bile salt sodium deoxycholate similarly induce apoptosis, indicating that apoptosis induction in the setting of this study may be not a feature peculiar to N-9 but a more general effect of the interaction of detergents with tissue  such damage could facilitate infection with bacterial or viral pathogens such as HIV.” [Emphasis added]

VacTruth Comment:

Apoptosis means cell death or cell ‘suicide’.

 

and

The N-9-triggered apoptosis of endometrial explants appears to be mediated through involvement of FAS/FASLG mechanism, followed by CASP3 activation leading to final cell death…These findings may have important practical implications to future microbicide development by demonstrating that vaginally administered agents may cause upper reproductive tract toxicity and possibly facilitate HIV infection.” [Emphasis added]

 

 

Solubilization of membranes by detergents

http://www.ncbi.nlm.nih.gov/pubmed/1091302

Lysis by surfactants has been studied mainly using erythrocytes [Red Blood Cells], since the process can be measured quantitatively by following the release of haemoglobin… The lytic process can, however, be divided into five stages: (1) The surfactant monomers absorb to, and (2) penetrate into the membrane, where (3) they induce a change in molecular organization. This leads to an alteration in permeability (4) and in the osmotic equilibrium, and finally (5) to the leakage of haemoglobin. Stages 2, 3 or 4 are rate limiting. It is generally believed that lysis results from an interaction between surfactant and the lipids of the membrane. Haydon and Taylor have suggested that surfactants may act as ‘wedges’ which destroy the natural orientation of the lipid bilayer.”

VacTruth Comment:

Lysis means dissolution or breakdown of cells.

 

 

Vascular endothelial dysfunction contributes to myocardial depression inischemia-reperfusion in the rat

http://www.ncbi.nlm.nih.gov/pubmed/9564547

This study was designed to evaluate whether the direct contractile modulatory effects of endocardial and (or) vascular endothelium were altered and whether these alterations contributed to contractile dysfunction in a model of ischemia-reperfusion. Sixty-two perfused rat hearts as Langendorff preparations were randomized to no intervention, intracoronary Triton X100 injection (to render vascular endothelium dysfunctional), ischemia (30 min)-reperfusion (20 min), and ischemia-reperfusion followed by intracoronary Triton X100 injection. Coronary endothelial-dependent vascular reactivity and vascular smooth muscle reactivity were assessed by serotonin and sodium nitroprusside, respectively. Myocardial damage was assessed by coronary effluent creatine phosphokinase and by morphologic studies. Papillary muscles were then excised and contractile characteristics evaluated at varying extracellular calcium concentration prior to and after endocardial endothelial removal with Triton X100…We conclude that vascular but not endocardial endothelial dysfunction contributes to the myocardial dysfunction that occurs during ischemia-reperfusion injury.” [Emphasis added]

VacTruth Comment:

Ischemia is tissue damage due to lack of adequate blood flow (which brings oxygen and nutrients to the tissue).

 

