Joni Mitchell- Morgellons victim

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Joni Mitchell- Morgellons victim

Postby catbirdsteed » Sun Feb 22, 2009 3:10 am

http://www.billboard.com/bbcom/news/jon ... 3464.story

"The Fiddle and the Drum" remains the primary focus for Mitchell, who's also in the midst of treatments for Morgellons syndrome, an infectious and potentially debilitating skin condition that's put other endeavors on hold for now.


Perhaps most of you have heard of this disease, and have heard where it MIGHT have come from. If your are curious, look it up. Certainly there is room for debate about what this disease might mean or indicate, but this is one of the highest profile cases yet come to light. it will be curious to see where this goes. Those following the rash of suspicious deaths in the microbiologist community might take special note of this mystery disease if you have not already heard of it or looked into it. This is very fresh news and I am not going to find anything else before posting this tonight. my heart goes out to Joni and her fans. As an appreciator of music I have found many Canadian artists who have made it to the top of my list and she is certainly among them. Of course, her new opera might be news too...
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Postby catbirdsteed » Sun Feb 22, 2009 4:07 am

Morgellons
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Morgellons (also called Morgellons disease or Morgellons syndrome) is a name given to a proposed infectious condition characterized by a range of cutaneous (skin) symptoms including crawling, biting, and stinging sensations; finding fibers on or under the skin; and persistent skin lesions (e.g., rashes or sores). Current scientific consensus holds that Morgellons is not a new disorder and is instead a new and misleading name for known illnesses. Most doctors,[1] including dermatologists[2] and psychiatrists,[3] regard Morgellons as a manifestation of known medical conditions, including delusional parasitosis,[4][5][6] although some health professionals say that an infectious cause could one day be found.[7] Illnesses such as delusional parasitosis can be serious and debilitating, but tested and effective treatments exist.

[edit]

Theories about the fibers

Randy Wymore, a former research director of the MRF and presently Director of the Oklahoma State University Center for Health Sciences' Center for the Investigation of Morgellons Disease, claims that Morgellons patients have masses of dark fibers visible at 60x magnification under the unbroken skin, while unaffected individuals do not.[2] Wymore sent samples of fibers supplied by Morgellons patients to the Police Crime Lab in Tulsa, Oklahoma for analysis. A forensic scientist at the Tulsa Police Crime Lab in Oklahoma searched the FBI's national database, but the Morgellons sample did not match any known fiber in the database.[12] Lab director Mark Boese said the fibers were "consistent with something that the body may be producing," adding, "These fibers cannot be manmade and do not come from a plant. This could be a byproduct of a biological organism."[12]

Dr. Rhonda Casey, chief of pediatrics at Oklahoma State University Hospital and part of the MRF research team at OSU, claimed that she has examined many patients' skin via a dermatoscope and performed biopsies on both lesions and apparently healthy skin, and that "she saw fibers embedded in both places. The white ones, she says, are hard to see. A dermatologist who either didn't look at all, or didn't use a dermatoscope, might not see them under the skin."[14]

Dermatologists say any fibers are from clothing embedded in self-imposed sores, and the fibers patients bring in bags are textile in nature.[14] [52]

[edit]

Environmental toxins

Richard Fagerlund, an entomologist who has a column titled "Ask the Bugman" in the San Francisco Chronicle and Albuquerque Journal, stated that he takes Morgellons disease seriously, and he receives letters from people with Morgellons symptoms daily. Twenty years ago, he got three to four letters like this a year. He believes the condition is reaching epidemic proportions and speculates only a small percentage of cases are delusional parasitosis, while the rest may be caused by something else, such as pollutants, especially pesticides.[56]

Conspiracy theories

Some self-identified Morgellons sufferers and various conspiracy theorists provide their own origin hypotheses: "Perhaps it is caused by chemical spills or bio-terror or even alien abductions. On a radio program called Coast to Coast--popular among people who believe in UFOs and ghosts--a New Mexico doctor reports that a former CIA agent told him the disease was caused by the French. A botched government experiment, he says, contaminated the water. All Evian drinkers are at risk."[18]

[edit]
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Postby catbirdsteed » Sun Feb 22, 2009 7:47 pm

A few years ago this condition was- to debunkers- seen as one of the ultimate paranoia conspiracy psychoses. It didn't help that people were saying it was delivered in chemtrails. Well, the medical community has come a long way since then regarding the existence of the condition as you can see from the excerpt below.

http://www.mayoclinic.com/health/morgel ... se/SN00043
Morgellons disease: Managing a mysterious skin condition
Morgellons disease is mysterious and controversial. Here you'll find answers to common questions about Morgellons disease — and suggestions for coping with it.

