Eczema as a Biomarker for a Genetically Susceptible Population

Did you know that you can put tetracycline in Rabies vaccine bait and when you x-ray the bones of the animals that consume it that they will fluoresce?

WHAT?

That Jordan dude jumps around topics like those little jitterbugs in summer on hot pavement.

Maybe.

Maybe not.  I did promise you in “Allergy-Immunity-Hypersensitivity the Hidden Link” that I would tie together the seemingly disparate conditions of immunity, hypersensitivity, allergy; and then reveal how it relates to the topic of eczema.  And I will.  So here it goes:

The 2002 Burton report on Autism [1] has testimony by Stejskal, a drug company insider, who said that their company did skin testing for thimerosal.  It turns out that EVERYONE is allergic to it but only about 20% of the population ARE GENETICALLY CAPABLE OF MOUNTING AN IMMUNE RESPONSE TO IT.  This response would be visible in the wheal and flare of allergy.  And there you go: I just brought you full circle back to the Rabies reference.  There are many ways that you can put a marker into biological agents like vaccines and laboratory created organisms.  You can tag the agents with specific DNA codes, immunofluorescent dyes, or radioactive tracers.  How do we know they aren’t looking for specific frequency flares and logging who has been dosed with what when they put you through a terahertz scanner at an airport?  Who, beyond me, ever even suggested such an outrageous cross-application of technology or ever brought the Stejskal data to your attention?  After all, I read the 2002 report word-for-word, cover-to-cover and nearly went unconscious from boredome (it seemed my dome had been bored out) when I came across their mention of the ICD-960 through ICD-999 codes for vaccine related diseases.  But I sense that you are dogpaddling, tasting seawater and still wondering what that triangular shape is that keeps circling, so let’s dig in:

BOY!  ARE YOU SENSITIVE!

Hypersensitivity Reactions

1)  Allergy/Anaphylaxis

2)  Delayed Hypersensitivity

3)  Serum Sickness

4)  Autoimmunity

EVERYONE is ALLERGIC to thimerosal (mercury SALICYLATE).  Salicylates provoke Serum Sickness.  Ahhh.  You can see that fin start to lower in the water a bit.  Allergy and Serum Sickness are 1 and 3 of the continuum of Hypersensitivity Reactions.  Ooooh.  The crowd makes satisfied noises even if they really don’t know what I just said.  So let me break it down because I am not here just to use 7-syllable words because my larynx might fracture.  This topic goes out in many directions like those modern fireworks with bursts and rings and stars — so put the clips on your Lederhosen and get ready:

Children are injected with vaccines containing thimerosal, a neurotoxic chemical.

MULTIPLE CAUSES OF NEUROLOGICAL DAMAGE

-There are those who say that measles virus is a myelin basic protein mimic that leads to nerve tissue destruction and Autism and they are right.

-There are those who say that vaccines damage intestinal tissue allowing for undigested food and antigens to cross over into the circulation causing symptomology in Autism victims and they are right.  [Except for the bit where he says that vaccines are OK they just need to be safer.  That’s just clinical insanity].

-There are those who say that Mercury in Thimerosal is bad and that it causes symptomology in Autism victims and they are half right.  Mercury SALICYLATE.  Who talks about Salicylate?  The functional part of magic is misdirection, so if the only topic is Mercury, Mercury, Mercury and NO ONE is talking about Salicylate then you know by default that you and the debate is being manipulated.  In my book ICD-999 (www.vaccinefraud.com) I go to great lengths to demonstrate if you ask the wrong questions it doesn’t matter what the answers are.  The reason they can’t find a link between Mercury and Autism is because the cannibals have been hired to run the soup kitchen so you know beans aren’t going to be on the menu.  Beyond that, Mercury has its own neurotoxic signature.  So if they were to be generous or honest then it would be part of the ‘Spectrum’ of brain damage caused by willful biological attack.  The firework is going off on tangents, so stay focused and I will bring you back to the point of ignition:  Salicylate causes Serum Sickness.  Serum Sickness can provoke: Circulating Immune Complex CIC implantation with inflammation and cell destruction; IgE/histamine reactions that cause cell permeability (Leaky Gut anyone? and I’m not talking the famous archeologist); capillary clogging resulting in visible inflammation on the surface of the skin.  Ohhh, now we are back to Stejskal, wheal (IgE/histamine edema) and flare (cytokine cascade erythema) AND Serum Sickness is the reason why you need a lawyer and a doctor for a mommy and daddy to win a case in adversarial court paying out tax money as an award for mitochondrial-associated vaccine sequelae.  (The Poling Case)  EVERY PERSON ON THIS PLANET IS UNIQUE.  That means they will respond in unique ways.  You have a 4 x 4 matrices of damage that can be done with the hypersensitivity reactions and 70 trillion cells in which for them to play out in.  When you factor in all of the Lord of The Rings goblins pouring from the cracks in the form of: Serum Sickness, molecular mimicry, heavy metal toxicity, bowel wall and Lymph Sickness attack, then it is a wonder that children in North America can rub two words together to make a sentence.

