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The Throwback Collection of Morgellons Specimens

In the first three years I suffered with Morgellons disease I was totally on my own.  All I knew was that I had something on and in my body that I could see and feel but my doctors were trying to tell me I was having delusions of parasites.  They also told me the ulcerous sores on my body were the results of self excoriation.  I made all of the classic moves like bringing in fibers to show the them.  The humiliating treatment I received from the medical profession only succeeded in making me very angry and fueled my great determination to prove them wrong.  I thought that I was the only person going through this misery and didn't learn for several years that other had these same symptoms.

In the beginning I was  looking for something with a logical and biological explanation.  I was not into any sort of  conspiracy theories.  I simply thought I would get a microscope and study what was on my body.  I believed  that with enough studying and looking through the scope that I would identify what disease I had from a known database of recognized diseases.  I began a 3 year study of all fungus, cyanobacteria, chytrids, rotifirs, algae or anything else I could learn about that might be a clue to this mystery.

Eventually I looked at the Internet and typed some symptoms into a search engine.  I was amazed and excited that I found Mary Leitao's Morgellons website.  I contacted Mary and started working with her.  I asked her about the name “Morgellons”.  She had taken it from a 1690 monograph by Sir Thomas Brown who described a condition in children that included copious growth of hair on their backs.  I can't say that I agreed with her choice to use that particular name for this illness but I supposed it sounded more medically correct than what I have been  calling it which was “the crap.”   

During the time I worked with Mary she was able to get some of my Morgellons samples into a lab at the University of Pittsburgh.  They underwent testing using Fourier Transform Infrared Spectroscopy.  They were found to be hollow, auto fluorescent and to contain cellulose but no chitin.  From my earlier study of mycology I knew that the absence chitin ruled out any fungus since all fungus contains chitin.  At that time I got a letter from Mary and with some micrograph images taken by the lab.  Due to a computer assault  from  an evil anti-Morgellons website I no longer have copies of these.  Apparently the samples were quite a sensation at the lab and could not be readily identified.  There were to be further studies done and frozen cross sections for further testing had already prepared by the lab.  Shortly thereafter I learned that the University had told Mary they had no time to work on it.  This was surprising since it was a unique material with many unanswered questions and this was, after all, a University where I would hope knowledge would be valued. I began to wonder why the Morgellons research had been dumped like a hot potato.  

Several years later more fiber samples from my body were determined to be made of HDPE ( high-density polyethylene) by another researcher who paid to have them tested at several accredited labs.  There are differences in the fibers since some are round and some are more ribbon-shaped.  There may also be a difference if a fiber directly enters the body from the environment or if it is a second or more generation product of self replication that occurs in the body. 

In later years it was apparent to me that the bizarre nature of my Morgellons  findings were unnatural and likely from a man-made source.  It was not a pleasant journey as I began to "wake up" to what was happening in this altered reality.  Much to my dismay, all roads carried me to the same conclusion and still do.  The pathogens in my body came from a bio-lab and have the hand of man written all over them.  It occurred to me that if these pathogens were being bioengineered in a lab that they were made of multiple components and that the mutated material might reproduce and intermittently send out a batch of identifiable debris much like the original genetics.  I call this type of debris “throwbacks”.
 

The multi-component part of my theory has proven to be true.  Read my paper entitled:

"Revelations From a Man Who Helped Design Morgellons Disease"

(RE: Dr Gwen Scott and her admissions from a government scientist)

It is my theory that when new life forms or designer diseases are created in bio-labs using the processes of gene splicing, mutation, bioengineering or nanotechnology that components of these mixtures can self replicate with varied results.  Components such as dictyolstelium discoidium, insect genes, and other pathogens will continue to make some new mutations in each generation of self replication.  I believe that some of these mutations "throw back" to expressions similar to the original materials used in the lab created mixture.  Specimens from Morgellons disease tissue can sometimes be identified as nearly identical to the original components used in this biological witches brew before the mutation process.  It is not unlike finding a child with flaming red hair in a family of people who do not have this characteristic. 

The information in this paper is only my personal theory but it is the best explanation I can find to make sense of all of the strange artifacts that come from people with Morgellons disease.  It is also why I think that some of these strange findings occur most frequently in the early phases of the disease and do not repeat as often in later years of the disease.  I will later discuss a strange cellular slime mold known as dictyostelium discoidium. It is all about using the genetic characteristics of this cellular slime mold to produce mutations in a bio-lab.  I believe it is one of many parts of the Morgellons story.

