Paul Offit - Falsely Defends Thimerosal
I just love Paul Offit. Don't you? What a guy. And children according to his calculations can as well safely tolerate 10,000 vaccines in one day? Here in this below article there is a video he has done, attempting to explain away any concern as to the thimerosal issue and in regard to the recent American Academy of Pediatrics push to keep thimerosal in all the vaccines used in such as other countries that are underdeveloped. So, to keep getting vaccines available across the globe, there is no other way, we must keep poisoning the infants, children, and adults, with mercury to do that and to provide those vaccines? I can understand that possibly single dose vials may be in reality a bit impractical and or more expensive, but really if that is all we can produce that is safe, then the vaccine makers can just go with less for profits. Poisoning the world with mercury containing vaccines has been going on for far to many years and decades already. In the year 2013, they still have no better option? Or is it just about making the least expensive vaccine in those countries, and profits? There has to be a better option, if they were seriously and actively looking. However, until the CDC the WHO and as well the AAP get on board and admit to the serious dangers of thimerosal nothing can nor likely will happen to change this.
So, in this Offit video right here, what are we actually witnessing? WE are witnessing Mr Offit again being a huge part of the problem by ignoring existing science, and again making denial of any problem with thimerosal. What we need is for him to get honest, for this to actually change. He needs to get it in his head that what he is actually doing is not only wrong, but it is as well a criminal act. To as continue to mislead the public, and all existing believed authorities, and the government/s as well, is additionally another criminal act.
So, they are telling us that they can find no other chemical (a neurotoxic heavy metal), on the planet earth to take the place of thimerosal/ mercury, and no substance to perform the same function in a vaccine??? And we are to actually believe that?
At the end of that article page however even though Offit claims that there are seven studies he is referencing, only this study is referenced to, and is NOT a physiological or epidemiological science study, it is only a their own opinion piece. Just look at what this QUACK gets away with. We all know as well that any of the CDC funded epidemiological studies they reference, were entire corrupt with predetermined outcomes and obvious study design flaws. The several analysis available on those studies, show that how and why that is only and the obvious actually thinking conclusion.
Offit's single reference on the page. (And he got away with that).
Orenstein WA, Paulson JA, Brady MT, Cooper LZ, Seib K. Global vaccination recommendations and thimerosal. Pediatrics. 2012;131:149-151.
Lets look at what the reality of some of the real existing science shows us, and a lot of this is also published right in Pubmed, so they obviously can not claim that they are only some obscure studies that do not deserve consideration and further follow up studies. That's right, studies that were needed already decades ago, funded by the CDC, with as well the participation of unbiased oversight.
Medscape Infectious Diseases > Offit on Vaccines
Thimerosal in Vaccines: What Are the Facts?
http://www.medscape.com/viewarticle/776762
Note worthy is as well that at the end of that article page, even though Offit claims that there are seven studies that he is referencing from; only one, this study below is referenced to. It is as well NOT a physiological or epidemiological science study, it is only a their own opinion piece. Just look at what this QUACK gets away with. We all know as well (should), that any of the CDC funded epidemiological studies they reference, were entirely corrupt with predetermined outcomes and obvious study design flaws. The several analysis available on those studies, show that how and why that is only and the obvious actually thinking conclusion.
Offit's article listed - References
Orenstein WA, Paulson JA, Brady MT, Cooper LZ, Seib K. Global vaccination recommendations and thimerosal. Pediatrics. 2012;131:149-151.
--------------------
Here are just a few of the many available and existing scientific studies Mr Offit and the CDC failed to recognize.
This below study, shows that even though ethyl mercury may be detoxed more quickly as far as the amount leaving the body; the study shows that both ethyl mercury and methyl mercury are still a significant concern as to potential toxicity. As well just because ethyl mercury left the body quicker, that would not tell you what level of mercury was left in the tissues, organs, and the brain. Such statements would as well clearly not take in account the children and adults who produce less that adequate levels of glutathione necessary to detox that ethyl mercury.
Arch Toxicol. 1985 Sep;57(4):260-7.
The comparative toxicology of ethyl- and methylmercury.
Magos L, Brown AW, Sparrow S, Bailey E, Snowden RT, Skipp WR.
Abstract
Neurotoxicity and renotoxicity were compared in rats given by gastric gavage five daily doses of 8.0 mg Hg/kg methyl- or ethylmercuric chloride or 9.6 mg Hg/kg ethylmercuric chloride. Three or 10 days after the last treatment day rats treated with either 8.0 or 9.6 mg Hg/kg ethylmercury had higher total or organic mercury concentrations in blood and lower concentrations in kidneys and brain than methylmercury-treated rats. In each of these tissues the inorganic mercury concentration was higher after ethyl- than after methylmercury. Weight loss relative to the expected body weight and renal damage was higher in ethylmercury-treated rats than in rats given equimolar doses of methylmercury. These effects became more severe when the dose of ethylmercury was increased by 20%. Thus in renotoxicity the renal concentration of inorganic mercury seems to be more important than the concentration of organic or total mercury. In methylmercury-treated rats damage and inorganic mercury deposits were restricted to the P2 region of the proximal tubules, while in ethylmercury-treated rats the distribution of mercury and damage was more widespread. There was little difference in the neurotoxicities of methylmercury and ethylmercury when effects on the dorsal root ganglia or coordination disorders were compared. Based on both criteria, an equimolar dose of ethylmercury was less neurotoxic than methylmercury, but a 20% increase in the dose of ethylmercury was enough to raise the sum of coordination disorder scores slightly and ganglion damage significantly above those in methylmercury-treated rats.
http://www.ncbi.nlm.nih.gov/pubmed/4091651
And how can they they at the CDC, keep on recommending the flu shot for all pregnant women that contains 25 mcg. of thimerosal, (mercury)????
Mercury Poisoning Is a Growing Menace
http://readersupportednews.org/opinion2/271-38/15500-focus-mercury-poisoning-is-a-growing-menace
Brain Dev. 2012 May 31. [Epub ahead of print]
Prenatal exposure to organomercury, thimerosal, persistently impairs the serotonergic and dopaminergic systems in the rat brain: Implications for association with developmental disorders.
Ida-Eto M, Oyabu A, Ohkawara T, Tashiro Y, Narita N, Narita M
.
Source:Department of Anatomy II, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.
Abstract
Thimerosal, an organomercury compound, has been widely used as a preservative. Therefore, concerns have been raised about its neurotoxicity. We recently demonstrated perturbation of early serotonergic development by prenatal exposure to thimerosal (Ida-Eto et al. (2011) [11]). Here, we investigated whether prenatal thimerosal exposure causes persistent impairment after birth. Analysis on postnatal day 50 showed significant increase in hippocampal serotonin following thimerosal administration on embryonic day 9. Furthermore, not only serotonin, striatal dopamine was significantly increased. These results indicate that embryonic exposure to thimerosal produces lasting impairment of brain monoaminergic system, and thus every effort should be made to avoid the use of thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/22658806
Mitochondrial Dysfunction
Wow, great information article, but not a mention of vaccines, even though Pubmed and multiple studies on the effect, and as well in regard to glutathione. And also not a mention of the success of biomedical treatment.
http://www.epidemicanswers.org/mitochondrial-dysfunction/
Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal.
Olczak M, Duszczyk M, Mierzejewski P, Wierzba-Bobrowicz T, Majewska MD.
Source
Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, ul. Sobieskiego 9, Warsaw, Poland.
Abstract
Thimerosal, an organomercurial added as a preservative to some vaccines, is a suspected iatrogenic factor, possibly contributing to paediatric neurodevelopmental disorders including autism. We examined the effects of early postnatal administration of thimerosal (four i.m. injections, 12 or 240 µg THIM-Hg/kg, on postnatal days 7, 9, 11 and 15) on brain pathology in Wistar rats. Numerous neuropathological changes were observed in young adult rats which were treated postnatally with thimerosal. They included: ischaemic degeneration of neurons and "dark" neurons in the prefrontal and temporal cortex, the hippocampus and the cerebellum, pathological changes of the blood vessels in the temporal cortex, diminished synaptophysin reaction in the hippocampus, atrophy of astroglia in the hippocampus and cerebellum, and positive caspase-3 reaction in Bergmann astroglia. These findings document neurotoxic effects of thimerosal, at doses equivalent to those used in infant vaccines or higher, in developing rat brain, suggesting likely involvement of this mercurial in neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/21225508
Vaccines and especially aluminum adjuvants cause over activation of the brains microlgia and resulting chronic brain inflammation, and has now been found in both those with ASD and ADHD, in several studies., (Those studies are found as well on this site).
