Simplified Brief:The adjuvant in vaccines, especially
aluminum hydroxide, is very efficient at activating the immune system, and the
resulting hormones are well documented in peer reviewed and published
literature. Inflammatory Interleukin-18 and Interleukin-1β (one beta)
produce inflammation in the gut (PMID: 17404311)
& (PMC1373865),
inflammation in the brain (PMID: 11898392)
& (PMID: 21184660),
and inflammation in the airways and lungs. Interleukin-18 and
Interleukin-1βhave been documented to be associated with asthma and
Chronic Obstructive Pulmonary Disease (COPD) (PMID: 15668323)
& (PMID: 10471611). Under most circumstances, the inflammation is self-limiting. In a growing
subset of people, this self-limiting does not occur, especially when multiple
vaccines are administered concomitantly. Two vaccines may result in a 200%
increase in inflammation of the glial cells in the brain, but five concomitant
vaccines may result in an increase in inflammation much greater than 500%, with
a proportional increase in inflamed oligodendrocytes, the cells in the brain
that produce myelin. To feed inflammation, the body needs additional
calcium, magnesium, etc., and may break apart mineral-rich biofilms. The
pathogens that were formerly encapsulated in
antibiotic resistant biofilms, including
vector-borne pathogens and co-infections transmitted by mosquitoes, fleas,
spiders, ticks, human or animal saliva, etc., are now exposed, and can
become virulent, resulting in a further cascade of inflammation. Viruses
and enteroviruses, such as Epstein Barr Virus (EBV), CMV, XMRV, etc., may also
be reactivated. Bartonella, FL1953 (Protozoa Rheumatica), Borrelia
burgdorferi, and other vector-borne pathogens have been observed in many of the
girls suffering adverse effects from the Gardasil HPV vaccine. Although these
pathogens may be reactivated or made virulent by a vaccination,
infants/children/adults are never tested for these potentially debilitating
pathogens during "wellness visits." These and other infections, especially
a history of Infectious Mononucleosis, present a higher risk for life
threatening reactions if the host receives one or more vaccinations, especially
since VEGF from Bartonella opens the Blood Brain Barrier (Phillips et al, 2010). From an autism standpoint,
the worst time to vaccinate an infant is while they are teething, because the
Blood Brain Barrier that protects the brain and CNS is permeated (opened), due to
the elevated histamine produced by teething. Histamine from mast cells in a
child with allergies also opens the Blood Brain Barrier. Compared to a 140
pound woman in good health, with no allergies, and a properly functioning Blood
Brain Barrier, levels of inflammation producing vaccine adjuvants are 2,000%
higher in a 7 pound infant. An infant girl receives greater
neuroprotection because of estrogen, while mercury accumulates in a male child,
due to testosterone binding (PMID:
15780490), as can be verified by the higher
incidence of autism and related disorders in vaccinated males. An infant/child/adult who was
healthy, may now encounter (flares of) debilitating and sometimes
life-threatening symptoms or events. In Phase II (chronic phase),
inflammation is typically diminished but
sustained, with sometimes intermittent acute flares of symptoms. Pathogen activity may increase.
Food sensitivities/allergies may increase as food proteins contact antibody
generating immune cells in the lining of an inflamed gut, resulting in food
allergies. The body may
become more acidic. As ph decreases, synapse firing is impaired,
especially in the presence of a Glutathione S-Transferase Deficiency, which can
impair mitochondrial activity, due to changes in electrolyte characteristics of body fluids,
caused by
elevated levels of contaminants and toxins, which affects the electrical charge
of the membrane of every cell in the body. Typical inflammatory markers may appear somewhat
lab-normal on a Comprehensive Cytokine Panel, except for LPS stimulated
cytokines, which may appear 1/4th lab normal, but cytokine base counts will
usually appear somewhat normal. Multiple Vector Borne pathogens have been
observed. Bartonella, HHV6, and several others, are suspect if seizures
are present. FL1953 is suspect if connective tissue disorders, joint pain, air
hunger, or fatigue are present,
with or with a positive Western Blot, especially when family pets or
livestock are present. Families with a history of Epstein Barr, Mononucleosis, arthritis, asthma, allergies,
or a Glutathione S-Transferase Deficiency (GSTM1, GSTT1, GSTP1, etc.
polymorphism) are at greatest risk. Through direct interviews, a high arch
on the foot, as seen in Charcot Marie Tooth Disease, is being observed in a
significant number of affected participants (Phillips et al, 2010), and appears
to be a risk factor.