Most of my “throwback” findings only appeared in the beginning of the disease when I had multiple lesions and things were at their worst.  That was about 7 years ago.  I had tentatively identified some of the debris as members of 3 varieties of the Oomycota phylum of pseudo fungus.  There are over 500 varieties and many of them can have ill effects of humans, animals and plants.

The varieties of oomycota can produce diseases like pythiosis, lagenidosis, rhinosporidosis, downy mildew, blue tobacco mold, the fish disease saprolegnia (Ich) and the infamous phytophthora infestans that had killed millions in the Irish Potato Famine by blighting the spuds. 

I had also found bizarre mutations of earthworms and other material that looked like dictyostelium discoidium.  The reason that the dictyostelium discoidium is important is because this cellular slime mold has unique properties that lend itself to mutating other substances.  These eukaryotic microorganisms have a simplistic genetic makeup and produces what are know as chemotaxis.  Dictyostelium is utilized in many labs to specifically mutate other material.  Dictyostelium has an amoeba form along with many other stages of varied shapes and configurations as the individual cells emerge into groupings that look like  larger single entities. 

“Dictyostelium amoebae grow as separate, independent cells but interact to form multicellular structures when challenged by adverse conditions such as starvation.  Up to 100,000 cells signal each other by releasing the chemoattractant cAMP and aggregate together by chemotaxis to form a mound that is surrounded by an extracellular matrix.  Processes depend on cell-cell communication in  Dictyostelium.  Many of the underlying molecular and cellular processes appear to have arisen in primitive precursor cells and to have remained fundamentally unchanged throughout evolution.  Basic processes of development such as differential cell sorting, pattern formation, stimulus-induced gene expression, and cell-type regulation are common to Dictyostelium.  It is used in gene research as well as other uses” (dictybase.org).

Even if you have never before heard of dictyostelium discoidium you may be quite impressed to go to this huge website that is well funded and part of the Human Genome Project and NIH.  This cellular slime mold is a major player in many aspects of medicine and cell research.  It is a good bit of information to have for future reference.  I encourage everyone to take a look at photos and videos of this substance at  http://dictybase.org/

    The many configurations of Dictyostelium: 

Each shape is comprised of hundreds to thousands of single motile amoeba cells acting in unison to form each of these configurations.

Take a good look at the photos below.  There is a definite presence of Dictyostelium in the tissue from Morgellons victims.  This can only mean that our disease is man made in a bio-lab.  The pathogens we have are no doubt a mixture of the Dictyostelium and other pathogens that were purposely mutated with it for a deliberate purpose.   Dictyostelium is not normally a pathogen to humans.  It feeds on bacteria and under normal circumstances a human is not a good host due to lack of bacteria and a body temperature that exceeds it's ideal gestation temperature of 72-77 degrees Fahrenheit.   It is obvious that the dictyostelium has been mutated to even be able survive on the human body.

 

A lawn of starved Dictyostelium amoeba cells is imaged using phase contrast microscopy. Cells signal via spiral waves of cAMP, and population territories form with a fruiting body in the center of each.

 

Dictyostelium Discoidium Life Cycle

cAMP receptor 1 (cAR1) of Dictyostelium couples to the G protein G2 to mediate activation of  chemotaxis, and cell aggregation.

Amoeba formation as found in Morgellons

Unusual antenna formation on amoeba

Spiral geometry of a signal transmitter cAMP in an amoeba population (Dictyostelium discoideum) leads to chemotactic movements of cells in direction of the spiral core. This is the signaling phase where cells communicate and aggregate.

