Boryana Stamova,corresponding author – 1,9,10
Peter G. Green,2
Yingfang Tian,1,9,10
Irva Hertz-Picciotto,3,9,10
Isaac N. Pessah,4,9,10
Robin Hansen,5,9,10
Xiaowei Yang,3
Jennifer Teng,1
Jeffrey P. Gregg,6,9,10
Paul Ashwood,7,9,10
Judy Van de Water,8,9,10
and Frank R. Sharp1,9,10
1 – Department of Neurology, University of California at Davis Medical Center, Sacramento, CA 95817 USA
2 – Department of Civil and Environmental Engineering, University of California at Davis, Sacramento, CA USA
3 – Department of Public Health Sciences, University of California at Davis Medical Center, Sacramento, CA USA
4 – Department of VM: Molecular Biosciences, University of California at Davis Medical Center, Sacramento, CA USA
5 – Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CA USA
6 – Department of Pathology, University of California at Davis Medical Center, Sacramento, CA USA
7 – Department of Medical Microbiology and Immunology, University of California at Davis Medical Center, Sacramento, CA USA
8 – Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis Medical Center, Sacramento, CA USA
9 – The MIND Institute, University of California at Davis Medical Center, 2805 50th Street, Room 2434, Sacramento, CA USA
10 – UC Davis Center for Children’s Environmental Health and Disease Prevention, Sacramento, CA USA
Abstract
Gene expression in blood was correlated with mercury levels in blood of 2- to 5-year-old boys with autism (AU) compared to age-matched typically developing (TD) control boys. This was done to address the possibility that the two groups might metabolize toxicants, such as mercury, differently. RNA was isolated from blood and gene expression assessed on whole genome Affymetrix Human U133 expression microarrays. Mercury levels were measured using an inductively coupled plasma mass spectrometer. Analysis of covariance (ANCOVA) was performed and partial correlations between gene expression and mercury levels were calculated, after correcting for age and batch effects. To reduce false positives, only genes shared by the ANCOVA models were analyzed. Of the 26 genes that correlated with mercury levels in both AU and TD boys, 11 were significantly different between the groups (P(Diagnosis*Mercury) ≤ 0.05). The expression of a large number of genes (n = 316) correlated with mercury levels in TD but not in AU boys (P ≤ 0.05), the most represented biological functions being cell death and cell morphology. Expression of 189 genes correlated with mercury levels in AU but not in TD boys (P ≤ 0.05), the most represented biological functions being cell morphology, amino acid metabolism, and antigen presentation. These data and those in our companion study on correlation of gene expression and lead levels show that AU and TD children display different correlations between transcript levels and low levels of mercury and lead. These findings might suggest different genetic transcriptional programs associated with mercury in AU compared to TD children.
US National Library of Medicine
National Institutes of Health – Nov 1982
Abstract
Cell-mediated immune response to human myelin basic protein was studied by the macrophage migration inhibition factor test in 17 autistic patients and a control group of 11 patients suffering from other mental diseases included in the differential diagnosis of the syndrome of autism. Of the 17 autistic patients, 13 demonstrated inhibition of macrophage migration, whereas none of the nonautistic patients showed such a response. The results indicate the existence of a cell-mediated immune response to brain tissue in the syndrome of autism.
US National Library of Medicine
National Institutes of Health – Apr 2000
Kawashima H, Mori T, Kashiwagi Y, Takekuma K, Hoshika A, Wakefield A.
Author information
Department of Paediatrics, Tokyo Medical University, Japan.
Abstract
It has been reported that measles virus may be present in the intestine of patients with Crohn’s disease. Additionally, a new syndrome has been reported in children with autism who exhibited developmental regression and gastrointestinal symptoms (autistic enterocolitis), in some cases soon after MMR vaccine. It is not known whether the virus, if confirmed to be present in these patients, derives from either wild strains or vaccine strains. In order to characterize the strains that may be present, we have carried out the detection of measles genomic RNA in peripheral mononuclear cells (PBMC) in eight patients with Crohn’s disease, three patients with ulcerative colitis, and nine children with autistic enterocolitis. As controls, we examined healthy children and patients with SSPE, SLE, HIV-1 (a total of eight cases). RNA was purified from PBMC by Ficoll-paque, followed by reverse transcription using AMV; cDNAs were subjected to nested PCR for detection of specific regions of the hemagglutinin (H) and fusion (F) gene regions. Positive samples were sequenced directly, in nucleotides 8393-8676 (H region) or 5325-5465 (from noncoding F to coding F region). One of eight patients with Crohn disease, one of three patients with ulcerative colitis, and three of nine children with autism, were positive. Controls were all negative. The sequences obtained from the patients with Crohn’s disease shared the characteristics with wild-strain virus. The sequences obtained from the patients with ulcerative colitis and children with autism were consistent with being vaccine strains. The results were concordant with the exposure history of the patients. Persistence of measles virus was confirmed in PBMC in some patients with chronic intestinal inflammation.
VAXXED TV – I gave up being a nurse because of vaccines
My mother was never the same after vaccinations
Two of my three children are injured by vaccines
My vaccinated child gave my 4 month old baby chickenpox
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
Study published in the Annals of Clinical Psychiatry suggests that Autism is likely triggered by a virus, and that measles virus (MV and/or MMR vaccine) might be a very good candidate. It supports the hypothesis that a virus-dincued autoimmune response may play a causal role in autism.
