Vaccine News – VAXXED TV – I’ve waited 30 years to tell my story & A PROFILE OF AUTISM IN AUSTRALIA

Journal of Molecular and Genetic Medicine – February 19, 2014

Study – Review of Vaccine Induced Immune Overload and the Resulting Epidemics of Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases

Abstract
There has been an epidemic of inflammatory diseases that has paralleled the epidemic on iatrogenic immune stimulation with vaccines. Extensive evidence links vaccine induced immune over load with the epidemic of type 1 diabetes. More recent data indicates that obesity, type 2 diabetes and other components of metabolic syndrome are highly associated with immunization and may be manifestations of the negative feedback loop of the immune system reacting to the immune overload. The epidemic of diabetes/prediabetes appears to be accelerating at a time when the prevalence of obesity has stabilized, indicating that the negative feedback system of the immune system has been over whelmed. The theory of vaccine induced immune overload can explain the key observations that have confounded many competing hypothesis. The current paper reviews the evidence that vaccine induced immune overload explains the disconnect between the increase in prediabetes and nonalcoholic fatty liver at a time when the obesity epidemic is waning in children.

 

 

 

 

Dr Dale Brown – A Young Doctor Dies after Receiving the Flu Shot
A doctor with a true heart of service to help people has died after suffering a serious paralytic injury after the flu vaccine. The US Court of Federal Claims “Vaccine Court” has awarded $500,000 to the beneficiary of this doctor after her vaccine injuries lead to her paralysis, multiple organ failure and eventual death.
This is heartbreak for anyone. To see such a good, caring, and servant to the Lord be taken from this world far before her time. I have read this doctor’s obituary and anyone can see that this woman was a very caring person who had a heart to serve others. What should upset and frustrate any of us is when you see the fact that vaccines like the flu vaccine are forces against unwilling nurses, doctors and other hospital staff.
The fact is that the flu vaccine is worthless, one could potentially argue that “yes the flu vaccine does cause injuries and even deaths, but it’s all for the ‘greater good’.” But the fact is the research proves that healthcare workers are not healthier and their patients are NOT protected by the vaccines.
Links to referenced research articles can be found at thewilddoc.com.
Visit thewilddoc.com or call 931-591-2010 to setup an online or in-office consultation.

Check out our other videos:
Are Vaccines Being Used For Population Control?

 

 

 

 

 

Flu Shots Are Fraud Part 1

 

 

A PROFILE OF AUTISM IN AUSTRALIA

Autism may present substantial challenges for those affected, their families and friends. It can also have an impact on a person’s education, as well as their social and economic participation.
In recent years an increasing number of Australians with Autism have been identified. There are numerous factors that may contribute to this increase in reporting. The results from the 2015 Survey of Disability, Ageing and Carers can provide insights into this complex and varied condition.

There were 164,000 Australians with Autism in 2015
The number of Australians with Autism increased by 42.1% since 2012
4 out of 5 people with Autism were male
More than 3/4 of those with Autism were young (5-24 years)
Almost 2/3 of those with Autismhad profound or severe disability
Almost 3/4 of those with Autism needed help with cognitive and emotional tasks
Almost of half of those with Autism needed help with communication
Around 4 out of 5 children2 with Autism had difficulties at school
40.8% of people with Autism participated in the workforce, compared with 83.2% people with no reported disability

Estimated Prevalence of Children With Diagnosed Developmental Disabilities in the United States, 2014–2016

Key findings Data from the National Health Interview Survey
● During 2014–2016, the prevalence of children aged 3–17 years who had ever been diagnosed with a developmental disability increased from 5.76% to 6.99%.
● During this same time, the prevalence of diagnosed autism spectrum disorder and intellectual disability did not change significantly.
● The prevalence of autism spectrum disorder, intellectual disability, other developmental delay, and any developmental disability was higher among boys compared with girls.
● The prevalence of any developmental disability was lower among Hispanic children compared with children in all other race and ethnicity groups.

 

 

 

VAXXED TV – Gardasil HPV vaccine killed my daughter

 

 

 

 

 

 

Multiple injuries in my family

My daughter is unvaccinated and super healthy

Immigration vaccines injured me

HERD IMMUNITY: Whooping Cough
Dr. Suzanne Humphries, MD discusses the fallacies about herd immunity and it’s relation to whooping cough.

Vaxxed/Unvaccinated in my family

 

Story and Q&A

I’ve waited 30 years to tell my story

My Unvaccinated 25 year old daughter

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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.

 

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Vaccine News – Study – The Blood-Brain Barrier Bottleneck in Brain Drug Development

Study – Systematic review and meta-analysis links autism and toxic metals and highlights the impact of country development status: Higher blood and erythrocyte levels for mercury and lead, and higher hair antimony, cadmium, lead, and mercury.

US National Library of Medicine
National Institutes of Health – 3 Oct 2017

Saghazadeh A – 1, Rezaei N – 2.
Author information
1 Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran; MetaCognition Interest Group (MCIG), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
2 Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Systematic Review and Meta-analysis Expert Group (SRMEG), Universal Scientific Education and Research Network (USERN), Boston, MA, USA. Electronic address: Rezaei_nima@tums.ac.ir.

