Spiritual News – End Times Productions – An ARMY Of Demons Are Forming RIGHT NOW For The FINAL BATTLE Between GOOD and EVIL!

End Times Productions – An ARMY Of Demons Are Forming RIGHT NOW For The FINAL BATTLE Between GOOD and EVIL!
UPDATE- My original video got flagged for “inappropriate content” and was removed. So i went through and edited out all the scary stuff. People are scared of reality.
WARNING: This video contains Foul Language, i didn’t want to censor reality so i left it in the video.
Time is running out! Turn to JESUS CHRIST before its too late!
Flakka is the zombie drug. People who smoke bath salts or flakka get possessed by demons.
Music from http://www.bensound.com

Vaccine News – VAXXED TV – Two of my three children are injured by vaccines & Study – Correlations Between Gene Expression and Mercury Levels in Blood of Boys With and Without Autism

US National Library of Medicine
National Institutes of Health – Jan 2011

Study – Correlations Between Gene Expression and Mercury Levels in Blood of Boys With and Without Autism

Boryana Stamova,corresponding author – 1,9,10
Peter G. Green,2
Yingfang Tian,1,9,10
Irva Hertz-Picciotto,3,9,10
Isaac N. Pessah,4,9,10
Robin Hansen,5,9,10
Xiaowei Yang,3
Jennifer Teng,1
Jeffrey P. Gregg,6,9,10
Paul Ashwood,7,9,10
Judy Van de Water,8,9,10
and Frank R. Sharp1,9,10
1 – Department of Neurology, University of California at Davis Medical Center, Sacramento, CA 95817 USA
2 – Department of Civil and Environmental Engineering, University of California at Davis, Sacramento, CA USA
3 – Department of Public Health Sciences, University of California at Davis Medical Center, Sacramento, CA USA
4 – Department of VM: Molecular Biosciences, University of California at Davis Medical Center, Sacramento, CA USA
5 – Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CA USA
6 – Department of Pathology, University of California at Davis Medical Center, Sacramento, CA USA
7 – Department of Medical Microbiology and Immunology, University of California at Davis Medical Center, Sacramento, CA USA
8 – Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis Medical Center, Sacramento, CA USA
9 – The MIND Institute, University of California at Davis Medical Center, 2805 50th Street, Room 2434, Sacramento, CA USA
10 – UC Davis Center for Children’s Environmental Health and Disease Prevention, Sacramento, CA USA

Abstract
Gene expression in blood was correlated with mercury levels in blood of 2- to 5-year-old boys with autism (AU) compared to age-matched typically developing (TD) control boys. This was done to address the possibility that the two groups might metabolize toxicants, such as mercury, differently. RNA was isolated from blood and gene expression assessed on whole genome Affymetrix Human U133 expression microarrays. Mercury levels were measured using an inductively coupled plasma mass spectrometer. Analysis of covariance (ANCOVA) was performed and partial correlations between gene expression and mercury levels were calculated, after correcting for age and batch effects. To reduce false positives, only genes shared by the ANCOVA models were analyzed. Of the 26 genes that correlated with mercury levels in both AU and TD boys, 11 were significantly different between the groups (P(Diagnosis*Mercury) ≤ 0.05). The expression of a large number of genes (n = 316) correlated with mercury levels in TD but not in AU boys (P ≤ 0.05), the most represented biological functions being cell death and cell morphology. Expression of 189 genes correlated with mercury levels in AU but not in TD boys (P ≤ 0.05), the most represented biological functions being cell morphology, amino acid metabolism, and antigen presentation. These data and those in our companion study on correlation of gene expression and lead levels show that AU and TD children display different correlations between transcript levels and low levels of mercury and lead. These findings might suggest different genetic transcriptional programs associated with mercury in AU compared to TD children.

US National Library of Medicine
National Institutes of Health – Nov 1982

Study – Abnormal immune response to brain tissue antigen in the syndrome of autism

Abstract
Cell-mediated immune response to human myelin basic protein was studied by the macrophage migration inhibition factor test in 17 autistic patients and a control group of 11 patients suffering from other mental diseases included in the differential diagnosis of the syndrome of autism. Of the 17 autistic patients, 13 demonstrated inhibition of macrophage migration, whereas none of the nonautistic patients showed such a response. The results indicate the existence of a cell-mediated immune response to brain tissue in the syndrome of autism.

US National Library of Medicine
National Institutes of Health – Apr 2000

Study – Detection and sequencing of measles virus from peripheral mononuclear cells from patients with inflammatory bowel disease and autism.

Kawashima H, Mori T, Kashiwagi Y, Takekuma K, Hoshika A, Wakefield A.
Author information
Department of Paediatrics, Tokyo Medical University, Japan.

Abstract
It has been reported that measles virus may be present in the intestine of patients with Crohn’s disease. Additionally, a new syndrome has been reported in children with autism who exhibited developmental regression and gastrointestinal symptoms (autistic enterocolitis), in some cases soon after MMR vaccine. It is not known whether the virus, if confirmed to be present in these patients, derives from either wild strains or vaccine strains. In order to characterize the strains that may be present, we have carried out the detection of measles genomic RNA in peripheral mononuclear cells (PBMC) in eight patients with Crohn’s disease, three patients with ulcerative colitis, and nine children with autistic enterocolitis. As controls, we examined healthy children and patients with SSPE, SLE, HIV-1 (a total of eight cases). RNA was purified from PBMC by Ficoll-paque, followed by reverse transcription using AMV; cDNAs were subjected to nested PCR for detection of specific regions of the hemagglutinin (H) and fusion (F) gene regions. Positive samples were sequenced directly, in nucleotides 8393-8676 (H region) or 5325-5465 (from noncoding F to coding F region). One of eight patients with Crohn disease, one of three patients with ulcerative colitis, and three of nine children with autism, were positive. Controls were all negative. The sequences obtained from the patients with Crohn’s disease shared the characteristics with wild-strain virus. The sequences obtained from the patients with ulcerative colitis and children with autism were consistent with being vaccine strains. The results were concordant with the exposure history of the patients. Persistence of measles virus was confirmed in PBMC in some patients with chronic intestinal inflammation.

 

 

 

 

 

 

VAXXED TV – I gave up being a nurse because of vaccines

 

 

 

 

 

My mother was never the same after vaccinations

 

Two of my three children are injured by vaccines

My vaccinated child gave my 4 month old baby chickenpox

The Lindermans – possible strong language!

 

 

 

 

 

 

 

Hep B vaccine made me sick

 

 

 

 

Joni Abbott interview

 

 

My niece is not vaccinated because of me

I am not having anymore vaccines

Vaccinated versus unvaxxed

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ONE FOR ISRAEL Ministry – Jewish Johnathan Ben-David forgave his killer and you would not believe why!!!

 

 

 

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

Isaiah 53 – Old testament Prophecy about Jesus

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.

Vaccine News – Study – B-Lymphocytes from a Population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal

VAXXED TV – VaxXed Stories: Eric and Ronnie in Denver, Colorado
Includes music and footage from Ronnie’s video for Eric, “Eric’s life before and after the Vaccine”. See it here:

Vaccines killed my 4 year old son

My own VaxXed versus unvaccinated

8 children- unvaccinated and healthy

Vaccine injuries

Vaxxed. Partially Vaxxed and unvaccinated

Hep B injured me

Unlocking key to autism

MMR vaccines gave my sons autism

Court ordered MMR on my son

A study published in the Journal of Toxicology and Environmental Health, Part A: Current Issues by the Department of Economics and Finance at the University of New York shows how researchers suspect one or more environmental triggers are needed to develop autism, regardless of whether individuals have a genetic predisposition or not. They determined that one of those triggers might be the “battery of vaccinations that young children receive.” Researchers found a positive and statistically significant relationship between autism and vaccinations. They determined that the higher the proportion of children receiving recommended vaccinations, the higher the prevalence of autism. A 1 % increase in vaccination was associated with an additional 680 children having autism. The results suggest that vaccines may be linked to autism and encourages more in depth study before continually administering these vaccines.

Study – A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population.

US National Library of Medicine
National Institutes of Health – 2011

Delong G.
Author information
Department of Economics and Finance, Baruch College/City University of New York, New York, New York, USA. gayle.delong@baruch.cuny.edu

Abstract
The reason for the rapid rise of autism in the United States that began in the 1990s is a mystery. Although individuals probably have a genetic predisposition to develop autism, researchers suspect that one or more environmental triggers are also needed. One of those triggers might be the battery of vaccinations that young children receive. Using regression analysis and controlling for family income and ethnicity, the relationship between the proportion of children who received the recommended vaccines by age 2 years and the prevalence of autism (AUT) or speech or language impairment (SLI) in each U.S. state from 2001 and 2007 was determined. A positive and statistically significant relationship was found: The higher the proportion of children receiving recommended vaccinations, the higher was the prevalence of AUT or SLI. A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI. Neither parental behavior nor access to care affected the results, since vaccination proportions were not significantly related (statistically) to any other disability or to the number of pediatricians in a U.S. state. The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted.

A study published in the Journal of Toxicology by the Department of Neurosurgery at The Methodist Neurological Institute in Houston has shown that ASD is a disorder caused by a problem in brain development. They looked at B-cells and their sensitivity levels to thimerosal, a commonly used additive in many vaccines. They determined that ASD patients have a heightened sensitivity to thimerosal which would restrict cell proliferation that is typically found after vaccination. The research shows that individuals who have this hypersensitivity to thimerosal could make them highly susceptible to toxins like thimerosal, and that individuals with a mild mitochondrial defect may be affected by thimerosal. The fact that ASD patients’ B cells exhibit hypersensitivity to thimerosal tells us something.

Study – B-Lymphocytes from a Population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal

Journal of Toxicology
Volume 2013 (2013), Article ID 801517, 11 pages

Martyn A. Sharpe, Taylor L. Gist, and David S. Baskin
Department of Neurosurgery, The Methodist Neurological Institute, 6560 Fannin Street, Scurlock Tower No. 944, Houston, TX 77030, USA

Abstract
The role of thimerosal containing vaccines in the development of autism spectrum disorder (ASD) has been an area of intense debate, as has the presence of mercury dental amalgams and fish ingestion by pregnant mothers. We studied the effects of thimerosal on cell proliferation and mitochondrial function from B-lymphocytes taken from individuals with autism, their nonautistic twins, and their nontwin siblings. Eleven families were examined and compared to matched controls. B-cells were grown with increasing levels of thimerosal, and various assays (LDH, XTT, DCFH, etc.) were performed to examine the effects on cellular proliferation and mitochondrial function. A subpopulation of eight individuals (4 ASD, 2 twins, and 2 siblings) from four of the families showed thimerosal hypersensitivity, whereas none of the control individuals displayed this response. The thimerosal concentration required to inhibit cell proliferation in these individuals was only 40% of controls. Cells hypersensitive to thimerosal also had higher levels of oxidative stress markers, protein carbonyls, and oxidant generation. This suggests certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like the vaccine preservative thimerosal.

A study published in the Journal of Biomedical Sciences determined that the autoimmunity to the central nervous system may play a causal role in autism. Researchers discovered that because many autistic children harbour elevated levels of measles antibodies, they should conduct a serological study of measles-mumps-rubella (MMR) and myelin basic protein (MBP) autoantibodies. They used serum samples of 125 autistic children and 92 controlled children. Their analysis showed a significant increase in the level of MMR antibodies in autistic children. The study concludes that the autistic children had an inappropriate or abnormal antibody response to MMR. The study determined that autism could be a result from an atypical measles infection that produces neurological symptoms in some children. The source of this virus could be a variant of MV, or it could be the MMR vaccine.

Study – Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with 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.

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How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

 

Vaccine News – Vaccine industry in panic as scientific study solves the riddle of why flu shots don’t work

Vaccine industry in panic as scientific study solves the riddle of why flu shots don’t work
Wednesday, November 01, 2017
The flu shot is a quack science medical hoax. While some vaccines do confer immunization effectiveness, the flu shot isn’t one of them. Recent studies, for example, have proven that flu shots sharply weaken immunity in subsequent years following immunization. In some years, the flu shot viral strains are completely wrong, offering no immunity at all to influenza strains circulating in the world. Even when flu shots are the “right” strain, flu vaccine insert sheets readily admit the shots have not been subjected to double blind placebo controlled studies, and there is no legitimate scientific evidence whatsoever that supports the claim that each year’s flu vaccine confers meaningful immunity.