US National Library of Medicine
National Institutes of Health – 2002
Singh VK, Lin SX, Newell E, Nelson C.
Author information
Department of Biology and Biotechnology Center, Utah State University, Logan, Utah 84322, USA. singhvk@cc.usu.edu
Abstract
Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal antibodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.
A study published in the American Journal of Clinical Nutrition determined that an increased vulnerability to oxidative stress and decreased capacity for methylation may contribute to the development and clinical manifestation of autism. It’s well known that viral infections cause increased oxidative stress. Research suggests that metals, including those found in many vaccines are directly involved in increasing oxidative stress.
S Jill James, Paul Cutler, Stepan Melnyk, Stefanie Jernigan, Laurette Janak, David W Gaylor, and James A Neubrander
Author Affiliations
From the Department of Pediatrics, University of Arkansas for Medical Sciences, and the Arkansas Children’s Hospital Research Institute, Little Rock, AR (SJJ, SM, and SJ); Niagara Falls, NY (PC); Colden, NY (LJ); Gaylor and Associates, LLC, Eureka Springs, AR (DWG); and Edison, NJ (JAN)
Abstract
Background: Autism is a complex neurodevelopmental disorder that usually presents in early childhood and that is thought to be influenced by genetic and environmental factors. Although abnormal metabolism of methionine and homocysteine has been associated with other neurologic diseases, these pathways have not been evaluated in persons with autism.
Objective: The purpose of this study was to evaluate plasma concentrations of metabolites in the methionine transmethylation and transsulfuration pathways in children diagnosed with autism.
Design: Plasma concentrations of methionine, S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), adenosine, homocysteine, cystathionine, cysteine, and oxidized and reduced glutathione were measured in 20 children with autism and in 33 control children. On the basis of the abnormal metabolic profile, a targeted nutritional intervention trial with folinic acid, betaine, and methylcobalamin was initiated in a subset of the autistic children.
Results: Relative to the control children, the children with autism had significantly lower baseline plasma concentrations of methionine, SAM, homocysteine, cystathionine, cysteine, and total glutathione and significantly higher concentrations of SAH, adenosine, and oxidized glutathione. This metabolic profile is consistent with impaired capacity for methylation (significantly lower ratio of SAM to SAH) and increased oxidative stress (significantly lower redox ratio of reduced glutathione to oxidized glutathione) in children with autism. The intervention trial was effective in normalizing the metabolic imbalance in the autistic children.
Conclusions: An increased vulnerability to oxidative stress and a decreased capacity for methylation may contribute to the development and clinical manifestation of autism.
A study published by the Department of Pharmaceutical Sciences at Northeastern University, Boston determined that a novel growth factor signalling pathway that regulates methionine synthase(MS) activity and thereby modulates methylation reactions. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins. You can read more about this here, and here. You can read more about the MS/autism link here
US National Library of Medicine
National Institutes of Health – Apr 2004
Waly M, Olteanu H, Banerjee R, Choi SW, Mason JB, Parker BS, Sukumar S, Shim S, Sharma A, Benzecry JM, Power-Charnitsky VA, Deth RC.
Author information
Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.
Abstract
Methylation events play a critical role in the ability of growth factors to promote normal development. Neurodevelopmental toxins, such as ethanol and heavy metals, interrupt growth factor signaling, raising the possibility that they might exert adverse effects on methylation. We found that insulin-like growth factor-1 (IGF-1)- and dopamine-stimulated methionine synthase (MS) activity and folate-dependent methylation of phospholipids in SH-SY5Y human neuroblastoma cells, via a PI3-kinase- and MAP-kinase-dependent mechanism. The stimulation of this pathway increased DNA methylation, while its inhibition increased methylation-sensitive gene expression. Ethanol potently interfered with IGF-1 activation of MS and blocked its effect on DNA methylation, whereas it did not inhibit the effects of dopamine. Metal ions potently affected IGF-1 and dopamine-stimulated MS activity, as well as folate-dependent phospholipid methylation: Cu(2+) promoted enzyme activity and methylation, while Cu(+), Pb(2+), Hg(2+) and Al(3+) were inhibitory. The ethylmercury-containing preservative thimerosal inhibited both IGF-1- and dopamine-stimulated methylation with an IC(50) of 1 nM and eliminated MS activity. Our findings outline a novel growth factor signaling pathway that regulates MS activity and thereby modulates methylation reactions, including DNA methylation. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins.
VAXXED TV – Vaccines gave my son autism
Vaccines while pregnant injured my daughter
Dr. Suzanne Humphries discusses smallpox from 1797 – 2005
MERCK’S DIRTY LITTLE SECRET – BY DR. SUZANNE HUMPHRIES
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.
VAXXED TV – VaxXed Stories: Eric and Ronnie in Denver, Colorado
Includes music and footage from Ronnie’s video for Eric, “Eric’s life before and after the Vaccine”. See it here:
Vaccines killed my 4 year old son
My own VaxXed versus unvaccinated
8 children- unvaccinated and healthy
Vaccine injuries
Vaxxed. Partially Vaxxed and unvaccinated
Hep B injured me
Unlocking key to autism
MMR vaccines gave my sons autism
Court ordered MMR on my son
A study published in the Journal of Toxicology and Environmental Health, Part A: Current Issues by the Department of Economics and Finance at the University of New York shows how researchers suspect one or more environmental triggers are needed to develop autism, regardless of whether individuals have a genetic predisposition or not. They determined that one of those triggers might be the “battery of vaccinations that young children receive.” Researchers found a positive and statistically significant relationship between autism and vaccinations. They determined that the higher the proportion of children receiving recommended vaccinations, the higher the prevalence of autism. A 1 % increase in vaccination was associated with an additional 680 children having autism. The results suggest that vaccines may be linked to autism and encourages more in depth study before continually administering these vaccines.