POST VACCINAL ACCIDENT PLAY-BY-PLAY WRAP-UP

You have to love that the govern mente as a corporate headquarters never takes responsibility for shooting biological weapons into people.  It is called a ‘vaccinal accident’ or they blame the patient as did Jenner for not having the right ‘constitution’ for accepting the gift of being poisoned.  After all it was Hanna Poling’s bad mitochondria that messed up their plans for a ‘successful’ vaccination.  However, in our universe: she was damaged.  That means that the vaccine was a success.  It was supposed to cause damage.  See the 1972 WHO memos.

http://www.vaccinefraud.com/uploads/WHO_Memo_1_searchable.pdf

http://www.vaccinefraud.com/uploads/WHO_Memo_2_Searchable.pdf

If you are wondering how the branch of the pine tree penetrated your car’s windshield because you avoided a swerving vehicle that made you run over some nails in the road that punctured your tire that put you out of control to careen into a ditch full of Firs then the answer becomes a bit furrier than just: The branch did it.

Hypersensitivity Reactions instant replay:

1) Allergy (thank you Clemons Von Pirquet — what? did you think I forgot the theme?),

2) Delayed Hypersensitivity

3) Serum Sickness

4) Autoimmunity.

We can see that Thimerosal will provide at least #3 Serum Sickness just from the Salicylate and #1 Allergy in 20% of the population and possibly #2 in the other 80%. Measles can attack any tissue thus the brain flame  = #4 instant autoimmunity and the gut buster = #1, 3, and 4.  So, this is where the sparkly stars of the fireworks fade and the planetary ring shoots out from the center:

IF there is gut damage what will happen next?  Well, the intestines contain 80% of the lymphatic system.  This was one clue to what I have coined as the phrase: Lymph Sickness.  Any derangement of the tissue of the intestines or the lymph lining the intestines will allow undigested food to pass into circulation thus being tagged as an antigen and thus causing said food, when consumed again (DELAYED HYPERSENSITIVITY = #2 — BONUS!!!!) to be recognized as a threat.  Do you see now that the classic definition of Allergy based on IgE responses is a fraud to keep you coming in to the clinic for SKIN TESTING to sensitize you to the next thing they want to sell you a neutralizer for ALL THE WHILE THEY ARE PUSHING THEIR FLU SHOTS!!!!!!!!!

Consider the lowly antigen shot used by an allergist.  Most of them contain the hair of the dog that bit you (literally in some cases.  Hope the dog wasn’t rabid) PLUS PHENOL as a preservative!  Now, phenol is one step down from formaldehyde as a potent embalming fluid.  The creators of Thimerosal: Eli Lily referred to Salicylate in their internal documents as PHENOLIC ACID!  So you can see that your allergist is basically VACCINATING you with what is promoted as a desensitizing agent.  The ‘allergy’ shot has all of the components of a vaccine: antigen and adjuvant.  What a scam.  Cause disaster and then profit from the fallout!  Yes, this ranks among the most heinous crimes on the planet that you can see more readily played out in the Veterinarian’s office.  They shoot vaccines into animals that are magnitudes more toxic than the human kind into the bum of Fluffy.  Then Fluffy either gets cancer or hip degeneration that, of course, requires surgery and lots of money.  They do it to people and hide behind the you-don’t-have-allergy lie because they didn’t find IgE.  Because Pirquet equated Hypersensitivity to Immunity to Allergy you know that these monsters that inject these poisons are liars, harmers, maimers and killers.  IgA, IgD, IgG, and IgM, are among the popular ones that you might know about.  The Ig means: immunoglobulins.  They are proteins that glue onto foreign invaders so that the white blood cells can find, recognize and destroy the antigens.  White blood cells even come with a memory so that the next time they recognize the mugshot they can take out single criminals before they turn into a gang.  This whole range of immunoglobulins combine as CICs for that immunity-allergy-hypersensitivity continuum that Pirquet talked about.  Circulating Immune Complexes are the antigen (bad guy) plus antibody (policeman) pairs that clog up the bloodstream, can plug the kidneys and even implant in tissue so that the body recognizes itself as being contaminated and attacks itself.  That last one is the very definition of autoimmunity.  They call it something different in medical texts to cover up the fact that they caused it with vaccines and don’t want anyone to know about it so they also lie and say they don’t know what causes autoimmunity.  The whole time they are describing in detail IgA, IgG and IgM pathologies. [4]  But these are just the named ones that show up in the textbooks.  I didn’t do the lab work so I don’t know if they are holding out on even more.  After all, I already exposed them as liars —

