“The doctors are very dismissive. One doctor sent the fibres off to a lab, but all she said was that nothing abnormal had been detected.” Among Morgellons sufferers, this is a common experience.
Most experts believe the condition is a psychological disorder called delusional parasitosis.
. . .
Note: I am updating this post as I learn more about Morgellons. Like many people, I had heard about it, but it just seemed too bizarre and inconclusive such that I didn’t want to get sidetracked by it. Well, here I am getting into it now. I still haven’t drawn any conclusions about it, but I will continue to share what I can here. Those who already know, or think they know, everything about it, humor me while I get up to speed on it.
PJ
. . .
Weird X-Files skin disease treated as a psychological disorder
Aftermath News | Sep 18, 2007
by PJ Walker
“Experts” write it off as a psychological disorder. Reminds me of the way vets with Agent Orange poisoning and Gulf War Syndrome have been treated as “delusional” too. That is the way the medical mafia treats anyone who exhibits symptoms that damn the Military/Industrial Complex’s radical disregard for human health and safety, human rights and the environment. Doctors also routinely pooh pooh deleterious drug side-effects that are literally killing hundreds of thousands of people in the US, conservatively speaking. So, as they say on the boob-tube, “Ask your doctor. He knows what’s best for you”.
Yes, in some cases, obsessive scratching can be caused by psychosis, be drug-induced with meth or crack, or by otherwise toxic abuse of one’s own body, but this is showing up in people without such behaviors or dispositions who are otherwise normal. And the wounds produce fibers or what appear to be mobile parasites in the shape of colored threads. These are not imaginary, but I believe if screaming alien babies came blasting out of a person’s skin and did a tap dance on the examining room floor, the typical doctor would still write it off as “paranoid delusion”. Such is their state of arrogant denial, and in some cases no doubt, deliberate cover-up.
If the AMA says it doesn’t exist, then it doesn’t exist. That’s the rule.
(photo Rense.com.)
I am not sure what this is, but I strongly suspect it has something to do with industrial pollutants (possibly nano-pollutants), runaway genetic experiments or with deliberate contamination of the human population at worst. Most of us know next to nothing about Morgellons, but it is gaining recognition as a real illness that needs treatment.
My first reflex is to recommend immune-boosting herbs and detoxification regimes for the body in the case of most disease conditions, because the body will usually respond favorably to anything that helps it dump overloads of toxins, parasites etc. But the problem is, if you inhale or ingest non-organic fibers or polymers, parasites, genetically engineered substances, etc, the body may not be able to break them down so the immune system will react trying to kick the invader out with very unpleasant symptoms including skin eruptions.
In that case, these types of things are going to have to migrate and work their way through the body until they emerge through the skin where they can be removed. And that’s the good news. The bad news is, well it’s something I don’t want to speculate on at the moment.
I doubt that there would be any effective treatment for Morgellons other than topical creams that would help sooth the itching and burning sensations. A commenter suggested sulphur, both internal and topical, and he claims it is a relatively harmless GM cotton “nematode”. For me, it remains to be seen. Some believe it is a nanotech bioweapon distributed by chemtrails. That is the farthest end of the conspiracy spectrum, but unfortunately, it could be true.
“‘Goldenhead’ A Nano Robotic Sensor” (Rense.com)
If someone (ie the Illuminati-controlled government) out there is deliberately releasing this malady on the human population, you can bet they have both vaccines and remedies for it that they won’t tell you about. Hell, they barely acknowledge that Morgellons even exists, so don’t expect any revelations from the media other than to misdirect us. Instead the establishment sends out their disinfo agents to “debunk” the illness and tell everybody that it’s a mental illness. So no surprise there folks.
Anyway, we all need to look into this further.
. . .
Main Article
Is this a disease or an episode of the X Files?
By DANIEL ELKAN
Morgellons disease: Sufferers complain of cuts which produce tiny red and blue fibres
It feels like insects crawling under your skin, but is this X-Files illness a reality?
The symptoms sound like something from The X Files – sufferers complain of a crawling sensation all over the body, egg-like lumps under the skin and, even more bizarrely, cuts which produce tiny red and blue fibres.
Many doctors, however, are highly sceptical – dismissing the symptoms as imaginary and patients as delusional.
But a growing number of experts believe the symptoms are genuine, and the U.S. government’s Centre for Disease Control and Prevention (CDC) is investigating the condition – Morgellons disease – as reported in the New Scientist.
This belated recognition comes as a great relief to the many thousands of sufferers, such as Beverley Warren, who have struggled for years with this debilitating condition.
“It feels like tiny insects crawling or biting under my skin,” says Beverley, 63, from Manchester.
As a result she hardly sleeps at night, constantly woken by the intense itching on her arms.
“I scratch and scratch, but it doesn’t help. I’ve suffered hundreds of nights like this. Sometimes I just lie awake, crying.”
Beverley’s arms are covered with dozens of sores. Some have tiny, white, egg-like lumps on them, just under the skin surface.
More bizarrely, when Beverley scratches her arms, small black specks, which look like tiny grains of pepper, appear from under the surface of the skin.
The problem appeared 11 years ago.
Doctors and dermatologists have been unable to give her a diagnosis, and two skin biopsies have provided no answer.
At the suggestion of a dermatologist, Beverley applies creams to try to soothe the itching and then bandages her arms for two days to protect the area.
Unfortunately, this hasn’t helped.
“The only thing that provides relief is when I put ice on my arms,” she says.
Then in April, Beverley discovered that she was not the only person with the problem.
After typing ‘itching on the arms’ into an internet search engine, she came across a website for Morgellons disease.
“My husband looked at the screen and said: ‘My God, those are all the symptoms you’ve described.'”
Incredibly, more than 10,000 people worldwide had registered on the website claiming they suffered, too.
But in addition to Beverley’s symptoms, many complained of something even stranger: tiny fibres, of various colours, growing out of their skin.
One of them is Rita, who lives in Somerset.
She says: “The fibres are 1mm or 2mm long and are either pinky red, blue, brown, black or transparent. They look like little hairs and most grow out of the lesions on my arms, legs and torso.”
Four years ago, Rita, 47, started being affected by what many sufferers describe as brain fog.
“My thinking became cloudy and forgetful,” she explains. “I jumble up my words and sometimes, if someone is talking to me, I can’t understand what they are saying so I have to ask them to repeat themselves.”
The condition forced Rita to give up her career as a legal secretary.
“The doctors are very dismissive. One doctor sent the fibres off to a lab, but all she said was that nothing abnormal had been detected.” Among Morgellons sufferers, this is a common experience.
The disease was named in 2002 by an American mother, Mary Leitao, whose two-year- old son one day pointed to his lip and said ‘bugs’.
Mary was alarmed to find fibres growing there, but soon became frustrated that no doctor would investigate her son’s condition.
She began researching it for herself, and came across a 17th-century article which described a condition, ‘The Morgellons’, where unusual hairs would grow out of the skin.
In the U.S., where the majority of cases are found, the number of people claiming to have the same symptoms – and the absence of a medical explanation – led to last month’s launch of the government’s CDC investigation, involving a team of specialists in epidemiology, environmental health, dermatology, chronic diseases, infectious diseases, pathology and mental health.
However, most experts believe the condition is a psychological disorder called delusional parasitosis.
Morgellons Disease “Alive with Intelligence”
Sufferers convince themselves the crawling sensations and fibres are evidence of an infection by a parasite.
“The brain tells them something is crawling on or under their skin,” says
Professor Lynn Kimsey, an expert on insects and disease at the University of California.
“The human brain is wired to make connections between events, but we don’t always draw the right conclusions. Only in a small proportion of cases do real parasites – such as mites – cause this type of thing.”
Instead, Prof Kimsey says, the skin sensations are likely to be the result of changes in brain and nerve chemistry, commonly triggered by drug or alcohol abuse or hormonal changes such as the menopause.
The patients constantly scratch their skin – a process called neurotic excoriation – creating sores that never get the chance to heal.