The Ohio State University – Wexner medical center
Study Charts Flu Shot’s Impact on Pregnant Women and Their Babies
In all, researchers followed 141 pregnant women, 91 of whom received a flu shot in the previous year, 50 who had not. “We actually found that those who didn’t get a flu shot had a better initial immune response to the vaccine,” said Christian. “On the other hand, for those who tend to get flu shots year after year, their peak antibody response becomes weakened over time.”

Study – A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States

US National Library of Medicine
National Institutes of Health – Dec 2013

David A Geier,1 Brian S Hooker,2 Janet K Kern,1,3 Paul G King,4 Lisa K Sykes,4 and Mark R Geiercorresponding author1
1 The Institute of Chronic Illnesses Inc, 14 Redgate Ct, Silver Spring, MD, USA
2 Simpson University, Redding, CA, USA
3 University of Texas Southwestern Medical Center at Dallas, Dallas, TX, USA
4 CoMeD Inc, Silver Spring, MD, USA
corresponding authorCorresponding author.
David A Geier: ten.tsacmoc@reiegnelladivad; Brian S Hooker: ude.unospmis@rekoohb; Janet K Kern: ten.riawfd@nrekj; Paul G King: moc.liamg@dhpgnikgluap; Lisa K Sykes: ten.nozrev@5enolkys; Mark R Geier: ten.tsacmoc@reiegm

Abstract

Background
Autism spectrum disorder (ASD) is defined by standardized criteria of qualitative impairments in social interaction, qualitative impairments in communication, and restricted and stereotyped patterns of behavior, interests, and activities. A significant number of children diagnosed with ASD suffer a loss of previously-acquired skills, which is suggestive of neurodegeneration or a type of progressive encephalopathy with an etiological pathogenic basis occurring after birth. To date, the etiology of ASD remains under debate, however, many studies suggest toxicity, especially from mercury (Hg), in individuals diagnosed with an ASD. The present study evaluated concerns about the toxic effects of organic-Hg exposure from Thimerosal (49.55% Hg by weight) in childhood vaccines by conducting a two-phased (hypothesis generating/hypothesis testing) study with documented exposure to varying levels of Thimerosal from vaccinations.

Methods
A hypothesis generating cohort study was undertaken to evaluate the relationship between exposure to organic-Hg from a Thimerosal-containing Diphtheria-Tetanus-acellular-Pertussis (DTaP) vaccine in comparison to a Thimerosal-free DTaP vaccine administered, from 1998 through 2000, for the risk of ASD as reported in the Vaccine Adverse Event Reporting System (VAERS) database (phase I). A hypothesis testing case–control study was undertaken to evaluate the relationship between organic-Hg exposure from Thimerosal-containing hepatitis B vaccines administered at specific intervals in the first six months of life among cases diagnosed with an ASD and controls born between 1991 through 1999 in the Vaccine Safety Datalink (VSD) database (phase II).

Results
In phase I, it was observed that there was a significantly increased risk ratio for the incidence of ASD reported following the Thimerosal-containing DTaP vaccine in comparison to the Thimerosal-free DTaP vaccine. In phase II, it was observed that cases diagnosed with an ASD were significantly more likely than controls to receive increased organic-Hg from Thimerosal-containing hepatitis B vaccine administered within the first, second, and sixth month of life.

Conclusions
Routine childhood vaccination is an important public health tool to reduce the morbidity and mortality associated with infectious diseases, but the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.

Study – Adverse event reports after tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccines in pregnant women.

Authors
Zheteyeva YA1, Moro PL, Tepper NK, Rasmussen SA, Barash FE, Revzina NV, Kissin D, Lewis PW, Yue X, Haber P, Tokars JI, Vellozzi C, Broder KR.
Author information
1 Immunization Safety Office, Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, Atlanta, GA, USA.

Abstract

OBJECTIVE: We sought to characterize reports to the Vaccine Adverse Event Reporting System (VAERS) of pregnant women who received tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccine (Tdap).

STUDY DESIGN: We searched VAERS for reports of pregnant women who received Tdap from Jan. 1, 2005, through June 30, 2010. We conducted a clinical review of reports and available medical records.

RESULTS: We identified 132 reports of Tdap administered to pregnant women; 55 (42%) described no adverse event (AE). No maternal or infant deaths were reported. The most frequent pregnancy-specific AE was spontaneous abortion in 22 (16.7%) reports. Injection site reactions were the most frequent non-pregnancy-specific AE found in 6 (4.5%) reports. One report with a major congenital anomaly (gastroschisis) was identified.

CONCLUSION: During a time when Tdap was not routinely recommended in pregnancy, review of reports to VAERS in pregnant women after Tdap did not identify any concerning patterns in maternal, infant, or fetal outcomes.

VAXXED TV – Doctors are all singing from the same hymn sheet
Mother shares her frustrations with the medical industry in trying to deal with her child’s vaccine injuries.
interview recorded on April 29th, 2017 in The United Kingdom Edited by TJ Jones

He was seizing over and over and over
Mother shares story of events of her son and his vaccine reactions.
interview recorded on April 29th, 2017 in The United Kingdom Edited by TJ Jones

All 3 of children are injured from vaccines

Vaccines gave my son autism

My grandson has autism from vaccines

Unvaccinated

My daughter has autism from vaccines

Flu vaccine killed my daughter

My daughter has diabetes from vaccines

Vaccines killed my baby boy

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How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

Vaccine News – I saw an immediate change – VAXXED TV

VAXXED TV – Andy Wakefield

I saw an immediate change
Mother recalls accounts of her son’s changes after vaccination.
Interview recorded on May 6th, 2017 in The United Kingdom

I could not shake the fatigue
Sharon recalls her own accounts of her vaccine responses as well as those of her children.
Interview recorded on May 6th, 2017 in The United Kingdom

Sheila Ealey brings down the house with the biblical story of Gideon! #TxMFA #TxMFA2017

Del Bigtree Speaks at #TxMFA2017 in Houston, Texas
Del Bigtree delivers an inspiring speech concerning the importance of the perception of one’s adversary. What do Tiger Woods, Mike Tyson, Paul Offit, Dorit Reiss, and Richard Pan all have in common?

Stephanie Seneff, PhD Computer Scientist at MIT speaks at #TxMFA #TxMFA2017
Dr. Stephanie Seneff, PhD Computer Scientist of Massachusetts Institute of Technology (MIT), conveys some of the issues surrounding the ubiquitous toxic herbicide, RoundUp (active ingredient, Glyphosate), and its shocking presence in vaccination samples.

Jim Meehan MD

Dr. Ted Fogarty #vaxxed #PrayBig

Joshua Coleman #vaxxed #PrayBig

Nation of Islam #vaxxed #PrayBig

Study – The toxicology of mercury: Current research and emerging trends.

US National Library of Medicine
National Institutes of Health – Nov 2017

Bjørklund G – 1, Dadar M – 2, Mutter J – 3, Aaseth J – 4.
Author information
1 Council for Nutritional and Environmental Medicine, Toften 24, 8610 Mo i Rana, Norway. Electronic address: bjorklund@conem.org.
2 Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
3 Paracelsus Clinica al Ronc, Castaneda, Switzerland.
4 Innlandet Hospital Trust and Inland Norway University of Applied Sciences, Elverum, Norway.

Abstract
Mercury (Hg) is a persistent bio-accumulative toxic metal with unique physicochemical properties of public health concern since their natural and anthropogenic diffusions still induce high risk to human and environmental health. The goal of this review was to analyze scientific literature evaluating the role of global concerns over Hg exposure due to human exposure to ingestion of contaminated seafood (methyl-Hg) as well as elemental Hg levels of dental amalgam fillings (metallic Hg), vaccines (ethyl-Hg) and contaminated water and air (Hg chloride). Mercury has been recognized as a neurotoxicant as well as immunotoxic and designated by the World Health Organization as one of the ten most dangerous chemicals to public health. It has been shown that the half-life of inorganic Hg in human brains is several years to several decades. Mercury occurs in the environment under different chemical forms as elemental Hg (metallic), inorganic and organic Hg. Despite the raising understanding of the Hg toxicokinetics, there is still fully justified to further explore the emerging theories about its bioavailability and adverse effects in humans. In this review, we describe current research and emerging trends in Hg toxicity with the purpose of providing up-to-date information for a better understanding of the kinetics of this metal, presenting comprehensive knowledge on published data analyzing its metabolism, interaction with other metals, distribution, internal doses and targets, and reservoir organs.

Study – Systematic Review and Meta-analysis: When One Study Is Just not Enough

Clinical Journal of the American Society of Nephrology

Amit X. Garg*, Dan Hackam † , Marcello Tonelli ‡
– Author Affiliations
*Division of Nephrology and Department of Epidemiology and Biostatistics, University of Western Ontario, London, and †Division of Clinical Pharmacology and Toxicology, University of Toronto, and Cardiac Rehabilitation and Secondary Prevention Program, Toronto Rehabilitation Institute, Toronto, Ontario, and ‡Division of Nephrology and Department of Public Health Sciences, University of Alberta, and Institute of Health Economics, Edmonton, Alberta, Canada

Conclusions
Like all types of research, systematic reviews and meta-analyses have both potential strengths and weaknesses. With the growth of renal clinical studies, an increasing number of these types of summary publications will certainly become available to nephrologists, researchers, administrators, and policy makers who seek to keep abreast of recent developments. To maximize their advantages, it is essential that future reviews be conducted and reported properly, with judicious interpretation by the discriminating reader.

Study – The association between mercury levels and autism spectrum disorders: A systematic review and meta-analysis

Journal of Trace Elements in Medicine and Biology
Volume 44, December 2017, Pages 289-297

Abstract

Background & aims
The relationship between mercury and autism spectrum disorders (ASD) has always been a topic of controversy among researchers. This study aimed to assess the relationship between ASD and mercury levels in hair, urine, blood, red blood cells (RBC), and brain through a meta-analysis.

Methods
A systematic search was performed in several databases including PubMed, ISI Web of Science, Cochrane register of controlled trials, Google Scholar, Scopus, and MagIran until June 2017. Case-control studies evaluating concentration of total mercury in different tissues of ASD patients and comparing them to the healthy subjects (control group) were identified. Necessary data were extracted and random effects model was used to calculate overall effect and its 95% corresponding confidence interval (CI) from the effect sizes.

Results
A total of 44 studies were identified that met the necessary criteria for meta-analysis. The mercury level in whole blood (Hedges = 0.43, 95% CI: 0.12, 0.74, P = 0.007), RBC (Hedges = 1.61, 95% CI: 0.83, 2.38, P < 0.001), and brain (0.61 ng/g, 95% CI, 0.02, 1.19, P = 0.043) was significantly higher in ASD patients than healthy subjects, whereas mercury level in hair (−0.14 mg/g, 95% CI: −0.28, −0.01, P = 0.039) was significantly lower in ASD patients than healthy subjects. The mercury level in urine was not significantly different between ASD patients and healthy subjects (0.51 mg/g creatinine, 95% CI: −0.14, 1.16, P = 0.121).

Conclusions
Results of the current meta-analysis revealed that mercury is an important causal factor in the etiology of ASD. It seems that the detoxification and excretory mechanisms are impaired in ASD patients which lead to accumulation of mercury in the body. Future additional studies on mercury levels in different tissues of ASD patients should be undertaken.