Abstract
BACKGROUND:
Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder that affects cognitive and higher cognitive functions. Increasing prevalence of ASD and high rates of related comorbidities has caused serious health loss and placed an onerous burden on the supporting families, caregivers, and health care services. Heavy metals are among environmental factors that may contribute to ASD. However, due to inconsistencies across studies, it is still hard to explain the association between ASD and toxic metals. Therefore the objective of this study was to investigate the difference in heavy metal measures between patients with ASD and control subjects.
METHODS:
We included observational studies that measured levels of toxic metals (antimony, arsenic, cadmium, lead, manganese, mercury, nickel, silver, and thallium) in different specimens (whole blood, plasma, serum, red cells, hair and urine) for patients with ASD and for controls. The main electronic medical database (PubMed and Scopus) were searched from inception through October 2016.
RESULTS:
52 studies were eligible to be included in the present systematic review, of which 48 studies were included in the meta-analyses. The hair concentrations of antimony (standardized mean difference (SMD)=0.24; 95% confidence interval (CI): 0.03 to 0.45) and lead (SMD=0.60; 95% confidence interval (CI): 0.17 to 1.03) in ASD patients were significantly higher than those of control subjects. ASD patients had higher erythrocyte levels of lead (SMD=1.55, CI: 0.2 to 2.89) and mercury (SMD=1.56, CI: 0.42 to 2.70). There were significantly higher blood lead levels in ASD patients (SMD=0.43, CI: 0.02 to 0.85). Sensitivity analyses showed that ASD patients in developed but not in developing countries have lower hair concentrations of cadmium (SMD=-0.29, CI: -0.46 to -0.12). Also, such analyses indicated that ASD patients in developing but not in developed lands have higher hair concentrations of lead (SMD=1.58, CI: 0.80 to 2.36) and mercury (SMD=0.77, CI: 0.31 to 1.23). These findings were confirmed by meta-regression analyses indicating that development status of countries significantly influences the overall effect size of mean difference for hair arsenic, cadmium, lead, and mercury between patients with ASD and controls.
CONCLUSION:
The findings help highlighting the role of toxic metals as environmental factors in the etiology of ASD, especially in developing lands. While there are environmental factors other than toxic metals that greatly contribute to the etiology of ASD in developed lands. It would be, thus, expected that classification of ASD includes etiological entities of ASD on the basis of implication of industrial pollutants (developed vs. developing ASD).

Study – Autism: A form of lead and mercury toxicity

Environmental Toxicology and Pharmacology
Volume 38, Issue 3, November 2014, Pages 1016–1024

Highlights
•Autism is a developmental disability characterized by severe, pervasive deficits in social interaction and communications.
•Lead and mercury two of the most common heavy metals in the environment.
•Lead and mercury can lead to autistic disorders.
•Many risk factors contribute to the high level of heavy metals in autistic children.
•Defect in the metabolism of the heavy metals in autistic children also contribute to the high level of these heavy metals in their body.
•Chelating agents can be used in the treatment of the autistic disorders.

Abstract
Aim
Autism is a developmental disability characterized by severe deficits in social interaction and communication. The definite cause of autism is still unknown. The aim of this study is to find out the relation between exposure to Lead and/or mercury as heavy metals and autistic symptoms, dealing with the heavy metals with chelating agents can improve the autististic symptoms.

Method
Blood and hair samples were obtained from 45 children from Upper Egypt with autism between the ages of 2 and 10 years and 45 children served as controls in the same age range, after taken an informed consent and fill a questionnaire to assess the risk factors. The samples were analyzed blindly for lead and mercury by using atomic absorption and ICP-MS. Data from the two groups were compared, then follow up of the autistic children after treatment with chelating agents were done.

Results
The results obtained showed significant difference among the two groups, there was high level of mercury and lead among those kids with autism. Significant decline in the blood level of lead and mercury with the use of DMSA as a chelating agent. In addition, there was decline in the autistic symptoms with the decrease in the lead and mercury level in blood.

Conclusion
Lead and mercury considered as one of the main causes of autism. Environmental exposure as well as defect in heavy metal metabolism is responsible for the high level of heavy metals. Detoxification by chelating agents had great role in improvement of those kids.

Study – The Blood-Brain Barrier: Bottleneck in Brain Drug Development

US National Library of Medicine
National Institutes of Health – Jan 2005

William M. Pardridge
Department of Medicine, UCLA, Los Angeles, California 90024
Address correspondence and reprint requests to William M. Pardridge, M.D., UCLA Warren Hall, 13-164, 900 Veteran Avenue, Los Angeles,

ABSTRACT
Summary: The blood-brain barrier (BBB) is formed by the brain capillary endothelium and excludes from the brain ∼100% of large-molecule neurotherapeutics and more than 98% of all small-molecule drugs. Despite the importance of the BBB to the neurotherapeutics mission, the BBB receives insufficient attention in either academic neuroscience or industry programs. The combination of so little effort in developing solutions to the BBB problem, and the minimal BBB transport of the majority of all potential CNS drugs, leads predictably to the present situation in neurotherapeutics, which is that there are few effective treatments for the majority of CNS disorders. This situation can be reversed by an accelerated effort to develop a knowledge base in the fundamental transport properties of the BBB, and the molecular and cellular biology of the brain capillary endothelium. This provides the platform for CNS drug delivery programs, which should be developed in parallel with traditional CNS drug discovery efforts in the molecular neurosciences.

VAXXED TV – Nick Johansen #vaxxed #PrayBig

Dr. Judy Mikovits, PhD Research Scientist at #TxMFA #TxMFA2017
Dr. Judy Mikovits, PhD research scientist, dives deep into the crude science of vaccination

Austin Bennett #vaxxed #PrayBig

Dawn Richardson

David Oldham

Barbara Loe Fisher #vaxxed #truth #science #praybig

Q&A vaccine syndrome

Global Vaccine Initiative Houston Protest #TxMFA #TxMFA2017
Jonathan Tommey and The Vaxxed Team hit the ground running at the Texas Medical Freedom Alliance world symposium in Housant, Texas.
They discusses vaccine safety concerns with our #TexasPeeps protesting on the ground and also interview medical doctor, Jim Meehan, M.D. with regard to his passion for exposing the deception endemic to the present vaccine paradigm.

Glaxo’s Vaccine Trials survivor speaks out
David tells his story and presents documentation of his history going through the Glaxo’s trials. His mother was told he had passed as an infant here they kept him as an orphan until 4 years old.
Interview recorded on May 5th, 2017 in The United Kingdom

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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 – Everything You’ll Need to Know about Vaccines

Pet owner spreading vaccination awareness after senior pet’s death
By Alyssa Goard and Nadine Bonewitz Published: September 29, 2017,
AUSTIN (KXAN) — Joann Saathoff’s 14-year-old Pomeranian, Lexy, died on Sept. 24, and she believes the round of vaccinations Lexy received 12 days earlier led to her death.
Now Saatoff is trying to raise awareness about the options owners of senior pets have when it comes to getting shots for their furry friends.
It all started when Lexy went in for her annual check up. She was evaluated by the vet first, who said Lexy was in good health. Then Lexy received five shots, the same exact group of shots she’d received the year before. Within a few hours, Saathoff said her active dog had grown lethargic.
She took Lexy back to the vet the next day and they said her reaction was common, so they gave her an antibiotic and fluids. But Lexy’s condition continued to decline, the six pound dog threw up everything she ate. When she died, she weighed only three pounds. Saathoff said the cause of Lexy’s death was starvation, but the veterinarian told her that it started with the vaccinations which were “too much for her system.”
Saathooff began researching.
“I found out there’s a lot of senior dogs out there that can’t handle the full regimen of vaccinations,” she said.
She says she doesn’t blame her vet, she just wishes she knew about other options. Now she’s urging other pet owners to ask about what is best for their pets.
“My message to the community is you have options with your senior level dogs,” she said.