As Professor Noah Scheinfeld, a dermatologist at Columbia University in the U.S., explains: “The skin becomes a sink for nervous energy and the slightest sensation can lead people to itch.”
Even the fibres have a simple explanation: “They inevitably turn out to be lint from clothes, household fibres or hair,” Kimsey says.
“Sores and scabs attract and trap these fibres.”
The sceptics say Morgellons is best treated with dermatological creams for the sores – and possibly anti-psychotic drugs in severe cases.
But a handful of experts have found evidence that seems to contradict conventional explanations.
Randy Wymore, assistant professor of pharmacology at Oklahoma State University, stumbled across the Morgellons website and, surprised by the number of people claiming to be affected, offered to test some of the fibres at his lab.
“I thought it would be easy to determine their origin,” he says.
But contrary to his expectations, the fibres did not match any common environmental ones.
So Wymore invited some Morgellons patients in to be examined by a colleague, Rhonda Casey.
She found that even under unbroken skin there were masses of fibres. After extensive tests, scientists including a police forensics team drew a blank as to their origin, despite comparing them to more than 90,000 organic compounds.
Meanwhile, at the State University of New York, Vitaly Citovsky, professor of biochemistry and cell biology, found that the lesions of Morgellons patients test positively for the presence of agrobacterium, a bacterium used in the commercial production of genetically modified food – but not normally found in skin sores.
Psychiatrist Robert Bransfield has studied a database of 3,000 Morgellons patients and argues that the psychological profile of Morgellons patients does not fit with a diagnosis of delusional parasitosis.
“Before the onset of their illness, their mental status appears to be quite representative of the general population,” says Bransfield.
“Later on they may become paranoid and delusional; but they don’t start out that way.”
Immunopsychology experts such as Bransfield are discovering that the body’s own immune reaction to invasion by a parasite can significantly affect levels of brain chemicals, such as serotonin.
In other illnesses, such as hepatitis C, this can result in altered psychological states and mental symptoms.
Morgellons could work this way, too, Bransfield suggests.
Some test results have led researchers to speculate that Morgellons may be caused by an unusual fungal parasite.
For Beverley, the new investigation cannot come soon enough.
“I’m not delusional,” she says. “I just want to find out what is happening to my body.”
. . .
Related
Morgellons – Part 1 – Nightline – CDC – Chemtrails nanotech
Morgellons – Part 2 – Nightline – CDC Skin Fiber chemtrails
Musical Artist Joni Mitchell being treated for Morgellons Syndrome
Artist Joni Mitchell battles Morgellon’s syndrome
Morgellons Disease May Be Linked to Genetically Modified Food
Morgellons: Terrifying New Disease Reaching Pandemic Status
CDC to Investigate Morgellons Mystery Skin Disease
The Staninger Report
Frightening Skin Disease Invades L.A.
Morgellons Research Foundation
Dr. Hildegarde Staniger PH.D Industrial Toxicologist/IH and Doctor of Integrative Medicine
Imagine your body pocked by erupting sores, the sensation of little bugs crawling just below the surface of your flesh, and worst of all, mysterious, hideous looking fibers sprouting from your skin. It may sound like a scene from a science fiction movie, but a growing legion of Americans, sixty thousand of them, now suffer from this condition. Join us as Dr. Hildegarde Staninger fills us in on the terrible affliction known as Morgellons”. Learn how what appear to be nanorobotic “assemblers” replicate from the inside out, from the digestive system to the skin, and how the composition of chemtrail fibers matches that of some of the fibers found on Morgellons sufferers. Are these nanorobots in our food? Can we protect ourselves from them? Dr. Hildegarde Staninger, Ph.D.’s websites:
http://www.morgellons.org/
Dr Hildegarde Staninger Interview (Part One)
Nanomachines Invasion
Morgellons – A Nano-911 Foreign Invader
MORGELLONS REPORTS
The New Morgellons Order
A Source For Morgellons Disease Information
Morgellons USA (see the videos)
MORGELLONS Disease is REAL…not associated with Delusions
Aftermath News 
If you can pry your mind opened, any, after all that…
http://morgellonswatch.com/about/
All I see on your site is the typical fuzzball/mental illness paradigm and no attempt to admit to a possible physical illness. Typical professional debunker. Why do you do it? Out of the goodness of your little heart? I’ll bet you’re a Fed or involved with Feds in some way. Ain’t that right?
I have seen enough to know this ain’t about lint and delusions. This is something bizarre that moves like it is a parasitic worm. At first, I thought maybe these were inorganic fibers migrating through the body, but fibers don’t have locomotion. Worms and possibly nanotubes, do. The more I learn, the more I will share here.
Yeah, if it looks like a Fed, writes like a Fed and smells like a Fed, then it probably is a Fed. Either that or it’s someone who is socio-pathic with a vendetta. Or both. Yeah, probably both.
I’m sorry. Does being so fearful, close-minded, and prejudiced feel as pleasurable to you as you make it seem? Please excuse me, if it’s something you actually don’t have any control over. For me, it would be absolutely torturous to feel like that. PJ, I don’t work. I’d had a two month bout with psychosis from a heat induced illness, including passing kidney stones, one time. Having gone through that, I know firsthand, like a lot of “morgellons disease” patients, what a hellish experience delusional parasitosis is. Please relax, I’m not employed by the government, or anybody.
Tens of thousands report Morgellons symptoms around the world, including these mobile “fibers” which are documented in hundreds of photos and videos of tissue samples, but you are the delusional parasitosis poster child, and out of the goodness of your heart, you as a “former psychotic” go around debunking Morgellons to save us from our delusions.
Sure makes loads of sense to me. Uhmhmmm…
if one investigates morgellons, one finds the horrific truth, it is a nanomonster from a lab, and it did not get out there by accident. it’s a bioweapon. operation depopulation i suppose. there is a massive coverup, but i see lately it’s beginning to fray around the edges. this thing is huge.
Morgellons is caused by a genetically modified nematode which was originally developed to increase the production of cotton fibers in the cotton plant.
It can be treated very effectively with topical sulphur and ingestion of sulphur drugs. It is not a mental disease.
The cotton most infected is now coming from South America.
GHamilton, not questioning your integrity, but could you give us some of your documentation on this genetically modified nematode and the efficacy of sulphur as a treatment? If it is simple as that, then I wonder why there is so much confusion, debunking and disinfo about Morgellons.
Americans deserve Morgellons. That’s all I have to say. Ignorance and hate deserves torture of the worst sort. Death to Chertoff and the Fed.
“Americans deserve Morgellons. That’s all I have to say. Ignorance and hate deserves torture of the worst sort.”
uh oh I think you fall within the domain of your own judgement…
I guess what goes around does come around.
Go to Rense . Com and look at the real research.
Listen to the mp3’s on program #10 and then contemplate the truth.
As for you Emma, Jewish people get this disease too. I know. Don’t be hateful!
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Smileykins is FAR from ‘open-minded’.
I’ve followed what he and his cohort have to say about this disease for well over a year and if they are NOT employed to professionally debunk, then the powers that be have sure missed out on employing these guys! I’ll give them their dues, they are GOOD at debunking. That includes ignoring and removing from their website information that contradicts them though.
By the way smileykins – having an open mind means being IMPARTIAL, something you are FAR from.
People in Britain are now coming down with this “imaginary” disease. But not to worry, ‘cos according to morgellonswatch.com, they’re just making it up…
Another thing about that far from impartial website – if you should go as far as to give the hosts any proof of the reality of morgellons, they just delete it from public view. Are these the actions of someone interested in the TRUTH, whatever it may be? I think not.
Absolutely. They have no counter to all the evidence, except denial. I have a nose for professional debunkers as I have dealt with so many of them. It’s like a sixth sense. No matter what the post is, I can feel it in my gut, a sick queasy feeling.
They are always haughty and single-minded and never admit any possibility other than their propaganda.
There is a new website that is just up and running from Dr Hildegarde Staninger. She is the researcher who has the real answers.
http://www.staningerreport.com/welcome.php
I suggest you go read about this if you want the scientific truth.
