Scabies

[divine_moments_of_truth]

Hey guys, I've been dealing with the nightmare bug Scabies for a few months now and have had very little progress. I'm pretty sure the over-the-counter Premethrin cream is total b/s so I've been experimenting with Tea Tree Oil and Neem Seed Oil. Anyone have any effective treatments or success stories?

Max

[white wizard]

Hey sorry to hear that I myself am in the process of fighting bed bugs with

Diatomaceous Earth and seems to be working. I would recommend neem soap for

them it is natural and cheap just apply it while you are showering. It worked for

me two years ago will take a little time to kill them but do not worry because it

does work. Here is were I bought mine.

http://www.islandlotions.com/Neem/maxsoap.html

[divine_moments_of_truth]

Thanks white wizard, I'm not to sure how to dillute the oil and I've heard the olive oil in the soap works well too.

[meeradas]

Yes, nightmare is an appropriate term.

You have my compassion.

[Trail]

Aren't you supposed to throw away your mattress and have your house decontaminated to be able to get rid of them?

[percival tyro]

Hi Dimotru. Secondary infected scabies. (After scratching), would consist of aerobic and anaerobic bacteria. (Oxygen tolerant and oxygen susceptible bacteria). So.... neem soap shower and dry, use towel once only. Apply mms solution or cider vinegar solution and allow to dry. Then use neem soap on a nail brush for hands and nails to prevent any further contamination. Wear airy clothing. This is just speculation Dimotru ...Best wishes.

[Siberia9]

I used to know a guy that was a bit of a hillbilly from the mountains. He was a funny character, and he had a lot of weird home remedy's that I used to ask him about. So any way one day back in the 1980's I went to see him and he told me his dog had some sort of skin parasite. I cant remember what kind now but he was pouring kerosene into a tub and said turpentine was better but he couldn't afford it. I said huh? what do you mean? he looked at me like I was stupid and said "to dunk that dawg in", and he did just that, much to my disbelief. "It'll kill the critters on him". His dog was clearly looking crusty and not looking well at all. He did not like being dunked in that tub repeatably either LOL. Anyway I came back a month later and his dog was clean shinny and looking brand new so I guess it worked.
So maybe some turpentine would work, seems worth a try to me although its just a guess.

[white wizard]

Aren't you supposed to throw away your mattress and have your house decontaminated to be able to get rid of them?

There are similar ways to get rid of bed bugs and scabies. I have dealt with

both. I can tell you that bed bugs are extremely difficult to get rid of and in

some cases have been confused for scabies, because there bite marks leave

red welts and in serious bed bug infestations bites can cover your whole body.

Bed bugs can infect your entire house while scabies tend to stay on the host.

One way to find out if you have BB's in search your mattress for blood stains

they leave behind after feeding on you. There favorite place to hide is in the

box spring. Like scabies they are killed within minutes of temperatures over

120F. Bed bugs are know becoming a major epidemic in the U.S. and like

scabies are highly immune to pesticides. I can tell you from first hand

experience I would rather deal with ten cases of scabies then one case of bed

bugs you wanna talk about a nightmare, I would't wish it on my worst enemy.

If you don't believe me go online a look up people dealing with these things

lives have been ruined. I got them five weeks ago, spent over 1700 USD

fighting them so far and I am not 100 percent sure there all gone. If anyone

has questions about BB's or scabies PM me or post here and I will answer your

questions to the best of my knowledge since I have had success fighting both.



And to answer your ? no you can buy a mattress cover to cover instead of throwing away

your bed or steam your mattress with a steamer which kills on contact. I also blanketed

my house in DE dust which dries them out and it seems to be working for BB's.

[conk]

Here is the answer: http://www.licebegone.net/

Proven track record of success! We use it to keep mosquitoes away and it works.

[pugwash84]

They get them a lot in nursing homes and it's best to boil wash sheets and the clothes worn and to steam clean the matress and furniture. They use a really strong lotion which is for headlice and scabies but it stinks to the high heaven I think its called Derbac or something. It absolutely stinks but it gets rid of them.

[kanishk]

Wash your all cloths with hot water and use new washed cloths daily.

Apply permathrin cream before and after bath.

Do not sscratch too much so that the blood will come out.

Do somthing that can boost the immune system.

get well soon..

[Heather2017]

Former BF got scabies after getting buried in sand at the beach. :p Sulfur powder and sulfur ointment really helped. Maybe you could also try putting MMS in bath water?

Hope you win the battle soon!

Love,
Heather

[Ki's]

Use the Elimite (permethrin) but you MUST cover every inch of skin from neck down... between fingers and toes, under nails, belly button, privates... every wrinkle and fold. It has to stay on for 12 hours before you shower. wash bedding and clothing...put pillows in dryer for 1/2 hour. The heat from the dryer will kill any lurking, however scabies don't usually stray very far from a human body.
You will probably itch for awhile after the scabies are dead because of the healing bites. Everyone in your household will need to be treated as well.
FYI: permethrin comes from the chrysanthemum flower.

[Arrowwind]

BTW, I've heard that beg bugs are spreading in movie theaters...
thank god for netflix!

[vilcabamba]

I thougt i had scabies too, then i found out it was nano-bots, a gift from the reptilian demons.. the whole bed bug scare is a cover up for the nanotechnology being put in our foods and sprayed in our air..and also sprayed on clothing..etc.

You can figure out if it's nano-bots by rubbing natures way coconut oil on the bump..if it's nano..then chances are stringy materials and black dots and pieces of plastic will come out of the skin..

you can read this report..

http://www.rense.com/general78/nano911.htm


Morgellons -
A Nano-911 Foreign Invader
By Hildegarde Staninger, PhD, RIET-1
Integrative Health Systems, LLC
415 3/4th N. Larchmont Blvd
LA, CA 90004
323-466-2599 323-466-2774 (fax)
All Material © 2007 Hildegarde Staninger
9-17-7

Presented at the
National Registry of Environmental Professionals
2007 Annual Conference, September 6, 2007, San Antonio, Texas
http://www.nrep.org

Abstract

There is an environmental disease on the horizon that will affect more humans and the environment than any one person will know. Its environmental impact will be far greater than DDT, PCBs and asbestos have ever been. It is called Morgellon's: A Nano-911 Foreign Invader. It has many names ­ fiber disease, mystery disease, delusional parasitosis and unknown dermatological skin disorder, to name a few. It is silent, smart, glistening ­ powered by its own transitional metal battery. And when it strikes its victim it feels like a piece of burning broken glass as it pierces the skin. Smaller than any of the 150 pieces of a virus (known as virons), it is invisible to the naked eye. So silent is it, only the one who has been invaded knows its true nature. Marked with the seal of man-made, self-assembling nano-size materials they can be used in forming drugs, pharmaceuticals, chemicals, biomaterials, artificial nerves, artificial brains, pseudo skin and molecular electronics. Yes, it was patterned after nature's many wonders, but it is still one hundred percent man-made. The nano-brew has been let loose from its scientific flask casting its woes upon an unsuspecting innocence.