Simple when I say it isn’t it?

Why isn’t anyone else presenting it this way?  Because they have programs to sell you.

But, we aren’t done.  Microbes and endotoxins (antigens secreted by bacteria) can also cross this damaged tissue into deeper tissue or circulation.  Therefore, what we see is not just a big old rubber stamp of Autism but a whole interlocking system of physiological disorders that should have the entire surface of the planet declared a triage zone.  So to complete my point: the endotoxins are proteins so they can provoke an immune response.  Isn’t allergy to Peanuts, and Wheat based on their proteins?  There is all this blather about Gluten when the Gliadin (rarely if never tested for) is the culprit in many cases.  Gliadin is the protein.  Because Gliadin and Gluten are a polymer, the difference is like that between a steel I-beam (Gliadin) and the rivets (Gluten) that hold it together.  Just because Junior doesn’t respond with IgE and balloon up like a beachball with anaphylaxis doesn’t mean there is not an immune component involved in a reaction to foods.  Beyond that, it doesn’t even need to be the food!  It could be that what you are eating feeds the microbes that have overgrown inside the gut allowing the microbes to produce their toxins that then affect the host.  Whether the genetic science behind Blood Type diets is because of the natural development of man or because of the genetic modification by vaccines, is simply academic to the observation that following your blood type with food restrictions works.  Authors go out of their way to delineate Food Allergy as an immune response but relegate digestive disorders, like intolerance and irritants, to other netherworlds.  If we look at an intolerance due to a substance that cannot be metabolized this would also qualify for an irritant.  Yet if there is inflammation associated with any irritant, aren’t we full circle back to an immune response?  Just not the holy cow of the IgE deception.  After all these things have to be processed out of the body.  The white blood cell army is the only way I know that the irritants can be processed inside the body, unless the undigested food in the gut is sluiced out by diarrhea.  I told you this was a very craftily packed firework.

I can only speak to the things I am familiar with.  You can reference anything that Jeffry has written on this topic.  In his multiple articles you will find that the causes and effects of so many other agents historically and in recent times have contributed to this ‘spectrum’ of intentional brain attacks that it really does seem like the goblins won’t end.

http://vactruth.com/2011/09/10/wwii-military-handbook-reveals-pesticide-chemicals-used-in-infant-vaccines/

http://vactruth.com/2011/08/23/vaccine-ingredients-non-ionic-surfactants-tween-80-triton-x-100-nonoxynol-9/

http://vactruth.com/2011/03/25/government-documents-show-ddt-contaminated-milk/

 

With all of this going on, all you need is time for the Autoimmunity to set in because the Hypersensitivity reactions are a CONTINUUM.  It is immediate with the measles virus mimicking nerve tissue.  It may take a while for the intestines as suggested by an internationally famous medical doctor.  We see that in the kidneys and other tissue it may also take some time for the damage to manifest, but the 1972 W.H.O. memos show that those reactions can be turned on or off by those who created the disease with the ease of someone throwing a light switch.  The gut bone is connected to the head bone.  Anyone who has ever had a Yeast overgrowth in their gut will know the autointoxication from the fungal bloom can just about put you to the floor.  So, why the dysbiosis?  Well, considering that Yeast of bread and beer was basically turned into a weapon in the 1980s via genetic engineering, this is one tough goblin to kill.  Beyond that, the immune system, as previously outlined, is so overwhelmed by the other distractions that it can’t multi-task such a strong invader.  It is hard to concentrate on the hot cup of coffee in the holder on your dashboard when you are careening towards a tree branch at 60 miles per hour when the speed limit is 55.

