Hepatitis B Vaccine for Infants: Is it Worth it, and the Risk?
Hepatitis B Vaccine for Infants: Is it Worth It?
In 1991, the American Council on Immunization Practices (ACIP) recommended universal vaccination of all U.S. infants with 3 doses of hepatitis B vaccine, beginning within 48 hours of birth. Hepatitis B is a sexually-transmitted disease and is spread the same way HIV and Hepatitis C are spread: through contact with body fluids such a semen, vaginal fluids, and blood. Those at high risk of infection include homosexual men, heterosexuals who have multiple sex partners, and healthcare workers who are exposed to body fluids. Infants whose mothers are actively infected with Hepatitis B are at increased risk of infection. (citation)
Pregnant women in the U.S. are screened for the disease.
Infants who are born to mothers who are not infected with hepatitis B are at very low risk for infection, by virtue of the fact that they are not engaging in high risk behaviors that are associated with the disease. (i.e., Infants are not having sex and they are not using injection drugs.)
The CDC states that the incidence of hepatitis B infection in U.S. children (age 0-19 years) has decreased by 89% as a result of mass vaccination of infants. This is misleading, in my opinion. When you say that the incidence of the illness has decreased by 89% it sounds like the vaccine has been extremely effective in improving the health of children who receive it. The opposite is actually the case.
Here are some studies that have investigated the health effects of hepatitis B vaccine in U.S. children.
Read more:
http://vaxtruth.org/2014/06/hepatitis-b-vaccine-for-infants-is-it-worth-it/
Written by a partner vaccine truth advocate: btw the CDC warns that if you have latex allergy to avoid the Hep B vaccine, one must ask how they know a newborn has a latex allergy and the common sense is that the vaccine is causing these allergies. My sister had a liver transplant last November, due to diagnosis over a decade ago of 'autoimmune hepatitis. Once said to be rare, I personally know 12 people with the diagnosis and all are healthcare professionals who were injected with Hep B vaccine decades ago. The physicians in the liver clinics have remarked how they are seeing this diagnosis more frequently. When informed of how many people we know with the diagnosis and how we think its due to the Hep B vaccine, rather than be dismissed, the doctors respond; "That's an interesting idea." We are lobbying the medical profession to include the question of whether they had the vaccine in the screening of patients. We believe that when the professionals see the high incidence in the vaccine populations this could result in further questioning and possible removal as mandatory.
Autoimmun Rev. 2005 Feb;4(2):96-100.
Autoimmune hazards of hepatitis B vaccine.
"According to Hippocratic tradition, the safety level of a preventive medicine must be very high, as it is aimed at protecting people against diseases that they may not contract. This paper points out that information on the safety of hepatitis B vaccine (HBV) is biased as compared to classical requirements of evidence-based medicine (EBM), as exemplified by a documented selectivity in the presentation or even publication of available clinical or epidemiological data. Then, a review is made of data suggesting that HBV is remarkable by the frequency, the severity and the variety of its complications, some of them probablyrelated to a mechanism of molecular mimicry leading to demyelinating diseases, and the others reproducing the spectrum of non-hepatic manifestations of natural hepatitis B. To be explained, this unusual spectrum of toxicity requires additional investigations based upon complete release of available data."
http://www.ncbi.nlm.nih.gov/pubmed/15722255
Hepatitis B Vaccine - What Are the Risks?
Adverse Reactions* and Deaths from Hepatitis B Vaccine between 1983-2012
*It is estimated that only 10% of vaccine reactions are ever reported to the CDC.
"As of March 2012, there was a total of 66,654 hepatitis B vaccine-related adverse events reported to the federal Vaccine Adverse Events Reporting System (VAERS), including reports of headache, irritability, extreme fatigue, brain inflammation, convulsions, rheumatoid arthritis, optic neuritis, multiple sclerosis, lupus, Guillain Barre Syndrome (GBS) and neuropathy. There have been more than 1500 hepatitis B vaccine-related deaths reported, including deaths classified as sudden infant death syndrome (SIDS)."
According to a similar report, the toxic metals in the Hepatitis B vaccine have varied in the years between 1983 and 2013. While the amount of one metal (mercury) in the vaccine decreased, another metal (aluminum) increased.
1,500 Deaths
1,359 Life Threatening Injuries
66,654 Total Injuries
Italy: “Hepatitis B vaccine is administered at birth only to children born to HBsAg + mothers. Otherwise immunisation starts at 3 months of age.”
Finland: “Hepatitis B vaccine is given only to infants of HbsAg carrier mothers or fathers at the age of 0, 1, 2 and 12 months.”
Denmark: “Vaccination against hepatitis B is recommended to children of HBsAg-positive mothers, starting at birth with both hepatitis B immunoglobulin and one dose of HepB.”
Norway: “HepB is recommended for risk groups only.”
Sweden: “HepB is only recommended to children considered high-risk groups. Vaccination is given at birth to infants of mothers positive for hepatitis B.”
The Netherlands: “Only for children born to HBsAg positive mothers.”
Read more:
http://www.ashotoftruth.org/vaccines/hepatitis-b-vaccine
Now, lets go to some real study science that you likely have not been told about, as to the actual efficacy of the vaccine and in and as to its preventing Hep B in an infant with an HBsAg-positive mother. Quite obviously the vaccine does not even protect a newborn in that situation, or with a quite lower than what would expected rate of efficacy. So, the point in giving it to a newborn then, is what? (Do you think or see yet that the pharma for profit vaccine program is just evil and out rightly, sick? And they have the experts behind them right, like the CDC and Paul Offit, how can it be wrong)?
FAIL: Infant Hep B Vaccines Perform Shamefully; Time To End Them?
http://www.greenmedinfo.com/blog/fail-infant-hep-b-vaccines-perform-shamefully-time-end-them
Hepatitis B vaccination with or without hepatitis B immunoglobulin at birth to babies born of HBsAg-positive mothers prevents overt HBV transmission but may not prevent occult HBV infection in babies: a randomized controlled trial.
Abstract (excerpt):
Women who were anti-HBe positive were a low-risk group, and their babies were most likely to remain free of HBV infection (occult or overt) and had good immune response to the vaccine. Maternal HBeAg-positive status and negativity for anti-HBe predicted not only overt but also any infection (both overt and occult) in babies. In addition, high maternal HBV DNA and treatment with vaccine alone were significant factors for overt HBV infection in babies. The current practice of administration of vaccine with HBIG at birth to babies born of HBsAg-positive mothers is not effective in preventing occult HBV infection in babies, which may be up to 40%.Because the most important risk factors for mother-to-baby transmission of HBV infection are the replicative status and high HBV DNA level in mothers; it will be worthwhile investigating the role of antivirals and HBIG administration during pregnancy to prevent mother-to-child transmission of HBV infection.
Read more:
http://www.greenmedinfo.com/article/hepatitis-b-vaccination-or-without-hepatitis-b-immunoglobulin-birth-babies
Hepatitis B vaccination with or without hepatitis B immunoglobulin at birth to babies born of HBsAg-positive mothers prevents overt HBV transmission but may not prevent occult HBV infection in babies: a randomized controlled trial
Summary
Vertical transmission of Hepatitis B virus HBV can result in a state of chronic HBV infection and its complications. HBV vaccination with or without hepatitis B immunoglobulin (HBIG) prevents transmission of overt infection to the babies. However, whether it also prevents occult HBV infection in babies is not known. Consecutive pregnant women of any gestation found to be HBsAg positive were followed till delivery, and their babies were included in the study. Immediately after delivery, babies were randomized to receive either HBIG or placebo in addition to recombinant HBV vaccine (at 0, 6, 10 and 14 weeks). The primary end-point of the study, assessed at 18 weeks of age, was remaining free of any HBV infection (either overt or occult) plus the development of adequate immune response to vaccine. The babies were further followed up for a median of 2 years of age to determine their eventual outcome. Risk factors for HBV transmission and for poor immune response in babies were studied. Of the 283 eligible babies, 259 were included in the trial and randomized to receive either HBIG (n = 128) or placebo (n = 131) in addition to recombinant HBV vaccine. Of the 222 of 259 (86%) babies who completed 18 weeks of follow-up, only 62/222 (28%) reached primary end-point. Of the remaining, 6/222 (3%) developed overt HBV infection, 142/222 (64%) developed occult HBV infection, and 12/222 (5%) had no HBV infection but had poor immune response. All 6 overt infections occurred in the placebo group (P = 0.030), while occult HBV infections were more common in the HBIG group (76/106 [72%] vs. 66/116 [57%]; P = 0.025). This may be due to the immune pressure of HBIG. There was no significant difference between the two groups in frequency of babies developing poor immune response or those achieving primary end-point. The final outcome of these babies at 24 months of age was as follows: overt HBV infection 4%, occult HBV infection 42%, no HBV infection but poor immune response 8% and no HBV infection with good immune response 28%. Women who were anti-HBe positive were a low-risk group, and their babies were most likely to remain free of HBV infection (occult or overt) and had good immune response to the vaccine. Maternal HBeAg-positive status and negativity for anti-HBe predicted not only overt but also any infection (both overt and occult) in babies. In addition, high maternal HBV DNA and treatment with vaccine alone were significant factors for overt HBV infection in babies. The current practice of administration of vaccine with HBIG at birth to babies born of HBsAg-positive mothers is not effective in preventing occult HBV infection in babies, which may be up to 40%. Because the most important risk factors for mother-to-baby transmission of HBV infection are the replicative status and high HBV DNA level in mothers; it will be worthwhile investigating the role of antivirals and HBIG administration during pregnancy to prevent mother-to-child transmission of HBV infection.
http://onlinelibrary.wiley.com/doi/10.1111/jvh.12102/abstract
How the CDC (and Dorit Reiss) Hyped Risk of Childhood Hep B Infection by 50-fold to Push Vaccines
By Cia Parker
Professional vaccine operatives like Dorit Reiss have been hard at work for some time to exaggerate the dangers of the vaccine-preventable diseases, while simultaneously denying the damage that the vaccines for them often do. A case in point was found in the comments on this article on the Mother Jones website last week:
The topic had turned to the hepatitis-B vaccine, given to all newborns in the U.S. while they were still at the hospital, beginning in 1991 (at the beginning of the autism epidemic). I put up information I had found in Dr. Bob Sears’ The Vaccine Book, a link to a CDC report with a chart at the bottom showing the rate of hep-B diagnosis in children 1-9 from 1986, five years before the vaccine program began.
The chart at the bottom of the report clearly shows that the rate at which hep-B was diagnosed in children was less than one per 100,000 or fewer than 360 a year in a childhood population of 36 million in 1990. The text at the top of the report, however, states: “Before 1982, an estimated 200,000--300,000 persons in the United States were infected annually with HBV, including approximately 20,000 children.” The source for this large number was an article in Pediatrics in 2001. It uses the word “estimated” because this is a purely speculative figure, not based on the disease being diagnosed by blood tests carried out by physicians.
Hepatitis B is a very dangerous disease when contracted in the first year. At that time, the only means of transmission, except in extremely unusual and almost unimaginable circumstances, is from contagion by an infected mother. It is usual to perform a blood test on a pregnant woman to learn whether her child is at risk, in which case it would probably be best to give the baby immunoglobulin and the vaccine when it was born. But instead it has become standard practice in the U.S. to give this dangerous vaccine to all newborns, even those born to healthy mothers, and very common to give the vaccine to the newborn without the permission or knowledge of the parents, making it harder to realize that the vaccine was the cause of the child’s autism, diagnosed years later.
The virus is transmitted like AIDS, by infected blood/body fluids to blood/mucus membrane contact. It is most commonly contracted by unsafe sex with a carrier or by shared use of needles used by illegal drug users. Medical personnel exposed to infected blood are at some increased risk, but it is not as great as is commonly believed. It is not spread by the sharing of eating utensils or drinking glasses, or sleeping in the same bed as an infected person. It may sometimes be transmitted by sharing toothbrushes or razors. Australia did a study which showed that it was not transmitted by children at school. (Burgess, MA and McIntosh, EDG, “Hepatitis-B in urban schoolchildren – No evidence of horizontal transmission between high-risk and low-risk groups,” Med J Australia, 5 Sept. 1993; 159: 315-319, quoted Wendy Lyall, Raising a vaccine-free child, p.178).
Hepatitis B is a very dangerous disease when contracted in the first year. At that time, the only means of transmission, except in extremely unusual and almost unimaginable circumstances, is from contagion by an infected mother. It is usual to perform a blood test on a pregnant woman to learn whether her child is at risk, in which case it would probably be best to give the baby immunoglobulin and the vaccine when it was born. But instead it has become standard practice in the U.S. to give this dangerous vaccine to all newborns, even those born to healthy mothers, and very common to give the vaccine to the newborn without the permission or knowledge of the parents, making it harder to realize that the vaccine was the cause of the child’s autism, diagnosed years later.
