Nestibo L, Lee BE, Fonseca K, Beirnes J, Johnson MM, Sikora CA.
Author information
Communicable Disease Control, Alberta Health Services;
Abstractin
In the midst of a local measles outbreak, a recently immunized child was investigated for a new-onset measles-type rash. Nucleic acid testing identified that a vaccine-type measles virus was being shed in the urine. Clinically differentiating measles from a nonmeasles rash is challenging, but can be supported by a thorough medical history evaluation. Rashes are expected to occur after immunization; nucleic acid testing can be used when it is difficult to differentiate between wild and attenuated strains.
US National Library of Medicine
National Institutes of Health – Jan 2009
Lederman E, Miramontes R, Openshaw J, Olson VA, Karem KL, Marcinak J, Panares R, Staggs W, Allen D, Weber SG, Vora S, Gerber SI, Hughes CM, Regnery R, Collins L, Diaz PS, Reynolds MG, Damon I.
Author information
Poxvirus and Rabies Branch, Division of Viral and Rickettsial Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA. edith.lederman@med.navy.mil
Abstract
On March 3, 2007, a 2-year-old boy was hospitalized with eczema vaccinatum. His two siblings, one with eczema, were subsequently removed from the home. Swabs of household items obtained on March 13th were analyzed for orthopoxvirus DNA signatures with real-time PCR. Virus culture was attempted on positive specimens. Eight of 25 household samples were positive by PCR for orthopoxvirus; of these, three yielded viable vaccinia virus in culture. Both siblings were found to have serologic evidence of orthopoxvirus exposure. These findings have implications for smallpox preparedness, especially in situations where some household members are not candidates for vaccination.
US National Library of Medicine
National Institutes of Health – Jan 2005
Minor PD, Dunn G, Ramsay ME, Brown D.
Author information
National Institute for Biological Standards and Control, Blanche Lane South Mimms, Potters Bar, Herts, EN6 3QG, UK. pminor@nibsc.ac.uk
Abstract
Excretion of live oral poliovaccine and molecular markers of increased virulence in the viruses isolated were examined in children who were either previously immunised with inactivated or live vaccine or were unimmunised. There appeared to be some effect of previous immunisation with either live or killed vaccine at the second dose of live vaccine. Where an effect was seen it took the form of reduced rates of excretion, shorter time periods of excretion and more rapid and complete reversion of the excreted virus. The data are consistent with the view that poliovirus is able to escape the immune pressure in the gut to some extent by improving its general fitness rather than direct evasion of immunity.
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
Tomljenovic L, Shaw CA.
Author information
Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, BC, V5Z 1L8, Canada. lucijat77@gmail.com
Abstract
Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted. Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences. In our opinion, the possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated, has not been rigorously evaluated in the medical and scientific community. We hope that the present paper will provide a framework for a much needed and long overdue assessment of this highly contentious medical issue.
A study published in the Journal Cell Biology and Toxicology by Kinki University in Osaka, Japan determined that in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.
US National Library of Medicine
National Institutes of Health – Apr 2010
Minami T, Miyata E, Sakamoto Y, Yamazaki H, Ichida S.
Author information
Department of Life Sciences, Kinki University, Higashi-osaka, Osaka, Japan. minamita@life.kindai.ac.jp
Abstract
Thimerosal, an ethyl mercury compound, is used worldwide as a vaccine preservative. We previously observed that the mercury concentration in mouse brains did not increase with the clinical dose of thimerosal injection, but the concentration increased in the brain after the injection of thimerosal with lipopolysaccharide, even if a low dose of thimerosal was administered. Thimerosal may penetrate the brain, but is undetectable when a clinical dose of thimerosal is injected; therefore, the induction of metallothionein (MT) messenger RNA (mRNA) and protein was observed in the cerebellum and cerebrum of mice after thimerosal injection, as MT is an inducible protein. MT-1 mRNA was expressed at 6 and 9 h in both the cerebrum and cerebellum, but MT-1 mRNA expression in the cerebellum was three times higher than that in the cerebrum after the injection of 12 microg/kg thimerosal. MT-2 mRNA was not expressed until 24 h in both organs. MT-3 mRNA was expressed in the cerebellum from 6 to 15 h after the injection, but not in the cerebrum until 24 h. MT-1 and MT-3 mRNAs were expressed in the cerebellum in a dose-dependent manner. Furthermore, MT-1 protein was detected from 6 to 72 h in the cerebellum after 12 microg/kg of thimerosal was injected and peaked at 10 h. MT-2 was detected in the cerebellum only at 10 h. In the cerebrum, little MT-1 protein was detected at 10 and 24 h, and there were no peaks of MT-2 protein in the cerebrum. In conclusion, MT-1 and MT-3 mRNAs but not MT-2 mRNA are easily expressed in the cerebellum rather than in the cerebrum by the injection of low-dose thimerosal. It is thought that the cerebellum is a sensitive organ against thimerosal. As a result of the present findings, in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.
