Archive for the ‘vaccines’ Category

Zika Puzzling Scientists

https://www.washingtonpost.com/amphtml/world/the_americas/scientists-are-bewildered-by-zikas-path-across-latin-america/2016/10/25/

The latest saga in the Zika Chronicles is that the Post states scientists are bewildered that Zika is

“not producing the wave of fetal deformities so widely feared….”

For those of you just tuning in, please read: https://madisonarealymesupportgroup.com/2016/03/08/fixation-on-zikapolio/.     The take home: 80% of those with Zika don’t even know they have it and 1 out of every 5 will have mild symptoms that last a week.

https://madisonarealymesupportgroup.com/2016/07/17/zika-in-the-land-of-oz/.  The take home: Brazil has been using WHOLE-CELL pertussis vaccines on impoverished pregnant women in the 27th, 36th, and up to 20 days of expected birth date. There is NO SIGN OF ZIKA in many cases of microcephaly and over 40 countries have Zika with no increased microcephaly. Brazil was spraying pyriproxyfen, a pyridine-based pesticide, on drinking water used by the affected population for 18 months prior to the microcephaly outbreak directly in that area. The transmission cycles for Zika in the U.S. is near zero.

https://madisonarealymesupportgroup.com/2016/04/08/zika-ebola-zombies-and-the-cdc/.  The take home: Based on TWO fetal tissue samples, the CDC has stated that Zika causes microcephaly. Meanwhile Physicians in the Crop-Sprayed villages Argentina debunk this theory altogether and state it’s more likely that the pesticides and vaccines are causing the issue.

The Post admits that 75% of babies born with microcephaly are in northeastern Brazil, a highly impoverished region where nutritional deficiencies are the norm not the exception. Of course they are looking for other viruses to blame but quietly mention that environmental, genetic, or immunological factors – of coursecombined with Zika may be issues.

Although they are puzzled, researchers and health officials remain cautious about the low U.N. numbers showing just 142 cases of birth defects linked to Zika outside Brazil. The article admits that the condition was initially over diagnosed.

Ernesto Marques, originally from Northern Brazil, is now an epidemiologist at the University of Pittsburgh who states that the focus on Zika has changed from causing microcephally to being a smoking gun. He admits they don’t know who is pulling the trigger, but true to form he is working on a vaccine. As for what is pulling the trigger, he hypothesizes that northern Brazilian mothers might have fewer antibodies to Zika or perhaps that sexual habits and hygiene play a role. Researchers state it will take years to identify the dangers.

I say the one armed man did it.

Peter Hotez, dean of the National School of Tropical Medicine at Baylor College of Medicine is complaining that they can’t even count how many actual people were infected because Congress didn’t approve Zika funding.

Now that’s the wisest thing I’ve heard all day.

Hotez is actually holding his breath to see what happens in the next few months.

Well, Peter, while you are holding your breath for something that isn’t going to happen, there are bodies piling up on the side of the road of people with tick borne illnesses that can’t get diagnosed, can’t get proper treatment, and if they miraculously do their medical insurance won’t cover a red cent.  Those who are chronically infected may lose everything trying to defeat an illness(es) that necessitates years of treatment.  
http://wapo.st/2c8cGiE  Here we have Wisconsin’s Paul Ryan accusing the Senate of “partisan filibustering” by not approving Zika funding.  Mr. Ryan you’ve been in Washington for too long and have obviously forgotten your fellow Wisconsinites who are contracting TBI’s at an alarming rate.

Zika isn’t even on the radar here.

NPRM – Act Now!

http://www.nvic.org/NVIC-Vaccine-News/September-2016/cdc-wants-to-expand-power-to-eliminate-measles.aspx

  Published on Sep 12, 2016

In one of the worse offenses against your rights yet, the CDC issued a Federal Register notice on August 15th to amend the Public Health Act. This notice states that CDC would like to expand their government police powers to apprehend people who look “unwell”. Public comment is only open until October 14, 2016.