Here is an excellent article about Morgellons that everyone should read.
http://theparanormalreport.com/morgellons-new-disease-or-manmade-weapon-of-terror.html
i experienced an extremely disturbing squirming sensation beneath my skin in my upper back & in my arms & legs for a day & a half. i had a bag of myrrh that my herbalist had given me & knowing that it is anti-fungal, anti-bactireal, anti-viral, etc., i chewed up 2 pebbles of myrrh each about the size of a dime & the squirming sensations were gone within the day.
My poo hole emitts a foul smelling odour sometimes; could this be Morgellons?
No, I don’t think so Hairy, but you’re getting warm. You see the problem is that somehow your head got stuck up there, so now you need to pull it out. Simply reach down and grasp your shoulders firmly and pull. This should dislodge your head from your rectum. If it doesn’t budge, just take a deep breath and pull harder and keep trying until it pops out.
But since your head has been stuck up there for so long, the real problem is that now your brain is full of crap, so for that, I recommend getting a very high enema.
This should clear it up for you. Let me know how everything comes out.
Ice Helps. Have cold showers, avoid heat. Go for a swim in the ocean. Start wearing only cotton and use only cotton bed sheets. Drink plenty of water and avoid anything synthetic as if it were the plague, especially perfumed soaps. Eat plenty of fruits and vegetables. Follow this advice and the crawling and itching will disappear. Trust me.
That sounds like what I have to do for eczema. Many “morgellons diseasers” are scared half to death of cotton, so get ready for someone to accuse you of working for Monsanto.
Isn’t it amazing how this guy Smileykins haas the time and effort to troll every website that posts about Morgellons? I can’t imagine someone so soulless.
Apparently, it’s his job. Probably gets paid per comment.
Dear PJ, I don’t see why you think the above is the work of a debunker. To me, the author does a wonderful job of exposing just how far the debunkers will go and what means they will employ to deny a palpably, visibly, demonstrably real condition. To me as a person with electrosensitivity, a far less visibly demonstrable condition, the success of these monsters (I don’t think “people” is an appropriate term for these so-called “debunkers”) in this case is very discouraging. People have been driven to suicide by the misery and lack of understanding of others around them. One important point made above is that people with Morgellons do not start out paranoid. I think a normal person would understand why the sufferers were being driven crazy if they knew the torment they had to suffer. Please keep up your spirits in any way you can. There is growing recognition among the public of something going terribly wrong despite the blackout on truthful reporting.
Pat
Iggy, PJ, and Goo:
Why, especially, if Goo has “followed me for well over a year”, am I being referred to as A MALE?
PEOPLE THAT DON’T HAVE MORGELLONS REALLY SHOULD FIND ANOTHER PLACE TO MAKE FUN OF THIS, NOT ALL SUFFERERS HAVE FIBERS. BUT THE MISERY IS PAINFUL AND HUMILIATING ENOUGH. THAT’S WHAT “BUGS” ME.
I had same symtoms without the hairs but constant itching especially at night, tried all kinds of drugs, beta blockers, creams, camomile lotion, finally used Derbac for scabies and it went. I threw out all my clothes and bedding, apart from a small holiday bag which I had forgot, some time later I used a pair of socks from this bag and symtoms came back, used Derbac and it dissappeared.
I don’t think nano-fibers that move on their own power can be equated with scabies. But that’s just me.
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Somehow, after looking for research on chestnut blight, I have come across this. Frankly, it is terrifying and I believe the sufferers are telling the truth. I’m of the opinion that this is caused by GMOs or nanotechnology (though I think the motive is the usual banal one–greed).
Please, does anyone know if there will be a way to stop this if it does turn out to be a GMO or a nano?
Does it really matter what it is called or whether or how bizarre it all sounds? What has happened to having a little compassion? Could all this denial boil down to nothing more than fear it self? I have suffered from this since October 2007. We are talking a life changing event. I have pretty much lost everything including my sanity. I suggest for your sake you wake up to what is happening before you or someone you care about comes down with this awful, awful, awful skin disease. Stop the denial and let’s work on a cure!! For everyone else, I love you, hang in there you are not alone!
The cure is to stop the psychotic elite and their eugenics/transhumanist insanity.
Touche PJ! Your witty response (9/27/07) to the Hairy ass had me lol.
Kudos!
I’ve once or twice wondered about Smileykins and thought ‘how pathetic this poor ol’ soul — no better way to occupy precious time, and so like a school-yard bully, resorts to the incessant chasing of those perceived as weaker, taunting them ’round and ’round the yard — clammoring for attention deprived. Or perhaps it’s morbid curiosity borne from a lack of stimulation (intellectual or otherwise) to help fill a dull life? How sad, what a loser. In any case, it is clear this person should consider a more fulfilling past-time. There are many wonderful spriritual/pyschological/inspirational self-help books out there. Why not get up, get out, and get over to the book store — enjoy a good cup of coffee and a nice read? A little fresh air may help to re-focus energy toward ways of improving upon the short-comings of the personal life-situations, rather than projecting misery on others.
Our misery does not love your company, Smileykins. Please, go work on getting a life and leave us to comfort each other in peace.
May divine guidance interceed on your behalf and offer you some grace.
If this was a psychotic phenomenon don’t you think there would be less cases with more diverse symptoms. But if any other cover-up were to be deployed for any other illness it would succeed in most cases. If the government tried to tell us that the Flu was just a psychotic illness then doctors will HAVE to tell the patients that lie. What people need to do is work their way around the “doctors” and find help from more humanly people. If doctors ARE trying to cover this up, there has to be some other crazy demented operation going on out there, like a depopulation test, or even worse human trials for a genetic war weapon. The psychological symptoms suggest a manipulation technique to render an enemy hopeless, and give up their campaign. On the flip side of that theory the article above pointed out a 17th century article on a similar disease, so maybe it’s a natural bioform. Aside these speculations, more on-hand examination, and testing has to be done with this peculiar occurrence. For comments please mail me at my myspace page listed above.
The picture of the hand and the open sores: It most definately looks like a man’s hand, but with lady’s sculptured nails. Most likely it’s some meth-up drag queen. The itching and scratching and open sores and paranoia are all symptoms of meth use.
Morgellons is a skin disorder that was first described more than 300 years ago. The disease is characterized by fiber-like strands extruding from the skin in conjunction with various dermatologic and neuropsychiatric symptoms. For support: http://www.morgellons-disease-research.com/
I have been studying Morgellons for 3 years and have spoken with hundreds of victims. I assure you that this disease is real.
Most victims tell me that the only thing that helps them is nutrasilver. It seems to heal the lesions in 3 weeks and eliminate the brain fog, depression and chronic fatigue in about 2 weeks or less. You may wish to give it a try: http://www.nutrasilver.com
Hello believers and non-believers alike….
Im here to impart my 2 cents on this topic.
I heard of morgellons quite some time before catching it myself. I was undecided at the time of reading the “facts” that neither clearly debunked nor proved if it exists or not.
Then I got a VERY strange sore. It started like an invisible bug bite, then it quickly became a lesion within a day and then it turned into a damn crater! Assuming it was a spider/skeeter bite I left it at that. But then it seemed to itch every few days and never heal.
Next I got many more, what I thought were bites, on my lower legs and ankles. I treated them like any bug bite and yet they did the same crazy things the arm bites had.. They swelled up and turned red, then lesion, then crater that VERY slowly heals. It wasnt until after re-seeing a video about it that it clicked. I started looking for fibers.. Wouldnt you know it they were there. Still not one to jump to conclusions I assumed the fibers could be from my clothing so I devised a series of experiments in which I would ultimately find the truth..
1. I wore ONLY red clothing from head to toe which I sealed at all ends hoping to reveal if red fibers were the only ones present and to keep any insects from easy access to most of my skin.
Results- Still I got more and more “bites” and there were more fibers, BUT NOT RED!
Still not sure I thought maybe somehow the fibers had gotten into my red clothing during wash etc. So I did my final test.