A study published in the Journal Neurochemical Research determined that since excessive accumulation of extracellular glutamate is linked with excitotoxicity, data implies that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders.
US National Library of Medicine
National Institutes of Health – Feb 2012
Author information
Michalina Duszczyk-Budhathoki – 1
Mieszko Olczak – 1,3
Malgorzata Lehner – 2
and
Maria Dorota Majewskacorresponding author – 1,4
1 – Marie Curie Chairs Program at the Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland
2 – Department of Neurochemistry, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland
3 – Department of Forensic Medicine, Medical University of Warsaw, Oczki 1 str., 02-007 Warsaw, Poland
4 – Department of Biology and Environmental Science, University of Cardinal Stefan Wyszynski, Wóycickiego Str. 1/3, 01-815 Warsaw, Poland Maria Dorota Majewska, Phone: +48-22-45-82-624, Fax: +48-22-45-82-842, Email: moc.liamg@akswejamdm
Abstract
Thimerosal, a mercury-containing vaccine preservative, is a suspected factor in the etiology of neurodevelopmental disorders. We previously showed that its administration to infant rats causes behavioral, neurochemical and neuropathological abnormalities similar to those present in autism. Here we examined, using microdialysis, the effect of thimerosal on extracellular levels of neuroactive amino acids in the rat prefrontal cortex (PFC). Thimerosal administration (4 injections, i.m., 240 μg Hg/kg on postnatal days 7, 9, 11, 15) induced lasting changes in amino acid overflow: an increase of glutamate and aspartate accompanied by a decrease of glycine and alanine; measured 10–14 weeks after the injections. Four injections of thimerosal at a dose of 12.5 μg Hg/kg did not alter glutamate and aspartate concentrations at microdialysis time (but based on thimerosal pharmacokinetics, could have been effective soon after its injection). Application of thimerosal to the PFC in perfusion fluid evoked a rapid increase of glutamate overflow. Coadministration of the neurosteroid, dehydroepiandrosterone sulfate (DHEAS; 80 mg/kg; i.p.) prevented the thimerosal effect on glutamate and aspartate; the steroid alone had no influence on these amino acids. Coapplication of DHEAS with thimerosal in perfusion fluid also blocked the acute action of thimerosal on glutamate. In contrast, DHEAS alone reduced overflow of glycine and alanine, somewhat potentiating the thimerosal effect on these amino acids. Since excessive accumulation of extracellular glutamate is linked with excitotoxicity, our data imply that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders. DHEAS may partially protect against mercurials-induced neurotoxicity.
VAXXED TV – Vaccines gave my son seizures
I am vaccine injured and so is my son
My baby is healthy and happy all the time
I’m a dad fighting the system
4 month vaccine injured my baby
James Neuenschwander M.D
He had a lump on his leg for a year A mother shares her observations of her son’s reactions to the vaccines given to him.
Interview recorded on May 5th, 2017 in The United Kingdom
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.
March 22, 2010 — GlaxoSmithKline’s Rotarix rotavirus vaccine contains DNA from an apparently harmless pig virus, the company and the FDA today announced.
The FDA estimates that 1 million U.S. kids have received the Rotarix vaccine.