Neurotoxicology. 2012 Mar;33(2):191-206. doi: 10.1016/j.neuro.2012.01.012. Epub 2012 Feb 2.
Microglia in the developing brain: a potential target with lifetime effects.
Harry GJ, Kraft AD.
Source:National Toxicology Program Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Abstract
Microglia are a heterogenous group of monocyte-derived cells serving multiple roles within the brain, many of which are associated with immune and macrophage like properties. These cells are known to serve a critical role during brain injury and to maintain homeostasis; yet, their defined roles during development have yet to be elucidated. Microglial actions appear to influence events associated with neuronal proliferation and differentiation during development, as well as, contribute to processes associated with the removal of dying neurons or cellular debris and management of synaptic connections. These long-lived cells display changes during injury and with aging that are critical to the maintenance of the neuronal environment over the lifespan of the organism. These processes may be altered by changes in the colonization of the brain or by inflammatory events during development. This review addresses the role of microglia during brain development, both structurally and functionally, as well as the inherent vulnerability of the developing nervous system. A framework is presented considering microglia as a critical nervous system-specific cell that can influence multiple aspects of brain development (e.g., vascularization, synaptogenesis, and myelination) and have a long term impact on the functional vulnerability of the nervous system to a subsequent insult, whether environmental, physical, age-related, or disease-related.
Published by Elsevier B.V.
http://www.ncbi.nlm.nih.gov/pubmed/22322212
Evidence of Parallels Between Mercury Intoxication and the Brain Pathology in Autism
http://www.bjorklundnutrition.net/2012/08/mercury-and-the-brain-pathology-in-autism/?fb_action_ids=3669587778013&fb_action_types=og.likes&fb_source=aggregation&fb_aggregation_id=246965925417366
New Japanese study confirms mercury in relation to damage in brain structures associated with autism
http://www.godlikeproductions.com/forum1/message2004889/pg1
Prenatal mercury exposure elevated risk for ADHD-related behavior
Sagiv SK. Arch Pediatr Adolesc Med. 2012;doi:10.1001/archpediatrics.2012.1286.
November 1, 2012
Excerpt:
“These results suggest that prenatal mercury exposure is associated with a higher risk of ADHD-related behaviors, and fish consumption during pregnancy is associated with a lower risk of these behaviors,” Sagiv and colleagues wrote. “Although a single estimate combining these beneficial vs. detrimental effects vis-à-vis fish intake is not possible with these data, these findings are consistent with a growing literature showing risk of mercury exposure and benefits of maternal consumption of fish on fetal brain development and are important for informing dietary recommendations for pregnant women.”
http://www.healio.com/pediatrics/add-adhd/news/online/%7B7EEB721F-166C-4DB8-B872-523CCB05ED2D%7D/Prenatal-mercury-exposure-elevated-risk-for-ADHD-related-behavior
J Toxicol. 2012; 2012: 373678.
Published online 2012 June 28. doi: 10.1155/2012/373678
PMCID: PMC3395253
Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes: Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA
Abstract
Thimerosal generates ethylmercury in aqueous solution and is widely used as preservative. We have investigated the toxicology of Thimerosal in normal human astrocytes, paying particular attention to mitochondrial function and the generation of specific oxidants. We find that ethylmercury not only inhibits mitochondrial respiration leading to a drop in the steady state membrane potential, but also concurrent with these phenomena increases the formation of superoxide, hydrogen peroxide, and Fenton/Haber-Weiss generated hydroxyl radical. These oxidants increase the levels of cellular aldehyde/ketones. Additionally, we find a five-fold increase in the levels of oxidant damaged mitochondrial DNA bases and increases in the levels of mtDNA nicks and blunt-ended breaks. Highly damaged mitochondria are characterized by having very low membrane potentials, increased superoxide/hydrogen peroxide production, and extensively damaged mtDNA and proteins. These mitochondria appear to have undergone a permeability transition, an observation supported by the five-fold increase in Caspase-3 activity observed after Thimerosal treatment.
1. Introduction
1.1. Thimerosal and Ethylmercury
Thimerosal is a preservative that is widely used in medical products, including as a preservative in vaccines, immunoglobulin preparations, skin test antigens, antivenins, ophthalmic and nasal products, and tattoo inks, and is composed of 49.6 percent ethylmercury by weight [1]. The widespread use of Thimerosal exposes many to its potential toxic effects, especially inutero and in neonates. We report the results of a series of experiments using cultured normal human astrocytes (NHA) exposed to Thimerosal to study the compound's effect on astrocyte mitochondria.
1.2. Oxidative Stress and Brain
Read more:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/
"Safe, and effective"???
NOVEMBER 11, 2003
Eli Lilly and Thimerosal
Excerpts:
In the 70 years since thimerosal/Merthiolate was developed, the FDA never required Eli Lilly to conduct clinical studies of its safety, despite ample evidence of its toxicity and its highly allergic properties. In fact, the FDA today still refers to the 1931 Powell and Jameison study on its Web site as indication of the “safety and effectiveness” of thimerosal as a preservative. Thimerosal/Merthiolate was widely used in over-the-counter products, including ointments, eye drops, nasal sprays and contact lens solution. In 1998, the FDA finally banned Thimerosal for use in OTC products—18 years after it began a safety review of mercury-containing products. It took another year before the CDC and the FDA would ask manufacturers to remove thimerosal from childhood vaccines. Eli Lilly stopped making Merthiolate-containing products in the mid-’80s but still profits from licensing agreements with pharmaceutical companies around the world.
Eli Lilly may be determined to avoid liability for thimerosal, but that doesn’t mean it has abandoned children with neurological problems. This year, the FDA approved Straterra, a new Eli Lilly drug for the treatment of Attention Deficit Hyperactivity Disorder. The irony that Eli Lilly profits from damaged children is not lost on parent Robert Krakow: “When Eli Lilly is promoting Straterra on TV, saying up to 10 percent of children can be helped, you realize what we are up against.”
http://www.inthesetimes.com/article/649/
VRM: Special Report
Those doctors who endorse the continued use of Thimerosal in vaccines, including the authors of the recent American Academy of Pediatrics article here-in (Walter A. Orenstein, MD, Jerome A. Paulson, MD, FAAP, Michael T. Brady, MD, FAAP, Louis Z. Cooper, MD, Katherine Seib, MSPH), should have their licences revoked immediately. But it’s also time for conscientious parents to consider walking away, once & for all, from the ENTIRE institution of Western Allopathic Medicine; all the trappings of this Medical Mafia monopoly. You have the evidence in hand.
http://vaccineresistancemovement.org/?page_id=11240
Crimes at the CDC
Excerpts:
According to Kennedy, in a July 1999 letter, vaccine producer SmithKline Beecham tells CDC that it is ready to produce non-Thimerosal DTP (Diptheria/Tetanus/Pertussis) vaccines immediately and has sufficient inventories to supply the entire U.S. market during the remainder of 1999 and the first half of 2000, by which time other vaccine manufacturers would have their Thimerosal-free DTP vaccines on line. Thimerosal-laden DTP vaccines containing 25 micrograms of mercury apiece (75 thousand trillion atoms of mercury) were then being administered to American infants at two months, four months and six months — far exceeding EPA’s recommended safe level for mercury. Had CDC accepted SmithKline’s offer, it could have immediately reduced the mercury exposures to vaccinated six-month-old children by 40%.
Kennedy continued, “However, in November, CDC mysteriously sent a letter back rejecting SmithKline’s offer. Then, on July 14, 2000 CDC published a deceptive press release promising to require that all vaccines be Thimerosal-free as soon as “adequate supplies are available.” This was a full 12 months after the agency had denied SmithKline’s proposal.”
CDC has allowed an entire generation of children to be injured.
“If CDC were basing its decision on safety alone, it would have taken SmithKline up on its offer. That’s a no-brainer,” said a federal health official to Kennedy anonymously. “So there were other considerations beside safety that were guiding their decision making.” “Among these “other considerations” were CDC’s important concerns for the preservation of the vaccine program, a bureaucratic impulse for self-preservation, and protecting the economic interests of its vaccine industry friends.”Immediate withdrawal would send a strong message; ‘We messed up!’” the health official told Kennedy. “And I don’t think they wanted to send that message to parents, the public or those considering legal action.” “There was also concern,” says the federal official, “that an immediate withdrawal might discredit the international vaccine programs for which CDC is an important partner.”