In South Korea, A “Japanese Encephalitis” booster vaccine
is given just 4 weeks after the first shot, and, like Gardasil, but then is also
given once each year until age 15. Like the HPV vaccine, it has a history of
causing adverse effects which INTERCELL, and its partner, MERCK, say are not
caused by their vaccine, and go on to say that this is “the wave of the future”
(http://www.medscape.com/viewarticle/414689_7
).
MERCK, the maker of the Gardasil HPV vaccine, is killing
and maiming American kids for profit, while protecting kids in foreign countries
from their dangerous vaccines, because they don't want to be sued. (whistle
blower)
MERCK is every lawyer's dream. MERCK
vaccinates any U.S. child that breathes -but- MERCK actually stated
they won't vaccinate any FOREIGN child with ANY allergies, or is sick, has an
autoimmune disease, or is pregnant. This means that virtually all 222,000
American children would still be healthy or still be alive if their parents
would have know that they could could be vaccinated in a foreign country.
Girl can
be vaccinated if she has a weakened immune
system
YES
NO
Girl can
be vaccinated if she receives other vaccines
YES
NO
Girl can
be vaccinated if she has allergies
YES
NO
Girl can be vaccinated if she
has asthma
YES
NO
Family can sue vaccine
manufacturer if a child dies or becomes ill from a vaccine
NO
YES
MERCK is far worse than the Tobacco Industry ever was.
At least the the tobacco industry never made smoking mandatory by bribing
politicians with "campaign contributions," and didn't pay people to lie and
discredit doctors who told the truth.
MERCK who also made Vioxx that caused 27,000 heart
attacks, but neglected to tell people that it caused a 200% increase in heart
attacks and strokes. MERCK is hell bent on vaccinating everything that
moves with its DNA contaminated HPV vaccine.
A girl with any of the following conditions should NOT
be vaccinated: "EXCLUSION CRITERIA" for the Gardasil HPV vaccine (taken
directly from the clinical trial):
AUTISM IS CURABLE WHEN YOU KNOW ITS CAUSE No child has ever caught autism from a chickenpox party!
Synopsis: Trauma to the immune system,
including vaccination, can initiate a systemic inflammatory condition that may
fail to self-limit, and become more aggressive in individuals with a Glutathione
S-Transferase (GST) deficiency and/or an impaired Cytochrome P450 pathway (CYP).
Acute inflammation may reactivate dormant pathogens, such as EBV, HHV6, XMRV,
etc., and cause a cascade of debilitating disorders, especially when vector
borne pathogens, such as FL1953 (Protomyxoa Rheumatica), are present. Protomyxoa
Rheumatica (destroys heme cells), Bartonella (seizures), and Babesia (parasite
that loves iron and causes "air hunger"), may enhance the activity of other
infections. During the second phase, inflammation may decrease, and CBC tests
may appear somewhat lab-normal. Malabsorption, from an inflamed gut, results in
Mitochondrial insufficiency, causing an additional cascade of debilitating
events. The multiple reactivated pathogens may present with multiple complex
symptoms, called "viral interference," making it difficult to diagnose any
single disorder. The patient may go undiagnosed for years, and may present with
symptoms of CFS, forgetfulness, ADD, ADHD, irritability, headache, nausea, joint
pain, photophobia, Mastocytosis, adrenal insufficiency, Gastroenteritis,
Colitis, Connective Tissue Disorders, flares of Lupus-like symptoms, and sometimes idiopathic seizures. These
individuals may typically have an intolerance to foods with a high fat content,
foods that contain wheat, and foods that contain citric acid. In severe cases,
decreasing barometric pressure, caused by approaching storm fronts, will result
in a flare of symptoms.