Notice of Proposed Rule Making – or NPRM – involves the participation of federally funded state health departments and state facilities giving police power to detain, isolate and quarantine US citizens.  

You Can Be Fined and Jailed for Disobeying CDC Orders
And if the CDC finds you guilty of disobeying their orders and they believe you transmitted an infection to someone else, you can be fined “$100,000 if the violation does not result in a death, or one year in jail, or both, or a fine of no more than $250,000 if the violation results in a death, or one year in jail or both.” Plus they have added this curious language without explanation: “Violations by organizations are subject to a fine of no more than $200,000 per event if the violation does not result in a death, or $500,000 per event it the violation results in a death.”

By the way, this is about far more than just measles.  The language is frighteningly vague and you could get in trouble for coughing too much on an airplane.

http://www.enhancedonlinenews.com/news/eon/20160913005591/en  If the NPRM becomes law, it will affect American and non-American travelers entering the U.S. or traveling between states, particularly on commercial airlines and ships. The CDC is proposing to enlist commercial airline and other public transportation personnel to step up surveillance on and report “unwell” passengers with rashes, cough, diarrhea and other symptoms of illness.  (oh goody, more surveillance)

If the NPRM becomes law, it appears U.S. health officials could hold a person in custody for 72 hours without the right to contact an attorney to appeal the detention. Detainees could be asked to sign a contract with the CDC that gives consent to the “public health measures” being applied to the adult or a minor child, which may include “quarantine, isolation, conditional release, medical examination, hospitalization, vaccination, and treatment.” However, the NPRM states that “the individual’s consent shall not be considered a prerequisite to any exercise of any authority” by the CDC. After release, the person can be electronically tracked and monitored, including by electronic tracking devices attached to the body.

Are you shaking yet?

This is a HUGE overreach of government power .  Americans have until Oct. 14, 2016 to make public comment to the CDC.

ACTION NEEDED:

1) Contact your U.S. Congressional Representative and both of your U.S. Senators Representatives and ask them to stop this outrageous federal overreach and unnecessary expansion of police powers by demanding the CDC withdraw the proposed rule. To find who represents you in the U.S. Congress and U.S. Senate, register/login to the NVIC Advocacy Portal, https://nvicadvocacy.org/members/Home.aspx, click on the “national” tab on the top of your home page, and the names of your personal U.S. Congressional Representative and your two U.S. Senators will be listed on the right hand side. Click on their names to be linked to all of their contact information. Send your letter by email, fax or regular mail then follow-up with a personal phone call expressing your concerns.

2) Submit public comments with your concerns directly to the CDC on the proposed rule by Oct. 14, 2016 11:59 pm EST.

3) Share this alert with family and friends by forwarding this email or sending them to http://NVICAdvocacy.org on our National page or to our note on National Vaccine Information Center Facebook.

SAMPLE LETTER TO U.S. LEGISLATORS:

Oct. 11, 2016

The Honorable FIRSTNAME LASTNAME
STREET ADDRESS
Washington, D.C. 20515

RE: Notice of Proposed Rulemaking (NPRM) by CDC and HHS Concerning Quarantine
CDC Docket No. CDC-2016-0068
Dear Representative or Senator LASTNAME,

As a constituent of yours, I am writing to you for your assistance. I have serious concerns about an overreaching proposed HHS/CDC Rule that would expand police powers to forcibly detain, isolate, vaccinate and quarantine citizens. This Notice of Proposed Rule Making was published in the Federal Register on 8/15/16 and is currently open for public comment until 10/14/16.

I am asking you to demand that the CDC withdraw this proposed rule for the following reasons:

· The proposed rule is a violation of civil liberties. U.S. health officials could hold a person in custody for 72 hours without the right to contact an attorney to appeal the detention. Detainees could be asked to sign a contract with the CDC that gives consent to the “public health measures” being applied to the adult or a minor child, which may include “quarantine, isolation, conditional release, medical examination, hospitalization, vaccination, and treatment.” The proposed rule states that “the individual’s consent shall not be considered a prerequisite to any exercise of any authority” by the CDC. After release, the person can be electronically tracked and monitored, including by electronic tracking devices attached to the body.