Introduction to Chemical Foreign Invaders

Plants, humans and other animals are constantly exposed in their environment to a vast array of chemicals that are foreign to their bodies. These foreign chemicals, or xenobiotics, can be of natural origin or they can be man-made. In general, the more lipophilic (fat loving) compounds are readily absorbed through the skin, across the lungs, or through the gastrointestinal tract. Constant or even intermittent exposure to these lipophilic chemicals could result in their accumulation within the organism, unless effective means of elimination are present. Indeed, chemicals can be excreted unchanged into urine, bile, feces, expired air, and perspiration. Except for exhalation, the ease with which compounds are eliminated from the body largely depends on their water solubility. This is particularly true for non-volatile chemicals that are eliminated in urine and feces, the predominant routes of elimination. Lipophilic compounds that are present in these excretory fluids tend to diffuse into cellular membranes and are reabsorbed, whereas water soluble compounds are excreted. Therefore, it is apparent why lipophilic xenobiotics could accumulate within the body; They are readily absorbed but poorly excreted.1

Fortunately, animal organisms have developed a number of biochemical processes that convert lipophilic compounds to more hydrophilic metabolites. These biochemical processes are termed biotransformation and are usually enzymatic in nature. It should be stressed that biotransformation is the sum of the processes by which a foreign invader such as a chemical is subjected to chemical change by living organisms (Figure 1 ­ 1). This definition implies that a particular chemical may undergo a number of chemical changes. It may mean that the parent molecule is chemically modified at a number of positions or that a particular metabolite of the parent compound may undergo additional modification. The end result of the biotransformation reaction(s) is that the metabolites are chemically distinct from the parent compound. Metabolites are usually more hydrophilic than the parent compound. This enhanced water solubility reduces the ability of the metabolite to partition into biologic membranes and thus restricts the distribution of the metabolites to the various tissues, decreases the renal metabolite(s), and ultimately promotes the excretion of the chemical by the urinary and biliary fecal routes.

Morgellons is a disease that affects humans and animals with a minimum of 93 or more symptoms. Humans experience different colored fibers growing out of their skin with the presence of lesions that ooze a gel like material or may have the feeling of hot burning glass ripping through the underside of their skin as a needle. Toxicological Pathology evaluations of specimens taken from a patient who was diagnosed with this disease and was having a knee replacement operation revealed that the specimen contained silica and silicone.2 Further analysis of these specimens using Micro Raman technology revealed that the fibers that grew out of this same patient were composed of a two part polyester, like a plastic straw within a straw with a head that was made up of silicone (Figure 1 -2 & 1-3). Polyester is a definite man-made material. It is "nylon" by another name. Nylon is a compound that is a lipophatic compound, just as silicone. In addition, high density polyethylene fibers were found in a different patient's heel of their foot. (Figure 1-4). The difference in these compounds and ones that are man-made in a chemical factory are that they have a size, which is measured at a "NANO" level.

Nano is nine decimals below the zero or 0.000,000,001.3 It is smaller than the width of a human hair. How can something so small be so harmful to humans?

Well this is were size counts Big Time. The nano material, which has many forms such as smart dust, nano gels, quantum dots, nano tube, nano wire, nano bots, nano horns are all part of the growing field of nanotechnology. If something is so small that it does not stimulate the immune system to react to its foreign invasion of the cell new cellular toxicological reactions will occur. Collectively these materials were found in specimens taken from the same patient who had the knee replacement operation. The individual had blue fibers that would not burn at 1,400 degrees F and harden gels that made lesions. The callus-like scab had cat-like claws on its underside. These specimens went through Toxicological Pathology and it is true, a picture says a thousand words (Figure 1-5).

No matter what the biological agent, chemical or foreign invader, the body is geared up to protect itself and remove the toxic material. The body is not ready for a nano foreign invader because one can not see it at any level. Normally the body would go through biotransformation and remove this toxic material from the body through biotransformation, but not in the case of Moregellons, which seems to have a mind of its own as it riddles the body with its fibers and continuous self- replication.

Normal Compounds vs Moregellons through Biotransformation

A number of enzymes in animal organisms are capable of biotransforming lipid-soluble xenobiotics in such a way as to render them more water soluble. These enzymatic reactions are of two types; phase I reactions, which involve oxidation, reduction, and hydrolysis, and phase II reactions, which consist of conjugation or synthetic reactions. Although phase I reactions generally convert foreign compounds to derivatives that are more water soluble than the parent molecule, a prime function of these reactions is to add or expose functional groups (e.g.,

- OH, - SH, _NH2, - COOH). These functional groups then permit the compound to undergo phase II reactions. Phase II reactions are biosynthetic reactions where the foreign compounds or a phase I ­ derived metabolite is covalently linked to an endogenous molecule, producing a conjugate. In these cases, the endogenous moieties (e.g. glucuronic acid, sulfate) usually confer upon the lipophilic xenobiotic or its metabolite increased water solubility and the ability to undergo significant ionization at physiologic pH. These conjugated moieties are normally added to endogenous products to promote their secretion or transfer across hepatic, renal, and intestinal membranes. The transport mechanisms that have developed recognize the conjugating moiety. Thus, the excretion of conjugated xenobiotics is enhanced by their ability to participate in transport systems that have evolved from the conjugated products of endogenous molecules.4

The relationship between phase I and phase II reactions is summarized in Figure 4-1. The fate of a particular chemical is determined by its physical/chemical products. Volatile organic compounds may be eliminated via the lungs with no biotransformation. Those with functional groups may be conjugated directly, whereas others undergo phase I reactions before conjugation. As implied, biotransformation is often integrated and can be complex. Because of this complexity, imbalances between phase I and phase II reactions or dose-related shifts in metabolic routes are often causes of chemical-induced tissue injury.5