US National Library of Medicine
National Institutes of Health – 2011
Delong G.
Author information
Department of Economics and Finance, Baruch College/City University of New York, New York, New York, USA. gayle.delong@baruch.cuny.edu
Abstract
The reason for the rapid rise of autism in the United States that began in the 1990s is a mystery. Although individuals probably have a genetic predisposition to develop autism, researchers suspect that one or more environmental triggers are also needed. One of those triggers might be the battery of vaccinations that young children receive. Using regression analysis and controlling for family income and ethnicity, the relationship between the proportion of children who received the recommended vaccines by age 2 years and the prevalence of autism (AUT) or speech or language impairment (SLI) in each U.S. state from 2001 and 2007 was determined. A positive and statistically significant relationship was found: The higher the proportion of children receiving recommended vaccinations, the higher was the prevalence of AUT or SLI. A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI. Neither parental behavior nor access to care affected the results, since vaccination proportions were not significantly related (statistically) to any other disability or to the number of pediatricians in a U.S. state. The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted.
A study published in the Journal of Toxicology by the Department of Neurosurgery at The Methodist Neurological Institute in Houston has shown that ASD is a disorder caused by a problem in brain development. They looked at B-cells and their sensitivity levels to thimerosal, a commonly used additive in many vaccines. They determined that ASD patients have a heightened sensitivity to thimerosal which would restrict cell proliferation that is typically found after vaccination. The research shows that individuals who have this hypersensitivity to thimerosal could make them highly susceptible to toxins like thimerosal, and that individuals with a mild mitochondrial defect may be affected by thimerosal. The fact that ASD patients’ B cells exhibit hypersensitivity to thimerosal tells us something.
Journal of Toxicology
Volume 2013 (2013), Article ID 801517, 11 pages
Martyn A. Sharpe, Taylor L. Gist, and David S. Baskin
Department of Neurosurgery, The Methodist Neurological Institute, 6560 Fannin Street, Scurlock Tower No. 944, Houston, TX 77030, USA
Abstract
The role of thimerosal containing vaccines in the development of autism spectrum disorder (ASD) has been an area of intense debate, as has the presence of mercury dental amalgams and fish ingestion by pregnant mothers. We studied the effects of thimerosal on cell proliferation and mitochondrial function from B-lymphocytes taken from individuals with autism, their nonautistic twins, and their nontwin siblings. Eleven families were examined and compared to matched controls. B-cells were grown with increasing levels of thimerosal, and various assays (LDH, XTT, DCFH, etc.) were performed to examine the effects on cellular proliferation and mitochondrial function. A subpopulation of eight individuals (4 ASD, 2 twins, and 2 siblings) from four of the families showed thimerosal hypersensitivity, whereas none of the control individuals displayed this response. The thimerosal concentration required to inhibit cell proliferation in these individuals was only 40% of controls. Cells hypersensitive to thimerosal also had higher levels of oxidative stress markers, protein carbonyls, and oxidant generation. This suggests certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like the vaccine preservative thimerosal.
A study published in the Journal of Biomedical Sciences determined that the autoimmunity to the central nervous system may play a causal role in autism. Researchers discovered that because many autistic children harbour elevated levels of measles antibodies, they should conduct a serological study of measles-mumps-rubella (MMR) and myelin basic protein (MBP) autoantibodies. They used serum samples of 125 autistic children and 92 controlled children. Their analysis showed a significant increase in the level of MMR antibodies in autistic children. The study concludes that the autistic children had an inappropriate or abnormal antibody response to MMR. The study determined that autism could be a result from an atypical measles infection that produces neurological symptoms in some children. The source of this virus could be a variant of MV, or it could be the MMR vaccine.
US National Library of Medicine
National Institutes of Health – 2002
Singh VK, Lin SX, Newell E, Nelson C.
Author information
Department of Biology and Biotechnology Center, Utah State University, Logan, Utah 84322, USA. singhvk@cc.usu.edu
Abstract
Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal antibodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.
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.
Vaccination debate arrives in Tacoma via documentary tour bus
Posted 4:44 PM, June 20, 2017, by Steve Kiggins, Updated at 05:38PM, June 20, 2017
TACOMA, Wash. – The number of mumps cases reported this year in Washington state outpaces totals from years past.
State health officials said one possible factor could be parents who haven’t gotten their children vaccinated.
Nearly 5 percent of kindergartners in Washington weren’t immunized for the 2016-2017 school year because of personal beliefs or medical reasons — that’s more than double the national average of 2 percent, according to the Washington State Department of Health.
But there is a group visiting our state who says this may not be a bad thing. Producers for a documentary called “Vaxxed” brought their tour bus to Tacoma`s Franklin Park to speak with parents who worry their kids were injured from vaccinations.
“I’m not here to tell parents not to vaccinate,” said Dr. Suzanne Humphries, who is touring with the documentary’s producers. “I’m here to tell parents there’s a bigger picture.”