· The proposed rule is a clear case of federal government overreach. Federal and state laws are already in place to address the control of outbreaks of serious communicable diseases. When similar rules have been proposed in the past they have been withdrawn over concerns of civil rights violations and the cost to implement. http://usatoday30.usatoday.com/news/washington/2010-04-01-quarantine_N.htm

The proposed rule has very subjective and unreasonably broad definitions of illness. The proposed rule defines a potentially “ill” person deserving of special government scrutiny to be someone with “areas of the skin with multiple red bumps, red, flat spots or blister like bumps filled with fluid or pus that are intact or partially crusted over,” warning ominously that “the presence of skin rash, along with fever, may indicate that the traveler has measles, rubella (German measles), varicella (chickenpox) meningococcal disease or smallpox.” These definitions (on pages 54239-40) are very subjective and will open the door for travelers to be detained for something as simple as a skin rash while suffering from a bad sunburn, acne, rosacea, eczema, psoriasis, the hives, or severe allergies and a mild fever that could be due to an old fashioned cold. Measles is not Ebola and chickenpox is not smallpox.

Sincerely,

YOUR NAME
YOUR STREET ADDRESS
YOUR CITY, STATE, ZIP
YOUR EMAIL
YOUR PHONE

 

 

 

 

Lyme Cryme Video – Powerful

Cryme Disease: The Lyme Cryme Against Humanity
TRUTH from the LYMErix whistleblower

https://youtu.be/f8DU1Z6R-ms  Published on Sep 2, 2016.  Powerful hour long video explaining how the CDC purposely rigged the case definition of Lyme so cases would be missed.

Stress is placed on the fact that spirochetes are fungal shedders not bacteria.  This is important in semantics because unless you are using the same linguistics you will never come to an agreement, and that’s right where we are:  NO AGREEMENT IN THE MEDICAL COMMUNITY.

CDC Widespread Abuse of Knowledge

This entire article was taken from:  https://lifebiomedguru.wordpress.com/.  It is one more example of how the CDC and others make public policy, and it should frighten all of us.

https://jameslyonsweiler.com/2016/05/17/science-and-policy-on-vaccine-safety-scienceabsence-of-evidence-abused-as-evidence-of-absence-part-1/

Science and Policy on Vaccine Safety Science:’Absence of Evidence’ Abused as ‘Evidence of Absence’: Part 1
by jameslyonsweiler

THERE IS A DISTURBING AND CONSISTENT trend in the vaccine safety literature for government-affiliated researchers in the misinterpretation of negative results from studies of specific, serious adverse events from vaccines, such as autism, encephalopathy, ADHD, and other serious neurological injuries.

Here’s the (il)logic flow:

*Conduct a retrospective epidemiological study (case/control, or cohort) with a relatively small samples size (few patients).

*Do not publish any power analysis showing that you had sufficient sampling effort to conduct significant effect.

*Analyze the data (we won’t go into cherry picking results here, but that, as well as “analyzing to result” both happen when a positive association is found, but the researchers wish to keep the result from public view).

*Find no or weak association.

*Lament the high confidence interval.

*Conclude something sciency-sounding, like:“The relative risk of severe neurologic disease in the 0–7 day risk period after meningococcal C conjugate vaccination was estimated at 1.28 (95% CI, 0.17–9.75). As evidenced by the wide confidence interval, the sample size is not large enough to get a more precise estimate of the relative risk. The authors concluded that administration of meningococcal C conjugate vaccine is not associated with an increased risk of severe neurologic disease within 0 to 7 days of vaccination” [1]

*Issue a official policy-sounding statement, such as:
Weight of Epidemiologic Evidence
The committee has limited confidence in the epidemiologic evidence, based on one study that lacked validity and precision, to assess an association between meningococcal vaccine and encephalitis or encephalopathy.[1]

*Create a policy of adoption of the vaccine, and give the following rationale:“There is no scientific evidence of serious neurological disease as result of this vaccine”.