I waited until I had a new “bite” and I literally dissected it out. I know it sounds horrible but it was the only way I could think to find out if there were any fibers inside the red bump BEFORE it turned into a lesion. Guess what? To my sheer horror, there was disgusting fibers deep within my living skin. The skin was unbroken until I removed it, I found the fibers on the underside of the lesion and they were VERY intertwined into the skin. It was very difficult to remove any of the fiber from the skin but I still got a good look at it under a microscope. Appeared to be 2 colors, clear/white and blueish/black. Some clear/white strands have what appears to be dark ends.
Furthermore, later my hair fell out on my head, I started feeling weak and older, my vision blurred rapidly then returns to full function (20×20), my eyes itched a lot, and I think I started getting them on the back of my head but was unable to see for sure. Smaller on the head but same effect, small crater, never heals even after months….
Lastly. I took action. I dont know for sure if its in remission or if its gone but it appears to be gone at least for now. Here is what I did.
1st I attempted nutrasilver, and while it appeared to help, no matter what they kept sporadically appearing but the itch was a bit less and they lasted just a few weeks shorter. 2-4 months average healing time without nutrasilver, 2-3 months with using it.
2nd I attempted shaving my head, using topical creams for skin conditions fungus etc. No help.
3rd times the charm… I ran across some videos by Dr. bob beck, they were unrelated videos since he died years before the discovery of morgellons. But he had systems for relieving extreme diseases so I gave the silver method a try. I suppose its a lot like nutrasilver but I get to choose the potency and delivery medium, IE cream, water for drinking water for topical, etc.
Its very simple and you can do it for nearly free.
You just need 2 items of pure silver, either .999 or .9999, (99.9% or 99.99%) and a small dc power adapter around 9-27 volts with low amps, something like 100-300 milliamps. Example 9v DC at 200ma. Then you attach 2 alligator clips to the positive and negative wires, clamping them onto the pure silver and dangling the pure silver in water for a few minutes. For internal colloidal silver I use only pure steam distilled water, for topical you can use tap water.
Take a gallon of steam distilled water and pour a massive cup full, add 2 tablespoons of tap water to get the juices flowing since pure water is a bad conductor unlike tap water. Leave it for 10-20 minutes and check your progress, upon stirring you should see some fog in the water, in fact a lot of fog since you will be pouring it back into the gallon shortly. Once you think it is clearly a cloudy liquid pour it back into the gallon and shake. This is your drinking silver take between 1-3 8oz glasses a day for 2-3 weeks.
For topical its much easier, get a shot glass near full of tap water, dangle the pure silver into the glass for a few minutes, unlike pure water, tap water will start dropping silver very rapidly. Once you have a shot glass full of VERY cloudy water check to see if a laser can make it through the water or not. Keep going until the laser doesnt shine through the other side. Then apply as needed, likely 1 shot glass a day on a shaved head, or a few drops on each lesion will do the trick. Honestly though once I started ingesting a glass a day they immediately started lightening and going away. Ive tested the topical method on so many things and people its not even funny. It is like some sort of miracle metal. Taking care of sores, scratches, BURNS
continued since I accidentally hit the submit button.
BURNS, zits, rashes, infections, non-healing wounds, athletes foot, busted lip, road rash, bites, mouth sores, cold sores, cuts, etc. etc. The list is literally too long to remember. Even had a friend swear by using it to relieve eye sty’s he occasionally gets, I personally wouldnt suggest this but he assures me it works like nothing hes ever tried. Once a few friends started using it then their friends and family etc.
Silver is known to kill over 600 different pathogens, bacterias, molds, fungus, parasites, etc. In petri dishes it even kills aids, cancer, and herpes.(scientific tests)
Finally I would like to say a few words to those who think its all in peoples heads, including those PIGHEADED DOCTORS out there…
Hey Im more of a skeptic than most and leaving my mind open I could neither dismiss nor prove the reports I had heard before it happened to me. It seemed totally plausible that either some pathogen was invading these people or that they really did have a mental psychosis causing insane scratching, lesions, etc. But there is clearly no denying it when you are the victim. I dont have mental problems, in fact Im considered a genius by many, I dont have paranoias, psychosis, delusions, etc. I simply had a problem and with a lot of effort I think I first found it then fixed it.
Hey im not out here saying buy my product, Im not saying buy their products, im not hiding the secret in a book for you to find. Its nearly free, make it yourself and see. I must add that if you do DRINK colloidal silver regularly you should take some macrobiotics and probiotics to replenish the healthy fauna of bacteria that aids in digestion, etc. Many special yogurts have tons of probiotics or you can take supplements after the silver treatment.
Warning- Do NOT use coins UNLESS they clearly state on them .999(silver eagle rounds or ingots) or .9999(canadian maple leaf coin or pure silver wires). The average “silver” coin for monetary use is actually only 92% silver and contains things like zinc tin and lead, so you dont want colloidal lead, zinc, etc.
That is all foks, looks like my 2 cents turned into a twelve dollars but I type fast, and if one person gets relief then it was worth it.
Einstein
well… my 2c is probly only good for about 1.5c, with inflation & all. plus i dont personally have this thing or know anyone who does (um, yet?)
but, did have a wierd experience with some kind of unidentified FUNGUS INFESTATION down in SoCa about 3 years ago. which dr’s didnt listen to either. people, listen to your own bodies. the experts really dont know everything, they just often act like they do. ADVICE: FIRST DO THE RESEARCH, & THEN TRUST YOUR OWN INSTINCTS (btw, ‘idiopathic’ only means, ‘medically dont know & frankly who cares’)
my story may or may not be relevant at all, altho some of the symptoms do seem to match up.
i live in Oregon, but grew up in SoCa. OC actually, & i can attest to how polluted the environment (air, soil & water) is there. my general health really improved after i moved to the generally cleaner ‘n much greener Pacific NW. several years ago, i went back down to OC for a summer to help out my aging parents- mom has FMS and suddenly seemed to be getting much worse, mildly delusional, severe anxiety, lots of new pain & fatigue, and what’s more… persistent, disturbing crawling sensations, or fire&ice, or twisting blade sensations, plus a ‘floater’ in one eye that sometimes she described as an oily blurring, and sometimes like a hair inside the eyeball. either way, it never showed on any test but was driving her nuts anyhow. did i mention her hair (never thick to begin with) was coming out too? so, i kept hearing all this for months in phone calls, getting more concerned until finally i went down. i planned on taking care of some house repairs & cleanup for them too, as mom had been complaining of a funny looking mildew problem that had recently been getting worse, affecting books & papers as well as as painted walls. lo & behold we soon discovered a much bigger problem than they had realized. these WIERD ORANGE SPOTS were everywhere!! all over books & papers(they were bibliophiles, we filled half a dumpster with ruined reading materials!), cotton linens & sheets, framed pencil art, and black & orange spotty mildew inside every closet in the house. torrential winter rains getting into a wall plus leaky pipes under the house had caused all this. the black stuff was plain ole mildew. but NO ONE COULD IDENTIFY THE ORANGE STUFF. one ‘expert’ said, he’d never seen it in 20 years therefore it wasnt mold. (so what did he think it was? rust??) And no one acknowledged that it could possibly be causing my dad’s asthma & certainly not my moms ‘idiopathic’ problems.
interesting thing tho… i was there with them for 2 months working to get the place clean and move out ready, and in that time i developed… yup… falling hair, mental fog & confusion, fatigue & joint pain, gritty eyes, bronchitis… and best of all, the constant sensation of itchy footed bugs crawling all over me! especially my face. sometimes ‘ice water’ pouring down my arms & legs too.
so, jump ahead 3 years… and my folks now live in Oregon, 20 minutes from my family, in a much cleaner ‘n greener place. ask how we feel. go ahead.
