AUTISM AND MANY "AUTOIMMUNE" AND VECTOR BORNE DISEASES CAN BE ARRESTED:
 THE ROLE OF POLYMORPHISMS, CYTOKINES, PATHOGENS, AND THE BLOOD BRAIN BARRIER
No child has ever caught autism using POWDERMED (PMED®) Vaccinations!

OMG! What would happen if we couldn't get all our vaccinations,
and only got a dozen, like in JAPAN, DENMARK, NORWAY, SWEDEN, or ICELAND????

We'd all be HEALTHIER and LIVE LONGER !
- and -
There would be less Autism !

PHILLIPS-OFFIT-WAKEFIELD Syndrome

a.k.a. GARDASIL SYNDROME
a.k.a. CERVARIX SYNDROME
a.k.a. VACCINE INDUCED AUTISM SYNDROME  (VIAS)
a.k.a. VACCINE INDUCED GULF WAR SYNDROME  (VIGWS)
Simplified Version  v1.261 Copyright©  January 17, 2012 - Working Copy; Publication Pending

PHILLIPS-OFFIT-WAKEFIELD Syndrome is commonly misdiagnosed as "Conversion Disorder"

Simplified Brief:   Trauma to the immune system may cause inflammation, an immune response.  If inflammation fails to self-limit, a cascade of debilitating or life-threatening events may follow.  Excessive or uncontrolled inflammation may be due to genetic polymorphisms or pathogen-hijacked cytokines, such as Interleukin-10, which may then become viral Interleukin-10 (vIL-10).  The adjuvant in vaccines, especially aluminum hydroxide, is very efficient at activating the immune system, but the resulting inflammatory hormones are now increasingly being documented for causing damage to the gut, brain, airways and lungs.  Peer reviewed and published literature shows that 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-1β have 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.  Five concomitant vaccines containing both aluminum and mercury adjuvants (different metals), may result in a synergistic increase in inflammation that is many times greater than the expected 500% (PMID: 731728).  While the primary Blood Brain Barrier consists of tightly packed endothelial cells in the walls of capillaries in the brain, Glial cells comprise the brain's secondary Blood Brain Barrier, and surround the capillaries of the brain.  Glial cells outnumber neurons 10 to 1, and regulate nutrients flowing to the brain by active transport.  When Glial cells are inflamed, a proportionate number of oligodendrocytes also become inflamed.  Oligodendrocytes are the macrophage cells in the brain that make the myelin sheath that surrounds nerves.  The continued ingestion of metals, including the use of aluminum based anti-perspirants, antacids, or foods containing aluminum, including baked goods using an aluminum baking powder, will now help to sustain inflammation, and some al(+3) may pass through the inflamed and permeated blood brain barrier, and contribute to a further debilitating neurodegenerative cascade of events.  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.  A fully intact Blood Brain Barrier passes Spirochetes, such as Borrelia, commonly referred to as Lyme Disease.  Viruses and enteroviruses, such as Epstein Barr Virus (EBV), CMV, XMRV, etc., may also be reactivated.  Fast growing Interleukin-17 cytokines, from the recently discovered TH-17 immune response, have now been documented as being capable of acting as incubators for viruses and pathogens, such as Epstein Barr, which may help explain the increase of autoimmune symptoms during flares of inflammation.  Attenuated viruses from vaccines may also multiply under these circumstances, as may be evidenced by the 83% increase of antibodies to the strain of measles found in the MMR vaccine in the serum of autistic children.  These antibodies are not found in normal children, nor in non-autistic siblings of autistic children (PMID: 12849883).  Infected leukocytes may now migrate into joints, and in the documented case of an eleven year old Canadian girl, resulted in Diffuse Pigmented Synovitis.  Bartonella, FL1953 (Protozoa Rheumatica), Borrelia burgdorferi, and other vector-borne pathogens have been observed in a significant number of the girls suffering adverse effects from the Gardasil HPV vaccine (Phillips et al, 2010).  According to recently peer reviewed and published data, the  arrogance, ignorance, negligence, and failure of the AMA, AAP, AHA, and some doctors to acknowledge, diagnose, and treat the epidemic of early Lyme Disease, is just now beginning to be addressed (PMID: 20508824), along with associated co-infections, such as Babesia, from infected vector-borne sources, and contaminated blood transfusions in the immunocompromised and elderly (CDC: Journal of Emerging Infectious Disease, Volume 18, Number 1—January 2012).  Infections, such as Babesia, may last from months to years (PMID: 9664092).  The multitude of antibiotics wrongfully prescribed to these patients appears to be contributing to making the growing incidence of Lyme Disease and its co-infections, antibiotic resistant (PMC: 2876246) (PMID: 18447934) (Reuters) (FOX NEWS).  Bartonella has recently been found in lice from the homeless in San Francisco (PMC: PMC2727331).  Persister cells, a form of antibiotic resistant dormant pathogen(s) (PMID: 20528688), may also be signaled to become virulent, and appear to be more readily reactivated in the presence of metals such as Pb(2+) and Al(3+), and also by metals typically found in mineral supplements such as Co(2+), Ni(2+), Cu(2+), and Zn(2+).  Because of peer reviewed and published abstracts, we find that the aluminum hydroxide adjuvant in vaccines, Al(3+),  allows biofilms and persister cells to become more accessible to re-infect the human body (PMID: 15946294), which may help explain chronic infectious disease.  The aluminum hydroxide adjuvant in a vaccine may actually increase the risk of infection or disease in a subset of the population harboring biofilms or persister cells (Phillips et al, 2010).  Although these latent and dormant pathogens have been shown to result in serious or life threatening reactions if provoked, and may be reactivated or made virulent by a vaccination, infants/children/adults are not tested for any of these potentially debilitating pathogens during "wellness visits."  These and other infections, especially a history of asthma or Infectious Mononucleosis, present a higher risk for life threatening reactions if the host receives one or more vaccinations, especially since VEGF from Bartonella and some other infections can permeate the Blood Brain Barrier (Phillips et al, 2010). Pathogens may also enter the brain and CNS through brain stem nerve terminations. 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 new food allergies.  Allergens may stimulate sensitized or overly abundant mast cells to overproduce histamine (Histadelia), which dilates blood vessels, and can produce MANY other symptoms, including Postural Orthostatic Tachycardia Syndrome (POTS).  Because of inflammation, elevated amounts of cortisol are also being released, resulting in short-term memory loss, irritability, fatigue, and much more.  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 in these in the 2010-2011 study of girls severely affected by the Gardasil HPV vaccine.  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 without 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.  Until aggressive therapy is started, Low Dose Naltrexone (3.5 mg/100 pounds of body weight before bed, but never exceeding 4.2 mg per day) has proven helpful, if started at a safe level of 0.5 milligrams (Phillips et al, 2010), increasing by 0.5 milligrams per week, until a 3.0 to 3.5 milligram per day maintenance dose is achieved (PMID: 20965606).  Low Dose Naltrexone has been found to help reduce glial cell inflammation in the brain, which helps restore a permeated blood brain barrier, and return the immune system to homeostasis in cases where an overproduction of T-lymphocytes has resulted in the immune system attacking self (autoimmune disease).