If you don’t the flaw in the logic of steps 1-7, you’ve been duped.

Scientific studies, whether they are prospective studies, or retrospective studies, are supposed to provide proof that the sample size – the number of patients included in the study – was large enough to detect a specific effect if it did indeed exist. This property of a study is called “STATISTICAL POWER” and the analysis they SHOULD be including in their publications is called “POWER ANALYSIS”. Statistical power is the ability of a test to detect a significant (difference, increase in relative risk, increase is odd ratio) and is a function of:

-Sample Size in each sample group (N1, N2)

-Stringency of the test – the p-value required for a result to be considered ‘significant’ – this is generally 5%

-The degree of intrinsic variability in the data within and between the two groups (population variance)

-The effect size (the size of the actual difference in the measure of interest between two groups).

In randomized prospective studies of adverse events of drugs, a power analysis is par for the course. Showing the no adverse reactions were found is easy with small sample sizes, because the variability estimated within and between the two groups (say, treated vs. untreated) is a mathematical function of sampling effort N1 and N2.

Any qualified data analyst, epidemiologist, statistician, or scientist knows this.

Any study in vaccine safety that demonstrates a negative result for any given adverse event may show a negative result for two reasons:

(1) No difference exists between the two populations under study with respect to rates of the adverse event of interest, or

(2) The study was conducted with a sample size that was too small to ensure detection of a difference in the frequency of adverse events between the two populations under study.

That is, the study had insufficient power.

Unless a power analysis is conducted, no one – NO ONE – interpreting the results has any position to choose between the two reasons as their interpretation of the results.

Any qualified data analyst, epidemiologist, statistician, or scientist knows all of this, too.

It is flabbergasting why, then, so many studies from the CDC and CDC-affiliated scientists make conclusions such as:

“The relative risk of severe neurologic disease in the 0–7 day risk period after meningococcal C conjugate vaccination was estimated at 1.28 (95% CI, 0.17–9.75). As evidenced by the wide confidence interval, the sample size is not large enough to get a more precise estimate of the relative risk. The authors concluded that administration of meningococcal C conjugate vaccine is not associated with an increased risk of severe neurologic disease within 0 to 7 days of vaccination.”[1]

And then issue a official policy-sounding statement, such as:
Weight of Epidemiologic Evidence
The committee has limited confidence in the epidemiologic evidence, based on one study that lacked validity and precision, to assess an association between meningococcal vaccine and encephalitis or encephalopathy.[1]

Leading to a policy of adoption of the vaccine, based on the rationale:“There is no scientific evidence of serious neurological disease as result of this vaccine” or “No scientific study has shown…”

The Safety Assumption

There is an expression that is sometimes a fallacy, and sometimes not. It goes like this:

“The absence of evidence is not evidence of absence”.

This is largely considered a general fallacy – due in large part to Carl Sagan’s use of it in arguing for consideration of the likelihood that we just have not discovered all of the missing pieces of the evolution of the cosmos, but we can nevertheless deduce from other evidence that those missing pieces – the absence of evidence – nevertheless occurred. And we can certainly use the absence of evidence to deduce that some events that have not occurred have, in fact, not occurred.

But when it comes to science, especially epidemiological comparisons of rates of biomedical events in populations, there is a set of conditions in which the absence of evidence MAY NOT be used as evidence of absence.

Those conditions are when the study has low statistical power.

According to the committee statement, they concluded no evidence of the suspected increase in neurological adverse events from the vaccine due in part to a lack of precision.

“Lack of precision” means “high variability”, as in that reported in the sentence in the study:

“As evidenced by the wide confidence interval, the sample size is not large enough to get a more precise estimate of the relative risk.”[1]

The specific committee statement is carefully selected so as to allow the errant policy interpretation. They committee could have, and should have written:

The committee has no ability to rule out can association between meningococcal vaccine and encephalitis or encephalopathy based on the study, due to a lack of precision, resulting from a small sample size used to assess an association between meningococcal vaccine and encephalitis or encephalopathy.

