Gardasil - The Damage is Done: From A Best Friend's View
UPDATE, AUGUST 17, 2013: IN 2012, A CLASS-ACTION LAWSUIT WAS BROUGHT AGAINST THE MANUFACTURER OF GARDASIL, MERCK, BY A 28 YEAR-OLD AUSTRALIAN WOMAN.
Naomi Snell began suffering autoimmune and neurological complications following injections with the HPV vaccine, Gardasil.
After receiving the first of three doses of the vaccine, Naomi suffered convulsions, severe back and neck pain, and lost her ability to walk.
Doctors actually diagnosed her with multiple sclerosis, which was later retracted and labeled a neurological reaction to the vaccine.
Seven other women, who say they have suffered various physical problems, including anaphylaxis and miscarriage, after receiving Gardasil may also join the civil lawsuit, and this is likely only the beginning, as Gardasil is being implicated in a growing number of serious, permanent and sometimes deadly adverse reactions.
Multiple Sclerosis-Like Symptoms and Paralysis Not Unusual After HPV Vaccination
Documents obtained from the U.S. Food and Drug Administration (FDA) under the provisions of the Freedom of Information Act (FOIA) detail 26 new deaths reported to the government following HPV vaccination between September 1, 2010 and September 15, 2011. That's 26 reported deaths of young, previously healthy, girls after Gardasil vaccination in just one year.
Other serious side effects reported during that time frame included:
Seizures, Paralysis, Blindness, Pancreatitis, Memory Loss, Speech problems, Ovarian Cysts,
Between May 2009 and September 2010, 16 deaths after Gardasil vaccination were reported. For that time-frame, there were also 789 reports of "serious" Gardasil adverse reactions, including 213 cases of permanent disability and 25 diagnosed cases of Guillain Barre Syndrome, Judicial Watch reported.
213 CASES OF PERMANENT DISABILITY TIED TO GARDASIL IN ONE YEAR!!!
THINK ABOUT THAT, PLEASE!
BLOGGER WILL NOT UPLOAD THIS VIDEO, SO YOU WILL HAVE TO CLICK ON THIS LINK TO VIEW IT:
HERE IS A MARCH, 2013 UPDATE ON THIS STORY:
Parents, PLEASE, please watch your children for these symptoms if you've already had them injected!
UPDATE APRIL 8, 2013
April 8, 2013“This new information from the government shows that the serious
safety concerns about the use of Gardasil have been well-founded,” said
Judicial Watch President Tom Fitton. “Public health officials should
stop pushing Gardasil on children.”
US vaccine court pays $6 million to Gardasil victims, most claims not yet settled
NEW YORK STATE LAST WEEK (see date of this post) TOOK UP A NEW BILL TO ALLOW MINORS, CHILDREN, THE "RIGHT" TO SEEK MEDICAL TREATMENT, INCLUDING VACCINES, FOR SEXUALLY TRANSMITTED DISEASE, FOR POSSIBLE DISEASE, ALL WITHOUT PARENTAL CONSENT, AND WITHOUT PARENTAL KNOWLEDGE.
THIS WILL INCLUDE THE VACCINATION OF MINORS WITH THE HEPATITIS B AND HUMAN PAPILLOMAVIRUS (HPV) , TWO VACCINES THAT ARE KNOWN KILLERS, TWO VACCINES THAT HAVE BEEN ADDED IN RECENT YEARS TO "REQUIRED" VACCINES IN SOME STATES, AND TWO VACCINES THAT HAVE A HISTORY OF CAUSING LIFELONG DEBILITATING SIDE EFFECTS AND/OR DEATH IN THOUSANDS WHO HAD THEM.
OUR CHILDREN DO NOT BELONG TO "THE STATE"!
THE STATE HAS NO RIGHT TO FORCE SUCH THINGS ON A FREE PEOPLE!
I WISH TO ADDRESS THE HAZARDS OF THE HPV VACCINE FIRST, THEN THE "HEP VAC" AFTERWARDS.
IF YOU VALUE YOUR CHILDREN PLEASE READ CAREFULLY.
THE HPV VACCINE, ALSO KNOWN AS GARDASIL, IS BANNED IN SOME NATIONS.