Organ and Cellular Location of Biotransformation

The enzymes or enzyme systems that catalyze the biotransformation of foreign compounds are localized mainly in the liver. This is not surprising, since a primary function of the liver is to receive and process chemicals absorbed from the gastrointestinal tract before they are distributed to other tissues. Liver receives all the blood that has perfused the splanchnic area, which contains nutrients and other foreign substances. Because of this, the liver has developed the capacity to extract these substances readily from the blood and to modify chemically many of these substances before they are stored, secreted into bile, or released into the general circulation. Other tissues can also biotransform foreign compounds. Nearly every tissue tested has shown activity toward some foreign chemicals (Figure 1-6). Extrahepatic tissues are limited with respect to the diversity of chemicals they can handle, and thus their contribution to the overall biotransformation of xenobiotics is limited. However, biotransformation of a chemical within an extrahepatic tissue may have an important toxicological implication for that particular tissue.6

Subcellular Localization of Biotransformation Enzymes

Biotransformation of foreign compounds within the liver is accomplished by several remarkable enzyme systems. These can chemically modify a wide variety of structurally diverse drugs and toxicants that enter the body through ingestion, inhalation, the skin, or injection. The phase I enzymes, those that add or expose functional groups, are located primarily in the endoplasmic reticulum, a network of interconnected channels present in the cytoplasm of most cells. These enzymes are membrane bound, since the endoplasmic reticulum is basically a contiguous membrane composed of lipids and proteins. The presence of enzymes within a lipoprotein matrix is critical, since lipophilic substances will preferentially partition into a lipid membrane, the site of biotransformation. 7

When liver is removed (in the laboratory) and homogenized, the tubular endoplasmic reticulum breaks up and fragments of the membrane are sealed off to form micro vesicles. These are referred to as microsomes, which can be isolated by differential centrifugation of the liver homogenate. If the supernatant fraction that results from centrifugation of the homogenate at 9000 x g (to remove nuclei, mitochondria, and lysosomes as well as unbroken cells and large membrane fragments) is subjected to centrifugation at 105,00 x g, a pellet highly enriched in microsomes is obtained. The resulting supernatant fraction, which contains a number of soluble enzymes, is referred to as the cytosol. This cytosol contains many of the enzymes of phase II biotransformation. Many of the important biotransformation enzymes are referred to as cytosolic or microsomal to indicate the subcellular location of the enzymes.

The microsomal enzymes that catalyze the phase I reactions were characterized primarily by their ability to metabolize drugs. Thus, much of the literature refers to these enzymes as the microsomal, as the microsomal enzymes will convert drugs to more polar products, but they also act on the numerous chemicals. Therefore, the word biotransformation is preferred to drug metabolism, since it conveys the more universal nature of the reactions. In addition, if delineates the normal process of metabolism of endogenous nutrients form the biotransformation of foreign chemicals.7

Detoxication ­ Toxication

Inasmuch as both phase I and phase II enzymes convert foreign chemicals to forms that can be more readily excreted, they are often referred to as detoxication enzymes. However, it should be emphasized that biotransformation is not strictly related to detoxicaiton. In a number of cases, the metabolic products are more toxic than than the parent compounds. This is particularly true for some chemical carcinogens, organo-phosphates, and a number of compounds that cause cell necrosis in the lung, liver, and kidney. In many instances, a toxic metabolite can be isolated and identified. In other cases, highly reactive intermediates are formed during the biotransformation of a chemical. The term toxication or bioactivation is often used to indicate the enzymatic formation of reactive intermediates. These reactive intermediates are thought to initiate the events that ultimately result in cell death, chemically induced cancer, teratogenesis and a number of other toxicities (Figure 1-7).

Moregellon affected individuals have the opposite reactions of phase I and II, because they experience specific physical parameters such as low body temperature, high blood pressure, urine conductivity high (20 -21), gels, fibers and fluorescents on the body as nano tattoo fluorescent shapes. All tell a tale of being injected with a burning glass needle through their skin as they suffer from severe itching.

Nanotechnology

Nanotechnology presents new opportunities to create better materials and products. Already, nano material containing products are available in U.S. markets including coatings, computers, clothing, cosmetics, sports equipment and medical devices. A survey of EmTech Research of companies working in the field of nanotechnology has identified approximately 80 consumer products, and over 600 raw materials, intermediate components and industrial equipment items that are used by manufacturers. Our economy will be increasingly affected by nanotechnology as more products containing nano materials move from research and development into production and commerce.8

Nanotechnology also has the potential to improve the environment, both through direct applications of nano materials to detect, prevent, and remove pollutants, as well as indirectly by using nanotechnology to design cleaner industrial processes and create environmentally friendly products. However, there are unanswered questions about the impacts of nano materials and nanoproducts on human health and the environment, and the US Environmental Protection Agency (EPA or "the Agency") has the obligation to ensure that potential risks are adequately understood to protect human health and the environment. As products made from nanomaterials become more numerous and therefore more prevalent in the environment, EPA is thus considering how to best leverage advances in nanotechnology to enhance environmental protection, as well as how the introduction of nano materials into the environment will impact the Agency's environmental programs, policies, research needs, and approaches to decision making. Currently, the only regulation that addresses to evaluate the environmental risk of nano materials/technology is the City of Berkley, California.9

Some examples of this technology that applied to a private research study addressed the composition of the fibers used current terminology to address the researcher's findings.10

Carbon nanotube injectors ­ a nano carbon nanotube, conjugated with streptavidin-coated quantum dots. Developed by Xing Chen, Andrax Kis, Alex Zetti, and Carolyn Bertozzi fromt eh University of California at Berklely. Unique feature is its ability to deliver genes.

