Legal Disclaimer and Limited Grant of Duplication: None of what is presented herein is to be construed as medical advice, nor is to be used for diagnostic purposes.  All information is provided for Education and Information only.  This work is copyrighted as a "work in progress" by the author. Full permission is granted by the author to any current member of the Yahoo "Lets Talk About Gardasil" group (Group)to duplicate this work, as long as: 1) it remains under your physical control [you may show it to someone, but they may not keep it or duplicate it] and 2) It remains unmodified.  No liability is extended for the use or interpretation of any part of this information. This information may not be used in any official proceedings by any person or jurisdiction, or for any other purpose(s), without the written consent of the author. A usage fee of $500,000.00 for each and every word of this work that is quoted or otherwise used or paraphrased without permission from the author, shall be assessed if used by a corporation, individual, or any entity as a plaintiff, or agent thereof, in any court of law or official proceeding, against any member or agent of this Group.  Lloyd W. Phillips, ABA ID#01291932

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sun -->  formic acid --> kills EBV --> pain and inflammation

The following is provided as information for educational purposes only.  It has had only limited peer review.  It is not meant to be a diagnostic tool.  This is rough draft VII, based on preliminary findings:

 ·         Changes since last version: 

·         Additions: phases and phase onset times

Latest revisions appear in RED

 

 

Vaccines and Adverse Effects: Focus on GARDASIL, --Preliminary Findings

DRAFT 7.40 -- NOT FOR PUBLICATION

Copyright© September 1, 2010, by Lloyd W. Phillips

PHILLIPS-OFFIT-WAKEFIELD SYNDROME 
a.k.a.
GARDASIL SYNDROME

Synopsis:  The Gardasil vaccine can cause severe and life threatening adverse reactions through multiple, sometimes simultaneous, pathways.  We will look at 2 overlapping pathways: Acute hypotension [observed bp=50/32] (septicemia), may result in syncope.  Fainting is a serious potential indication of septic shock, which can lead to Systemic Inflammatory Response Syndrome (SIRS), which can result in Multiple Organ Dysfunction Syndrome (MODS).  Another pathway, an acute TH17 cytokine response, can be evoked when the recipient of the vaccine has or has had a reactive exposure to a filamentous member of the Fungal Kingdom.   Hypercytokinemia can result from either pathway, affecting the Brain, Central Nervous System, and Peripheral Nervous System.  Inflammation and autoimmune symptoms may appear, along with new or heightened sensitivities, especially to the fungal kingdom.  Signs of adrenal insufficiency (Addison's) is a key symptom. The TH17 Response causes downregulation of the TH1 Immune Response, leaving the patient open to bacterial and sometimes uncontrolled fugal growth and infections.  The condition is made worse (Lupus-like flares) by exposure to fungal metabolites present in cereal grains, corn, and virtually all commercially made citric acid (including supplements bound to a citrate), because 99% of commercial citric acid is prepared by using the Aspergillus Niger  fungus in the fermenting process.  Debilitating head pressure, migraine aura, neuropathy, cognitive dysfunction (brain fog), mood swings, and depression are typically present.  Fixed pupils and (lower) motor control inhibition may present in the more severe cases, yet Nerve Conduction Tests (EMG) may appear lab-normal (but weak).  Like MS, EBV, and the Herpes family infections, flares wax and wane with stress, viral infections, and heat, strongly suggesting the possible involvement of HHV-6 ( citation ) ( citation-2 ), which might also account for involvement of the cardiovascular system ( citation ).

ABSTRACT

Vaccinations, environmental factors, pathogens, plus resident microbiomes, can trigger the immune system to produce inflammatory cytokines.  In young girls, vaccinated with the GARDASIL vaccine, increased evidence of Hypercytokinemia, accompanied by the proliferation of autoimmune disorders, has been observed and documented. (Janak et al., 2010 )  The majority of severely affected individuals develop an extreme sensitivity to commercially prepared citric acid, due to the fact that 99% of citric acid is currently produced by adding the Aspergillus Niger fungus to corn oil.  These individuals recount a history of exposure to fungus and sometimes mouse droppings, and/or pathogens such as Streptococcus, Mononucleosis, or Pneumonia:

Case 1:  An 11 yr old B.C. Canadian female went into a basement and breathed a cloud of "dust" while her mother was cleaning a basement where mold spores and mouse/dog/cat feces was left in a locked, undisturbed basement for 2 years.