IN EUROPE, AUSTRALIA, AND THE PHILIPPINES, THE GLAXOSMITHKLINE DRUG CERVARIX IS USED INSTEAD OF GARDASIL.
NOTE TO EUROPEAN READERS: Cervarix has been responsible for more than 9,000 cases of serious, adverse reactions and at least 3 PROVEN deaths since this vaccine has been in use. One of the worst cases involved 14-year-old Natalie Morton, who collapsed and died in school in England just one hour after receiving the vaccine.
To date, 15,037 girls have OFFICIALLY reported adverse side effects from Gardasil to the Vaccine Adverse Event Reporting System (VAERS).
ASK YOURSELF, HOW MANY HAVE NOT "OFFICIALLY" REPORTED SIDE EFFECTS, AND HOW MANY HAVE DIED FROM "UNKNOWN CAUSES" WHERE DOCTORS DON'T LOOK AT GARDASIL AS A POSSIBLE CAUSE OF DEATH, OR OF SERIOUS ILLNESS FOLLOWING INJECTION?
These 'OFFICIALLY REPORTED' adverse effects include Guilliane Barre, lupus, seizures, paralysis, blood clots, brain inflammation and many others.
The CDC acknowledges that there have been 44 reported deaths. REPORTED DEATHS.
BUT LOOK AT FACTS! The rate of serious adverse events is greater than the incidence rate of cervical cancer.
The National Vaccine Information Center’s has said that “though nearly 70 percent of all Gardasil reaction reports were filed by Merck (Gardasil's creator), a whopping 89 percent of the reports Merck did file were so incomplete there was not enough information for health officials to do a proper follow-up and review.”
In the clinical studies alone, BEFORE GARDASIL WENT PUBLIC, BEFORE IT BECAME 'MANDATORY', 23 girls died after receiving either Gardasil or the Aluminum control injection. 15 of the 13,686 girls who received Gardasil died, while 8 died among the 11,004 who received the Aluminum shot.
What this means is that 1 out of every 912 who received Gardasil, in the CLINICAL study ALONE, died.
The numbers of deaths and adverse effects are undoubtedly underestimated.
TOO MANY ARE CHALKED-UP TO "UNKNOWN CAUSES" AND TOO FEW CORONERS KNOW WHAT TO LOOK FOR TO LINK THESE DEATHS TO GARDASIL.
ONE PHYSICIAN HAS FOUND A WAY TO LINK THE DEATHS TO GARDASIL, PERHAPS. READ DR. LEE'S FINDINGS BELOW.
ALMOST NO ONE IS DOING EXTENSIVE TESTING TO SEE WHAT REALLY CAUSES SO MANY TO SUCCUMB TO "MYSTERY AILMENTS" OR EVEN DEATH AFTER GARDASIL INJECTIONS.
WE DO KNOW A FEW KEY THINGS THAT SHOULD ALARM US ALL.
~Polysorbate 80, an ingredient in the vaccine, has been observed in a European clinical study to cause INFERTILITY in rats. DOES GARDASIL CAUSE INFERTILITY IN HUMANS?
NO STUDIES AVAILABLE!!!
~MERCK ADMITS THAT NO STUDIES OF THE VACCINE'S EFFECT ON THOSE UNDER 15 YEARS OF AGE WERE CONDUCTED BEFORE THE FDA APPROVED IT. EVEN LESS WAS DONE TO SEE WHAT ITS EFFECTS ON MALES WOULD BE IN THE LONG RUN.
~WE ALSO KNOW THAT ALUMINUM IS PART OF THE VACCINE. ALUMINUM, A METAL IS USED TO BIND THE VACCINE. "Aluminum may reach toxic levels with prolonged parenteral administration [this means injected into the body] if kidney function is impaired . . . Research indicates that patients with impaired kidney function, including premature neonates [babies], who received parenteral levels of aluminum at greater than 4 to 5 micrograms per kilogram of body weight per day, accumulate aluminum at levels associated with central nervous system and bone toxicity [for a tiny newborn, this toxic dose would be 10 to 20 micrograms."
INJECTED ALUMINUM KILLS!
~GARDASIL IS A TRANSGENIC VACCINE! IT CARRIES VIRAL DNA THAT CAN BE FOUND INTACT IN HUMAN BODIES, POSTMORTEM.