Nano motor - Carlo Montemagno of Cornell University made a molecular motor less than one-fifth the size of a red blood cell. The key components are protein from E. coli attached to a nickel spindle and propeller a few nanometers across, which is powered by ATP, the energy-intermediate that the body itself uses to power all living activities. But this molecular motor works with the efficiency of only 1 to 4 percent, comparing poorly with those in living organisms that could work at close to 100 percent efficiency.11

Nanobombs - Researchers in Michigan have designed smart "nanobombs" that are said to evade the immune system, to hone in on diseased cells to kill them or deliver drugs to them.11

Nanoelectrosensor - Electronic devices that can tell cells to make specific hormones when the body needs them, and electricity generators that self-assembling inside the cell. 11

Nano-pharmaceuticals ­ Another idea is to interact directly with cells, so they can be harnessed as pharmaceutical factories to produce drugs on demand. Milan Mrksich, chemist at the University of Chicago, plans to hook up cells to electronic circuits by tethering them to a carpet of molecular arms. Carbon chains between 10 to 20 atoms long attached to a gold-plated glass plate with sulphur atoms. The strands are packed so tightly that they have to stand upright on the surface. That creates a thicket of free sticky molecular ends to capture and manipulate cells.11

Quantum dots, nanoparticles, carbon nanotubes (in microelectronics) and other throw-away nanodevices may constitute whole new classes of non-biodegradable nano-junk and nanosmog, environmental pollutants that could make cancer-causing asbestos seem tame.11

The prospect of adverse immune reactions has already been pointed out. Scientists have yet to develop artificial materials that don't cause at least some problems when inserted into the body, starting with silicone breast implants.11 Nanoscale devices are worse. As David Williams an advisor to the European Union on problems of public perceptions of medical technologies says, "The human body is best designed to repel or attack things the size of a cell." Worse yet, the devices could clog up our immune system for good.

And if so small as to not stimulate the immune system at all, "What will be the effects upon the cellular membranes, organelles or the nuclear material (DNA) or its membrane. If the nano material is made up of DNA plasmids of fungi, bacteria or viruses will this new material mix and bind to our own internal cell constituents?

Nano and the Enviornment

In the NIOSH white paper on Nano Technology, it specifically states that the nano material is so small that it will not do any harm to living cells. Current studies on the use of nano tubes on rat lungs have shown that the rats become ill or died after the procedure.12

In Project FMM two individuals who had Morgellons submitted samples for analysis using scanning electron microscope technology along with a sample of a chemtrail cottoncandy-like material that fell from the sky in Texas. The test revealed that the materials in all 3 samples were various stages of development or degradation of the material within the host (Anna and Lily), while the chemtrail sample matched the ladies'. The samples were over 1,500 miles from each other.13

Our environment has seen the results of chemicals upon its land, waters and air. DDT and how it almost whipped out the American Bald Eagle almost 40 years ago was a perfect example of how a chemical could do harm in the food chain of other animals. Nano materials that are dumped into the streams and air are a time bomb of environmental problems. It is important for both scientists and the general public to keep a close track on the developments of nanotechnology and to distinguish the real facts of this technology. And determine if it can really improve our lives without compromising our dignity, integrity and the human race.
REFERENCE(s)

1. Amdur, Mary O., J. Doull, and C.D. Klaassen. Casarett and Doull's Toxicology: The Basic Science of Poisons, 4th Edition. Chapter 4: Biotransformation of Toxicants by I. Glenn Sipes and A. Jay Gandolfi. Pergamon Press. New York. © 1991. Pgs. 88 ­ 126.

2. Staninger, Hildegarde. Far-Infrared Radiant Heat (FIR RH) Type Remediation for Mold and Other Unique Diseases. National Registry of Environmental Professionals. Annual Conference in Nashville, Tennessee. NREP, Des Plaines, IL © October 18, 2006,
http://www.dldewey.com/stan.htm
3. Staninger, Hildegarde. 'Size Matters'
http://www.rense.com/morgphase/sizematters.htm © March 2007

4. Dutton, G.J. Glucuronidation of Drugs and Other Compounds. CRC Press, Inc.. Boca Raton, FL. © 1980

5. Guengerich, F.P. and Liebler, D.C. Enzymatic activation of chemicals to toxic metabolites. CRC Crit. Rev. Toxicol. 14:259-307. © 1985

6. Hawkins, D.R. (ed): Biotransformaitons. Vol. 1: A Survey of the Biotransformations of Drugs and chemicals in Animals. Royal Society of Chemistry. London. © 1988

7. Weber, W.W. The Acetylator Genes and Drug Response. Oxford University Press. New York. © 1987

8. U.S. EPA Environmental Protection Agency. External Review Draft Nanotechnology White Paper. Science Policy Council. U.S. EPA, Washington, D.C. December 2, 2006, http://www.epa.gov/osa/nanotech.htm

9. City of Berkley, California County Commissioner's Meeting. Testimony of
Dr. Edward Spencer and other public citizens on the risk of
nanotechnology to the environment. (City developed an
ordinance/regulation to evaluate the risk to the environment from
nanotechnology.) Berkley, California © 2006, http://www.seektress.com/berkeley.htm

10. Staninger, Hildegarde. Project: Fiber, Meteroite & Morgellons. Phase I and II. http://www.rense.com/morgphase/phase2_1.htm, © March 2007.

11. Ho, Mae-Wan. Nanotecnology, a Hard Pill to Swallow.
http://www.i-sis.org.uk/nanotechnology.php © July 16, 2007

12. Lam, et. al. Pulmonary Toxicity of Single-Walled Carbon Nanotubes in Mice 7 and 90 Days after Intratracheal Instillation. Toxicol. Sci. 77:126-134 © 2004

13. Staninger, Hildegarde. Project: Fiber, Meteroite & Morgellons. Phase I and II. http://www.rense.com/morgphase/phase2_1.htm © March 2007

14. Environmental Defense Fund & Dupont. Brochure: NANO Risk Framework. (www.dupont.com & www.environmentaldefensefung.com )

[Flash]

I used to know a guy that was a bit of a hillbilly from the mountains. He was a funny character, and he had a lot of weird home remedy's that I used to ask him about. So any way one day back in the 1980's I went to see him and he told me his dog had some sort of skin parasite. I cant remember what kind now but he was pouring kerosene into a tub and said turpentine was better but he couldn't afford it. I said huh? what do you mean? he looked at me like I was stupid and said "to dunk that dawg in", and he did just that, much to my disbelief. "It'll kill the critters on him". His dog was clearly looking crusty and not looking well at all. He did not like being dunked in that tub repeatably either LOL. Anyway I came back a month later and his dog was clean shinny and looking brand new so I guess it worked.
So maybe some turpentine would work, seems worth a try to me although its just a guess.

My old mom (80) told me that when she was small, her grand mother would take kerosene with a comb and comb the children with it to get rid of hair lices. It worked.

[pugwash84]

For head lice I use olive oil and a fine tooth comb through the hair but wash it well 3 times after to get all the oil out. This way gets the eggs out too. My daughter is always bringing home "unwanted guests" .