A LOT BETTER! no more crawly bugs or hot ice! no more floaters or itchy, gritty ‘hot rock’ eyeballs. a lot less anxiety & confusion. hair quit falling. we still have fatigue & joint pain, but hey, thats just FMS for ya. we can live with that.
so my thoughts are, if a mystery fungus could cause all that, could that be what is going on with Morgellons too? i notice that LA is the US hotspot, along with urban areas in TX & FL… pollution must have some part in this, either direct or indirect. and if leaving the contaminated area was key to relief for my mom & i, with our fungus issue, could getting away from the hotspot areas bring relief to Morgellons sufferers too? has anyone been able to id a link to certain locales, or in getting away from them?
my brother’s family still lives down there, and he has a baby girl who has suffered with intense rashes almost since she was born. their dr said its eczema, but i am keeping posted on this morgellons thing all the same. after all, no one who has it ever thought they ever would. nano, gmo, environmental pollutants, bis-A, you name it… there is just a lot to look out for these days, isnt there.
ALL my sympathies to the sufferers. and to the so-called d’bunkers i just have to say… wait until you get sick. then see how you feel about these things. in the meantime, enjoy your good health with out getting snarky on those who no longer have theirs, for goodness sake! health is a privilege, not a ‘right’- and is appreciated most by those who dont have it. GOD bless you & keep you & give you HIS HOPE.
um, by LA i meant LosAngeles, not Lousiana. i should be more clear. oops
I think morgies are some of the best people in the whole wide world. Just ask a few of ’em, and they’ll tell ya so, in the same breath they tell ya to rot in hell with.
Hey Smileykins,
Rot in hell…
why condemn Americans we were born here i am a full blooded Indian I have no qualms of with any race religions yes but this is also none of my damn business .. Children are being hurt with this are they too blame too .. there needs to love and understanding if one is too heal .. it hurts and i aint no hitler!! ya i play with myself from time to time but shit i dont hurt no one.. we need help as you will too in your countries and i wouldnt be surprised if this is where it comes from please stop debunking americans
How is it that this Smileykins person, who supposedly doesn’t have this but instead suffered through delusions, can not only follow this article 2 years after it was written, but continues the exact same debate despite thousands more sufferers and mounds of more proof? SK must have some sort of software that flags whenever the subject is breached. It makes no sense.
Also, bo’nana…. I live in the So Cal area and all that you describe sounds exactly like what I’ve experienced. Since the year 2000, I had always had ONE hepa air-filter in my home. For years, it would take at least 3 months for the filter to become dirty enough to need cleaning. Beginning in Oct. 2005 though, after heavy chemtrailing began in my area for 9 months straight, my air filter became completely clogged with some sort of filament fibers. Similiar to spider webs. I bought 2 more air-filters… No matter, all 3 become completely dirty within a few days. I had all the physical symptoms you described. Eye floaters, joint pain, crawling bug sensation under the skin, 3 years of a throbbing in my gums under my left incisor tooth, etc. The only thing that has made it tolerable is pain killers. Unfortunately this is expensive and addictive. I have thought many times that i should try to move out of the area. The problem is I am so weakened and fatigued, it is impossible to do this on my own. I don’t have any help. I wish there was some way to email bonana….
Smileykins is an agent provacateur, a mind-controlled zombie or a demon-possessed psychotic or all the above.
hello from australia!@ i recently have started finding fibres (black and blue) and am suffering from skin lesions but have no itching as of yet.. i found “morgellons” from searching symptoms and lack of conventional help.. and to the people (neil & smiley) who question sufferers and voice their negative opinion i ask you why? noone wants to hear from you, you arent helping anyone and how would you feel if you or someone you loved (probly noone loves you is why you comment here) was called a “junkie” or dug abuser after reaching out for help by people who are nobodies? it is truely sad that people like you who obviously arent human show no compassion for your fellow brothers and sisters who are suffering and it is scarey.. why dont you join in on the search for knowledge? are you afraid? or maybe you are just immature.. if so i hope you grow out of it.. if you are older than it puzzles my why you try to hinder the united human quest for answers and abuse such beauty of the internet.. then again maybe because you found this you are showing symptoms yourself and are in denial.. it is big what is going on but together we will find answers for a better tomorrow .. :D peace
AIDS, H1N1, Morgellons, etc, all these “emerging” illnesses are actually bioweapons unleashed on the general public to either depopulate the planet gradually or to otherwise weaken people physically and mentally. There is a war on humanity which is the real war being waged globally.
….and depopulation through suicide…
A Challenge to Celebrities Who Quietly Suffer From Morgellons Disease
I have a challenge to Celebrities around the world that are silently and privately suffering from Morgellons Disease; when your symptoms have been reduced or eliminated, who among you will become the “Spokesperson for Morgellons?”
Morgellons disease is just as real as HIV was 30 years ago. The only difference is 30 years of research and study by the medical community that has gone in HIV. This will only occur when Morgellons hits a certain ‘plateau’ of patients and research attention.
What is truly needed now is a celebrity who has Morgellons and is willing to tell the world about this horrific disease. This will only work if the celebrity has Morgellons and has eliminated their symptoms to the point where they can really function in this capacity.
Let’s tell the truth here; 99.99% of the medical profession has never even heard the word ‘Morgellons’ yet alone has been willing to open their minds to the possibility that it might even exist. Only those who have experienced Morgellons can truly ‘know’ what this is unless they are living with some one who suffers every waking moment of their lives with this terrible disease on their minds. How could they not? The feeling of biting and scratching 24/7 will certainly draw anyone’s attention.
The author of this post deals with Morgellons victims daily, hundreds each month as this pandemic explodes across our planet. He hears their cries of pain and suffering, the loneliness and isolation they experience and most horrific is the way the medical community is quick to diagnose Delusions of Parasitosis (DOP) without the benefit of an exam or lab tests (to date all known lab test result in nothing being found).
What the MD’s have forgotten is that in order to have DOP, the patient must be schizophrenic because DOP is a sub-set of schizophrenia BEFORE they can be diagnosed with DOP. If their patient is not schizophrenic, DOP is not possible.
What is missing here is public awareness. To date 40 US Senators have written to the US CDC requesting an investigation. It took 6 years for the CDC to begin their investigation into this new disease. It has now been nearly a year and a half since the CDC began the investigation and their conclusions are expected in May of 2009. The question to the reader is: What sort of conclusion might you expect if you funded such an investigation if you only funded it to the tune of $338,000? You decide.
There is a safe and effective way for Morgellons victims to reduce or eliminate their Morgellons symptoms; Nutrasilver. This natural mineral has proven in thousands of cases to eliminate most, if not all cognitive and lesion symptoms within a few short weeks. Although not a cure, Nutrasilver has an amazing ability to push this disease out of the body from the inside rather than treating with lotions and potions. This can be very frightening, but the good news is that it is coming out of the body.
I am aware of several Celebrities who have become “symptom-free” from Morgellons disease using Nutrasilver and I challenge them to step forward and become the “Poster-child” of this grass-roots movement of Morgellons suffers. There are obvious personal benefits to doing this, but the most important thing a Celebrity can do for the Morgellons movement is to step up and make the world aware of this life-stealing disease and let Morgellons victims know they can get their lives back using Nutrasilver. http://www.nutrasilver.com
To see proof of how Nutrasilver affects Morgellons victims, please click here: http://morgellonstreatment.blogspot.com/ Caution; this site is NOT for the faint-of-heart.
I have no idea if Morgellans is a real disease or not. I am highly troubled by Smileykins though. I can’t for the life of me understand what motive he/she has for remaining on this site (for four months) to so strongly refute the existance of something that he/she doesn’t believe in. If you don’t believe that it exists than go along your merry way and get a life. And about that website that Smileykins supports: How does simulating pictures of a a perported illness prove that the illness doesn’t actually exist? Here’s a history lesson–it was once a firm belief that those who 1)thought the world was round, or 2)that the sun was the center of our solar system, or 3)that flies infact did not grow from dead pig flesh, were suffering from some form of obvious psychosis. You can’t prove that something doesn’t exist by merely saying so and then telling others to prove you wrong. Smileykins acts as if he/she is personally at risk of something if Morgellans does exist. It almost sounds like he/she works for some as-of-yet unidentified organization that caused Morgellans in the first place and is worried that they will be held acountable for their wrong doing.