In other words, a firm “We Don’t Know Because the Sample Size was Not Large Enough”.

This policy-like statement has a higher degree of fidelity to the limits of knowledge (LOK) imposed on interpretation of the study due to small sample size.

Policy based on a lack of evidence that results from a lack of statistical power, or destruction of validity of conclusions of studies via cherry-picking results after applying “kitchen-sink” statistics, is dangerous, because it requires the Safety Assumption: that a lack of evidence implies evidence of absence. The Safety Assumption only applies after a negative result has been found AND a power analysis has demonstrated that a positive result WOULD have been found given the sample sizes (N1, N2) and a priori estimate of the effect size.

Of course, if you control the sample size, you control the power…

ALERT!

There are many parents who know full well that their child suffered seizures, encephalopathy, and autism as a direct result of the vaccine – (aka “Vaccine-Induced Encephalopathy-Mediated Autism, or VIEMA). They know the vaccines cause their child’s autism as sure as they would be able to tell you their child was injured if they saw the child get hit by a moving car. They don’t need a significant result, nor a p-value, nor a power analysis. As the number of these parents in the population explode, an army of misled, misinformed parents are created. Fairly rapidly, however, these parents are waking up and becoming informed. When they attend courses to learn about statistical power – and how ridiculously simple is it to execute power analysis with available software, including many free online applications – they will have their time in the sun, their day in court, and they will re-dedicate their lives to righting the wrongs of the CDC and preventing further injuries. They, unlike scientists in academia, or not dependent on a culture of turning a blind eye to these willful acts of misinterpretation in the name of a ‘common good’ of vaccination. And, as I pointed out, they are growing in number every day, possibly by as many as 250,000 vaccine injured people/day.

Vaccine Safety Science as an Archery Contest

Imagine an archery contest in which a choice prize – a bag of gold – is given for hitting a hitting a bull eye’s on a target. In each round, a contestant gets a single draw. Each time a contestant hits hits the bull’s eye, they get another bag of gold.

A contestant lines up, draws, aims, and lets go. They miss the bull’s eye because their aim is not good. No bag of gold for them.

Another contestant lines up, draws, aims, and lets go. They hit the bull’s eye because their aim was good, and their pull was strong. All in witness of the tournament can see that the bag of gold is well-earned.

The CDC lines up, aims, draws a little, and the arrow flies about three feet, falling far short of the target. “Bullseye!” they claim!

In reality, they neither hit, nor missed the bull’s eye because they did not draw with sufficient power to enable an appropriate assessment of their aim.

The CDC’s widespread abuse of knowledge – because that’s what it is – leads to the situation where it appears as if a positive study has been conducted upon which public policy is based, when, in reality, the study might as well not even ever been conducted.

In reality, the above analogy is better fit if the goal of the contestants is to MISS the bull’s eye (no positive result), but you get the idea: The amount of empirical information generated by underpowered studies with negative results is zero.

What is even more disturbing is that the practice of Steps 1-7 have been repeated over, and over… and over. And worse than that – there is a pattern of CDC analysts taking the extraordinary step of changing study designs by omitting specific patients from studies for arbitrary reasons – with the result being a reduction in the sample size, yielding a corresponding drop in statistical power – AFTER finding a positive association with the full sample available for analysis.

In Part 2, I will enumerate examples in which current public policy on vaccines are based on the illogical, unwarranted Safety Assumption.

In Part 3, I will review the evidence that CDC officials and collaborators committed scientific fraud by taking extraordinary steps to corrupt otherwise robust study designs to reduce statistical power, and publish only the final, negative results, with no reference to the initial positive association.

These abuses of science are widely known as ‘heinous crimes’ in the biostatistics literature. So far, the academic community of statisticians have been oddly silent on these issues, but I will be sharing this series of posts with them for their consideration.