Why will CDC inject millions of minority kids in America’s poorest neighborhoods with poison proven to kill brain tissue and cause learning disorders when child-safe vaccines are available?
- Robert F. Kennedy Jr.
http://imva.info/index.php/vaccines/crimes-at-the-cdc/
Would THIS make you want to get a flu shot??? Your doctor didn't tell you this? So, you develop and egg allergy you didn't have before, oh no big deal; just trust the for profit authorities, right?
[The results obtained indicate possible contamination of vaccine products with allergens of egg origin and a potential risk of allergic manifestation after influenza vaccination.]
Serological examination of IgE- and IgG-specific antibodies to egg protein during influenza virus immunization.
N. Yamane and H. Uemura
Abstract
The concentrations of serum IgE (PRIST) and IgE- and IgG-specific antibodies to egg protein were determined in paired sera taken from students who had received influenza virus vaccine. Although persons who gave a history of allergy to egg or to chicken feathers were excluded, 10-16% of vaccinees possessed higher titres of serum IgE and IgE-specific antibody (RAST) to egg white (F1) allergen before vaccination. The titres of IgG-specific antibody to egg protein (ovalbumin and ovomucoid antigens) were negligible, and did not show any significant response after vaccination. In contrast, IgE-specific antibody to F1 allergen rose significantly in a considerable number of the vaccines. The results obtained indicate possible contamination of vaccine products with allergens of egg origin and a potential risk of allergic manifestation after influenza vaccination.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2249232/
So obviously you can become IgE response allergic to anything in a vaccine. Latex included.
The Man-Made Food Allergy Epidemic (It's NOT just PEANUTS!!)
http://barbfeick.com/vaccinations/
[PDF] Influenza Vaccination During Pregnancy: A Critical Assessment of the Recommendations of the Advisory Committee on Immunization Practices (ACIP)
ABSTRACT
Influenza vaccination during all trimesters of pregnancy is now universally recommended in the United States. We critically
reviewed the influenza vaccination policy of the CDCs Advisory Committee on Immunization Practice (ACIP) and the citations that were used to support their recommendations. The ACIPs citations and the current literature indicate that influenza infection is rarely a threat to a normal pregnancy. There is no convincing evidence of the effectiveness of influenza vaccination during this critical period. No studies have adequately assessed the risk of influenza vaccination during pregnancy, and animal safety
testing is lacking. Thimerosal, a mercury-based preservative present in most inactivated formulations of the vaccine, has been implicated in human neurodevelopment disorders, including autism, and a broad range of animal and experimental reproductive toxicities including teratogenicity, mutagenicity, and fetal death. Thimerosal is classified as a human teratogen.The ACIP policy recommendation of routinely administering influenza vaccine during pregnancy is ill-advised and unsupported by current scientific literature, and it should be withdrawn. Use ofthimerosal during pregnancy should be contraindicated.
www.jpands.org/vol11no2/ayoub.pdf
In Vaccines We Trust? Paul Offit threatens religious and philosophical vaccine exemptions. A response by Suzanne Humphries, MD
http://www.vaccinationcouncil.org/2012/08/26/paul-offit-threatens-religious-and-philosphical-vaccine-exemptions-a-respose-by-suzanne-humphries-md/
What's coming through that needle? Dr Sherri Tenpenny
http://youtu.be/ZlX2O_-ZEu4
What Is Coming Through That Needle? The Problem of Pathogenic Vaccine Contamination, Benjamin McRearden
http://www.scribd.com/doc/42722540/Vaccine-Contamination-Mcrearden
Medical evidence shows that pregnant mothers exposed to mercury in vaccines are more likely to have children with ADHD
Learn more: http://www.naturalnews.com/038037_pregnancy_vaccines_ADHD.html
Multiple studies link autism to mercury, which is still present in most flu vaccines
Learn more: http://www.naturalnews.com/031678_mercury_autism.html
Exposed: CDC deliberately manipulated, covered up scientific data showing link between vaccines containing mercury and autism
Learn more: http://www.naturalnews.com/034038_vaccines_autism.html
Government report links thimerosal laden vaccines to neurological disorders
Learn more: http://www.naturalnews.com/036748_thimerosal_vaccines_neurological_disorders.html
Vaccines And Immune Suppression.
http://preventdisease.com/news/articles/vaccines_and_immune_suppresion.shtml
The misinformation and the lies we have been fed, are just unimaginable; but are all to real.
Basics of the Human Immune System Prior to Introduction of Vaccines: Are Vaccines Turning Our Children’s Immune Systems Inside Out?
http://www.vaccinationcouncil.org/2011/06/10/basics-of-the-human-immune-system-prior-to-introduction-of-vaccines-are-vaccines-turning-our-children%E2%80%99s-immune-systems-inside-out/
Basics of the Human Immune System Prior to Introduction of Vaccines: Are Vaccines Turning Our Children’s Immune Systems Inside Out? Part 2
http://www.vaccinationcouncil.org/2011/06/21/risks-damage-basics-of-the-human-immune-system-prior-to-introduction-of-vaccines-are-vaccines-turning-our-childrens-immune-systems-inside-out-part-2/
Vaccines and Brain Inflammation
http://www.vaccinationcouncil.org/2011/06/01/vaccines-and-brain-inflammation/
Do Vaccines Disable The Immune System?
http://www.healthychild.com/do-vaccines-disable-the-immune-system
Vaccines and neonatal immune development
Hilary Butler - Monday, May 23, 2011
http://www.beyondconformity.org.nz/_blog/Hilary's_Desk/post/Vaccines_and_neonatal_immune_development/
Vaccination does not equal immunisation.
http://nocompulsoryvaccination.com/2012/12/24/vaccination-does-not-equal-immunisation/
VIDS – Vaccine Induced Diseases
http://www.vaccinesuncensored.org/vids.php
A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.
Abstract
J Toxicol Environ Health A. 2007 May 15;70(10):837-51.
A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.
Geier DA, Geier MR.
Source:Institute of Chronic Illnesses, Inc., Silver Spring, Maryland, USA.
Abstract
Impairments in social relatedness and communication, repetitive behaviors, and stereotypic abnormal movement patterns characterize autism spectrum disorders (ASDs). It is clear that while genetic factors are important to the pathogenesis of ASDs, mercury exposure can induce immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with ASDs. The Institutional Review Board of the Institute for Chronic Illnesses (Office for Human Research Protections, U.S. Department of Health and Human Services, IRB number IRB00005375) approved the present study. A case series of nine patients who presented to the Genetic Centers of America for a genetic/developmental evaluation are discussed. Eight of nine patients (one patient was found to have an ASD due to Rett's syndrome) (a) had regressive ASDs; (b) had elevated levels of androgens; (c) excreted significant amounts of mercury post chelation challenge; (d) had biochemical evidence of decreased function in their glutathione pathways; (e) had no known significant mercury exposure except from Thimerosal-containing vaccines/Rho(D)-immune globulin preparations; and (f) had alternate causes for their regressive ASDs ruled out. There was a significant dose-response relationship between the severity of the regressive ASDs observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing biologic/vaccine preparations during their fetal/infant developmental periods, and subsequently, between 12 and 24 mo of age, these previously normally developing children suffered mercury toxic encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.
http://www.ncbi.nlm.nih.gov/pubmed/17454560
Pubmed index of more related studies
http://www.ncbi.nlm.nih.gov/pubmed?term=Geier+DA%5BAuthor%5D&cauthor=true&cauthor_uid=17454560
Evidence of Parallels Between Mercury Intoxication and the Brain Pathology in Autism
http://www.bjorklundnutrition.net/2012/08/mercury-and-the-brain-pathology-in-autism/?fb_action_ids=3669587778013&fb_action_types=og.likes&fb_source=aggregation&fb_aggregation_id=246965925417366
The Severity of Autism Is Associated with Toxic Metal Body Burden and Red Blood Cell Glutathione Levels
Abstract
This study investigated the relationship of children's autism symptoms with their toxic metal body burden and red blood cell (RBC) glutathione levels. In children ages 3–8 years, the severity of autism was assessed using four tools: ADOS, PDD-BI, ATEC, and SAS. Toxic metal body burden was assessed by measuring urinary excretion of toxic metals, both before and after oral dimercaptosuccinic acid (DMSA). Multiple positive correlations were found between the severity of autism and the urinary excretion of toxic metals. Variations in the severity of autism measurements could be explained, in part, by regression analyses of urinary excretion of toxic metals before and after DMSA and the level of RBC glutathione (adjusted in all cases). This study demonstrates a significant positive association between the severity of autism and the relative body burden of toxic metals.
