(Natural News) In today’s Situation Update podcast (below), I share passages from the Old Testament that are highly relevant today when it comes to protecting children against being sacrificed to Satan.
In Leviticus, God explains (through Moses) that not only is child sacrifice sinful and evil, but that communities have an obligation to stop parents who are sacrificing their children to Moloch (“Molek”).
Societies that fail to stop the practice of child sacrifice face the wrath of God. Here’s Leviticus 20:2-5 (emphasis added)
Say to the Israelites: ‘Any Israelite or any foreigner residing in Israel who sacrifices any of his children to Molek is to be put to death. The members of the community are to stone him. I myself will set my face against him and will cut him off from his people; for by sacrificing his children to Molek, he has defiled my sanctuary and profaned my holy name. If the members of the community close their eyes when that man sacrifices one of his children to Molek and if they fail to put him to death, I myself will set my face against him and his family and will cut them off from their people together with all who follow him in prostituting themselves to Molek.’
As you can see, God calls for harsh punishment for parents who sacrifice their own children. In Exodus, God also shows that he is willing to unleash plagues upon entire nations that fail to follow his teachings. His plagues become increasingly severe as his warnings are ignored. In Exodus, God commanded the Pharaoh to set free the Israelites, and the Pharaoh refused until the tenth plague finally changed his mind.
Notably, at least two of these plagues are biological weapons attacks (livestock disease and the plague of the boils). Other plagues unleashed by God against Egypt include locusts, flies, gnats, frogs and finally, the mass death of all first-born sons.
Spike protein vaccines are biological weapons aimed at human children
Covid vaccines contain instructions for the body to manufacture spike protein nanoparticles. Those toxic nanoparticles attack the body from the inside and even damage the DNA repair mechanism found in the nuclei of human cells. Accordingly, covid vaccines are a biological weapon being used to destroy human lives.
When they are injected into children with the permission of their parents, those parents are sacrificing their children and condemning them to death. God has already chimed in on his disdain for those parents who sacrifice their own children, and if the modern world does not stop this medical violence being committed against children, it’s quite clear that God will unleash his wrath against the nations of our world.
Nathalie Lussier, MD, Anne-Marie Bourgault, MD FRCPC, Christiane Gaudreau, MD FRCPC, and Pierre Turgeon, MD FRCPC
Department of Microbiology and Infectious Diseases, Centre Hospitalier de l’Université de Montréal, Pavillon St-Luc, Montréal, Québec
Correspondence and reprints: Dr Anne-Marie Bourgault, Centre Hospitalier de l’Université de Montréal, Pavillon Saint-Luc, 1058, rue Saint-Denis, Montréal, Québec H2X 3J4. Telephone 514-281-2100, fax 514-281-2443
Abstract
The attenuated bacille Calmette-Guérin (BCG) vaccine is administered to prevent tuberculosis. Complications of vaccination are uncommon. A case of cutaneous abscess due to BCG is presented in a 24-year-old woman. The abscess developed at the inoculation site four weeks after vaccination. Routine Gram stain and bacterial cultures of the pus were negative. The auramine stain was positive. Mycobacterial cultures were positive after 14 and 18 days, using the BACTEC 12B bottle and Löwenstein-Jensen media, respectively. The mycobacteria were identified as Mycobacterium bovis, vaccinal strain by high-performance liquid chromatography and DNA probe assays.
The Ontario Ministry of Health and Long Term Care
Hon. Dr. Eric Hoskins, Minister of Health
Dr. Bob Bell, Deputy Minister of Health
Ontario Medical Association
150 Bloor Street West, Suite 900
Toronto, Ontario, M5S 3C1
To the Attention of:
Dr. Shawn Whatley, OMA President
Dr. Nadia Alam, OMA President Elect
Dr. Timothy Nicholas, Chair, OMA Board of Directors
The Pediatric Alliance of Ontario
Dr. Hirotaka Yamashiro, President
Dr. Sharon Burey, Interim Vice President
To Whom It May Concern:
It is my assumption that the intention of this document is to provide Ontario parents with accurate and up-to-date information about the safety, effectiveness and necessity of the current recommended vaccination schedule. Unfortunately your document contains numerous inaccuracies and makes many statements and claims about vaccine safety and effectiveness that are not supported by the evidence. If this document represents the best and most up-to-date information available from the Ontario Ministry of Health, the Ontario Medical Association and the Pediatric Alliance of Ontario, it indicates that health consumers in Ontario are being given inaccurate, deceptive, and dishonest information with which to make their vaccination decisions.