Citation

[1] Committee to Review Adverse Effects of Vaccines; Institute of Medicine; Adverse Effects of Vaccines: Evidence and Causality. Stratton K, Ford A, Rusch E, et al., editors. Washington (DC): National Academies Press (US); 2011 Aug 25. Chapter 11. Meningococcal Vaccine. http:// http://www.ncbi.nlm.nih.gov/books/NBK190008/

jameslyonsweiler | May 17, 2016 at 7:53 pm | Categories: Cures | URL: http://wp.me/p5Qzty-13O

Gardasil and Bartonella

Taken from “Bartonella Associated Cutaneous Lesions in People With Neuropsychiatric Symptoms

http://www.thevaccinereaction.org/2016/03/study-linking-gardasil-to-behavioral-abnormalities-pulled-from-vaccine-journal/

Recently a peer-reviewed article linking Gardasil to behavior abnormalities via its aluminum adjuvant and HPV antigens and may “trigger neuroinflammation and autoimmune reactions” in mice was removed. The article was replaced with the following notice:

“This article has been withdrawn at the request of the Editor-in-Chief due to serious concerns regarding the scientific soundness of the article. Review by the Editor-in-Chief and evaluation by outside experts, confirmed that the methodology is seriously flawed, and the claims that the article makes are unjustified. As an international peer-reviewed journal we believe it is our duty to withdraw the article from further circulation, and to notify the community of this issue.”

The study’s lead author has stated this action is due to a conflict of interest with Merck & Co and the publication’s editor who chaired a safety evaluation committee for vaccine trials by Merck as well as provided consulting services on vaccine development to Merck and several other pharmaceutical companies. He also conducted four studies in direct affiliation with Merck including a pro-HPV trial in 2005. The following link lists more retracted news stories on Gardasil. The American College of Pediatricians has also released a statement expressing concerns in relation to premature ovarian failure or premature menopause and 213 reports in the Vaccine Adverse Reaction Database since Gardisil’s approval in 2006.
http://www.thevaccinereaction.org/2016/03/blacklisting-of-gardasil-studies-to-silence-the-safety-debate/

The retracted study highlights:

“the necessity of proceeding with caution with respect to further mass-immunization practices with a vaccine of yet unproven long-term clinical benefit which is capable of inducing immune-mediated cross-reactions with neural antigens of the human host. Especially considering the continually increasing number of serious disabling neurological adverse events linked to HPV vaccination reported in the current medical literature and vaccine surveillance databases.”

https://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM111263.pdf  This official package insert reveals on page 7 that the clinical study had 40 DEATHS. “The following adverse events have been spontaneously reported during post-approval use of GARDASIL. Because these events were reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or to establish a causal relationship to vaccine exposure. Blood and lymphatic system disorders: Autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura, lymphadenopathy. Respiratory, thoracic and mediastinal disorders: Pulmonary embolus. Gastrointestinal disorders: Nausea, pancreatitis, vomiting. General disorders and administration site conditions: Asthenia, chills, death, fatigue, malaise. Immune system disorders: Autoimmune diseases, hypersensitivity reactions including anaphylactic/anaphylactoid reactions, bronchospasm, and urticaria. Musculoskeletal and connective tissue disorders: Arthralgia, myalgia. Nervous system disorders: Acute disseminated encephalomyelitis, dizziness, Guillain-Barré syndrome, headache, motor neuron disease, paralysis, seizures, syncope (including syncope associated with tonic-clonic movements and other seizure-like activity) sometimes resulting in falling with injury, transverse myelitis. Infections and infestations: cellulitis. Vascular disorders: Deep venous thrombosis.

http://www.thevaccinereaction.org/2016/04/victims-of-hpv-vaccine-in-japan-will-sue-state-and-vaccine-makers/  Also worth mentioning is Japan’s decision to withdraw its HPV vaccine recommendation due to numerous reports that formerly healthy vaccine recipients were experiencing alarming side effects ranging from short-term memory loss to paralysis.  Further, The Japan Times recently reported that a class action lawsuit will be filed after June 2016 against the Japanese government and Merck and GlaxoSmithKline by victims who have suffered severe side effects as a result of receiving the former government recommended vaccine.  One college student told the Japan Times:

“I felt acute pain as if someone was squashing my internal organs … Such conditions have only gotten worse,” Sonoda told a court while sitting in her wheelchair. “I received the shots because the government recommended it. I want the government to take seriously its responsibility for causing us (to suffer from) such symptoms.”  http://www.japantimes.co.jp/news/2017/02/13/national/crime-legal/suit-opens-tokyo-court-cervical-cancer-vaccine-side-effects/#.WLYHaRE0r_w

http://www.healthnutnews.com/olympic-medalist-dies-of-cervical-cancer-despite-being-vaccinated-for-hpv-years-before/  Australian, London Olympics medallist rower, Sarah Tait died after a battle with cervical cancer at 33 despite having regular pap smears and the HPV vaccine.

http://www.thevaccinereaction.org/2016/06/gardasil-injured-teen-in-ireland-gets-no-help-from-countrys-public-health-service/   One girl from Ireland is now in a wheelchair, remains in constant pain, and reportedly sleeps up to 23 hours a day after receiving the three recommended doses of Gardisil. Ireland’s Health Service stands behind the safety of the HPV vaccine, noting that “seizures, muscle weakness, leg pain and chronic fatigue are not mentioned as known side effects to Gardasil in the Patient Information Leaflet,” but there are 27 symptoms highlighted in the leaflet and approximately 350 girls in Ireland are suffering from chronic health problems following HPV vaccination.  http://www.thevaccinereaction.org/2017/10/irish-girls-harmed-by-gardasil-vaccine/  As of October, 2017, Irish girls account for 1 in 5 of reported Gardasil vaccine reactions.  In 2010 Irish Gardasil vaccination rate was 87%, today it is 50%.

http://healthimpactnews.com/2014/gardasil-vaccine-one-more-girl-dead/  Sudden death of 12 year old girl in Waukesha, Wisconsin just hours after receiving the HPV Gardasil vaccine.  After this news story broke, another local parent contacted a news station to report her 17-year old daughter needed urgent care at the hospital.  

Studies have shown that Gardasil can make women MORE likely to get the high risk strains of HPV that lead to the deadly cancer, than women who’ve received no vaccine at all. Even CBS was forced to admit this on the national news. The Solution? Merck says MORE shots. http://www.healthnutnews.com/cbs-women-vaccinated-with-gardasil-can-be-more-likely-to-be-infected-with-high-risk-strain-new-study-shows/

And it’s not just women who are suffering.

http://www.vaccines.news/2016-09-07-boy-completely-paralyzed-from-the-neck-down-due-to-gardasil-vaccine.html

“Colton finished his last round of the Gardasil series on February 1, 2014. In the following weeks, he would eventually become paralyzed from the neck down. On February 17th, just over two weeks after his final vaccine, Colton was admitted to the hospital and proceeded to spend 88 days in intensive care.  The young teen has spent many, many months trying to recover from this horrible experience, but he still requires assistance from a breathing apparatus and suffers from some paralysis.”

Currently under U.S. federal law, no one can directly sue a vaccine manufacturer in civil court after a vaccine causes the injury or death of a minor child or adult.

Isn’t that convenient?

http://www.vaccines.news/2015-09-29-hpv-vaccine-alert-lead-developer-warns-that-it-is-all-a-big-scam.html

Lead developer of Gardasil & Cervarix, Dr. Diane Harper, states that cervical cancer is extremely rare in the U.S., and 70% of cases resolve naturally without treatment.  She also warns that if 11 year olds are vaccinated and the protection doesn’t last, they have been put at harm for no benefit.