http://www.hindawi.com/journals/jt/2009/532640/
Oxidative Stress Causes Renal Dopamine D1 Receptor Dysfunction and Hypertension via Mechanisms That Involve Nuclear Factor-?B and Protein Kinase C
http://jasn.asnjournals.org/content/18/5/1446.long
Low natural killer cell cytotoxic activity in autism: The role of glutathione, IL-2 and IL-15
http://www.sciencedirect.com/science/article/pii/S0165572808003986
Oxidative stress in autism
NYS Institute for Basic Research in Developmental Disabilities
Excerpt: Several studies have suggested alterations in the activities of antioxidant enzymes such as superoxide dismutase, glutathione peroxidase, and catalase in autism. Additionally, altered glutathione levels and homocysteine/methionine metabolism, increased inflammation, excitotoxicity, as well as mitochondrial and immune dysfunction have been suggested in autism
http://www.sciencedirect.com/science/article/pii/S0928468006000538
Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism
Excerpt: These results suggest that the autism LCLs exhibit a reduced glutathione reserve capacity in both cytosol and mitochondria that may compromise antioxidant defense and detoxification capacity under prooxidant conditions.
http://www.fasebj.org/content/23/8/2374.short
Neurotoxicology. 2005 Jan;26(1):1-8.
Thimerosal neurotoxicity is associated with glutathione depletion: protection with glutathione precursors.
http://www.ncbi.nlm.nih.gov/pubmed/15527868
Neurosurgeon issues public challenge to vaccine zealots: Inject yourselves with all shots you say children should get!
http://www.naturalnews.com/035335_vaccines_Dr_Blaylock_children.html
THE CENTRAL ROLE OF IMMUNOEXCITOTOXICITY IN ALUMINUM AND MERCURY-CONTAINING ADJUVANT-TRIGGERED NEURODEVELOPMENTAL AND NEURODEGENERATIVE DISORDERS
Dr. Russell Blaylock is a board certified neurosurgeon, author and lecturer. He attended the Louisiana State University School of Medicine in New Orleans and completed his general surgical internship and neurosurgical residency at the Medical University of South Carolina in Charleston, South Carolina. During his residency training he worked with the eminent neurosurgeon, Dr. Ludwig Kempe. Together they developed the transcallosal removal of intraventricular tumors, a technique still used today. For the past 25 years he has practiced neurosurgery in addition to having a nutritional practice. He recently retired from his neurosurgical duties to devote his full attention to nutritional studies and neuroscience research.
https://www.youtube.com/watch?v=u9DkcpEEBPI
Published Papers – Dr. Russell Blaylock
http://www.russellblaylockmd.com/
Vaccines Contaminated with Mycoplasma's - by Garth Nicolson microbiologist
http://www.youtube.com/watch?v=Tk-RMI4qNvA
Dr. Sherri Tenpenny: What's Coming Through That Needle
http://www.youtube.com/watch?v=6KkQ6sf9tY4
http://drtenpenny.com/home/
What Is Coming Through That Needle? The Problem of Pathogenic Vaccine Contamination
Benjamin McRearden
http://www.scribd.com/doc/42722540/Vaccine-Contamination-Mcrearden
Vaccines And Immune Suppression
http://preventdisease.com/news/articles/vaccines_and_immune_suppresion.shtml
December 31, 2012
SaneVax: Newly Developed Same-Nested PCR Method May Help Answer Questions Regarding HPV Vaccine Safety
TROY, Mont.--(BUSINESS WIRE)--SaneVax Inc. announces the development of a new PCR methodology described in “Detection of human papillomavirus L1 gene DNA fragments in post-mortem blood and spleen after Gardasil vaccination – A case report,” authored by Dr. Sin Hang Lee of Milford Hospital, Connecticut. This method may provide a way for concerned scientists to determine whether or not HPV vaccines are linked to serious adverse events and death. The study undertaken to develop this method was commissioned and sponsored by SaneVax Inc. for a future payment not to exceed one US dollar, as disclosed in the article.
Read more:
http://www.businesswire.com/news/home/20121231005212/en
And it is NOT just about the thimerosal (mercury) issue
Aluminum information, toxicity, safety, danger, benefit and risk
From: History of crime against the Food Laws (1929) by Dr. Riley, the prime mover behind the original Pure Food Law and Director of the FDA. He resigned in disgust in 1912 over exceptions granted to the law and lack of enforcement.
Aluminum has been exempted from testing for safety by the FDA under a convoluted logic wherein it is classified as GRAS. (Generally Regarded As Safe.) It has never been tested by the FDA on its safety and there are NO restrictions whatever on the amount or use of aluminum. Diseases Associated with Aluminium Intoxication. H. Tomlinson, M.B., Ch.B., MRCS., LRCP. Since that time thousands of studies have been published indicating aluminum is involved in neurological dysfunction, immunocompetence, as well as a host of other morbidities. I cannot begin to reference them all. Sepsis: a cause of aluminum release from tissue stores associated with acute neurological dysfunction and mortality. Davenport A. – Williams P.S. – Roberts N.B. – Bone J.M. From: Clin Nephrol (1988 Jul) 30(1):48-51. We report six cases of patients with renal failure and exposure to aluminum who developed septicemia. In all cases the serum aluminum increased markedly. This may have contributed to the neurological dysfunction seen in five, and the deaths of four of the patients. We suggest that the rise in serum aluminum was due to the release of tissue-bound aluminum, resulting in an increase in free, diffusable aluminum and that this jeopardized both neurological function and immunocompetence.
Understanding Colloidal Suspensions - Help from Frank Hartman & Thomas Riddick (What does injecting aluminum do to the blood, aluminum is a coagulant, and blood is a fluid)
http://www.raysahelian.com/aluminum.html
Vaccine Caused Ischemia/Hypoxia, (the as a fact, now silenced information)
http://www.vacfacts.info/vaccine-caused-ischemiahypoxia.html
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Understanding Colloidal Suspensions - Help from Frank Hartman & Thomas Riddick
Aluminum toxicity is a widespread problem in all forms of life, including humans, animals, fish, plants and trees, and causes widespread degradation of the environment and health. Over 7000 reference articles on aluminum toxicity exist in various data bases; ( as of 1996 ) all recognizing the toxicity but concluding the mechanism of action is unknown. — [ Search results - scirus.com ]
http://www.scirus.com/srsapp/search?q=%22aluminum+toxicity%22&ds=web#results
Aluminum information, toxicity, safety, danger, benefit and risk
http://customers.hbci.com/~wenonah/info/colloid.htm
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Here is of course what the Offit video was based on and what it actually regarded.
Pediatricians: Keep Thimerosal in Vaccines
TRUST ...THEM, The American Academy of Pediatrics??? They know whats best, right? They have all the science, right? And do you actually believe that? What a bunch of criminal, sick, and irresponsible, to much to lose, bullshit.
Excerpts:
The American Academy of Pediatrics has endorsed the World Health Organization's stance that thimerosal -- a mercury-based preservative -- should be left in vaccines and should not be subject to a ban contained in a draft treaty from the United Nations Environment Program (UNEP).
In a brief statement published online in Pediatrics, the academy supported the recommendations drafted by the WHO's Strategic Advisory Group of Experts (SAGE) on immunization at an April meeting. An AAP spokesperson said that the endorsement was adopted unanimously by the academy's infectious diseases committee.