Morgellons disease is a mysterious skin disorder characterized by disfiguring sores and crawling sensations on and under the skin. Although Morgellons disease isn't widely recognized as a medical diagnosis, experts from the Centers for Disease Control and Prevention (CDC) are investigating reports of the condition, which they refer to as unexplained dermopathy.

If you suspect that you have Morgellons disease, you may have many questions about the condition. Here's what you need to know about Morgellons disease, including practical tips for managing your signs and symptoms.
What are the signs and symptoms of Morgellons disease?

According to the Morgellons Research Foundation, primary signs and symptoms of Morgellons disease include:

* Skin lesions, often accompanied by pain or intense itching
* Fibers — which may be white, blue, red or black — in and on the lesions
* Crawling sensations on and under the skin, often compared to insects moving, stinging or biting
* Joint and muscle pain
* Fatigue significant enough to interfere with daily activity
* Inability to concentrate and difficulty with short-term memory
* Behavioral changes

Other signs and symptoms may include:

* Changes in vision
* Stomach pain or other gastrointestinal symptoms
* Changes in skin texture and color

Morgellons disease shares characteristics with various recognized conditions, including attention-deficit disorder, chronic fatigue syndrome, Lyme disease, obsessive-compulsive disorder and a mental illness involving false beliefs about infestation by parasites (delusional parasitosis).
How long has Morgellons disease been around?

In 1674, English physician and writer Sir Thomas Browne used the term "Morgellons disease" to describe "black hairs" emerging from childhood skin lesions. Today, the Morgellons Research Foundation doesn't claim that the disorder described by Browne is the same as Morgellons disease. Rather, the foundation adopted the term as a convenient label for a set of signs and symptoms.
How widespread is Morgellons disease?

Reports of Morgellons disease have been made in every state in the United States and various countries around the world. Most reported cases are clustered in California, Texas an


I see there are a lot of views to this so far, anyone else been interested tn this in the past and let it get under their radar, like I did? It is odd that the Joni Mitchell link came up yesterday ,as just the night before I was looking at some vids and the morgellons reference came up again and I thought ' I gotta look into this again" Bam!
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Postby justdrew » Sun Feb 22, 2009 8:19 pm

the subject is too horrifying, I'm keeping it in my denial basket.

Really I can see how it's a complex interaction of stress, psychosomatic origins and real bacteria. but then, it could also be be alien nano-machines infiltrating bodies and re-wiring/re-building them for unknown purpose. Perhaps everyone has them and only a few people are showing abnormal reactions.

too many unknowns. What's going on with the first cases that now must be nearly 10 years old or more? Are those first cases still suffering? Are they all dead? Are they better?
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Postby seemslikeadream » Sun Feb 22, 2009 8:50 pm

http://abcnews.go.com/Primetime/Story?id=2283503&page=3

''Morgellons' Mystery
Mysterious Colored Fibers Grow on Their Skin Like Hair -- It's a Medical Mystery.
Aug. 9, 2006

Brandi Koch of Clearwater Beach, Fla., says she feels as if she's living in a horror movie. She claims she has colored fibers coming out of her skin.

Mary Leitao refused to accept medical skepticism. She took matters into her own hands after noticing an odd sore on her son's lip that would not heal. Her son pointed at his lip and said "bugs."
(ABC)Brandi is married to Billy Koch, a former Major League baseball player who was one of a handful of pitchers who could throw a ball at more than 100 mph. Koch says her life was good, until one day in the shower she noticed something strange -- tiny fibers running through her skin.

"The fibers look like hair, and they're different colors," Koch says.

Koch says she knows that what she's experiencing "sounds crazy," but it's true. "If I had a family member call me up and say, 'I have this stuff,' I'd say, 'I'm sending a straitjacket over. You need some help.'"

Related
Your Thoughts On MorgellonsAnne Dill describes a similar condition. Looking at Dill's life, it appears as if she's living an idyllic existence in a home on Florida's Lake Mary. Her three daughters excel in sports and are straight-A students.