Streaming pattern
of cells towards the aggregation center

 

Jan's Photo  Tentacles (dictyostelium)

The left photo shows the beginning and ending phases of dictyostelium metamorphosis.  The photo on the right is the translation of mutated dictyostelium as found inside a lesion on the human body. The formation of the dictyostelium component continues to mutate and vary. This one throws back to to the original morphology.  Other specimens  take the tentacle form and do not   elongate and produce the bulb on the end. The basic forms are apparent but the actual function of bulb on the top producing sporulation is now gone. 

~~~~~~~~~~

From: "Texas Medical Center News"
Vol. 21, No. 18  October 1, 1999
Genome Studies of Slug Might be Applicable to Humans
"Dictyostelium consists of only six chromosomes and approximately 8,000 genes. The DNA in those genes comprises 34 million pairs of chemicals called bases that contain instructions for the role each gene plays. "
"By "knocking out" or deleting a gene and observing the effect of the mutation on Dictyostelium's development, Dr. Kuspa can determine the gene's function. It takes only a month to generate a mutation in Dictyostelium, but in a more complicated genome, such as that of a mouse, the process can require six months to a year.
"We have developed methods that enable one laboratory researcher to mutate 100 Dictyostelium genes within a month," Dr. Kuspa says."
~~~~~~~~~~~~~~

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Here are some of the “throwbacks” I found in my own tissue from the phylum oomycota (o-o-my-CO-ta)  3 photos of saprolegnia zoosporangium.   

1.Saprolegnia from my body 200x

 

 

Saprolegnia  oospores web photo

 

 

 

2. Saprolegnia zoosporangium 60x

    from my body.

 

  3. Cluster saprolegnia 200x from

        my body.

 

These are not the original coloration as shown except for small image on lower left fibers were dark  blue, bulbs on the ends of fibers were brown/red.  The bulbs (zoosporangium) would fall off as a separate component.  I only found this formation twice, about 5 years ago.

 

Saprolegnia  oospores - 200x my body

 

Saprolegnia oospores web photo

 

The photo below is not from my body but I did find a specimen exactly like this.  I was able to get a drop of the clear sticky liquid that came out of a lesion onto a slide.  At a magnification of 350x I found a tiny but uniquely distinct shape on the slide. I could not then identify it but I described it to Mary Leitao as a clear snake skin with tiny round circles in it. I was sure this slide would be a breakthrough for the research but unfortunately that did not happen.

 

I did not have a microscope that I could take a digital image with at that time. I did have a scientific microscope.  I sent this slide to Mary Leitao who is a trained biologist.  She looked at it and acknowledged the specimen on the slide.  She forwarded that slide and many others to Dr. William Harvey who was then in private practice.  The slides were said to have been “lost” during a move by his office.  Formerly Dr. Harvey had worked for NASA full time and at that time was still the Chairman of their Educational Advisory Board.  I must admit that I still question what happened to my slides.  I later identified the missing specimen myself as Dictyuchus from a web photo.    

 

Dictyuchus  Species of Oomycota

 

All of the varieties of oomycota  I have mentioned thus far are related to the fish disease known as Ich or Saprolegnia.  I do not believe that Morgellons victims have a pure strain of this disease but I do believe that some of the genetics were used from this disease in the bioengineered mixture.

 

Fish with saprolegnia (Ich) lesion ,,,,,,,,

 

Saprolegnia Fibers in Nature (blue and red)

 

I believe that other varieties of the oomycota family have been put into the mix as well.  I have previously found this star fish shape in my lesions. I know that others have found them as well

 

Top photo: Oomycota Peronospora Tabacina or blue tobacco mold

 

 

Photo from " Blue" Morgellons victim.

 

 

This is the last of the oomycota from my body.  I have found a few of these grooved, coffee bean shaped pieces in the past but this one was found only a few weeks ago.  This zoospore is Phytophthora infestans, the villain in the Irish potato famine. This is a motile zoospore powered by two flagellum. One is a long whiplash flagella and a shorter one is the shorter tinsel flagella.  When these zoospores are threatened they encyst and can hide out in their encapsulated form for a very long while.  Sometimes they release the flagellum and in other instances they retract the flagellum and they become encysted as well.  The whiplash flagella has a shape similar to a worm-like structure I often find which I call the motile strand. The composition of oomycota is cellulose and glucans which store mycolaminarin and is a form of sugar.  If glucans and cellulose are added to the human body could the results of this addition = excess sugars and carbohydrates = diabetes? I wonder since I have recently been diagnosed with it and there is an epidemic of it in this country.  I will search for answers and write a follow up.

Web photos of phytophthora infestans compared to Morgellons motile strand.

This is what I found in a lesion on my body.