* INTERMISSION *

Worn out?  Take a break.  I’ll be here when you come back.

AND NOW BACK TO OUR SHOW:

So what about the immunity, the allergy (Pirquet said that they were one in the same), and the markers, and the Rabies, and the lions and tigers and bears, OH MY!  ?  In my last book “Assaulted” (www.cafepress.com/icd999) I uncovered a very disturbing pattern in the testimony to congress that was being given by dermatologists who specialized in syphilology. [2]  The dermatologists said that Iodine in certain populations provoked severe acne and herpetiform lesions on the faces of those who consumed it.    Being a nondoctor, I had to reach deep into that mystery bag, feel around for something with a familiar shape and pull out a Hahnemann bunny by the ears.  In homeopathy there are three chronic/inherited miasms of interest to me:  Tuberculosis, Syphilis, and Psora!!!!

Psora is said to be an ancient miasm. [5] Skin lesions like eczema — see I told you this firework had a lot loaded in it — psoriasis, etc.  The focus organs are the bowel and skin, however, the condition can show as asthma with eczema.

The Tuberculinum miasm was called anti-psora before it was renamed.  Whereas Psora is a deficiency condition and Syphilis is a destructive condition, Tuberculinum is a combination of both.  Tuberculosis and its miasm is one part of my theory of why our lymph systems are clogged leading to the disease state that I coined the term: Lymph Sickness.  Coffee antidotes any attempt to bring the Psora out by remedy so it is no wonder to me why such a dangerous and suppressive drink is mandatory for Slave Work Units to keep them functional and without the obvious MARKERS (the theme of this article) of disease that Hahnemann suspected affected around 85% of the population.

A reviewer of my work offered an insight that when children with deep neurological autistic conditions are healing then eczema often surfaces as a sign of the exit of the miasm and healing.  However, doctors love to drive it back in with a steroid.  Avoidance of chasing the condition back in from the surface is warned about in reference #5 and the work of those using Iodine therapy who claim that fungus being chased out from the lymph system should not be treated topically because it risks pushing it deep into tissue where it may not be able to be removed.

When you look at the history of vaccination you find that syphilis (while typically attributed to lonely sheppards and invading colonists) was engrafted directly into the human population via cow pus or human pus since the days of Jenner [3], which coincidentally crossed over with Sam Hahnemann’s time period.  The implication being that if you were operating in the days before computerized labs with immunofluorescent tags, radioisotopes or other ways of tracking who got what poison, then the simple heartbreaking outbreak of acne vulgaris or skin rashes on the face would tell the smug observing Overlords that their experiment and population coverage was successful.  It would be a MARKER.  TB as you will find in the work of Crookshank (www.cafepress.com/icd999) came from the milk supply, vaccination, and just poor hygiene.  Within a generation later our buddy Pirquet would make sure that everyone got a nice miasmic dose of it with his TB ‘test’.  In my previous article “Allergy-Immunity-Hypersensitivity the Hidden Link” it is my nonmedical view that skin testing GIVES you a disease that you may have never had before.  When you consider the continuum of allergy, immunity and hypersensitivity even if there are no outward manifestations of disease or provocation as seen in the wheal and flare after the allergist attempts to conjure a reaction, the substance may be sitting there quiescent until there is a resensitization resulting in delayed hypersensitivity and then the continuum, well — continues.  You will have left the office with the assurance that you are not sensitive, allergic or reactive to a substance when you might have been primed for a new condition by the very person you went to and paid to relieve you of an unrelated but active condition.  This is brilliantly Evil.  We need only look at the work of Richet in 1902 where he claimed that taking a toxin from a sea urchin and injecting it into a test subject (victim) causes immunization that was said to be prophylactic.  A protection against the substance or disease.  However, if he repeatedly injects the toxin into the same victim they become anaphylactic.  This is precisely Clemens Von Pirquet’s continuum of hypersensitivity.  So you tell me how much sense it makes to submit to allergy ‘testing’?

Now pay attention:  In the first article I mentioned that Pirquet was studying Scarlet Fever infection that led to nephritis, which he called KIDNEY ECZEMA!!!

Put that in the mystery bag, shake it up a bit (don’t mind the noises and squirming) and we can see that Stejskal saying that EVERYONE was allergic to thimerosal but only 20% of the population was genetically capable of mounting a skin reaction to it should scare the ureen out of you.  That means that 80% of the population could be harboring this SYSTEMIC REACTION, for that is what Serum Sickness is, INSIDE their bodies festering like Kidney Eczema but completely unseen and unknown until it is too late.