The virus is transmitted like AIDS, by infected blood/body fluids to blood/mucus membrane contact. It is most commonly contracted by unsafe sex with a carrier or by shared use of needles used by illegal drug users. Medical personnel exposed to infected blood are at some increased risk, but it is not as great as is commonly believed. It is not spread by the sharing of eating utensils or drinking glasses, or sleeping in the same bed as an infected person. It may sometimes be transmitted by sharing toothbrushes or razors. Australia did a study which showed that it was not transmitted by children at school. (Burgess, MA and McIntosh, EDG, “Hepatitis-B in urban schoolchildren – No evidence of horizontal transmission between high-risk and low-risk groups,” Med J Australia, 5 Sept. 1993; 159: 315-319, quoted Wendy Lyall, Raising a vaccine-free child, p.178).
Read more:
http://www.ageofautism.com/2014/03/how-the-cdc-and-dorit-reiss-hyped-risk-of-childhood-hep-b-infection-by-50-fold-to-push-vaccines-.html
Hepatitis B Vaccine: An Unmitigated Disaster
By J.B. Handley
http://www.ageofautism.com/2009/10/hepatitis-b-vaccine-an-unmitigated-disaster-.html
When We Know Better, We Do Better. Marcella Piper-Terry’s Speech, We the Parents Rally, West Virginia
(The REAL Hepatitis B vaccine statistics-extensive article)
http://vaxtruth.org/2012/02/when-we-know-better-we-do-better-or-do-we/
Should Infants be Vaccinated Against Hepatitis B? How Much Aluminum is Safe for Infants?
INFANTS IN THE UNITED STATES ARE NOT AT RISK FOR HEPATITIS B!
In 1991, there were 18,003 cases of hepatitis B reported in the U.S. out of a total U.S. population of 248 million. According to the October 31, 1997 Morbidity and Mortality Weekly Report published by the CDC, in 1996 there were 10,637 cases of hepatitis B reported in the U.S. with 279 cases reported in children under the age of 14 and the CDC stated that “Hepatitis B continues to decline in most states, primarily because of a decrease in the number of cases among injecting drug users and, to a lesser extent, among both homosexuals and heterosexuals of both sexes.”
But the CDC and vaccines’ biggest proponent, Dr. Paul Offit wants ALL babies vaccinated for Hepatitis B, not once but three times. I wonder if that’s because if they are going in for their Hep. B shots, they are also more likely to receive the Rotavirus Vaccine, for which Dr. Offit developed the patent, which sold for 182 MILLION dollars. Imagine how much money would be lost on rotavirus vaccination if parents started questioning and as a result, did not follow the currently mandated schedule.
If you think babies should be vaccinated against a sexually transmitted disease at birth, with a vaccine that contains up to 125 times the “safe” limit of aluminum (according to the EPA regulations), watch this video from ABC News 20-20, Part 1 of Who’s Calling The Shots?
and this video from ABC News 20-20, Part 2 of Who’s Calling The Shots?
Read more:
http://vaxtruth.org/2012/01/should-infants-be-vaccinated-against-hepatitis-b-how-much-aluminum-is-safe-for-infants/
ABC News 20-20 1999 Hep B part 1 (both videos are the same as the above)
http://www.youtube.com/watch?v=hNy5VmeaGNw
ABC News 20-20 1999 Hep B part 2
http://www.youtube.com/watch?v=78b1rFJgyXI
Meet Timmy: A beautiful little boy who was seriously injured by the Hepatitis B vaccine administered in infancy.
http://vaxtruth.org/2011/09/meet-timmy/
PHYSICIANS OPPOSE MANDATORY HEPATITIS B VACCINE FOR OHIO SCHOOLCHILDREN
PARENTS, NOT GOVERNMENT, SHOULD DECIDE
The Association of American Physicians and Surgeons (AAPS) opposes efforts in Ohio and other states to force all schoolchildren to receive three doses of hepatitis B vaccine. Too few children contract the disease to justify exposing all children to the risk of adverse vaccine reactions. AAPS urges Ohio legislators to support Ohio House Bill 200, which would repeal Ohio's hastily mandated hepatitis B vaccine requirement, and add informed consent for all vaccines.
In the United States, hepatitis B is primarily an adult disease, and risk is highly dependent on lifestyle. Risk factors include: multiple sex partners, drug abuse, an occupation involving frequent exposure to blood, or having a hepatitis-B infected mother. The disease is not spread by casual contact. More than 99.7 percent of Ohioans are free of this virus. No Ohio school has ever reported hepatitis B transmission.
Read more:
http://www.aapsonline.org/press/nrohvac.htm
Shots in the dark.
Author: Blevins, Sue A.
Source: Reason v. 31 no3 (July 1999) p. 49-51
Lyla Rose Belkin was an alert and lively baby at five weeks old. Her parents, Michael and Lorna Belkin, say she had never been sick until she received a mandatory hepatitis B shot on September 16, 1998. "That night she became agitated and feisty," her father recalls. "Then she fell asleep and never woke up." Doctors told the Belkins that Lyla must have died from Sudden Infant Death Syndrome, a catchall diagnosis.
Vaccine Casualty: Five-week-old Lyla Rose Belkin died after receiving a mandatory hepatitis B shot. Since 1991, at least 274 newborns have died and 2,600 infants have suffered serious medical problems after getting the vaccine.
Read more:
http://www.utmb.edu/pedi_ed/healthdev/OtherPages/shots-in-dark.asp
Mindless Vaccination Bureaucracy
By Michael Belkin
http://www.nvic.org/vaccines-and-diseases/Hepatitis-B/fatherstory.aspx
Michael Belkin Testimony to Congress on Hepatitis B Vaccine-Congressional Testimony
http://therefusers.com/refusers-newsroom/michael-belkin-testimony-to-congress-on-hepatitis-b-vaccine/
Uploaded on Apr 14, 2008
Hepatitis B Vaccine, May 18, 1999 The House Reform Committee. 2 Congressman Mica D-FL. 1st Michael Belkin
https://www.youtube.com/watch?v=sgtXNnevorg
Hepatitis B Vaccine
The Untold Story
http://www.nvic.org/nvic-archives/newsletter/untoldstory.aspx
Is the Hepatitis B Vaccine a Deadly Roll of the Dice?
http://www.thelibertybeacon.com/2014/04/13/is-the-hepatitis-b-vaccine-a-serious-or-deadly-roll-of-the-dice/
Hepatitis B Vaccine Side Effects
http://www.childhoodshots.com/Hepatitis-B-Vaccine-Side-Effects-s/64.htm
The Hepatitis B Vaccine Scam
http://healthwyze.org/index.php/component/content/article/83-the-hepatitis-b-vaccine-scam.html
The vaccine science on hepatitis B vaccine
View the Evidence: Problematic Actions
http://www.greenmedinfo.com/anti-therapeutic-action/vaccination-hepatitis-b
VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body
http://vaccineresistancemovement.org/?p=8787
Vaccine Truth Informational Brochures:
Do not allow all of the vaccine-injured childrens injuries to be in vain. Educate others in honor of them. Be the Voice for those who don't have one. Do not be silent. You can inform other parents. We provide multiple free brochures you can give to educate other parents.
Download and print them now.
http://www.educate4theinjured.org/eric/4571993523
We Want The Vaccine Facts And the Real Science, (and here it is)
http://www.educate4theinjured.org/#!the-factsscience/cc2d
Memorial to Victims of the Silent War ~ VACCINES ~
Cease for Peace! ~ Interviews with Sallie O. Elkordy
http://billiontoddlermarchforsurvival.blogspot.com/
20 Top-selling Vaccines -- H1 2012 (Big money)
http://www.fiercevaccines.com/special-report/20-top-selling-vaccines/2012-09-25
Blood on Their Hands: The World’s Slickest Con Job and a Stack of Deadly LIES...
Has More Vaccination Led to More Health?
Follow the Money
The Alliance Between the Vaccine Industry and the Government
Always Look for Hidden Motivations
Why Isn't This ILLEGAL?
Protect Your Right to Informed Consent and Defend Vaccine Exemptions
http://articles.mercola.com/sites/articles/archive/2010/11/04/big-profits-linked-to-vaccine-mandates.aspx
Who Says There is No Money in Making Vaccines? At Least $5.7 Billion Given to Vaccine Manufacturers in 2011 by US Gov’t
http://vactruth.com/2012/11/30/2011-billions-vaccine-manufacturers/
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Hepatitis B vaccine
1. The graph below shows that the annual incidence of IDDM rose following Hepatitis B immunization in New Zealand.
The Center for Disease Control, CDC, published data which supports a link between timing of immunization and the development of diabetes (Pharmacoepidemiology and Drug Safety Vol 6 Suppl. 2, S60; 1998). The data from the CDC's preliminary study supports published data that immunization starting after 2 months is associated with an increased risk of diabetes. The US government study showed Hep B immunization starting after 2 months was associated with an almost doubling of the risk of IDDM, odds ratio of 1.9. The results were also consistent with data that immunization starting at birth is associated with a decreased risk of diabetes compared to immunization starting after 2 months of life (odds ratio of 1.3 vs 1.9). The children immunization at birth in the CDC study were followed on average less than 2 years. By contrast the BCG data from Sweden showed the ability of immunization at birth to prevent diabetes is only seen clearly after about age seven.
Read more:
http://www.vaccines.net/hepatiti.htm
Congress Told Hepatitis B Vaccine Linked to Rise in Diabetes.
http://www.vaccines.net/toppage1.htm
Juvenile Diabetes and Vaccination: New Evidence for a Connection
http://www.nvic.org/vaccines-and-diseases/Diabetes/juvenilediabetes.aspx
Review of Vaccine Induced Immune Overload and the Resulting Epidemics of
Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent
Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases
J Barthelow Classen MD
3637 Rockdale Road, Manchester, MD 21102, USA
Abstract
There has been an epidemic of inflammatory diseases that has paralleled the epidemic on iatrogenic immune stimulation with vaccines. Extensive evidence links vaccine induced immune over load with the epidemic of type 1 diabetes. More recent data indicates that obesity, type 2 diabetes and other components of metabolic syndrome are highly associated with immunization and may be manifestations of the negative feedback loop of the immune system
reacting to the immune overload. The epidemic of diabetes/prediabetes appears to be accelerating at a time when the prevalence of obesity has stabilized, indicating that the negative feedback system of the immune system has been over whelmed. The theory of vaccine induced immune overload can explain the key observations that have confounded many competing hypothesis. The current paper reviews the evidence that vaccine induced immune overload explains the disconnect between the increase in prediabetes and nonalcoholic fatty liver at a time when the obesity epidemic is waning in children.
http://www.vaccines.net/vaccine-induced-immune-overload.pdf
Vaccine-induced immune overload now affects majority of US children, study finds.
Read article here: http://www.thelibertybeacon.com/?p=21474
Saying No to Vaccines: Your Rights
http://naturalsociety.com/your-rights-saying-no-vaccines/
Aluminum: The Neurotoxin Far Worse than Mercury...
http://www.thelibertybeacon.com/?p=16598
Aluminum in Vaccines Found to be Deadly for Children and Adults Alike
http://naturalsociety.com/aluminum-in-vaccines-found-to-be-deadly-for-children-and-adults-alike/
Vaccines Don’t Protect: Exposing the Vaccination for Immunity Fraud
http://naturalsociety.com/exposing-vaccination-for-immunity-fraud/
10 outrageous (but true) facts about vaccines the CDC and the vaccine industry don't want you to know
http://www.naturalnews.com/042012_vaccine_facts_vaccine-damaged_children_cdc.html#
Dissolving Illusions - paints a historic portrait with quotes from the pages of long overlooked medical journals, books, newspapers, and other sources to reveal a startling history that has been disregarded. With this historic information and originally researched data in the form of myth-shattering graphs, Dissolving Illusions shines new light onto issues that are assumed to be clear-cut and settled long ago.
http://www.dissolvingillusions.com/
50 Reasons NOT To Vaccinate Your Children
http://www.fhfn.org/50-reasons-not-to-vaccinate-your-children/
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Check out the ingredients in the Hepatitis B vaccine.
Hepatitis B (HBV) Vaccine Ingredients: (All of them contain, aluminum hydroxide or aluminum phoshate in the injection. Do you really want to be giving your just born infant this substance injected in any vaccine? Where are the safety studies; there are none.)
http://novaccine.com/specific-vaccines/hepatitis-b-hbv-vaccines/
Vaccine aluminum adjuvant causation of neuroglial activation and neuroinflammation in the brain of patients with autism. (Long list of independent unbiased physiologically based studies)
http://www.vacfacts.info/vaccine-aluminum-adjuvant-causation-of-neuroglial-activation-and-neuroinflammation-in-the-brain-of-patients-with-autism.html
Vaccine aluminum adjuvant causation of neuroglial activation and neuroinflammation in the brain of patients with autism - Page 2
http://www.vacfacts.info/vaccine-aluminum-adjuvant-causation-of-neuroglial-activation-and-neuroinflammation-in-the-brain-of-patients-with-autism--page-2.html
Zeta Potential
http://en.wikipedia.org/wiki/Zeta_potential
Using "Zeta Potential" as a Healing Tool
http://customers.hbci.com/~wenonah/new/mcdaniel.htm
— You Must Avoid Aluminum —
In Your Water, Your Food, and in things you put "In" and "On" Your Body !