PATHOGENESIS OF HIPPOCAMPAL NEURONAL DEATH AFTER HYPOXIA–ISCHEMIA CHANGES DURING BRAIN DEVELOPMENT

http://www.ncbi.nlm.nih.gov/pubmed/15219674

Apoptotic neuronal death takes place during brain development under genetic control. Nuclear chromatin condensation or clumping characterized by electron microscopy (EM) is a hallmark of apoptosis and is remarkably conserved among cell types (Kerr et al., 1972; Wyllie, 1997). It is well documented that pathological conditions including brain hypoxia–ischemia (HI) are able to initiate apoptotic machinery to facilitate cell death through activation of caspase-3 (Blomgren et al., 2003; Olney, 2003). In comparison with apoptosis, necrotic cell death occurs always under pathological conditions.Two types of neuronal injury-induced necrotic morphologies characterized by EM have been described in the literature: one is the conventional cellular lysis with cell swelling followed by rupture to release cell contents; the second type of necrosis is characterized by dilation of subcellular organelles followed by shrinkage of the entire cell. Neuronal cell lysis takes place in the infarct core area after focal brain ischemia (Dodson et al., 1974), while the shrinkage type of necrosis occurs in a delayed manner in vulnerable brain regions after transient brain ischemia, in the penumbral regions after focal ischemia, as well as in regions of excitotoxic neuronal death (Siesjo¨, 1985; Deshpande et al., 1992; Fukuda et al., 1999; Colbourne et al., 1999; Hu et al., 2000b; Olney, 2003). In some cases, mixed features of apoptosis and necrosis can be seen in the same neurons after brain injury (Martin et al., 1998;Ishimaru et al., 1999). The neurons dying during development also adopt one of at least three different morphological types: “apoptotic,” “autophagic,” and “non-lysosomal vesiculate,” which probably reflect the various mechanisms underlying both nuclear and cytoplasmic destruction during cell death in developing neurons (Clarke, 1990). [Emphasis added]

….

It is, therefore, likely that immature neurons are liable to apoptosis after injury (Ikonomidou et al., 1989; Johnston, 1995), and thus both necrosis and apoptosis remain effective therapeutic targets for developing neurons after brain injury (Han et al., 2000; Cheng et al., 1998; Nakajima et al., 2000; Northington et al., 2001; Blomgren et al., 2001). However, both apoptotic morphology and biochemical machinery fade out during brain development. Therefore, traditional approaches targeting to necrotic cell death mechanisms such as energy failure, acidosis, calcium influx, oxidative stress and protein aggregation in adult brain remain valid.”

 

 

Ischemic preconditioning prevents protein aggregation after transient cerebral ischemia.

http://www.ncbi.nlm.nih.gov/pubmed/15939539

A short period of ischemia (ischemic preconditioning) that does not lead to neuronal death (sublethal), is able to induce neuronal tolerance to a subsequent longer or lethal period of ischemia. This phenomenon is known as “ischemic tolerance.” Although definitive mechanisms underlying ischemic tolerance remain incompletely understood, induction of molecular chaperones and folding enzymes has long been proposed to contribute to the acquisition of ischemic tolerance.” [Emphasis added]

  • Catherine J Frompovich

    What documentation! And ALL is taken from sources that cannot be disputed.  This information needs to be printed by every parent, saved, and presented by parents to every MD, school district/nurse, state representative, and member of Congress to understand: 1) Why there is so much neurological damage to kids today; 2) Why there is so much chronic disease in children today; 3) Why parents don’t want to vaccinate their kids–ALL the POISONS that are injected into their sweet babies and toddlers, which cause life-long health problems, including possible cancers.
    It’s about time that HHS, CDC, FDA and CONGRESS realize there’s a problem with not only the cost of healthcare that will sink the USA, but they have to get out of Big Pharma’s deep pockets and start protecting the public, not vested interests that apparently have no compunction about ruining health with neurotoxins and poisons under the guise of supposed
    prophylactic ‘health’ practices. 
    Suggestion to Everyone: Please print out this information and send it everywhere: the media,
    news reporters, your clergy, community health centers, and get people to know what really is in vaccines.  It’s not pretty healthy stuff, as you can readily see.
    Remember: You CANNOT poison a body into wellness.  Just read the above information.

  • Blackkobra2

    That’s why my baby wasn’t vaccinated. My gp want’s 2 convince me but no way he will. I saw movies on u tube about vaccinated kids and really bad side effects and i was crying. http://youtu.be/L1f8XTTsrpU So no vaccine for my baby she is not a laboratory rat. And the companies who make vaccines don’t care if they ppl would die more important is to get the money. Monsters!

  • Blackkobra2

    That’s why my baby wasn’t vaccinated. My gp want’s 2 convince me but no way he will. I saw movies on u tube about vaccinated kids and really bad side effects and i was crying. http://youtu.be/L1f8XTTsrpU So no vaccine for my baby she is not a laboratory rat. And the companies who make vaccines don’t care if they ppl would die more important is to get the money. Monsters!