But life in the Dill household is far from idyllic. Anne's 40-year-old husband, Tom, died in January and she believes his death was due to a contagious illness that has infected her entire family.


Dill describes her family's skin: "There's this fibrous material. It's in layers." Dill says the skin on their hands is particularly bad, very swollen and itchy. She says it feels as if bugs are crawling underneath the skin.


Consulting Doctors
Dr. Greg Smith of Gainesville, Ga., has been a pediatrician for the past 28 years. He claims a fiber is coming out of his big toe, and he has video footage to prove it. "It felt like somebody stuck a pin in my toe and wiggled it and it just continued to hurt," Smith says. He says he never thought he had bugs. "I've certainly had those crawling sensations, and the fibers which come out of the skin are really bizarre, and really odd."

When Koch, Dill and Smith consulted doctors, they received diagnoses that they call wrong or dismissive. Dill's doctor told her to stop scratching, even though many of her sores were in places she could not reach.

Koch went to the Mayo Clinic, where doctors didn't believe that the fibers she'd brought them had grown from her body. "I saw the infectious disease doctor, and I showed him some samples that I had and he snickered. I can't go through another doctor blowing me off or looking at me like I'm crazy. I know I'm not," says Koch.


Smith -- a doctor himself -- was handed over to a hospital psychiatrist when he went to the emergency room complaining of a fiber in his eye. He admits that he, too, would be skeptical if a patient came to him with the same story. "I would wonder if they'd taken their medicine that day. It makes no sense. It's totally bizarre. It's something that -- just telling the story is so outlandish on the face of it -- that no one would believe it," Smith says.

Dr. Vincent DeLeo, chief of dermatology at New York's St. Lukes-Roosevelt Medical Center, weighed in on what he'd say to someone who came to him with this condition. "I don't think this is any different than many patients I've seen who have excoriations and believe that there is something in their skin causing this."

DeLeo says the open lesions are a result of scratching the skin.

But for biologist Mary Leitao of Surfside Beach, S.C., medical skepticism was something she refused to accept.


Relying on Your Own Research
Her son, Drew, was just 2 years old when Leitao noticed an odd sore on his lip that would not heal.

"He very simply said 'bugs,' and he pointed to his lips," says Leitao.

Leitao never expected to find herself at the center of a medical storm. But when her son complained about that strange sore, the biologist, who once ran the electron microscope at Massachusetts General Hospital in Boston, did what any scientist would do. She took a closer look.

"What I saw were bundles of fibers, balls of fibers," Leitao says. "There was red and blue." Even stranger, they glowed under ultraviolet light.

Armed with research, Leitao took her son to a doctor at one of the country's leading hospitals. He dismissed her tale of fibers and wrote to her pediatrician, saying that her son needed Vaseline for his lips and that his mother needed a thorough psychiatric evaluation.

Undaunted, Leitao began poring through the medical literature looking for clues. What she discovered was a 17th-century reference to a strange disease with "harsh hairs" called "Morgellons."


She named the strange fibers Morgellons disease and put the information on a Web site, Morgellons.org. Since then, more than 4,500 people have contacted Leitao, claiming they have Morgellons-type symptoms. The name has stuck, and the disease was featured on the television show "ER."

But do these fibers grow from inside the body -- as Morgellons patients believe -- or do they come from the external environment -- a kind of lint -- as the medical skeptics say?


Searching for an Answer
Forensic scientist Ron Pogue at the Tulsa Police Crime Lab in Oklahoma checked a Morgellons sample against known fibers in the FBI's national database. "No, no match at all. So this is some strange stuff," Pogue says. He thinks the skeptics are wrong. "This isn't lint. This is not a commercial fiber. It's not."

The lab's director, Mark Boese, says the fibers are "consistent with something that the body may be producing." He adds, "These fibers cannot be manmade and do not come from a plant. This could be a byproduct of a biological organism."

While they wait for evidence that they hope will convince the medical community to take them seriously, some Morgellons sufferers wear pink bracelets that say, simply, "Fortitude."