ABSTRACT: The PHILLIPS-OFFIT-WAKEFIELD SYNDROME
is a condition in which inflammation moves from physiologic to pathologic,
resulting in a cascade of symptoms of various degrees of Developmental Disorders
and possible seizures in infants and toddlers, and cognitive impairment,
CFS, with flares of Lupus/SLE, Urticaria, Mastocytosis, Schizophrenia, and possible
seizures in older children and adults. Please be aware that these multiple
pathogens skew symptoms (viral interference), making it difficult to diagnose a specific disorder. Self-sustained and sometimes uncontrolled inflammation may be due to
the failure of T-Reg cells such as STAT3, which may cause
Hyper IgE Syndrome;
(RAD51 enhanced) BRACA2 gene, which inhibits human p53 (p53 may also be
inhibited by Stat3, Bartonella, Protomyxoa Rheumatica* (PR) [formerly called FL1953],
etc.); dysfunctional Interleukin 10; SEPS1; or other genetic or environmentally
induced variant or variable. The inflammation is initiated by an acute immune response,
which may be caused by close-spaced, concomitant, or repetitive vaccination(s),
which cause hyperactivity in T-Cells and B-cells. A significant number of
patients recall exposure to places where a mold or fungus was present, such as a
classroom or building where mold was found, possibly resulting in their immune
system becoming highly sensitive to vaccines that use a yeast/fungus to grow
viruses, such as the Gardasil HPV vaccine. Subsequent flares of inflammation and
new autoimmune-like symptoms may be triggered by newly acquired food allergies
from food proteins coming into contact with antibody-producing immune cells in
the lining of an inflamed gut. These immune cells may produce antibodies to
favorite foods, causing new food allergies. Histamine-producing mast cells may
become highly sensitized and more abundant, limiting food choices, especially
foods containing histamine-stimulating citric acid. Malabsorption and enzyme
deficiencies may become common, and result in a further cascade of debilitating
and/or life-threatening conditions and events. Dormant viruses, retroviruses,
and enteroviruses, such as Protomyxoa Rheumatica (a protozoan common to North
America, in the Malaria family, formerly called FL1953), XMRV, EBV, HHV6, and vector borne pathogens
such as Borrelia,
may be reactivated during periods of inflammation. (Vaccination against HPV with
Gardasil®, and vaccination against Lyme (Borrelia) with Lymerix®, are
unfortunately proving to be a new source of neurological disorders and adverse
effects, due to the Recombinant Outer Surface Protein (Osp)
(PMID: 21673416)). These pathogens may be
incubated and thrive within pro-inflammatory cytokines, such as Interleukin 17,
resulting in obligate intracellular bacteria, such as Mycoplasma Pneumonia and
Chlamydia Pneumonia, Babesia, (the seizure causing) Bartonella, which may also
attack heme cells (discovered 2 decades ago - 24 strains have now been
identified), and Protomyxoa Rheumatica, which feeds on lipids in the blood, and
has an affinity for the arginine
found in wheat, also causes coagulation disorders and biofilm growth, and is
quickly spreading across North America. These reactivated pathogens may enhance
the activity of currently active infections. Bartonella is the only genus that
infects human erythrocytes and elevates monocyte-macrophage chemoattractant
protein-1 (MCP-1), which is produced upon infection of endothelial cells with
Bartonella henselae. Bartonella triggers pathological angiogenesis in the vascular bed, due
to mitogenic levels of vascular endothelial growth factor (VEGF) that are able
to cause endothelial cell proliferation. The elevated level of MCP-1 is
sufficient to result in the migration of macrophages to the infected endothelial
cells. The Bartonella bacteria stimulates the growth of its host cells, and may
actually attract
pro-inflammatory Interleukin 21 cytokines to epithelial cells in the gut
(PMID:
PMC2915423),
(PMID:
17241869), which may lead to gastroenteritis, IBS, and Chron's. In
this manner, Bartonella (and possibly other pathogens), attract pro-inflammatory
cytokines to a site, and use these fast growing cells as incubators
(Phillips et al, 2010). Pathogen infected leukocytes may now penetrate and infect joints,
and may result in disorders ranging from RA to rare disorders, such as Pigmented
Villonodular Synovitis, or Ankylosing spondylitis. Elevated and/or waves of
histamine from sensitized or overly abundant mast cells may cause syncope and
lowered blood pressure, due to vascular dilation. Histamine permeates the Blood
Brain Barrier, allowing pathogen access to the brain and CNS. Elevated cortisol
can inhibit and/or kill neurons in the hippocampus, resulting in short-term
memory loss and poor concentration, but fatigue, GI distress, head pressure,
migraines, joint pain, seizures, photophobia, lightheadedness (check for POTS),
insomnia, and mood swings are the most common complaints. Elevated cortisol can
disrupt the pineal gland, inhibit melatonin production, and result in insomnia
and decreased neuroprotection. A Glutathione S-Transferase (GST) deficiency has
been observed in a significant number of these patients, typically due to a
GSTM1, GSTP1, or other GST polymorphism. Other genetic variants that cause
enzyme deficiencies, have been observed in these patients, and may appear and be
exacerbated during this time. Genetic variants such as CYP1A1, CYP1B1, and
CYP2C9, have been observed in the Cytochrome P450 Pathway. These genetic
variants form a bottleneck for the metabolism of nutrients and medications.