  • Carmen

    Hi everyone, this info is so important for all children and parents. My beloved son Damien is 29 and is now suffering from so-called schizophrenia. My poor son developed this disorder about 4 years ago. He was born perfect, meaning he was every mother’s dream. He was always healthy, did exceptional in school, musician, became an electrician and did cable with his dad as well. He was married and had a son, my beloved grandson. He was extra loving and also very handsome. Now his life is ruined by this so-called disorder. My heart is so broken now I can’t bare the pain. This is the first time I have ever written about this in a forum. Damien now also from time to time suffers myaclonic jerks of the neck and shoulders. I love him so much and have done so much research on this subject matter that now I am convinced that Damien is vaccine injured. What I have seen in his symtems are like a latent form of so-called Autism. I need your imput. I am calling for help.

  • Carmen

    Hi everyone, this info is so important for all children and parents. My beloved son Damien is 29 and is now suffering from so-called schizophrenia. My poor son developed this disorder about 4 years ago. He was born perfect, meaning he was every mother’s dream. He was always healthy, did exceptional in school, musician, became an electrician and did cable with his dad as well. He was married and had a son, my beloved grandson. He was extra loving and also very handsome. Now his life is ruined by this so-called disorder. My heart is so broken now I can’t bare the pain. This is the first time I have ever written about this in a forum. Damien now also from time to time suffers myaclonic jerks of the neck and shoulders. I love him so much and have done so much research on this subject matter that now I am convinced that Damien is vaccine injured. What I have seen in his symtems are like a latent form of so-called Autism. I need your imput. I am calling for help.

  • can

    Would be helpful if there was a way to easily share this on facebook & other media.
    Is it possible to put such lnks in to the pages to help spread the information world-wide?

  • http://vactruth.com Jeffry John Aufderheide

    Hi Can,

    You can use the Facebook “Like” this post right above the comments section here. You’ll see where it says “Share This:” and there are other options available. Thank you for spreading this information.

  • http://vactruth.com Jeffry John Aufderheide

    Hi Carmen,

    Thank you for sharing your story. Seriously consider looking into Autism. The common theme, or thread, is a damaged gut. One resource that has helped many parents is a book called Breaking the Vicious Cycle, by Elaine Gottschall.

    Website-1: http://www.breakingtheviciouscycle.info
    Website-2: http://www.pecanbread.com/
    Book: http://www.amazon.com/Breaking-Vicious-Cycle-Intestinal-Through/dp/0969276818

    Dr. Mario Capecchi has also won a Nobel Prize for showing a direct correlation between psychological disorders and impairment of the gut.
    http://capecchi.genetics.utah.edu/

    I hope this helps you on your journey. God Bless.

  • http://vactruth.com Jeffry John Aufderheide

    Thank you Catherine! You’re spot on with your last comment, as usual.

  • B. St. Marie

    This information is very disturbing. I’m not sure which is worse, the harmful effects these ingredients can have, or the fact that experts widely acknowledge the harm these ingredients can cause and STILL recommend usage!

    This comment in particular stood out to me: “The words inert or inactive may be misnomers for some excipients because some have been shown to cause adverse effects. Neonates and young children are at risk for such effects because they may not be able to metabolize or eliminate an ingredient in a pharmaceutical product in the same manner as an adult.”While I’m extremely grateful for this information, I’m also furious at the same time. If these effects are commonly known and accepted by the “experts,” why are parents often left in the dark about it all?

  • Cara

    Jeffry, I just wanted to say thank you for your efforts in research and bravery in sharing this information. You are Awesome .. and this autism mom thanks you from the bottom of her heart !

  • Cara

    Jeffry, I just wanted to say thank you for your efforts in research and bravery in sharing this information. You are Awesome .. and this autism mom thanks you from the bottom of her heart !