Brunel PA1, Argaw T.
Author information
Ahmanson Pediatrics Department, Cedars Sinai Medical Center, Los Angeles, California, USA. pbrunell@niaid.nih.gov
Abstract
Five months after 2 siblings were immunized with varicella vaccine, 1 developed zoster. Two weeks later the second sibling got a mild case of chicken pox. Virus isolated from the latter was found to be vaccine type. Thus, the vaccine strain was transmitted from the vaccinee with zoster to his sibling. Vaccinees who later develop zoster must be considered contagious.
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My sons vaccinations at 22 months caused his autism
HighWire with Del Bigtree
Vaccines Cause Autism, And So Can You
New scientific research suggests that not only can vaccine ingredients cause autism, but pinning a screaming child down to a table and forcing a needle into their body may actually have more to do with autism and other neurological injuries than realized.
Watch the whole explanation at:
areyoucrooked.com
There are a few different ways your child might exhibit cranial nerve lesions. Although there are a few others, these are the most common faces to look out for. Use your phone to document your child’s face and see if you can notice when it changed
FOR ISRAEL Ministry – Jewish Johnathan Ben-David forgave his killer and you would not believe why!!!
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
French scientists sound the alarm about aluminum in vaccines — crickets from media and health authorities
PARIS, France — Roman K. Gherardi and his colleagues from the Université Paris Est Créteil (“UPEC”)in France issued a worldwide warning in late 2016 about the aluminum adjuvant used in childhood vaccines. Their paper, published in the highly-respected journal Toxicology, is deeply distrubing for any parent contemplating vaccinating their child according to the present schedule recommended by the American Centers for Disease Control (“CDC”). And, it’s highly likely that this is the first time you’ve ever heard about it.It’s safe to say that this study’s conclusions have revolutionized our understanding of aluminum adjuvant, the kind used in most children’s vaccines.The French study authors were very concerned about the widespread use of aluminum adjuvant: “Concerns about its [aluminum adjuvant’s] safety emerged following recognition of its unexpectedly long-lasting biopersistence within immune cells in some individuals, and reports of chronic fatigue syndrome, cognitive dysfunction, myalgia, dysautonomia and autoimmune/inflammatory features temporally linked to multiple Al-containing vaccine administrations.”
Journal of Toxicology – 28 November 2016
Study – Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity
Guillemette Crépeaux a , b , * , 2 , Housam Eidi a , c , Marie-Odile David c , Yasmine Baba-Amer a , Eleni Tzavara d , Bruno Giros d , François-Jérôme Authier a , Christopher Exley e , Christopher A. Shaw f , Josette Cadusseau a , g , 1 ,Romain K. Gherardi a,1
a Inserm U955 E10, Université Paris Est Créteil (UPEC), Créteil, France
b Ecole Nationale Vétérinaire d’Alfort,Maisons-Alfort,France
c Inserm U1204, Université Evry Val d’ Essonne (UEVE),Evry,France
d Inserm U1130, CNRS UMR 8246, UPMC UM CR18,Paris, France
e Birchall Centre, Keele University,Staffordshire,UK
f Department of Ophthalmology, University of British Columbia,Vancouver,BC,Canada
g Faculté des Sciences&TechnologiesUPEC,Créteil,France
Abstarct
Aluminium (Al) oxyhydroxide (Alhydrogel 1), the main adjuvant licensed for human and animal vaccines, consists of primary nanoparticles that spontaneously agglomerate. Concerns about its safety emerged following recognition of its unexpectedly long-lasting biopersistence within immune cells in some individuals, and reports of chronic fatigue syndrome, cognitive dysfunction, myalgia, dysautonomia and autoimmune/inflammatory features temporally linked to multiple Al-containing vaccine administrations. Mouse experiments have documented its capture and slow transportation by monocyte-lineage cells from the injected muscle to lymphoid organs and eventually the brain. The present study aimed at evaluating mouse brain function and Al concentration 180 days after injection of various doses of Alhydrogel 1 (200, 400 and 800 mg Al/kg of body weight) in the tibialis anterior muscle in adult female CD1 mice. Cognitive and motor performances were assessed by 8 validated tests, microglial activation by Iba-1 immunohistochemistry, and Al level by graphite furnace atomic absorption spectroscopy. An unusual neuro-toxicological pattern limited to a low dose of Alhydrogel 1 was observed. Neurobehavioural changes, including decreased activity levels and altered anxiety-like behaviour, were observed compared to controls in animals exposed to 200 mg Al/kg but not at 400 and 800 mg Al/kg. Consistently, microglial number appeared increased in the ventral forebrain of the 200 mg Al/kg group. Cerebral Al levels were selectively increased in animals exposed to the lowest dose, while muscle granulomas had almost completely disappeared at 6 months in these animals. We conclude that Alhydrogel 1 injected at low dose in mouse muscle may selectively induce long-term Al cerebral accumulation and neurotoxic effects. To explain this unexpected result, an avenue that could be explored in the future relates to the adjuvant size since the injected suspensions corresponding to the lowest dose, but not to the highest doses, exclusively contained small agglomerates in the bacteria-size range known to favour capture and, presumably, transportation by monocyte-lineage cells. In any event, the view that Alhydrogel 1 neurotoxicity obeys “ the dose makes the poison ” rule of classical chemical toxicity appears overly simplistic.