PLEASE PAY ATTENTION TO THIS! IT MAY BE ONE OF THE MOST IMPORTANT THINGS YOU READ ESPECIALLY YOU PARENTS AND THOSE WHO CARE ABOUT CHILDREN.
<<Fragments of foreign DNA and other substances from vaccinations found in sick, disabled and dying children.
Foreign DNA is a term most medical consumers are not aware of. However, common sense alone raises questions about the dangers of foreign DNA – otherwise known as recombinant DNA.
The American Biologic Safety Association (ABSA) has classified recombinant DNA a biohazard and has outlined specific directives over the handling of such contaminants.
Researchers have identified the contamination of live viral vaccines for use in healthy children, with viral nucleic acids; the findings have since been confirmed by the vaccine manufacturers and the data reported to the FDA.
Contaminating nucleic acids include retroviral sequences from the producer CHICKEN AND PRIMATE CELLS used to manufacture vaccines.
Specifically, Avian leucosis virus (ALV) was present as RNA in viral particles while simian retrovirus (SRV) was present as genetically defective DNA. (BIRD AND APE DNA!)
Rotarix, an orally administered rotavirus vaccine, contained nucleic acids from porcine (PORK) circovirus-1 (PCV1), virus. Since this report, a second rotavirus vaccine (RotaTeq) has been shown to contain nucleic acids from both PCV1 and PCV2, A PATHOGEN IN PIGS that is associated with wasting and immunodeficiency.
“The MMR II vaccine is contaminated with human DNA from the cell line in which the rubella virus is grown. This human DNA could be the cause of the spikes in incidence. An additional increased spike in incidence of autism occurred in 1995 when the chicken pox vaccine was grown in human [ABORTED] FETAL tissue,” wrote Dr. Helen Ratajczak, Ph.D. in support of this belief. She published two papers regarding this subject in the Journal of Immunotoxicology. (Merck and Co. Inc., 2001; Breuer, 2003)
In June of 2001, a paper was published in Emerging Infectious Diseases entitled: “Adventitious Agents and Vaccines” stating that: “Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines. The challenge of identifying potential adventitious agents in vaccines closely parallels the challenge of identifying the agents causing particular emerging infectious diseases.”
War of the DNA
IN A DIFFERENT VEIN, IS IT JUST A LITTLE 'SICK' TO GIVE A 9-YEAR-OLD CHILD A VACCINE THAT IS ONLY EFFECTIVE FOR 5 YEARS, SUGGESTING THAT A 3RD GRADER IS GOING TO BE HAVING SEX? OR A 4TH GRADER WILL BECOME 'SEXUALLY ACTIVE"?
The most frightening aspect of all is
that government health agencies do not have the testing nor do they have
understanding as to what happens when a recombinant DNA particle
infects a cell with ‘normal’ DNA. What are the mechanisms of action that
determine who wins the DNA wars? What if the normal ‘DNA’ loses? Are
the skyrocketing rates of autism and the increasing Post-Gardasil and
Post-Cervarix Syndromes examples of DNA gone bad?
Even more frightening is that scientists
do not know how to isolate or even remove the foreign DNA particles
from the body. What lies ahead is a crap shoot for medical consumers who
are left with a ‘damned if I do or damned if I don’t scenario.’>>
OR THAT EVEN A 6TH GRADER HAVING SEX IS 'NORMAL' AND TO BE EXPECTED?
IF THE VACCINATED CHILD DOESN'T BECOME SEXUALLY ACTIVE BY AGE 14, DARE WE IMAGINE THAT THE HIGH RISK OF DEATH OR HARM FROM THIS VACCINE IS WORTH VACCINATING THESE GRADE-SCHOOLERS ON A "WHAT-IF"?
WHO ARE WE REALLY PROTECTING?
WHO ARE WE KIDDING?
NO 9-YEAR-OLD CHILDREN ARE "CONSENTING ADULTS"!
ANYONE WHO HAS SEX WITH A MINOR IS GUILTY OF STATUTORY RAPE IN MOST OF AMERICA, AND OF CHILD MOLESTATION!