Part of that bigger picture includes hundreds of names scribbled on the side of the Vaxxed tour bus. The names represent those who claim to have been injured by vaccinations.
According to Humphries, parents should do their research before vaccinating their child.
Truth About Tetanus Infection and the Vaccine
Step on a rusty nail … go get a Tetanus shot, Right? Wrong!
Tetanus has nothing to do with rust! No amount of rust rubbed on your body or eaten or injected will cause Tetanus.
(It will likely cause some other type of harm though.)
Horse droppings always contain tetanus bacteria. It lives in a horses intestines. Horses are the main source of the bacteria.
If a deep wound is infected with tetanus, a toxin may be produced. It is this toxin that causes problems.
Was that rusty nail you stepped on covered in horse manure? In the days of the horse and carriage, streets were covered in horse droppings. But unless you live on a hobby farm or ranch today, that is likely not a problem.
Dr. Suzanne Humphries’s video
FDA approved: Human cancer cells added to vaccines
Posted by: Lori Alton, staff writer in Vaccine Dangers December 6, 2014
(NaturalHealth365) Consumers already concerned about vaccine dangers are likely to find little reassurance in recent reports that Food and Drug Administration (FDA) officials are giving vaccine manufacturers the green light to use human cancer cells to produce future vaccines.
But, the big question to ask is ‘why?’ The FDA, with this approval, shows no regard for basic safety issues.
Looks like profits are more important than human health concerns
The FDA’s approval is not related to any effort to make vaccines safer or more effective. Not surprisingly, the latest situation to fuel the fire over vaccine use comes down to cost of production.
To manufacture vaccines through the use of human cancer tumor cells – sadly, in ready supply – is less expensive than prior methods of breeding lab animals to provide culture media. Therefore, vaccine manufacturers are more likely to rake in millions of dollars in the process.
While downplaying the concern that vaccines made from cancer cells could transfer cancer to vaccine recipients, proponents of the use of human cancer cells as an additional substrate for the manufacture of vaccines claim there are several ‘advantages’. The primary argument is that cancer cell substrate would offer greater virus yield and production potential for new vaccines – otherwise unavailable through the use of previous substrates.
Official transcripts reveal an uncertain future for humanity
A recently uncovered transcript, from a September 19, 2012 meeting of the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) within the agency’s Center for Biologics Evaluation and Research (CBER), reveals misgivings even among the experts as to the safety of vaccines manufactured from human cancer cells.
A committee member identified in the transcript only as ‘Dr. H’, from the University of North Carolina, is quoted as stating, “I’m guessing the safety concerns we have are ones that you typically wouldn’t observe in humans on the time scale that a Phase I trial takes place on…We are worried about these vaccines causing cancer in people many years down the road, well beyond the conclusion of the Phase I study.”
Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents: A Pilot Case–Control Study
Results: Subjects with newly diagnosed AN were more likely than controls to have had any vaccination in the previous 3 months [hazard ratio (HR) 1.80, 95% confidence interval 1.21–2.68]. Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of AN, OCD, and an anxiety disorder. Several other associations were also significant with HRs greater than 1.40 (hepatitis A with OCD and AN; hepatitis B with AN; and meningitis with AN and chronic tic disorder).
Natural News – Incredibly disturbing animation reveals how vaccines are really made… WARNING: this will turn your stomach
Wednesday, April 05, 2017 by: Mike Adams
interesting how so many people scrutinize the ingredients in the groceries they buy, yet they allow themselves to be injected with vaccines without having any clue what ingredients they contain?
Vaccines are deliberately made with all sorts of bizarre ingredients, the CDC confirms. These ingredients include toxic heavy metals, animal blood components, human fetal tissue, monkey kidney cells, inflammatory chemicals that harm nerve cells, chemical preservatives, taste-enhancing chemicals (like MSG) and much more.
Even more shockingly, the way vaccines are made is beyond merely gross… it’s inhumane! Did you know that African Green Monkeys are raised in cages, infected with disease, murdered by drug companies then organ harvested to extract diseased kidneys that are used to make Smallpox vaccines?
Did you know that the human chickenpox vaccine is made from human tissue harvested from aborted human babies? Did you know that the abortion industry and the vaccine industry work to make sure a steady supply of aborted baby parts is supplied to vaccine manufacturers to keep the factories humming?
33 Fragen an deinen Impfarzt
Diese Fragen können schon vorab per Fax oder Email an deinen Impfarzt gesendet werden, damit er/sie sich auf das kommende Impfberatungsgespräch vorbereiten kann. Gegebenenfalls kann ja der Thermin nach hinten verschoben werden, sollte der Arzt diese Fragen nicht beantworten können.
International Journal of Vaccines and Vaccination – New Quality-Control Investigations on Vaccines Micro-and Nanocontamination
Abstract
Vaccines are being under investigation for the possible side effects they can cause. In order to supply new information, an electron-microscopy investigation method was applied to the study of vaccines, aimed at verifying the presence of solid contaminants by means of an Environmental Scanning Electron Microscope equipped with an X-ray microprobe. The results of this new investigation show the presence of micro- and nanosized particulate matter composed of inorganic elements in vaccines’ samples which is not declared among the components and whose unduly presence is, for the time being, inexplicable. A considerable part of those particulate contaminants have already been verified in other matrices and reported in literature as non biodegradable and non biocompatible. The evidence collected is suggestive of some hypotheses correlated to diseases that are mentioned and briefly discussed
What did the new Italian study find?