The contamination was discovered by researchers developing a new technique for detecting viral material. GlaxoSmithKline confirmed that the pig virus, porcine circovirus type 1 or PCV-1, has been in the vaccine since it was developed.
This means that pig virus DNA was in the vaccine throughout clinical trials. No safety issues emerged from these international studies with 90,000 participants or, GlaxoSmithKline says, in post-marketing surveillance covering more than 69 million doses of the vaccine.
Nevertheless, as a precaution the FDA is asking doctors to stop using the two-dose Rotarix vaccine, which it approved in 2008.
“The message is clearly not a message of safety but of caution going forward,” FDA Commissioner Margaret Hamburg, MD, said at a news conference. “We believe the vaccine is both safe and effective and we strongly encourage vaccination against rotavirus. But we want to more deeply understand the finding of this unexpected material in the product, and that is why we are putting a clinical pause on its use.”
A study published in the Journal Annals of Epidemiology has shown that giving the Hepatitis B vaccine to newborn baby boys could triple the risk of developing an autism spectrum disorder compared to boys who were not vaccinated as neonates. The research was conducted at Stony Brook University Medical Centre, NY.
US National Library of Medicine
National Institutes of Health – 2010
Gallagher CM, Goodman MS.
Author information
PhD Program in Population Health and Clinical Outcomes Research, Stony Brook University Medical Center, State University of New York at Stony Brook, Stony Brook, New York, USA. cmgallagher@notes.cc.sunysb.edu
Abstract
Universal hepatitis B vaccination was recommended for U.S. newborns in 1991; however, safety findings are mixed. The association between hepatitis B vaccination of male neonates and parental report of autism diagnosis was determined. This cross-sectional study used weighted probability samples obtained from National Health Interview Survey 1997-2002 data sets. Vaccination status was determined from the vaccination record. Logistic regression was used to estimate the odds for autism diagnosis associated with neonatal hepatitis B vaccination among boys age 3-17 years, born before 1999, adjusted for race, maternal education, and two-parent household. Boys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life. Non-Hispanic white boys were 64% less likely to have autism diagnosis relative to nonwhite boys. Findings suggest that U.S. male neonates vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. Nonwhite boys bore a greater risk.
A study published in the Journal of Inorganic Biochemistry by researchers at the Neural Dynamics Group, Department of Ophthalmology and Visual Sciences at the University of British Columbia determined that Aluminum, a highly neurotoxic metal and the most commonly used vaccine adjuvant may be a significant contributing factor to the rising prevalence of ASD in the Western World. They showed that the correlation between ASD prevalence and the Aluminum adjuvant exposure appears to be the highest at 3-4 months of age. The studies also show that children from countries with the highest ASD appear to have a much higher exposure to Aluminum from vaccines. The study points out that several prominent milestones of brain development coincide with major vaccination periods for infants. These include the onset of synaptogenesis (birth), maximal growth velocity of the hippocampus and the onset of amygdala maturation. Furthermore, major developmental transition in many bio-behavioural symptoms such as sleep, temperature regulation, respiration and brain wave patterns, all of which are regulated by the neuroendocrine network. Many of these aspects of brain function are known to be impaired in autism, such as sleeping and brain wave patterns.
Lucija Tomljenovic a,
Christopher A. Shaw a,b
a Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia, 828 W. 10th Ave, Vancouver, BC, Canada V5Z 1L8
b Departments of Ophthalmology and Visual Sciences and Experimental Medicine and the Graduate Program in Neuroscience, University of British Columbia, Vancouver, British Columbia, 828 W. 10th Ave, Vancouver, BC, Canada V5Z 1L8
Abstract:
Autism spectrum disorders (ASD) are serious multisystem developmental disorders and an urgent global public health concern. Dysfunctional immunity and impaired brain function are core deficits in ASD. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the potential to induce neuroimmune disorders. When assessing adjuvant toxicity in children, two key points ought to be considered:
(i) children should not be viewed as “small adults” as their unique physiology makes them much more vulnerable to toxic insults;
and
(ii) if exposure to Al from only few vaccines can lead to cognitive impairment and autoimmunity in adults, is it unreasonable to question whether the current pediatric schedules, often containing 18 Al adjuvanted vaccines, are safe for children? By applying Hill’s criteria for establishing causality between exposure and outcome we investigated whether exposure to Al from vaccines could be contributing to the rise in ASD prevalence in the Western world.