And just when you think it’s really bad, it gets worse.

http://wearechange.org/bill-gatesphilanthropy-30000-indian-girls-used-guinea-pigs-test-cancer-vaccine/

In 2009, thanks to the Gates Foundation, about 16,000 girls from ages 9-15 from the Khammam district in Andhra Pradesh were given three shots of vaccine, (manufactured by Merck) by the state health department. The girls were told that they were being given “well-being” shots.  Five died and several girls’ health deteriorated. Similar cases of deaths were reported from Vadodara, Gujarat, where 14,000 tribal children were also vaccinated with the HPV vaccine Cervarix, made by Glaxo SmithKline.

http://sanevax.org/gardasil-and-bartonella-a-dirty-little-secret/ 

There is further damning evidence that Gardasil can produce life-threatening reactions in those who have been close to a cat, fleas, or ticks, since many of these animals are infected with Bartonella, Babesia, or Lyme (borrelia). Also, since many MSIDS patients (multi systemic infectious disease syndrome) also struggle with viruses such as Mono or active EBV, a cytokine storm can result with mucus being over manufactured in lungs and airways and well as wide-spread inflammation.

Asymptomatic girls after receiving Gardasil activated dormant Bartonella which was confirmed by testing.

“Gardasil contains aluminum adjuvant nano-prticle substrates, bound to HPV16-L1 protein fragments, that appear to have mutated at binding sites, possibly resulting in excessive inflammation. The mutation attaches to the endothelial lining of blood vessels and organs, including the brain, if the host lacks sufficient active glutathione, or similar complimentary attractant, or does not readily clear toxins. Inflammatory HPV16-L1 DNA protein particles were found in autopsy tissue samples from two different teenage girls, six months after receiving her last vaccination, in the case of one deceased girl. Our findings indicate that if the blood brain barrier is open, commonly due to allergies or the common cold, these man-made inflammatory vaccine nano-particles may enter the brain, and cause additional damage, and possible demyelination.”

Statistics indicate that 50% of domestic cats in the US are infected with Bartonella, and humans can contract Bartonella and have no symptoms at all. It can lie dormant until a stressor, such as a vaccine, triggers an active infection.

Symptoms such as fatigue, pain, memory loss, cysts, Inflammatory Breast Cancer, and much more can be caused by Bartonella. For more information please read:

https://madisonarealymesupportgroup.wordpress.com/2015/07/23/understanding-bartonella/

https://madisonarealymesupportgroup.wordpress.com/2016/01/03/bartonella-treatment/

https://madisonarealymesupportgroup.wordpress.com/2011/09/25/the-bartonella-checklist-copyrighted-2011-james-schaller-md-version-11/
http://www.thevaccinereaction.org/2015/08/uprising-against-hpv-vaccine-mandate-sweeps-rhode-island/ Some states are mandating this vaccine despite the fact it has three times more reported adverse reactions than all other vaccines combined – including deaths and permanent disabilities, without proof it has stopped a single case of cervical cancer.

https://madisonarealymesupportgroup.com/2017/07/02/hpv-after-vaccines/  Dr. Lapenta states:

*Invented vaccines only protect against less than 50% of the oncogenic types of HPV described; therefore, they do not have scientific justification from the point of view of prevention.

*The invention is badly implemented since proteins are used for every type of HPV, the ideal have been a protein or antigen common to all types of HPV.  

*Mixing these antigens of each type of HPV in a single solution seems to me like a biological bomb, which has provoked death and thousands of affected everywhere on the planet, many of those have not recovered.

*Using aluminum as adjuvant was another error as it is known that it is involved in inflammatory and auto-immune reactions.  

*It causes severe side effects.

*The vaccination campaigns were misleading and amounted to saying they are the “salvation of humanity against HPV.”

*They were not well tested because in most studies almost everyone concludes that they are safe.  This is nothing but false.

In this case of VACCINES AGAINST HPV, I also very responsibly say that:
THEY WERE A BIG FAILURE AND WILL CONTINUE TO KILL AND DAMAGING THE HEALTH OF THE POPULATION THAT ACCESSES THESE VACCINES … 

For more information on vaccines in general read:
https://madisonarealymesupportgroup.wordpress.com/2015/06/19/a-word-on-vaccines/

A post dedicated to women who have lost their lives too early: http://truthaboutgardasil.org/breaking-news-truth-about-gardasil-makes-headlines/