  • Cara

    Jeffry, I just wanted to say thank you for your efforts in research and bravery in sharing this information. You are Awesome .. and this autism mom thanks you from the bottom of her heart !

  • Carmen

    Thank you so very much Jeffery for these important links. I so appreciate that people like you really care.

  • Carmen

    Thank you so very much Jeffery for these important links. I so appreciate that people like you really care.

  • Christina England

    Well done Jeff a brilliant piece of research which I will spread to others. Thank you
    Christina

  • Christina England

    Well done Jeff a brilliant piece of research which I will spread to others. Thank you
    Christina

  • http://vactruth.com Jeffry John Aufderheide

    Cara, you are welcome! Thank you for reading and sharing this important information. It’s ‘Warrior Moms’ like you that make all of the difference.

  • http://vactruth.com Jeffry John Aufderheide

    Cara, you are welcome! Thank you for reading and sharing this important information. It’s ‘Warrior Moms’ like you that make all of the difference.

  • http://vactruth.com Jeffry John Aufderheide

    Thank you for reading, Christina :)

  • Discouraged

    After working my tail off for almost a year to get great information to some pregnant friends and family members, I could not be more discouraged. Had anyone given me the same information when I had my children many years ago, I would have been horrified. But these moms, as far as I know, trust their pediatricians and just don’t see the truth. Young mothers are not very discerning I’m afraid. They are too afraid NOT to vaccinate.

  • Iowa

    Could you provide the link to the Nobel Prize you are referring to? The only one I can find has nothing to do with what you say. The Nobel Prize in Physiology or Medicine 2007 was awarded jointly to Mario R. Capecchi, Sir Martin J. Evans and Oliver Smithies “for their discoveries of principles for introducing specific gene modifications in mice by the use of embryonic stem cells”.  

  • http://vactruth.com Jeffry John Aufderheide

    Hoxb8 Is Required for Normal Grooming Behavior in Mice
    http://www.ncbi.nlm.nih.gov/pubmed/11779477

    Hematopoietic Origin of Pathological Grooming in Hoxb8 Mutant Mice
    http://www.ncbi.nlm.nih.gov/pubmed/20510925

    Utah scientist makes breakthrough in mental illness research
    http://www.ksl.com/?nid=148&sid=10947928

  • Iowa

    You said, “Dr. Mario Capecchi has also won a Nobel Prize for showing a direct correlation between psychological disorders and impairment of the gut.” His Nobel prize doesn’t mention the gut, nor does any of the links you provided later. His work involves bone marrow transplant. Can you provide substantiation of what you say or am I wasting my time asking for it?

  • http://vactruth.com Jeffry John Aufderheide

    My sincerest apologies. I was incorrect on saying Capecchi’s work was on gut flora – my intention was to state bone marrow.

  • Chrisb

    Quite a read!  Fantastic. I believe that the VitK shot sets up the immune system to “better recieve” vaccinations.

  • Chrisb

    Quite a read!  Fantastic. I believe that the VitK shot sets up the immune system to “better recieve” vaccinations.

  • Brother Sun

    Jeffry: First sentence: “used to prevent contraception” should be “used to prevent conception”.

  • LAdsit

    Thank you for posting. this information is so important. Keep sharing……

  • creeves

    Most of the information presented here is “true” but is out of context. The specific experimental situation matters. Reminding people that apoptosis means cell death after a quote about how apoptosis was induced by a surfactant in some experiment is really meant to alarm those who don’t understand biochemistry. Vaccines and other formulations for injection often contain surfactants and they have been shown, after many studies, to be harmless excipients. The FDA would not approve them otherwise.

  • http://vactruth.com Jeffry John Aufderheide

    Fantastic. I’m glad you made this comment. Your assumption is that if the FDA approves the product it must be safe. You and I both know that is not true as previously approved products have been recalled in the past.

    Please provide the safety information regarding the excipients.