The Pediatrics Infectious Diseases Society and the International Pediatric Association have also thrown their support behind the guidance.
http://www.medpagetoday.com/infectiousdisease/vaccines/36480
Protect Your Children – The AAP and WHO Want to Keep Poisonous Mercury in Vaccines
http://vactruth.com/2012/12/23/mercury-in-vaccines/
Petitioning Rep. Darrell Issa
American Academy of Pediatrics (AAP): The AAP must reverse support for unrestricted use of mercury in vaccines.
http://www.change.org/petitions/american-academy-of-pediatrics-aap-the-aap-must-reverse-support-for-unrestricted-use-of-mercury-in-vaccines
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Federal Response to the Increase in Autisn 1 in 99 (hearings in which the CDC was questioned about the situation. Their responses are of course entirely pathetic)
http://www.c-spanvideo.org/program/AutismRa
I just love Paul Offit. Don't you? What a guy. And children according to his calculations can as well safely tolerate 10,000 vaccines in one day? Here in this below article there is a video he has done, attempting to explain away any concern as to the thimerosal issue and in regard to the recent American Academy of Pediatrics push to keep thimerosal in all the vaccines used in such as other countries that are underdeveloped. So, to keep getting vaccines available across the globe, there is no other way, we must keep poisoning the infants, children, and adults, with mercury to do that and to provide those vaccines? I can understand that possibly single dose vials may be in reality a bit impractical and or more expensive, but really if that is all we can produce that is safe, then the vaccine makers can just go with less for profits. Poisoning the world with mercury containing vaccines has been going on for far to many years and decades already. In the year 2013, they still have no better option? Or is it just about making the least expensive vaccine in those countries, and profits? There has to be a better option, if they were seriously and actively looking. However, until the CDC the WHO and as well the AAP get on board and admit to the serious dangers of thimerosal nothing can nor likely will happen to change this.
So, in this Offit video right here, what are we actually witnessing? WE are witnessing Mr Offit again being a huge part of the problem by ignoring existing science, and again making denial of any problem with thimerosal. What we need is for him to get honest, for this to actually change. He needs to get it in his head that what he is actually doing is not only wrong, but it is as well a criminal act. To as continue to mislead the public, and all existing believed authorities, and the government/s as well, is additionally another criminal act.
So, they are telling us that they can find no other chemical (a neurotoxic heavy metal), on the planet earth to take the place of thimerosal/ mercury, and no substance to perform the same function in a vaccine??? And we are to actually believe that?
At the end of that article page however even though Offit claims that there are seven studies he is referencing, only this study is referenced to, and is NOT a physiological or epidemiological science study, it is only a their own opinion piece. Just look at what this QUACK gets away with. We all know as well that any of the CDC funded epidemiological studies they reference, were entire corrupt with predetermined outcomes and obvious study design flaws. The several analysis available on those studies, show that how and why that is only and the obvious actually thinking conclusion.
Offit's single reference on the page. (And he got away with that).
Orenstein WA, Paulson JA, Brady MT, Cooper LZ, Seib K. Global vaccination recommendations and thimerosal. Pediatrics. 2012;131:149-151.
Lets look at what the reality of some of the real existing science shows us, and a lot of this is also published right in Pubmed, so they obviously can not claim that they are only some obscure studies that do not deserve consideration and further follow up studies. That's right, studies that were needed already decades ago, funded by the CDC, with as well the participation of unbiased oversight.
Medscape Infectious Diseases > Offit on Vaccines
Thimerosal in Vaccines: What Are the Facts?
http://www.medscape.com/viewarticle/776762
Note worthy is as well that at the end of that article page, even though Offit claims that there are seven studies that he is referencing from; only one, this study below is referenced to. It is as well NOT a physiological or epidemiological science study, it is only a their own opinion piece. Just look at what this QUACK gets away with. We all know as well (should), that any of the CDC funded epidemiological studies they reference, were entirely corrupt with predetermined outcomes and obvious study design flaws. The several analysis available on those studies, show that how and why that is only and the obvious actually thinking conclusion.
Offit's article listed - References
Orenstein WA, Paulson JA, Brady MT, Cooper LZ, Seib K. Global vaccination recommendations and thimerosal. Pediatrics. 2012;131:149-151.
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Here are just a few of the many available and existing scientific studies Mr Offit and the CDC failed to recognize.
This below study, shows that even though ethyl mercury may be detoxed more quickly as far as the amount leaving the body; the study shows that both ethyl mercury and methyl mercury are still a significant concern as to potential toxicity. As well just because ethyl mercury left the body quicker, that would not tell you what level of mercury was left in the tissues, organs, and the brain. Such statements would as well clearly not take in account the children and adults who produce less that adequate levels of glutathione necessary to detox that ethyl mercury.
Arch Toxicol. 1985 Sep;57(4):260-7.
The comparative toxicology of ethyl- and methylmercury.
Magos L, Brown AW, Sparrow S, Bailey E, Snowden RT, Skipp WR.
Abstract
Neurotoxicity and renotoxicity were compared in rats given by gastric gavage five daily doses of 8.0 mg Hg/kg methyl- or ethylmercuric chloride or 9.6 mg Hg/kg ethylmercuric chloride. Three or 10 days after the last treatment day rats treated with either 8.0 or 9.6 mg Hg/kg ethylmercury had higher total or organic mercury concentrations in blood and lower concentrations in kidneys and brain than methylmercury-treated rats. In each of these tissues the inorganic mercury concentration was higher after ethyl- than after methylmercury. Weight loss relative to the expected body weight and renal damage was higher in ethylmercury-treated rats than in rats given equimolar doses of methylmercury. These effects became more severe when the dose of ethylmercury was increased by 20%. Thus in renotoxicity the renal concentration of inorganic mercury seems to be more important than the concentration of organic or total mercury. In methylmercury-treated rats damage and inorganic mercury deposits were restricted to the P2 region of the proximal tubules, while in ethylmercury-treated rats the distribution of mercury and damage was more widespread. There was little difference in the neurotoxicities of methylmercury and ethylmercury when effects on the dorsal root ganglia or coordination disorders were compared. Based on both criteria, an equimolar dose of ethylmercury was less neurotoxic than methylmercury, but a 20% increase in the dose of ethylmercury was enough to raise the sum of coordination disorder scores slightly and ganglion damage significantly above those in methylmercury-treated rats.
http://www.ncbi.nlm.nih.gov/pubmed/4091651
And how can they they at the CDC, keep on recommending the flu shot for all pregnant women that contains 25 mcg. of thimerosal, (mercury)????
Mercury Poisoning Is a Growing Menace
http://readersupportednews.org/opinion2/271-38/15500-focus-mercury-poisoning-is-a-growing-menace
Brain Dev. 2012 May 31. [Epub ahead of print]
Prenatal exposure to organomercury, thimerosal, persistently impairs the serotonergic and dopaminergic systems in the rat brain: Implications for association with developmental disorders.
Ida-Eto M, Oyabu A, Ohkawara T, Tashiro Y, Narita N, Narita M
.
Source:Department of Anatomy II, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.
Abstract
Thimerosal, an organomercury compound, has been widely used as a preservative. Therefore, concerns have been raised about its neurotoxicity. We recently demonstrated perturbation of early serotonergic development by prenatal exposure to thimerosal (Ida-Eto et al. (2011) [11]). Here, we investigated whether prenatal thimerosal exposure causes persistent impairment after birth. Analysis on postnatal day 50 showed significant increase in hippocampal serotonin following thimerosal administration on embryonic day 9. Furthermore, not only serotonin, striatal dopamine was significantly increased. These results indicate that embryonic exposure to thimerosal produces lasting impairment of brain monoaminergic system, and thus every effort should be made to avoid the use of thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/22658806
Mitochondrial Dysfunction
Wow, great information article, but not a mention of vaccines, even though Pubmed and multiple studies on the effect, and as well in regard to glutathione. And also not a mention of the success of biomedical treatment.
http://www.epidemicanswers.org/mitochondrial-dysfunction/
Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal.
Olczak M, Duszczyk M, Mierzejewski P, Wierzba-Bobrowicz T, Majewska MD.
Source
Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, ul. Sobieskiego 9, Warsaw, Poland.
Abstract
Thimerosal, an organomercurial added as a preservative to some vaccines, is a suspected iatrogenic factor, possibly contributing to paediatric neurodevelopmental disorders including autism. We examined the effects of early postnatal administration of thimerosal (four i.m. injections, 12 or 240 µg THIM-Hg/kg, on postnatal days 7, 9, 11 and 15) on brain pathology in Wistar rats. Numerous neuropathological changes were observed in young adult rats which were treated postnatally with thimerosal. They included: ischaemic degeneration of neurons and "dark" neurons in the prefrontal and temporal cortex, the hippocampus and the cerebellum, pathological changes of the blood vessels in the temporal cortex, diminished synaptophysin reaction in the hippocampus, atrophy of astroglia in the hippocampus and cerebellum, and positive caspase-3 reaction in Bergmann astroglia. These findings document neurotoxic effects of thimerosal, at doses equivalent to those used in infant vaccines or higher, in developing rat brain, suggesting likely involvement of this mercurial in neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/21225508
Vaccines and especially aluminum adjuvants cause over activation of the brains microlgia and resulting chronic brain inflammation, and has now been found in both those with ASD and ADHD, in several studies., (Those studies are found as well on this site).