Aluminum is used to treat waste water. It is added to waste water to cause materials to come out of solution and settle to the bottom of the tank.
The same thing can happen inside your body. 3–4 parts per million* of Aluminum in our blood Will Cause materials to come out of the blood plasma solution forming plaque on blood vessel walls. It also causes blood cells to clump together, thereby blocking blood flow to organs — causing strokes, heart attacks and other problems!
[ * About 27 milligrams of elemental aluminum in our body's 7 liters of blood will cause coagulation. ]
The reason this happens, is because Aluminum has a strong effect on Zeta Potential.
Aluminum is used in many Vaccinations as a stabilizer, and is known to cause learning disabilities. It can also STOP CELL DIVISION during the "S Phase".
Aluminum is Especially Harmful to Children! (And they are injecting multiple vaccines with aluminum adjuvants).
4 ppm of aluminum in human blood can cause it to colagulate.
Aluminum in humans is documented to inhibit learning.
http://customers.hbci.com/~wenonah/new/mcdaniel.htm
Zeta Potential is a measure of the electrical force that exists between atoms, molecules, particles, suspensoids, cells, etc., in a fluid.
Understanding Colloidal Suspensions - Help from Frank Hartman & Thomas Riddick
SOME EFFECTS OF REDUCED CARRYING CAPACITY
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 the results] -
http://www.sciencedirect.com/science?_ob=ArticleListURL&_method=list&_ArticleListID=-591300251&_sort=r&_st=13&view=c&md5=941c110d6231749e7d8ba96b96450263&search
Despite the number of references to aluminum toxicity, the FDA has always exempted it from testing from testing by putting it on their "Generally Regarded as Safe" ( GRAS ) list. Aluminum can be added to foods, medicines or water without restriction from the FDA.
[ Aluminum is known to stop cell division during the "S Phase", at levels less than 4 ppm. ]
The mechanism of action of aluminum toxicity is aluminum’s effect on carrying capacity or Zeta Potential. Aluminum is relatively non-toxic in and of itself. However, it destroys the carrying capacity of a liquid.
Aluminum has three ( 3 ) positive ions, so a single ion of aluminum will reduce surface charge, reduce carrying capacity and increase surface tension by 6,000 times the amount that an ion of Sodium, which has one ( 1 ) positive charge, would.
Read more:
http://customers.hbci.com/~wenonah/info/colloid.htm#Altox
The Chemistry of Aluminum toxicity, side effects
As I understand the literature, most aluminum is eliminated renally, bound to albumin or transferrin. If this system is fully utilized, the excess aluminum is sequestered in various organ systems, the brain being one, with highest concentrations in the limbic system. As aluminum levels are not often called for, many primary care physicians might not know to use a mobilizing agent prior to checking the blood level, and miss the presence of the metal altogether. (I know of such a case).
Generally, findings from an aluminum level blood test are unreliable, as most of the body's stores are bound in bone and tissue and are not reflected in the serum value. A deferoxamine infusion test can be performed but may take more than 48 hours to yield a result (see Medical Care). Deferoxamine liberates aluminum from tissues by chelating it and leads to an increased serum level compared to one taken prior to infusion. The combination of a baseline immunoreactive parathyroid hormone level of less than 200 mEq/mL and a change in serum aluminum value of 200 ng/mL after deferoxamine is 90% specific and has a positive predictive value of 85% for aluminum toxicity. From WEBMD Michael R. Edwards M.D. Bebe Medical Center. Further complicating the issue, regarding aluminum (aluminium, for any Brits reading this) the FDA has never tested this element for safety!
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.
Read more:
http://www.raysahelian.com/aluminum.html
Aluminum Adjuvants - Lack of Safety Data - Lack of Aluminum Adjuvant Safety Studies
http://www.vacfacts.info/aluminum-vaccine-adjuvants.html
Multiple scientific study links/ Blaylock RL.
Journal of American Nutraceutical Association 6: 21-35, 2003.
Interaction of Cytokines, Excitotoxins, and Reactive Nitrogen and Oxygen Species in Autism Spectrum Disorders Russell Blaylock, MD* Medical Director, Advanced Nutritional Concepts Ridgeland, Mississippi
ABSTRACT
There is growing and compelling evidence that excessive peripheral as well as central immune activation of brain microglia can result in alterations in brain growth and connectivity during rapid brain growth, the so-called "brain growth spurt." A considerable amount of evidence, presented in this paper, demonstrates the deleterious effects of immune factors, such as cytokines, chemokines, and excitotoxins, when present in excess. The interaction between excitotoxicity, ROS and RNS injury and immune dysfunction is discussed. It is concluded that excessive activation of the brain's immune system during critical growth periods can occur when vaccines are given as combination vaccines, using schedules that are too close together or by the use of certain live viruses in the vaccines.
http://www.nutrimedical.com/news.jhtml?method=view&news.id=1084
The Mechanisms of Vaccine Injury and Via Cytokine Storm, (my site page)
http://www.vacfacts.info/the-mechanisms-of-vaccine-injury-and-via-cytokine-storm.html
Session 22, The Vaccine Safety Conference: Dr. Russell Blaylock, MD, CCN
THE CENTRAL ROLE OF IMMUNOEXCITOTOXICITY IN ALUMINUM AND MERCURY-CONTAINING ADJUVANT-TRIGGERED NEURODEVELOPMENTAL AND NEURODEGENERATIVE DISORDERS
http://www.youtube.com/watch?v=u9DkcpEEBPI
Dr. Russell Blaylock, MD, CCN, video presentation - (same video as above, for an alternate source).
http://www.vaccinesafetyconference.com/videos.html#BlaylockVideo
How Vaccines Harm Child Brain Development - Dr Russell Blaylock MD
http://www.youtube.com/watch?v=7QBcMYqlaDs
Although this next study does not pertain to nor mention vaccines, look at how similar the findings are to that found in vaccine injury? Also review the other pages here on this site pertaining to the studies in regard to aluminum adjuvants, etc.
Surg Neurol Int. 2011; 2: 107.
Published online 2011 July 30. doi: 10.4103/2152-7806.83391
PMCID: PMC3157093
Immunoexcitotoxicity as a central mechanism in chronic traumatic encephalopathy—A unifying hypothesis
Published online 2011 July 30. doi: 10.4103/2152-7806.83391
PMCID: PMC3157093
Russell L. Blaylock* and Joseph Maroon1
Abstract
Some individuals suffering from mild traumatic brain injuries, especially repetitive mild concussions, are thought to develop a slowly progressive encephalopathy characterized by a number of the neuropathological elements shared with various neurodegenerative diseases. A central pathological mechanism explaining the development of progressive neurodegeneration in this subset of individuals has not been elucidated. Yet, a large number of studies indicate that a process called immunoexcitotoxicity may be playing a central role in many neurodegenerative diseases including chronic traumatic encephalopathy (CTE). The term immunoexcitotoxicity was first coined by the lead author to explain the evolving pathological and neurodevelopmental changes in autism and the Gulf War Syndrome, but it can be applied to a number of neurodegenerative disorders. The interaction between immune receptors within the central nervous system (CNS) and excitatory glutamate receptors trigger a series of events, such as extensive reactive oxygen species/reactive nitrogen species generation, accumulation of lipid peroxidation products, and prostaglandin activation, which then leads to dendritic retraction, synaptic injury, damage to microtubules, and mitochondrial suppression. In this paper, we discuss the mechanism of immunoexcitotoxicity and its link to each of the pathophysiological and neurochemical events previously described with CTE, with special emphasis on the observed accumulation of hyperphosphorylated tau.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157093/
Download PDF: Immunoexcitotoxicity as a central mechanism in chronic traumatic encephalopathy-A unifying hypothesis
http://www.surgicalneurologyint.com/downloadpdf.asp?issn=2152-7806%3Byear%3D2011%3Bvolume%3D2%3Bissue%3D1%3Bspage%3D107%3Bepage%3D107%3Baulast%3DBlaylock%3Btype%3D2
Vaccination and brain inflammation
http://www.heartmdinstitute.com/prevention/immunity/vaccinations/167-vaccines-depression-neurodegeneration-after-age-50-years?showall=&
Danger of live virus vaccines
http://www.heartmdinstitute.com/prevention/immunity/vaccinations/167-vaccines-depression-neurodegeneration-after-age-50-years?showall=&
A Mechanism of Toxicity of Aluminium-based Adjuvants?
Consumer Summary | by Chris Exley
http://www.vaccinesafetyconference.com/exley
Exley & House (2011) Aluminium in the human brain. Monatsh Chem (In press)
http://www.springerlink.com/content/9550512205128414/
Aluminum as a Neurotoxin: The Evidence from Cell Culture, In Vivo, & Human Studies
http://www.vaccinesafetyconference.com/pdf/Shaw/Shaw_PPT.pdf
Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
Lucija Tomljenovic a, Christopher A. Shaw a,b
http://pop.1796kotok.com/pdfs/Aluminum_autism.pdf
Abstract for talk: Aluminum as a neurotoxin: the evidence from cell culture, in vivo, and
human studies
http://www.vaccinesafetyconference.com/pdf/Shaw/Shaw_CS.pdf
Autism Spectrum Disorders and Aluminum Vaccine Adjuvants
Lucija Tomljenovic, Russell L. Blaylock, Christopher A. Shaw
Abstract
Impaired brain function, excessive inflammation, and autoimmune manifestations are common in autism. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the necessary properties to induce neuroimmune disorders. Because peripheral immune stimuli in the postnatal period can compromise brain development and cause permanent neurological impairments, the possibility that such outcomes could also occur with administration of Al vaccine adjuvants needs to be considered. In regard to the risk of adjuvant toxicity in children, the following should be noted: (i) children should not be viewed as “small adults” as their unique physiology makes them more vulnerable to toxic insults; (ii) in adult humans Al adjuvants can cause a variety of serious autoimmune and inflammatory conditions including those affecting the brain, yet children are routinely exposed to much higher amounts of Al from vaccines than adults; (iii) compelling evidence has underscored the tight connection between the development of the immune system and that of the brain. Thus, it appears plausible that disruptions of critical events in immune development may also play a role in the establishment of neurobehavioral disorders; (iv) the same immune system components that play key roles in brain development appear to be targeted for impairment by Al adjuvants. In summary, research data suggests that vaccines containing Al may be a contributing etiological factor in the increasing incidence of autism.
http://link.springer.com/referenceworkentry/10.1007%2F978-1-4614-4788-7_89
Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes
C.A. Shawa,b,c, ⁎, Y. Li a , L. Tomljenovic a
Abstract:
Our previous ecological studies of autism spectrum disorder (ASD) has demonstrated a correlation between increasing ASD rates and aluminium (Al) adjuvants in common use in paediatric vaccines in several Western countries. The correlation between ASD rate and Al adjuvant amounts appears to be dose-dependent and satisfies 8 of 9 Hill criteria for causality. We have now sought to provide an animal model to explore potential behavioural phenotypes and central nervous system (CNS) alterations using s.c. injections of Al hydroxide in early postnatal CD-1 mice of both sexes. Injections of a “high” and “low”Al adjuvant levels were designed to correlate to either the U.S. or Scandinavian paediatric vaccine schedules vs. control saline-injected mice. Both male and female mice
in the “high Al” group showed significant weight gains following treatment up to sacrifice at 6 months of age. Male mice in the “high Al” group showed significant changes in light–dark box tests and in various measures of behaviour in an open field. Female mice showed significant changes in the light–dark box at both doses, but no significant changes in open field behaviours. These current data implicate Al injected in early postnatal life in some CNS alterations that may be relevant for a better understanding of the aetiology of ASD. © 2013 Elsevier Inc
http://myofasciite.fr/Contenu/Divers/201307_CAShaw_YLee_LTomljenovic.pdf
PRESENTATIONS
http://www.vaccinesafetyconference.com/presentation.html
Study RESOURCES - Dr Russell Blaylock
http://www.vaccinesafetyconference.com/resources.html
The Danger of Excessive Vaccination During Brain Development
The Case for a Link to Autism Spectrum Disorders
By Russell L. Blaylock, M.D.
http://articles.mercola.com/sites/articles/archive/2008/03/14/the-danger-of-excessive-vaccination-during-brain-development.aspx
Immune-Glutamatergic Dysfunction as a Central Mechanism of the Autism Spectrum Disorders
http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.317.7642&rep=rep1&
http://www.utdallas.edu/~mxa049000/lessons/research/literature/Autism/new/Blaylock%20autism%20rev%20CMC%2009.pdf
Chronic Microglial Activation and Excitotoxicity Secondary to Excessive Immune Stimulation:
Possible Factors in Gulf War Syndrome and Autism
The Role of Excitotoxicity
Page 47. Damage to neuronal mechanisms is not limited to direct cytokine effects. The excitotoxicity initiated by microglial activation is even more important. In cases of HIV-1 dementia, it is known that brain quinolinic acid, an excitotoxin secreted by activated microglia, can increase more than 300-fold. In addition, glutamate is released in concentrations that are known to destroy neurons and/or synaptic connections.