A VERY IMPORTANT ADMISSION :
According to Diane Harper, an international expert in HPV science, its vaccines, its clinical disease and treatment and the leading professional involved in the clinical trials of the HPV vaccinations, the duration for the effectiveness of the HPV vaccination Gardasil is just five years. In an interview with Marcia G. Yerman she states:
If the vaccinated person is not sexually active during the five years of its efficacy, then the vaccine has not protected her from disease (as we do not have evidence that Gardasil offers efficacy any longer than five years). Its faults include tiny antibody titers for all HPV types other than HPV 16; limited protection; limited duration of efficacy; and safety concerns (as outlined in my opening statement).If this is correct, a child vaccinated at age eleven will not be protected on any level unless she becomes sexually active before the age of sixteen. Quite shocking, isn't it?
OR MAYBE NOT SHOCKING AT ALL IN OUR SEX-ORIENTED AMERICAN SOCIETY?
Are the proponents of "sexual liberation" so determined not to let mere disease—or even death—stand in the way of their pleasures? Is our nation vaccinating 9-year-olds with the belief that they are WILLFULLY or will be WILLFULLY sexually active within the SHORT 5-year period that Gardasil is "good for"?
Do people really believe that there must be 'technological solutions' to the diseases that have arisen from the relentless promotion of promiscuity, childhood 'sexual freedom', or is all this to protect ADULTS who may want sex with 9-year-olds?
WHY ELSE VACCINATE ELEMENTARY SCHOOL CHILDREN FOR SEXUALLY TRANSMITTED DISEASE?
After all, IS the alternative is too horrible to contemplate?
THE ALTERNATIVE BEING THAT ADULTS AND TEENAGERS MIGHT HAVE TO LEARN TO CONTROL THEIR SEXUAL APPETITES, THAT PARENTS AND SCHOOLS AND FAMILY PHYSICIANS OR CLINICIANS MIGHT HAVE TO TEACH ABSTINENCE INSTEAD?
ABSTAIN? PERISH THE THOUGHT!
ABSTINENCE GUARANTEES PEOPLE WON'T CONTRACT SOME SEXUALLY TRANSMITTED DISEASE, DOESN'T IT?
AND WE JUST DON'T HAVE PROOF THAT ANYONE HAS EVER DIED FROM ABSTINENCE, DO WE?
THERE IS PROOF PEOPLE HAVE DIED FROM THIS VACCINE...THAT CHILDREN HAVE DIED!
Until August 2012 this vaccine was produced only in the United States: There were over 265,000 KNOWN adverse events ( 264,162 females, 9490 males ); permanent disability 8,910( 8890 females, 90 males ); almost 1220 deaths (1011 females, 70 males); abnormal PAP in 4,930; cervical dysplasia in 1,970, and cervical cancer in 570.
WHAT ARE THE ODDS OF THE HPV DOING MORE HARM THAN GOOD?
RUN THE STATISTICS!
PARENTS, PLEASE READ THIS BEFORE YOU AGREE TO VACCINATE YOUR CHILD!
Merck did not disclose that the vaccine was transgenic.
IT CONTAINS RECOMBINANT HPV DNA, AND ALUMINUM.
A coroner investigating the unexplained death of a teenager following a Gardasil HPV vaccination has announced the disturbing finding of Gardasil HPV DNA fragments in post-mortem samples.
“The finding of these foreign DNA fragments in the post-mortem samples six months after vaccination indicates that some of the residual DNA fragments from the viral gene or plasmid injected with Gardasil have been protected from degradation in the form of DNA-aluminum complexes in the macrophages; or via integration into the human genome.
Undegraded viral and plasmid DNA fragments are known to activate macrophages, causing them to release tumor necrosis factor, a myocardial depressant which can induce lethal shock in animals and humans.”
Dr. Lee did not claim the HPV-16 L1 gene DNA he discovered in the post-mortem blood and spleen samples was the cause of the sudden and unexplained death of the New Zealand teenager in her sleep. He did note that since the full autopsy analysis had ruled out all known causes of death, his discovery presented a plausible mechanism of action that needed further investigation in all cases of unexplained deaths following Gardasil vaccinations.