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How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

Vaccine News – Mother-of-two dies from flu despite being vaccinated

World Renowned Genetics Doctor Sees Relationship Between Fetal Cells Used in Vaccines and Increasing Autism Rates
Health Impact News
Dr. Theresa Deisher recently granted an interview with the VAXXED team to discuss, among other things, vaccines and autism.
Theresa Deisher, Ph.D., is the president of Sound Choice Pharmaceutical Institute (SCPI), a cutting edge biomedical research organization.
Dr. Deisher is a genetic engineer with over 20 years experience in the pharmaceutical industry, from basic human biology through clinical trials.
Dr. Deisher obtained her Ph.D. in Molecular and Cellular Physiology from Stanford University and has spent over 20 years in commercial biotechnology. Prior to founding AVM Biotechnology and Sound Choice Pharmaceutical Institute (SCPI), she worked with leading biotechnology companies, including Genentech, Repligen, ZymoGenetics, Immunex and Amgen.
Dr. Deisher is an inventor on 23 issued U.S. patents, and her discoveries have led to clinical trials of FGF18 for osteoarthritis and cartilage repair, and for Factor XIII for surgical bleeding. Dr. Deisher was the first person to discover adult cardiac derived stem cells, and has been a champion of adult stem cell research, both professionally and privately, for two decades. Dr. Deisher was a plaintiff in the U.S. federal lawsuit to prohibit use of federal tax payer dollars for embryo destructive research, which was instrumental in steering science towards adult stem cell research, which has led to 14 U.S. FDA approved adult stem cell products and the Washington Post Dec 2013 headline “Scientists Go Ethical in 2013.”
AVM Biotechnology is the marquee prolife biotech company worldwide, certifying that it does not use morally illicit material in any process. SCPI’s mission is to end human trafficking in biomedical research.
Discovering the Link Between Fetal Tissue in Vaccines and Autism
Dr. Deisher states in her VAXXED interview that she looked at the rise in autism rates in the U.K. and its link to the MMR vaccine, originally discovered and published by Dr. Andrew Wakefield, and how the medical establishment tried to discredit Dr. Wakefield’s research.
She notes that one reason given to try and discredit Dr. Wakefield’s research was that MMR vaccination rates remained steady both prior to and after the spike in autism rates in 1988.
However, what she discovered that was not reported was that the manufacturer of the MMR vaccine switched from animal cells to develop cultures to human fetal cells from aborted babies in 1988.

Infant Twins Die Simultaneously After Vaccines, Medical Board Rules ‘Just a Coincidence’
By Erin Elizabeth – February 1, 2017
Given that the sudden and simultaneous deaths of twins rarely occur, you would think- especially given the fact that they had been recently vaccinated– that it would receive quite a bit of attention. However, this story went largely unreported. (In order for twins to meet the criteria for simultaneous SIDS both babies must have died independently and within the same 24 hour time period.)
PubMed reports that identical twin girls, aged 3.5-months and delivered via c-section, were found dead (by their poor momma) in their crib, both laying face up. Not surprisingly, both babies were healthy will no serious medical history. Two days before their death, both of the girls had received their second dose of oral polio, DPT, and their first dose of hepatitis B vaccines. They had a fever the day after the vaccines and were given a teaspoon of acetaminophen.
All that and yet, “the death scene investigation, judicial investigation, parental assessment, macroscopic and microscopic autopsy findings and the toxicological analysis didn’t yield any specific cause of death.” Because the case was so rare it was referred to a board of multidisciplinary medical professionals at the Institute of Forensic Medicine, in the Ministry of Justice, in Istanbul. And yet, the Board still decided that the data they had was consistent with SIDS.

Babys werden mit gedrosseltem Immunsystem geboren
Datum: 02.05.2017
Das Immunsystem von Säuglingen arbeitet augenscheinlich im ersten Jahr nach der Geburt absichtlich auf Sparflamme. Das zeigt eine Studie der Medizinischen Hochschule Hannover sowie der Universitäten Bonn und Münster. Dadurch verhindert die Natur vermutlich, dass die Immunabwehr nach der Geburt zu stark auf Bakterien und Fremdstoffe außerhalb des Mutterleibs reagiert. Die Ergebnisse könnten auch neue therapeutische Ansätze ermöglichen, um Säuglinge vor einer so genannten Sepsis zu schützen. Dabei handelt es sich um eine lebensgefährliche Entzündungsreaktion, die besonders häufig Frühgeborene trifft. Die Arbeit ist in der renommierten Fachzeitschrift „Nature Immunology“ erschienen.
Dass die Immunzellen von Neugeborenen nur in sehr geringem Maße Entzündungen auslösen, ist schon lange bekannt. Bislang dachte man, das Immunsystem sei bei Säuglingen noch nicht ganz ausgereift und daher nicht besonders schlagkräftig. Die Ergebnisse der neuen Studie werfen an dieser Deutung Zweifel auf: „Wir vermuten, dass dieser verminderten Entzündungsantwort eine spezifische und sinnvolle Programmierung zugrunde liegt“, erklärt Dr. Thomas Ulas vom LIMES-Institut der Universität Bonn.
Sobald das Neugeborene den Mutterleib verlässt, kommt es schlagartig mit zahllosen unbekannten Bakterien und Fremdstoffen in Kontakt. „Das »Spar-Programm« verhindert vermutlich, dass die körpereigenen Abwehrtruppen in unzählige Scharmützel verwickelt werden“, sagt Dr. Sabine Pirr von der Medizinischen Hochschule Hannover. Folge könnte sonst nämlich eine lebensgefährliche starke Entzündungsreaktion sein, eine Sepsis. Zudem sind viele der unbekannten Mikroorganismen gar keine Krankheitserreger. So funktioniert der Darm nur dann so, wie er soll, wenn er mit bestimmten Bakterien besiedelt wurde. Auch aus diesem Grund muss sich das Immunsystem zurückhalten.

Mother-of-two dies from flu despite being vaccinated
3:51pm Sep 26, 2017
A touching tribute to a Canberra mother who died of influenza has been posted online after she became the latest victim of Australia’s horror flu season.
Mother-of-two Jennifer Thew spent a week suffering from bad influenza symptoms before she died at Calvary Hospital on Saturday.
It’s understood her daughter Estella, aged 7, has also been sick with the virus.
Thew, who moved to Australia from Germany, was a medical receptionist who had reportedly been vaccinated.
A Go Fund Me page has been set up for the Thew Family by her daughter’s dance school.

Vaccines Produce Homosexuality, Says Italian Scientist Gian Paolo Vanoli
An Italian scientist is arguing that vaccinations produce homosexuality.
Gian Paolo Vanoli, a 70-year-old scientist, journalist and opponent of vaccinations, says that vaccines make people gay.
Vanoli, who’s a proponent of alternative medicine, recently spoke with Vice Italy’s Matteo Lenardon about his ideals.
Via a Huffington Post translation of the Vice interview:

The vaccine is introduced into the child, the child then grows and tries to find its own personality, and if this is inhibited by mercury or other substances present in the vaccine which enter the brain, the child becomes gay. The problem will especially be present in the next generations, because when gays have children, the children will carry along with them the DNA of their parent’s illness. Because homosexuality is a disease, even though the WHO has decided that it is not. Who cares! The reality is that it is so. Each vaccination produces homosexuality, because it prevents the formation of one’s personality. It is a microform of autism, if you will. You will see how many gays there will be in the next generation, it will be a disaster.

Despite these views, Vanoli insists he supports same-sex marriage and gay adoption. He doesn’t “blame” gay people for their “illness,” just as he wouldn’t blame someone who “suffers from cancer or a heart attack,” he told GayStarNews.

“My Family Was Devastated By Vaccines” Tasha Dāvid, AVN President
Tasha has 6 vaccine injured kids and 2 healthy vaccine free kids. Her 6 vaccine injured kids include diagnoses of Autism, ADHD, severe mood swings and severe language disorder, as well as gastrointestinal issues, skin problems, chronic ear infections, chemical sensitivities, and many other health issues. However, her vaccine free kids are very healthy. Her 6 kids who were vaccinated always had more health issues after vaccination, but Tasha never understood that the vaccines were destroying her children because the doctors never told her. Tasha Dāvid is President of Australian Vaccination-skeptics Network Inc. and advocates that parents have complete choice over whether or not to vaccinate. She believes that a vaccine free lifestyle is a healthy lifestyle. Tasha Dāvid suggests that parents do their own research into vaccines and vaccination. Australian Vaccination-skeptics Network Inc. https://www.avn.org.au A http://www.stopmandatoryvaccination.com video production. Copyright © 2017 Larry Cook

Former Merck Rep Says Mandatory Vaccination Is For Profit and Not Public Health
http://www.StopMandatoryVaccination.com – Brandy Vaughan is a former sales rep for Merck & Co. – a vaccine maker – and she details how vaccine companies are using vaccines as a vehicle for massive profit and not public health. Brandy researched the safety of vaccines and found that not only do vaccines contain known toxins that can cause neurological damage, but that vaccine makers do not create the same safety studies for vaccines as they do for other drugs. This lack of true safety research of vaccines combined with the known adverse reactions to vaccination has helped Brandy to decide to never vaccinate her own child. Brandy says giving children a vaccine is like playing Russian roulette with our children and that mandatory vaccination is simply a way for vaccine makers to profit off of our children. Don’t be fooled: we do not need mandatory vaccination.
Stop Mandatory Vaccination
Produced by Larry Cook
Founder and Director of http://www.StopMandatoryVaccination.com
Contribute here: http://www.gofundme.com/ohwupg

 

