Association

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.

****************************************************

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 – VAXXED TV – What If I Harmed My Children

Study – Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal

Environmental Health – Apr 2005

Thomas M. Burbacher, Danny D. Shen, Noelle Liberato,
Kimberly S. Grant, Elsa Cernichiari, and Thomas Clarkson

Abstract
Thimerosal is a preservative that has been used in manufacturing vaccines since the 1930s. Reports have indicated that infants can receive ethylmercury (in the form of thimerosal) at or above the Environmental Protection Agency (EPA) guidelines for methylmercury (MeHg) exposure, depending on the exact vaccinations, schedule, and size of the infant. This study compared the systemic disposition and brain distribution of total and inorganic mercury in infant monkeys following thimerosal exposure with infants exposed to MeHg. Monkeys were exposed to MeHg (via oral gavage) or vaccines containing thimerosal (via i.m. injection) at birth and 1, 2, and 3 weeks of age. Total blood mercury (Hg) levels were determined 2, 4 and 7 days after each exposure. Total and inorganic brain Hg levels were assessed 2, 4, 7 or 28 days after the last exposure. The initial and terminal half-life of Hg in blood following thimerosal exposure was 2.1 and 8.6 days, which are significantly shorter than the elimination half-life of Hg following MeHg exposure at 21.5 days. Brain concentrations of total Hg were significantly lower by ~3-fold for the thimerosal-exposed infants when compared to the MeHg infants, while the average brain-to-blood concentration ratio was slightly higher for the thimerosal-exposed infants (3.5±1.0 vs. 2.5±0.6). A higher percentage of the total Hg in the brain was in the form of inorganic mercury for the thimerosal-exposed infants (34% vs 7%). The current study indicates that MeHg is not a suitable reference for risk assessment from exposure to thimerosal derived Hg. Knowledge of the toxicokinetics and developmental toxicity of thimerosal is needed to afford a meaningful assessment of the developmental effects of thimerosal-containing vaccines.

Study – Evolution of multiple sclerosis in France since the beginning of hepatitis B vaccination

US National Library of Medicine
National Institutes of Health – 14 Nov 2014

Dominique Le Houézeccorresponding author
REVAHB (“Réseau Vaccin Hépatite B” in French), 32 rue du Clos Herbert, 14000 Caen, France

Abstract
Since the implementation of the mass vaccination campaign against hepatitis B in France, the appearance of multiple sclerosis, sometimes occurring in the aftermath of vaccinations, led to the publication of epidemiological international studies. This was also justified by the sharp increase in the annual incidence of multiple sclerosis reported to the French health insurance in the mid-1990s. Almost 20 years later, a retrospective reflection can be sketched from these official data and also from the national pharmacovigilance agency. Statistical data from these latter sources seem to show a significant correlation between the number of hepatitis B vaccinations performed and the declaration to the pharmacovigilance of multiple sclerosis occurring between 1 and 2 years later. The application of the Hill’s criteria to these data indicates that the correlation between hepatitis B vaccine and multiple sclerosis may be causal.

Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents: A Pilot Case–Control Study

Douglas L. Leslie1*, imageRobert A. Kobre2, imageBrian J. Richmand2, imageSelin Aktan Guloksuz2 and imageJames F. Leckman2*

1 Department of Public Health Sciences, Pennsylvania State University College of Medicine, Hershey, PA, USA
2 Yale Child Study Center, Yale University School of Medicine, New Haven, CT, USA

Background: Although the association of the measles, mumps, and rubella vaccine with autism spectrum disorder has been convincingly disproven, the onset of certain brain-related autoimmune and inflammatory disorders has been found to be temporally associated with the antecedent administration of various vaccines. This study examines whether antecedent vaccinations are associated with increased incidence of obsessive–compulsive disorder (OCD), anorexia nervosa (AN), anxiety disorder, chronic tic disorder, attention deficit hyperactivity disorder, major depressive disorder, and bipolar disorder in a national sample of privately insured children.

Methods: Using claims data, we compared the prior year’s occurrence of vaccinations in children and adolescents aged 6–15 years with the above neuropsychiatric disorders that were newly diagnosed between January 2002 and December 2007, as well as two control conditions, broken bones and open wounds. Subjects were matched with controls according to age, gender, geographical area, and seasonality. Conditional logistic regression models were used to determine the association of prior vaccinations with each condition.