23 ‘must-see’ vaccine documentaries
By Britny Murray
In no particular order, here are 23 highly informative, must-see vaccine documentaries that you could share with your firends.
They all have to do with various factors of vaccination – evidence,, efficacy, injuries, health effects and medicinal politics.
They come with a brief description pulled from YouTube. Most of them are free and featured here in-full.

Deadly Immunity – Government Cover-Up Of A Mercury/Autism Scandal
Sep 30, 2017
World Mercury Project note: With the ongoing mainstream media blackout on questions regarding vaccine safety, we want to remind our followers of the publication–and subsequent retraction–of Robert F. Kennedy, Jr.’s 2005 article “Deadly Immunity” in Salon. The history of repression of crucial vaccine safety data runs deep. The article laid out the scientific link between thimerosal and childhood neurological disorders and published explosive excerpts from the transcripts from the CDC’s secretive June 2000 Simpsonwood conference which brought together government public health officials, vaccine manufacturers and professional medical associations. The article was groundbreaking at the time and received lots of media attention for uncovering the cozy relationship between government and industry at the expense of children’s health. Even though a dozen years have passed, the article’s facts have stood the test of time. An important read for people new to the movement and long-time advocates alike.

Transcript – Scientific Review of Vaccine Safety Datalink Information

Everything You’ll Need to Know about Vaccines
With this enormous effort in marketing vaccines and the money spent sponsoring large cohort studies showing that vaccines are always safe and effective, never expressing anything negative, and in some countries enforcing mandatory vaccine schedules wouldn’t any normal sensible person become a little suspicious and ask themselves..ARE THEY TRYING TO HIDE SOMETHING ??. It took the medical mafia 12 years to remove the evidence in Wakefield and Walker smith’s study analysis of 12 children with serious intestinal abnormalities that their parents confirmed had developed after receiving the MMR vaccine. The British media found a scapegoat using British journalist Brian Deer to uncover a potential conflict of interest to ‘blow the smoke away ‘ from the findings of the study. At the time autism was on the rise without explanation 6.2/10,000 births in 1990 to 42.5/10,000 births in 2001..for the most part the vaccine marketing machine ignored any correlation or causality toward their glorious vaccines. Why was Merck allowed to manufacture a Vaccine that included a benign children’s disease when the CDC confirmed there was no need to protect against Mumps, but the MMR vaccine was allowed anyway to be included in CDC’s vaccine schedule.

Appology to Polly Tommy
Gross misconduct from the Australian Government

Hammond vaccine terror #vaxxed #vaxxedperiscope

Donations to help our case and cause
Hi,
My name is Tanya and on the 26th of September 2012, James my son was born 8 weeks premature weighing in at just 2.4oz.
We live in a remote mining community in southern WA called Kalgoorlie and Ben, my beautiful husband, worked in the mines and because our son was born prem, he had to have a dTap vaccination and that’s just what you do. So just to be safe, as our entire family was protected and as good parents we believed we were, we always did the right thing.
James ended up and is doing fine but Ben, a healthy 34-year-old loving father and beautiful husband, sadly and totally unknowingly suffered the worst fate possible.
Both reported and recorded by the CDC (Centre for Disease Control) on their website, Ben had developed post vaccination ADEM (Acute Disseminated Encephalomyelitis) – our lives were shattered!
By October the 11th, 2012, Ben was classified a quadriplegic and since then, his health mentally, emotionally and physically has deteriorated so bad, that our lives will never be the same again.
Our vows in sickness and in health, no longer see any of the later and I’m now a full-time carer for Ben, no different than he would have done for me because our love for each other was so strong, but this curveball of life has put us to the test.
We’ve lost so much and are on the brink of extinction. We’re in surmounting debt, unable to work because we have 5 children and can’t afford childcare to work and bring home anything because the growing costs to care for Ben are not met with any government support.

Girl, 8, left with no skin after horrific allergic reaction to childhood vaccination meant it fell off when mum touched her
By Erin Elizabeth – September 26, 2017
At 18 months old, Isabel Olesen of Melbourne, Australia was taken to her pediatrician’s office for routine vaccinations (the kind that almost never cause a reaction and yet, our website is FULL of children who have suffered or died from very “rare” vaccine reactions) that ended up leaving her partially blind and covered with painful blisters all over her body, just 48 hours later.
Part of the problem with the one size fits all vaccine schedule is that you can’t tell when a child has Stevens-Johnson Syndrome (SJS) – a rare but life-threatening allergic reaction to medication or an infection. And Isabel had the worst form of SJS that doctors had ever seen. In fact, when Mom Edwina would touch her daughter, her skin would fall off. 1
It took three months of fighting for her life in the hospital, but even though Isabel lost the majority of her sight (SJS can break down the membranes around the eyes and cause them to become extremely dry) and needed to learn to walk, eat, and talk all over again- she’s now a healthy second grader who loves to ride her bike and run triathlons.

Real News with David Knight – EXPOSED: Secretive Vax Court
Wayne Rohde, author of “The Vaccine Court”, exposing the origins of the little known court that is the only recourse to those who have been harmed by vaccines. Wayne also explains what happened with the Somali population in Minnesota and why they refused vaccines.

TWO CHILDREN MURDERED VIA VACCINES IN KENYA!