Examining 30 vaccines — representing 44 samples in total — the researchers found particulate matter, in aggregates and clusters, of micro- and nano-sized particulate matter in 43 of the 44 samples whose presence was not declared in the leaflets delivered in the package of the product.
The scientists were “baffled” by their findings of lead, tungsten, gold, chromium, stainless steel, gold-zinc aggregate, platinum, silver, bismuth, iron, silicon and many others. The investigations revealed that some particles are embedded in a biological substrate. As soon as a particle comes in contact with proteic fluids, an interaction occurs and a bigger-sized compound is created that is not biodegradable and can induce adverse effects, since it is not recognized as self by the body. The authors conclude the following from their findings:
This new investigation represents a new quality control that can be adopted to assess the safety of a vaccine. Our hypothesis is that this contamination is unintentional, since it is probably due to polluted components or procedures of industrial processes (e.g. filtrations) used to produce vaccines, not investigated and not detected by the Producers.
The analyses carried out showed that, in all samples checked, vaccines contain non-biocompatible and bio-persistent foreign bodies which are not declared by the producers.
Here are some gentle detox ideas for a child who has been vaccinated (to help counteract the harmful effects of vaccines):
Detoxification bath – This bath can be used to pull bacteria and viruses from the spine, and cellular waste, metals and chemicals from the body. Add 5 drops of “Lavender“ to your child’s bath with a 1/4 cup of epsom salt. You can also do this as a foot bath.
Probiotics – A probiotic is essential to restore gut flora and balance the immune system. This is very important especially if a child experienced an adverse reaction to a vaccine (like eczema, ear infections, arthritis, diabetes, gastrointestinal disease, etc.). I love “Life Start” by Natren (for babies/young children) and this probiotic by Garden of Life.
Omega 3 Oil – This is especially important to take if your child suffered an adverse reaction or had MMR, DPT, Dtap, or Varicella vaccines. Cod liver oil is thought to be the most superior of all fish oils but with the cost of CLO and potential rancidity, I use Udo’s Oil.
Cilantro Chelation Therapy – Dr. Yoshiaki Omura discovered that the leaves of the coriander plant can accelerate the excretion of mercury and aluminum from the body. If you give the body what it needs, it will heal itself, and cilantro has a molecular bond that binds to heavy metals and pulls them from the body. Cilantro therapy is gentle and inexpensive.
To use: Incorporate cilantro into your detoxing regimen by juicing with cilantro consuming it raw. Your child should have a minimum of 1 teaspoon daily for 2-3 weeks. You can also do a detox bath with two drops of coriander and epsom salt.
Elderberry – This is an excellent herb for children and can be taken as a syrup or in supplement form. Research shows that elderberry inhibits enzymes used by viruses to penetrate and infect healthy cells. Another option is Elderberry Defense which contains Echinacea, royal jelly, and olive leaf. Echinacea strengthens the immune system, fights viral infections in the body, and increases the production of T-lymphocytes to fight bacterial toxins, and stimulates macrophages (that filter out and destroy foreign particles, bacterial and toxins in the lymph system).
Royal jelly contains many nutrients and all 8 essential amino acids, helps prevent illness, and combats the stress on the body caused by vaccines. Olive leaf has been shown to be an effective remedy against almost every type of disease-causing microorganism, relieves many health problems, and has exhibited microbial effects against over 130 infectious diseases. It would be pertinent to take this remedy if your child has had any of the live vaccines including MMR, Varicella, Flu Vaccine, OPV, DPT, and would also be indicated in Dtap.
There are several ways to take elderberry: You can make your own elderberry syrup for children under two, purchase elderberry in soft chew or herbal form (2 capsules daily mixed in applesauce), or drink an elderberry-infused tea.
Vitamin C helps counteract the damage of heavy metals, chemicals, and toxins contained in vaccines and strengthens the immune system. The best way to get vitamin C is through food but since we’re detoxing, adding a supplement and taking it frequently throughout the day is beneficial. I typically recommend vitamin C chewables but powdered form and liposomal form is also an option.
Silica helps gently pull toxins out of the tissues and into the blood stream to be eliminated from the body. Studies on silicic acid show that it is an effective non-invasive therapy for reducing the burden of aluminum in the body, that it slows down the accumulation of aluminum in brain tissue and the gastrointestinal tract, substantially reduces aluminum bioavailability to humans, reduces toxicity in plants and animals, and enhances the excretion of aluminum in urine without negative side-effects. In other words, silica can only help a good detox. You can purchase silica in liquid mineral form, as a cell salt, or as an herbal supplement (horsetail).
Homeopathic Antidotes – Some children benefit greatly from homeopathic antidotes. Typically, a homeopath or naturopathic doctor will either recommend a remedy based on the constitutional type of your child and side effects they experienced as a result of vaccinations, or will recommend a vaccine potentized as a homeopathic remedy known as a “vaccine antidote.”
If your child was vaccinated against chicken pox, measles, mumps, rubella, and polio, you would want a Varicella antidote, MMR antidote, and IPV antidote. If they were injected with vitamin K or Hepatitis B, you would want a vitamin K and Hep B antidote. Antidotes generally have no negative side-effects and are in an easy-to-take sugar pellet form that can be dissolved under the tongue or crushed up.