[wynderer]

i have a friend who has Morgellon's -- i understand the medical mafia calls it a 'parasitic delusion' -- she believes she got it while in the hospital , used as a kind of guinea pig [& she is not into all the NWO stuff as on Avalon]

there's a woman who posts on Rumor Mill News about all thse new Designer Diseases, as i call them -- she has suggested that we are all getting these little nano-bots/nano-particles in our bodies, & that those w/symptoms are like the canaries in the mines, warning of what awaits all

you probably know that Joni Mitchell, the singer, has Morgellon's


I thougt i had scabies too, then i found out it was nano-bots, a gift from the reptilian demons.. the whole bed bug scare is a cover up for the nanotechnology being put in our foods and sprayed in our air..and also sprayed on clothing..etc.

You can figure out if it's nano-bots by rubbing natures way coconut oil on the bump..if it's nano..then chances are stringy materials and black dots and pieces of plastic will come out of the skin..

you can read this report..

http://www.rense.com/general78/nano911.htm


Morgellons -
A Nano-911 Foreign Invader
By Hildegarde Staninger, PhD, RIET-1
Integrative Health Systems, LLC
415 3/4th N. Larchmont Blvd
LA, CA 90004
323-466-2599 323-466-2774 (fax)
All Material © 2007 Hildegarde Staninger
9-17-7

Presented at the
National Registry of Environmental Professionals
2007 Annual Conference, September 6, 2007, San Antonio, Texas
http://www.nrep.org

Abstract

There is an environmental disease on the horizon that will affect more humans and the environment than any one person will know. Its environmental impact will be far greater than DDT, PCBs and asbestos have ever been. It is called Morgellon's: A Nano-911 Foreign Invader. It has many names ­ fiber disease, mystery disease, delusional parasitosis and unknown dermatological skin disorder, to name a few. It is silent, smart, glistening ­ powered by its own transitional metal battery. And when it strikes its victim it feels like a piece of burning broken glass as it pierces the skin. Smaller than any of the 150 pieces of a virus (known as virons), it is invisible to the naked eye. So silent is it, only the one who has been invaded knows its true nature. Marked with the seal of man-made, self-assembling nano-size materials they can be used in forming drugs, pharmaceuticals, chemicals, biomaterials, artificial nerves, artificial brains, pseudo skin and molecular electronics. Yes, it was patterned after nature's many wonders, but it is still one hundred percent man-made. The nano-brew has been let loose from its scientific flask casting its woes upon an unsuspecting innocence.

Introduction to Chemical Foreign Invaders

Plants, humans and other animals are constantly exposed in their environment to a vast array of chemicals that are foreign to their bodies. These foreign chemicals, or xenobiotics, can be of natural origin or they can be man-made. In general, the more lipophilic (fat loving) compounds are readily absorbed through the skin, across the lungs, or through the gastrointestinal tract. Constant or even intermittent exposure to these lipophilic chemicals could result in their accumulation within the organism, unless effective means of elimination are present. Indeed, chemicals can be excreted unchanged into urine, bile, feces, expired air, and perspiration. Except for exhalation, the ease with which compounds are eliminated from the body largely depends on their water solubility. This is particularly true for non-volatile chemicals that are eliminated in urine and feces, the predominant routes of elimination. Lipophilic compounds that are present in these excretory fluids tend to diffuse into cellular membranes and are reabsorbed, whereas water soluble compounds are excreted. Therefore, it is apparent why lipophilic xenobiotics could accumulate within the body; They are readily absorbed but poorly excreted.1

Fortunately, animal organisms have developed a number of biochemical processes that convert lipophilic compounds to more hydrophilic metabolites. These biochemical processes are termed biotransformation and are usually enzymatic in nature. It should be stressed that biotransformation is the sum of the processes by which a foreign invader such as a chemical is subjected to chemical change by living organisms (Figure 1 ­ 1). This definition implies that a particular chemical may undergo a number of chemical changes. It may mean that the parent molecule is chemically modified at a number of positions or that a particular metabolite of the parent compound may undergo additional modification. The end result of the biotransformation reaction(s) is that the metabolites are chemically distinct from the parent compound. Metabolites are usually more hydrophilic than the parent compound. This enhanced water solubility reduces the ability of the metabolite to partition into biologic membranes and thus restricts the distribution of the metabolites to the various tissues, decreases the renal metabolite(s), and ultimately promotes the excretion of the chemical by the urinary and biliary fecal routes.

Morgellons is a disease that affects humans and animals with a minimum of 93 or more symptoms. Humans experience different colored fibers growing out of their skin with the presence of lesions that ooze a gel like material or may have the feeling of hot burning glass ripping through the underside of their skin as a needle. Toxicological Pathology evaluations of specimens taken from a patient who was diagnosed with this disease and was having a knee replacement operation revealed that the specimen contained silica and silicone.2 Further analysis of these specimens using Micro Raman technology revealed that the fibers that grew out of this same patient were composed of a two part polyester, like a plastic straw within a straw with a head that was made up of silicone (Figure 1 -2 & 1-3). Polyester is a definite man-made material. It is "nylon" by another name. Nylon is a compound that is a lipophatic compound, just as silicone. In addition, high density polyethylene fibers were found in a different patient's heel of their foot. (Figure 1-4). The difference in these compounds and ones that are man-made in a chemical factory are that they have a size, which is measured at a "NANO" level.

Nano is nine decimals below the zero or 0.000,000,001.3 It is smaller than the width of a human hair. How can something so small be so harmful to humans?

Well this is were size counts Big Time. The nano material, which has many forms such as smart dust, nano gels, quantum dots, nano tube, nano wire, nano bots, nano horns are all part of the growing field of nanotechnology. If something is so small that it does not stimulate the immune system to react to its foreign invasion of the cell new cellular toxicological reactions will occur. Collectively these materials were found in specimens taken from the same patient who had the knee replacement operation. The individual had blue fibers that would not burn at 1,400 degrees F and harden gels that made lesions. The callus-like scab had cat-like claws on its underside. These specimens went through Toxicological Pathology and it is true, a picture says a thousand words (Figure 1-5).

No matter what the biological agent, chemical or foreign invader, the body is geared up to protect itself and remove the toxic material. The body is not ready for a nano foreign invader because one can not see it at any level. Normally the body would go through biotransformation and remove this toxic material from the body through biotransformation, but not in the case of Moregellons, which seems to have a mind of its own as it riddles the body with its fibers and continuous self- replication.