Results: Subjects with newly diagnosed AN were more likely than controls to have had any vaccination in the previous 3 months [hazard ratio (HR) 1.80, 95% confidence interval 1.21–2.68]. Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of AN, OCD, and an anxiety disorder. Several other associations were also significant with HRs greater than 1.40 (hepatitis A with OCD and AN; hepatitis B with AN; and meningitis with AN and chronic tic disorder).

Conclusion: This pilot epidemiologic analysis implies that the onset of some neuropsychiatric disorders may be temporally related to prior vaccinations in a subset of individuals. These findings warrant further investigation, but do not prove a causal role of antecedent infections or vaccinations in the pathoetiology of these conditions. Given the modest magnitude of these findings in contrast to the clear public health benefits of the timely administration of vaccines in preventing mortality and morbidity in childhood infectious diseases, we encourage families to maintain vaccination schedules according to CDC guidelines.

VAXXED TV – I can’t believe they are doing this!
Patricia Gua tells of her injuries from receiving the HEP-B vaccination.
Interview recorded on May 5th, 2017 in The United Kingdom

What If I Harmed My Children
Kelly Johnson, author of “What If?: I Harmed My Children” gives detailed accounts of her experiences with her kids which inspired her to write the book. You can find a copy of it for purchase or download here: http://a.co/6Fy23cJ
Interview recorded on May 5th, 2017 in The United Kingdom

I had every reaction documented
Liola shares about the details of her children’s reactions to vaccinations and the challenges they faced.
Interview recorded on May 5th, 2017 in The United Kingdom

It’s sad we have to learn the hard way
A mother shares her story about her children’s reactions to the vaccines.
Interview recorded on May 5th, 2017 in The United Kingdom

Know Your Body

Drunk on Toxins

Mark Blaxill

A Tribute To Polly Tommey

Dr Suzanne- more herd immunity

Vaccinated versus unvaccinated

****************************************************

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

****************************************************

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

Vaccine News – Study – Association of spontaneous abortion with receipt of inactivated influenza vaccine containing H1N1pdm09 in 2010-11 and 2011-12

Study – Human papilloma virus vaccine and primary ovarian failure: another facet of the autoimmune/inflammatory syndrome induced by adjuvants.

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

Colafrancesco S – 1, Perricone C, Tomljenovic L, Shoenfeld Y.
Author information
1 Zabludowicz Center for Autoimmune Diseases Sheba Medical Center, Tel-Hashomer, Israel; Rheumatology Unit, Department of Internal Medicine and Medical Specialities, Sapienza University of Rome, Rome, Italy.

Abstract
PROBLEM:
Post-vaccination autoimmune phenomena are a major facet of the autoimmune/inflammatory syndrome induced by adjuvants (ASIA) and different vaccines, including HPV, have been identified as possible causes.
METHOD OF STUDY:
The medical history of three young women who presented with secondary amenorrhea following HPV vaccination was collected. Data regarding type of vaccine, number of vaccination, personal, clinical and serological features, as well as response to treatments were analyzed.
RESULTS:
All three patients developed secondary amenorrhea following HPV vaccinations, which did not resolve upon treatment with hormone replacement therapies. In all three cases sexual development was normal and genetic screen revealed no pertinent abnormalities (i.e., Turner’s syndrome, Fragile X test were all negative). Serological evaluations showed low levels of estradiol and increased FSH and LH and in two cases, specific auto-antibodies were detected (antiovarian and anti thyroid), suggesting that the HPV vaccine triggered an autoimmune response. Pelvic ultrasound did not reveal any abnormalities in any of the three cases. All three patients experienced a range of common non-specific post-vaccine symptoms including nausea, headache, sleep disturbances, arthralgia and a range of cognitive and psychiatric disturbances. According to these clinical features, a diagnosis of primary ovarian failure (POF) was determined which also fulfilled the required criteria for the ASIA syndrome.
CONCLUSION:
We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry.

Study – Association of spontaneous abortion with receipt of inactivated influenza vaccine containing H1N1pdm09 in 2010-11 and 2011-12.