Vaccine News – Study – Gender-selective toxicity of thimerosal

PubMed.gov – Mar.2009
Abstract
A recent report shows a correlation of the historical use of thimerosal in therapeutic immunizations with the subsequent development of autism; however, this association remains controversial. Autism occurs approximately four times more frequently in males compared to females; thus, studies of thimerosal toxicity should take into consideration gender-selective effects. The present study was originally undertaken to determine the maximum tolerated dose (MTD) of thimersosal in male and female CD1 mice. However, during the limited MTD studies, it became apparent that thimerosal has a differential MTD that depends on whether the mouse is male or female. At doses of 38.4-76.8mg/kg using 10% DMSO as diluent, seven of seven male mice compared to zero of seven female mice tested succumbed to thimerosal. Although the thimerosal levels used were very high, as we were originally only trying to determine MTD, it was completely unexpected to observe a difference of the MTD between male and female mice. Thus, our studies, although not directly addressing the controversy surrounding thimerosal and autism, and still preliminary due to small numbers of mice examined, provide, nevertheless, the first report of gender-selective toxicity of thimerosal and indicate that any future studies of thimerosal toxicity should take into consideration gender-specific differences.
PubMed.gov – 15.Mar.2010
Abstract
Mercury (Hg) exposure from dental amalgam fillings and thimerosal in vaccines is not a major health hazard, but adverse health effects cannot be ruled out in a small and more susceptible part of the exposed population. Individual differences in toxicokinetics may explain susceptibility to mercury. Inbred, H-2-congenic A.SW and B10.S mice and their F1- and F2-hybrids were given HgCl2 with 2.0 mg Hg/L drinking water and traces of (203)Hg. Whole-body retention (WBR) was monitored until steady state after 5 weeks, when the organ Hg content was assessed. Despite similar Hg intake, A.SW males attained a 20-30% significantly higher WBR and 2- to 5-fold higher total renal Hg retention/concentration than A.SW females and B10.S mice. A selective renal Hg accumulation but of lower magnitude was seen also in B10.S males compared with females. Differences in WBR and organ Hg accumulation are therefore regulated by non-H-2 genes and gender. Lymph nodes lacked the strain- and gender-dependent Hg accumulation profile of kidney, liver and spleen. After 15 days without Hg A.SW mice showed a 4-fold higher WBR and liver Hg concentration, but 11-fold higher renal Hg concentration, showing the key role for the kidneys in explaining the slower Hg elimination in A.SW mice. The trait causing higher mercury accumulation was not dominantly inherited in the F1 hybrids. F2 mice showed a large inter-individual variation in Hg accumulation, showing that multiple genetic factors influence the Hg toxicokinetics in the mouse. The genetically heterogeneous human population may therefore show a large variation in mercury toxicokinetics.
US National Library of Medicine – National Institutes of Health – Feb.2015
Results
Developmental Domain: ASD Diagnostic Criteria
Social Communication/Social Interaction
Deficits in social communication and social interaction are core factors in the diagnostic criteria of ASD. Impairments in social communication may present as abnormalities in eye contact, poor integration of verbal and nonverbal behaviors, and difficulties understanding the nonverbal communication of others (American Psychiatric Association, 2013). In some cases, persons with ASD may not participate in conversation or struggle with pragmatic language (American Psychiatric Association, 2013). Impairments in social interaction include difficulties with social-emotional reciprocity, failure to develop peer relationships, and reduced empathetic understanding and/or response (American Psychiatric Association, 2013).
There were 21 articles reviewed on social communication and social interaction in persons with ASD published between 1993 and 2013: 13 case-control studies, 7 cross-sectional studies, and 1 surveillance study. Nine studies were conducted in the United States and 12 studies were conducted at outside of the US. Of these 21 articles, 14 address social communication or other language abilities. In samples of children with varying cognitive abilities, some studies showed no significant differences in communication, conversational deficits, and language levels between males and females with ASD (Andersson et al., 2013; Dawson et al., 2007; Nicholas et al., 2008; Pilowsky et al., 1998; Park et al., 2012a, 2012b; Mayes and Calhoun, 2011; Mandy et al., 2012; Sipes et al., 2011; Solomon et al., 2012; Amr et al., 2011). One study found that males with ASD had greater expressive and receptive language skills than females with ASD (Carter et al., 2007) and another study found that females with ASD had more impaired social communication skills than males with ASD (Hartley and Sikora, 2009). Conversely, Park et al. (2012b) found that females with ASD had stronger non-verbal communication abilities than males with ASD. The majority of the literature reviewed on social communication found no difference between males and females with ASD, but there is some inconsistency.
The literature on sex differences in social interaction among persons with ASD (13 of 21 articles reviewed) is also inconsistent but generally suggests no significant sex differences in social interaction skills (Andersson et al., 2013; Dawson et al., 2007; Nicholas et al., 2008; Pilowsky et al., 1998; Mayes and Calhoun, 2011; Park et al. 2012b; Mandy et al., 2012; Sipes et al., 2011; Solomon et al., 2012). In population-level surveillance of eight-year olds, 80 % of children with ASD had poor social-emotional reciprocity with no significant difference between males and females (Nicholas et al., 2008). Szatmari et al. (2012) also found no sex differences in social-emotional reciprocity for children with varying cognitive abilities in a study from the Autism Genome Project. Oppositely, in an age and IQ matched case–control study, female adults with ASD were found to have fewer socio-communication difficulties during interpersonal interaction than male adults with ASD (Lai et al., 2013). Lastly, no sex differences have been noted in emotional reactiveness or being withdrawn (Hartley and Sikora, 2009) and in empathetic understanding and responses (Auyeung et al., 2009).
Cognitive functioning is likely to play a role in these social processes. Lower intellectual abilities are often linked with greater social impairment regardless of sex (Dawson et al., 2007). Among children with high functioning autism (IQ≥70), social skills have been found to be more impaired in female children than male children (Holtmann et al., 2007) and more severe as children aged (McLennan et al., 1993). In contrast, other studies found adult females with high functioning autism to have less socio-communication issues compared to males (Lai et al., 2011) or there were no sex differences in socio-communication skills in older children and adolescents (Holtmann et al., 2007; Kopp and Gillberg, 2011).
Overall, the 21 articles reviewed suggest no difference in social interaction between males and females with ASD and inconsistent differences in social communication between males and females with ASD, although both social interaction and social communication may be influenced by intellectual ability and age.
Restricted, Repetitive Patterns of Behavior, Interests, or Activities
There were 18 articles reviewed on restricted and repetitive patterns of behaviors and interests (RRBI) published between 1993 and 2013: nine cross-sectional studies, seven case–control studies, one cohort study, and one surveillance study. Eleven studies were conducted in the United States and seven studies were conducted in other countries. Based on this review, the literature suggests that males with ASD have more RRBI than females with ASD (Hattier et al., 2011; Carter et al., 2007). When assessing individual facets of RRBI, restricted interests are seen more often in males with ASD than females with ASD independent of cognitive ability (Kohane et al., 2012; May et al., 2012; Mandy et al., 2012; Szatmari et al., 2012). Males with ASD are also more likely to have more routines, rituals, and fascination with parts of objects than females with ASD (Nicholas et al., 2008; Park, et al., 2012b; Beuker et al., 2013). The literature on repetitive motor movements is less consistent: adult males with high functioning autism or Asperger’s syndrome had more repetitive motor movements than adult females with high functioning autism or Asperger’s syndrome in one case-control study (May et al., 2012), but there were no sex differences in repetitive motor movements among persons with autism in two other case-control studies (McLennan et al., 1993; Worley and Matson, 2011), one cross-sectional study (Auyeung et al., 2009), and one population-based cross-sectional study (Nicholas et al., 2008).
Age may influence the presentation of RRBI in males and females with ASD. One study found no sex difference among RRBI in toddlers (Sipes et al., 2011), whereas a different study found significantly more RRBI among adult males with ASD compared to females with ASD (Hattier et al., 2011). In summation, most studies reviewed suggested that males with ASD are likely to have more RRBI than females with ASD across levels of cognitive ability, although RRBI may be influenced by age.
Sensory issues are prevalent among persons with ASD (Nicholas et al., 2008) and are included as a RRBI in the DSM 5 (American Psychiatric Association, 2013). Common issues are oversensitivity to touch, sound, smell, taste, and attraction to certain tactile stimuli (American Psychiatric Association, 2013; Baranek et al., 2006; Rogers et al., 2003). Abnormal sensory reactions have been reported to occur in up to 47 % of persons with ASD, which is a rate ten times higher than reported in the general population (Nicholas et al., 2008). Additionally, there is a significant correlation between sensory issues in each of the individual senses (Kern et al., 2007); therefore, impairment is compounded for persons with ASD and sensory abnormalities.
Cross-sectional studies found no observed differences between males and females in sensitivity to sound (Mandy et al., 2012) or sensory sensitivity in general (Louisa et al., 2012; Mayes and Calhoun, 2011; Baranek et al., 2006). Mandy et al. (2012) examined RRBI in children and adolescents 3 to 18 years of age and found that age did not influence the presentation of RRBI. However, Lai et al. (2011) found that adult females with high functioning autism had more lifetime sensory issues than males with ASD. Overall, the majority of articles reviewed that addressed sensory issues in ASD do not suggest a sex difference, although aging may be a factor and should be further explored.
Developmental Domain: other Developmental Endophenotypes
Attention Deficit Hyperactivity Disorder
Attention deficit hyperactivity disorder (ADHD) and corresponding symptoms are common in children with ASD (Bradley and Isaacs, 2006; Nicholas et al., 2008). Previous studies show that 50 % to 83 % of children and teenagers with ASD had hyperactivity and attention problems (Nicholas et al., 2008; Bradley and Isaacs, 2006). There were seven articles that met search criteria and addressed ADHD. These seven articles were published between 2008 and 2012 with five cross-sectional studies and two cohort studies. Two studies were conducted in the United States and five were conducted in other countries.
A study of 7 to 12 year-olds with varying cognitive abilities found that males with ASD had higher levels of hyperactivity and impulsivity than females with ASD and this difference was more pronounced at younger ages (May et al., 2012). Males with high functioning autism from middle childhood to adolescence had higher levels of hyper-activity and inattention in teacher reports as compared to female peers, but there was no difference in parental reports (Mandy et al., 2012). A study of children and young adults aged 5 to 20 with high functioning autism found females had more attention problems (Bryson et al., 2008). A majority of studies found no difference in ADHD co-occurrence between males and females with ASD (Simonoff et al., 2008; Sinzig et al., 2009; Mayes and Calhoun, 2011; Horovitz et al., 2011). In summary, the current literature leans toward no sex differences in the co-occurrence of ADHD and ASD, but there is still inconsistency in the literature and thus, the sex difference is largely inconclusive
Challenging Behavior (Aggressiveness/Temper Tantrums/Oppositional Tendencies)
Challenging behavior is a common associated feature of ASD and includes aggression expressed toward other people, temper tantrums, and oppositional and defiant tendencies. Aggression expressed toward other people and temper tantrums are found in 50 % and 54 % of children with ASD compared to only 28 % and 23 % of children without ASD (Nicholas et al., 2008). The 12 articles in this review that met search criteria and addressed challenging behaviors were published between 2005 and 2012 and included six cross-sectional studies, four case–control studies, one clinical trial, and one surveillance study. Six studies were conducted in the United States and six were conducted in other countries. In general, there were no differences in aggression, temper tantrums, or anger between child sexes, regardless of age or cognitive ability (Kozlowski et al., 2012; Worley and Matson, 2011; Carter et al., 2007; Murphy et al., 2009; Mandy et al., 2012; Quek et al., 2012; Mayes and Calhoun, 2011; Horovitz et al., 2011). One study found that females with ASD had more “challenging behaviors” than males with ASD, although challenging behaviors were not explicitly defined (Dworzynski et al., 2012). Delinquent behavior (Park et al., 2012b) and oppositional defiance (Gadow et al., 2005) were more prevalent in males than in females with ASD in two studies reviewed.
Cognitive Skills and Intellectual Disability
In a review from 1966 to 2001, Fombonne (2003) found that the median prevalence of intellectual impairment in persons with ASD was 70 % in the studies evaluated. More recent population-based studies have found lower rates of ID in persons with ASD, with a range from 18 % to 55 % (Charman et al., 2011). The National Health Interview Study found 0.71 % of all children aged 3 to 17 from 1998 to 2007 had an ID (Boyle et al., 2011). Our review found 12 articles that met the search criteria and addressed ID or specific cognitive skills. These 12 articles were published between 1983 and 2011, and included seven cross-sectional studies, four case–control studies, and one-surveillance study. Four studies were conducted in the United States and eight were conducted in other countries.
The 12 articles reviewed support a relationship between child sex and co-occurring ID in children with ASD. The sex ratio between males and females without ID is greater than the sex ratio for all levels of cognitive ability combined (Nicholas et al., 2008; Hartley and Sikora, 2009). Consequently, the male to female ratio is lower when there is co-occurring ID compared to when there is no co-occurring ID (Hartley and Sikora, 2009; Nicholas et al., 2008; Yeargin-Allsopp et al., 2003). The ratio of males to females with ASD and co-occurring ID has been seen to range from 1.3:1 (Tsai and Beisler, 1983) to 2.8:1 (Bryson et al., 2008) with a trend toward fewer sex differences as ID becomes more severe (Yeargin-Allsopp et al., 2003). This differential sex difference in ID results in females with ASD, on average, having lower intelligence test scores than males with ASD (Banach et al., 2009; Volkmar et al., 1993).