Our results show that:
(i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines;
(ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades (Pearson r=0.92, pb0.0001);
and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3–4 months of age (Pearson r=0.89–0.94, p=0.0018–0.0248). The application of the Hill’s criteria to these data indicates that the correlation between Al in vaccines and ASD may be causal. Because children represent a fraction of the population most at risk for complications following exposure to Al, a more rigorous evaluation of Al adjuvant safety seems warranted
According to the FDA, vaccines represent a special category of drugs as they are generally given to healthy individuals. Further according to the FDA, “this places significant emphasis on their vaccine safety”. While the FDA does set an upper limit for Aluminum in vaccines at no more that 850/mg/dose, it is important to note that this amount was selected empirically from data showing that Aluminum in such amounts enhanced the antigenicity of the vaccine, rather than from existing safety. Given that the scientific evidence appears to indicate that vaccine safety is not as firmly established as often believed, it would seem ill advised to exclude paediatric vaccinations as a possible cause of adverse long-term neurodevelopment outcomes , including those associated with autism.
VAXXED TV – My brother has autism from vaccines
I’m a pharmacist and I will never vaccinate again
Vaccines caused my daughters autism and epilepsy
My 3 children are unvaccinated
I’m a nurse and I didn’t know
Type 1 diabetes, autoimmunity and vaccines
The one and only Ginger Taylor
Vaccines gave my children autism, tics, allergies and eczema
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.
War Room – Mumps Vaccine Causes Mumps Outbreak In Colleges
Should we continue to pretend vaccines are risk free when they’re now causing outbreaks of the exact thing they’re supposed to prevent?
Help us spread the word about the liberty movement, we’re reaching millions help us reach millions more. Share the free live video feed link with your friends & family: http://www.infowars.com/show
VAXXED TV – Too many coincidences #vaxxed #DidYouKnow #praybig
Dr Cammy Benton MD #didyouknow #knowtherisk
I will not vaccinate #vaxxed #didYouKnow #praybig
Single Rubella vaccine injured my son #vaxxed #DidYouKnow #praybig
I will not vaccinate my little boy #vaxxed #DidYouKnow #praybig
Vaccines gave my children autism, food allergies, type 1 diabetes and speech disorders #DidYouKnow
My 3 boys are injured from vaccines #vaxxed #DidYouKnow #Praybig
RV mechanics wife – it’s a God thing #vaxxed #DidYouKnow #praybig
Vaccines gave my son eczema #vaxxed #DidYouKnow #Praybig
TDap vaccine during pregnancy killed my baby #vaxxed #DidYouKnow #Praybig
Hot Lots #SIDS and what every parent deserves to know.
Study – ECZEMA VACCINATUM
Audrey H. Reynolds, Howard A. Joos
Abstract
Nine cases of eczema vaccinatum are presented, including two fatalities. Seven were caused by contact of a child with eczema with a recently vaccinated sibling.
Suddenly appearing umbilicated vesicles superimposed upon atopic eczema are almost diagnostic of eczema vaccinatum or eczema herpeticum. These do not occur with mere secondary bacterial infection.
Hyperimmune vaccinal gamma-globulin is now available for specific therapy.
Eczema vaccinatum is frequently iatrogenic and uniformly preventable.
The following steps are recommended for prophylaxis: 1) No child with atopic eczema or other skin disorder should be vaccinated. 2) No child should be vaccinated if any member of his family has eczema or other skin disorder. 3) Parents of children with eczema should be notified at the onset of the disease of the danger from vaccination contact. 4) If a sibling of a child with atopic eczema is vaccinated, he must be completely separated from that child for at least 21 days. 5) Forms used by state and local health departments for parents’ consent to vaccination should include an appropriate warning of the contraindications. 6) Eczema vaccinatum should be a reportable disease. 7) Patients recently vaccinated must be excluded from pediatric wards containing patients with atopic eczema, other diseases of the skin, burns or healing surgical incisions. 8) Vaccination may be recommended at 2 months of age, especially for babies from strongly allergic families.