Because glutamate can also activate microglia and enhance cytokine-induced neurodegeneration, a vicious cycle is created in which immune cytokines can stimulate release of glutamate, and glutamate in turn enhances cytokine production and release. Moreover, cytokines inhibit glutamate transporters, which play a critical role in removal of excess extracellular glutamate. Intimately linked to excitotoxicity is the generation of destructive free radicals, especially the reactive nitrogen species such as peroxynitrite and nitrosoperoxycarbonate. Much of the injury to dendrites, synapses and neurons, by both cytokines and excitotoxicity, is caused by free radicals.
The Role of Vaccines, page 49
Read more:
http://www.jpands.org/vol9no2/blaylock.pdf
Entropy 2012, 14(8), 1399-1442; doi:10.3390/e14081399
Review
The Initial Common Pathway of Inflammation, Disease, and Sudden Death
Robert M. Davidson 1,* and Stephanie Seneff
Abstract: In reviewing the literature pertaining to interfacial water, colloidal stability, and cell membrane function, we are led to propose that a cascade of events that begins with acute exogenous surfactant-induced interfacial water stress can explain the etiology of sudden death syndrome (SDS), as well as many other diseases associated with modern times. A systemic lowering of serum zeta potential mediated by exogenous cationic surfactant administration is the common underlying pathophysiology. The cascade leads to subsequent inflammation, serum sickness, thrombohemorrhagic phenomena, colloidal instability, and ultimately even death. We propose that a sufficient precondition for sudden death is lowered bioavailability of certain endogenous sterol sulfates, sulfated glycolipids, and sulfated glycosaminoglycans, which are essential in maintaining biological equipose, energy metabolism, membrane function, and thermodynamic stability in living organisms. Our literature review provides the basis for the presentation of a novel hypothesis as to the origin of endogenous bio-sulfates which involves energy transduction from sunlight. Our hypothesis is amply supported by a growing body of data showing that parenteral administration of substances that lower serum zeta potential results in kosmotropic cationic and/or chaotropic anionic interfacial water stress, and the resulting cascade.
http://www.mdpi.com/1099-4300/14/8/1399 (Also view full text from that link by clicking full study)
file:///C:/Users/TEMP/Downloads/entropy-14-01399.pdf
The Initial Common Pathway of Inflammation, Disease, and Sudden Death, (full study source)
Pay particular attention to reading pages, Page 414-415 in regard to vaccine aluminum adjuvants, and as well pages 419-420 in regard to Gardasil.
http://www.mdpi.com/1099-4300/14/8/1399
http://people.csail.mit.edu/seneff/Entropy/Entropy1_downloaded.pdf
Is Encephalopathy a Mechanism to Renew Sulfate in Autism?
Stephanie Seneff 1,*, Ann Lauritzen 2 , Robert M. Davidson 3 and Laurie Lentz-Marino 4
Entropy; Jan2013, Vol. 15 Issue 1, p372
ABSTRACT This paper makes two claims: (1) autism can be characterized as a chronic lowgrade encephalopathy, associated with excess exposure to nitric oxide, ammonia and glutamate in the central nervous system, which leads to hippocampal pathologies and resulting cognitive impairment, and (2), encephalitis is provoked by a systemic deficiency in sulfate, but associated seizures and fever support sulfate restoration. We argue that impaired synthesis of cholesterol sulfate in the skin and red blood cells, catalyzed by sunlight and nitric oxide synthase enzymes, creates a state of colloidal instability in the blood manifested as a low zeta potential and increased interfacial stress. Encephalitis, while life-threatening, can result in partial renewal of sulfate supply, promoting neuronal survival. Research is cited showing how taurine may not only help protect neurons from hypochlorite exposure, but also provide a source for sulfate renewal. Several environmental factors can synergistically promote the encephalopathy of autism, including the herbicide, glyphosate, aluminum, mercury, lead, nutritional deficiencies in thiamine and zinc, and yeast overgrowth due to excess dietary sugar. Given these facts, dietary and lifestyle changes, including increased sulfur ingestion, organic whole foods, increased sun exposure, and avoidance of toxins such as aluminum, mercury, and lead, may help to alleviate symptoms or, in some instances, to prevent autism altogether.
http://www.mdpi.com/1099-4300/15/1/372
Autism: A neuroepigenetic disorder, By Richard C. Deth, PhD
http://www.autismone.org/sites/default/files/Deth_ASD03.pdf
Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure
Stephanie Seneff, Robert M. Davidson, and Jingjing Liu
http://www.mdpi.com/1099-4300/14/11/2227
http://people.csail.mit.edu/seneff/Entropy/entropy-14-02227.pdf
GLUTATHIONE Scientific Research
Our findings suggest that acetaminophen administration selectively depletes (within 2 hr) mitochondrial glutathione, and produces local toxicity by altering membrane permeability and decreasing the efficiency of oxidative phosphorylation. This renders mitochondria more susceptible to oxidative damage… PMID: 8937421
http://www.readisorb.com/science/glutathione_scientific_researc.html
Biochem Pharmacol. 1996 Oct 25;52(8):1147-54.
Effect of acetaminophen administration on hepatic glutathione compartmentation and mitochondrial energy metabolism in the rat.
http://www.ncbi.nlm.nih.gov/pubmed/8937421
Scientific Research, 2nd Page
http://www.readisorb.com/science/
Tim Guilford, MD
Glutathione in Health and Disease
http://www.svhi.com/newsletters/2005/slf-122005.pdf
Glutathione
http://www.readisorb.com/
Glutathione, Tylenol, Vaccine Adverse Reactions, and ASD
http://www.vacfacts.info/glutathione-tylenol-vaccine-adverse-reactions-and-asd.html
Neurodegenerative Diseases: Neurotoxins as Sufficient Etiologic Agents?
Christopher A. Shaw and Günter U. Höglinger
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814816/
Neuroscience and Biobehavioral Reviews
Analysis of neurological disease in four dimensions: insight from ALS-PDC epidemiology and animal models
The causal factor(s) responsible for sporadic neurological diseases are unknown and the stages of disease progression remain undefined and poorly understood. We have developed an animal model of amyotrophic lateral sclerosis-parkinsonism dementia complex which mimics all the essential features of the disease with the initial neurological insult arising from neurotoxins contained in washed cycad seeds. Animals fed washed cycad develop deficits in motor, cognitive, and sensory behaviors that correlate with the loss of neurons in specific regions of the central nervous system. The ability to recreate the disease by exposure to cycad allows us to extend the model in multiple dimensions by analyzing behavioral, cellular, and biochemical changes over time. In addition, the ability to induce toxin-based neurodegeneration allows us to probe the interactions between genetic and epigenetic factors. Our results show that the impact of both genetic causal and susceptibility factors with the cycad neurotoxins are complex. The article describes the features of the model and suggests ways that our understanding of cycad-induced neurodegeneration can be used to decipher and identify the early events in various human neurological diseases.
http://yadda.icm.edu.pl/yadda/element/bwmeta1.element.elsevier-a4f127e4-0c75-3f6d-bb32-9406a3136a76
And to realize that in any of the studies that the CDC has considered as to vaccine toxicity, none of that has been studied, and nor as well has any basic physiological science like this been addressed nor even acknowledged. They are yet by CHOICE, in the dark ages, as to their known and accepted knowledge, and of the human body, and its immune system
Dr Blaylock, a Board-certified neurosurgeon, Visiting Professor of Biology at Belhaven College, Jackson, Mississippi, and member of the Editorial Board of the Journal of the American Nutraceutical Association (JANA), is the author of three books on excitotoxicity: Excitoxicity: the taste that kills, Health and nutrition secrets, and Natural strategies for cancer patients.
EXCITOTOXICITY: A POSSIBLE CENTRAL MECHANISM IN FLUORIDE NEUROTOXICITY, (the fluoride and aluminum connection)
by Russell L Blaylocka, Ridgeland, MS, USA
SUMMARY: Recent evidence indicates that fluoride produces neuronal destruction and synaptic injury by a mechanism that involves free radical production and lipid peroxidation. For a number of pathological disorders of the central nervous system (CNS), excitotoxicity plays a critical role. Various studies have shown that many of the neurotoxic metals, such as mercury, lead, aluminum, and iron also injure neural elements in the CNS by an excitotoxic mechanism. Free radical generation and lipid peroxidation, especially in the face of hypomagnesemia and low neuronal energy production, also magnify excitotoxic sensitivity of neurons and their elements. This paper reviews briefly some of the studies that point to a common mechanism for the CNS neurotoxic effects of fluoride and calls for research directed toward further elucidation of this mechanism.
http://www.fluorideresearch.org/374/files/374301-314.pdf
Toxic Overload: Children Vaccinated To Extreme
http://www.thelibertybeacon.com/?p=16643
Vaccinations Cause Chronic Immune System Dysregulation
http://www.thelibertybeacon.com/?p=16251
There Is No Such Thing As a Safe Vaccine and There Never Will Be
http://wp.me/p2X3AR-47a
Vaccines Are Causing Mutations That May Jeopardize
The Health of Future Generations
http://www.thelibertybeacon.com/?p=16698
Forced Vaccination is Equivalent to Human Experimentation
and Subject to the Nuremberg Code
http://www.thelibertybeacon.com/?p=13171
Multiple Infant Vaccines Linked To Dramatically Increased Mortality ~ By: Sayer Ji
http://wp.me/p2X3AR-4dx
Vaccination During Pregnancy: Is It Safe?
http://wp.me/p2X3AR-4bT
The Vaccine Mafia and Its Jury of Thugs: Your Rulers
Read this scathing critique here: http://wp.me/p2X3AR-47x
Are Vaccines Safe: Bracing Ourselves for More Sham Vaccine Studies
Read this very critical article here: http://wp.me/p2X3AR-43O
The Hidden Connection Behind Viruses, Vaccines and Cancer
By: Dr. Tyson Perez
Mainstream medicine tells us that the hepatitis B virus (HBV) causes liver cancer which is why it is so necessary for US newborns to be vaccinated within hours of birth. We are told that the human papillomavirus (HPV), which is supposedly so prevalent in our population, causes cervical cancer which is why there is such a push to vaccinate girls and boys in the US as early as 9 years old. Let’s not forget about Simian Virus 40 (SV40) which is known to have contaminated polio vaccines and is associated with a wide variety of human cancers. Conventional wisdom tells us that viruses cause cancer. But is this true? Let’s investigate the story further.
The first recorded cases of HBV infection occurred following the administration of the smallpox vaccine containing human lymph to shipyard workers in Germany in 1883. HBV is transmitted through contact with infected bodily fluids. It is estimated that over 2 billion people worldwide have been infected and that approximately 350 million are chronic carriers. Chronic HBV infection is believed to cause up to 80% of all hepatocellular carcinomas. Sounds scary right? But when you look deeper you find that, in the US, HBV is found predominantly in adults who are either I.V. drug users or engaging in high-risk sexual behavior.
Read more:
http://www.thelibertybeacon.com/2013/02/09/the-hidden-connection-behind-viruses-vaccines-and-cancer/
VRM: The Rise of Mutagenic Viruses
http://vaccineresistancemovement.org/?p=13124
Your Immune System, How It Works And How Vaccines Damage It
"Chronic illnesses are now so common, having a sick child seems to be the “new normal.”Children are supposed to be vibrant, healthy, free of disease." - Janet Levatin MD, Pediatrician.
http://www.vaccineriskawareness.com/Your-Immune-System-How-It-Works-And-How-Vaccines-Damage-It
Vaccines Are Causing Mutations That May Jeopardize The Health of Future Generations
By: Dave Mihalovic
Vaccines are causing an unprecedented number of mutations creating superbugs and potent viruses and bacteria that may eventually threaten future generations and humanity itself. Evidence continues to mount from the scientific community who now admit that certain vaccines are in-fact causing both viral and bacterial mutations. Ironically, the same researchers assert that “better” vaccines are needed to offset the rise in persistent mutations.
Life-threatening pathogens are capable of evolving rapidly and developing genetic decoys that serve to disguise them from even the most powerful drugs. University of Oxford researcher Rory Bowden found that pathogens switch genetic material with other bacteria, but predominantly for the part of the genome responsible for making the cell coating, which is the area targeted by vaccines.
Former post-doctoral researcher of the Center for Infectious Disease Dynamics, Grainne Long found that vaccination led to a 40-fold enhancement of B. parapertussis colonization in the lungs. His data suggested that the vaccine may be contributing to the observed rise in whooping cough incidence over the last decade by promoting B. parapertussis infection.
Whooping Cough
An acellular whooping cough vaccine actually enhances the colonization of Bordetella parapertussis in mice; pointing towards a rise in B. parapertussis incidence resulting from acellular vaccination, which may have contributed to the observed increase in whooping cough over the last decade.
Despite widespread vaccination, whooping cough incidence is on the rise worldwide, making it a disease virtually immune to vaccines.