Big Pharma Executive Blows Whistle on Vaccines: ‘Vaccinations are Deadly’ Pfizer Vice

President Dr. Peter Rost exposes dangers of Gardsil inoculation By: Jay Greenberg |@NeonNettle on 23rd September 2017
The former vice president of the world’s largest pharmaceutical company has blown the whistle to expose the true dangers of mandatory vaccinations. Dr. Peter Rost lifted the lid on vaccines and revealed that the Gardasil inoculation, in particular, is in fact, “deadly”. In a shocking exposé from one of the highest-ranking whistleblowers to date, Rost has also claimed that Big Pharma is purposely keeping the public unhealthy so they can make a fortune from continual treatments of illnesses rather than curing them. Dr. Rost made the revelations during an interview for the “One More Girl” documentary in which he candidly discussed how the main objective for vaccines and pharmaceutical drugs is to keep the public in a constant state of dis-ease. Rost also likened mandatory vaccinations to “child abuse” saying; “I would never vaccinate my children”

 

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 – Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013

An interview with Robert Kennedy Jr. on vaccines
By Helen Branswell
In the early days of 2017, proponents of vaccination were deeply concerned. Donald Trump, who has long espoused a debunked link between vaccines and autism, was set to enter the White House. He met with environmental activist Robert Kennedy Jr., who has for years argued that vaccines can cause a range of developmental and other health conditions. Kennedy emerged to report he’d been asked to chair a commission into vaccine safety.
But seven months later, no such commission has been appointed and the crisis-mired White House has declined to say whether the plan has been shelved.
STAT contacted Kennedy to see where plans stood. He would only speak on condition that STAT publish the interview in a Q&A format. He argued that his assertions — which are disputed as a misreading of the scientific literature by many mainstream scientists — have been misquoted and misrepresented in the media.
Here is STAT’s conversation with Kennedy. It has been lightly edited, for length and readability.
The question I want to ask you relates to the vaccine safety commission that you had announced in January that you were going to head, after you met with then President-elect Trump. It’s been a number of months now, and there hasn’t been any further public announcement. And so we’ve been wondering: Where does this stand?
I’ve had no discussions specifically about the vaccine safety commission, probably since February. I’ve spoken to the White House about other issues of vaccine safety and had a number of follow-up meetings.

Study – The putative role of environmental aluminium in the development of chronic neuropathology in adults and children. How strong is the evidence and what could be the mechanisms involved?
Abstract
The conceptualisation of autistic spectrum disorder and Alzheimer’s disease has undergone something of a paradigm shift in recent years and rather than being viewed as single illnesses with a unitary pathogenesis and pathophysiology they are increasingly considered to be heterogeneous syndromes with a complex multifactorial aetiopathogenesis, involving a highly complex and diverse combination of genetic, epigenetic and environmental factors. One such environmental factor implicated as a potential cause in both syndromes is aluminium, as an element or as part of a salt, received, for example, in oral form or as an adjuvant. Such administration has the potential to induce pathology via several routes such as provoking dysfunction and/or activation of glial cells which play an indispensable role in the regulation of central nervous system homeostasis and neurodevelopment. Other routes include the generation of oxidative stress, depletion of reduced glutathione, direct and indirect reductions in mitochondrial performance and integrity, and increasing the production of proinflammatory cytokines in both the brain and peripherally. The mechanisms whereby environmental aluminium could contribute to the development of the highly specific pattern of neuropathology seen in Alzheimer’s disease are described. Also detailed are several mechanisms whereby significant quantities of aluminium introduced via immunisation could produce chronic neuropathology in genetically susceptible children. Accordingly, it is recommended that the use of aluminium salts in immunisations should be discontinued and that adults should take steps to minimise their exposure to environmental aluminium.

Australia Bans Truth-Telling Mother From Country For Three Years…And It Backfired
The date was August 8th and the Vaxxed team had just wrapped up a two-week tour of Australia, where the communities of parents received their info with great interest. It was time for the team, consisting of a medical doctor, a scientist, a videographer, and a mother of a vaccine-injured son to pass through Australia’s Department of Immigration within the airport on the way to their flight to New Zealand. Three passed through unhassled, one didn’t. Vaxxed team member Polly Tommey describes what happened to her:
“I get taken to one side and that’s when two immigration police take me into a room and tell me that I’ve been detained and ask for my phone…and then they told me that I was in violation of my Visa and they took my phone and went right through everything in my phone. They typed in ‘Australia’ they went through every contact and every email that there had been with myself and the team. They took my phone away and photographed everything.”
In an instant Tommey was a persecuted individual who moments later would find out she was officially banned from Australia for three years. Next, it came time for airport security immigration officers to address one of the reasons Tommey was being harassed:
“Then they asked me about Vaxxed. Did I have a copy of it? Endless questions about Vaxxed being a very dangerous film with lies…I’m a mother recording stories from parents. And parents come to me to tell their stories. I didn’t seek them out, they come to me. And that is more of a threat than anything else?”
How did we get to the point where a mother can be banned from a western country for simply offering a voice to families?

The Wild Doc – What Officials Can Do To End Unnecessary Drug Overdoses/ Vaccine Awareness Month Brings New Confirmation That Vaccines Are Causing SIDS.

Relevant to the back-end profits (and back-end injuries) industry is generating from the autism epidemic. Abilify is in the class of second generation antipsychotics frequently pushed on individuals with autism by mainstream doctors as part of the $5 billion (and rising) “autism drug” market.

Dr.Russell Blaylock Exposes The Gardasil, HPV Vaccine Fraud
A shocking interview by Mike Adams (The health ranger) with Dr. Russell Blaylock who exposes to total criminal fraud of HPV vaccines and the vaccine industry.

Hear Why He Calls The HPV Vaccine a Crime Against Kids!
The HPV vaccine continues to be a hotly debated issue. Robert Scott Bell, popular radio host and homeopathic practitioner, discusses the theory behind the HPV vaccine and whether or not he thinks it’s safe.
http://www.ihealthtube.com

The Health Ranger – Gardasil HPV Vaccine Hoax Exposed
This video exposes the truth about Gardasil and HPV vaccinations: They don’t work and may actually be dangerous to women. The FDA knew HPV did not cause cervical cancer in 2003.