Case 2:  A 20 Yr old Ohio girl had a history of exposure to mold in a basement classroom where she attended junior high school.  In her later teens, she recounts becoming very ill after volunteering for an intercity restoration project, when she crawled through a previously undisturbed crawl space under an older residence to replace a window sill.  During this time, she was exposed to mouse droppings and mold spores, and additional mold spores from the previously undisturbed soil.

Case 3:  A 21 yr old girl recounts living in the Southwestern United States, where a good portion of the long-time residents are exposed to a soil fungus called Coccidioides immitis/posadasii, which causes coccidioidomycosis (valley fever, desert fever) in humans.

Case 4:  A 32 yr old female nurse with a history of mold exposure and a prior vaccine reaction was given a seasonal flu vaccine (No Gardasil).  She reported Lupus like symptoms.  After receiving various protocols, including chelation, she began presenting with additional symptoms, including angina and arrhythmias.

Case 5:  A 14 yr old girl with prior fungal exposure had a lab-normal CBC after presenting with multiple autoimmune symptoms.  A Cytokine Panel revealed high ANA, low (1/4x normal) IL-17 (Stimulated-LPS), and 4x high TNF-a (Stimulated-LPS). After receiving the Gardasil vaccine, she slowly declined until she could not walk for a period of 11 months until a protocol was started.  An EMG had shown normal nerve conduction activity, but with reduced amplitude (slightly lower voltage in the nerve, but lab-normal F-Wave delay and Velocity).