Read more:
http://www.thelibertybeacon.com/2014/02/10/vaccines-are-causing-mutations-that-may-jeopardize-the-health-of-future-generations/
In 1991, the American Council on Immunization Practices (ACIP) recommended universal vaccination of all U.S. infants with 3 doses of hepatitis B vaccine, beginning within 48 hours of birth. Hepatitis B is a sexually-transmitted disease and is spread the same way HIV and Hepatitis C are spread: through contact with body fluids such a semen, vaginal fluids, and blood. Those at high risk of infection include homosexual men, heterosexuals who have multiple sex partners, and healthcare workers who are exposed to body fluids. Infants whose mothers are actively infected with Hepatitis B are at increased risk of infection. (citation)
Pregnant women in the U.S. are screened for the disease.
Infants who are born to mothers who are not infected with hepatitis B are at very low risk for infection, by virtue of the fact that they are not engaging in high risk behaviors that are associated with the disease. (i.e., Infants are not having sex and they are not using injection drugs.)
The CDC states that the incidence of hepatitis B infection in U.S. children (age 0-19 years) has decreased by 89% as a result of mass vaccination of infants. This is misleading, in my opinion. When you say that the incidence of the illness has decreased by 89% it sounds like the vaccine has been extremely effective in improving the health of children who receive it. The opposite is actually the case.
Here are some studies that have investigated the health effects of hepatitis B vaccine in U.S. children.
Read more:
http://vaxtruth.org/2014/06/hepatitis-b-vaccine-for-infants-is-it-worth-it/
Written by a partner vaccine truth advocate: btw the CDC warns that if you have latex allergy to avoid the Hep B vaccine, one must ask how they know a newborn has a latex allergy and the common sense is that the vaccine is causing these allergies. My sister had a liver transplant last November, due to diagnosis over a decade ago of 'autoimmune hepatitis. Once said to be rare, I personally know 12 people with the diagnosis and all are healthcare professionals who were injected with Hep B vaccine decades ago. The physicians in the liver clinics have remarked how they are seeing this diagnosis more frequently. When informed of how many people we know with the diagnosis and how we think its due to the Hep B vaccine, rather than be dismissed, the doctors respond; "That's an interesting idea." We are lobbying the medical profession to include the question of whether they had the vaccine in the screening of patients. We believe that when the professionals see the high incidence in the vaccine populations this could result in further questioning and possible removal as mandatory.
Autoimmun Rev. 2005 Feb;4(2):96-100.
Autoimmune hazards of hepatitis B vaccine.
"According to Hippocratic tradition, the safety level of a preventive medicine must be very high, as it is aimed at protecting people against diseases that they may not contract. This paper points out that information on the safety of hepatitis B vaccine (HBV) is biased as compared to classical requirements of evidence-based medicine (EBM), as exemplified by a documented selectivity in the presentation or even publication of available clinical or epidemiological data. Then, a review is made of data suggesting that HBV is remarkable by the frequency, the severity and the variety of its complications, some of them probablyrelated to a mechanism of molecular mimicry leading to demyelinating diseases, and the others reproducing the spectrum of non-hepatic manifestations of natural hepatitis B. To be explained, this unusual spectrum of toxicity requires additional investigations based upon complete release of available data."
http://www.ncbi.nlm.nih.gov/pubmed/15722255
Hepatitis B Vaccine - What Are the Risks?
Adverse Reactions* and Deaths from Hepatitis B Vaccine between 1983-2012
*It is estimated that only 10% of vaccine reactions are ever reported to the CDC.
"As of March 2012, there was a total of 66,654 hepatitis B vaccine-related adverse events reported to the federal Vaccine Adverse Events Reporting System (VAERS), including reports of headache, irritability, extreme fatigue, brain inflammation, convulsions, rheumatoid arthritis, optic neuritis, multiple sclerosis, lupus, Guillain Barre Syndrome (GBS) and neuropathy. There have been more than 1500 hepatitis B vaccine-related deaths reported, including deaths classified as sudden infant death syndrome (SIDS)."
According to a similar report, the toxic metals in the Hepatitis B vaccine have varied in the years between 1983 and 2013. While the amount of one metal (mercury) in the vaccine decreased, another metal (aluminum) increased.
1,500 Deaths
1,359 Life Threatening Injuries
66,654 Total Injuries
Italy: “Hepatitis B vaccine is administered at birth only to children born to HBsAg + mothers. Otherwise immunisation starts at 3 months of age.”
Finland: “Hepatitis B vaccine is given only to infants of HbsAg carrier mothers or fathers at the age of 0, 1, 2 and 12 months.”
Denmark: “Vaccination against hepatitis B is recommended to children of HBsAg-positive mothers, starting at birth with both hepatitis B immunoglobulin and one dose of HepB.”
Norway: “HepB is recommended for risk groups only.”
Sweden: “HepB is only recommended to children considered high-risk groups. Vaccination is given at birth to infants of mothers positive for hepatitis B.”
The Netherlands: “Only for children born to HBsAg positive mothers.”
Read more:
http://www.ashotoftruth.org/vaccines/hepatitis-b-vaccine
Now, lets go to some real study science that you likely have not been told about, as to the actual efficacy of the vaccine and in and as to its preventing Hep B in an infant with an HBsAg-positive mother. Quite obviously the vaccine does not even protect a newborn in that situation, or with a quite lower than what would expected rate of efficacy. So, the point in giving it to a newborn then, is what? (Do you think or see yet that the pharma for profit vaccine program is just evil and out rightly, sick? And they have the experts behind them right, like the CDC and Paul Offit, how can it be wrong)?
FAIL: Infant Hep B Vaccines Perform Shamefully; Time To End Them?
http://www.greenmedinfo.com/blog/fail-infant-hep-b-vaccines-perform-shamefully-time-end-them
Hepatitis B vaccination with or without hepatitis B immunoglobulin at birth to babies born of HBsAg-positive mothers prevents overt HBV transmission but may not prevent occult HBV infection in babies: a randomized controlled trial.
Abstract (excerpt):
Women who were anti-HBe positive were a low-risk group, and their babies were most likely to remain free of HBV infection (occult or overt) and had good immune response to the vaccine. Maternal HBeAg-positive status and negativity for anti-HBe predicted not only overt but also any infection (both overt and occult) in babies. In addition, high maternal HBV DNA and treatment with vaccine alone were significant factors for overt HBV infection in babies. The current practice of administration of vaccine with HBIG at birth to babies born of HBsAg-positive mothers is not effective in preventing occult HBV infection in babies, which may be up to 40%.Because the most important risk factors for mother-to-baby transmission of HBV infection are the replicative status and high HBV DNA level in mothers; it will be worthwhile investigating the role of antivirals and HBIG administration during pregnancy to prevent mother-to-child transmission of HBV infection.
Read more:
http://www.greenmedinfo.com/article/hepatitis-b-vaccination-or-without-hepatitis-b-immunoglobulin-birth-babies
Hepatitis B vaccination with or without hepatitis B immunoglobulin at birth to babies born of HBsAg-positive mothers prevents overt HBV transmission but may not prevent occult HBV infection in babies: a randomized controlled trial
Summary
Vertical transmission of Hepatitis B virus HBV can result in a state of chronic HBV infection and its complications. HBV vaccination with or without hepatitis B immunoglobulin (HBIG) prevents transmission of overt infection to the babies. However, whether it also prevents occult HBV infection in babies is not known. Consecutive pregnant women of any gestation found to be HBsAg positive were followed till delivery, and their babies were included in the study. Immediately after delivery, babies were randomized to receive either HBIG or placebo in addition to recombinant HBV vaccine (at 0, 6, 10 and 14 weeks). The primary end-point of the study, assessed at 18 weeks of age, was remaining free of any HBV infection (either overt or occult) plus the development of adequate immune response to vaccine. The babies were further followed up for a median of 2 years of age to determine their eventual outcome. Risk factors for HBV transmission and for poor immune response in babies were studied. Of the 283 eligible babies, 259 were included in the trial and randomized to receive either HBIG (n = 128) or placebo (n = 131) in addition to recombinant HBV vaccine. Of the 222 of 259 (86%) babies who completed 18 weeks of follow-up, only 62/222 (28%) reached primary end-point. Of the remaining, 6/222 (3%) developed overt HBV infection, 142/222 (64%) developed occult HBV infection, and 12/222 (5%) had no HBV infection but had poor immune response. All 6 overt infections occurred in the placebo group (P = 0.030), while occult HBV infections were more common in the HBIG group (76/106 [72%] vs. 66/116 [57%]; P = 0.025). This may be due to the immune pressure of HBIG. There was no significant difference between the two groups in frequency of babies developing poor immune response or those achieving primary end-point. The final outcome of these babies at 24 months of age was as follows: overt HBV infection 4%, occult HBV infection 42%, no HBV infection but poor immune response 8% and no HBV infection with good immune response 28%. Women who were anti-HBe positive were a low-risk group, and their babies were most likely to remain free of HBV infection (occult or overt) and had good immune response to the vaccine. Maternal HBeAg-positive status and negativity for anti-HBe predicted not only overt but also any infection (both overt and occult) in babies. In addition, high maternal HBV DNA and treatment with vaccine alone were significant factors for overt HBV infection in babies. The current practice of administration of vaccine with HBIG at birth to babies born of HBsAg-positive mothers is not effective in preventing occult HBV infection in babies, which may be up to 40%. Because the most important risk factors for mother-to-baby transmission of HBV infection are the replicative status and high HBV DNA level in mothers; it will be worthwhile investigating the role of antivirals and HBIG administration during pregnancy to prevent mother-to-child transmission of HBV infection.
http://onlinelibrary.wiley.com/doi/10.1111/jvh.12102/abstract
How the CDC (and Dorit Reiss) Hyped Risk of Childhood Hep B Infection by 50-fold to Push Vaccines
By Cia Parker
Professional vaccine operatives like Dorit Reiss have been hard at work for some time to exaggerate the dangers of the vaccine-preventable diseases, while simultaneously denying the damage that the vaccines for them often do. A case in point was found in the comments on this article on the Mother Jones website last week:
The topic had turned to the hepatitis-B vaccine, given to all newborns in the U.S. while they were still at the hospital, beginning in 1991 (at the beginning of the autism epidemic). I put up information I had found in Dr. Bob Sears’ The Vaccine Book, a link to a CDC report with a chart at the bottom showing the rate of hep-B diagnosis in children 1-9 from 1986, five years before the vaccine program began.
The chart at the bottom of the report clearly shows that the rate at which hep-B was diagnosed in children was less than one per 100,000 or fewer than 360 a year in a childhood population of 36 million in 1990. The text at the top of the report, however, states: “Before 1982, an estimated 200,000--300,000 persons in the United States were infected annually with HBV, including approximately 20,000 children.” The source for this large number was an article in Pediatrics in 2001. It uses the word “estimated” because this is a purely speculative figure, not based on the disease being diagnosed by blood tests carried out by physicians.
Hepatitis B is a very dangerous disease when contracted in the first year. At that time, the only means of transmission, except in extremely unusual and almost unimaginable circumstances, is from contagion by an infected mother. It is usual to perform a blood test on a pregnant woman to learn whether her child is at risk, in which case it would probably be best to give the baby immunoglobulin and the vaccine when it was born. But instead it has become standard practice in the U.S. to give this dangerous vaccine to all newborns, even those born to healthy mothers, and very common to give the vaccine to the newborn without the permission or knowledge of the parents, making it harder to realize that the vaccine was the cause of the child’s autism, diagnosed years later.
The virus is transmitted like AIDS, by infected blood/body fluids to blood/mucus membrane contact. It is most commonly contracted by unsafe sex with a carrier or by shared use of needles used by illegal drug users. Medical personnel exposed to infected blood are at some increased risk, but it is not as great as is commonly believed. It is not spread by the sharing of eating utensils or drinking glasses, or sleeping in the same bed as an infected person. It may sometimes be transmitted by sharing toothbrushes or razors. Australia did a study which showed that it was not transmitted by children at school. (Burgess, MA and McIntosh, EDG, “Hepatitis-B in urban schoolchildren – No evidence of horizontal transmission between high-risk and low-risk groups,” Med J Australia, 5 Sept. 1993; 159: 315-319, quoted Wendy Lyall, Raising a vaccine-free child, p.178).
Hepatitis B is a very dangerous disease when contracted in the first year. At that time, the only means of transmission, except in extremely unusual and almost unimaginable circumstances, is from contagion by an infected mother. It is usual to perform a blood test on a pregnant woman to learn whether her child is at risk, in which case it would probably be best to give the baby immunoglobulin and the vaccine when it was born. But instead it has become standard practice in the U.S. to give this dangerous vaccine to all newborns, even those born to healthy mothers, and very common to give the vaccine to the newborn without the permission or knowledge of the parents, making it harder to realize that the vaccine was the cause of the child’s autism, diagnosed years later.