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

Donahue JG – 1, Kieke BA – 2, King JP – 3, DeStefano F – 4, Mascola MA – 5, Irving SA – 6, Cheetham TC – 7, Glanz JM – 8, Jackson LA – 9, Klein NP – 10, Naleway AL – 11, Weintraub E – 12, Belongia EA – 13.
Author information
1 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: donahue.james@mcrf.mfldclin.edu.
2 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: kieke.burney@mcrf.mfldclin.edu.
3 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: king.jennifer@mcrf.mfldclin.edu.
4 Centers for Disease Control and Prevention, Immunization Safety Office, 1600 Clifton Road NE, MS-D26 Atlanta, GA 30333, United States. Electronic address: fxd1@cdc.gov.
5 Marshfield Clinic, Department of Obstetrics and Gynecology, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: mascola.maria@marshfieldclinic.org.
6 Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, United States. Electronic address: stephanie.a.irving@kpchr.org.
7 Kaiser Permanente Southern California, 100 S. Los Robles Ave., 2nd Floor, Pasadena, CA 91101, United States. Electronic address: craig.t.cheetham@kp.org.
8 Kaiser Permanente Colorado, 10065 E. Harvard, Suite 300, Denver, CO 80231, United States. Electronic address: jason.m.glanz@kp.org.
9 Group Health Research Institute, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101, United States. Electronic address: jackson.l@ghc.org.
10 Kaiser Permanente Northern California, 1 Kaiser Plaza, 16th Floor, Oakland, CA 94612, United States. Electronic address: Nicola.Klein@kp.org.
11 Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, United States. Electronic address: Allison.Naleway@kpchr.org.
12 Centers for Disease Control and Prevention, Immunization Safety Office, 1600 Clifton Road NE, MS-D26 Atlanta, GA 30333, United States. Electronic address: eiw8@cdc.gov.
13 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: belongia.edward@marshfieldclinic.org.

Abstract

INTRODUCTION:
Inactivated influenza vaccine is recommended in any stage of pregnancy, but evidence of safety in early pregnancy is limited, including for vaccines containing A/H1N1pdm2009 (pH1N1) antigen. We sought to determine if receipt of vaccine containing pH1N1 was associated with spontaneous abortion (SAB).
METHODS:
We conducted a case-control study over two influenza seasons (2010-11, 2011-12) in the Vaccine Safety Datalink. Cases had SAB and controls had live births or stillbirths and were matched on site, date of last menstrual period, and age. Of 919 potential cases identified using diagnosis codes, 485 were eligible and confirmed by medical record review. Exposure was defined as vaccination with inactivated influenza vaccine before the SAB date; the primary exposure window was the 1-28days before the SAB.
RESULTS:
The overall adjusted odds ratio (aOR) was 2.0 (95% CI, 1.1-3.6) for vaccine receipt in the 28-day exposure window; there was no association in other exposure windows. In season-specific analyses, the aOR in the 1-28days was 3.7 (95% CI 1.4-9.4) in 2010-11 and 1.4 (95% CI 0.6-3.3) in 2011-12. The association was modified by influenza vaccination in the prior season (post hoc analysis). Among women who received pH1N1-containing vaccine in the previous influenza season, the aOR in the 1-28days was 7.7 (95% CI 2.2-27.3); the aOR was 1.3 (95% CI 0.7-2.7) among women not vaccinated in the previous season. This effect modification was observed in each season.
CONCLUSION:
SAB was associated with influenza vaccination in the preceding 28days. The association was significant only among women vaccinated in the previous influenza season with pH1N1-containing vaccine. This study does not and cannot establish a causal relationship between repeated influenza vaccination and SAB, but further research is warranted.

VAXXED TV – My son seized on the table after vaccines #vaxxed #DidYouKnow #Praybig

My 2 month old son died following vaccinations #vaxxed #DidYouKnow #Praybig

Mandates would have killed my son #vaxxed #DidYouKnow #Praybig

One of my children is vaccinated and one is not #vaxxed #DidYouKnow #Praybig

Vaccinated without my consent #vaxxed #DidYouKnow #Praybig

Vaccines injured my family #vaxxed #DidYouKnow #Praybig

Flu shot injured me #vaxxed #DidYouKnow #Praybig

My son has autism from vaccines #vaxxed #DidYouKnow #Praybig

Vaccines destroyed my family #vaxxed #DidYouKnow #praybig

The medical profession killed my son #vaxxed #DidYouKnow #Praybig

How to accept Jesus Christ as your personal Saviour

Vaccine News – BREAKING: Robert F. Kennedy Jr. calls for extradition of CDC vaccine criminal mastermind Poul Thorsen to face charges of criminal scientific misconduct

Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis
Abstract
Routine childhood vaccination against measles, mumps and rubella has virtually abolished virus-related morbidity and mortality. Notwithstanding this, we describe here devastating neurological complications associated with the detection of live-attenuated mumps virus Jeryl Lynn (MuVJL5) in the brain of a child who had undergone successful allogeneic transplantation for severe combined immunodeficiency (SCID). This is the first confirmed report of MuVJL5 associated with chronic encephalitis and highlights the need to exclude immunodeficient individuals from immunisation with live-attenuated vaccines. The diagnosis was only possible by deep sequencing of the brain biopsy. Sequence comparison of the vaccine batch to the MuVJL5 isolated from brain identified biased hypermutation, particularly in the matrix gene, similar to those found in measles from cases of SSPE. The findings provide unique insights into the pathogenesis of paramyxovirus brain infections

To my friends in Australia: the vaccine war deepens
by Jon Rappoport
September 20, 2017
The string of abuses laid on citizens of Australia by their government grows almost week by week.
Now, parental rights to raise children, without interference from the State, is under a new form of attack. This must be resisted.
Schools are bringing doctors on board, as a permanent feature. Young children will be subjected to medical diagnoses and treatment, without consent or approval from parents, even if those parents actively object. The State is stealing the role of guardian.
The Herald Sun reports. Read carefully:
“DOCTORS will have the power to treat students as young as 12 in schools even if parents refuse their consent.”
“GPs will consult at 100 Victoria high schools for up to one day a week as part of a $43.8 million program.”
“Guidelines released on Thursday show that even if a parent ‘expressly states’ that a doctor should not [examine] their child, the GP can if they deem the teen mature enough.”
“’Any student who wants to see the GP will be permitted to make an appointment,’ the policy said.”
“The GP will decide if the young person is mature enough to provide consent to any medical treatment for the prevailing issue.”
A young child “giving consent?” This is supposed to be “informed consent” when facing off with an adult doctor?

AUSTRALIAN BABY GIRL MURDERED BY VACCINE!

Australian Medical Association: Class Action against the AMA for Vaccine Injury
Why this is important
The health and well being of our beautiful and innocent Australian children are paramount to all Australians.
It’s obvious to anyone with intelligence that there is an epidemic of ill health occurring with children around the World and particularly, with our Australian children which can be traced to Vaccine Injury through multiplying forced application of a large and growing number of untested combined vaccines riddled with known carcinogens and poisons being directly administered into the blood streams of our Australian babies and children.
Modern medical, psychological, health and nutritional sciences have grave questions as to the efficacy of these vaccines and in fact clearly, illustrate that these vaccines are in general unnecessary and poisonous and in fact interfere with the natural immune system of the human being.
We call for a moratorium of forced vaccination of Australian children and the initiation of major testing initiatives in Australia and elsewhere to prove any efficacy of injecting these poisons into our Children.
We are appalled at the support of the Australian Medical Association of these unscientific and abusive injurious procedures causing epidemic harm to our beautiful and innocent

Australian Children and demand:
1. The AMA stop all support for these appalling procedures.
2. Pay full and appropriate damages to the Australian Parents and Children injured by these AMA supported procedures.
3. Instigate a full review of these appalling procedures, based particularly on the evidence presented in the film ‘VAXXED’ and the documentation series ‘The Truth about Vaccines’, ‘Vaccines Revealed’, ‘Trace Amounts’, and ‘Vaccine Syndrome’.
4. Place the health and well‐being of our Australian children as paramount before commercial gain by Pharmaceutical and Medical industries and professionals

HEROIC #ANTIVACCINE WARRIORS SMACKDOWN EUGENICISTS!

BOMBSHELL: Flu vaccines don’t work in the elderly, new science shows … U.S. media

Tuesday, September 19, 2017
(Natural News) The Centers for Disease Control and Prevention (CDC), the same authority that determines the national vaccination schedule, notes that those most at risk of complications from the flu virus are children younger than 5, but particularly those under the age of 2; pregnant women; people in nursing homes; and adults over the age of 65. The elderly are therefore among the most vulnerable members of society when it comes to influenza. It makes sense, therefore, to believe that the flu vaccination would need to be especially effective for that demographic.
A recent report by Public Health England (PHE), however, has revealed that though it seems to have been slightly more effective at preventing influenza among children than in previous years, last year’s flu shot was totally ineffective for the elderly.
Experts believe that the shot was ineffective because it did not protect against the most common circulating strain – the H3 strain. This is because the flu shot is essentially a game of chance each year; experts have to try to predict in advance which three strains of the virus will be in circulation in the coming winter. Even in a good year, their strike rate is only 50 percent.
Of course, instead of admitting the uselessness of the vaccine, health professionals are blaming the elderly themselves.