Neurotoxicology. 2012 Mar;33(2):191-206. doi: 10.1016/j.neuro.2012.01.012. Epub 2012 Feb 2.
Microglia in the developing brain: a potential target with lifetime effects.
Harry GJ, Kraft AD.
Source:National Toxicology Program Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Abstract
Microglia are a heterogenous group of monocyte-derived cells serving multiple roles within the brain, many of which are associated with immune and macrophage like properties. These cells are known to serve a critical role during brain injury and to maintain homeostasis; yet, their defined roles during development have yet to be elucidated. Microglial actions appear to influence events associated with neuronal proliferation and differentiation during development, as well as, contribute to processes associated with the removal of dying neurons or cellular debris and management of synaptic connections. These long-lived cells display changes during injury and with aging that are critical to the maintenance of the neuronal environment over the lifespan of the organism. These processes may be altered by changes in the colonization of the brain or by inflammatory events during development. This review addresses the role of microglia during brain development, both structurally and functionally, as well as the inherent vulnerability of the developing nervous system. A framework is presented considering microglia as a critical nervous system-specific cell that can influence multiple aspects of brain development (e.g., vascularization, synaptogenesis, and myelination) and have a long term impact on the functional vulnerability of the nervous system to a subsequent insult, whether environmental, physical, age-related, or disease-related.
Published by Elsevier B.V.
http://www.ncbi.nlm.nih.gov/pubmed/22322212
Evidence of Parallels Between Mercury Intoxication and the Brain Pathology in Autism
http://www.bjorklundnutrition.net/2012/08/mercury-and-the-brain-pathology-in-autism/?fb_action_ids=3669587778013&fb_action_types=og.likes&fb_source=aggregation&fb_aggregation_id=246965925417366
New Japanese study confirms mercury in relation to damage in brain structures associated with autism
http://www.godlikeproductions.com/forum1/message2004889/pg1
Prenatal mercury exposure elevated risk for ADHD-related behavior
Sagiv SK. Arch Pediatr Adolesc Med. 2012;doi:10.1001/archpediatrics.2012.1286.
November 1, 2012
Excerpt:
“These results suggest that prenatal mercury exposure is associated with a higher risk of ADHD-related behaviors, and fish consumption during pregnancy is associated with a lower risk of these behaviors,” Sagiv and colleagues wrote. “Although a single estimate combining these beneficial vs. detrimental effects vis-à-vis fish intake is not possible with these data, these findings are consistent with a growing literature showing risk of mercury exposure and benefits of maternal consumption of fish on fetal brain development and are important for informing dietary recommendations for pregnant women.”
http://www.healio.com/pediatrics/add-adhd/news/online/%7B7EEB721F-166C-4DB8-B872-523CCB05ED2D%7D/Prenatal-mercury-exposure-elevated-risk-for-ADHD-related-behavior
J Toxicol. 2012; 2012: 373678.
Published online 2012 June 28. doi: 10.1155/2012/373678
PMCID: PMC3395253
Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes: Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA
Abstract
Thimerosal generates ethylmercury in aqueous solution and is widely used as preservative. We have investigated the toxicology of Thimerosal in normal human astrocytes, paying particular attention to mitochondrial function and the generation of specific oxidants. We find that ethylmercury not only inhibits mitochondrial respiration leading to a drop in the steady state membrane potential, but also concurrent with these phenomena increases the formation of superoxide, hydrogen peroxide, and Fenton/Haber-Weiss generated hydroxyl radical. These oxidants increase the levels of cellular aldehyde/ketones. Additionally, we find a five-fold increase in the levels of oxidant damaged mitochondrial DNA bases and increases in the levels of mtDNA nicks and blunt-ended breaks. Highly damaged mitochondria are characterized by having very low membrane potentials, increased superoxide/hydrogen peroxide production, and extensively damaged mtDNA and proteins. These mitochondria appear to have undergone a permeability transition, an observation supported by the five-fold increase in Caspase-3 activity observed after Thimerosal treatment.
1. Introduction
1.1. Thimerosal and Ethylmercury
Thimerosal is a preservative that is widely used in medical products, including as a preservative in vaccines, immunoglobulin preparations, skin test antigens, antivenins, ophthalmic and nasal products, and tattoo inks, and is composed of 49.6 percent ethylmercury by weight [1]. The widespread use of Thimerosal exposes many to its potential toxic effects, especially inutero and in neonates. We report the results of a series of experiments using cultured normal human astrocytes (NHA) exposed to Thimerosal to study the compound's effect on astrocyte mitochondria.
1.2. Oxidative Stress and Brain
Read more:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/
"Safe, and effective"???
NOVEMBER 11, 2003
Eli Lilly and Thimerosal
Excerpts:
In the 70 years since thimerosal/Merthiolate was developed, the FDA never required Eli Lilly to conduct clinical studies of its safety, despite ample evidence of its toxicity and its highly allergic properties. In fact, the FDA today still refers to the 1931 Powell and Jameison study on its Web site as indication of the “safety and effectiveness” of thimerosal as a preservative. Thimerosal/Merthiolate was widely used in over-the-counter products, including ointments, eye drops, nasal sprays and contact lens solution. In 1998, the FDA finally banned Thimerosal for use in OTC products—18 years after it began a safety review of mercury-containing products. It took another year before the CDC and the FDA would ask manufacturers to remove thimerosal from childhood vaccines. Eli Lilly stopped making Merthiolate-containing products in the mid-’80s but still profits from licensing agreements with pharmaceutical companies around the world.
Eli Lilly may be determined to avoid liability for thimerosal, but that doesn’t mean it has abandoned children with neurological problems. This year, the FDA approved Straterra, a new Eli Lilly drug for the treatment of Attention Deficit Hyperactivity Disorder. The irony that Eli Lilly profits from damaged children is not lost on parent Robert Krakow: “When Eli Lilly is promoting Straterra on TV, saying up to 10 percent of children can be helped, you realize what we are up against.”
http://www.inthesetimes.com/article/649/
VRM: Special Report
Those doctors who endorse the continued use of Thimerosal in vaccines, including the authors of the recent American Academy of Pediatrics article here-in (Walter A. Orenstein, MD, Jerome A. Paulson, MD, FAAP, Michael T. Brady, MD, FAAP, Louis Z. Cooper, MD, Katherine Seib, MSPH), should have their licences revoked immediately. But it’s also time for conscientious parents to consider walking away, once & for all, from the ENTIRE institution of Western Allopathic Medicine; all the trappings of this Medical Mafia monopoly. You have the evidence in hand.
http://vaccineresistancemovement.org/?page_id=11240
Crimes at the CDC
Excerpts:
According to Kennedy, in a July 1999 letter, vaccine producer SmithKline Beecham tells CDC that it is ready to produce non-Thimerosal DTP (Diptheria/Tetanus/Pertussis) vaccines immediately and has sufficient inventories to supply the entire U.S. market during the remainder of 1999 and the first half of 2000, by which time other vaccine manufacturers would have their Thimerosal-free DTP vaccines on line. Thimerosal-laden DTP vaccines containing 25 micrograms of mercury apiece (75 thousand trillion atoms of mercury) were then being administered to American infants at two months, four months and six months — far exceeding EPA’s recommended safe level for mercury. Had CDC accepted SmithKline’s offer, it could have immediately reduced the mercury exposures to vaccinated six-month-old children by 40%.
Kennedy continued, “However, in November, CDC mysteriously sent a letter back rejecting SmithKline’s offer. Then, on July 14, 2000 CDC published a deceptive press release promising to require that all vaccines be Thimerosal-free as soon as “adequate supplies are available.” This was a full 12 months after the agency had denied SmithKline’s proposal.”
CDC has allowed an entire generation of children to be injured.
“If CDC were basing its decision on safety alone, it would have taken SmithKline up on its offer. That’s a no-brainer,” said a federal health official to Kennedy anonymously. “So there were other considerations beside safety that were guiding their decision making.” “Among these “other considerations” were CDC’s important concerns for the preservation of the vaccine program, a bureaucratic impulse for self-preservation, and protecting the economic interests of its vaccine industry friends.”Immediate withdrawal would send a strong message; ‘We messed up!’” the health official told Kennedy. “And I don’t think they wanted to send that message to parents, the public or those considering legal action.” “There was also concern,” says the federal official, “that an immediate withdrawal might discredit the international vaccine programs for which CDC is an important partner.”