Study – Spontaneous Integration of Human DNA Fragments into Host GenomeK. Koyama, T. A. DeisherSound Choice Pharmaceutical Institute, Seattle, WA
Introduction A trio of recent publications in the journal NEURON reports the presence of hundreds of diverse de novo gene mutations indicating that autism spectrum disorder (ASD) may be a disease of genomic instability, with a significant environmental component. Altered double strand break formation and repair pathways (DSB) may be a commonality among the diverse genetic mutations that have been documented in ASD. US birth year change points in AD are apparent in 1980, 1988 and 1996, coinciding with the switch to or introduction of childhood vaccines contaminated with human endogenous retrovirus K (HERVK) and human fetal DNA fragments (6). We hypothesize that the HERVK and human fetal DNA contaminants could contribute to the genomic instability of ASD as demonstrated by de novo mutations. Cell free DNA can be taken up by healthy cells via receptor mediated uptake or may spontaneously penetrate cell membranes that have altered permeability, for instance, during inflammatory reactions. Nuclear uptake of cell free DNA fragments is thought to provide a source for maintenance of DNA integrity during rescue of collapsed replication forks or base lesion repair. Spontaneous extracellular DNA uptake has also been exploited for gene therapy as well as for cellular gene correction (2,4,5,7,8, and 9). While free DNA uptake has been used advantageously, the process has also been associated with generation of mutations and chromosomal aberrations (3). Vaccines manufactured using human fetal cells contain residual DNA fragments (50-500 bp) (Table I). It is possible that these contaminating fragments could be incorporated into a child’s genome and disrupt normal gene function, leading to autistic phenotypes. In this study we demonstrate foreign DNA uptake in human cells and genomic integration by incubating the cells with Cy3-labeled human Cot1 (placental) DNA fragments which represents contaminating residual human fetal DNA in vaccines
Conclusion
Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and be integrated into host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through vaccination. Vaccine must be safe without any human DNA contaminations or reactivated viruses, and must be produced in ethically approved manufacturing processes
Study – Abortive and subclinical poliomyelitis in a family during the 1992 epidemic in The Netherlands
AuthorsKroon FP1, Weiland HT, van Loon AM, van Furth R.
Author informationDepartment of Infectious Diseases, University Hospital Leiden, The Netherlands.
AbstractWe describe a case of abortive poliomyelitis due to poliovirus type 3 (PV3) in an unvaccinated woman and a subclinical poliovirus infection in her family during an epidemic in the Netherlands. The woman excreted the epidemic strain (PV3) for 7 weeks. Her two children received oral attenuated poliovirus vaccine and were subsequently found to excrete PV1 and PV2 vaccine strains in addition to the epidemic PV3 strain. Her husband, who had neutralizing antibodies to all three poliovirus types because of previous vaccination, initially excreted no virus; subsequently, however, the vaccine strain PV1 and the epidemic strain PV3 could be cultured from his feces. These observations demonstrate the ease with which poliovirus circulates among family members, including those with neutralizing antibodies.
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
Study published in the Annals of Clinical Psychiatry suggests that Autism is likely triggered by a virus, and that measles virus (MV and/or MMR vaccine) might be a very good candidate. It supports the hypothesis that a virus-dincued autoimmune response may play a causal role in autism.