HPV Gardasil Vaccine Proves Lethal – 236 Girls have now Died
236 Girls have now died in America – http://sanevax.org/
Irish Times 8.1.2012-Schoolgirl vaccine uptake of 82% beats target figures http://j.mp/zuYds8
236 girls have now died in America and the rest of the World, But the Irish Times keeps this quite, Irish Dr Kevin Kelleher, assistant national director of health protection at the HSE, welcomed the high uptake on Gardisil Vaccinations, he fails to give the facts also, says its excellent!
The 82 per cent uptake was “excellent” and was equal to or greater than those achieved in the first year of programmes in other countries such as the United Kingdom and Australia. He said the figures were great credit to the vaccination teams.

MMR gave our boy organ failure and then loss of legs #vaxxed #truth #science #Praybig

Why My Wife and I Decided Not To Vaccinate Our Daughter
Author: Jason Christoff
When my wife was pregnant we knew the vaccine issue was coming our way and we put it off as long as possible. As the day fast approached, I started to investigate and compile some information for my wife because she trusted that I would make sure she understood what the main issues were regarding vaccination. We had heard vaccinations were potentially dangerous but we didn’t know if that applied to all children or just some. We weren’t aware if vaccination was beneficial for some babies and maybe not for others. We were new to being parents and we didn’t want to make any mistakes. We certainly didn’t want our baby getting sick if we could do something about it proactively. We wanted our baby to have the most comfortable journey through life possible and if that meant giving our new born vaccines, so she could avoid disease now and in the future, then that’s what we were going to do. After researching for a couple of days, we were more than shocked at what we were uncovering.

Study – Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden.
RESULTS:
Excess risks among vaccinated compared with unvaccinated people were of low magnitude for Bell’s palsy (hazard ratio 1.25, 95% confidence interval 1.06 to 1.48) and paraesthesia (1.11, 1.00 to 1.23) after adjustment for age, sex, socioeconomic status, and healthcare utilisation. Risks for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, and rheumatoid arthritis remained unchanged. The risks of paraesthesia and inflammatory bowel disease among those vaccinated in the early phase (within 45 days from 1 October 2009) of the vaccination campaign were significantly increased; the risk being increased within the first six weeks after vaccination. Those vaccinated in the early phase were at a slightly reduced risk of death than those who were unvaccinated (0.94, 0.91 to 0.98), whereas those vaccinated in the late phase had an overall reduced mortality (0.68, 0.64 to 0.71). These associations could be real or explained, partly or entirely, by residual confounding.
CONCLUSIONS:
Results for the safety of Pandemrix over 8-10 months of follow-up were reassuring -notably, no change in the risk for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, or rheumatoid arthritis. Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign. Small numbers of children and adolescents with narcolepsy precluded any meaningful conclusions.

Injecting Aluminum Official Trailer
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In the early 90s, a mysterious muscular disease with symptoms that included severe muscle and joint pain began to surface among multiple patients in France. In 1993, a team of doctors in Paris discovered that these patients had developed a new disease called Macrophagic Myofascitis, or MMF, which occurs when the aluminum hydroxide adjuvant from a vaccine remains embedded in the muscle tissue and causes an immune reaction. Featuring interviews with patients, doctors, scientists, and influential politicians, Injecting Aluminum calls in to question the public health policies around aluminum in vaccines and examines aluminum’s devastating effects on the human body.

IMPFEN MUSS FREIWILLIG BLEIBEN!
In vielen Ländern Europas dürfen Eltern schon jetzt nicht mehr frei entscheiden, ob, wann und wogegen ihre Kinder geimpft werden. Auch in Deutschland werden die Daumenschrauben angezogen, aktuell wird diskutiert, man solle Eltern, die ihre Kinder nicht impfen, das Kindergeld entziehen!
Da Impfungen schwere Nebenwirkungen haben können, darf kein Staat und keine Institution Eltern vorschreiben dürfen, welche Pharma-Produkte ihren Kindern einverleibt werden!
Um den drohenden Impf-Zwang zu verhindern, rufen wir zur Teilnahme auf und bitten um Unterstützung:
Demonstration am 16.9.2017 in Berlin
FÜR EINE FREIE ZUKUNFT GESUNDER MENSCHEN!

Vaccination must be voluntary!
In many countries of Europe, parents are no longer allowed to decide whether, when and what their children are vaccinated. In Germany, too, the squeeze are being drawn up, and it is currently being discussed that parents who do not vaccinate their children should withdraw child benefit.
Since vaccination can have serious side effects, no state and no institution must be allowed to require parents to have the pharmaceutical products incorporated into their children.
In order to prevent the threat of vaccination, we call to participate and ask for support:
Demonstration on 16.9.2017 in Berlin
For a free future of healthy people!

Movie Vaxxed gets up QUEENSLAND Health Minister’s nose
By Brent Melville
QUEENSLAND Health Minister Cameron Dick was either seriously misinformed, ignorant, or flat out lying when, in response to the touring movie Vaxxed: From Coverup to Catastrophe, he said “there is no shred of credible scientific evidence to support claims that vaccinations are dangerous” (Gold Coast Bulletin, 15/7/17).
The same with Victorian Health Minister Jill Hennessy who stated on Seven News in February last year: “There are no risks in vaccinating your children – the science is really clear”.
Dr Hooker, who joined the Vaxxed tour, says there are in fact more than 100 studies on PubMed on autism, neurological developmental disorders (NDDs) and vaccination. But here’s a few specific studies our blind, deaf and dumb health ministers and their advisers refuse to look at.
1. Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden. https://www.ncbi.nlm.nih.gov/pubmed/21994316 Conclusion in part: “… Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign…”.
2. Autoimmune disorders (AIDs) after immunisation with Influenza A/H1N1 vaccines with and without adjuvant: EudraVigilance data and literature review. https://www.ncbi.nlm.nih.gov/pubmed/23022149 From abstract: “Of the 50,221 adverse reactions received in EudraVigilance for A/H1N1 vaccines (adjuvanted: 46,173, non-adjuvanted: 4048), 314 were AID (adjuvanted: 276, non-adjuvanted: 38). GBS was the AID with the highest number of reports (125, adjuvanted: 109, non-adjuvanted: 16).
3. Serious adverse events rarely reported after trivalent inactivated influenza vaccine (TIV) in children 6-23 months of age. https://www.ncbi.nlm.nih.gov/pubmed/19450636 From results: “During 1991-2001, VAERS received 128,717 reports…A total of 14.2% of all reports described serious adverse events, which by regulatory definition include death, life-threatening illness, hospitalization or prolongation of hospitalization, or permanent disability.”
4. “Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013.” https://www.ncbi.nlm.nih.gov/pubmed/25598306 Study results found: “VAERS received 29,747 reports after Hib vaccines; 5179 (17%) were serious, including 896 reports of deaths. Median age was 6 months (range 0-1022 months). Sudden infant death syndrome was the stated cause of death in 384 (51%) of 749 death reports with autopsy/death certificate records. The most common non-death serious AE categories were neurologic (80; 37%), other noninfectious (46; 22%) (comprising mainly constitutional signs and symptoms); and gastrointestinal (39; 18%) conditions.”