Water – When toxins are pulled from the body, they need to be flushed out. Full kidney function is dependent upon there being enough water in the body. Avoid soda, dairy, and junk juices and encourage your child to drink plenty of water (5-8 cups) throughout the day. You can sweeten it with a little honey and lemon (for increased vitamin C) or add some liquid chlorophyll.
Massage – During a detox it is especially important to “milk the lymph nodes” through gentle massage. The Lymphatic system is the clean-up crew of the body and massage helps remove cell wastes, proteins, excess fluid, viruses, and bacteria trapped in the lymph nodes.
Dandelion Root (herbal or tincture)- Supporting the liver during a detox is very important because the liver performs over 5,000 functions – including toxin filtration. Although there are several herbs that can support and cleanse the liver, none are safer, more effective, or as inexpensive as dandelion. Dandelion helps the liver and gallbladder filter out toxins, purifies the blood, stimulates the kidneys to eliminate toxins through the urine, and assists with cell metabolism.
You can purchase dandelion greens from the store (to use in juices and smoothies) or purchase in pill form, as an herbal tea, or pick them from your own back yard. If you have a hard time believing that the “weed” in your yard could serve such an important purpose, might I recommend reviewing the studies on dandelion in the PubMed database? They are quite impressive.
Raw Food, Juices, & Smoothies – The absolute best way to counteract the harmful effects of a vaccine is through food, and my favorite way of doing this for children is through raw smoothies and juices. Shoot for at least 2-3 raw juices or smoothies per day during a detox, in addition to their normal meals. You can check out my Pinterest for some of my favorite juices and smoothies and “Ergonomics of a Smoothie” for smoothie tips. Try to include foods like broccoli, collards and kale, daikon radish, garlic, onions, spices, and sunny-side up eggs from free-range chickens in their diet during this time.
Dutch whistle-blower reveals Big Pharma’s “business model” — Creating pandemics to sell their vaccines, with zero liability for their poisons, while their excess vaccines are disposed of with the same safety precautions used with hazardous waste.
Why you can fuck off when you say I NEED to vaccinate my children….
June 20, 2017
Vaccines are not scientific, because there has never been – I repeat, NEVER – been a published study that used an unvaccinated controlled/placebo group, to demonstrate the long-term efficacy, and long-term safety of any vaccine used in the U.S. Not one controlled study in any scientific journal evaluating the long-term benefits and risks vs. dangers of vaccination vs. unvaccinated (Dr. Hugh Fudenberg, M.D. world-leading in Immunogenetics, speech at the NVIC International Vaccine Conference, Arlington Virginia, Sept. 1997.
Also, there has been no long-term study done on the safety of multiple vaccines given at the same time, or the carcinogenic and reproductive complications that may occur. Thus, no doctor or other health professional can honestly tell you your baby will be safe and there is no future cancer risk.
For those of you who remember science class, the use of a control (untreated or “placebo”) group to test results was considered fundamental in producing scientific findings. This bizarre absence of scientific method in vaccine studies tells you something vaccine industry integrity.
I ask you to show me one, just ONE, scientific study on any routine childhood vaccination showing that vaccinated kids are better off in the long-term than unvaccinated kids. You have to read all the raw data on the study and make sure that the control group is actually unvaccinated and the “placebo” they are using isn’t just another vaccine, or a vaccine that has just had the somewhat safe antigen removed and all the poisonous, toxic ingredients left in.
In fact, most general non-“big-pharma” health studies show that non-vaccinated people are healthier all around, and more disease resistant than vaccinated people. A 2011 German study (The Kiggs Study) examined 17,461 children aged 0-19 across Germany, and found vaccinated kids were 2-5 times more likely to suffer from a range of diseases such as otitis media, allergies, asthma, bronchitis, migraines, and experience ten times the number of epileptic seizures than unvaccinated kids. The study also found that many parents who did not vaccinate subsequent children due to side effects in the first children, stated the unvaccinated younger siblings were much healthier. You can argue that the correlation does not always equal causation. However, if you are a pro-vaxxer, please be fair and balanced, and use your same line of critical analysis toward non-placebo big pharma vaccination studies.
The one and only published comparison (non-controlled) study I have found comparing vaccinated kids to unvaccinated kids, was one in 2008 which showed that infants who were vaccinated with the Hepatitis B vaccine with Thimerosal (Thimerosal is 50% Mercury by weight) had nine times higher rate of developmental disabilities than unvaccinated children (The Journal of Toxicological and Environmental Chemistry, Sept. 2008 entitled Hepatitis B triple series vaccine and developmental disability in U.S. children aged 1 to 9 years by Gallagher and Goodman.).
Our society celebrates the historical conquests of vaccines over disease. However, the data shows this celebration may not be deserved. National Morbidity Reports, from the U.S. Public Health Reports, show the rise and fall of deaths related to disease epidemics. In most cases, the death rate was decreasing significantly before vaccines were even introduced.
Gardasil May Cause Cancer NOT TESTED FOR CARCINOGENICITY
Information in the package insert states that the vaccine has not been tested for carcinogenicity. (2) Why has this not been done? Absence of evidence is not evidence of absence! There appears to be no official requirement for vaccines to be tested for carcinogenicity and no incentive for manufacturers to do so. Many experts consider that vaccines are conducive towards the dramatic worldwide increase in cancer cases. REPLACEMENT MAY CAUSE DEVELOPMENT OF CANCER
A normal phenomenon in virology is that virus strains which have been removed are replaced by new ones. It is not known by anyone, including the vaccine manufacturer whether the new virus strains are more carcinogenic than the original ones which have been removed.