Normal Compounds vs Moregellons through Biotransformation

A number of enzymes in animal organisms are capable of biotransforming lipid-soluble xenobiotics in such a way as to render them more water soluble. These enzymatic reactions are of two types; phase I reactions, which involve oxidation, reduction, and hydrolysis, and phase II reactions, which consist of conjugation or synthetic reactions. Although phase I reactions generally convert foreign compounds to derivatives that are more water soluble than the parent molecule, a prime function of these reactions is to add or expose functional groups (e.g.,

- OH, - SH, _NH2, - COOH). These functional groups then permit the compound to undergo phase II reactions. Phase II reactions are biosynthetic reactions where the foreign compounds or a phase I ­ derived metabolite is covalently linked to an endogenous molecule, producing a conjugate. In these cases, the endogenous moieties (e.g. glucuronic acid, sulfate) usually confer upon the lipophilic xenobiotic or its metabolite increased water solubility and the ability to undergo significant ionization at physiologic pH. These conjugated moieties are normally added to endogenous products to promote their secretion or transfer across hepatic, renal, and intestinal membranes. The transport mechanisms that have developed recognize the conjugating moiety. Thus, the excretion of conjugated xenobiotics is enhanced by their ability to participate in transport systems that have evolved from the conjugated products of endogenous molecules.4

The relationship between phase I and phase II reactions is summarized in Figure 4-1. The fate of a particular chemical is determined by its physical/chemical products. Volatile organic compounds may be eliminated via the lungs with no biotransformation. Those with functional groups may be conjugated directly, whereas others undergo phase I reactions before conjugation. As implied, biotransformation is often integrated and can be complex. Because of this complexity, imbalances between phase I and phase II reactions or dose-related shifts in metabolic routes are often causes of chemical-induced tissue injury.5

Organ and Cellular Location of Biotransformation

The enzymes or enzyme systems that catalyze the biotransformation of foreign compounds are localized mainly in the liver. This is not surprising, since a primary function of the liver is to receive and process chemicals absorbed from the gastrointestinal tract before they are distributed to other tissues. Liver receives all the blood that has perfused the splanchnic area, which contains nutrients and other foreign substances. Because of this, the liver has developed the capacity to extract these substances readily from the blood and to modify chemically many of these substances before they are stored, secreted into bile, or released into the general circulation. Other tissues can also biotransform foreign compounds. Nearly every tissue tested has shown activity toward some foreign chemicals (Figure 1-6). Extrahepatic tissues are limited with respect to the diversity of chemicals they can handle, and thus their contribution to the overall biotransformation of xenobiotics is limited. However, biotransformation of a chemical within an extrahepatic tissue may have an important toxicological implication for that particular tissue.6

Subcellular Localization of Biotransformation Enzymes

Biotransformation of foreign compounds within the liver is accomplished by several remarkable enzyme systems. These can chemically modify a wide variety of structurally diverse drugs and toxicants that enter the body through ingestion, inhalation, the skin, or injection. The phase I enzymes, those that add or expose functional groups, are located primarily in the endoplasmic reticulum, a network of interconnected channels present in the cytoplasm of most cells. These enzymes are membrane bound, since the endoplasmic reticulum is basically a contiguous membrane composed of lipids and proteins. The presence of enzymes within a lipoprotein matrix is critical, since lipophilic substances will preferentially partition into a lipid membrane, the site of biotransformation. 7

When liver is removed (in the laboratory) and homogenized, the tubular endoplasmic reticulum breaks up and fragments of the membrane are sealed off to form micro vesicles. These are referred to as microsomes, which can be isolated by differential centrifugation of the liver homogenate. If the supernatant fraction that results from centrifugation of the homogenate at 9000 x g (to remove nuclei, mitochondria, and lysosomes as well as unbroken cells and large membrane fragments) is subjected to centrifugation at 105,00 x g, a pellet highly enriched in microsomes is obtained. The resulting supernatant fraction, which contains a number of soluble enzymes, is referred to as the cytosol. This cytosol contains many of the enzymes of phase II biotransformation. Many of the important biotransformation enzymes are referred to as cytosolic or microsomal to indicate the subcellular location of the enzymes.

The microsomal enzymes that catalyze the phase I reactions were characterized primarily by their ability to metabolize drugs. Thus, much of the literature refers to these enzymes as the microsomal, as the microsomal enzymes will convert drugs to more polar products, but they also act on the numerous chemicals. Therefore, the word biotransformation is preferred to drug metabolism, since it conveys the more universal nature of the reactions. In addition, if delineates the normal process of metabolism of endogenous nutrients form the biotransformation of foreign chemicals.7

Detoxication ­ Toxication

Inasmuch as both phase I and phase II enzymes convert foreign chemicals to forms that can be more readily excreted, they are often referred to as detoxication enzymes. However, it should be emphasized that biotransformation is not strictly related to detoxicaiton. In a number of cases, the metabolic products are more toxic than than the parent compounds. This is particularly true for some chemical carcinogens, organo-phosphates, and a number of compounds that cause cell necrosis in the lung, liver, and kidney. In many instances, a toxic metabolite can be isolated and identified. In other cases, highly reactive intermediates are formed during the biotransformation of a chemical. The term toxication or bioactivation is often used to indicate the enzymatic formation of reactive intermediates. These reactive intermediates are thought to initiate the events that ultimately result in cell death, chemically induced cancer, teratogenesis and a number of other toxicities (Figure 1-7).

Moregellon affected individuals have the opposite reactions of phase I and II, because they experience specific physical parameters such as low body temperature, high blood pressure, urine conductivity high (20 -21), gels, fibers and fluorescents on the body as nano tattoo fluorescent shapes. All tell a tale of being injected with a burning glass needle through their skin as they suffer from severe itching.