Excuse me, Smileykins has been hovering around for 2 years and 4 months… This is somehow very personal to him/her.
MisterWhiskers –
That is an interesting spin on the usual interpretation of Smileykins et al. Most think they are simply paid disinformation agents. (and well paid, evidently, given all the effort that group has put into their blog!!!).
But fear of being killed (or, WORSE, infected with Morgellons) are pretty powerful motivators.
I’ve thought about Smileykins some more and I have a couple of thoughts to share. My best guess is that Smileykins is working on an educational dissertation–probably a doctoral degree requirement or something similar–and his/her (Smileykins’) basis is that Morgellons doesn’t exist. I don’t know that this is the case. Regardless, his/her view is severely biased–but so is the view that you hold (each of you that believe that you have Morgellons). My view is biased too, but hear me out…I believe this can help you. Smileykins doesn’t need help because he/she isn’t suffering from the disease.
I am a Gulf War veteran of the Desert Shield/Desert Storm era (1990-1991). I came home with many undiagnosed illnesses with numerous physical and mental symptoms. Like many of you, I became extremely frustrated at the lack of medical attention. Specifically, I was told over and over again that there was nothing wrong and that I was depressed. Of course I was depressed. I was depressed because I couldn’t get any help! Well, I got out of the Army 1-1/2 years later–still sick. Within a couple of more years, it became apparent that I was not alone. Using the newly available Internet I met many veterans who were suffering just as I was.
I can tell you that I came into contact with MANY doctors who “believed” that there was a “Gulf War Illness,” and they could “cure” me. The truth is, most of them only wanted to cure me of what little money I had left. Still, a couple of doctors worked with me for free, and really did look for answers. Some of those doctors found answers—for other veterans, but not for me. To this day I still don’t know what caused the majority of my symptoms.
This is the part that is likely to sting… Until I got away from all of those other “supportive” veterans and started working with an Internal Medicine doctor, a neurologist, and a psychiatrist (each in a one-on-one relationship), I found no relief for my symptoms. It took doctors willing to treat each symptom independently at first before I improved. The problem with the support groups is that when each person lists all of his/her symptoms in the community blog, you identify with and confuse their symptoms with your own. At least I did. That’s because when they list things like constipation, and headache, and fatigue you think to yourself, “Hey, I had constipation! I had a headache! I have fatigue! I didn’t know that was because of {insert disease of choice here}!” All of a sudden, you have the exact same symptoms. Granted, I don’t, and never did, have fibers growing through my skin.
Your help will not come from the Internet. Keep a symptom journal! It’s the only way you’ll begin to understand YOUR disease. It will also immensely help your primary care provider to treat each symptom. It will also help you learn what side effects can be attributed to your medications.
I am NOT disease free, but if you are interested in my semi-success story, email me at gmail dot com (use my username above). Keep your hard earned money.
I don’t believe for a minute that you are who you say you are. First – Smileykins working on a graduate thesis???
Secondly, you seem to entirely miss the point. It wasn’t until all the medical steps were taken that most of us even researched what our symptoms were.
This is horrifying beyone words, and when you are shunned by the medical community, it is look for help wherever you can find it or suicide – an option taken far too many times with this nightmare.
Yes, I did learn that the lipoma I had excised 3 months before my Morgellons erupted is a common occurrence (gosh – even the dermatologist who did the surgery had the delusion I had – even CUT and stiched me!). And the explosion of floaters that appeared two years before the Morgellons (no – I didn’t go to a doctor about them right away; I learned on the groups that this, too, was a common symptom – and the opthamologist I eventually visited saw them easily when he dilated my pupils)
An awful lot of doctors seem to be reading from these groups and contributing to the hysteria.
By the way, if you have been diagnosed with Gulf War Syndrome, you should get a 30X – 60X magnifier and go out into the sunlight. The fibers are visible beneath unbroken skin; lesions are not necessary.
number one advice to people with skin issues. there are about 1000s ailments that cause similar reactions in humans. luckily many of them are treated the exact same way. you could have scabies, herpies, bedbugs, be in withdrawal from many street or perscripton drugs or simply be insane. the nano fibers thing is like hog wash. i stumbled upon this article because i recently had a similar skin irritation for three days all over my body it had all the symptoms of scabies and i thought it was but i took a few baths with a cup of bleach and self medicated whatever it was away. i do not think it was scabies because i didn’t even wash my bedding. people stop jumping to so many conclusions just because you want to believe the government is responsible for all your problems. I would leave my country for far less than this if i believed it were true. only a dermatologist is gonna take you seriously regular doctors don’t know anything about skin ailments.
There is only one disease that causes the fibers (that are not any known substance) to grow out of and under unbroken skin. That is Morgellons.
The fibers were taken to the Tulsa Crime Lab and compared to 800 textiles (both natural and synthetic) that are in the FBI database. There is no match.
When they were subjected to FTIR elemental analysis, again, they did not match any of the known 96,000 substances.
There is much more, but no more needs to be said. If a person has these hallmark fibers, they have Morgellons – a newly emerging pandemic.
It is time for the world to wake up. This is not only incredibly bizarre and more frightening than can be put into words, but it is something that the world has never seen before.
We desperately need professionals who can suspend their understandable disbelief and LOOK at the evidence. So much more research needs to be done.
Any amount of money that you can afford to donate to either the MRF or OSU would be greatly appreciated.
Recently, a single donation of $12,000 was given to OSU for two targeted research projects. Both of these projects are replications of previous studies, and will be written up for publication in peer-reviewed journals.
In addition to a high profile sufferer to step forward to give Morgellons a face, objective research must be done.
The first reason is to prove beyond any doubt that this disease is real and unlike anything that has ever existed. The second reason is to begin to understand the nature of it so that appropriate treatments can be developed.
Some info directed to those in, what I refer to as; “Morgellon’s Denial”
On August 1, 2007, the CDC issued the following statement regarding Morgellons Disease: “Morgellons is an unexplained and debilitating condition that has emerged as a public health concern. Recently, the CDC has received an increased number of inquiries from the public, health care providers, public health officials, Congress, and the media regarding this condition. Persons who suffer from this condition report a range of coetaneous symptoms including crawling, biting and stinging sensations; granules, threads or black speck-like materials on or beneath the skin; and/or lesions (e.g., rashes or sores) and some sufferers also report systemic manifestations such as fatigue, mental confusion, short term memory loss, joint pain, and changes in vision. Moreover, some who suffer from this condition appear to have substantial morbidity and social dysfunction, which can include decreased work productivity or job loss, total disability, familial estrangement, divorce, loss of child custody, home abandonment, and suicidal ideation.”
The government is paying to have the patients who have the disease studied and the “fibers” analyzed.
Stop wasting your time denying this condition (that has nothing to do with you anyway) and just wait and see what the study and analysis will reveal like the rest of us.
Morgellons Attacks Teenagers Too;
Danny Shares His Story of How He Got His Life Back
Dear fellow Morgellons victims,
I’m writing on behalf of all the young people and the elderly with Morgellons who have been shunned, criticized, and outcasted by society thinking we suffers of this horrible disease are crazy. I personally knew absolutely nothing about this disease until I came home from school one day of September 2007 and noticed granule-like crystals on my hands. I also noticed clear fibers that appeared to be coming out of my hands as well. I went to the computer and typed in “black crystals on hands?” or something to that extent. I stumbled upon a few websites that had details of Morgellons symptoms and the blue, black, clear, and red fibers with granules coming out of hands, body, and or hair. I didn’t automatically assume I have this disease after a couple months of thorough personal research I had whatever this bizarre disease was. Every single symptom I had matched everything I read. I had everything from the physical identification of Morgellons right down to all the mental and cognitive disorders of Morgellons; brain fog, I slept constantly, depression, insomnia at night (slept all through the days), lost a lot of weight, everything aliment you could imagine I had. But by far the worst symptoms was the anxiety that would come out of nowhere, it literally felt like I was even in my body at times.