Study: Vaccine Induced Inflammation Cause of Obesity Epidemic – Not Diet
Childhood obesity is now a reason why the state could take away children from their parents. The rationale is that if a child is obese, it is the parents’ fault, because they failed to feed them properly. It is assumed that all childhood obesity is a result of diet.
However, most of us have probably seen first-hand just how different children are when it comes to food and putting on weight. Some children can eat junk food most of the time and never add weight, while some children can eat a healthy, organic diet and still add pounds.
Dr. J. Bart Classen has published a study claiming that the evidence for the overwhelming problem of childhood obesity is not diet, but “vaccine induced inflammation.”

Vaccines, not Diet, are Causing Epidemic of Obesity and Type 2 Diabetes According to New Paper from Classen Immunotherapies
MANCHESTER, Md., June 26, 2017 /PRNewswire/ — A newly published paper in June’s Journal of Endocrinology, Diabetes & Obesity, 5(3): 1107, by immunologist J. Bart Classen, MD of Classen Immunotherapies provides further proof of the dangers of vaccines. The paper reviews the growing evidence that many cases of obesity, type 2 diabetes and metabolic syndrome are inflammatory conditions and that vaccine induced inflammation is the cause of the epidemic of these diseases. Upon receiving a vaccine some individuals’ immune system becomes hyper active leading to autoimmune destruction of insulin secreting cells and the development of type 1 diabetes. Many other individuals produce increased cortisol and other immune suppressing molecules, to suppress the vaccine induced inflammation. This increased production leads to type 2 diabetes, obesity and metabolic syndrome. The new paper reviews evidence supporting vaccines, not diet, as a cause of the epidemics of obesity, type 2 diabetes and metabolic syndrome.

Study – Cause of the Obesity, Type 2 Diabetes and Metabolic Syndrome Epidemics, Vaccine Induced Immune Overload versus Nutrition Overload
Abstract
There is an epidemic of obesity, type 2 diabetes, metabolic syndrome and associated conditions. Patients with these conditions often have markers of
increased inflammation. Many researchers have published that nutrition overload caused the epidemic of obesity and the associated inflammation which
leads to type 2 diabetes and metabolic syndrome. A contrasting view has provided extensive evidence that vaccine induced immune overload has caused an
epidemic of inflammation and this inflammation caused epidemics of obesity, type 2 diabetes and metabolic syndrome. The data reviewed in these manuscripts
provides proof that immune overload, not nutrition overload has been the major contributing factor for the epidemics and inflammation associated with the
epidemics. Several lines of evidence are reviewed including evidence that inflammation precedes obesity in many patients, the lack of inflammation in many
obese patients, an epidemic of inflammation in thin patients, and an epidemic of obesity in children under 6 months of age. The failure to control the obesity
epidemic is blamed on the focus on nutrition and ignoring the root cause, vaccine induced immune overload. Once a patient has developed metabolic syndrome
with type 2 diabetes providers are too frequently subjecting their patients to further immune overload by administering yearly influenza vaccines and many
other vaccines. This action makes metabolic syndrome more difficult to reverse. The plan to reduce obesity must be focused on preventing immune overload
and not blaming patients for their diet. The epidemic of obesity can be reversed through discontinuation of vaccine practices that result in immune overload.

 

Vaccine News – “It took me 7 years to teach him how to chew”

Big Pharma is the biggest, baddest, most dangerous drug dealer in the world.

Study – Clinical clues for autoimmunity and neuroinflammation in patients with autistic regression.
RESULTS:
The charts of 206 children with ASD and 33 diagnosed with autistic regression variant were reviewed. The incidence of febrile illness in the 6 months prior to initial parental concern was significantly higher in the children with autistic regression compared with those with ASD (30% vs 0%; p<0.001). The overall prevalence of familial autoimmunity was also higher in children with autistic regression compared with those with ASD (33% vs 12%; p<0.001). Type 1 diabetes and autoimmune thyroiditis were both more common in families with children with autistic regression. Other non-immune risk factors did not differ between the two groups.
INTERPRETATION:
Our findings suggest that predisposition to autoimmunity, and immune/inflammatory activation, may be associated with autistic regression.

The Vaccine Science Contradiction
The modern human race has been thriving and evolving for at least the last 200,000 years according to Anthropologists. Vaccines have only been around for less than 200 years. So how did humans survive for the 199,800 years before that. The answer is that you are born with a fully functioning immune system, capable of self-immunization. Vaccines are not required for immunization. Your body does it automatically. Just like 10,000 generations of your ancestors who also survived without vaccines. If your immune system didn’t work automatically to keep you alive then you would have never been born.

The Amazing Dr. Franz from Orlando.
#gooddoctor #pediatrician #vaxxed #praybig

Episode 7 of The Truth About Vaccines is NOW PLAYING. Tonight’s episode is all about Vaccine alternatives and Freedom of Choice. Super important for you to see.