Nanotechnology

Nanotechnology presents new opportunities to create better materials and products. Already, nano material containing products are available in U.S. markets including coatings, computers, clothing, cosmetics, sports equipment and medical devices. A survey of EmTech Research of companies working in the field of nanotechnology has identified approximately 80 consumer products, and over 600 raw materials, intermediate components and industrial equipment items that are used by manufacturers. Our economy will be increasingly affected by nanotechnology as more products containing nano materials move from research and development into production and commerce.8

Nanotechnology also has the potential to improve the environment, both through direct applications of nano materials to detect, prevent, and remove pollutants, as well as indirectly by using nanotechnology to design cleaner industrial processes and create environmentally friendly products. However, there are unanswered questions about the impacts of nano materials and nanoproducts on human health and the environment, and the US Environmental Protection Agency (EPA or "the Agency") has the obligation to ensure that potential risks are adequately understood to protect human health and the environment. As products made from nanomaterials become more numerous and therefore more prevalent in the environment, EPA is thus considering how to best leverage advances in nanotechnology to enhance environmental protection, as well as how the introduction of nano materials into the environment will impact the Agency's environmental programs, policies, research needs, and approaches to decision making. Currently, the only regulation that addresses to evaluate the environmental risk of nano materials/technology is the City of Berkley, California.9

Some examples of this technology that applied to a private research study addressed the composition of the fibers used current terminology to address the researcher's findings.10

Carbon nanotube injectors ­ a nano carbon nanotube, conjugated with streptavidin-coated quantum dots. Developed by Xing Chen, Andrax Kis, Alex Zetti, and Carolyn Bertozzi fromt eh University of California at Berklely. Unique feature is its ability to deliver genes.

Nano motor - Carlo Montemagno of Cornell University made a molecular motor less than one-fifth the size of a red blood cell. The key components are protein from E. coli attached to a nickel spindle and propeller a few nanometers across, which is powered by ATP, the energy-intermediate that the body itself uses to power all living activities. But this molecular motor works with the efficiency of only 1 to 4 percent, comparing poorly with those in living organisms that could work at close to 100 percent efficiency.11

Nanobombs - Researchers in Michigan have designed smart "nanobombs" that are said to evade the immune system, to hone in on diseased cells to kill them or deliver drugs to them.11

Nanoelectrosensor - Electronic devices that can tell cells to make specific hormones when the body needs them, and electricity generators that self-assembling inside the cell. 11

Nano-pharmaceuticals ­ Another idea is to interact directly with cells, so they can be harnessed as pharmaceutical factories to produce drugs on demand. Milan Mrksich, chemist at the University of Chicago, plans to hook up cells to electronic circuits by tethering them to a carpet of molecular arms. Carbon chains between 10 to 20 atoms long attached to a gold-plated glass plate with sulphur atoms. The strands are packed so tightly that they have to stand upright on the surface. That creates a thicket of free sticky molecular ends to capture and manipulate cells.11

Quantum dots, nanoparticles, carbon nanotubes (in microelectronics) and other throw-away nanodevices may constitute whole new classes of non-biodegradable nano-junk and nanosmog, environmental pollutants that could make cancer-causing asbestos seem tame.11

The prospect of adverse immune reactions has already been pointed out. Scientists have yet to develop artificial materials that don't cause at least some problems when inserted into the body, starting with silicone breast implants.11 Nanoscale devices are worse. As David Williams an advisor to the European Union on problems of public perceptions of medical technologies says, "The human body is best designed to repel or attack things the size of a cell." Worse yet, the devices could clog up our immune system for good.

And if so small as to not stimulate the immune system at all, "What will be the effects upon the cellular membranes, organelles or the nuclear material (DNA) or its membrane. If the nano material is made up of DNA plasmids of fungi, bacteria or viruses will this new material mix and bind to our own internal cell constituents?

Nano and the Enviornment

In the NIOSH white paper on Nano Technology, it specifically states that the nano material is so small that it will not do any harm to living cells. Current studies on the use of nano tubes on rat lungs have shown that the rats become ill or died after the procedure.12

In Project FMM two individuals who had Morgellons submitted samples for analysis using scanning electron microscope technology along with a sample of a chemtrail cottoncandy-like material that fell from the sky in Texas. The test revealed that the materials in all 3 samples were various stages of development or degradation of the material within the host (Anna and Lily), while the chemtrail sample matched the ladies'. The samples were over 1,500 miles from each other.13

Our environment has seen the results of chemicals upon its land, waters and air. DDT and how it almost whipped out the American Bald Eagle almost 40 years ago was a perfect example of how a chemical could do harm in the food chain of other animals. Nano materials that are dumped into the streams and air are a time bomb of environmental problems. It is important for both scientists and the general public to keep a close track on the developments of nanotechnology and to distinguish the real facts of this technology. And determine if it can really improve our lives without compromising our dignity, integrity and the human race.
REFERENCE(s)

1. Amdur, Mary O., J. Doull, and C.D. Klaassen. Casarett and Doull's Toxicology: The Basic Science of Poisons, 4th Edition. Chapter 4: Biotransformation of Toxicants by I. Glenn Sipes and A. Jay Gandolfi. Pergamon Press. New York. © 1991. Pgs. 88 ­ 126.

2. Staninger, Hildegarde. Far-Infrared Radiant Heat (FIR RH) Type Remediation for Mold and Other Unique Diseases. National Registry of Environmental Professionals. Annual Conference in Nashville, Tennessee. NREP, Des Plaines, IL © October 18, 2006,
http://www.dldewey.com/stan.htm
3. Staninger, Hildegarde. 'Size Matters'
http://www.rense.com/morgphase/sizematters.htm © March 2007

4. Dutton, G.J. Glucuronidation of Drugs and Other Compounds. CRC Press, Inc.. Boca Raton, FL. © 1980

5. Guengerich, F.P. and Liebler, D.C. Enzymatic activation of chemicals to toxic metabolites. CRC Crit. Rev. Toxicol. 14:259-307. © 1985

6. Hawkins, D.R. (ed): Biotransformaitons. Vol. 1: A Survey of the Biotransformations of Drugs and chemicals in Animals. Royal Society of Chemistry. London. © 1988

7. Weber, W.W. The Acetylator Genes and Drug Response. Oxford University Press. New York. © 1987

8. U.S. EPA Environmental Protection Agency. External Review Draft Nanotechnology White Paper. Science Policy Council. U.S. EPA, Washington, D.C. December 2, 2006, http://www.epa.gov/osa/nanotech.htm

9. City of Berkley, California County Commissioner's Meeting. Testimony of
Dr. Edward Spencer and other public citizens on the risk of
nanotechnology to the environment. (City developed an
ordinance/regulation to evaluate the risk to the environment from
nanotechnology.) Berkley, California © 2006, http://www.seektress.com/berkeley.htm

10. Staninger, Hildegarde. Project: Fiber, Meteroite & Morgellons. Phase I and II. http://www.rense.com/morgphase/phase2_1.htm, © March 2007.