According to Wikepedia
Phytophthora infestans Potato blight was one of more than 17 agents that the United States researched as potential biological weapons before the nation suspended its biological weapons program.[15][dead link] France, Canada, USA and the Soviet Union also researched P. infestans as a biological weapon in the 1940s and 50s.[16]
Do we really believe that this former candidate as a biological weapon was discontinued by the Government? What a coincidence that it is turning up in the tissue of Morgellons victims.
 

What I do know thus far is that some of the motile (moving) strands found on my body were tested with Raman Spectroscopy in the labs at  SUNY Stony Brook.  The results were surprising to me at the time since I expected the fibers to be silicon or HDPE (high density polyethylene) due to previous results of other types of Morgellons samples that had undergone professional lab analysis.  

These strands were made of an indeterminate kind of polysaccharide (sugar substance- polymer and other unknowns).  More testing was to be done on this material but this was not possible since the researcher, quite suddenly, was no longer allowed to use their lab.  Funny how any progress on Morgellons research seems to end suddenly as soon as the research results are posted on the Internet.

I wondered how many sugar/polysaccharide based organisms could produce motile strands with independent movement.   Once again I could only think of the zoospores of the polysaccharide based oomycota and the whiplash flagella of pythium insidiosum.  There are some chytrids that produce motile zoospores but not in long stranded fibers.  All roads lead me back to my original conclusion of oomycota.

The researcher, Biologist Mark Darrah, nicknamed these Sugar Snakes.  The coloration varies with these strands.  They are sometimes a white crystal-laden translucent coloration and vary to brown or black as well as striped mixtures of several colors. The high magnification that was used by Mark Darrah clearly shows a striped banding on the structures.  Mark shined a laser light on one of the strands and it literally melted.  There is a deformity in it's surface at the top left of the photo below.  Here is what he stated to me in about this: “This is a pimple that formed when the laser light hit it demonstrating heat sensitivity.”

To see more of Mark's work go to: Mark Darrah Research

There are 7 pages of his lab photos at this site. 

Sugar Snake #2 (note tiny crystals)

Sugar Snake  #3 (note red fiber)

 

 

 

 

The question I have now is are the materials in these strands related to the beta glucans in the oomycota?  The cellulosic compounds and Beta-1,3-Glucans in oomycota form a natural polymer in it's original state.  In this bioengineered state what is the purpose of the material as it is being introduced to our bodies through many vectors?  The answers are rapidly coming into focus. 

After further research I have determined that the specific strains of oomycota that I have found in my body all contain soluble Beta-1,3-Glucans.  This is an important new discovery since out of the 500 species of oomycota only a small percentage contain this Beta-1,3-Glucans characteristic.  All of the oomycota species I identified as throwbacks have this Beta-1,3-Glucans in their makeup.

What are the odds of that?

At the original time I did the oomycota research which started 5 years ago there was no immediate connection I could even imagine to link my oomycota samples to biotechnology or nanotechnology.  I had not yet found the other nanotechnology items that surfaced in my body which I have since identified.  Read "Living With a Nightmare" for more information.  It has only been lately that I revisited the past and decided to see if there was somehow a nano or bio lab connection with my earlier finds.

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These are the types oomycota I believe I have found :

Saprolegnia,

Dictyuchus,

 Phytophthora.

Peronospora Tabacina

I identified these oomycota species 5 years ago with no thought in mind to ever match them to any data.  The odds against finding these particular oomycota specimens and making a meaningful match for them is astronomical.  The article below regarding cothe surprising characteristics of Beta-1-3 glucans  was a fortuitous find in my recent research.

Oomycota will support the self replication process of the nanos.

"A soluble Beta-1,3-Glucan Found in Selected Genera of Oomycetes"
From here: http://mic.sgmjournals.org/cgi/reprint/72/2/393.pdf
“The polysaccharide extracted from each organism was water soluble and had an infrared spectrum very similar to the glucan of Phytophthora and Achlya. The infrared spectra of the glucans of Phytophthora, Saprolegnia, Dictyuchus and Pythium are identical."
Further investigation from other sources state that Peronospora Tabacina or blue tobacco mold also contains the Beta-1,3 Glucans.