Aluminium Adjuvants Have Never Been Approved For Use In Vaccination
In a press release, describing Professor Exley’s latest paper, the founder of the Dwoskin Family Foundation, Mrs. Claire Dwoskin wrote:
“Research at Keele University led by Professor Christopher Exley aims to understand the toxicity of aluminum adjuvants in vaccinations and their latest findings are now published in Nature’s ‘Scientific Reports.
In a project funded by the Medical Research Council (MRC) and the Dwoskin Foundation the group at Keele investigated the relationship between the physicochemical properties of aluminum adjuvants and the immune response. Specifically, they show that the reaction of the aluminum adjuvant at the injection site will determine its subsequent fate and therefore its activity both at the injection site and away from the injection site.
One form of aluminum adjuvant which is most commonly used in vaccines is an aluminum hydroxyphosphate salt and is more toxic at the injection site than the second form of aluminum adjuvant, also commonly used in vaccines, aluminum oxyhydroxide salt. However, the latter is more easily loaded into immune reactive cells with the possibility to be transported throughout the body. It is suggested by the Keele research that this loading of aluminum into viable cells offers a mechanism whereby significant amounts of aluminum, a known neurotoxin, might be translocated throughout the body and even across the blood brain barrier and into the central nervous system.” [2, 3, 4]
Countless Childhood Vaccinations Contain Aluminum

Shingles Vaccine Zostavax Is Causing What It’s Designed To Prevent
April 19, 2017
By now I think most people have seen the commercials on television telling us that if we’ve ever had the chicken pox at any point in our lives, then the shingles virus is already inside of us. As it stands right now, there is a vaccine for shingles called Zostavax, but what we’re finding out now about this vaccine makes it seem like it might be pretty dangerous or at least cause some side effects that are actually the same as what we’d see from shingles. Ring of Fire’s Farron Cousins talks with Attorney Troy Bouk about the dangers associated with Zostavax

Dying 13 Year Old Diagnoses Her Own HPV Vaccine Injury that Stumped Doctors
April 20, 2017
Health Impact News Editor Comments
One of the true tragedies in modern medicine is the refusal to consider vaccine injuries when diagnosing or treating disease. The U.S. government acknowledges that people die and are injured by vaccines, as is evidenced from the Department of Justice’s quarterly reports on settlements in vaccine court: http://vaccineimpact.com/vaccine-injuries-and-deaths-compensated-through-vaccine-court/
However, medical students are given no training in recognizing or treating vaccine injuries, and no studies are ever conducted to find out why some children suffer from vaccines while others do not.
In this story out of the U.K., a 13 year old girl accomplishes something her doctors could not do, and that was diagnose her own life-threatening disease by researching all of the possibilities, without excluding vaccine injuries, something that apparently handicapped her doctors. She discovered that she suffered from an autoimmune disease after receiving the HPV vaccine.

Professor Hamamoto talks about the persecution he faces at UC Davis after speaking the truth to his students. #Vaxxed #DarrylHamamoto #SenatorPan #SB277 #OperationPaperClip
Camera, editing and sound by Joshua Coleman.
YOUTUBE:

It took me 7 years to teach him how to chew
Nancy Kirkman’s son was severely injured by vaccines at 3 months of age. The family has been subjected to immense heartache and cruelty.
Interview recorded on February 2, 2017 in San Diego, California.
YOUTUBE LINK:

#VaxxedNation #VaxxedNationTour #RFKcommission #Truth #Science #Vaxxed #Tears #VaxxedTears

Baby’s Health Rapidly Declines After Receiving 13 Vaccines at One Time – Mom Accused of Abuse for Disagreeing with Doctors
April 20, 2017
Durenda and her son KJ on his 1st birthday, before he had 8 shots in one day.
by Health Impact News/MedicalKidnap.com Staff
A young Georgia mother had no idea that a routine trip to the pediatrician’s office for her son’s 1 year check-up would change her son’s life forever, and leave her fighting the state for custody of her own son. When the nurse-practitioner told her that her son was a little behind on his shots and they would need to catch up, Durenda Whitehead didn’t question the need for the vaccines. She did, however, question the safety of giving 13 vaccines at once.
Durenda’s pediatrician assured her that it was fine:
I can give up to 20 at one time.
Durenda was unaware of a research study published in the summer 2016 edition of the Journal of American Physicians and Surgeons by Neil Z. Miller entitled, “Combining Childhood Vaccines at One Visit Is Not Safe.” In a press release, Miller wrote:
Our study showed that infants who receive several vaccines concurrently…are significantly more likely to be hospitalized or die when compared with infants who receive fewer vaccines simultaneously.
Baby’s Health Declines After 13 Vaccines in One Day
During his first year of life, little KJ had a few bouts with respiratory illness, but on January 16, 2017, he was healthy, happy, and active.

Study – Combining Childhood Vaccines at One Visit Is Not Safe
Neil Z. Miller

#VaXism NEWS
#Texas Well done Texans For Vaccine Choice!!
Thank you freedom Reps!
Zedler let TIP have it!!
#HB2249

Skip that Newborn Vitamin K Shot
How much synthetic vitamin K is in the shot? Shockingly, the national standard mandated by most states for US hospitals to administer is over 100 times the infant’s RDA of this nutrient. Since studies have linked large doses of vitamin K with childhood cancers and leukemia, this large dose of synthetic K administered within minutes of birth seems questionable at best.
The fact is that medical science still does not know that much about the metabolic fate of vitamin K. Little to no unmetabolized vitamin K shows up in urine or bile. This is disturbing given the fact that vitamin K is a fat soluble vitamin and therefore has the potential to accumulate in body tissues. More disturbing is that the liver of a newborn does not begin to function until 3 or 4 days after birth. As a result, this little being has very limited to no ability to detoxify the large dose of synthetic vitamin K and all other the dangerous ingredients in the injection cocktail including:

– Phenol (carbolic acid – a poisonous substance derived from coal tar)
– Benzyl alcohol (preservative)
– Propylene glycol (better known as “edible” antifreeze)
– Acetic acid (astringent, antimicrobial agent)
– Hydrochloric acid
– Lecithin
– Castor oil

The manufacturer’s insert included with the shot includes the following warning:
Severe reactions, including fatalities, have occurred during and immediately after intravenous injection of phytonadione [synthetic Vitamin K] even when precautions have been taken to dilute the vitamin and avoid rapid infusion ….
The manufacturer’s insert is no exaggeration of the risks. On October 17, 2013, a case of anaphylactic shock in a newborn from the synthetic vitamin K shot was reported making the possibility of death from this shot a a very real side effect
Source:
Anaphylactic shock due to vitamin K in a newborn and review of literature
Abstract
Newborn infants are born with an immature innate immunity. They are less likely to develop anaphylaxis since their immune system is weaker than older infants and children. There are only a few reports of side effects after vitamin K injection in neonates although prophylaxis against hemorrhagic disease of the newborn with this drug has been in routine practice in all over the world for many years. We herein report a case of anaphylactic shock developing after the intramuscular administration of vitamin K1 in a newborn. To our knowledge, this patient is the first case of neonatal anaphylactic shock developing due to intramuscular administration of vitamin K1. We suggest the clinicians should be aware of this possibility of potentially fatal adverse effect occurring with intramuscular administration of vitamin K1.
Does this make any sense to you? It makes absolutely no sense to me. How could anyone say that this shot is safe and effective for newborns?