11. Ho, Mae-Wan. Nanotecnology, a Hard Pill to Swallow.
http://www.i-sis.org.uk/nanotechnology.php © July 16, 2007

12. Lam, et. al. Pulmonary Toxicity of Single-Walled Carbon Nanotubes in Mice 7 and 90 Days after Intratracheal Instillation. Toxicol. Sci. 77:126-134 © 2004

13. Staninger, Hildegarde. Project: Fiber, Meteroite & Morgellons. Phase I and II. http://www.rense.com/morgphase/phase2_1.htm © March 2007

14. Environmental Defense Fund & Dupont. Brochure: NANO Risk Framework. (www.dupont.com & www.environmentaldefensefung.com )

[wynderer]

Penn Herb, an old & reputable herb company, sells a soap created by a Japanese [i think] Dr which directly affects any parasites on the skin -- i can't remember if scabies was one of the conditions it works on, but maybe give it a try

[indigopete]

Hey guys, I've been dealing with the nightmare bug Scabies for a few months now and have had very little progress. I'm pretty sure the over-the-counter Premethrin cream is total b/s so I've been experimenting with Tea Tree Oil and Neem Seed Oil. Anyone have any effective treatments or success stories?
Max

A few MONTHS ??!! :eek:

Jeez - I had this 20 years ago and just about scratched myself out of existence in a week !

I know this is an 'alternative medicine' thread, but I would forget that stuff in this case - you might as well be stripping car paint with soap & water.

You need some serious chemistry to get rid of those suckers - in this case Benzyle Benzoate, otherwise known as "Ascabiol". That will get rid of it in about 72 hours,
http://www.netdoctor.co.uk/skin-and-hair/medicines/ascabiol-emulsion.html

De-contaminate everything:

- smear it on every inch of your body (it stings but that's because its doing something usefull)
- wash all your clothes and bedclothes in a dilute solution (I did it 3 times in a triple concentration out of sheer paranoia)

I can tell you, I was never so glad in my life for modern chemistry. I also never had any adverse effects since then (that I know off - I may of course be off my head without realising it).

Of course, usual disclaimers apply - go to your doc and get a proper diagnoisis and prescription (I think you'd need one anyway). Then come back here and resume the search for alternative therapies in relaxed tranquility, free from playing host to a million little breeders trying to burn your a**s off.

Pete

P.S. When you paste that stuff on, don't go too near to your "privates" unless your looking for an interesting "Out of Body" experience :)

[GoodETxSG]

My GF said that when on a ship deployed in WWII if one of the guys did not bathe all of the time and especially if they got lice they were held down, dowsed with some sort of gas or fuel and scrubbed with a wire brush... not only did it work but they guy NEVER ever wen a day w/out bathing again.... juts made me think of it.

[Connecting with Sauce]

If these are a parasite you may want to try urine therapy... David Jubb states it is one of the best parasite cleanses bar none... I started a thread with some info and links you may or may not find interesting.

[genevieve]

divine moments of truth:

In February 2011 I discovered I had scabies and researched the curse on the internet. Many people said the medications they got from their doctors didn't work, and since I hadn't been to an M.D. since 1979, I immediately went my usual alternative route.

I started off with Dermisil for Scabies from Amazon.com, which I rated three stars, and then went on to many other things. What finally got the job done was CLOVE OIL in conjunction with protocols for bathing, laundering and disinfecting. I'm absolutely positive that the clove oil was the most important element in the cure.

Some scientists in Australia studied four different oils for the treatment of permethrin-resistant scabies and found that a 6% solution of clove oil killed all scabies after only 15 minutes. The study is here: http://www.plosone.org/article/info:doi/10.1371/journal.pone.0012079

I mixed 3/4 tsp clove oil with 4 TBS olive oil (or almond or coconut oil). I had a mind-deranging (no kidding!) infestation in almost all areas of my body from my ankles to my chin (!!!). So even though the clove oil kills the scabies after only 15 minutes, I applied the oil mix after an MMS bath three times daily for two months. It worked.

I also accidentally increased the clove oil percentage by too much and burned myself. Be careful--it is really strong!

If you go to Jennifer's three star review of Dermisil for Scabies on Amazon, you will find my complete protocols and helpful information from others. The most important thing for you to know is 6% CLOVE OIL (also extremely important: you WILL transport the beasties from one place to another unless you are careful how you scratch, and men need to be especially careful to clean their hands BEFORE urinating).

Best wishes!

Peace Love Joy & Harmony
Genevieve

[kanishk]

Can Hulda Clark's Zapper be useful in scabies?

I heard that some good oils can kill these parasites. When I had scabies I tried Kerosene once but it didn't worked.

Nowadays I don't find hair lice problems, because once a time 100-200 lices came out of my head daily for may be two weeks.

[genevieve]

kanishk--

I used a zapper--not Hulda Clark's--and it didn't do a thing for me.

Clove oil was the answer to my prayers for the scabies, and perhaps it would be helpful for lice as well.

Peace Love Joy & Harmony,
Genevieve

[Mark]

This stuff has worked very well for me:

http://www.scabies-killer.com/

The $37 package worked fine. Not only does it work wonderfully, it smells great and feels awesome on your body.

[FraZZleD]

An old lady down the street had scabies and said everything the doctor gave her didn't work. I told her to try Turmeric

This yellow orange spice has seasoned food for millennia. You may even have heard about the use of turmeric for cardiovascular health. But, did you know that it's also a mite fighter? Science has just begun to understand the magic of turmeric. A paste of turmeric powder and water applied scabies rashes will zap your mites in no time!

1 Heaping teaspoon full in the morning and 1 heaping teaspoon full at night. Take it internally. I usually eat it in a taco and once I got use to the taste I can now drink it in my coffee.

It got rid of the old ladies scabies.... She was so grateful!

My son got MRSA and almost died from it. The hospital couldn't get rid of it. I spent 5 minutes on the internet looking for a natural cure and found it. I told my son to leave the hospital went to the grocery store and bought 3 bottles of Turmeric and started him on 1 heaping teaspoon in the morning and 1 heaping teaspoon at night. Within a week the MRSA was almost gone. My son now makes his own Turmeric pills and if he gets any boils starts taking Turmeric and they go away.

So now I can say it works for MRSA AND SCABIES. I hope it works for you too!

FraZZleD