It began to slowly but surely rule my life. I noticed the fibers everywhere in my home, friend’s homes, family member’s homes, these fibers were everywhere but I was one of the only that had symptoms to this extent. My friends and family had the fibers on there body and hair as well. My friends were the only ones who believed me about the fibers and knew I was sick. I tried to express to my mother and stepfather what was going on but surely my mother thought I was loosing my mind which I can completely understand because of how bizarre this disease sounds to the layman. Finally after convincing my mom I had this disease I stumbled upon a website called “NutraSilver”. My mother personally thought I was crazy but my stepfather said “whether its in his head or not we can see if this helps”
So my stepdad bought a bottle of NutraSilver and it came with another for free. The first night I tried the NutraSilver I had to lie down in bed with my mother I trembled so bad. When I woke up the next morning I felt slightly better. I started to use the NutraSilver a couple times a day and just put some drops in my daily routine of drinking water. Everyday progressively got better, I started to forget completely about Morgellons and live my life. It ruled my life, I am an 18 year old male (at the time I was 17). I also stumbled across an amazing doctor and friend named Dr. Susan Kolb. I found her website when I was researching about Morgellons and even though I lived many states away and was very embarrassed I deciding to just call her and tell her what was going on. She talked to my parents, talked to my family and tried to express to them that this is a real disease. Still after all of that they still did not believe. She gave me great tips to get slowly but surely better as well. I slowly started being able to go to school more and focus more on my life. Everyday with NutraSilver and Dr. Kolb’s advice made everyday easier to get through. As last summer came along (2008), I was very confident I was Morgellons-free. I completely forgot about the disease and was able to live my life.
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This is actually some thing that is done to you. I cannot disclose who I am for fear of loosing my security clearance. Those sores are something that is done directly to you. It is administered by way of clear fluid that comes off of thier finger tips and flicked on you. The more concentrated version is delivered by an aerosaul can. The fact that this is going on is a highly gaurded secret. I have tryed to put a stop to this sort of thing in the past and have found it to be a rather dawnting task. If you want to put a stop to this, please email me at unificationv@gmail.com
NEMATODES!!!
Its a Fungal infection
complicated by miasis.
Theard like fungus grows in top layer of skin exploding giving a stinging biting feeling. The constant growing exploding reattaching itself to your skin causes constant unrest.
buy 1 sanding wet sponge fine /medium
in a blender, blend to a smooth mixture
2 yellow onions with skin
1 avocado with skin and seed
3 limes peel seeds and all
1 cup collodial oatmeal
soak whole body hair too
wash with oatmeal bar and sanding sponge
sores start to heal, fugus starts to die
3 to 4 baths should do it, but your house, car, cloths are a source of reinfection. Use white vinegar to clean 9% spray floor, car
Oh, one more thing cuticurri oatmeal soap with castil soap cleans skin.
hi again,
i wrote awhile back about how moving out of the soCal area greatly improved me & my family’s health & quality of life….
well it did. for several years. but portland has been inviting a great deal of expansion over the past few years, there has been a real population explosion in our valley… and the effects are becoming noticeable: we now have Traffic, Overcrowding in many areas, and SMOG. our water has had issues with contaminants, and now they are talking about adding new chemicals to the stuff we drink in an effort to combat the other chemicals etc. because of our wet climate, molds are something we have always had to be vigilant against. i dont know about morgellons in portland yet, but we are the lucky recipients of the boobyprize for having the most victims of MS (just as nasty).
this has been an interesting year for my own family: my ADHD/Tourette’s son landed in emergency twice with severe asthma attacks (something that only happens to him in periods of bad air: smog, fires, etc)… both my husband and i have experienced a great deal of unexplained hairloss (over the course of the year we have gone to approximately half of what we had before)…. and this past spring i was diagnosed with Morphea, which is a type of Scleroderma.
so, in case anyone was thinking portland might be the place to go to get away from pollution, think again before moving here- our valley is well on its way to being the next “LA Basin”. oh, and we have major issues with jet Contrails overhead too. plus now i am finding out that we have stuff drifting over from japan too…. and even eastern oregon has big problems with smog, becoz of the coal-fired Boardman Power plant which supplies electricity to most everyone in this part of the state.
grrrrr…. is there no way to escape!
i guess we are all reaping according to how we have sown, eh. somehow its ALL going to turn out to be POLLUTION related. even the crazy wierd funguses, becoz they feed on our chemicals and our toxins and then infect us with our own poisons.
Stephanie- i like your suggestions. i am allready using castille soap becoz my hair and scalp no longer tolerate the chems in ordinary shampoos. i am going to try your scrub and see if it helps the wierd little sores i keep getting on my face and under my arms (also something new to my whole family this year) that might be mrsa? they start like pimples but burn like fire and refuse to heal. maybe your recipe will work for that too!
cheers
That’s odd; I was diagnosed with Morphea in the early 90’s and often wonder if that was the beginning of this mess. I was also diagnosed with MS in 1982. Just lucky, I guess…
yikes! Claire! i would love to hear more of your personal story, i bet a lot of readers would. if you wouldnt mind sharing…
bo’nana –
Give me a little time. I’ve been meaning to write it up for some time now, instead of re-writing it over and over and thrown together. I’ll do it on word pad, then copy and paste.
Just curious – have you ever heard of a connection between Borrelia burgdorferi and Morphea? Google it. Very interesting, because I don’t have Lyme, but I got Morphea while living very close to Lyme, CT. A nurse I worked with had Lyme Disease.
Will get back to you…
Claire
claire-
was wondering how you were able to discern that you are definitely Lyme free… that can be tricky- and expensive!
yes, i do know of the connection, and have considered that i may have one of the milder variants (there are several).
Unfortunately, i know of no medical insurance that is willing to cover the kind of testing required, the results are often iffy at best, and frankly, my pockets just arent that deep…
but i think that having grown up in tick-heaven is grounds enough for vague suspicion, anyway.
another thing i learned about Morphea is that there is a genetic connection to several family lines of Oklahoma Choctaw. i am of choctaw descent, altho several generations removed and not sure of specific family ties… but i found that an interesting coincidence, at least.
as far as autoimmune illnesses go… morphea doesnt seem that bad when so many are just horrible! so far mine hasn’t manifested worse than an occasional inconvenience, brought on by various combinations of stress, hormone imbalances, dietary deficiencies and/or chemical toxins. as far as i can tell, anyway.
how has your condition progressed? how long afterward did Morgellon’s develop, and what sort of connections have you made there? i am so intrigued by the fungus hypotheses… or has it been confirmed now?
no morg’s here, but i certainly do know what its like to have all kinds of wierd skin sensations from exposure to mystery fungus- and how frustrating it feels to be patronized and ignored by your doctor!
looking forward to your eventual response….
until then, and to all readers on this column-
i wish you a very Merry CHRISTmas, and a New Year filled with Hope!
Rest to the Weary,
hannah
how do i find out if the photos of morgellan pt may be of me. i dont care if they are but the clinic doctor who took those pictures and i may have to go back to them for service because we live in a small rural town and they are the only clinic within 60 miles.
Quote: “Then I got a VERY strange sore. It started like an invisible bug bite, then it quickly became a lesion within a day and then it turned into a damn crater! Assuming it was a spider/skeeter bite I left it at that. But then it seemed to itch every few days and never heal.”
Interesting. I was looking up morgellons out of curiosity to see what it is about. The pictures astounded me, because I have a lesion on my lower right leg that looks just like a ‘morgellons sore’. The scenario was the same for me as described in the above quote, though less of a crater, and more of a hardened below-skin callous and surface rash/lesion with a lot of itching. I used cold-pressed castor oil on my lesion and it is halfway healed from only two applications.
I don’t know if it’s morgellons or not, but in any case, castor oil is great for clearing up all kinds of sores and itchy-skin problems and could be helpful for those who definitely have it.