The chief editor of the Journal of the Norwegian Medical Association, immunologist Charlotte Haug writes about several unanswered questions including that of replacement in her article “We Need to Talk about HPV Vaccination – Seriously”:
Abhorred vacuum.There is another serious question that may be answered sooner: what effect will the vaccine have on the other cancer-causing strains of HPV? Nature never leaves a void, so if HPV-16 and HPV-18 are suppressed by an effective vaccine, other strains of the virus will take their place. The question is, will these strains cause cervical cancer?
Results from clinical trials are not encouraging. Vaccinated women show an increased number of precancerous lesions caused by strains of HPV other than HPV-16 and HPV-18. The results are not statistically significant, but if the trend is real – and further clinical trials should tell us in a few years – there is reason for serious concern. (3)
In an article in the New England Journal of Medicine “ Human Papilloma Virus Vaccination – Reasons for Caution”, Dr. Haug again poses the question of replacement:
“How will the vaccine affect other oncogenic strains of HPV? If HPV-16 and HPV-18 are effectively suppressed, will there be selective pressure on the remaining strains of HPV? Other strains may emerge as significant oncogenic serotypes”. (4)
Replacement was obviously one of several unanswered questions when FDA, Merck and the Norwegian government signed a contract which involved research studies on thousands of young Norwegian schoolgirls. The agreement was that Gardasil would be approved in US under the condition that extensive research projects were carried out in Norway. There was implication of corruption in connection with introduction of Gardasil in the childrens’ vaccination program. (5)
The contract includes this statement from FDA to Merck:
“You have committed to conduct a study in collaboration with the Norwegian Government, if GARDASIL is approved in the European Union and the Government of Norway incorporates HPV vaccination into its national guidelines, to assess the impact of HPV vaccination on the following in Norway … to assess whether administration of GARDASIL will result in replacement of these diseases due to vaccine HPV types with diseases due to non-vaccine HPV types.” (6) ABNORMAL PAP SMEARS AFTER GARDASIL VACCINATION
Corrupt Vaccine “Safety Testing” Explained By Dr. Andrew Wakefield
Dr. Andrew Wakefield gives a short overview of why vaccine “safety testing” is fraudulent on so many levels, including the fact that vaccines are NOT tested the same way pharmaceutical drugs are tested: double blind placebo tests. This video is of a Q&A after the screening of his documentary Vaxxed: From Cover-Up to Catastrophe – a MUST SEE documentary by everyone. http://www.vaxxedthemovie.comhttp://www.stopmandatoryvaccination.com — with Andrew Wakefield, Del Bigtree and Polly Tommey.
Cherai doesn’t vaccinate because vaccines contain harmful ingredients that maim and kill children. Cherai is not worried about infectious diseases because she keeps her child healthy, and therefore, protected. If you are on the fence about vaccination and would like to learn more, start here: http://www.GoVaccineFree.org.
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“I used to work at an Urgent Care center and I can tell you that vaccines are pushed for profit, not health. And when parents called to say their child was having a vaccine reaction, the doctor didn’t even want to know. We were instructed to tell them everything was normal.” — Lupita Salazar
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Dr. Andrew Moulden: Every Vaccine Produces Harm
by John P. Thomas
Health Impact News
Canadian physician Dr. Andrew Moulden provided clear scientific evidence to prove that every dose of vaccine given to a child or an adult produces harm. The truth that he uncovered was rejected by the conventional medical system and the pharmaceutical industry. Nevertheless, his warning and his message to America remains as a solid legacy of the man who stood up against big pharma and their program to vaccinate every person on the Earth.
Dr Moulden died unexpectedly in November of 2013 at age 49.
Because of the strong opposition from big pharma concerning Dr. Moulden’s research, I became concerned that the name of this brilliant researcher and his life’s work had nearly been deleted from the internet. His reputation was being disparaged, and his message of warning and hope was being distorted and buried without a tombstone.
I prepared a series of articles as a tribute to a great physician and as a memorial to a courageous individual who was not afraid to speak the truth about medical corruption and a flawed healthcare system that does more to harm health than it does to cure disease.
This is the first in a series of four articles about Dr. Moulden — the man, the physician, and the powerful advocate for ending all vaccine use. In future articles, I will summarize his detailed scientific evidence, which shows how vaccine damage occurs. I will explain the common mechanisms behind vaccine damage and how vaccines harm the health of everyone who receives them regardless of whether or not they notice any adverse reactions at the time they take the shots.
Dr. Moulden stated:
What we have done to each other [with vaccines] has produced the most profound damage to humankind by humankind in the history of humanity. And the reason why we got here is partly because of:
Our arrogance in thinking that we know everything. In physiology and medicine we do not know everything!
[Our greed] to advance our own self-interest to make money, to sell products and to advance corporate alliances. Commercialization has overtaken the fundamental human value of “do unto others as you would have others do unto you.” When society turns toward this human value, then we would all be working together for the greater good of each other. [However, other values have become more important] I don’t care whose feet I step on or how I get there as long as my American dream is realized. I don’t care who has to pay for it on the way of getting there. [1]
Dr. Moulden’s Credibility
Was Dr. Moulden a crackpot as some sources claim, or was he a brilliant physician and researcher? This series of articles will set the record straight, and summarize the contribution that his work has made to medical knowledge.