Dill says she looks at pictures of her family from just four years ago and finds them unrecognizable. "My kids have to see not only their dad but their mom disintegrating, and that's gotta be really scary."
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Postby catbirdsteed » Sun Feb 22, 2009 11:37 pm

Then again, I suppose it could be this...

http://psy.psychiatryonline.org/cgi/con ... ll/50/1/90

Psychosomatics 50:90, January-February
doi: 10.1176/appi.psy.50.1.90
© 2009 Academy of Psychosomatic Medicine


Letter
Morgellons Disease as Internet Meme
Andrew Lustig, M.D., FRCP(C), Sherri Mackay, Ph.D., and John Strauss, M.D., M.Sc., FRCP(C), Centre for Addiction and Mental HealthToronto, Ontario, Canada

TO THE EDITOR: In 1690, Sir Thomas Browne, an English physician, made mention of a pediatric medical condition that he called "the Morgellons:"1 "Hairs which have most amused me have not been in the face or head, but on the back, and not in men, but children, as I long ago observed in that endemial[sic] distemper of little children in Languedock, called the Morgellons, wherein they critically break out with harsh hairs on their backs, which takes off the unquiet symptoms of the disease, and delivers them from coughs and convulsions."

The Morgellons faded into obscurity and was rarely mentioned until 2002, when the mother of a child with a skin condition resurrected the term and began the Morgellon Research Foundation (http://www.morgellons.org). According to the Morgellon Research Foundation, Morgellons disease is a newly-described illness first noted in 2002. It is characterized by a number of symptoms, such as fatigue, skin lesions, diffuse musculoskeletal pain, cognitive dysfunction, and emotional lability.2 Notably, patients with the illness describe filaments of various colors spontaneously growing from the skin, as well as the sensation that insects are crawling under the skin. There has been much debate over the nature of Morgellons: infectious, environmental, and psychiatric etiologies have been posited.

The term meme was coined in 1976.3 "Meme" was chosen to be phonetically similar to the word gene in order to highlight the similarities between the two terms. It is an amalgam of the words memory and gene. Genes can be considered as units of genetic material that "compete" with each other for survival. Similarly, Dawkins suggested, ideas are engaged in an analogous struggle with each other to attain dominance in the marketplace of ideas.

The recent success of the Morgellons-disease meme is, in part, explained by the fact that the Morgellons label resonates with symptomatic individuals. In one person’s words: "I felt so relieved. I found all these people talking about the same thing I was."4 Accordingly, Morgellons disease has been considered a rapport-enhancing term in clinical medicine.5 The dermatology literature indicates that Morgellons disease is likely the equivalent of "delusional parasitosis," a psychiatric illness in which patients erroneously believe that their skin is infested with parasites.5,6 This competing conventional meme has been unpopular among individuals identifying themselves as having Morgellons disease.

For Morgellons disease, most information available to patients exists on the Internet; thus, the World Wide Web is a second important contributor to the proliferation of the Morgellons moniker. With widespread reports dating back only about 3 years, Morgellons has seen explosive growth for a concept dormant for more than 300 years. A large CDC-supported descriptive study is underway: a first formal clinical epidemiologic investigation of the Morgellons phenomenon, involving skin biopsies and fiber analysis (http://www.cdc.gov/unexplaineddermopath ... ation.html).4 Results will characterize Morgellons as either a novel illness or an internet meme synonymous with one or more previously described disorders.

REFERENCES

1. Keynes G (ed): A Letter to a Friend, in: The Works of Sir Thomas Browne, Vol. 1. London, UK, Faber & Gwyer, 1931, p 171
2. Savely VR, Leitao MM, Stricker RB: The mystery of Morgellons disease: infection or delusion? Am J Clin Dermatol 2006; 7:1–5[CrossRef][Medline]
3. Dawkins R: The Selfish Gene. Oxford, U.K., Oxford University Press, 1976
4. Marris E: Mysterious "Morgellons disease" prompts U.S. investigation. Nature Med 2006; 12:982[Medline]
5. Murase JE, Wu JJ, Koo J: Morgellons disease: a rapport-enhancing term for delusions of parasitosis. J Am Acad Dermatol 2006; 55:913–914[CrossRef][Medline]
6. Waddell AG, Burke W: Morgellons disease? J Am Acad Dermatol 2006; 55:914–915[CrossRef][Medline]



but I am not surprised that the afflicted would be offended at such an insinuation. It was not that long ago that the psychiatric world thought that autism was a result of bad parenting, ala: the refrigerator mother.