The virus is transmitted like AIDS, by infected blood/body fluids to blood/mucus membrane contact. It is most commonly contracted by unsafe sex with a carrier or by shared use of needles used by illegal drug users. Medical personnel exposed to infected blood are at some increased risk, but it is not as great as is commonly believed. It is not spread by the sharing of eating utensils or drinking glasses, or sleeping in the same bed as an infected person. It may sometimes be transmitted by sharing toothbrushes or razors. Australia did a study which showed that it was not transmitted by children at school. (Burgess, MA and McIntosh, EDG, “Hepatitis-B in urban schoolchildren – No evidence of horizontal transmission between high-risk and low-risk groups,” Med J Australia, 5 Sept. 1993; 159: 315-319, quoted Wendy Lyall, Raising a vaccine-free child, p.178).
Read more:
http://www.ageofautism.com/2014/03/how-the-cdc-and-dorit-reiss-hyped-risk-of-childhood-hep-b-infection-by-50-fold-to-push-vaccines-.html
Hepatitis B Vaccine: An Unmitigated Disaster
By J.B. Handley
http://www.ageofautism.com/2009/10/hepatitis-b-vaccine-an-unmitigated-disaster-.html
When We Know Better, We Do Better. Marcella Piper-Terry’s Speech, We the Parents Rally, West Virginia
(The REAL Hepatitis B vaccine statistics-extensive article)
http://vaxtruth.org/2012/02/when-we-know-better-we-do-better-or-do-we/
Should Infants be Vaccinated Against Hepatitis B? How Much Aluminum is Safe for Infants?
INFANTS IN THE UNITED STATES ARE NOT AT RISK FOR HEPATITIS B!
In 1991, there were 18,003 cases of hepatitis B reported in the U.S. out of a total U.S. population of 248 million. According to the October 31, 1997 Morbidity and Mortality Weekly Report published by the CDC, in 1996 there were 10,637 cases of hepatitis B reported in the U.S. with 279 cases reported in children under the age of 14 and the CDC stated that “Hepatitis B continues to decline in most states, primarily because of a decrease in the number of cases among injecting drug users and, to a lesser extent, among both homosexuals and heterosexuals of both sexes.”
But the CDC and vaccines’ biggest proponent, Dr. Paul Offit wants ALL babies vaccinated for Hepatitis B, not once but three times. I wonder if that’s because if they are going in for their Hep. B shots, they are also more likely to receive the Rotavirus Vaccine, for which Dr. Offit developed the patent, which sold for 182 MILLION dollars. Imagine how much money would be lost on rotavirus vaccination if parents started questioning and as a result, did not follow the currently mandated schedule.
If you think babies should be vaccinated against a sexually transmitted disease at birth, with a vaccine that contains up to 125 times the “safe” limit of aluminum (according to the EPA regulations), watch this video from ABC News 20-20, Part 1 of Who’s Calling The Shots?
and this video from ABC News 20-20, Part 2 of Who’s Calling The Shots?
Read more:
http://vaxtruth.org/2012/01/should-infants-be-vaccinated-against-hepatitis-b-how-much-aluminum-is-safe-for-infants/
ABC News 20-20 1999 Hep B part 1 (both videos are the same as the above)
http://www.youtube.com/watch?v=hNy5VmeaGNw
ABC News 20-20 1999 Hep B part 2
http://www.youtube.com/watch?v=78b1rFJgyXI
Meet Timmy: A beautiful little boy who was seriously injured by the Hepatitis B vaccine administered in infancy.
http://vaxtruth.org/2011/09/meet-timmy/
PHYSICIANS OPPOSE MANDATORY HEPATITIS B VACCINE FOR OHIO SCHOOLCHILDREN
PARENTS, NOT GOVERNMENT, SHOULD DECIDE
The Association of American Physicians and Surgeons (AAPS) opposes efforts in Ohio and other states to force all schoolchildren to receive three doses of hepatitis B vaccine. Too few children contract the disease to justify exposing all children to the risk of adverse vaccine reactions. AAPS urges Ohio legislators to support Ohio House Bill 200, which would repeal Ohio's hastily mandated hepatitis B vaccine requirement, and add informed consent for all vaccines.
In the United States, hepatitis B is primarily an adult disease, and risk is highly dependent on lifestyle. Risk factors include: multiple sex partners, drug abuse, an occupation involving frequent exposure to blood, or having a hepatitis-B infected mother. The disease is not spread by casual contact. More than 99.7 percent of Ohioans are free of this virus. No Ohio school has ever reported hepatitis B transmission.
Read more:
http://www.aapsonline.org/press/nrohvac.htm
Shots in the dark.
Author: Blevins, Sue A.
Source: Reason v. 31 no3 (July 1999) p. 49-51
Lyla Rose Belkin was an alert and lively baby at five weeks old. Her parents, Michael and Lorna Belkin, say she had never been sick until she received a mandatory hepatitis B shot on September 16, 1998. "That night she became agitated and feisty," her father recalls. "Then she fell asleep and never woke up." Doctors told the Belkins that Lyla must have died from Sudden Infant Death Syndrome, a catchall diagnosis.
Vaccine Casualty: Five-week-old Lyla Rose Belkin died after receiving a mandatory hepatitis B shot. Since 1991, at least 274 newborns have died and 2,600 infants have suffered serious medical problems after getting the vaccine.
Read more:
http://www.utmb.edu/pedi_ed/healthdev/OtherPages/shots-in-dark.asp
Mindless Vaccination Bureaucracy
By Michael Belkin
http://www.nvic.org/vaccines-and-diseases/Hepatitis-B/fatherstory.aspx
Michael Belkin Testimony to Congress on Hepatitis B Vaccine-Congressional Testimony
http://therefusers.com/refusers-newsroom/michael-belkin-testimony-to-congress-on-hepatitis-b-vaccine/
Uploaded on Apr 14, 2008
Hepatitis B Vaccine, May 18, 1999 The House Reform Committee. 2 Congressman Mica D-FL. 1st Michael Belkin
https://www.youtube.com/watch?v=sgtXNnevorg
Hepatitis B Vaccine
The Untold Story
http://www.nvic.org/nvic-archives/newsletter/untoldstory.aspx
Is the Hepatitis B Vaccine a Deadly Roll of the Dice?
http://www.thelibertybeacon.com/2014/04/13/is-the-hepatitis-b-vaccine-a-serious-or-deadly-roll-of-the-dice/
Hepatitis B Vaccine Side Effects
http://www.childhoodshots.com/Hepatitis-B-Vaccine-Side-Effects-s/64.htm
The Hepatitis B Vaccine Scam
http://healthwyze.org/index.php/component/content/article/83-the-hepatitis-b-vaccine-scam.html
The vaccine science on hepatitis B vaccine
View the Evidence: Problematic Actions
http://www.greenmedinfo.com/anti-therapeutic-action/vaccination-hepatitis-b
VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body
http://vaccineresistancemovement.org/?p=8787
Vaccine Truth Informational Brochures:
Do not allow all of the vaccine-injured childrens injuries to be in vain. Educate others in honor of them. Be the Voice for those who don't have one. Do not be silent. You can inform other parents. We provide multiple free brochures you can give to educate other parents.
Download and print them now.
http://www.educate4theinjured.org/eric/4571993523
We Want The Vaccine Facts And the Real Science, (and here it is)
http://www.educate4theinjured.org/#!the-factsscience/cc2d
Memorial to Victims of the Silent War ~ VACCINES ~
Cease for Peace! ~ Interviews with Sallie O. Elkordy
http://billiontoddlermarchforsurvival.blogspot.com/
20 Top-selling Vaccines -- H1 2012 (Big money)
http://www.fiercevaccines.com/special-report/20-top-selling-vaccines/2012-09-25
Blood on Their Hands: The World’s Slickest Con Job and a Stack of Deadly LIES...
Has More Vaccination Led to More Health?
Follow the Money
The Alliance Between the Vaccine Industry and the Government
Always Look for Hidden Motivations
Why Isn't This ILLEGAL?
Protect Your Right to Informed Consent and Defend Vaccine Exemptions
http://articles.mercola.com/sites/articles/archive/2010/11/04/big-profits-linked-to-vaccine-mandates.aspx
Who Says There is No Money in Making Vaccines? At Least $5.7 Billion Given to Vaccine Manufacturers in 2011 by US Gov’t
http://vactruth.com/2012/11/30/2011-billions-vaccine-manufacturers/
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Hepatitis B vaccine
1. The graph below shows that the annual incidence of IDDM rose following Hepatitis B immunization in New Zealand.
The Center for Disease Control, CDC, published data which supports a link between timing of immunization and the development of diabetes (Pharmacoepidemiology and Drug Safety Vol 6 Suppl. 2, S60; 1998). The data from the CDC's preliminary study supports published data that immunization starting after 2 months is associated with an increased risk of diabetes. The US government study showed Hep B immunization starting after 2 months was associated with an almost doubling of the risk of IDDM, odds ratio of 1.9. The results were also consistent with data that immunization starting at birth is associated with a decreased risk of diabetes compared to immunization starting after 2 months of life (odds ratio of 1.3 vs 1.9). The children immunization at birth in the CDC study were followed on average less than 2 years. By contrast the BCG data from Sweden showed the ability of immunization at birth to prevent diabetes is only seen clearly after about age seven.
Read more:
http://www.vaccines.net/hepatiti.htm
Congress Told Hepatitis B Vaccine Linked to Rise in Diabetes.
http://www.vaccines.net/toppage1.htm
Juvenile Diabetes and Vaccination: New Evidence for a Connection
http://www.nvic.org/vaccines-and-diseases/Diabetes/juvenilediabetes.aspx
Review of Vaccine Induced Immune Overload and the Resulting Epidemics of
Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent
Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases
J Barthelow Classen MD
3637 Rockdale Road, Manchester, MD 21102, USA
Abstract
There has been an epidemic of inflammatory diseases that has paralleled the epidemic on iatrogenic immune stimulation with vaccines. Extensive evidence links vaccine induced immune over load with the epidemic of type 1 diabetes. More recent data indicates that obesity, type 2 diabetes and other components of metabolic syndrome are highly associated with immunization and may be manifestations of the negative feedback loop of the immune system
reacting to the immune overload. The epidemic of diabetes/prediabetes appears to be accelerating at a time when the prevalence of obesity has stabilized, indicating that the negative feedback system of the immune system has been over whelmed. The theory of vaccine induced immune overload can explain the key observations that have confounded many competing hypothesis. The current paper reviews the evidence that vaccine induced immune overload explains the disconnect between the increase in prediabetes and nonalcoholic fatty liver at a time when the obesity epidemic is waning in children.
http://www.vaccines.net/vaccine-induced-immune-overload.pdf
Vaccine-induced immune overload now affects majority of US children, study finds.
Read article here: http://www.thelibertybeacon.com/?p=21474
Saying No to Vaccines: Your Rights
http://naturalsociety.com/your-rights-saying-no-vaccines/
Aluminum: The Neurotoxin Far Worse than Mercury...
http://www.thelibertybeacon.com/?p=16598
Aluminum in Vaccines Found to be Deadly for Children and Adults Alike
http://naturalsociety.com/aluminum-in-vaccines-found-to-be-deadly-for-children-and-adults-alike/
Vaccines Don’t Protect: Exposing the Vaccination for Immunity Fraud
http://naturalsociety.com/exposing-vaccination-for-immunity-fraud/
10 outrageous (but true) facts about vaccines the CDC and the vaccine industry don't want you to know
http://www.naturalnews.com/042012_vaccine_facts_vaccine-damaged_children_cdc.html#
Dissolving Illusions - paints a historic portrait with quotes from the pages of long overlooked medical journals, books, newspapers, and other sources to reveal a startling history that has been disregarded. With this historic information and originally researched data in the form of myth-shattering graphs, Dissolving Illusions shines new light onto issues that are assumed to be clear-cut and settled long ago.
http://www.dissolvingillusions.com/
50 Reasons NOT To Vaccinate Your Children
http://www.fhfn.org/50-reasons-not-to-vaccinate-your-children/
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Check out the ingredients in the Hepatitis B vaccine.
Hepatitis B (HBV) Vaccine Ingredients: (All of them contain, aluminum hydroxide or aluminum phoshate in the injection. Do you really want to be giving your just born infant this substance injected in any vaccine? Where are the safety studies; there are none.)
http://novaccine.com/specific-vaccines/hepatitis-b-hbv-vaccines/
Vaccine aluminum adjuvant causation of neuroglial activation and neuroinflammation in the brain of patients with autism. (Long list of independent unbiased physiologically based studies)
http://www.vacfacts.info/vaccine-aluminum-adjuvant-causation-of-neuroglial-activation-and-neuroinflammation-in-the-brain-of-patients-with-autism.html
Vaccine aluminum adjuvant causation of neuroglial activation and neuroinflammation in the brain of patients with autism - Page 2
http://www.vacfacts.info/vaccine-aluminum-adjuvant-causation-of-neuroglial-activation-and-neuroinflammation-in-the-brain-of-patients-with-autism--page-2.html
Zeta Potential
http://en.wikipedia.org/wiki/Zeta_potential
Using "Zeta Potential" as a Healing Tool
http://customers.hbci.com/~wenonah/new/mcdaniel.htm
— You Must Avoid Aluminum —
In Your Water, Your Food, and in things you put "In" and "On" Your Body !