When I evaluate the credibility of people who are unknown to me, I begin by seeking answers to a few basic questions. For example: Is this person offering opinion, or can he or she back up the claims with valid science? Does he have educational credentials? Are there other physicians and scientists who support his or her beliefs and recommendations? Is this person controlled by the pharmaceutical industry, allopathic medical associations, or the US FDA (US Food and Drug Administration)? And finally, what do Quackwatch and their friends have to say about the person?
Dr. Moulden had a PhD in Clinical Psychology and Neuropsychology. He had a master’s degree in child development, and was also a medical doctor. [2] His work was respected by other researchers who don’t march to the drumbeat of the pharmaceutical companies. Dr. Moulden was a threat to the pharmaceutical industry, and their Quackwatch family of 21 related websites treated him as an enemy. [3, 4]
Vaccine Contraindications: Six People Who Should Not Be Vaccinated
The debate surrounding vaccinations is a fierce one, and personally, I don’t like to argue about it. I’m happy to make the right choices for my family while you make the right ones for yours. (I personally have suffered adverse reactions to vaccinations.) It’s ok to have different opinions, really it is. But there are a lot of folks out there who think everyone should be vaccinated, period, and those who choose not to vaccinate should be penalized or worse.
Listen. I get that people are scared and there’s a lot of fear-mongering in the media. But let’s be realistic here: vaccinations are a medical procedure. There are risks. Vaccinations are not right for everyone. There are at least six types of people in particular who should avoid vaccinations, and below, I’ll spell it out.
Vaccine Contraindications
Just like a particular surgery or prescription medication won’t work well for everyone, vaccinations are not a good choice for everyone.
Some people, in particular, are much more likely to have adverse reactions to vaccinations, including:
– Those with an autoimmune disease
– Children born to a mother with an autoimmune disease
– Anyone who is sick
– Pregnant women
– Those who have previously had a reaction to a vaccination
One size does not fit all
Clearly, vaccinations are not the right choice for everyone, and each family should decide what is right for them and their children. When parents are aware of vaccine contraindications, they can make informed and safer choices for their children.
Please share this post so that other parents can learn about vaccine contraindications and decide if vaccination is right for their children.
USA: Highest Vaccination Rate in the World Has the Worst Health
by PAUL FASSA
That “worst health” label includes a ranking of 34th in the world with infant mortality. In other words, the USA has the 34th worst infant survival with its highest rate of vaccinations. Some are directly from multiple vaccinations administered.
But the USA leads the world in infant vaccinations, those administered during the first year after their births – 26 vaccinations during that time.
The only vaccination I recall receiving during early childhood, circa 1948, was the smallpox vaccine, the one that left a circle of shallow pockmarks on the upper arm, a non-ink tattoo that proved you had received that vaccine. Months later there was the booster shot which gave me a vacation of several days away from my first grade teacher while sitting out the chicken pox.
During Naval training the mass vaccination high pressure hand held gun that replaced syringes and needles was tried on us with the polio shot. I wound up with a vacation in the base infirmary with an extended period of the flu. Between those two, there may have been a tetanus shot or two.
From the Healthy Home Economist:
-In1950, there were 3 childhood vaccines typically given when a child entered school.
-In 1983, there were 10 recommended vaccines by the age of 6 years old (24 doses, 7 injections, 4 oral doses for polio).
-In 2010, the CDC vax schedule totaled 68 doses with more than half given by the time a child was only a year and a half old.
-In 2016, the schedule has increased to 74 doses by age 17 with 53 injections and 3 oral doses of rotavirus.
The number of vaccines included in the current childhood vaccine schedule has quadrupled over the past 60 years, with several demanding multiple injections and boosters. During this exponential rise of CDC “recommended” schedules, the health of American children has plummeted.
Autoimmune diseases, learning disabilities, food allergies, chronic ailments, and childhood obesity have all risen. The overall health of this nation ranks very low compared to all other industrialized nations, dead last in most areas.
Vaccine false dogma is so heavy hardly anyone with authority, even in mainstream media, makes the connection between poor health with high vaccination rates. Instead, more, three added for 2016, are getting enforced by mandate or coerced by pediatricians who have the right to refuse medical care on kids who aren’t vaccinated.
Destroying Health with Vaccines is Good Business
50 Studies the AAP Avoided to Mention
There is a robust, worldwide body of published science from highly esteemed scientists questioning the safety of many different aspects of vaccines-how come we never hear from them? The majority of the most compelling science has been published since 2010. Below find 50 such studies to consider, sorted chronologically, and note that these studies only represent a portion of the published work implicating vaccinations in a wide variety of negative health outcomes.
The American Academy of Pediatrics made representations to President Trump in a letter dated 2/7/2017 that are utterly indefensible and inaccurate, as any rational review of the studies below quickly demonstrates. For example, the AAP wrote:
“Claims that vaccines are unsafe when administered according to expert recommendations have been disproven by a robust body of medical literature…we write to express our unequivocal support for the safety of vaccines.”
We contend that the AAP’s statements to the President are baseless, reckless, and easily refuted. The AAP’s letter alone supports the President’s desire to field a Vaccine Safety Commission and do all we can to make vaccines as safe as possible. Please click here for a list of all 50 studies detailed below.
the news network 