Dr. Suzanne Humphries who has written brilliant papers on the topics of vaccines and renal disease commented:

“Too late’ meaning they go to the doctor because they smell like urea, or are extremely ill because their kidneys no longer filter the blood.  Death will then ensue without dialysis.  This process can take weeks, months, years.”

http://drsuzanne.net/

For those trying to decide on the use of vaccines or not: These are the Door Prizes that EVERYBODY leaves with.  This is not a russian roulette of syringes where maybe you might dodge the boulette.  You are going to get damaged whether you see it or not.  For all of the grief that eczema and other outward signs of internal disease causes us consider this:

EVERYONE who told me they had stage 4 cancer said they were never sick a day in their lives.  If you have no functional immune system you have no immune reaction and Pirquet taught us:  Measles rash is NOT the disease.  It is the result of the impact of antibody/antigen pairs clogging the capillaries!  Can you see it?  I hope you do.  I know I am verbous, but it is really hard to capture the sparklies and push them back into the firework package so that you can see it as a whole.  The skin rashes are the body’s System Status Board that tell you that something is wrong on a systemic level.  Let us examine local vs. global reactions to the Hypersensitivities:  Allergy can be a runny nose or red eyes (local), or where-the-hell-is-the-epi-pen? anaphylaxis.  Serum Sickness can be the ‘some adverse reactions may be swelling and inflammation at the injection site, fever, joint pain, malaise’ (false local) because Serum sickness, by the time it gets to your joints, has already gone systemic.  The word “serum” implies systemic because the blood vessels and the blood are considered connective tissue.  In simple terms it means that they connect to every single cell in your body and sent the message to your brain to heat up.  Your body wouldn’t mount a fever unless the invader overwhelmed the entire system.  And Autoimmunity — well, who cares if it is just your brain or your pancreas or your bowel?  It is your body eating itself up because it saw its own cells as the enemy due to the CICs and then released oxidative chemicals to dissolve the CICs and the cells.

SO WHAT ABOUT THE ECZEMA?

Thanks.  Glad you asked.  For a while there I thought you had forgotten.

Got your knickers cinched up?  Because this is going to be another of those wild rides.

Because the hawkers have their programs to sell, and they make disclaimers that the results may vary for the different desperate doers of their doctoring, they will attribute the cause of the skin lesions to one thing.  When you evaluate the Atkins diet against the Blood Type Diet, of course it will work for the majority of the population in the USA because they are Type-O.  That is just probability.  I am compiling a list of symptoms that are common to those who claim that if you have them then you JUST have Candida, or JUST a thyroid condition, or JUST a clogged gallbladder, or JUST chemical allergies (ooh, hey, back to allergies).  But, when you peel back the layers you find that a primary failure of the thyroid can lead to bad bile that leads to gallbladder problems that lead to the gut not being sterile that leads to microbial overgrowth that leads to food and chemical allergies.  So, then wouldn’t the prudent question be: What took out the thyroid?  (or other primary organ).  Given that Congress was obsessed with causing undetectable goiter, they held the 1947 Hearing [2] in which a large topic during the testimony was skin lesions of the face.  The thyroid seems like a likely place to start.

But, I won’t even bother to try to pin the tail on the eczema.  Just like the Autism spectrum that is nothing but a cover for a total attack on the brain via as many agents as they can possibly deploy, the eczema is just one of those MARKERS that proves they were successful in their deployment.  More insidious than that is that they can track you by these skin reactions as being “One Of Those!”  “Those”, would mean the kind of people who genetically respond to their poisons thus making it difficult for the enemy to hide their poisonings below the threshold of perception.  After all, 80% of the population is completely unaware that they are suffering from systemic Serum Sickness and festering a long term illness like a fermenter vat.  Think about this: skin rashes from Iodine would prevent people from taking Iodine that is essential for health.  The rash tells the victim that something is wrong and needs to be taken care of, but the results of that specific intervention causes a negative feedback thus dooming them to the ill health inflicted on their ancestors and them.  The manifestation of the disfiguring skin lesion tells those who caused it that the Miasm has been set in the genome or deep in the tissue.  Personally, I don’t care about appearances — I want resolution.  I continue to take nascent Iodine to chase the disease out from inside the lymph so that it will be exorcised from the body.  Remember the warning that some practitioners advise to not treat these skin conditions from on the outside because if they are from something like Candida you can drive it deeper into the tissue where it is nearly impossible to extract.