Why will CDC inject millions of minority kids in America’s poorest neighborhoods with poison proven to kill brain tissue and cause learning disorders when child-safe vaccines are available?
- Robert F. Kennedy Jr.
http://imva.info/index.php/vaccines/crimes-at-the-cdc/
Would THIS make you want to get a flu shot??? Your doctor didn't tell you this? So, you develop and egg allergy you didn't have before, oh no big deal; just trust the for profit authorities, right?
[The results obtained indicate possible contamination of vaccine products with allergens of egg origin and a potential risk of allergic manifestation after influenza vaccination.]
Serological examination of IgE- and IgG-specific antibodies to egg protein during influenza virus immunization.
N. Yamane and H. Uemura
Abstract
The concentrations of serum IgE (PRIST) and IgE- and IgG-specific antibodies to egg protein were determined in paired sera taken from students who had received influenza virus vaccine. Although persons who gave a history of allergy to egg or to chicken feathers were excluded, 10-16% of vaccinees possessed higher titres of serum IgE and IgE-specific antibody (RAST) to egg white (F1) allergen before vaccination. The titres of IgG-specific antibody to egg protein (ovalbumin and ovomucoid antigens) were negligible, and did not show any significant response after vaccination. In contrast, IgE-specific antibody to F1 allergen rose significantly in a considerable number of the vaccines. The results obtained indicate possible contamination of vaccine products with allergens of egg origin and a potential risk of allergic manifestation after influenza vaccination.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2249232/
So obviously you can become IgE response allergic to anything in a vaccine. Latex included.
The Man-Made Food Allergy Epidemic (It's NOT just PEANUTS!!)
http://barbfeick.com/vaccinations/
[PDF] Influenza Vaccination During Pregnancy: A Critical Assessment of the Recommendations of the Advisory Committee on Immunization Practices (ACIP)
ABSTRACT
Influenza vaccination during all trimesters of pregnancy is now universally recommended in the United States. We critically
reviewed the influenza vaccination policy of the CDCs Advisory Committee on Immunization Practice (ACIP) and the citations that were used to support their recommendations. The ACIPs citations and the current literature indicate that influenza infection is rarely a threat to a normal pregnancy. There is no convincing evidence of the effectiveness of influenza vaccination during this critical period. No studies have adequately assessed the risk of influenza vaccination during pregnancy, and animal safety
testing is lacking. Thimerosal, a mercury-based preservative present in most inactivated formulations of the vaccine, has been implicated in human neurodevelopment disorders, including autism, and a broad range of animal and experimental reproductive toxicities including teratogenicity, mutagenicity, and fetal death. Thimerosal is classified as a human teratogen.The ACIP policy recommendation of routinely administering influenza vaccine during pregnancy is ill-advised and unsupported by current scientific literature, and it should be withdrawn. Use ofthimerosal during pregnancy should be contraindicated.
www.jpands.org/vol11no2/ayoub.pdf
In Vaccines We Trust? Paul Offit threatens religious and philosophical vaccine exemptions. A response by Suzanne Humphries, MD
http://www.vaccinationcouncil.org/2012/08/26/paul-offit-threatens-religious-and-philosphical-vaccine-exemptions-a-respose-by-suzanne-humphries-md/
What's coming through that needle? Dr Sherri Tenpenny
http://youtu.be/ZlX2O_-ZEu4
What Is Coming Through That Needle? The Problem of Pathogenic Vaccine Contamination, Benjamin McRearden
http://www.scribd.com/doc/42722540/Vaccine-Contamination-Mcrearden
Medical evidence shows that pregnant mothers exposed to mercury in vaccines are more likely to have children with ADHD
Learn more: http://www.naturalnews.com/038037_pregnancy_vaccines_ADHD.html
Multiple studies link autism to mercury, which is still present in most flu vaccines
Learn more: http://www.naturalnews.com/031678_mercury_autism.html
Exposed: CDC deliberately manipulated, covered up scientific data showing link between vaccines containing mercury and autism
Learn more: http://www.naturalnews.com/034038_vaccines_autism.html
Government report links thimerosal laden vaccines to neurological disorders
Learn more: http://www.naturalnews.com/036748_thimerosal_vaccines_neurological_disorders.html
Vaccines And Immune Suppression.
http://preventdisease.com/news/articles/vaccines_and_immune_suppresion.shtml
The misinformation and the lies we have been fed, are just unimaginable; but are all to real.
Basics of the Human Immune System Prior to Introduction of Vaccines: Are Vaccines Turning Our Children’s Immune Systems Inside Out?
http://www.vaccinationcouncil.org/2011/06/10/basics-of-the-human-immune-system-prior-to-introduction-of-vaccines-are-vaccines-turning-our-children%E2%80%99s-immune-systems-inside-out/
Basics of the Human Immune System Prior to Introduction of Vaccines: Are Vaccines Turning Our Children’s Immune Systems Inside Out? Part 2
http://www.vaccinationcouncil.org/2011/06/21/risks-damage-basics-of-the-human-immune-system-prior-to-introduction-of-vaccines-are-vaccines-turning-our-childrens-immune-systems-inside-out-part-2/
Vaccines and Brain Inflammation
http://www.vaccinationcouncil.org/2011/06/01/vaccines-and-brain-inflammation/
Do Vaccines Disable The Immune System?
http://www.healthychild.com/do-vaccines-disable-the-immune-system
Vaccines and neonatal immune development
Hilary Butler - Monday, May 23, 2011
http://www.beyondconformity.org.nz/_blog/Hilary's_Desk/post/Vaccines_and_neonatal_immune_development/
Vaccination does not equal immunisation.
http://nocompulsoryvaccination.com/2012/12/24/vaccination-does-not-equal-immunisation/
VIDS – Vaccine Induced Diseases
http://www.vaccinesuncensored.org/vids.php
A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.
Abstract
J Toxicol Environ Health A. 2007 May 15;70(10):837-51.
A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.
Geier DA, Geier MR.
Source:Institute of Chronic Illnesses, Inc., Silver Spring, Maryland, USA.
Abstract
Impairments in social relatedness and communication, repetitive behaviors, and stereotypic abnormal movement patterns characterize autism spectrum disorders (ASDs). It is clear that while genetic factors are important to the pathogenesis of ASDs, mercury exposure can induce immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with ASDs. The Institutional Review Board of the Institute for Chronic Illnesses (Office for Human Research Protections, U.S. Department of Health and Human Services, IRB number IRB00005375) approved the present study. A case series of nine patients who presented to the Genetic Centers of America for a genetic/developmental evaluation are discussed. Eight of nine patients (one patient was found to have an ASD due to Rett's syndrome) (a) had regressive ASDs; (b) had elevated levels of androgens; (c) excreted significant amounts of mercury post chelation challenge; (d) had biochemical evidence of decreased function in their glutathione pathways; (e) had no known significant mercury exposure except from Thimerosal-containing vaccines/Rho(D)-immune globulin preparations; and (f) had alternate causes for their regressive ASDs ruled out. There was a significant dose-response relationship between the severity of the regressive ASDs observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing biologic/vaccine preparations during their fetal/infant developmental periods, and subsequently, between 12 and 24 mo of age, these previously normally developing children suffered mercury toxic encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.
http://www.ncbi.nlm.nih.gov/pubmed/17454560
Pubmed index of more related studies
http://www.ncbi.nlm.nih.gov/pubmed?term=Geier+DA%5BAuthor%5D&cauthor=true&cauthor_uid=17454560
Evidence of Parallels Between Mercury Intoxication and the Brain Pathology in Autism
http://www.bjorklundnutrition.net/2012/08/mercury-and-the-brain-pathology-in-autism/?fb_action_ids=3669587778013&fb_action_types=og.likes&fb_source=aggregation&fb_aggregation_id=246965925417366
The Severity of Autism Is Associated with Toxic Metal Body Burden and Red Blood Cell Glutathione Levels
Abstract
This study investigated the relationship of children's autism symptoms with their toxic metal body burden and red blood cell (RBC) glutathione levels. In children ages 3–8 years, the severity of autism was assessed using four tools: ADOS, PDD-BI, ATEC, and SAS. Toxic metal body burden was assessed by measuring urinary excretion of toxic metals, both before and after oral dimercaptosuccinic acid (DMSA). Multiple positive correlations were found between the severity of autism and the urinary excretion of toxic metals. Variations in the severity of autism measurements could be explained, in part, by regression analyses of urinary excretion of toxic metals before and after DMSA and the level of RBC glutathione (adjusted in all cases). This study demonstrates a significant positive association between the severity of autism and the relative body burden of toxic metals.