Fungus (yeast) exposure can evoke an aggressive TH17 immune response, and cause autoimmune symptoms to appear ( citation ).  Inflammatory cytokines may be produced following the activation of the TH1/TH17 immune response, producing NF-Kappa-B.  The TH17/IL-23 pathway, however, increases inflammation and inhibits the body's TH1 immune response from fighting infection , Candida albicans, and Aspergillus fumigatus.  The same researchers also noted a molecular connection between IL-23 and uncontrolled fungal growth ( citation )This may account for some vaccinated children presenting with increased ear-infections, and why people who receive the Gardasil vaccine (that is made with a fungus), become highly sensitive to commercially made citric acid, which is made using the Aspergillus fungus. The TH17/IL-23 pathway may help contribute to the increased autoimmune prevalence in females.  Historically, 80% of autoimmune cases occur in females, and sex hormones are known modulators of NF-Kappa-B ( citation ).  NF-Kappa-B can trigger the production of pro-inflammatory IL-1, IL-6, TNF-α, etc., which results in the signaling of microglia to produce inflammatory cytokines.  If not controlled by a feedback mechanism such as Interleukin-10 (IL-10), these microglia cells can cause a runaway flood of cytokines, called Hypercytokinemia, a.k.a., Cytokine Storm. When left unchecked, or held in the "on" state by adjuvants from (multiple) vaccinations, together with a condition or disorder where the immune system may be hypersensitive (allergies), and/or deficient in Interleukin 10 (IL-10), and/or otherwise marginally keeping up with other body burdens, a wasting condition may ensue.  Some Genetic Variants (polymorphisms) are credited with causing an increase in body burdens that occur in an estimated 2% of the population.  These genetic variants are found in COMT, NAT1, NAT2, GSTM1, GSTP1, SOD1 and SOD2, CPOX4, BDNF, 5HTTLPR, and other Genes, and contribute to an increased body burden from pesticides, heavy metals, and other toxins, especially when Glutathione S-Transferase is compromised (GSTP1 and GSTM1 Genes).  Low GSH and heavy metals have been observed in a significant number of cases, along with polymorphisms of some of the Genes listed. Body burdens also include, but are not limited to, possibly infected leukocytes ( citation ), dormant or active pathogens/microbiomes, and persister cells. One possible underlying cause of this syndrome might be an RNase-L Defect. Patients with the RNase-L Defect overproduce normal Rnase-L, which then degrades into the 37kDa lower weight version. The 80kDA protein can then break into three parts. The middle drops out, and the first and third parts bind into the new, 37kDA Rnase-L protein, leaving the body without its normal antiviral defenses, and subject to the reactivation of viruses that should be dormant (Horvath et. al).  Virii like the meningitis causing Coxsackie B and the Echovirus (rash on face and chest), which also target the heart and cause chest pain and potentially life threatening viral myocarditis and pericarditis, may then become virulent.  There are three overlapping phases to this syndrome.  The First Phase may involve an immediate or delayed allergic IgE (T-Cell/Beta Cell) response  to one or more vaccine components, especially yeast (fungi) and fungal metabolites, resulting in fainting (syncope) caused by acute hypotension from septicemia( OBSERVATION ), seizure, thrombosis, etc., and may generally last up to about a month.  The Second Phase (overlapping) involves the host's attempt to make antibodies to the vaccine, while other (dormant) pathogens are already present in the host, resulting in the intermittent or continuous presentation of debilitating multiple autoimmune symptoms and variants, plus any number of the symptoms listed below.  The Third Phase, or Extended Phase, involves debilitating "flares" of autoimmune symptoms, plus may include involvement of the CNS and Peripheral Nervous System, adrenals, and thyroid function.  These Phases may become more serious and life threatening with each additional vaccination or series of vaccine injections.  The continuous or intermittent cytokine cascade may result in the failure of multiple organ systems, due to prolonged inflammation and/or compromised nutrient, enzyme, and hormone availability.  The primary cause is nutrient malabsorption from an inflamed or compromised GI tract, caused in most cases by acquiring a sensitivity to very small amounts of commercially made citric acid, especially those with a history of HHV-4 or when HHV-6 or the Rotavirus is present ( citation ).   The NO/ONOO Cycle, which mediates intracellular iron signaling in NF-Kappa-B, may also be effected, resulting in a further increase in inflammatory cytokines, due to increased NF-Kappa-B activity ( citation ).  With changed conditions in the body, and the immune system further compromised by decreased nutrients, together with IL-17/IL-23 causing a decreased TH-1 immune response to bacteria and fungi, dormant organisms may be signaled to replicate and become virulent.  Upon replication, some of these organisms, viruses, Rotaviruses, and RETROVIRUSES, and fungi - such as Coccidioides, Aspergillus fumigatus, plus  XMRV, can activate receptors, such as Toll-Like Receptor 3 (TLR3), and further intensify or prolong Hypercytokinemia.  In the brain and nervous system, inflammation caused by inflammatory cytokines from microglia cells, can damage neurons.  There are also indications that heavy metals are also being freed during the rapid production of cytokines, and by the inflammation process ( hypothesis ), because high levels of heavy metals, such as aluminum, have been found in hair samples ( observation ).  Aluminum is a known disruptor in MS ( citation ),  and an adjuvant in many vaccines, including GARDASIL.  Unchecked Hypercytokinemia may cause microglia to originate a massive calcium wave, resulting in a seizure ( hypothesis ).  The resulting signs or symptoms presented by a patient with this scenario may come on slowly or suddenly, may come in "flare ups," be mild or severe, and may be temporary or permanent, and is the culmination of SYMPTOMS from (Pathogen 1) + (Pathogen 2) + (Pathogen 3-n), ie: if EBV, Mononucleosis, attenuated viruses, microbiomes, etc., were all present, the multiple symptoms of the patient may be the cumulative sum/result of symptoms for all pathogens present, or which he acquires, caused by each individual pathogen flipping multiple genetic switches - but all symptoms may not appear simutaneously.  This includes, but is not limited to death; (acute) hypotension (septicemia), blood clots; encephalitis; seizures; tachycardia; paralysis; fatigue (adrenal insufficiency-Addison's); irritability; arrhythmias; fainting; shortness of breath; fixed/dilated pupils; auditory hypersensitivity; head and eye pressure (aura); seeing colorful displays and/or flashes of color; swelling and/or redness about the face and neck; specific and/or general swelling of the skin and internal organs; a sometimes noticeable sensitivity and/or swelling around the spleen; disdented abdomen; specific and/or generalized severe pain, especially about the head and eyes; rash; inability to concentrate; lupus like symptoms; global pain, which may first present as joint pain and/or pain around pressure points;  severe head pressure accompanied by a protrusion at the base of the skull that the patient describes as a "baggie" or "water sack" (in severe cases); numbness / tingling / pain (sometimes pounding pain) in legs and thighs; weakness in extremities - legs and thighs especially;  failure of brain to communicate with hands or legs (a Nerve Conduction Test [EMG]may disclose a weak signal, and the professional may have difficulty locating a signal, but "F Wave" and "Velocity" are within lab-normal); weakness in hands; photophobia; hair loss; skewed/compromised nutrient absorption due to poor GI tract absorption; GI tract inflammation; Gastroenteritis; a perceived EMF sensitivity, due to stimulation of the skin by photons (light) or by Radio Frequency energy (RF or EMF), including cell phones, hot stoves (Infra Red [IR] Radiation), bright TV screens, etc., which produces formic acid on exposed skin (note: RF energy passes through clothes), which causes a microbial (spirochete/strep/staph/parasite) disregulation.   In this case, the patient may also become nauseous for days after ingesting foods containing commercially prepared citric acid.  ** An estimated 99% of commercially prepare citric acid is made by combining corn oil with the Aspergillus Niger Fungus, a member of the Fungal Kingdom. The host may develop an extreme fungal sensitivity.  Various amounts of the fungal metabolites and mycotoxins of the Aspergillus Niger Fungus appear in Commercially prepared Citric Acid, and contaminate many foods and prepared drinks, and medications.**  These contaminants can also be found in many vitamin and mineral supplements, including some digestive enzyme supplements recommended by DAN doctors (DAN=Defeat Autism Now).  In addition, anything ingested that would cause an increase and/or redistribution of heavy metals (chelation), especially aluminum (Tums, Mylanta, aluminum containing deodorants), can result in great pain and/or swelling in the patient. This would be a daunting task for any practitioner to diagnose, especially since most symptoms are varied and intermittent, and may never occur simultaneously.  The administration of a drug such as Intercept, which decreases TNF-a, may actually prove life threatening if not carefully monitored, due to opportunistic fungi, bacteria, virii, etc, like Coccidioides, C. albicans or A. fumigatus. To more easily describe this disorder, and place a name, we will simply refer to this as the  Phillips-Offit-Wakefield Syndrome.   In younger, vaccinated children, the Phillips-Offit-Wakefield Syndrome may account for the similar symptoms that are observed in some types of "AUTISM."