Specific cognitive skills posited to vary between males and females with ASD include cognitive flexibility, response inhibition, working memory, and attention to detail (Geurts et al., 2004). Female adolescents with high functioning autism were seen to have superior information processing, multiple conceptual tracking, divided attention, and cognitive flexibility compared to male adolescents with high functioning autism (Bolte et al., 2011). In contrast, studies show males with ASD have superior attention to detail, visuo-spatial skills (Auyeung et al., 2009), and inhibitory control (Lemon et al., 2011) compared to females with ASD. There were no sex differences between adults with ASD in the “eyes test” which measures ability to infer mental states through the eyes (Lai et al., 2011). In summary, the 12 journal articles reviewed in this section suggest that females with ASD generally have lower intelligence test scores than males with ASD and that specific cognitive skills may vary by sex.
Developmental Regression
Parents of some children with ASD report a period of typical development followed by a loss in language, social, motor, self-help, imaginative play, or other skills. This developmental regression is usually reported to occur between 15 and 24 months of age (Meilleur and Fombonne, 2009). Our review found six articles that met search criteria and addressed developmental regression. These six articles were published between 2007 and 2013 and comprised two cohort studies, three cross-sectional studies, and one surveillance study. In a population-based surveillance study of children with ASD, 17 % of children had documented developmental regression and that percentage rose if the child had a previous ASD diagnosis (Wiggins et al., 2009). Males had significantly more regression than females and were more likely to regress at a younger age (Wiggins et al., 2009). This higher risk of regression in males was also seen in smaller, non-population based studies (n=4, 8, and 17 female children) (Bernabei et al., 2007; Ekinci et al., 2012; Zhang et al., 2012). In contrast, a cross-sectional study found that females aged 18 months to 15 years had significantly higher occurrence of regression as compared to males (30 % vs. 19 %) (Ben-Itzchak et al., 2013). No difference in the presence of developmental regression between males and females with ASD was observed in a small clinical sample of 20 females (Meilleur and Fombonne, 2009). In sum, the review of sex differences of developmental regression is contradictory and thus inconclusive.
Excess/Absence of Fear
Excess or absence of fear is more common in children with ASD than other children (Evans et al. 2005; Nicholas et al., 2008). In a population-based surveillance of eight-year olds, Nicholas et al. (2008) found that 32 % of children with ASD had atypical fear noted in service records compared to 6 % of children with ASD symptoms but no ASD diagnosis. Three articles met search criteria and addressed excess or absence of fear. All three of these articles were published in the United States between 1990 and 2011 and were two cross-sectional studies and one case–control study. In these studies, females with ASD had more specific phobias than males with ASD (Gadow and DeVincent, 2012; Matson and Love, 1990) and more unusual fears (Mayes et al., 2013). One study conducted by Matson and Love (1990) found more fear in typically developing female children compared to male children and no significant difference in fear between typically developing female children and female children with ASD. Given the sparse amount of research on this topic, further exploration is warranted to understand sex differences in fear among persons with ASD.
Safety Issues (Self-Injury/Elopement)
About 50 % of children with ASD engage in self-injurious behavior (Richards et al., 2012; Baghdadli et al., 2003; Duerden et al., 2012). Four studies met search criteria and three pertained to self-injurious behavior. All three of these studies were cross-sectional designs with two being conducted in Europe and one in the United States. No difference in self-injurious behavior was found between males and females with ASD (Richards et al., 2012; Baghdadli et al., 2003; Duerden et al., 2012).
Elopement, also known as wandering off, is a rising concern among parents of children with ASD. One online survey addressing elopement met our search criteria. This survey was conducted in the United States in 2013 and found that 49 % of parents reported that their child with an ASD wandered off at least once after the age of four years (Anderson et al., 2012). Results also found that sex did not influence the prevalence of elopement, although children with more intellectual impairment were more likely to elope (Anderson et al., 2012). Few conclusions can be drawn since there is little research on elopement and other safety issues in children with ASD and associated sex differences.
Psychiatric Domain
Anxiety/Mood Disorders
Symptoms of anxiety and mood disorders are more prevalent in children with ASD than in typically developing children (Worley and Matson, 2011; Nicholas et al., 2008). Among children who met a surveillance definition for an ASD, 55 % had abnormal mood or affect compared to 26 % of children with at least one symptom of an ASD but no ASD diagnosis (Schendel et al., 2009). The Special Needs Autism Project in the UK found 44 cases of emotional disorder per 100 children with ASD (Simonoff et al., 2008). Moreover, among eight-year-old children who met a surveillance definition for an ASD, 3 % had anxiety, 2 % had emotional disorder, 2 % had mood disorder, and less than 2 % had obsessive-compulsive disorder (OCD), depression, bipolar, or oppositional defiant disorder (Levy et al., 2010). Nine studies were found that met search criteria and addressed anxiety or mood disorders. These nine studies were published between 2005 and 2012 and included five cross-sectional studies and four case–control studies. Four of the studies were conducted in the United States and five were conducted in other countries.
The literature on sex differences in co-occurring anxiety or mood disorders and ASD is mixed and dependent on cognitive abilities. In some studies, females with high functioning autism were at greater risk for internalizing psychopathology than both male children with ASD and typically developing female children (Solomon et al., 2012; Mandy et al., 2012). These studies are supported by a Finnish report that found female children with ASD had lower scores on a test associated with major depressive disorder compared to male children with ASD (Mattila et al., 2010). Other studies found no sex differences in the of co-occurrence of anxiety or depression in children with ASD and varying cognitive abilities (Quek et al., 2012; Gadow et al., 2005; Park et al., 2012b; Simonoff et al., 2008; Mayes and Calhoun, 2011; Lai et al., 2011). In the general population, females have more panic attacks, generalized anxiety disorders and males have more social anxiety (American Psychiatric Association, 2013). Based on this review, the current literature is inconclusive on whether a sex difference in children with ASD and co-occurring anxiety or mood disorders exists, although a few studies suggest more anxiety and mood disorders in females than males with ASD.
Schizophrenia
Schizophrenia is a mental disorder that involves delusions, disorganized behavior, disorganized speech, hallucinations, and restrictions in the range and intensity of emotions (American Psychiatric Association, 2013). Schizophrenia typically presents between 18 and 30 years of age with earlier onset associated with male sex. Lifetime prevalence of schizophrenia is near 0.2 % (American Psychiatric Association, 2013) The prevalence of schizophrenia in eight-year olds with ASD is less than 1 % (Levy et al., 2010). Two articles met search criteria and addressed schizophrenia. These two articles were published in 2005 and 2010 and were both case–control studies. Review of the two studies found conflicting results on sex differences and the co-occurrence of ASD and schizophrenia or schizophrenia spectrum traits. A parental survey of 6 to 12 year olds with ASD found schizophrenia spectrum traits to be twice as prevalent in females compared to males (57 %: 28 %) independent of ID (Gadow and DeVincent, 2012). Conversely, in a group of 6 to 12 year olds with ASD and ID, schizophrenia was more common in males than females (Tsakanikos et al., 2011). Again, the literature is relatively sparse due to the late onset of schizophrenia and the rarity of co-occurring schizophrenia: future research is warranted.
Medical Domain
Birth defects/Chromosomal Disorders /Genetic Disorders
Population-based surveillance data from the 2008 ADDM report found that among children with ASD, less than 1 % had a co-occurrence of fragile X syndrome, Down syndrome, chromosomal disorders, or other genetic and congenital diagnoses (Levy et al., 2010). It is likely that these rates are under-reported because investigation of ASD co-occurring conditions was not the focus of the ADDM surveillance effort. However, a cohort study of children in Georgia found a similar prevalence of chromosomal disorders and Down syndrome in persons with ASD (Schendel et al., 2009).
There were four studies reviewed that met search criteria and addressed ASD sex differences in birth defects, chromosomal disorders, and genetic disorders: two systematic reviews, one case–control study, and one surveillance study. Co-occurring birth defects, such as impairments to the central nervous system, cardiovascular system, genitourinary system, or musculoskeletal system, appear more often in males than females with ASD. Among children with ASD, the male to female ratio was 9:1 if a child had a co-occurring birth defect and 3.6:1 if the child did not have a co-occurring birth defect (Schendel et al., 2009).
A review conducted by Reilly (2009) found that males with ASD have more co-occurring Down syndrome than females with ASD and the male to female ratio among children with both ASD and Down syndrome may be near the overall ASD prevalence ratio of 4:1. A review conducted by Wiznitzer (2004) found no difference between males and females with ASD and the co-occurrence of tuberous sclerosis. Clifford et al. (2007) found that about 70 % of males aged 5 to 80 with fragile X syndrome had co-occurring ASD while 23 % of females in the same age range with fragile X had co-occurring ASD. The difference in co-occurrence of ASD between males and females may suggest a greater association between the two conditions in males as compared to females.
It is important to note that birth defects, chromosomal disorders, and genetic disorders are rare and seldom studied. Therefore, the results on sex differences for co-occurring ASD and chromosomal and genetic conditions are inconclusive.
Head Size / Encephalopathy
Head size, specifically an enlarged head circumference or macrocephaly, has been associated with ASD (Wallace and Treffert, 2004). Three articles were reviewed that examined differences in head size between males and females with ASD. Studies include two case–control studies and one cross-sectional study. Two studies were conducted in the US and one study was conducted in Italy. A cross-sectional study by Fombonne et al. (1999) found no difference in head size between males and females aged 2 to 16 with ASD. Sacco et al. (2007) also found no difference in head size between males and females aged 3 to 16 with ASD. In contrast, Aylward et al. (2002) found larger head sizes in male adults and children compared to female adults and children with ASD, but the female sample size was low (n=9).
Abnormal Eating and Gastrointestinal Issues
In a population-based study conducted by Nicholas et al. (2008), about 54 % of children with ASD had an abnormality in eating, drinking, or sleeping, which is nearly 40 % higher than that of children with at least one symptom of ASD but no diagnosis (Nicholas et al., 2008). Some studies have shown an increase in certain gastrointestinal symptoms among persons with ASD, including constipation (Ibrahim et al., 2009) and diarrhea (Wang et al., 2006), while other studies found no significant increase in overall gastrointestinal symptoms or symptoms such as esophageal reflux, vomiting, and abdominal discomfort (Ibrahim et al., 2009; Wang et al., 2006; Valicenti-McDermott et al., 2007). However, little research on gastrointestinal issues has been conducted at a population level and no studies were found that compared males to females on gastrointestinal response. More research is needed to determine if there is an association between gastrointestinal symptoms and ASD and whether the association differs between the sexes.
Four studies were found that compared the sexes and addressed food selectivity. These four studies were conducted in the United States between 2006 and 2010 and included one case–control and three cross-sectional designs. In general, review of these studies found food selectivity and feeding issues to be more frequent in children with ASD than children without ASD (Valicenti-McDermott et al., 2007; Ibrahim et al., 2009), although limited research is available in this area. There was no difference between child sexes in over or under-eating in a study of children with high functioning autism (Worley and Matson, 2011) and no differences between the sexes in eating abnormalities in two studies conducted in children with ASD and varying cognitive abilities (Mayes and Calhoun, 2011; Horovitz et al., 2011). Based on this limited review, it appears unlikely that there is a difference in eating habits between males and females with ASD.
Seizures/ Epilepsy
Epilepsy and other seizure disorders co-occur in 5 % to 40 % of children with ASD and there is differential prevalence based on ID (Baird et al., 2008; Nicholas et al., 2008). This review found three articles that met search criteria and addressed seizures or epilepsy. These three articles were published between 2008 and 2013 and consist of a cohort study, one cross-sectional study, and one meta-analysis. Females with ASD were found to have more epilepsy than males with ASD; the male to female ratio drops to near 2:1 in children with ASD and co-occurring epilepsy, but this may be partly due to differential ID (Amiet et al., 2008; Bolton et al., 2011; Ben-Itzchak et al., 2013). There may be an increased likeliness in females with ASD to have co-occurring epilepsy or seizure disorder; however, the literature is sparse so a conclusion cannot be drawn. Further research is needed to enhance current knowledge of sex differences in children with ASD and epilepsy or seizure disorder.
Sleep Disturbances
In a systematic review of parental sleep surveys, sleep problems were present in 50 % to 80 % of children with ASD compared to 9 % to 50 % in matched typically developing children (Kotagal and Broomall, 2012). There were six articles reviewed that met search criteria and addressed sleep disturbances. These six articles were published between 2004 and 2012 and included two case–control studies, two cohort studies, and two cross-sectional studies. Four were conducted in the United States and three were conducted in other countries. Based on this review, some studies found no sex differences in sleep problems among persons with ASD (Liu et al., 2006; Wiggs and Stores, 2004; Mayes and Calhoun, 2011; Horovitz et al., 2011), one study found that female children with ASD have less sleep problems than male children with ASD (Sivertsen et al., 2012), and one study found female children with ASD have more sleep problems than male children with ASD (Hartley and Sikora, 2009). The minimal amount of research in this area leads to inconsistent results and prevents definitive conclusions on whether a sex difference exists in sleep disturbance.