http://www.hindawi.com/journals/jt/2009/532640/
Oxidative Stress Causes Renal Dopamine D1 Receptor Dysfunction and Hypertension via Mechanisms That Involve Nuclear Factor-?B and Protein Kinase C
http://jasn.asnjournals.org/content/18/5/1446.long
Low natural killer cell cytotoxic activity in autism: The role of glutathione, IL-2 and IL-15
http://www.sciencedirect.com/science/article/pii/S0165572808003986
Oxidative stress in autism
NYS Institute for Basic Research in Developmental Disabilities
Excerpt: Several studies have suggested alterations in the activities of antioxidant enzymes such as superoxide dismutase, glutathione peroxidase, and catalase in autism. Additionally, altered glutathione levels and homocysteine/methionine metabolism, increased inflammation, excitotoxicity, as well as mitochondrial and immune dysfunction have been suggested in autism
http://www.sciencedirect.com/science/article/pii/S0928468006000538
Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism
Excerpt: These results suggest that the autism LCLs exhibit a reduced glutathione reserve capacity in both cytosol and mitochondria that may compromise antioxidant defense and detoxification capacity under prooxidant conditions.
http://www.fasebj.org/content/23/8/2374.short
Neurotoxicology. 2005 Jan;26(1):1-8.
Thimerosal neurotoxicity is associated with glutathione depletion: protection with glutathione precursors.
http://www.ncbi.nlm.nih.gov/pubmed/15527868
Neurosurgeon issues public challenge to vaccine zealots: Inject yourselves with all shots you say children should get!
http://www.naturalnews.com/035335_vaccines_Dr_Blaylock_children.html
THE CENTRAL ROLE OF IMMUNOEXCITOTOXICITY IN ALUMINUM AND MERCURY-CONTAINING ADJUVANT-TRIGGERED NEURODEVELOPMENTAL AND NEURODEGENERATIVE DISORDERS
Dr. Russell Blaylock is a board certified neurosurgeon, author and lecturer. He attended the Louisiana State University School of Medicine in New Orleans and completed his general surgical internship and neurosurgical residency at the Medical University of South Carolina in Charleston, South Carolina. During his residency training he worked with the eminent neurosurgeon, Dr. Ludwig Kempe. Together they developed the transcallosal removal of intraventricular tumors, a technique still used today. For the past 25 years he has practiced neurosurgery in addition to having a nutritional practice. He recently retired from his neurosurgical duties to devote his full attention to nutritional studies and neuroscience research.
https://www.youtube.com/watch?v=u9DkcpEEBPI
Published Papers – Dr. Russell Blaylock
http://www.russellblaylockmd.com/
Vaccines Contaminated with Mycoplasma's - by Garth Nicolson microbiologist
http://www.youtube.com/watch?v=Tk-RMI4qNvA
Dr. Sherri Tenpenny: What's Coming Through That Needle
http://www.youtube.com/watch?v=6KkQ6sf9tY4
http://drtenpenny.com/home/
What Is Coming Through That Needle? The Problem of Pathogenic Vaccine Contamination
Benjamin McRearden
http://www.scribd.com/doc/42722540/Vaccine-Contamination-Mcrearden
Vaccines And Immune Suppression
http://preventdisease.com/news/articles/vaccines_and_immune_suppresion.shtml
December 31, 2012
SaneVax: Newly Developed Same-Nested PCR Method May Help Answer Questions Regarding HPV Vaccine Safety
TROY, Mont.--(BUSINESS WIRE)--SaneVax Inc. announces the development of a new PCR methodology described in “Detection of human papillomavirus L1 gene DNA fragments in post-mortem blood and spleen after Gardasil vaccination – A case report,” authored by Dr. Sin Hang Lee of Milford Hospital, Connecticut. This method may provide a way for concerned scientists to determine whether or not HPV vaccines are linked to serious adverse events and death. The study undertaken to develop this method was commissioned and sponsored by SaneVax Inc. for a future payment not to exceed one US dollar, as disclosed in the article.
Read more:
http://www.businesswire.com/news/home/20121231005212/en
And it is NOT just about the thimerosal (mercury) issue
Aluminum information, toxicity, safety, danger, benefit and risk
From: History of crime against the Food Laws (1929) by Dr. Riley, the prime mover behind the original Pure Food Law and Director of the FDA. He resigned in disgust in 1912 over exceptions granted to the law and lack of enforcement.
Aluminum has been exempted from testing for safety by the FDA under a convoluted logic wherein it is classified as GRAS. (Generally Regarded As Safe.) It has never been tested by the FDA on its safety and there are NO restrictions whatever on the amount or use of aluminum. Diseases Associated with Aluminium Intoxication. H. Tomlinson, M.B., Ch.B., MRCS., LRCP. Since that time thousands of studies have been published indicating aluminum is involved in neurological dysfunction, immunocompetence, as well as a host of other morbidities. I cannot begin to reference them all. Sepsis: a cause of aluminum release from tissue stores associated with acute neurological dysfunction and mortality. Davenport A. – Williams P.S. – Roberts N.B. – Bone J.M. From: Clin Nephrol (1988 Jul) 30(1):48-51. We report six cases of patients with renal failure and exposure to aluminum who developed septicemia. In all cases the serum aluminum increased markedly. This may have contributed to the neurological dysfunction seen in five, and the deaths of four of the patients. We suggest that the rise in serum aluminum was due to the release of tissue-bound aluminum, resulting in an increase in free, diffusable aluminum and that this jeopardized both neurological function and immunocompetence.
Understanding Colloidal Suspensions - Help from Frank Hartman & Thomas Riddick (What does injecting aluminum do to the blood, aluminum is a coagulant, and blood is a fluid)
http://www.raysahelian.com/aluminum.html
Vaccine Caused Ischemia/Hypoxia, (the as a fact, now silenced information)
http://www.vacfacts.info/vaccine-caused-ischemiahypoxia.html
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Understanding Colloidal Suspensions - Help from Frank Hartman & Thomas Riddick
Aluminum toxicity is a widespread problem in all forms of life, including humans, animals, fish, plants and trees, and causes widespread degradation of the environment and health. Over 7000 reference articles on aluminum toxicity exist in various data bases; ( as of 1996 ) all recognizing the toxicity but concluding the mechanism of action is unknown. — [ Search results - scirus.com ]
http://www.scirus.com/srsapp/search?q=%22aluminum+toxicity%22&ds=web#results
Aluminum information, toxicity, safety, danger, benefit and risk
http://customers.hbci.com/~wenonah/info/colloid.htm
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Here is of course what the Offit video was based on and what it actually regarded.
Pediatricians: Keep Thimerosal in Vaccines
TRUST ...THEM, The American Academy of Pediatrics??? They know whats best, right? They have all the science, right? And do you actually believe that? What a bunch of criminal, sick, and irresponsible, to much to lose, bullshit.
Excerpts:
The American Academy of Pediatrics has endorsed the World Health Organization's stance that thimerosal -- a mercury-based preservative -- should be left in vaccines and should not be subject to a ban contained in a draft treaty from the United Nations Environment Program (UNEP).
In a brief statement published online in Pediatrics, the academy supported the recommendations drafted by the WHO's Strategic Advisory Group of Experts (SAGE) on immunization at an April meeting. An AAP spokesperson said that the endorsement was adopted unanimously by the academy's infectious diseases committee.
The Pediatrics Infectious Diseases Society and the International Pediatric Association have also thrown their support behind the guidance.
http://www.medpagetoday.com/infectiousdisease/vaccines/36480
Protect Your Children – The AAP and WHO Want to Keep Poisonous Mercury in Vaccines
http://vactruth.com/2012/12/23/mercury-in-vaccines/
Petitioning Rep. Darrell Issa
American Academy of Pediatrics (AAP): The AAP must reverse support for unrestricted use of mercury in vaccines.
http://www.change.org/petitions/american-academy-of-pediatrics-aap-the-aap-must-reverse-support-for-unrestricted-use-of-mercury-in-vaccines
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Federal Response to the Increase in Autisn 1 in 99 (hearings in which the CDC was questioned about the situation. Their responses are of course entirely pathetic)
http://www.c-spanvideo.org/program/AutismRa