Aluminum is used to treat waste water. It is added to waste water to cause materials to come out of solution and settle to the bottom of the tank.
The same thing can happen inside your body. 3–4 parts per million* of Aluminum in our blood Will Cause materials to come out of the blood plasma solution forming plaque on blood vessel walls. It also causes blood cells to clump together, thereby blocking blood flow to organs — causing strokes, heart attacks and other problems!
[ * About 27 milligrams of elemental aluminum in our body's 7 liters of blood will cause coagulation. ]
The reason this happens, is because Aluminum has a strong effect on Zeta Potential.
Aluminum is used in many Vaccinations as a stabilizer, and is known to cause learning disabilities. It can also STOP CELL DIVISION during the "S Phase".
Aluminum is Especially Harmful to Children! (And they are injecting multiple vaccines with aluminum adjuvants).
4 ppm of aluminum in human blood can cause it to colagulate.
Aluminum in humans is documented to inhibit learning.
http://customers.hbci.com/~wenonah/new/mcdaniel.htm
Zeta Potential is a measure of the electrical force that exists between atoms, molecules, particles, suspensoids, cells, etc., in a fluid.
Understanding Colloidal Suspensions - Help from Frank Hartman & Thomas Riddick
SOME EFFECTS OF REDUCED CARRYING CAPACITY
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 the results] -
http://www.sciencedirect.com/science?_ob=ArticleListURL&_method=list&_ArticleListID=-591300251&_sort=r&_st=13&view=c&md5=941c110d6231749e7d8ba96b96450263&search
Despite the number of references to aluminum toxicity, the FDA has always exempted it from testing from testing by putting it on their "Generally Regarded as Safe" ( GRAS ) list. Aluminum can be added to foods, medicines or water without restriction from the FDA.
[ Aluminum is known to stop cell division during the "S Phase", at levels less than 4 ppm. ]
The mechanism of action of aluminum toxicity is aluminum’s effect on carrying capacity or Zeta Potential. Aluminum is relatively non-toxic in and of itself. However, it destroys the carrying capacity of a liquid.
Aluminum has three ( 3 ) positive ions, so a single ion of aluminum will reduce surface charge, reduce carrying capacity and increase surface tension by 6,000 times the amount that an ion of Sodium, which has one ( 1 ) positive charge, would.
Read more:
http://customers.hbci.com/~wenonah/info/colloid.htm#Altox
The Chemistry of Aluminum toxicity, side effects
As I understand the literature, most aluminum is eliminated renally, bound to albumin or transferrin. If this system is fully utilized, the excess aluminum is sequestered in various organ systems, the brain being one, with highest concentrations in the limbic system. As aluminum levels are not often called for, many primary care physicians might not know to use a mobilizing agent prior to checking the blood level, and miss the presence of the metal altogether. (I know of such a case).
Generally, findings from an aluminum level blood test are unreliable, as most of the body's stores are bound in bone and tissue and are not reflected in the serum value. A deferoxamine infusion test can be performed but may take more than 48 hours to yield a result (see Medical Care). Deferoxamine liberates aluminum from tissues by chelating it and leads to an increased serum level compared to one taken prior to infusion. The combination of a baseline immunoreactive parathyroid hormone level of less than 200 mEq/mL and a change in serum aluminum value of 200 ng/mL after deferoxamine is 90% specific and has a positive predictive value of 85% for aluminum toxicity. From WEBMD Michael R. Edwards M.D. Bebe Medical Center. Further complicating the issue, regarding aluminum (aluminium, for any Brits reading this) the FDA has never tested this element for safety!
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.
Read more:
http://www.raysahelian.com/aluminum.html
Aluminum Adjuvants - Lack of Safety Data - Lack of Aluminum Adjuvant Safety Studies
http://www.vacfacts.info/aluminum-vaccine-adjuvants.html
Multiple scientific study links/ Blaylock RL.
Journal of American Nutraceutical Association 6: 21-35, 2003.
Interaction of Cytokines, Excitotoxins, and Reactive Nitrogen and Oxygen Species in Autism Spectrum Disorders Russell Blaylock, MD* Medical Director, Advanced Nutritional Concepts Ridgeland, Mississippi
ABSTRACT
There is growing and compelling evidence that excessive peripheral as well as central immune activation of brain microglia can result in alterations in brain growth and connectivity during rapid brain growth, the so-called "brain growth spurt." A considerable amount of evidence, presented in this paper, demonstrates the deleterious effects of immune factors, such as cytokines, chemokines, and excitotoxins, when present in excess. The interaction between excitotoxicity, ROS and RNS injury and immune dysfunction is discussed. It is concluded that excessive activation of the brain's immune system during critical growth periods can occur when vaccines are given as combination vaccines, using schedules that are too close together or by the use of certain live viruses in the vaccines.
http://www.nutrimedical.com/news.jhtml?method=view&news.id=1084
The Mechanisms of Vaccine Injury and Via Cytokine Storm, (my site page)
http://www.vacfacts.info/the-mechanisms-of-vaccine-injury-and-via-cytokine-storm.html
Session 22, The Vaccine Safety Conference: Dr. Russell Blaylock, MD, CCN
THE CENTRAL ROLE OF IMMUNOEXCITOTOXICITY IN ALUMINUM AND MERCURY-CONTAINING ADJUVANT-TRIGGERED NEURODEVELOPMENTAL AND NEURODEGENERATIVE DISORDERS
http://www.youtube.com/watch?v=u9DkcpEEBPI
Dr. Russell Blaylock, MD, CCN, video presentation - (same video as above, for an alternate source).
http://www.vaccinesafetyconference.com/videos.html#BlaylockVideo
How Vaccines Harm Child Brain Development - Dr Russell Blaylock MD
http://www.youtube.com/watch?v=7QBcMYqlaDs
Although this next study does not pertain to nor mention vaccines, look at how similar the findings are to that found in vaccine injury? Also review the other pages here on this site pertaining to the studies in regard to aluminum adjuvants, etc.
Surg Neurol Int. 2011; 2: 107.
Published online 2011 July 30. doi: 10.4103/2152-7806.83391
PMCID: PMC3157093
Immunoexcitotoxicity as a central mechanism in chronic traumatic encephalopathy—A unifying hypothesis
Published online 2011 July 30. doi: 10.4103/2152-7806.83391
PMCID: PMC3157093
Russell L. Blaylock* and Joseph Maroon1
Abstract
Some individuals suffering from mild traumatic brain injuries, especially repetitive mild concussions, are thought to develop a slowly progressive encephalopathy characterized by a number of the neuropathological elements shared with various neurodegenerative diseases. A central pathological mechanism explaining the development of progressive neurodegeneration in this subset of individuals has not been elucidated. Yet, a large number of studies indicate that a process called immunoexcitotoxicity may be playing a central role in many neurodegenerative diseases including chronic traumatic encephalopathy (CTE). The term immunoexcitotoxicity was first coined by the lead author to explain the evolving pathological and neurodevelopmental changes in autism and the Gulf War Syndrome, but it can be applied to a number of neurodegenerative disorders. The interaction between immune receptors within the central nervous system (CNS) and excitatory glutamate receptors trigger a series of events, such as extensive reactive oxygen species/reactive nitrogen species generation, accumulation of lipid peroxidation products, and prostaglandin activation, which then leads to dendritic retraction, synaptic injury, damage to microtubules, and mitochondrial suppression. In this paper, we discuss the mechanism of immunoexcitotoxicity and its link to each of the pathophysiological and neurochemical events previously described with CTE, with special emphasis on the observed accumulation of hyperphosphorylated tau.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157093/
Download PDF: Immunoexcitotoxicity as a central mechanism in chronic traumatic encephalopathy-A unifying hypothesis
http://www.surgicalneurologyint.com/downloadpdf.asp?issn=2152-7806%3Byear%3D2011%3Bvolume%3D2%3Bissue%3D1%3Bspage%3D107%3Bepage%3D107%3Baulast%3DBlaylock%3Btype%3D2
Vaccination and brain inflammation
http://www.heartmdinstitute.com/prevention/immunity/vaccinations/167-vaccines-depression-neurodegeneration-after-age-50-years?showall=&
Danger of live virus vaccines
http://www.heartmdinstitute.com/prevention/immunity/vaccinations/167-vaccines-depression-neurodegeneration-after-age-50-years?showall=&
A Mechanism of Toxicity of Aluminium-based Adjuvants?
Consumer Summary | by Chris Exley
http://www.vaccinesafetyconference.com/exley
Exley & House (2011) Aluminium in the human brain. Monatsh Chem (In press)
http://www.springerlink.com/content/9550512205128414/
Aluminum as a Neurotoxin: The Evidence from Cell Culture, In Vivo, & Human Studies
http://www.vaccinesafetyconference.com/pdf/Shaw/Shaw_PPT.pdf
Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
Lucija Tomljenovic a, Christopher A. Shaw a,b
http://pop.1796kotok.com/pdfs/Aluminum_autism.pdf
Abstract for talk: Aluminum as a neurotoxin: the evidence from cell culture, in vivo, and
human studies
http://www.vaccinesafetyconference.com/pdf/Shaw/Shaw_CS.pdf
Autism Spectrum Disorders and Aluminum Vaccine Adjuvants
Lucija Tomljenovic, Russell L. Blaylock, Christopher A. Shaw
Abstract
Impaired brain function, excessive inflammation, and autoimmune manifestations are common in autism. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the necessary properties to induce neuroimmune disorders. Because peripheral immune stimuli in the postnatal period can compromise brain development and cause permanent neurological impairments, the possibility that such outcomes could also occur with administration of Al vaccine adjuvants needs to be considered. In regard to the risk of adjuvant toxicity in children, the following should be noted: (i) children should not be viewed as “small adults” as their unique physiology makes them more vulnerable to toxic insults; (ii) in adult humans Al adjuvants can cause a variety of serious autoimmune and inflammatory conditions including those affecting the brain, yet children are routinely exposed to much higher amounts of Al from vaccines than adults; (iii) compelling evidence has underscored the tight connection between the development of the immune system and that of the brain. Thus, it appears plausible that disruptions of critical events in immune development may also play a role in the establishment of neurobehavioral disorders; (iv) the same immune system components that play key roles in brain development appear to be targeted for impairment by Al adjuvants. In summary, research data suggests that vaccines containing Al may be a contributing etiological factor in the increasing incidence of autism.
http://link.springer.com/referenceworkentry/10.1007%2F978-1-4614-4788-7_89
Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes
C.A. Shawa,b,c, ⁎, Y. Li a , L. Tomljenovic a
Abstract:
Our previous ecological studies of autism spectrum disorder (ASD) has demonstrated a correlation between increasing ASD rates and aluminium (Al) adjuvants in common use in paediatric vaccines in several Western countries. The correlation between ASD rate and Al adjuvant amounts appears to be dose-dependent and satisfies 8 of 9 Hill criteria for causality. We have now sought to provide an animal model to explore potential behavioural phenotypes and central nervous system (CNS) alterations using s.c. injections of Al hydroxide in early postnatal CD-1 mice of both sexes. Injections of a “high” and “low”Al adjuvant levels were designed to correlate to either the U.S. or Scandinavian paediatric vaccine schedules vs. control saline-injected mice. Both male and female mice
in the “high Al” group showed significant weight gains following treatment up to sacrifice at 6 months of age. Male mice in the “high Al” group showed significant changes in light–dark box tests and in various measures of behaviour in an open field. Female mice showed significant changes in the light–dark box at both doses, but no significant changes in open field behaviours. These current data implicate Al injected in early postnatal life in some CNS alterations that may be relevant for a better understanding of the aetiology of ASD. © 2013 Elsevier Inc
http://myofasciite.fr/Contenu/Divers/201307_CAShaw_YLee_LTomljenovic.pdf
PRESENTATIONS
http://www.vaccinesafetyconference.com/presentation.html
Study RESOURCES - Dr Russell Blaylock
http://www.vaccinesafetyconference.com/resources.html
The Danger of Excessive Vaccination During Brain Development
The Case for a Link to Autism Spectrum Disorders
By Russell L. Blaylock, M.D.
http://articles.mercola.com/sites/articles/archive/2008/03/14/the-danger-of-excessive-vaccination-during-brain-development.aspx
Immune-Glutamatergic Dysfunction as a Central Mechanism of the Autism Spectrum Disorders
http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.317.7642&rep=rep1&
http://www.utdallas.edu/~mxa049000/lessons/research/literature/Autism/new/Blaylock%20autism%20rev%20CMC%2009.pdf
Chronic Microglial Activation and Excitotoxicity Secondary to Excessive Immune Stimulation:
Possible Factors in Gulf War Syndrome and Autism
The Role of Excitotoxicity
Page 47. Damage to neuronal mechanisms is not limited to direct cytokine effects. The excitotoxicity initiated by microglial activation is even more important. In cases of HIV-1 dementia, it is known that brain quinolinic acid, an excitotoxin secreted by activated microglia, can increase more than 300-fold. In addition, glutamate is released in concentrations that are known to destroy neurons and/or synaptic connections.