http://www.plantphysiol.org/cgi/content/full/117/2/585
Now that I have established the probable presence of the Beta-1,3-Glucans by way of oomycota in Morgellons victims, the following article which I recently found is not a coincidence.  The law of averages ran out a long time ago for this to be coincidental.  I believe we are looking at a huge puzzle piece in the Morgellons mystery. 
What could oomycota possibly have to do with biotechnology or nanotechnology? Please read the following article.
"Beta-1,3-glucan polysaccharides as novel one-dimensional hosts for DNA/RNA, conjugated polymers and nanoparticles."
Sakurai K, Uezu K, Numata M, Hasegawa T, Li C, Kaneko K, Shinkai S
 http://www.ncbi.nlm.nih.gov/pubmed/16136229
Department of Chemical Processes and Environments, Faculty of Environmental Engineering, The University of Kitakyushu, Hibikino, 1-1 Wakamatsu-ku, Kitakyushu, Fukuoka, 808-0135, Japan.
Beta-1,3-glucan polysaccharides have triple-stranded helical structures whose sense and pitch are comparable to those of polynucleotides. We recently revealed that the beta-1,3-glucans could interact with certain polynucleotides to form triple-stranded and helical macromolecular complexes consisting of two polysaccharide-strands and one polynucleotide-strand. This unique property of the beta-1,3-glucans has made it possible to utilize these polysaccharides as potential carriers for various functional polynucleotides. In particular, cell-uptake efficiency of the resultant polysaccharide/polynucleotide complexes was remarkably enhanced when functional groups recognized in a biological system were introduced as pendent groups. The beta-1,3-glucans can also interact with various one-dimensional architectures, such as single-walled carbon nanotubes, to produce unique nanocomposites, in which the single-walled carbon nanotubes are entrapped within the helical superstructure of beta-1,3-glucans. Various conductive * polymers and gold nanoparticles  also entrapped within the helical superstructure in a similar manner. 
 *The original "goldenhead fiber" came from my body. I subjected this HDPE fiber to a 30 second burn test which revealed the gold nanoparticles. It also demonstrated the heat resistance of the material it is made of. I later sent this burn experiment fiber to researchers who identified the composition of materials.
In addition, diacetylene monomers entrapped within the helical superstructure can be photo-polymerized to afford the corresponding poly(diacetylene)-nanofibers with a uniform diameter. These findings indicate that the beta-1,3-glucans are very attractive and useful materials not only in biotechnology but also in nanotechnology. These unique properties of the beta-1,3-glucans undoubtedly originate from their inherent, very strong helix-forming character which has never been observed for other polysaccharides. (Editors Note: human DNA is a helix)
(This article was found at Pubmed the rest of the article is only available by subscription)
Note: The number 3 in Beta-1,3 glucans indicates 3 carbon atoms. The next articles is also about the use of sugars with 3 carbon atoms in nanotechnology applications aimed at DNA replacement.
http://www.scientificblogging.com/news_releases/gna_
dnas_chemical_cousin_is_a_nanotechnology_building_block
Chemical Cousin of DNA Provides New Nanotechnology Building Block
“In the case of GNA, the sugar is the only difference with DNA.  The five carbon sugar commonly found in DNA, called deoxyribose, is substituted by glycerol, which contains just three carbon atoms.”
“The only chemical difference between DNA and a synthetic cousin, GNA, is in the sugar molecule. GNA uses a three-carbon sugar called glycerol rather than the five-carbon deoxyribose used in DNA. The sugar provides the chemical backbone for nucleic acid polymers, anchoring a phosphate molecule and nitrogenous base (B). Credit: Biodesign Institute at Arizona State University.”
There is proof that not only do I have nanotechnology on my body but there is significant proof that the other pathogens I am finding

 