Dr. Lee had previously tested a total of 16 Gardasil samples from around the world under contract with the non-profit organization SaneVax Inc. Five of those Gardasil samples were distributed in New Zealand, each with a different lot number. Dr Lee found HPV-16 L1 gene DNA fragments admixed with HPV-18 and/or HPV 11 L1 gene DNA in all samples.>>
[NOTE:Dr. Lee is known for using the nested PCR/DNA sequencing technology for reliable detection and genotyping of HPV in clinical specimens. He is the author of the chapter, “Guidelines for the Use of Molecular Tests for the Detection and Genotyping of Human Papillomavirus from Clinical Specimens” in a Methods in Molecular Biology volume published by Humana Press in July 2012.]
Fragments of HPV rDNA firmly attached to the aluminum adjuvant have been found in 100% of Gardasil samples tested. 100%!!!
Various regulatory agencies agree these particles ARE in the vaccine!
Does this HPV rDNA have the capability of integrating with the host DNA and causing mutations that may lead to cancer?
According to Dr. Lee:
“There are only two known ways these HPV DNA fragments would remain in post-mortem tissue. Either the fragments are attached to the aluminum adjuvant and unable to be degraded by the DNA nucleases, or the fragments were integrated into the human genome. Either of these options may have harmful and potentially lethal consequences, and need further investigation.”
Medical consumers worldwide have every right to demand these questions be answered.
Until answers are provided the human right to informed consent is being violated.
MERCK DOES NOT TELL PARENTS (OR POTENTIAL VICTIMS) THAT 70% of HPV infections resolve themselves WITHOUT ANY TREATMENT in one year.
After two years, this rate climbs to 90%.
Of the remaining 10% of HPV infections, only half coincide with the development of cervical cancer.
Using data from trials funded by Merck, THEIR OWN SPOKESPERSON, Dr. Harper informed attendees at a recent conference that “with the use of Gardasil, there will be no decrease in cervical cancer until at least 70% of the population is vaccinated, and in that case, the decrease will be very minimal. The highest amount of minimal decrease will appear in 60 years.”
THE DECREASE WILL BE MINIMAL AND WILL TAKE 60 YEARS TO MAKE A DIFFERENCE?
Let’s do the math. If the 4% annual decline in cervical cancer death continues AS IT HAS, in 60 years there will have been a 91.4% decline in cervical cancer death just from current cancer monitoring and treatment. Comparing this rate of decline to Gardasil’s projected “very minimal” reduction in the rate of cervical cancer of only 70 % of incidences in 60 years, it is hard to resist the conclusion that Gardasil does almost nothing for the health of American women...EXCEPT MAYBE SUBJECT THEM TO UNNECESSARY RISK.
DID YOU KNOW THAT IT HAS NEVER BEEN FIRMLY ESTABLISHED THAT THE HPV CAUSES CERVICAL CANCER, THAT THIS IS WHY LESS THAN 1/2 OF 10% OF WOMEN WITH ACTIVE HPV EVER DEVELOP CERVICAL CANCER?
On the Merck website, the "KNOWN" side effects of Gardasil are listed as pain, swelling, itching, bruising and redness at the injection site; headache, fever, nausea, dizziness, vomiting and fainting. Sometimes fainting is accompanied by falling with injury, as well as shaking or stiffening and other seizure-like activity. The product information also says that patients who are severely allergic to yeast should not take Gardasil.
Is the current rate of death, sterility and serious immune dysfunction from Gardasil worth the potential that in 60 years a minimal amount of a cervical disease (that is already decreasing on its own) may perhaps be reduced?
COULD GARDASIL, AS MANY HAVE SUGGESTED, SIMPLY BE A NEW MEANS OF CONTROLLING HUMAN POPULATION? SINCE IT IS BASICALLY USELESS AS A CERVICAL CANCER PREVENTION, IS ITS PRIMARY USE TO REDUCE WORLDWIDE FERTILITY?
BEFORE WE ALLOW NEW YORK STATE OR ANY OTHER ENTITY THE RIGHT TO VACCINATE OUR CHILDREN AS THEY PLEASE, WE NEED TO DETERMINE WHY THIS ONE VACCINE HAS BEEN CRAMMED DOWN AMERICAN THROATS, WHY IT'S CLOSE "SISTER" DRUG, CERVARIX IS BEING PUSHED IN EUROPE, AND WHY ANY AGENCY OR ANY PHYSICIAN UNDER A HIPPOCRATIC OATH WOULD WANT TO TAKE OVER INDISCRIMINATE, ACROSS-THE-BOARD VACCINATIONS OF OUR CHILDREN?