Vaccine News – This is the Best Explanation of the Vaccine/Autism Connection I’ve Ever Heard!

The Only Vaccine Guide a New Parent Will Ever Need
BY J.B. HANDLEY
First, a disclaimer: I’m not a doctor, and the final decision about vaccinating your child should take place between you and your healthcare provider. I’m not giving you medical advice; I’m stating my opinion.
I am a dad. And, I write this without benefitting in anyway from what is said here. I have no book to peddle, no profits to protect, and there’s no doubt that writing this will result in some amount of hate directed in my general direction for challenging a popular narrative that vaccines are only safe and effective and should be administered the same way to all children without consideration for the unique biology of each and every child. So be it.
Do your own research. Understand the risks and benefits of everything you are putting into your child.
Find a healthcare provider who doesn’t believe “one size fits all” when it comes to vaccines

The Vaccine Studies That Have Never Been Done.
1. Study Proving the Existing Vaccine Schedule Is Safe – NEVER DONE
2. Study Proving Safety of Childhood Vaccines For Children – NEVER DONE
3. Study Proving Safety of Infant Vaccines For Infants – NEVER DONE
4. Study Proving Vaccines Safe for Pregnant Women – NEVER DONE
5. Study Proving Vaccines Safe For Unborn Fetus – NEVER DONE
6. Study Comparing the Health of Vaccinated vs Un-Vaccinated – NEVER DONE
7. Study to Prove Combining Several Vaccines at One Doctor’s Visit Is Safe – NEVER DONE
8. Study That Exposes Vaccinated People to Targeted Virus (to see if they get sick or not) – NEVER DONE
9. Study That Proves Vaccinated People Don’t Acquire the Targeted Disease – NEVER DONE
10. Study Proving Thimerosal (mercury) or Aluminum Are Safe to Inject Into Children – NEVER DONE
Read # 8 again and then read it again…….and then think about that.
These are the studies the average person assumes were already done decades ago and they have NEVER been done. If you’re not concerned, you’re not paying attention.
~ Chris Kirckof

Disturbing tape-recording of an immunologist having a laugh over the numerous and useless vaccines they inject for a child’s first year of life, in order to keep parents compliant and unquestioning of what is being done to their baby. Research is KEY and education is empowerment

Pro-Vaccine Immunologist Admits a Shocking Truth About Vaccines
For several years, until April of this year, I had been lecturing nationally to health professionals about the great vaccine hoax. Attending one such seminar was a board member of an association of health professionals, who invited me to speak on this subject at their national conference. I did, and had 90 minutes to present the most salient points from my 7-hour seminar. It caused quite a stir, and several clinicians thanked me for having the courage to speak the truth about this controversial subject.
Later that day, I sat on a panel of four experts to answer questions from conference attendees. Many of the questions were directed at the PhD immunologist on the panel, asking if the statements I had made in the morning presentation were true. To my surprise, the immunologist confirmed every assertion I had made.
The first was that it is pointless to administer drugs intended to stimulate antibody production to babies who are too young to produce antibodies. Infants in their first year mostly depend on generalized, non-specific immunity, including (hopefully) immunoglobulins from breast milk, to protect their young bodies from infection. They do not produce antibodies of their own until about age one. Despite this basic fact, the medical establishment insists administering a total of 19 shots, containing 24 vaccines, to infants on the 2, 4 and 6 month pediatric visits (Source: cdc.gov). Somehow, the basic facts of human physiology and development do not apply to vaccines.
You can listen to an audio file of an exchange between an attendee and the immunologist about this question. She declined to be identified in my presentations, including this post, perhaps because she knows that anyone who speaks the truth about vaccines is savaged by the medical establishment and their compliant lapdogs in the mainstream media. It is professional suicide for anyone in conventional medicine to question the unquestionable (yet unproven) assumptions about vaccines: that they are effective, safe and necessary. I have stopped lecturing publicly on this subject for the same reason, because the attacks in recent years have become particularly vicious; and because my main message in my teachings is about personal responsibility, innate wholeness and opening to the largeness of who we are, not just vaccines.

Study – A modified self-controlled case series method to examine association between multidose vaccinations and death
Abstract
The self-controlled case series method (SCCS) was developed to analyze the association between a time-varying exposure and an outcome event. We consider penta- or hexavalent vaccination as the exposure and unexplained sudden unexpected death (uSUD) as the event. The special situation of multiple exposures and a terminal event requires adaptation of the standard SCCS method. This paper proposes a new adaptation, in which observation periods are truncated according to the vaccination schedule. The new method exploits known minimum spacings between successive vaccine doses. Its advantage is that it is very much simpler to apply than the method for censored, perturbed or curtailed post-event exposures recently introduced. This paper presents a comparison of these two SCCS methods by simulation studies and an application to a real data set. In the simulation studies, the age distribution and the assumed vaccination schedule were based on real data. Only small differences between the two SCCS methods were observed, although 50 per cent of cases could not be included in the analysis with the SCCS method with truncated observation periods. By means of a study including 300 uSUD, a 16-fold risk increase after the 4th dose could be detected with a power of at least 90 per cent. A general 2-fold risk increase after vaccination could be detected with a power of 80 per cent. Reanalysis of data from cases of the German case-control study on sudden infant death (GeSID) resulted in slightly higher point estimates using the SCCS methods than the odds ratio obtained by the case-control analysis.

The Top 10 Reasons To Never Take A Vaccine
There are many, many good reasons to never take a vaccine. Whether you want to protect yourself against carcinogenic hidden ingredients, disallow toxic adjuvants into your body, defend your immune system against a chemical onslaught or refuse to be part of any sinister schemes of sterilization-depopulation agenda, this information is vitally important.
More and more, we are learning the truth about vaccines, what they are really composed of and what they really do to the human body – and the more we learn about them, the more we see just how dangerous and harmful they are. Whatever they may have been or could be, as it stands, they are a weapon of medical destruction that makes billions of dollars for the Rockefeller Medicine Big Pharma cartel. Here is my list of the top 10 reasons for an ordinary person to never take a vaccine, unless they were in a life-threatening situation where somehow the benefit outweighed the risk.

Reason #1 to Never Take a Vaccine: Toxic Ingredients – Formaldehyde, MSG, Antibiotics, GMOs, Polysorbate, Mercury, Squalene and More
Reason #2 to Never Take a Vaccine: Toxic Adjuvants – Aluminum
Reason #3 to Never Take a Vaccine: Hidden Ingredients – Immunity-Destroying Nagalese
Reason #4 to Never Take a Vaccine: Injection of Human and Animal Cells
Reason #5 to Never Take a Vaccine: Blood Sludge, Hypoxia, Ischemia and Localized “Strokes” in Your Body
Reason #6 to Never Take a Vaccine: The Herd Immunity Myth Busted
Reason #7 to Never Take a Vaccine: Viral Shedding
Reason #8 to Never Take a Vaccine: Possible Side Effects of Paralysis and Death
Reason #9 to Never Take a Vaccine: Insufficient Legal Recourse
Reason #10 to Never Take a Vaccine: The Vaccine-Sterilization-Depopulation Connection

Remember that Bill Gates himself, point man for the NWO agenda, has slipped up and admitted there is a vaccine-depopulation link on at least 2 occasions:

“… if we do a really great job on new vaccines … we could lower that (i.e. population growth) perhaps by 10-15% …”
“… the benefits (of vaccines) are there in terms of reducing sickness, reducing population growth …”

WEM NÜTZT DAS IMPFEN?
Zeit für einen Shitstorm gegen die Impfstoffhersteller! In deren Prospekten stimmt kein einziger Satz, schwere Nebenwirkungen werden mit Hilfe einer Armada von Lobbyisten verschwiegen, damit der Rubel rollt. Es ist Zeit, den Verletzungen an Körper, Geist und Seele, die von Impfungen verursacht werden, ein Ende zu bereiten!
Impfungen haben keine einzige Seuche ausgerottet – das zeigen Statistiken des Bundes. Jede Seuche war aufgrund des wachsenden Wohlstands nach dem 2. WK schon so gut wie verschwunden, BEVOR die entsprechende Impfung auf den Markt kam!
Schluss mit den Lügen der Pharma-Industrie und staatlich organisierten Subventionen wie bei den “Schweinegrippe-Impfstoffen”!
Konkret sind im ersten Lebensjahr von der Lobbygruppe “StIKo” empfohlen:4 x 6-fach-Impfung, 4 x Pneumokokken, 1 x MMRV (4-fach), dazu kommen optionale Impfungen wie gegen “Rotaviren” oder Influenza, die viele Ärzte zusätzlich verimpfen. Macht maximal 34 Impfungen im ersten Lebensjahr. Und im 2. Lebensjahr wird dann munter weitergeimpft…
FÜR EINE FREIE ZUKUNFT GESUNDER MENSCHEN! IMPFEN MUSS FREIWILLIG BLEIBEN!
http://www.facebook.com/FIEGZ
http://www.freie-impfentscheidung.blogspot.com

Study – What is regressive autism and why does it occur? Is it the consequence of multi-systemic dysfunction affecting the elimination of heavy metals and the ability to regulate neural temperature?
Abstract
There is a compelling argument that the occurrence of regressive autism is attributable to genetic and chromosomal abnormalities, arising from the overuse of vaccines, which subsequently affects the stability and function of the autonomic nervous system and physiological systems. That sense perception is linked to the autonomic nervous system and the function of the physiological systems enables us to examine the significance of autistic symptoms from a systemic perspective. Failure of the excretory system influences elimination of heavy metals and facilitates their accumulation and subsequent manifestation as neurotoxins: the long-term consequences of which would lead to neurodegeneration, cognitive and developmental problems. It may also influence regulation of neural hyperthermia. This article explores the issues and concludes that sensory dysfunction and systemic failure, manifested as autism, is the inevitable consequence arising from subtle DNA alteration and consequently from the overuse of vaccines.

Study – A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States
Abstract
Background
Autism spectrum disorder (ASD) is defined by standardized criteria of qualitative impairments in social interaction, qualitative impairments in communication, and restricted and stereotyped patterns of behavior, interests, and activities. A significant number of children diagnosed with ASD suffer a loss of previously-acquired skills, which is suggestive of neurodegeneration or a type of progressive encephalopathy with an etiological pathogenic basis occurring after birth. To date, the etiology of ASD remains under debate, however, many studies suggest toxicity, especially from mercury (Hg), in individuals diagnosed with an ASD. The present study evaluated concerns about the toxic effects of organic-Hg exposure from Thimerosal (49.55% Hg by weight) in childhood vaccines by conducting a two-phased (hypothesis generating/hypothesis testing) study with documented exposure to varying levels of Thimerosal from vaccinations.
Methods
A hypothesis generating cohort study was undertaken to evaluate the relationship between exposure to organic-Hg from a Thimerosal-containing Diphtheria-Tetanus-acellular-Pertussis (DTaP) vaccine in comparison to a Thimerosal-free DTaP vaccine administered, from 1998 through 2000, for the risk of ASD as reported in the Vaccine Adverse Event Reporting System (VAERS) database (phase I). A hypothesis testing case–control study was undertaken to evaluate the relationship between organic-Hg exposure from Thimerosal-containing hepatitis B vaccines administered at specific intervals in the first six months of life among cases diagnosed with an ASD and controls born between 1991 through 1999 in the Vaccine Safety Datalink (VSD) database (phase II).
Results
In phase I, it was observed that there was a significantly increased risk ratio for the incidence of ASD reported following the Thimerosal-containing DTaP vaccine in comparison to the Thimerosal-free DTaP vaccine. In phase II, it was observed that cases diagnosed with an ASD were significantly more likely than controls to receive increased organic-Hg from Thimerosal-containing hepatitis B vaccine administered within the first, second, and sixth month of life.
Conclusions
Routine childhood vaccination is an important public health tool to reduce the morbidity and mortality associated with infectious diseases, but the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.

#VaxXed #medical #Oregon
Dr Paul Thomas interview with Polly Tommey
June 17, 2017

The Shift Episode 8: Del Bigtree
Join host Doug McKenty as he discusses the controversial movie Vaxxed with producer Del Bigtree. Listen in as the conversation includes the real story behind Dr. Andrew Wakefield’s study of the MMR vaccine that started it all, the realization that regulatory agencies have been corrupted at the highest levels, as well as the real reasons behind the mainstream media’s complicity in covering up the actual science behind vaccine safety. Find out more about it at http://www.vaxxedthemovie.com, and as always help out at http://www.patreon.com/theshift or visit http://www.theshiftnow.com for more information about making The Shift.