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 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) (Phillips et al, 2010).   Acute inflammation may reactivate dormant pathogens, such as EBV, CMV, HHV6, XMRV, picornaviruses, etc., and cause a cascade of debilitating disorders, especially when vector borne pathogens, such as FL1953 (Protomyxoa Rheumatica), are present.  People who suffer multiple or repetitive insect bites, or a single bite from a tick, are at greater risk.  Protomyxoa Rheumatica (destroys heme cells), Bartonella (seizures), and Babesia (parasite that loves iron, leaves oxidized iron deposits in joints, and causes "air hunger"), may enhance the activity of other infections.  Because of increased airway and lung mucus, patients living in arid climates, or in coastal salt-water areas, may experience lighter symptoms, compared to those living in inland areas with higher humidity. In many individuals, oxygen levels may appear normal, but will decrease to below 85% with light to moderate exercise in severe cases.  Decreased exhaled NO levels may be used to monitor an underlying pulmonary inflammatory condition.  During the second phase, inflammation may decrease, and CBC tests may appear somewhat lab-normal.    New food allergies may result when proteins from favorite foods contact antibody producing immune cells in an inflamed gut lining, resulting in newly sensitized mast cells releasing increased amounts of histamine when those foods are later eaten.  This causes new and additional inflammation, which further elevates cortisol that destroys short term memory neurons in the hippocampus of the brain, and inhibits the pineal gland from producing the melatonin that is necessary for sleep.  Malabsorption, caused by the 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 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.

Contact Lloyd W. Phillips for further information or recovery protocol information:   PPL@Mailbox7.net  or phone (954) 370-3500 (USA).

 

Note:  The average patient presenting with this syndrome has seen approximately 30+ doctors, is told that she has a "Conversion Disorder" (it's all in her mind), is typically between 11 and 22 years of age, has received the HPV or other vaccine, and frequently appears to be in good health. 

 

 

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MMR vaccine pushes autism rate to 1 in 38

The CDC proudly announced in 2007 that South Korea was free of measles, because of the MMR vaccine. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5613a3.htm

In 2011,  1 in 38 South Korean children now have autism
(http://www.ctv.ca/CTVNews/Health/20110509/south-korea-autism-prevalence-rate-study-110509/ ). 