One person wrote me to say that my first article allowed them to see patterns that had bothered them for some time but were unexplained.  The goal of this article is to show that if you are upset about the eczema on your skin that makes you or your child look bad and hesitant to be seen in public, plus causes pain and discomfort, then how much more should you be alarmed at the eczema INSIDE your body that you cannot see that is destroying you or your child from the inside?

I have no program to sell, so I will also cite Hulda Clark who says that if you have a very tough infection of roundworms that their molting chemicals cause eczema.  Until you get rid of the worms you will never get rid of the skin lesions.  So which one is it?  This is why I don’t take sides or make a declarative statement.  It could be either or both!  How would I know?  Everyone who has ever been vaccinated has been permanently damaged.  Anyone who has ever owned pets or goes anywhere other than a hermetically sealed bubble will be exposed to roundworms (yes, in North America where even the Merck Manual says you can get Dog Heartworm).  [ok, that bears explanation: Visceral Larval Migrans is where the larvae crawl through the human body like a pile of dirt looking for the genetic material of dog heart.  This can go on for several years until the worms die inside your now-swiss-cheesed body.  This intense crawling feeling will, of course, be attributed to a psychiatric disorder (like Morgellons is) because the Psychiatrists are the lowest paid of the medical profession and they need market share.  After all, no one REALLY reads the Merck Manual—]

Summary:  What caused our problems?  The hypersensitivity continuum.  Where did this continuum come from?  One source: the end of a needle.

Strategies?

This is the second in a series of scary articles on what they did to us, so what can we do about it?  Of course number one would be to avoid the assault.  Number two would be to remove the allergens.  Number three would be to dampen or shut off the hyperimmune response.  Generalizations, I know, but not a bad plan.  But not a good one.  We are living in a world where they invent new diseases faster than designer jeans.  Even if that were not so, then my latest postulate that I think is unique in the world of Alternative Machinations is that the lymphatic system is a reservoir of disease.  So, that even if  you were to clean out your bowels of Candida or other offenders, that this then becomes new grazing land for the amoeba, bacteria, fungus and other organisms that were waiting back stage behind the curtain.  This may be why Lyme victims treat and then relapse (well, beyond the indiscriminate use of antibiotics taking off the cell walls of the organisms making them go stealth deeper into the tissue).  See, I told you this firework was complicated.  What does that mean, though?  It means that no matter what ‘therapy’ you try, there is an unlimited supply of goblins waiting to come out the cracks of the lymph system (hence my concept: Lymph Sickness) so that you have to continually mow them down as you would a lawn until you can come out with the tiller and take it out at the roots.

Do you remember that ALL of the goblins retreated when the Fire creature awakened?

 

References:

1. The Status of Research into Vaccine Safety and Autism, The Burton Report, 2002.

2. Hearing before a subcommittee of the committee on interstate and foreign commerce house of representatives eightieth congress first session on h. R. 2717 a bill to amend section 301 of the federal food, drug, and cosmetic act, so as to prohibit the introduction into interstate commerce of salt, for table use, not having a required content of iodides ; JUNE 11, 1947

3. The History and Pathology of Vaccination, 1889, Edgar March Crookshank; and Jenner and Vaccination; A Strange Chapter of Medical History, 1886, The Natural History of Cow-Pox and Vaccinal Syphilis, 1887, Charles Creighton

4. Oxford Textbook of Clinical Nephrology, 1992, Volumes 1-3.

5. http://www.homeoint.org/morrell/articles/pm_psori.htm

 

 

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About the author

Patrick Jordan

Patrick Jordan likes to call himself an Illinois Farmboy. Regardless of truncated higher education, and his experience in a wide variety of american industry employment, pattern recognition is the only thing that sets apart those who are intelligent from those who will perish for the lack of such a survival trait. Memory, too, is a survival trait, for, if you had vast life experience and 30+ years of investigative research to draw from but could not remember it, then you would still be fodder for the machine that intends to consume us all. Patrick has found that it took 6 books to explain just the basics of what he calls Planetary Military Occupation using the Medical Manhattan Project that goes beyond singular topics of Autism, Morgellons, Cancer, etc. to show that it is all a combined generational plan to subjugate and genetically engineer mankind. Knowledge is power so the first step is to identify the Predator, next alert the herd, then neutralize the threat. That last part is up to you.