Billy D Live with Del Bigtree
Watch Billy D and Del Bigtree talk about vaccines
Go to https://caljamnetwork.org/ to watch Jeremy’s Stretch video series.

Follow Billy D. on
facebook – https://www.facebook.com/billy.demoss1/
website – http://www.californiajam.org/

Vaccine’s Safety: A Crime Against Humanity
Dr. Sherri J Tenpenny warns about the perils of vaccination

This is the Best Explanation of the Vaccine/Autism Connection I’ve Ever Heard!
Dr. Stephanie Seneff discusses the potential connection between vaccines and autism. It’s a hotly-debated topic. Here she gets specific into what ingredient in the vaccine may be linked to autism and other conditions. Find out what her research has found. You may think differently after watching this!

Trace Amounts: Ethyl Mercury | Educational Documentary
Has Ethyl Mercury Caused One of the Worst Health Crises in American History? During the past 20 years, the frequency of autism occurring in children has .
This video shares facts about the devastating mercury based preservative, thimerosal, used in vaccines. .
For this EP of Zero Doubt Zone, host Dane Sorenson, circles back to the subject of vaccines. On the heels of viewing the documentary, ‘Trace Amounts’, .
Courtesy of AAE tv Documentary filmmaker and researcher, Eric Gladen. Ethann and Eric discuss his new film “Trace Amounts”. They talk about the scientific .

Shots In The Dark: Silence on Vaccine
Following the increase in cases of autism and other immune disorders among some particularly vulnerable people, several recognized specialists are questioning the safety of large-scale vaccination. Despite the serious side effects, pharmaceutical companies, the medical profession and government authorities continue to bury their heads in the sand, refusing to see a serious problem. In Quebec, the United States and France, as in most industrialized countries, victims are almost without recourse despite the high toxicity of substances such as mercury and aluminum contained in vaccines. With this hard-hitting documentary, Lina B. Moreco highlights a very worrying public health problem.
Since they were introduced in the early 20th century, vaccines have been a tremendous medical and scientific success. Today perceived as a necessity, they are so familiar to us that their potential risks are rarely mentioned.
However, the stakes are significant. Based on recommendations of health agencies, North American children receive about 48 doses of 14 different vaccines before the age of 6 — double the amount prescribed 25 years earlier. Despite this extraordinary increase, few studies independent of the pharmaceutical industry have been conducted into their long-term side effects. This is a disturbing situation given the numerous toxins, including mercury and aluminum, contained in some commonly administered vaccines.
Several worried pediatricians and scientists are sounding the alarm. Some of the research underway indicates that vaccination is directly responsible for immune or neurological disorders among certain people genetically or neurologically predisposed to react badly to vaccine components. Cases of autism, multiple sclerosis, Guillain-Barré syndrome, macrophagic myofasciitis, encephalitis, paralysis and neuropathies indicate the seriousness of the situation.
Despite these findings, the pharmaceutical industry and government authorities deny there is a serious problem. Relying on perfunctory studies, some of which date back to the late 1920s, they reject out of hand any cause-and-effect relationship. Given the known fact that adding preservatives such as thimerosal (mercury) helps reduce production costs, the reaction of the pharmaceutical industry is at the very least puzzling. Preferring not to question a system that has proved its worth, a majority of the medical profession’s members reject any potential toxicity in vaccines.
http://films.nfb.ca/shots-in-the-dark/
FAIR USE NOTICE: These Videos may contain copyrighted (© ) material the use of which has not always been specifically authorized by the copyright owner. Such material is made available to advance understanding of ecological, political, human rights, economic, democracy, scientific, moral, ethical, and social justice issues, etc. It is believed that this constitutes a ‘fair use’ of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, this material is distributed without profit to those who have expressed a prior general interest in receiving similar information for research and educational purposes. For more information go to: http://www.law.cornell.edu/uscode

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The truth about vaccines and Big Pharma, and info on GMO foods

Se cere demisia ministrului Sănătăţii. Motivul – legea care prevede vaccinarea obligatorie
In nicio țară din Uniunea Europeană nu sunt obligatorii 8 vaccinuri!
In Germania, Austria, Olanda, Spania, Portugalia, Marea Britanie, Luxemburg, Suedia, Danemarca, Italia, Irlanda, Finlanda, Suedia, Croația, Cipru, Estonia și Lituania, părinții decid dacă &icirc;și vaccinează copiii!
Vaccinul este un medicament, dar poate fi și o armă biologică!
Peste 180.000 de copii vor fi obligați, in primul an de viață, să primească 26 de vaccinuri!
in cazul unui copil contraindicația definitivă la un vaccin sau mai multe se acordă numai la București de către GTCAV!
Pana la varsta de 6 ani un copil trebuie să primească 33 de vaccinuri!
Vaccinurile provoacă boli autoimune: un copil din patru suferă de o boală alergică, iar un copil din zece suferă de astm bronșic!
Asociația Pro Consumatori are o activitate de peste 27 de ani in domeniul apărării drepturilor și intereselor economice ale consumatorilor.

 

Vaccine News – Biopersistence in the Brain of Aluminum Nanoparticles from Vaccines

Dr. Brownstein on CDC Corruption: “I am Tired of Writing About This – I See Patients Damaged by Vaccines”
CDC Whistleblower Case Three Years Later: Nothing Happening
by Dr. Brownstein’s
Holistic Medicine
I honestly cannot believe I am still writing about this. It was three years ago that a senior CDC scientist, Dr. William Thompson, claimed whistleblower protection after he issued a statement that he and his fellow colleagues altered, hid, and threw out data that showed a direct association between the MMR vaccine and autism.

CDC Whistleblower Case Three Years Later: Nothing Happening
I honestly cannot believe I am still writing about this. It was three years ago that a senior CDC scientist, Dr. William Thompson, claimed whistleblower protection after he issued a statement that he and his fellow colleagues altered, hid, and threw out data that showed a direct association between the MMR vaccine and autism. In August, 2014, I wrote in a blog post, “Now, there may be proof that the CDC not only knew about the link between the MMR vaccine and autism but they changed the data in a landmark 2004 study to hide the damning data. What did the heads of the CDC do? They altered the data and reported in 2004 (1) that there was no association between autism and the MMR vaccine. Who wrote this article? William Thompson, PhD, the whistleblower, was one of the authors of that 2004 study. He is reported to be suffering with regret and remorse over the damage that has been done to our children over the last ten years.”
The data that was altered showed a whopping 240% increase in autism cases among African American males who received the MMR vaccine before 36 months of age. Furthermore, there was a 69% increase risk in any male injected with MMR before 36 months of age. Guess which racial group has the highest incidence of autism? If you guessed African American males, you win the prize. Guess who suffers with more autism, boys or girls? If you guessed boys, you win again.

‘I would rather be dead than like this’: Teenager’s agony as she is left wheelchair-bound and feeling like an ’80-year-old’ as her parents claim controversial HPV vaccine is to blame
Zara Beattie, from Wigton, Cumbria was once a promising football player
Now the teenager struggles to stand up on her own and is largely bed bound
Her parents believe her symptoms started after she had the HPV vaccine
Since the jab, Zara suffers heart palpitations and severe pain all over her body
Experts say there is no link between the HPV vaccine and chronic illness
By Daisy Dunne For Mailonline

Mia, left paralyzed from the neck down after suffering a reaction to the HPV vaccine, has no feeling in her arms or legs and is unable to lift her head. Her Mother, Gini Blesky, says the symptoms of her debilitating illness all began after being given Gardasil. Parents! Please BE INFORMED now and share this crucial information with everyone you love. View this newly available docu-series right now and protect your beloved children: tinyurl.com/VaccinationEducation
#Gardasil #Cervarix #RevolutionForChoice #HearThisWell #VaccineInjury #VAXXED #INFORMEDconsent

Johns Hopkins Researcher Releases Shocking Report On Flu Vaccines
In 2015, a whole new slew of flu vaccines found themselves getting approved by the Federal Drug Administration. This isn’t an uncommon practice; most flu vaccines pass inspection every year. It’s well known advice that has been passed down from doctor to patient that the flu vaccine is something that we all should get, but it has been quickly surfacing that what’s in the vaccines–especially those from 2015 and after–might actually be more damaging then simply rolling the dice on getting the flu.
The ingredient that is getting the most flack is called an adjuvant. The particular one involved is called Squalene, and it has been linked to auto-immune disease side effects. In fact, it may have been used during chemical attacks in the Gulf War. Symptoms include chronic fatigue, muscle aches, and neurologic damage.
While it may be a contested subject, it remains that we aren’t really sure what’s going into these vaccines we’re being convinced should be used. A scientist who has been working at the Johns Hopkins School of Medicine, released a report sharing his views on the subject. And they aren’t pretty.
Here is an excerpt from yournewswire.com that summarizes aspects of Peter Doshi’s report. You can find the original report at the British Medical Journal’s site. Determine for yourself if the evidence he presents is credible or not…

WATCH NOW: http://bit.ly/2wqaSvA – Watch this free 7-part miniseries featuring over 60 vaccine experts to hear both sides of the vaccine debate. Playing through August 23rd. WATCH NOW: http://bit.ly/2wqaSvA

INFERTILITY – DISEASE – DEATH … Laura Hayes, Mother of vaccine-injured children, on a mission to end the vaccine holocaust! Share this LIFE-SAVING information with your loved ones and stay informed with this groundbreaking docu-series happening now: tinyurl.com/VaccinationEducation
“Would you allow something that could cause infertility, such as nonstick chemicals and solvents, to be injected into your child? Of course not. You know that you would never want to destroy your child’s future reproductive capabilities. However, millions of mothers across America are allowing doctors to inject their children with polysorbate 80, known to adversely affect fertility. And who knows what propylene glycol (antifreeze), Triton X100 (detergent), aluminum, mercury, foreign DNA fragments, and the myriad other vaccine ingredients do to one’s future reproductive ability, especially when injected in conjunction with polysorbate 80.
We know that the HPV vaccine has caused Primary Ovarian Failure (which is premature menopause) and amenorrhea (the prolonged cessation of a female’s menstrual cycle) in girls and young women, rendering them infertile, and possibly sterile for life. We know that tetanus vaccines given to girls and women in Kenya were laced with Human Chorionic Gonadotropin (HCG), rendering them sterile. How? Administering HCG via vaccination stimulates the production of antibodies to HCG, and these antibodies then cause the woman’s body to reject embryos, effectively sterilizing her. Such an HCG-laced tetanus vaccine is in actuality a contraception vaccine.
Do you think any of these Kenyan women was told that prior to vaccination? To add to the evilness and deception, the Kenyan women were given a 5-dose tetanus program spread over a number of years, versus the 2-3 dose norm. Clearly, those vaccines were being used for induced sterility and birth control without the girls’ and women’s knowledge or consent.
Does any parent or vaccine recipient really know what is in the vaccines being injected into their child or themselves? It’s no wonder pharmaceutical companies don’t test to see whether or not their vaccine products cause infertility, they already know the answer. Instead, they simply write “not tested for impairment of fertility” on their package inserts, and our unethical government regulators let them get away with that. Interestingly, we are seeing record numbers of couples struggling with infertility issues. Coincidence?
Would you allow something that could kill your baby to be injected into your otherwise healthy child? Of course not! Mothers would lay down their lives for their children, they don’t purposefully put them in harm’s way. However, millions of mothers across America are allowing doctors to inject their children with more and more vaccines, not knowing that each and every one carries the risk of death, even more so when combined, as they most often are.
Interestingly, we are seeing record numbers of babies who are dying before their 1st birthday in the U.S., including many of “SIDS” and “SBS” (the labels that unethical doctors and unethical medical examiners use for vaccine-induced deaths instead of calling them what they are…i.e. vaccine-induced deaths). Coincidence?
Now that we have discussed what is actually in vaccines, let’s talk once more about how parental instincts have been demeaned, grossly manipulated, and obliterated, specifically, about how parents have been grievously lied to and misled, to the point where parents are now allowing things that simply do not make sense.
Imagine looking from the outside in, and seeing a tiny newborn, small infant, or trusting toddler, being held down, painfully stuck with a needle multiple times, screaming so that its face is beet red with tears, all while the child’s parents not only watch, but due to being lied to and coerced, they participate in this atrocity! What must this do to the psyche and stress hormones of a child to have this happen, time and again, while the person he trusts most is not only allowing it, but participating in it?
What would you say if you walked by the window to my house, peered in, and saw my husband and me holding down our tiny baby on the dining room table, then roughly jabbing and injecting it multiple times with toxic cocktails and true witches’ brews of ingredients…all while our baby, or child of any age, screamed bloody murder, trying to escape our grip and savagery? I imagine you would whip out your cell phone, call the police, then try to barge into our home to stop the abuse! How is what I just described any different than what goes on every minute of every day in doctors’ offices and hospitals in our country and across the world? To be very clear, it isn’t.
To state it very plainly, vaccination is child abuse in the form of medical assault and battery. With regard to adults, when vaccination is carried out against one’s will or wishes, say for school admittance, job requirements, elder care and housing, or military admission, or when carried out with one who is hesitant, or with one who is unsuccessful in resisting and refusing, it also meets the legal definition for assault and battery.
We must begin to label these vaccine atrocities for what they are: blatant and inexcusable child abuse; medical assault and battery; and when death is the result for the vaccine recipient, involuntary manslaughter. These vaccine-induced injuries, illnesses, and deaths are iatrogenic in nature, meaning they are caused by doctors and nurses. Vaccinations are crimes against humanity, and there is no time to mince words about this fact.”
This is a MUST SEE docu-series – totally free! tinyurl.com/VaccinationEducation
#RevolutionForChoice #VaccineInjury #TheTruthAboutVaccines #VAXXED #Infertility