WHAT MOTIVE DO THEY HAVE TO ROB PARENTS OF CONSENT OR BEING INFORMED?
WE CONCEIVED AND BIRTHED OUR CHILDREN, NOT THE FEDERAL OR STATE GOVERNMENTS, NOT PHYSICIANS!
HEPATITIS VACCINE, A KNOWN KILLER
Hepatitis B Vaccine
The Untold Story
Parents Question Forced Vaccination As Reports of
Hepatitis B Vaccine Reactions Multiply
Appeared in NVIC's Printed Newsletter - Vaccine Reaction, Sept 1999
In increasing numbers, parents across the country are contacting the National Vaccine Information Center (NVIC) to report opposition to regulations being enacted by state health department officials that legally require children to be injected with three doses of hepatitis B vaccine before being allowed to attend daycare, kindergarten, elementary school, high school or college. Simultaneously, as more schools and employers bow to pressure from government health officials and require individuals to show proof they have been injected with hepatitis B vaccine before being allowed to get an education or a job, reports of serious health problems following hepatitis B vaccination among children and adults are multiplying.
Hepatitis B Not Highly Contagious - Unlike other infectious diseases for which vaccines have been developed and mandated in the U.S., hepatitis B is not common in childhood and is not highly contagious. Hepatitis B is primarily an adult disease transmitted through infected body fluids, most frequently infected blood, and is prevalent in high risk populations such as needle using drug addicts; sexually promiscuous heterosexual and homosexual adults; residents and staff of custodial institutions such as prisons; health care workers exposed to blood; persons who require repeated blood transfusions and babies born to infected mothers.
According to CDC Prevention Guidelines: A Guide to Action (1997), a book written by federal public health officials at the U.S. government Centers for Disease Control (CDC), "the sources of [hepatitis B] infection for most cases include intravenous drug use (28%), heterosexual contact with infected persons or multiple partners (22%) and homosexual activity (9%)." According to Harrison's Principles of Internal Medicine (1994), mother to child transmission of hepatitis B "is uncommon in North America and western Europe."
Although CDC officials have made statements that hepatitis B is easy to catch through sharing toothbrushes or razors, Eric Mast, M.D., Chief of the Surveillance Section, Hepatitis Branch of the CDC, stated in a 1997 public hearing that: " although [the hepatitis B virus] is present in moderate concentrations in saliva, it's not transmitted commonly by casual contact."
SO WHY DID THE CDC LIE?
WHY DON'T PEDIATRICIANS INFORM PARENTS OF THE RARE POSSIBILITY OF THEIR NEWBORN BABIES CONTRACTING "HEP B"? WHY PUT NEWBORNS AT RISK? WHY PUT TODDLERS AND CHILDRFEN, ANYONE AT RISK?
<<According to Harrison's, in cases of acute hepatitis B "most patients do not require hospital care" and "95 percent of patients have a favorable course and recover completely" with the case-fatality ratio being "very low (approximately 0.1 percent)."
Those who recover completely from hepatitis B infection acquire life-long immunity. Of those who do not recover completely, fewer than 5 percent become chronic carriers of the virus with just one quarter of these in danger of developing life threatening liver disease later in life, according to Robbins Pathologic Basis of Disease (1994), a medical college textbook. The U.S. and western Europe have always had among the lowest rates of hepatitis B disease in the world (0.1% to 0.5% of the general population).>>
SO WHO MAINLY GETS HEP B? I.V. DRUG ABUSERS, THE SEXUALLY PROMISCUOUS (HETERO- AND HOMO-SEXUAL), PEOPLE WHO REQUIRE REPEATED BLOOD TRANSFUSIONS...NOT BABIES, NOT KIDS, NOT THE MAJORITY OF PEOPLE!
Even though hepatitis B is an ADULT disease, is NOT highly contagious, is NOT deadly for THE VAST MAJORITY who contract it, and is NOT in epidemic form in the U.S. (except among high risk groups such as IV drug addicts), in 1991 the Advisory Committee on Immunization Practices (ACIP) of the Centers for Disease Control (CDC) recommended that ALL INFANTS be injected with the first dose of hepatitis B vaccine at birth before being discharged from the hospital newborn nursery. MOST HOSPITALS WILL NOT RELEASE A NEWBORN UNLESS IT RECEIVES THIS POTENTIALLY DEADLY VACCINE! A similar recommendation was also made by the Committee on Infectious Diseases of the American Academy of Pediatrics (AAP). This, despite the fact almost nothing is known about the health and integrity of an individual baby's immune and neurological systems at birth.