DISCUSSION

Virtually all diseases are the result of a virus or bacteria that enters the mucous membranes of the nose, mouth, pulmonary passages,  or GI tract. When activated by a pathogen, the membranes that line these passages produce an IgA immune response.   The  IgA immune system is the body’s first line of defense, and helps reduce the need for a more intense activation of the body's immune system. The IgA immune system can often contain and eliminate many localized pathogens.

A vaccination works differently, and injects an antigen (sometimes further contaminated) into the body, along with a chemical additive called an “adjuvant.”  The adjuvant forces the immune system to turn “on,” and stay on for a period of time.  This “on” state varies in both aggression and duration, according to the sensitivity of the immune system of the individual vaccine recipient.

There is a critical window that must be calculated for the adjuvant in a vaccine.  An adjuvant is a chemical that causes the human immune system to react to the vaccine and form antibodies.  Too little immune system stimulation, and the vaccine fails to produce antibodies in infants and the elderly.  Too strong an adjuvant, and many healthy people will suffer adverse reactions.  The adjuvant, then, must be calculated for the average person, with an average immune system. 

The administration of a vaccine is actually a very serious medical procedure.  There are additional problematic variables that are encountered in humans, that are not seen in lab animals.  Although vaccine manufactures know that the human body is in homeostasis with numerous pathogens present as miniscule amounts of DNA, such as found in the saliva and joints of all humans, the unique sensitivity of the homeostatic balance of the vaccine recipient is not taken into account, nor is it usually known by either the medical community or the vaccine recipient. 

Syncope (fainting) is seen in many Gardasil vaccine recipients.  On closer inspection of this phenomenon, it was discovered that the Blood Pressure of one Med student plummeted to 50/32.  This acute hypotension immediately following the Gardasil vaccine is a marker for septicemia: the body reacting to a foreign pathogen, and that pathogen can be the the fungal medium used to cultivate the viruses in the vaccine, the virus-like particles, or the aluminum containing adjuvant.  This may then cause Systemic Inflammatory Response syndrome (SIRS), which can eventually cause Multiple Organ Dysfunction Syndrome (MODS).

There is no attempt to measure existing antibodies, sensitivity to vaccine components, CRP, SED Rate, or Interleukin 10, all factors that could predict an immune system that could already be stressed, and might result in an adverse reaction to a vaccine, a "perfect storm," with a possible deadly outcome caused by hypercytokinemia. 