STUDY: Reality Trumping Establishment Vaccine “Facts”
The past week has offered glimpses of hope for the growing number of people who know they are being lied to by the mainstream medical establishment about vaccine safety. More people are now aware that the kind of rigorous testing required for drugs to be put on the market does not apply to vaccines, or that vaccines like the HPV shot were not properly tested against a saline placebo before approval by the US Food and Drug Administration (FDA).
Yet, the medical establishment continues to omit these facts and instead focuses on why vaccine hesitancy is on the rise. Studies are being done in an attempt to understand vaccine hesitancy and come up with solutions to the “problem” of poor vaccine uptake. In 2014, the Boston Globe ran the headline Doctors Still Hesitant to Urge HPV Vaccine for Teenagers, highlighting a survey from the US Centers for Disease Control and Prevention (CDC), in which the agency stated that the inoculation rate is ‘unacceptably low.’ In 2015, NPR ran the story titled Doctors, Not Parents, Are the Biggest Obstacle to the HPV Vaccine in response to a study published in the journal Cancer Epidemiology, Biomarkers & Prevention, which found that more than a quarter of pediatricians and family doctors do not strongly endorse the HPV vaccine.
A new study in the journal PLOS One titled Misinformation Lingers in Memory: Failure of Three Pro-vaccination Strategies is an eye-opener at how clueless the medical establishment appears to be as to why its vaccine propaganda is being rejected. In this study, the researchers compared three strategies in vaccine promotion: a) contrasting myths vs. “facts,” b) employing “fact” and icon boxes, and c) showing images of non-vaccinated sick children. It should be noted that when the study’s authors refer to “facts,” they are using the term to mean vaccine propaganda. Beliefs in the autism-vaccine link and in vaccines side effects, along with intention to vaccinate a future child, were evaluated both immediately after the “correction intervention” and after a 7-day delay to reveal possible backfire effects. The study concluded the following:
“Results show that existing strategies to correct vaccine misinformation are ineffective and often backfire, resulting in the unintended opposite effect…”

Study – The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
Highlights
•When DTP and OPV were introduced in Guinea-Bissau in 1981, allocation by birthday resulted in a natural experiment of being vaccinated early or late.
•Between 3 and 5 months of age, children who received DTP and OPV early had 5-fold higher mortality than still unvaccinated children.
•In the only two studies of the introduction of DTP and OPV, co-administration of OPV with DTP may have reduced the negative effects of DTP.
Few studies have examined what happened to child survival when DTP and OPV were introduced in low-income countries. These vaccines were introduced in 1981 in an urban community in Guinea-Bissau from 3 months of age in connection with 3-monthly weighing sessions. Children were therefore allocated by birthday to receive vaccines early or late between 3 and 5 months of age. In this natural experiment vaccinated children had 5-fold higher mortality than not-yet-DTP-vaccinated children. DTP-only vaccinations were associated with higher mortality than DTP + OPV vaccinations. Hence, DTP may be associated with a negative effect on child survival.
Results
Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) compared with not-yet-DTP-vaccinated children. Differences in background factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19)).
Conclusion
DTP was associated with increased mortality; OPV may modify the effect of DTP.

Dr. Buchwald testimony before the Quebec College of Physicians Medical Board:
Dr. Gerhard Buchwald takes the stand
A physician from Germany, Dr. Buchwald testifies through an interpreter. Dr. Lanctot tables his credentials as well as a copy of his book entitled “Vaccination: Business Based on Fear”. He is recognized as an expert on vaccination by the Committee.
Dr. Buchwald testifies that his experience includes being a medical counselor to an association of parents whose children have been injured or killed by vaccinations. He adds that he is aware of a thousand vaccination related injury cases and has had personal contact with 350 cases. In 150 of these cases, he wrote the medical opinion and acted as an advisor during the legal proceedings.
Dr Lanctot (L).: If you take this stand in your country, have you been reprimanded by the medical authorities?
B.: I wrote a paper entitled, “Vaccinations: A Crime Against our Children”. I received written reprimands from the College of Physicians… In Germany, we have a law called “Kronegesetz” in the Civil Code, which stipulates that everyone has the right to freely voice his or her opinion. When I was fed up with this nonsense with the College, I drew their attention to the fact that their responses were actually a breach of those sections of the law. German judges, who deal with these issues, are very touchy on this issue… It is impossible to suppress the free speech of a physician in a free country which is why the College knew that it would lose. They also knew that the press would really have a field day. Since then I’ve heard nothing more…
L.: You mentioned earlier that the first criterion in medicine is to do no harm… And you referred to these ethics in
He continues with a brief history of his experiences in general and describes how he got interested in the whole question of immunization. He recalls that after graduating from medical school, he was a supporter of vaccination policies, as was everyone else he knew. Then he relates to the Committee the story of the eldest of his three children, born in 1957, who at eighteen months received a smallpox vaccination and who, eight days later was no longer able to stand up in his crib. Until then, his son’s development had been absolutely normal:
“He fell sick with a post-vaccination encephalitis, and ever since, I have a completely destroyed human being at home.”
It was at that time that someone approached him to become a member of a protective association in Germany. It was through this group that he got to know other vaccination damage cases.

Study – Human papillomavirus vaccination and risk of autoimmune diseases: A large cohort study of over 2million young girls in France.
RESULTS:
Among 2,252,716 girls, 37% received HPV vaccine and 4,096 AID occurred during a mean follow-up time of 33months. The incidence of AID was not increased after exposure to HPV vaccination, except for Guillain-Barré syndrome (GBS) (incidence rate of 1.4 among exposed [20 cases] versus 0.4 per 100,000 PY among unexposed [23 cases]; adjusted HR: 3.78 [1.79-7.98]). This association persisted across numerous sensitivity analyses and was particularly marked in the first months following vaccination. Under the hypothesis of a causal relationship, this would result in 1-2 GBS cases attributable to HPV vaccine per 100,000 girls vaccinated.
CONCLUSIONS:
Our study provides reassuring results regarding the risk of AID after HPV vaccination, but an apparently increased risk of GBS was detected. Further studies are warranted to confirm this finding.

Study – Detection of contaminants in cell cultures, sera and trypsin.
Abstract
The aim of this study was standardization and application of polymerase chain reaction (PCR) for the detection of contaminants in cell cultures, sera and trypsin. Five PCR protocols were standardized to assess the presence of genetic material from mycoplasma, porcine circovirus 1 (PCV1), bovine leukemia virus (BLV) or bovine viral diarrhea virus (BVDV) in cell culture samples. PCR reactions for the genes GAPDH and beta-actin were used to evaluate the efficiency of nucleic acid extraction. The PCR protocols were applied to 88 cell culture samples from eight laboratories. The tests were also used to assess potential contamination in 10 trypsin samples and 13 fetal calf serum samples from different lots from five of the laboratories. The results showed the occurrence of the following as DNA cell culture contaminants: 34.1% for mycoplasma, 35.2% for PCV1, 23.9% for BVDV RNA and 2.3% for BLV. In fetal calf sera and trypsin samples BVDV RNA and PCV1 DNA was detected. The results demonstrated that cell culture, sera and trypsin used by different laboratories show a high rate of contaminants. The results highlight the need for monitoring cell cultures and controlling for biological contaminants in laboratories and cell banks working with these materials.

C-Span – April 6, 2000
Autism and Childhood Vaccines Witnesses testified about a theory that routine vaccinations may cause autism in a growing number of children. Parents spoke about their experiences with their own autistic children. Medical experts and researchers then testified about the scientific evidence of a link between vaccines and autism, often disagreeing on whether a causal link existed.

Alfred Lambremont Webre – EXPERT PANEL Forced Adult vaccinations are component of extermination program Refuse all vaccines

Vaccines-The True Weapons Of Mass Destruction
Dr.Rebecca Carley.
ADVERSE REACTIONS to immunizations are more common than many people realize.
Please visit her website: http://www.drcarley.com/

Biopersistence in the Brain of Aluminum Nanoparticles from Vaccines
Posted by Merinda Teller, Ph.D, MPH on Aug 14, 2017
In the 1990s, French clinicians and researchers began noticing and reporting on a mysterious inflammatory muscle disorder with a distinctive pathological pattern that later earned the name “macrophagic myofasciitis” or MMF.1 Myofasciitis refers to inflammation of muscles and their connective tissue (fascia).
Initially, the cause and features of MMF were unknown. Subsequent research by French investigators elucidated that the deltoid muscle lesions characteristic of MMF were secondary to intramuscular injection with vaccines containing aluminum hydroxide adjuvants.2 The lesions revealed both an ongoing local immune reaction along with long-term persistence of aluminum hydroxide at the injection site.2
An ongoing series of admirably methodical studies also have confirmed a number of other post-vaccination clinical symptoms associated with MMF.3 These disabling health problems include not just muscle pain but joint pain, chronic fatigue, autonomic nervous system dysfunction, autoimmunity, and cognitive dysfunction.4 The cognitive deficiencies experienced by MMF patients mirror the cognitive impairments that have been observed to result from chronic exposure to aluminum particles.5 Together, all of these dysfunctions are “paradigmatic” of an emerging aluminum-adjuvant-related syndrome that has come to be known as ASIA (autoimmune/inflammatory syndrome induced by adjuvants).

Finally! I’ve teased around the real reason polio began to paralyze people in the late 1800s and in this video, I explain it completely. It’s a crazy simple answer that’s so obvious, most people have looked right past it.
Watch Part 1:
https://www.facebook.com/MyIncredibleOpinionWithForrestMaready/videos/1902971670026604/
Watch Part 2:
https://www.facebook.com/MyIncredibleOpinionWithForrestMaready/videos/1903458489977922/
Watch Part 3:
https://www.facebook.com/MyIncredibleOpinionWithForrestMaready/videos/1904022136588224
Watch Part 4:
https://www.facebook.com/MyIncredibleOpinionWithForrestMaready/videos/1904510039872767/
Watch Part 5:
https://www.facebook.com/MyIncredibleOpinionWithForrestMaready/videos/1904999419823829/
Watch Part 6:
https://www.facebook.com/MyIncredibleOpinionWithForrestMaready/videos/1905574199766351/

#VaxXed #Tennessee #flu #medical
chiropractor fed up with vaccine harm!
Dr Humphries outs flu shot fail:https://youtu.be/QhNTV4ekYVc?t=157

#VaxXed #NorthCarolina #Nebraska