SO WHY PUSH THE HEP VAC?
I WISH I COULD SAY THAT THE FOLLOWING TRAGIC STORY IS UNIQUE THAT IT HAS ONLY HAPPENED TO THIS ONE NEWBORN, BUT IT HAS HAPPENED MANY TIMES.
I WARN YOU THE PHOTOS ALONE OF THIS PRECIOUS BABY BOY WILL BREAK YOUR HEART, IF YOU HAVE ANY FEELINGS AT ALL.
IT WAS PREVENTABLE, IT WAS SENSELESS THAT THIS CHILD PERISHED AFTER 47 AGONIZING DAYS FROM THE HEPATITIS VACCINE HE SHOULD NEVER HAVE BEEN GIVEN.
LET US ALWAYS REMEMBER LITTLE IAN, AND SO MANY OTHERS LIKE HIM.
THE FDA HAS LONG KNOWN THAT ALUMINUM INJECTED OR INGESTED IS TOXIC, SOMETIMES FATALLY TOXIC! YOU CAN SEE THIS FOR YOURSELF BY GOING TO www.fda.gov AND SEARCH "ALUMINUM TOXICITY". THEE ARE MANY DOCUMENTS THERE.
THE FDA KNOWS, YET KEEPS PUSHING VACCINES THAT CONTAIN ALUMINUM!
Aluminum TOXICITY Information from The Vaccine Book
<<The American Academy of Pediatrics published a policy in 1996 called Aluminum Toxicity in Infants and Children (See Resource 5). Here are several keys items found in this paper:
Aluminum can cause neurologic harm.
A study from 30 years ago showed that human adults will increase their urine excretion of aluminum when exposed to higher levels (suggesting adults can clear out excess aluminum).
Adults taking aluminum-containing antacids don't build up high levels in their body.
There have been reports of infants with healthy kidneys showing elevated blood levels of aluminum from taking antacids.
The AAP found that people with kidney disease who build up levels of aluminum greater than 100 micrograms per liter in their bloodstream are at risk of toxicity.
The AAP also states that the toxic threshold may be lower than this.
The paper states that aluminum loading (meaning tissue build up) has been seen even in patients with healthy kidneys who receive IV solutions containing aluminum over extended periods.
Completely absent from this paper was any mention whatsoever of aluminum in vaccines.
No one has ever measured the levels of aluminum absorption into the bloodstream, then excretion into the urine and out of the body, when it is injected into the skin and muscle of human infants. All the FDA and AAP documents say is it may be a problem, but we haven't studied it yet, so we should limit aluminum in injectible solutions. But no one is talking about the levels in vaccines.
What I think may have happened is that aluminum used to be in only one vaccine (DTP), so no one thought much about it. Then along came PedVaxHib brand of HIB vaccine in the 80s with aluminum, but the other brands of HIB did not have aluminum, so no one thought much about it. Then we started using Hep B vaccine in the 90s, Pc vaccine in the 2000s, and recently Hep A vaccine. Giving one aluminum vaccine at a time doesn't amount to much aluminum, but giving four all together really adds up. It seems this issue has simply escaped everyone's attention. Or has it?>>
Hep B Vaccine Licensed By FDA Without Adequate Proof of Long Term Safety - In 1986, the FDA gave Merck & Co. a license to market the first recombinant DNA hepatitis B vaccine, which replaced the old hepatitis B vaccines made from blood taken from human chronic hepatitis B virus carriers. In awarding Merck & Co. and, later, SmithKline Beecham Pharmaceuticals, licenses to market their genetically engineered hepatitis B vaccines in the U.S., the FDA allowed both drug companies to use "safety" studies which only included a few thousand children monitored for only four or five days after vaccination to check for reactions. As "proof" their hepatitis B vaccine is safe to be used in children, Merck & Co. stated in their 1993 product insert that "In a group of studies, 1636 doses of RECOMBIVAX HB were administered to 653 healthy infants and children (up to 10 years of age) who were monitored for 5 days after each dose."