In this scenario of hypercytokinemia, an already present fungal pathogen, together with  acne vulgaris, plus (dormant) mononucleosis, Epstein Barr Virus, etc., in addition to other resident microbiomes, are held at bay by a healthy immune  system.  The pathogen(s) cause a downregulation of Interleukin 10, but the body remains in homeostasis because of the good health of the human host.  When a fungus (yeast) grown vaccine is introduced, a "cytokine storm"  (hypercytokinemia) may result, and because immune downregulators such as Interleukin 10 levels have been depleted, cytokines continue to be produced by microglia.  Increased levels of cortisol further fuel the production of inflammatory cytokines, as does NF-Kappa-B, when serum iron becomes deficient.  Nearby neurons are damaged if levels of Vitamin K, a potent neuroprotector, are also low.  Additional systems and organs in the body become affected, and with nutrition absorption compromised by an inflamed GI tract, inflammation runs rampant.

 Researchers have documented a decreased production of Interleukin-10 in girls with acne vulgaris (cit)).  Interleukin 10, like the brake on a car going downhill, keeps the speed of the immune system and cytokine production, under control.  The adjuvant in the Gardasil vaccine, acts like a lead foot on the car's accelerator.  when a very healthy person with acne vulgaris receives a Gardasil vaccination, the body’s immune system produces a TH1/TH17 pro-inflammatory immune response.   With low interleukin 10, the immune system can go out of control, and produce a cytokine storm (hypercytokinemia), and the vaccine’s adjuvant further prevents the immune system from shutting down in a timely manner.

ACNE as a risk factor for autoimmune disease(s) with the Gardasil vaccine:

"Furthermore, activation of TLR2 [Toll Like Receptor 2] on monocytes releases proinflammatorysup> cytokines,.... ....Overproduction of Th1 cytokines such as IL-12 has been implicated in the development of tissue injury in certain autoimmune and inflammatory diseases (28, 29, 30, 31, 32, 33, 34). " http://www.jimmunol.org/cgi/content/full/169/3/1535 

"In rare cases, Propionibacterium species have been implicated as a cause of brain abscess,2 subdural empyema, dental infections, endocarditis .... conjunctivitis ( important Citation ) associated with contact lenses, peritonitis, and breast-implant infections." (cit)

Birth Control Pills as a risk factor with the Gardasil vaccine

Birth control pills increase inflammation as noted by increased C-Reactive Protein [CRP] blood levels, decrease glutathione, and decrease the body’s ability to control additional inflammation caused by the Gardasil vaccine (cit).  Birth control pills may also increase the risk of clotting from the Gardasil or accompanying vaccination(s).

An important component of the immune system of the brain and Central Nervous System (CNS), are the macrophages called microglia, which surround neurons.  Microglia can produce cytokines, hormones that regulate and control the immune system.  Pro-inflammatory cytokines are known to be switched “on” by the TH1 and/or TH17 immune system response.  This response can produce inflammation, and cause cell death (apoptosis) in the same cells of the brain and Central Nervous System that generated the inflammation, causing damage to surrounding neurons.  Aluminum and mercury in vaccines are also known to stimulate microglia to produce inflammatory cytokines and excitotoxins. 

This is a very serious, all-out effort by the immune system to contain and destroy a pathogen.  It was only intended to be a very brief event.  If the immune system is not shut down, severe damage and disruption to the brain, the Central Nervous System, the Blood Brain Barrier [the TH17 Immune Response has only recently been documented in lab animals], and other organs, plus damage and disruption to the vascular system, the NO/ONOO and Methylation cycles, etc., may follow. This same immune response can disrupt the production of the body’s powerful anti-inflammatory, glutathione (GSH).  This condition is also referred to as a “Cytokine Storm,” or hypercytokinemia, and markers are readily seen in the more serious adverse reactions in formerly active and healthy girls, to the Gardasil vaccine, with an immune system out of control, and being forced to stay “on” by a chemical adjuvant from a man-made vaccine. 