US National Library of Medicine
National Institutes of Health – 2002
Singh VK, Lin SX, Newell E, Nelson C.
Author information
Department of Biology and Biotechnology Center, Utah State University, Logan, Utah 84322, USA. singhvk@cc.usu.edu
Abstract
Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal antibodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.
A study published in the American Journal of Clinical Nutrition determined that an increased vulnerability to oxidative stress and decreased capacity for methylation may contribute to the development and clinical manifestation of autism. It’s well known that viral infections cause increased oxidative stress. Research suggests that metals, including those found in many vaccines are directly involved in increasing oxidative stress.
S Jill James, Paul Cutler, Stepan Melnyk, Stefanie Jernigan, Laurette Janak, David W Gaylor, and James A Neubrander
Author Affiliations
From the Department of Pediatrics, University of Arkansas for Medical Sciences, and the Arkansas Children’s Hospital Research Institute, Little Rock, AR (SJJ, SM, and SJ); Niagara Falls, NY (PC); Colden, NY (LJ); Gaylor and Associates, LLC, Eureka Springs, AR (DWG); and Edison, NJ (JAN)
Abstract
Background: Autism is a complex neurodevelopmental disorder that usually presents in early childhood and that is thought to be influenced by genetic and environmental factors. Although abnormal metabolism of methionine and homocysteine has been associated with other neurologic diseases, these pathways have not been evaluated in persons with autism.
Objective: The purpose of this study was to evaluate plasma concentrations of metabolites in the methionine transmethylation and transsulfuration pathways in children diagnosed with autism.
Design: Plasma concentrations of methionine, S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), adenosine, homocysteine, cystathionine, cysteine, and oxidized and reduced glutathione were measured in 20 children with autism and in 33 control children. On the basis of the abnormal metabolic profile, a targeted nutritional intervention trial with folinic acid, betaine, and methylcobalamin was initiated in a subset of the autistic children.
Results: Relative to the control children, the children with autism had significantly lower baseline plasma concentrations of methionine, SAM, homocysteine, cystathionine, cysteine, and total glutathione and significantly higher concentrations of SAH, adenosine, and oxidized glutathione. This metabolic profile is consistent with impaired capacity for methylation (significantly lower ratio of SAM to SAH) and increased oxidative stress (significantly lower redox ratio of reduced glutathione to oxidized glutathione) in children with autism. The intervention trial was effective in normalizing the metabolic imbalance in the autistic children.
Conclusions: An increased vulnerability to oxidative stress and a decreased capacity for methylation may contribute to the development and clinical manifestation of autism.
A study published by the Department of Pharmaceutical Sciences at Northeastern University, Boston determined that a novel growth factor signalling pathway that regulates methionine synthase(MS) activity and thereby modulates methylation reactions. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins. You can read more about this here, and here. You can read more about the MS/autism link here
US National Library of Medicine
National Institutes of Health – Apr 2004
Waly M, Olteanu H, Banerjee R, Choi SW, Mason JB, Parker BS, Sukumar S, Shim S, Sharma A, Benzecry JM, Power-Charnitsky VA, Deth RC.
Author information
Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.
Abstract
Methylation events play a critical role in the ability of growth factors to promote normal development. Neurodevelopmental toxins, such as ethanol and heavy metals, interrupt growth factor signaling, raising the possibility that they might exert adverse effects on methylation. We found that insulin-like growth factor-1 (IGF-1)- and dopamine-stimulated methionine synthase (MS) activity and folate-dependent methylation of phospholipids in SH-SY5Y human neuroblastoma cells, via a PI3-kinase- and MAP-kinase-dependent mechanism. The stimulation of this pathway increased DNA methylation, while its inhibition increased methylation-sensitive gene expression. Ethanol potently interfered with IGF-1 activation of MS and blocked its effect on DNA methylation, whereas it did not inhibit the effects of dopamine. Metal ions potently affected IGF-1 and dopamine-stimulated MS activity, as well as folate-dependent phospholipid methylation: Cu(2+) promoted enzyme activity and methylation, while Cu(+), Pb(2+), Hg(2+) and Al(3+) were inhibitory. The ethylmercury-containing preservative thimerosal inhibited both IGF-1- and dopamine-stimulated methylation with an IC(50) of 1 nM and eliminated MS activity. Our findings outline a novel growth factor signaling pathway that regulates MS activity and thereby modulates methylation reactions, including DNA methylation. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins.
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1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
the news network 