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 ).   

Clinical trials on another MERCK – INTERCELL joint venture, a Staphylococcus aureus Vaccine called V710, was halted because it was too obvious that the vaccine was causing multiple organ failure and death, instead of the usual vaccine collateral damage: autism, paralysis, SIDS, plus deaths that can more easily be covered up  (http://www.intercell.com/main/forbeginners/news/news-full/article/merck-and-intercell-ag-announce-termination-of-phase-iiiii-clinical-trial-of-investigational-staphy/ ).

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http://www.betterhealthguy.com/joomla/blog/243-dr-stephen-fry-on-fl1953

 

"FL1953" is the name of the protozoan that loves the ARGENINE found in Gluten. In a person receiving multiple vaccines at the same time (concomitant), Interleukin-18 is released by the immune system to the gut, and starts inflaming the lining of the intestines that contains immune cells. The inflammed gut causes immune cells to be exposed to food proteins, which then can produce antibodies to y...our child's favorite food(s). Cortisol is then released by the body to help stop inflammation, but cortisol kills neurons in the brain (to stop you from remembering trauma). Unfortunately, Cortisol also effects the pineal gland, and stops it from producing the melatonin needed for good sleep. You now have autism, as long as this condition exists.

An acquaintence, Dr. Stephen Fry ( http://FryLabs.com/ ) has discovered a common protozoan found in people presenting with MS, CFS, autism, and more, but this protozoan keeps them from improving. He has temporary called this "FL1953" and has researched this for the past 10 years, and it loves the ARGENINE found in GLUTEN, and fats found in the blood. FL1953 can be delivered to your child by the bite of a flea, mosquito, tick, spider, etc. See More

Welcome to Fry Labs - Fry Laboratories

FryLabs.com

Fry Labs is a diagnostic lab based in Scottsdale Arizona specializing in vector borne diseases including lyme disease, lupis, and chronic fatigue syndrome

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>>> Please copy this to other groups <<<

To see even more improvement in autistic children, use the "INFLAMMATION FACTOR" found with each food on http://NutritionData.com/ for planning meals. You simply want to try come out with a positiv...e number for each meal. This will not be mainstreamed for another 5 to 10 years. Each food will either contribute or subtract from inflammation in the body. Inflammation causes the body to release the anti-inflammatory compound "cortisol." If you google "cortisol hippocampus neurons NIH" you will be presented with some very technical peer reviewed and published studies that all say that elevated cortisol levels are responsible for killing the neurons (wiring) that connect different parts of the brain, and cause autism and Alzheimer's ! ! !See More

Nutrition facts, calories in food, labels, nutritional information and analysis – NutritionData.com

nutritiondata.self.com

Find nutrition facts, including food labels, calories, nutritional information a...nd analysis that helps promote healthy eating by telling you about the foods you eat.See More

 

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By Julie Bailey Obradovic:

"Imagine you are the victim of a violent crime. You don't remember it happening, but you are left with permanent, life-altering damage.

Your parents were eye witnesses. Your friends and extended family members were too. They all positively identified the perpetrator. They are willing to go under oath to testify to what they saw. You go to the police. They reluctantly investigate, but low and behold, they find the finger prints and DNA on the weapon and all over the crime scene. Your wounds match the weapon precisely. You hire a private investigator who finds the same things. The case is a no brainer. You are not worried.

But then, something strange happens. The police give the investigation over to the accused. They start interpreting the evidence their own way. Slowly, they are being exonerated. You object. They don't care. 

The case goes to trial. At the trial, the judge dismisses all of the eye witness testimony as irrelevant. He dismisses the evidence from your doctor. He dismisses the original police findings. He dismisses your private investigator. All that he uses to decide the guilt or innocence of the accused is the accused's version of events. They walk free.

The judge tells you and your family you are pathetic, desperate, money-grubbing low-lifes who are immoral and dangerous. They warn you not scare others. The police and the accused go after your private investigator. They go after your doctor. They go after your reputation.  They tell everyone they are the victim, not you. You continue on anyway.

In your quest for justice, you discover there are thousands and thousands of people just like you with the exact same story. You discover the police, the judge and the perpetrator are all best friends. You discover the evidence has been tampered with, destroyed, or lost. You discover some victims, whose evidence was so damning and so over the top, secretly got compensated but had to agree to never speak of it again if they wanted their money. 

You have nowhere left to go. All you have left is the truth and your voice to warn others, but doubt has been planted. People who have known you and your family your whole life wonder if you've lost your mind. They wonder what the truth is anymore. Congratulations. You now understand the Autism controversy perfectly."