Baby Boy Suffers From Seizures After Getting Vaccines
It’s Just a Tetanus Shot
Posted on July 16, 2016
A story from a heart broken mother, Christie:
I am up. It’s 5am here. I stopped researching at 1 am and fell asleep crying after throwing my phone across the room in tears. I was furious. I was devastated. And I still am. But now I’m sick to my stomach and I’m up.
My son has been having trouble medically since he received two DTaP shots (yes 2) in the ER back in August. That was 11 months ago when he was 3 years old, after getting some stitches. He has been having seizures, weight loss, social regression, migraines lasting multiple days, increase in irritability, increased sleep (up to 18 hours some days), vomiting, very thirsty and more.
We have been doing non-stop testing for over a month with more tests scheduled: an MRI, another EEG, glucose testing, a 24 HR EEG and another heavy metals test. Yesterday I got a call from one of our doctors saying that he had test results in about heavy metals and essential minerals. This was the test I was most excited to see as I thought for sure it was going to be aluminum poisoning from the DTaP overdose that was causing the problems.
To my surprise, he did not have aluminum toxicity. Or mercury,…..or lead……. or iron. I was shocked, but also curious what could be causing these problems in a previously healthy and virtually vax-free organic free-range wild child. But the test results did show immense toxicity in another heavy metal that I had never heard of. Cadmium.
The doctor was perplexed. Cadmium poisoning?!?? From where? No smoking in our family. No exposure to places or things where cadmium would be around to cause that. The doctor left me with a list of foods that chelate cadmium and said to return in a month for follow up testing to see if it detoxes from his body. We were both also curious if his body was for some reason not able to naturally detox itself.
So I started to do detailed research. I was on my computer/iPhone for 7 hours. And I found it. At 12:38 am today I found it. And I got angry. And here’s why-
POLYSORBATE 80!
Polysorbate 80 prevents the body from being able to excrete cadmium. And if cadmium toxicity gets high enough it can cause death.
He also had other essential minerals missing entirely. We are still researching and chelating, hoping for success. We are also hiring an attorney for VICP (vaccine Injury court).
I hate the CDC. I HATE pharma. I am heartbroken. I am furious.
DPT vaccine killed my son at 32 years old #vaxxed #peoplesStudy #Praybig #truth #science
Film documentar de lung metraj. Filmul este despre efectele adverse ale vaccinurilor si despre proiectul de lege privind obligativitatea vaccinurilor. Filmul are o durata totala de 150 de minute.
Partea I
Partea II
Partea III
As Lawsuits Against Cholesterol Drugs Mount, Big Pharma Develops a Cholesterol Vaccine
June 30, 2017
by Paul Fassa
Health Impact News
As we have reported frequently here at Health Impact News, sales of drugs to lower cholesterol are the top selling drugs of all time. It is a $100 billion a year industry.
The cholesterol-lowering drug Lipitor is the best-selling drug of all time, grossing over $140 billion, with no serious close competitors in the history of pharmaceutical drugs.
One out of every four Americans over the age of 50 is taking a statin drug to lower their cholesterol. However, these blockbuster drugs have run through their patent life, and now generics dominate the market.
So Big Pharma is looking at new ways to patent new drugs to lower your cholesterol.
The latest? A vaccine is being developed to lower your cholesterol.
Unfortunately, this vaccine is based on the bogus lipid theory of obesity and heart disease fostered by physiologist Ancel Keys’ flawed Seven Countries Study circa 1961. The lipid theory of saturated fats causing obesity and heart disease led to vilifying cholesterol, which is an important pre-hormone and tissue building block substance created by our bodies.