Because glutamate can also activate microglia and enhance cytokine-induced neurodegeneration, a vicious cycle is created in which immune cytokines can stimulate release of glutamate, and glutamate in turn enhances cytokine production and release. Moreover, cytokines inhibit glutamate transporters, which play a critical role in removal of excess extracellular glutamate. Intimately linked to excitotoxicity is the generation of destructive free radicals, especially the reactive nitrogen species such as peroxynitrite and nitrosoperoxycarbonate. Much of the injury to dendrites, synapses and neurons, by both cytokines and excitotoxicity, is caused by free radicals.
The Role of Vaccines, page 49
Read more:
http://www.jpands.org/vol9no2/blaylock.pdf
Entropy 2012, 14(8), 1399-1442; doi:10.3390/e14081399
Review
The Initial Common Pathway of Inflammation, Disease, and Sudden Death
Robert M. Davidson 1,* and Stephanie Seneff
Abstract: In reviewing the literature pertaining to interfacial water, colloidal stability, and cell membrane function, we are led to propose that a cascade of events that begins with acute exogenous surfactant-induced interfacial water stress can explain the etiology of sudden death syndrome (SDS), as well as many other diseases associated with modern times. A systemic lowering of serum zeta potential mediated by exogenous cationic surfactant administration is the common underlying pathophysiology. The cascade leads to subsequent inflammation, serum sickness, thrombohemorrhagic phenomena, colloidal instability, and ultimately even death. We propose that a sufficient precondition for sudden death is lowered bioavailability of certain endogenous sterol sulfates, sulfated glycolipids, and sulfated glycosaminoglycans, which are essential in maintaining biological equipose, energy metabolism, membrane function, and thermodynamic stability in living organisms. Our literature review provides the basis for the presentation of a novel hypothesis as to the origin of endogenous bio-sulfates which involves energy transduction from sunlight. Our hypothesis is amply supported by a growing body of data showing that parenteral administration of substances that lower serum zeta potential results in kosmotropic cationic and/or chaotropic anionic interfacial water stress, and the resulting cascade.
http://www.mdpi.com/1099-4300/14/8/1399 (Also view full text from that link by clicking full study)
file:///C:/Users/TEMP/Downloads/entropy-14-01399.pdf
The Initial Common Pathway of Inflammation, Disease, and Sudden Death, (full study source)
Pay particular attention to reading pages, Page 414-415 in regard to vaccine aluminum adjuvants, and as well pages 419-420 in regard to Gardasil.
http://www.mdpi.com/1099-4300/14/8/1399
http://people.csail.mit.edu/seneff/Entropy/Entropy1_downloaded.pdf
Is Encephalopathy a Mechanism to Renew Sulfate in Autism?
Stephanie Seneff 1,*, Ann Lauritzen 2 , Robert M. Davidson 3 and Laurie Lentz-Marino 4
Entropy; Jan2013, Vol. 15 Issue 1, p372
ABSTRACT This paper makes two claims: (1) autism can be characterized as a chronic lowgrade encephalopathy, associated with excess exposure to nitric oxide, ammonia and glutamate in the central nervous system, which leads to hippocampal pathologies and resulting cognitive impairment, and (2), encephalitis is provoked by a systemic deficiency in sulfate, but associated seizures and fever support sulfate restoration. We argue that impaired synthesis of cholesterol sulfate in the skin and red blood cells, catalyzed by sunlight and nitric oxide synthase enzymes, creates a state of colloidal instability in the blood manifested as a low zeta potential and increased interfacial stress. Encephalitis, while life-threatening, can result in partial renewal of sulfate supply, promoting neuronal survival. Research is cited showing how taurine may not only help protect neurons from hypochlorite exposure, but also provide a source for sulfate renewal. Several environmental factors can synergistically promote the encephalopathy of autism, including the herbicide, glyphosate, aluminum, mercury, lead, nutritional deficiencies in thiamine and zinc, and yeast overgrowth due to excess dietary sugar. Given these facts, dietary and lifestyle changes, including increased sulfur ingestion, organic whole foods, increased sun exposure, and avoidance of toxins such as aluminum, mercury, and lead, may help to alleviate symptoms or, in some instances, to prevent autism altogether.
http://www.mdpi.com/1099-4300/15/1/372
Autism: A neuroepigenetic disorder, By Richard C. Deth, PhD
http://www.autismone.org/sites/default/files/Deth_ASD03.pdf
Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure
Stephanie Seneff, Robert M. Davidson, and Jingjing Liu
http://www.mdpi.com/1099-4300/14/11/2227
http://people.csail.mit.edu/seneff/Entropy/entropy-14-02227.pdf
GLUTATHIONE Scientific Research
Our findings suggest that acetaminophen administration selectively depletes (within 2 hr) mitochondrial glutathione, and produces local toxicity by altering membrane permeability and decreasing the efficiency of oxidative phosphorylation. This renders mitochondria more susceptible to oxidative damage… PMID: 8937421
http://www.readisorb.com/science/glutathione_scientific_researc.html
Biochem Pharmacol. 1996 Oct 25;52(8):1147-54.
Effect of acetaminophen administration on hepatic glutathione compartmentation and mitochondrial energy metabolism in the rat.
http://www.ncbi.nlm.nih.gov/pubmed/8937421
Scientific Research, 2nd Page
http://www.readisorb.com/science/
Tim Guilford, MD
Glutathione in Health and Disease
http://www.svhi.com/newsletters/2005/slf-122005.pdf
Glutathione
http://www.readisorb.com/
Glutathione, Tylenol, Vaccine Adverse Reactions, and ASD
http://www.vacfacts.info/glutathione-tylenol-vaccine-adverse-reactions-and-asd.html
Neurodegenerative Diseases: Neurotoxins as Sufficient Etiologic Agents?
Christopher A. Shaw and Günter U. Höglinger
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814816/
Neuroscience and Biobehavioral Reviews
Analysis of neurological disease in four dimensions: insight from ALS-PDC epidemiology and animal models
The causal factor(s) responsible for sporadic neurological diseases are unknown and the stages of disease progression remain undefined and poorly understood. We have developed an animal model of amyotrophic lateral sclerosis-parkinsonism dementia complex which mimics all the essential features of the disease with the initial neurological insult arising from neurotoxins contained in washed cycad seeds. Animals fed washed cycad develop deficits in motor, cognitive, and sensory behaviors that correlate with the loss of neurons in specific regions of the central nervous system. The ability to recreate the disease by exposure to cycad allows us to extend the model in multiple dimensions by analyzing behavioral, cellular, and biochemical changes over time. In addition, the ability to induce toxin-based neurodegeneration allows us to probe the interactions between genetic and epigenetic factors. Our results show that the impact of both genetic causal and susceptibility factors with the cycad neurotoxins are complex. The article describes the features of the model and suggests ways that our understanding of cycad-induced neurodegeneration can be used to decipher and identify the early events in various human neurological diseases.
http://yadda.icm.edu.pl/yadda/element/bwmeta1.element.elsevier-a4f127e4-0c75-3f6d-bb32-9406a3136a76
And to realize that in any of the studies that the CDC has considered as to vaccine toxicity, none of that has been studied, and nor as well has any basic physiological science like this been addressed nor even acknowledged. They are yet by CHOICE, in the dark ages, as to their known and accepted knowledge, and of the human body, and its immune system
Dr Blaylock, a Board-certified neurosurgeon, Visiting Professor of Biology at Belhaven College, Jackson, Mississippi, and member of the Editorial Board of the Journal of the American Nutraceutical Association (JANA), is the author of three books on excitotoxicity: Excitoxicity: the taste that kills, Health and nutrition secrets, and Natural strategies for cancer patients.
EXCITOTOXICITY: A POSSIBLE CENTRAL MECHANISM IN FLUORIDE NEUROTOXICITY, (the fluoride and aluminum connection)
by Russell L Blaylocka, Ridgeland, MS, USA
SUMMARY: Recent evidence indicates that fluoride produces neuronal destruction and synaptic injury by a mechanism that involves free radical production and lipid peroxidation. For a number of pathological disorders of the central nervous system (CNS), excitotoxicity plays a critical role. Various studies have shown that many of the neurotoxic metals, such as mercury, lead, aluminum, and iron also injure neural elements in the CNS by an excitotoxic mechanism. Free radical generation and lipid peroxidation, especially in the face of hypomagnesemia and low neuronal energy production, also magnify excitotoxic sensitivity of neurons and their elements. This paper reviews briefly some of the studies that point to a common mechanism for the CNS neurotoxic effects of fluoride and calls for research directed toward further elucidation of this mechanism.
http://www.fluorideresearch.org/374/files/374301-314.pdf
Toxic Overload: Children Vaccinated To Extreme
http://www.thelibertybeacon.com/?p=16643
Vaccinations Cause Chronic Immune System Dysregulation
http://www.thelibertybeacon.com/?p=16251
There Is No Such Thing As a Safe Vaccine and There Never Will Be
http://wp.me/p2X3AR-47a
Vaccines Are Causing Mutations That May Jeopardize
The Health of Future Generations
http://www.thelibertybeacon.com/?p=16698
Forced Vaccination is Equivalent to Human Experimentation
and Subject to the Nuremberg Code
http://www.thelibertybeacon.com/?p=13171
Multiple Infant Vaccines Linked To Dramatically Increased Mortality ~ By: Sayer Ji
http://wp.me/p2X3AR-4dx
Vaccination During Pregnancy: Is It Safe?
http://wp.me/p2X3AR-4bT
The Vaccine Mafia and Its Jury of Thugs: Your Rulers
Read this scathing critique here: http://wp.me/p2X3AR-47x
Are Vaccines Safe: Bracing Ourselves for More Sham Vaccine Studies
Read this very critical article here: http://wp.me/p2X3AR-43O
The Hidden Connection Behind Viruses, Vaccines and Cancer
By: Dr. Tyson Perez
Mainstream medicine tells us that the hepatitis B virus (HBV) causes liver cancer which is why it is so necessary for US newborns to be vaccinated within hours of birth. We are told that the human papillomavirus (HPV), which is supposedly so prevalent in our population, causes cervical cancer which is why there is such a push to vaccinate girls and boys in the US as early as 9 years old. Let’s not forget about Simian Virus 40 (SV40) which is known to have contaminated polio vaccines and is associated with a wide variety of human cancers. Conventional wisdom tells us that viruses cause cancer. But is this true? Let’s investigate the story further.
The first recorded cases of HBV infection occurred following the administration of the smallpox vaccine containing human lymph to shipyard workers in Germany in 1883. HBV is transmitted through contact with infected bodily fluids. It is estimated that over 2 billion people worldwide have been infected and that approximately 350 million are chronic carriers. Chronic HBV infection is believed to cause up to 80% of all hepatocellular carcinomas. Sounds scary right? But when you look deeper you find that, in the US, HBV is found predominantly in adults who are either I.V. drug users or engaging in high-risk sexual behavior.
Read more:
http://www.thelibertybeacon.com/2013/02/09/the-hidden-connection-behind-viruses-vaccines-and-cancer/
VRM: The Rise of Mutagenic Viruses
http://vaccineresistancemovement.org/?p=13124
Your Immune System, How It Works And How Vaccines Damage It
"Chronic illnesses are now so common, having a sick child seems to be the “new normal.”Children are supposed to be vibrant, healthy, free of disease." - Janet Levatin MD, Pediatrician.
http://www.vaccineriskawareness.com/Your-Immune-System-How-It-Works-And-How-Vaccines-Damage-It
Vaccines Are Causing Mutations That May Jeopardize The Health of Future Generations
By: Dave Mihalovic
Vaccines are causing an unprecedented number of mutations creating superbugs and potent viruses and bacteria that may eventually threaten future generations and humanity itself. Evidence continues to mount from the scientific community who now admit that certain vaccines are in-fact causing both viral and bacterial mutations. Ironically, the same researchers assert that “better” vaccines are needed to offset the rise in persistent mutations.
Life-threatening pathogens are capable of evolving rapidly and developing genetic decoys that serve to disguise them from even the most powerful drugs. University of Oxford researcher Rory Bowden found that pathogens switch genetic material with other bacteria, but predominantly for the part of the genome responsible for making the cell coating, which is the area targeted by vaccines.
Former post-doctoral researcher of the Center for Infectious Disease Dynamics, Grainne Long found that vaccination led to a 40-fold enhancement of B. parapertussis colonization in the lungs. His data suggested that the vaccine may be contributing to the observed rise in whooping cough incidence over the last decade by promoting B. parapertussis infection.
Whooping Cough
An acellular whooping cough vaccine actually enhances the colonization of Bordetella parapertussis in mice; pointing towards a rise in B. parapertussis incidence resulting from acellular vaccination, which may have contributed to the observed increase in whooping cough over the last decade.
Despite widespread vaccination, whooping cough incidence is on the rise worldwide, making it a disease virtually immune to vaccines.
Read more:
http://www.thelibertybeacon.com/2014/02/10/vaccines-are-causing-mutations-that-may-jeopardize-the-health-of-future-generations/