After the initial eruption of symptoms in which ANA, TNF-a, SED rate, and other
inflammatory markers may test high, the inflammation becomes attenuated,
possibly due to pathogen “hijacked cytokines” (ie: Interleukin 17 is converted
to viral Interleukin 17 (vIL-17), which may slow the inflammation process and/or
inhibit apoptosis. Slightly lowered body temperature may be observed, possibly due
in part to the
leaching of Bromine and other halides from the surge in cell apoptosis due to
inflammation. Bromine, Fluorine, and Chlorine now compete for iodine receptors and
thyroid related functions, and body temperature regulation may (briefly) become
unstable. During this chronic second phase, in addition to
developing new food allergies and symptoms, a Cytochrome P-450 pathway
deficiency may cause additional flares of debilitating symptoms when fats and
sugars are ingested. Medications metabolized through the Cytochrome P450
pathway may fail, and accumulate to toxic levels in the blood. Typical CBC lab
tests may appear lab-normal, but an “NK-CD57” test (Natural Killer Cell, Marker
57) may display a very low count, indicative of viral activity from HPV viruses
and/or opportunistic or formerly dormant pathogens.
NK-CD57 test counts from four females were 51, 22,
15, and 8. The NK-CD57 test may then be administered at 6 month
intervals to gauge the progress of the patient’s recovery. The girl with
the NK-CD57 count of 51 subsequently tested positive for Protomyxoa Rheumatica,
while the others remain untested. A “COMPREHENSIVE
CYTOKINE PANEL” may reveal that, while cytokine base counts are somewhat normal,
Lipopolysaccharide (LPS) Stimulated IL-17 and other pro-inflammatory cytokines
may test far below acceptable lab limits, thus confirming an underlying and
continuing inflammatory condition. FRY LABS is currently the only lab that
is capable of testing for Protomyxoa Rheumatica (FL1953 Protozoa), and it is
suggested to use "PCR for FL1953, with Advanced Stain,
Panels A and B" (skip the NK-CD57 Panel if you use this test).
Protomyxoa Rheumatica, is widespread and is usually overcome by a healthy immune
system, but presents with symptoms similar to Malaria when reactivated from a
dormant state. Indications of a DOMINANT TH1 immune
system may also surface, making certain dietary choices potentially
life-threatening. Intestinal disorders, including gastroenteritis, are not
uncommon, and gastroparesis has also been diagnosed, which appears to confirm
that intestinal and other problems may become exacerbated without dietary and
drug intervention, such as Low Dose Naltrexone (LDN). LDN affects membrane of
fast-growing cells. LDN *MUST* be started VERY gradually: 0.5 Milligram for the
first two weeks, then doubling the dose each following week, until a maintenance
dose of approximately 3.5 milligrams per 100 pounds of body weight is reached,
but in no case should the daily dose exceed 4.5 milligrams. Increasing the dose
beyond 4.5 milligrams has been found to decrease its effectiveness.
Risk Factors include, but are not limited to:
Families with a history of autoimmune disease
Families with a history of allergies or asthma
Families living in areas with an abundant mosquito, flea,
or tick population
Families with a high arch on their foot, with or without a
diagnosis of Charcot Marie Tooth (CMT) Disease
Families with a history of Mononucleosis among its members
*Protomyxoa Rheumatica is a vector borne protozoan similar to
Malaria, typically transmitted to humans by fleas and mosquitoes. Protomyxoa
Rheumatica is normally encapsulated by a biofilm.
Contact Lloyd W. Phillips for further information or recovery
protocol informtion:
PPL@Mailbox7.net or phone (954) 370-3500 (USA).
Note regarding girls who have received the Gardasil HPV vaccine; The
average patient presenting with this syndrome has seen approximately 30+
doctors, is young, has received the Gardasil HPV or other vaccine within the
past two years, and frequently appears to be in good health.