Is There Vaccine Cause-And-Correlation Regarding The Dramatic Rise In Children’s Chronic Diseases?
Posted on April 18, 2017
Since the introduction of CDC’s hyper-vaccine schedule, which saw children’s vaccines schedules increase from 10 to 69 vaccines after the 1986  National Childhood Vaccine Injury Act was passed into law, very young children are contracting chronic “old age type” diseases early in life—an anomaly heretofore not experienced demographically.
First off, obesity rates (2013-2014) for U.S. children between the ages of 6 and 11 years was 17.4% [1]  Three leading causes of death in children between 1 and 4 years of age were congenital malformations, deformations and chromosomal abnormalities. [1]   Mandatory pregnancy vaccines have impact upon growing fetuses.  For children 5 to 14 years of age, it’s cancer! [1]   However, according to Contemporary Pediatrics [2] 2014 published data, cancer was the second leading cause of death for children between 1 and 9 years of age (11.8% of deaths).  For infants, the third leading cause of death was sudden infant death syndrome (SIDS, 8.4%)—something that seemingly appeared in pediatric medicine context concomitantly with the increase in mandated vaccines, specifically with multi-valent vaccines, i.e., numerous vaccines given at one time.  However, the CDC’s information about SIDS claims vaccines do not cause SIDS.  Try telling that to many parents.
According to Focus for Health, 27% of U.S. children live with chronic diseases! [3]   That website asks the question, “Why are today’s children sicker than ever before?”  The answer: “While genes may play a role in obesity, asthma and ADHD, environmental and social changes are behind the surge, researchers said.”5 [Children Sicker Now Than in Past, Harvard Report Says] [4]   That Harvard Report found a fourfold increase in childhood obesity; twice the asthma rate since the 1980s; and regarding diabetes: White children’s rate was 26.1 per 100,000; black children, 25.4 per 100,000; American Indian youth, 25 per 100,000 including the highest rate of type-2 diabetes. [4] According to the CDC, one in six children in the USA has a developmental disability, which represents a 17% rise between 1997 and 2008. [7]
Furthermore, are you aware the cost of fully vaccinating a child has increased by 2,700% during the last decade?  Vaccines are extremely profitable for manufacturers, but very costly in terms of adverse health effects, medical bills for parents, and social issues (day care, school, jobs, welfare benefits, etc.) for infants, toddlers, teens and adults.

The Dangers Of Vaccines and Vaccination
Vaccines Are Unavoidably Unsafe
According to the US Food and Drug Administration, safety assessments for vaccines have not often included toxicity studies because vaccines have not been viewed as inherently toxic. Yet vaccines are legally defined as unavoidably unsafe.
It is not just childhood vaccines that come with substantial risk. Influenza vaccines, vaccines for sexually transmitted diseases, and others contain similar risks for adverse events. Also troubling is that vaccination is recommended now for pregnant women, even though vaccine package inserts clearly state they have not been tested on pregnant women, so the effects on the fetus can’t be known.
In the 1960s only a handful of childhood vaccines were given. The current CDC recommended vaccine schedule for children now has over 30 vaccines by the time a child turns 6 and an additional potential for up to 30 more by the time they reach 18. Could this increase be linked to our declining health? For example, currently:

    One in six children in the US has a learning disability
Over 50% suffer from some type of chronic illness.
Cancer is the leading cause of death in our children
Autism rates have soared from 1 in 10,000 in 1990 to 1 in 68 today

Since genetic mutations change slowly over generations, we must look to environmental causes for these changes. While other environmental toxins certainly are at play in these statistics, disregarding the potential role to the amounts of toxin injected into children through vaccines is not only bad public policy, it is bad science. By disregarding the role of vaccines in our statistics for infant mortality and chronic diseases, we could be doing more harm than good in mandating, or even advising, them.
Vaccine Adverse Effects: Known Risks
The list of adverse side effects for vaccines is long and troubling. A quick scan of the Vaccine Injury Table kept by the Health Resource Center for the U.S. Department of Health and Human Services reveals that compensation for injury is possible from a variety of the most common vaccines given to children.
Adverse events are the reason the Vaccine Injury Compensation Program has paid out over 3 billion dollars from 1988 – 2016 despite the fact that only 1 in 5 claims receives any compensation at all. Studies reveal that a small fraction of those injured by vaccines ever file any claim at all since most doctors reject the notion that a problem was caused by a vaccine despite the reality that such problems are listed on the manufacturers product insert. You can learn more by reading this fficial document: National Vaccine Injury Compensation Program.
Vaccines: Adverse Effects List
Various vaccines are linked to the following serious adverse reactions:

    Anaphylactic shock
Aseptic meningitis, meningitis
Bell’s palsy, facial palsy, isolated cranial nerve palsy
Blood disorders such as thrombocytopenic purpura (a disease that destroys platelets need for clotting)
Brachial neuritis
Cerebrovascular accident (stroke)
Chronic rheumatoid arthritis
Convulsions, seizures, febrile seizure
Death
Encephalopathy and encephalitis (brain swelling)
Hearing loss
Guillain-Barré syndrome
Immune system disorders
Lymphatic system disorders
Multiple sclerosis
Myocarditis
Nervous system disorders
Neurological syndromes including autism
Paralysis and myelitis including transverse myelitis
Peripheral neuropathy
Pneumonia and lower respiratory infections
Skin and tissue disorders including eczema
Sudden infant death syndrome (SIDS)
Tinnitus (ringing in the ears)
Vaccine-strain versions of chicken pox, measles, mumps, polio, influenza, meningitis, yellow fever, and pertussis
Vasculitis (inflammation of blood vessels)