Merck & Co. found that injection site and systemic complaints, such as fatigue and weakness, fever, headache and arthralgia (joint pain), were reported following up to 17 percent of all hepatitis B injections. Because the FDA did not require drug companies to provide scientific evidence that hepatitis B vaccine does not compromise the immune and neurological systems of children and adults over weeks, months or years post-vaccination, Merck & Co. warns in the 1996 product insert that "As with any vaccine, there is the possibility that broad use of the vaccine could reveal adverse reactions not observed in clinical trials" and SmithKline Beecham (1993) has a similar warning that "it is possible that expanded commercial use of the vaccine could reveal rare adverse reactions.
WHY DIDN'T THESE DRUG COMPANIES DO THE TESTS? WHY WAS THEIR INITIAL STUDY SO LAX? WHY DIDN'T THEY PUBLISH ALL THEIR FINDINGS?
WHY DIDN'T THE FDA DEMAND NEW AND LONGER AND MORE THOROUGH STUDIES?
Another warning in the Merck 1996 product insert is "it is also not known whether the vaccine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity" and "it is not known whether the vaccine is excreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when the vaccine is administered to a nursing woman."
And, although doctors routinely inject hepatitis B vaccine into children along with many other vaccines such as DPT, HIB, MMR and chicken pox vaccine, Merck & Co. state in the 1996 product insert: "Specific data are not yet available for the simultaneous administration of RECOMBIVAX HB with other vaccines."
IOM Report Reveals Lack Of Adequate Scientific Studies - In Adverse Events Associated with Childhood Vaccines published in 1994 by the Institute of Medicine, National Academy of Sciences, observations about the limitations of hepatitis B vaccine studies included the statements that "it is important to note that individual trials usually involved a few hundred subjects for study...when larger vaccination programs were monitored, observations of adverse events were necessarily less detailed and less accurately reported" and "the studies were not designed to assess serious, rare adverse events; the total number of recipients is too small and the follow-up generally too short to detect rare or delayed serious adverse reactions."
The IOM report also noted that no controlled observational studies or controlled clinical trials have ever been held to evaluate repeated reports that hepatitis B vaccine can cause Guillain-Barre syndrome; arthritis; transverse myelitis, optic neuritis, multiple sclerosis and other central demyelinating diseases of the nervous system (degeneration of the myelin sheath of the brain that helps transmit nerve impulses); or sudden infant death syndrome (SIDS).
A major conclusion of the Institute of Medicine report was that almost no basic science research has been undertaken to define at the cellular and molecular level the biological mechanism of vaccine-induced injury and death. The report concluded that "The lack of adequate data regarding many of the adverse events under study was of major concern to the committee...the committee encountered many gaps and limitations in knowledge bearing directly or indirectly on the safety of vaccines. These include inadequate understanding of the biologic mechanisms underlying adverse events following natural infection or immunization, insufficient or inconsistent information from case reports and case series...and inadequate size or length of follow-up of many population-based epidemiologic studies…."
WAKE UP PARENTS!
WAKE UP, PEOPLE!
WE DON'T KNOW THESE THINGS BECAUSE WE JUST DON'T QUESTION THOSE WHO SHOVE VACCINES AT US!
WE'RE LOSING OUR YOUNG PEOPLE IN MORE WAYS THAN ONE!
SOMEONE NEEDS TO PROTECT THEM FROM THE CONSTANT ONSLAUGHT OF VACCINES THAT DO MORE HARM THAN GOOD!
IF WE ARE NOT THAT 'SOMEONE', WHO WILL BE?
OUR CHILDREN DO NOT BELONG TO "THE STATE"!
THE STATE HAS NO RIGHT TO FORCE SUCH THONGS ON A FREE PEOPLE!
DO SOMETHING, PLEASE!
FROM THE MOTHER'S WEB PAGE http://www.ageofautism.com/2009/02/managing-editors-note-below-is-the-story-of-iam-gromowski-a-boy-who-lived-47-days-after-his-hepatitis-b-vaccination-thank.html , LITTLE IAN BEFORE THE HEP VAC, A NORMAL LITTLE NEWBORN BOY.