Medical Bullying: “Fired” by My GYN for Saying No
Posted on June 29, 2017 by Thinking Moms’ Revolution
There have been signs for a long time that the mainstream medical system in this country has lost whatever soul it may have once possessed: pediatricians “firing” patients who are not vaccinated according to the CDC-recommended schedule; doctors of all stripes denying what is right in front of their faces; the proliferation of iatrogenic (doctor-caused) illness to the point where medical mishap is considered the third leading cause of death in the U.S.; the continued push for pharmaceutical or surgical Band-Aids for the chronically ill to mask ever-increasing symptoms and side effects instead of a studied effort to seek out and address root causes. But I was personally rocked by a recent in-your-face example of the worst attitudes in modern medical practice.
A little backstory: Unlike many others with two copies of the MTHFR mutation that significantly reduces the ability to methylate when activated, I had no problem getting pregnant. In fact, between the ages of 37 and 43, I was pregnant four times and two of them went full-term. But one of those full-term pregnancies was my son Zane whose brief life story I have told before. Zane’s absence made me long for another child, and after a miscarriage at 43 I knew that time was running out. My regular gynecologist happened to also be a reproductive endocrinologist (RE), and in a last-ditch Hail Mary pass, we decided to take advantage of the fact that my insurance company would cover one round of in vitro fertilization (IVF).
Treating autism by targeting the gut
Date: June 19, 2017
Source: Frontiers
Summary:
Therapies to change the bacteria in the gut, through diet, pro-and prebiotic supplements, fecal matter transplants or antibiotics, could treat autism. A review of six decades of research linking the gut to brain development could pave the way for cheap and effective treatment.
A cheap and effective treatment?
Many of the papers reviewed support the idea of a gut-brain axis — a way in which factors in the gut can affect processes in the brain. So these gastro-intestinal problems may have a more sinister side. The overgrowth of bad bacteria in the gut inevitably leads to an overproduction of by-products — including toxins. These can make the gut lining more permeable. Then toxins, by-products and even undigested food can get into the bloodstream and travel to the brain.
In a child under three years old, whose brain is at the height of development, the presence of these chemicals can impair neuro-development, leading to ASD.
Dedicated to all the victims of vaccines.
Vaccine pioneer admits adding cancer-causing virus to Vaccine
In this interview Dr. Maurice Hilleman reveals some astounding revelations. He admits that Merck drug company vaccines (Polio) had been deliberately contaminated with SV40, a cancer-causing monkey virus from 1953 – 63.
For years, researchers suggested that millions of vials of polio vaccine, contaminated with SV40, infected individuals which caused human tumors, and by 1999, molecular evidence of SV40 infections were showing up in children born after 1982. Some experts now suggest the virus may have remained in the polio vaccine until as late as 1999.
In 2002, the journal Lancet published compelling evidence that contaminated polio vaccine was responsible for up to half of the 55,000 non-Hodgkin’s lymphoma cases that were occurring each year. And there is the likelihood that there was an importing and spreading of the AIDS virus in the same manner, as revealed in the video.
At first no one could fathom how the virus had been transmitted into the human population, but this shocking video proves that it was deliberately added to the vaccine by Dr. Maurice Hilleman, which was “good science” at that time.
Just Who is Dr. Maurice Hilleman?
Now, for those of you who may think Dr. Hilleman was just another crackpot (he passed away in 2005), think again. He was, and still is, the leading vaccine pioneer in the history of vaccines. He developed more than three dozen vaccines—more than any other scientist in history—and was the developer of Merck’s vaccine program.
He was a member of the U.S. National Academy of Science, the Institute of Medicine, the American Academy of Arts and Sciences, and the American Philosophical Society, and received a special lifetime achievement award from the World Health Organization.
When he was chief of the Department of Respiratory Diseases with what’s now the Walter Reed Army Institute of Research, he discovered the genetic changes that occur when the influenza virus mutates, known as shift and drift. He was also one of the early vaccine pioneers to warn about the possibility that simian viruses might contaminate vaccines.So Dr. Hilleman knew what he was talking about. And in his own words, “vaccines have to be considered the bargain basement technology for the 20th Century.”