Glial cells in the brain and CNS can quickly signal other sites(cit), including vascular cells, perhaps accounting for  fainting, plus they might also *initiate* the calcium wave and/or the glial intracellular potassium changes implicated in seizures.(cit)  If the vaccine recipient is deficient in Vitamin K [or K2], developing neurons and oligodendrocytes may be damaged.(cit

"Vitamin K status is important in the maintenance of normal biosynthesis of lipid sulfatide, an important component of CNS myelin, in young animals (Sundaram et al., 1996). Moreover, exposure to the vitamin K antagonist warfarin in utero causes CNS malformations and mental retardation (Hall et al., 1980). These observations suggest a possible unidentified role of vitamin K in the developing brain. In this study, we report the discovery of a novel and potent protective action of vitamin K in preventing oxidative injury to primary OL precursors and to immature cortical neurons that appears to be independent of the current known function of vitamin K." (cit

In younger children, the medical profession terms this vaccination induced degenerative cascade "autism."   If death occurs after a reactive vaccination, Sudden Infant Death Syndrome, or SIDS is identified as the cause of death, not the vaccination.

One of the primary causes of this continuing degenerative cascade is the exposure of the sensitized host to small amounts of citric acid, fungi such as mold, mushrooms, aged foods, etc., and/or excitotoxins such as aspartic acid, aspartame, glutamates such as monosodium glutamate or its 70 other names, and aluminum compounds such as Mylanta, Tums, or aluminum containing deodorants.

The children who live through a cytokine storm now risk hosting activated, formerly dormant, viruses which they have acquired over a lifetime.  These virii also include those from attenuated vaccines.  This outcome is not common, but may be observed during and following hypercytokinemia, and may have lead to the findings of active virii in research by Dr. Andrew Wakefield.  Some of these pathogens appear to have the capability of taking over VDR receptors, turning the immune system into their host.   These virii and bacteria may now become virulent mutations of the original virus or bacteria, and the host presents with an unbelievable amount of endless symptoms, which are actually the sum total of the symptoms for each individually activated pathogen.

When a foreign gene is introduced into a human during a vaccination, the vaccine manufacture makes no warranty that the immune system of the human can read and/or error correct for INTRONS contained within the [genetically modified] DNA, upon Gene replication.(cit)  The concept of INTRONS introduces a vast, new, uncharted universe, full of additional uncertainties, and many more good reasons for reserving vaccines for all but the most serious of REAL pandemics.

Every Drug that has ever been Recalled,
Has been proven to be Safe and Effective by the FDA

As a vaccine manufacturer, the burden of proof is on the vaccine recipient.  As a vaccine manufacturer, you cannot be sued under a law signed by George W. Bush, while Donald Rumsfeld, former board member of a pharmaceutical company called Gilead Sciences, held office as Secretary Of Defense.  Gilead Sciences not only makes vaccines such as the H1N1, they also make TAMIFLU.  John McCain’s wife, Cindy McCain, owns an estimated $25,000,000.00 worth of stock in Gilead Sciences, as of 2008.   England’s Tony Blair, NBC’s Tom Brokaw, and former Republican House Leader, William First [Tennessee], whose family founded the American Hospital Association which was fined over $600 Million for cheating Medicare, are also heavy investors in Gilead Sciences. 

Dr. Andrew Wakefield was one of the first to recognize the link between autism and vaccines.  Dr. Wakefield has been publicly discredited by the U.S. Government and the politicians cited above, and his medical license has been revoked for publishing his findings.  Those findings caused a parents to question the safety of vaccines, resulting in a worldwide decrease in vaccine sales for pharmaceutical companies. 

MERCK, maker of Vioxx, the drug proven to be Safe and Effective by the FDA but had caused 27,000 heart attacks, is also the maker of GARDASIL.  During investigations into fraud, doctors and scientists stated that MERCK had fraudulently used their names on fake clinical tests and drug trials.  They also stated that some drug trials never existed.(cit)

 I recently spoke with Dr. David Soper, an OBGYN (not a virologist or immunologist) at the Medical University of South Carolina, who is conducting a clinical test for MERCK.  MERCK obtained the services of the University to prove that Gardasil caused antibodies to be formed from the strains of HPV contained in the Gardasil vaccine.  The trial subject criteria was based on girls who had received all three Gardasil injections, and was restricted to girls in good health.  This eliminates the thousands of girls who died or are suffering from Gardasil's many adverse effects.  After this trial, MERCK might erroneously claim, through careful pre-screening, that Gardasil is 100% safe and effective.  However, this applies only to the test group, and not to the general public, who have reported a 71.3% problem rate.

It should further be noted that to make Gardasil appear safer, the "placebo" that Gardasil was compared to was purposely tainted with aluminum and various chemicals, as allowed by law. to make Gardasil appear less dangerous than it actually is.

Respectfully,

 Lloyd W. Phillips

954-370-3500

PPL@Mailbox7.net