It’s real, not imagined. My first contact with it was in the Seattle area about 1998, before 911. It is a parasite that can move rapidly like a microscopic snake and punches into the skin; it doesn’t “bite”, it enters the body and feels EXACTLY like a flea bite. If you can bare it long enough, you actually feel them “wiggle” their way in. they sense body heat. Some people are oblivious to it, while it torments some of us. I suspect that has something to do with skin pore size. It seems to have some intelligence, as it knows what areas are vulnerable and can’t easily be scratched, like mosquitos do. I sometimes pick them up from riding the bus and I know immediately when I have them, they waste no time when it comes to “feeding”. I do a “decontamination” of me and everything on me! Heat kills them and rubbing alcohol either stuns them (so they can be washed off) or kills them. Wash your hats and everything, they live for days off of the body.
I believe they are a cross-over parasite from insects, similar to the nematode that attacks the date wasp. They spread quickly over the body and breed rapidly. I’m buying a microscope and I’m going to catch one of the little suckers. They can’t be seen under a 10x loupe, I’ve tried that already! Whatever it is, it’s an epidemic and being dismissed or ignored. If they are a living parasite, they can carry bacteria and viruses…that creates some scary thoughts.
The sad part about this is the children that are picking these up and trying to get someone to help them because “bugs are crawling” and people are saying these tormented children are “delusional”!
rick, i agree- those experiencing these problems know it is real!
i am wondering tho, if what you are describing might actually be related to Demodex mite infestation?
…that is not to minimize what you said in any way… the constant itching and ‘crawling’ sensations can drive a person to feeling a little nuts! and it doesnt help that few people who are not/have never experienced some sort of wierd mystery ailment ever seem to really listen to the sufferers, merely chalking it off as imaginary delusions and suggesting psychiatric meds instead of any real help.
however, everything in your post pretty much describes what i have been experiencing for the past couple years- for all i know, that is how i ended up on this site in the first place- i too itch and have wierd little slow-healing sores, but i know i do not have Morgellons. (a simple test: if the plug that comes out of a pore can be burned with a match, then it isnt morgs)
it took ages to figure it out, there is just not a lot of good info about the problem on the net, unless you allready have a name for it and know where to look. so demodex is like morgellons in those ways. but it seems nowhere as severe… ive been fighting the mites without knowing it for at least a couple years now, and so far it has been more infuriating and inconveniencing than actually life threatening or incapacitating.
some of the symptoms of both conditions match up, although i’m sure they are caused by different organisms…. with Demodex, i have experienced a constant tickling and crawling that used to come and go but over time became constant over first my face and scalp and eventually my whole body. after that happened, my face began to develop small pustules which would crater out and take forever to heal. later on, they also began to sting and burn like fire… similar feeling to fire ant bites… they felt much worse than they looked, but the sores all over my chin and here and there on my forehead made me look embarrassingly like a ‘meth-mama’! (i avoid pharma like the plague- the hardest thing i do is my morning coffee)
believe me when this stage kicked in i started wondering about morgellons. but as i said, if the stuff burns then that aint it: occasionally the sores will produce a small whitish ‘seed’ – the biggest one like a small grain of rice- which can be plucked with tweezers. the sores bleed like crazy afterward, but always seems to help move them toward healing a little faster than the ones which produce only a milky fluid instead of a solid core.
from what ive been learning of Demodex, it would seem that probly everyone has the little buggers, but for some reason overgrowth is becoming more common. (my guess- pollution. pollution. pollution!) they dont seem to cause any problems for people until and unless overgrowth occurs. probly a lot like Candidiasis/yeast overgrowth in your innards. which also used to be a whole lot less common than now, btw.
and like monica, for the past couple months i too have been having good success in at least controlling the darn kritters with oils like Castor, olive, and Sea Buckthorn. i also started using Neem oil bar soap for washing hair & skin, and have gotten rid of all other lotions, serums, cleansers, shampoos, conditioners, etc etc etc as it ALL seems to make the condition worse and i have FINALLY been noticing some relief. my rosacea is much better, altho it still flares whenever the buggers have an opportunity to act up, such as when my routine is off.
i also was using Witch Hazel as a toner, but have recently switched to diluted organic Apple Cider Vinegar and that has helped ‘dry’ the condition some. and ive just started using the dilute vinegar solution in place of conditioner, which was my last hold out, and my hair and scalp seem better too- less hair loss and itching.
i dont know if any of these ideas would be the least bit beneficial to actual morgellons sufferers, but it couldnt hurt to try, if you havent allready- some of you may discover that it was ‘only’ demodex after all and be able to heave HUGE sighs of relief :) …and wouldnt it be fabulous if any of the stuff that works for the mites ended up being effective on the morgellons parasites as well!!
here is one link offering additional info for anyone who is thinking that perhaps this post applies to them too:
http://rosacea-support.org/demodex-mites-treatment/comment-page-3#comment-44690
blessings in all your searches… may you discover TRUTH!
And everybody wondered after the beast-whose wound was healed. They create a disease in secret-just to get power for having the cure-only the cure also includes the chip-the real agenda. People in power are not people you can trust-it takes a completely dishonest sociopath to climb the ladder of success. Nice guys finish last. The meek shall inherit the earth. The elite are creating their future Hell in the afterlife, a place where they really belong. Those who can only make earth a Hell-the people in power=TPTB.
the problem i have with all this is the blurry photos, and much of this information about morgellans is coming from disinfo outlets such as rense.com
where did this information originate? how about focusing on that? i do not beleive any of this because it looks like you fed off of renses plate for this article…just sayin…..
and if your still getting fooled by disinfo websites and feeding off of their material – well, what should we say about your website now?
see how disinfo works? they trick you into wasting your time writing about it and spreading it to more people to spread even more…
better wise up quick people
Well, “a new world order “,
The article is from the Daily Mail and I cite a wide variety of links and videos which should stimulate people to go out and check facts and do their own research which is what I encourage constantly. As for trying to smear me with the “disinfo” label go right ahead and keep trying. Only a fool would listen to you. It doesn’t worry me in the slightest what you post on this site.
im not trying to smear you with a disinfo label, but alot of this came from proven disinfo websites. and if this came from the daily mail thats even worse. where are the actual people? i want to see actual people, actual accounts. i dont want to see some blurry photos from rense and daily mail, and some account from someone we will never be able to see for ourselves or contact, or interview ourselves.
the only people i see in any documentaries loo like they were paid to say the things they are and anyways any “conspiracy” documentary ever released to the public it is proven they are loaded with disinfo and other lies. why do you think they now have all these conspiracy shows like with jessie ventura, and websites like rense, alex jones.it’s so they can intentionally spread disinfo, fears, lies, mix half truths.
just sayin i think this whole morgellans fear is just that – FEAR from the NWO
almost everything i have seen on this has had NWO disinfo written all over it. just something to think about further.
PLEASE EVERYONE TRY WASHING IN NEEM & GUMBI GUMBI
IF YOU HAVE MORGELLANS
WASH AS MANY TIMES A DAY AS YOU CAN STAND, LEAVE ON FOR 10 MINUTES BEFORE WASHING OFF
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@ NWO underground
Agreed sir.
@ Every Else
NWO is commming, and for this there is so much dis-information to stray your eyes from what may really be going on. Another article I read on this site said that the John Birch Society was endorsed by the rockafellers (citation needed) to mislead the public on the real NWO. Whats the difference with citing everything from a car-crash to stepping on a spider as a conspiracy for a NWO? Most of these posts sound like the movie “bug” and I strongly suggest watching this. I have no doubt that Morgellons is real, but common…. these articles will get everyone beliving they have “bugs” inside them. Stop being a fear-monger and seek the real truth! Not your own version of the “truth”
Myself… im a Christian, my NWO scenario falls with what I believe from Revelations and such. You will also not see me saying “ANTI-CHRIST IS COMMING FEAR THE 666!!!!” on EVERY news article or every blog. Grow up and stop saying everything from a-z is a NWO. Help these true sufferers out by giving them credit and helping them find a cure, instead of saying “the government designed morgellons and AIDS…. GOOD LUCK WITH A CURE”
Take a shower, you stink of stupid. Much love, peace!
Has anyone tried to put lemon juice all over there body to stop itching.