Repeal Immunity for Drug Companies Against Vaccine Injuries
Why should the drug companies be above the law? If vaccines are safe, there would be no need to grant the drug companies immunity. In 1986 Congress gave the drug companies immunity against all lawsuits from vaccine related injuries. The Federal Government is now paying out billions in damages to some parents whose children have been hurt by vaccines. While the drug companies continue to rack up huge profits, most families continue to pay for the damages with their own money.
Vaccine Ingredients — A Comprehensive Guide
Posted on August 15, 2011 by Megan
If the above document does not display use this link! cdc vaccine ingredients You will need the updated Adobe Reader if you don’t already have it.
By: Megan Pond
So what does the above document mean?
To find out the question to that, let’s dissect just a few of the ingredients on the list.
A devastasting report from The European Citizen’s Initiative, (Initiative Citoyenne) details of the potential horrors of GSK’s Infanrix 6-in-1 Vaccine. An internal GSK document marked Confidential usually reserved for regulatory bodies only, the 1,271 page document details the adverse effects associated with the vaccine over a 2 year period.
Infanrix is used in Ireland by the HSE for Infants with repeated doses at 2, 4 and 6 months. It is intended to protect newborns and infants from six different illnesses: Diphtheria, Tetanus, Whooping Cough, Polio, Haemophilius Influenza B (HIB) and Hepatitis B.
The GSK document in question details the adverse effects of this vaccine, reported back to the manufacturer from various European countries between the 23rd of October 2009 and the 22nd of October 2011.
GSK received 1,742 reports of adverse effects, of which 503 were serious effects not listed and 56 were serious adverse effects listed.The events registered included 36 deaths (over the two-years period), most of which occurred within three days after the child received the Infanrix Hexa vaccine.
Adverse events include autism, encephalitis, heart failure, gaze palsy (indicative of neurological damage), gastrointestinal hemorrhage, jaundice, mental retardation (classed as not serious!), removal of part of the intestine (also defined as not serious!), opisthotonos (yet again labeled as not serious!), paralysis. Guillain Barré syndrome, convulsions, and many others.
Of course, not all the reported events were actually caused by Infanrix. GSK reported that the number of reported adverse events was only 14.6 per 100,000 doses distributed (not per 100,000 administered). However, as reported by Initiative Citoyenne, the doctors’ publication, Revue française du Practicien, reports that this figure is likely only 1-10% of the reality.
So you think the above figures are not correct?
See links here:
Why Is Informed Consent to Vaccination A Human Right?
Civil liberties: They include the legal right to exercise freedom of thought, speech, conscience and religious belief.
Autonomy: Protection of autonomy and bodily integrity includes the human right to exercise informed consent to medical risk taking.
What is informed consent?
Informed consent means you have the legal right to be fully and accurately informed about the benefits and risks of a medical intervention, including a pharmaceutical product, and are free to make a voluntary decision about whether to accept the risk for yourself or your minor child without being coerced or punished for the decision you make.
Informed consent has guided the ethical practice of medicine since the Doctor’s Trial at Nuremberg after World War II, where the informed consent principle was internationally acknowledged as a human right for individuals participating in scientific research. Today, informed consent to medical risk taking also means you have the legal right to be fully and accurately informed by a doctor or medical facility about the benefits and risks of a lab test, surgical procedure, prescription drug or other medical intervention performed on you or your minor child and give your voluntary permission.
Why is informed consent to vaccine risk taking a human right?
Vaccines are biological products manufactured by pharmaceutical corporations. Like other pharmaceutical products, vaccines carry a risk of injury or death, which can be greater for some people than others, and often doctors cannot predict who will be harmed.
One-size-fits-all vaccine policies and laws, which force you to risk your health or your child’s health without your voluntary, informed consent and with the threat of punishment for declining a vaccine, violate human rights.
It is important to protect civil liberties, including the freedom to exercise voluntary, informed consent to medical risk taking. Without the legal right to protect autonomy and bodily integrity, without the legal right to freedom of thought, speech, conscience and religious belief, we are no longer free.
Within NVIC.org, learn more about vaccines, diseases and the human right to informed consent to medical risk taking.
Empower yourself today with well-referenced information that can help you make educated decisions about vaccination.
It’s your health. Your family. Your choice.
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