 

~~~~~~~~~~~~~~~~~~~~~~~~~~

 

The Indications of Annelids (earthworms) in Morgellons Debris

Here are some odd finds I made a few years back. I am only glad that I have not seen any of these recently.

Web photo of an earthworm cocoon

Cocoon mutation from inside wrist lesion view 1

Cocoon view 2

Cocoon view 3

Cocoon view 4

Mutation 2 Cocoon view 1

Mutation 2 Cocoon view 2

More clues about earthworm    genes 60x   

Creepy worm fiber replaced hair bulb 200x

It is no surprise to me that people with Morgellons often find insect-like creatures in their lesions. I believe these throwbacks can be whatever genetics are part of the brew. It may vary in different people as to what they may find. There are vectors that seem to be actual mutated insects that carry Morgellons.  It may be a function of their own genetics as to what manifestations develop.  Could these worm genes now be a part of the polysaccharide “Sugar Snake?”  Here are more mutations to ponder.  Which part is the worm and which is the polysaccharide?  Some throwbacks can't make up their minds.

 Plastic-like worm 

 

Polysaccharide Strand with swelling.

Points to ponder:   Many people with Morgellons disease have noted that they rarely get any bacterial or secondary infections in the lesions.  The dictyostelium are eukaryotic microorganisms that eat bacteria as their sole food source. (they also produce ammonia)  Normally there would not be enough bacteria on the human body to keep dictyostelium adequately supplied with it's fuel.  There have been findings in Morgellons victims  by other researchers of mycoplasma and chlamydia pneumoniae which are both bacteria that are especially difficult to kill on the human body.

Recent reports have come in from others with Morgellons disease who state that in clinical testing there is a nearly complete a lack of healthy bacteria in their intestines but there other harmful bacteria in their bodies.

The need for probiotics and Diflucan or cellulose eating products that contain cellulase and hemicellulase like Candex or NSI Candida yeast Management Capsules becomes necessary.  These types of products may be helpful for overgrowth of cellulose combined with the lack of beneficial  bacterial flora in the body.

 This lack of beneficial bacterial flora would be further evidence of the dictyostelium feeding on the beneficial bacteria in the body.  There is anecdotal evidence that that if sugars and carbohydrate consumption are lessened it may help to lessen the negative impact of lesions and symptoms.  The pathogen that I believe many have is a mixture of oomycota and the dictyostelium.  Just like Candida which has cellulose as a component the oomycota has cell walls of cellulose.  The human body has no way to rid itself of cellulose.  Feeding the body carbohydrates which will ultimately become sugar overgrowth due to lack of good bacteria in the gut, seems support this cellulose growth.  To lessen the cellulose growth, carbohydrates are best kept to a minimum.  Since I have had type 2 diabetes this past year and have had to alter my carbohydrate intake, my skin manifestations have lessened.  Two other people I know have tried this and have had many of their skin symptoms abate.  It is certainly not a cure but it may be helpful to know if skin symptoms are especially aggressive.   Unfortunately the internal nano wiring and and other body symptoms have remained largely unchanged. 

Could it be that some symbiotic balance is being kept in the grand scheme of things to create a favorable environment for the dictyostelium,  oomycota and other genetic bio-mixtures to live well and prosper?  In the bigger picture most things found are serving a purpose and act together.  These are not all random things thrown into the mix without thought or  purpose.  To find the answers, all of the components must be looked at as a whole system. 

Along with that we have the presence of Beta-1,3-Glucans from the oomycota varieties which are known for their anti-tumor effects and beneficial effects on the immune system.  How nice of them to throw out a health bonus.  As I have just mentioned it is also known for it's ability to produce an environment for the development of nano machines and bio-engineering.  Take a look at my photo journal and see the many categories of wires and components inhabiting the human body.  This is not random.

Consider the implications of the bigger picture and the fact that most people without symptoms have had the same exposure to the same chemtrails and tainted food as Morgellons victims.  These people may simply be assimilating the technology without problems or symptoms.  Morgellons disease may actually be the lack of ability to assimilate the crap they are dumping on us due to an aberration in our immune systems or our genetics.  This aberration was probably unforeseen by those who are doing this to us.  As such it is an unwelcome circumstance that is being ignored, ridiculed and constantly monitored by professionals.  Reality is not always apparent until it is in hindsight.  Further, all "people" we meet are not necessarily what they appear to be.  If all is as I suppose it to be considering what I see coming out of my own body on a daily basis,  there would be a small army in place to contain the Morgellons information from the public. 

Morgellons is not a one-component disease but a system of synergistic pathogens with a purpose.

As an update, I want the public to understand that there is no valid funded research being done by our government.  A handful of people are trying to make progress with their own time and money but it seems that there is a brick wall placed in front of us at every turn.  I believe the term for this is that we are being "contained".   A number of medical professionals have found that involvement with the Morgellons issue has led to government shakedowns of their records in attempts to find any reason to close them down.  Other researchers have been threatened and more.  There is a dark underbelly of evil that is calling the shots regarding this man-made disease.  It is time to wake up and discern the truth.

Let's spread the truth and the love - they just hate that.

"Greema"

      

 

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