BREAKING: Robert F. Kennedy Jr. calls for extradition of CDC vaccine criminal mastermind Poul Thorsen to face charges of criminal scientific misconduct
Thursday, September 21, 2017
(Natural News) Robert F. Kennedy Jr. (RFK Jr.) and his team at World Mercury Project have drafted up a new report that reveals the criminal conduct of CDC consultant and vaccine cultist Poul Thorsen. With an overwhelming body of evidence, RFK Jr is calling for Attorney General Jeff Sessions to take action and extradite Poul Thorsen so he can face up to his numerous crimes. In a statement, RFK Jr declared, “World Mercury Project calls upon Attorney General Jeff Sessions to extradite Thorsen back to the U.S. to face prosecution. We also call upon Secretary of Health and Human Services Dr. Tom Price to retract the Thorsen-affiliated autism research papers that are the fruit of illegally conducted research.”
What has World Mercury Project (WMP) uncovered? In addition to evidence of criminal activity, new findings by WMP show that Thorsen and his team never obtained permission from the Institutional Review Board (IRB) to do their studies, published in 2002 by the New England Journal of Medicine and in 2003 by the journal Pediatrics. As WMP explains, this alone detracts from the validity of their research, but to make matters worse, records indicate that the CDC was complicit in covering up this little “mistake.” According to the WMP report, CDC staff realized that no IRB approval had ever been granted for Thorsen’s research, but the error was simply ignored and the studies were never retracted. Freedom of Information Act documents show that supervisors at the CDC looked the other way and actively tried to conceal what transpired.

Criminal Conduct – Poul Thorsen
Robert F. Kennedy, Jr. and World Mercury Project Issue Report Regarding New Evidence of Ongoing Corruption and Scientific Misconduct at CDC
Kennedy hopes new evidence and a fresh look at criminal misconduct will result in law enforcement action, rigorous and transparent vaccine safety science, and safer vaccines.
In a new report released September 18, 2017, Robert F. Kennedy, Jr. and his team outlined various criminal acts on the part of employees and consultants for the Centers for Disease Control and Prevention (CDC) whose questionable ethics and scientific fraud have resulted in untrustworthy vaccine safety science.

PDF – Poul Thorsen Fugitive Researcher
UPDATE AUGUST 2017
BETH CLAY FOR THE WORLD MERCURY PROJECT

HighWire with Del Bigtree – Jimmy Kimmel the Hypocrite. Vaccine Risk Now Mainstream!

One vaccine injection could carry many doses
Microparticles created by new 3-D fabrication method could release drugs or vaccines long after injection.
Anne Trafton | MIT News Office
September 14, 2017
MIT engineers have invented a new 3-D fabrication method that can generate a novel type of drug-carrying particle that could allow multiple doses of a drug or vaccine to be delivered over an extended time period with just one injection.
The new microparticles resemble tiny coffee cups that can be filled with a drug or vaccine and then sealed with a lid. The particles are made of a biocompatible, FDA-approved polymer that can be designed to degrade at specific times, spilling out the contents of the “cup.”
“We are very excited about this work because, for the first time, we can create a library of tiny, encased vaccine particles, each programmed to release at a precise, predictable time, so that people could potentially receive a single injection that, in effect, would have multiple boosters already built into it. This could have a significant impact on patients everywhere, especially in the developing world where patient compliance is particularly poor,” says Robert Langer, the David H. Koch Institute Professor at MIT.
Langer and Ana Jaklenec, a research scientist at MIT’s Koch Institute for Integrative Cancer Research, are the senior authors of the paper, which appears online in Science on Sept. 14. The paper’s lead authors are postdoc Kevin McHugh and former postdoc Thanh D. Nguyen, now an assistant professor of mechanical engineering at the University of Connecticut.

the news network

the news network

Association

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

Vaccine News – VAXXED TV – What If I Harmed My Children

Vaccine News – I saw an immediate change – VAXXED TV

Vaccine News – BREAKING: Robert F. Kennedy Jr. calls for extradition of CDC vaccine criminal mastermind Poul Thorsen to face charges of criminal scientific misconduct