As a note, there was no other googlemews story about morgellons but the billboard article and the above, save for one article in French
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Postby Col. Quisp » Mon Feb 23, 2009 12:02 am

Wonder what treatment Joni Mitchell is getting?? Since this condition is not recognized as a disease??
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Postby compared2what? » Mon Feb 23, 2009 12:55 am

According to the National Pediculosis Association's research, it's caused by extremely tiny parasites called collembola (or springtails). You can read about it over at the bluntly named headlice.org.

Apparently, this doesn't interest the Morgellons Research Foundation, which is the organization that brought the syndrome to the attention of the world and is still the go-to source for the media. I have no idea why that it, although (also, apparently) entomologists assert that collembola can't be human parasites.

To which the NPA says: But, hey: There was a case study of human springtail infestation in a Swedish medical journal in 1955. (Translation linked here.)

People with Lyme Disease used to be thought of as crazy, too. In very much the same way, actually, except that it was in the pre-rumors-on-the-internet era, so it wasn't as intensely controversial.

Personally, I don't have any idea if the springtail hypothesis is correct or not. But there's some clinical evidence for it, and....It has the virtue of being a possible explanation, at least. And that's not a small consideration, given the circumstances, obviously.
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Postby compared2what? » Mon Feb 23, 2009 2:17 pm

An addendum: I did some research on the Morgellons Research Foundation after posting last night, and just wanted to add that there are a lot of small but distinct red flags wrt various aspects of that organization. Among the things that caught my eye were:

* Its curiously narrowcast focus on personal media appearances for the same three to six key members.

* The website's dedication to the collection of personal data of little-to-no clinical value from visitors to the site.

* The disparity between the six-person board of directors listed on the website and the two-person board of directors (Mary Leitao, Douglas Buckner) it reports on its IRS filings, on which information is submitted under penalty of perjury.

* Some minor inconsistencies and/or misleading representations of fact, such as literature that sometimes refers to board member Douglas Buckner as a Ph.D, sometimes as an MD. Or the prominence given to the failure of the Tulsa PD to match the fibers to anything in the FBI database without mentioning that there are only 800 samples in that database, which is kind of relevant, given that there are a lot more than 800 kinds of fiber. Stuff like that.

* The several indicators that there are some internal organizational problems over there, including (inter alia)the resignation early on of two board members (including the chairman) following Leitao's refusal to show them financial records and -- more recently -- the decision of pro-Morgellons OSU neuroscientist Randy Wymore to dissociate himself from the foundation for unstated reasons.

* I was also kind of disturbed to see that the website is fundamentally unchanged from what it was in (approximately) 2005, when I first looked at it. I mean, surely they could have managed to come up with some more photographs to add to the ones Leitao took of her son something like a decade ago at some point in the last four years, come on.


* And so forth.

None of that stuff is incredibly horrible. And some of it isn't even that out of the ordinary. (There's no IRS enforcement to speak of wrt the accuracy of non-profit filings, so they're (unsurprisingly) often not very rigorously filled out.) Still. All of it taken together suggests that (at best) it's not an entity that has the capabilities or resources to responsibly serve as the primary source of information about and/or advocacy on behalf of Morgellons research. Or it does to me, anyway.

So fwiw: Hey, heads up. The Morgellon's Research Foundation -- which is the source of almost all the widely disseminated info on the subject -- has too many discomfiting signs of unreliability and/or lack of transparency for it to be a one hundred percent safe assumption that it's doing a good job in that position. That's just by my standards. I should emphasize. Because I'm not saying I see any smoking guns or anything like that. In fact, I should also emphasize that I don't.

However, I do think that it certainly couldn't hurt to make a habit of looking for unrelated, third-party sources of verification wrt any info that has its origins on that website. Because for whatever reason, it's an organization that's spent the last six or so years making as many people as it can sensitive to the possibility that they've got a problem for which there's no known solution and to which the world in general is so hostile that practically the only place they can hope to find any help is the Morgellons Research Foundation. Where the main (if not the only) form of help on offer is whatever comfort comes from joining a community of problem-having individuals who put almost all their energy and resources into validating and reinforcing their identity as problem-havers while barely even making a pro-forma attempt also to organize a campaign of solution-seeking.

And, you know. That's not really what I'd call an ideal standard of helpfulness. Plus, for whatever percentage of the people who are attracted to it by the media campaigning that either have some other difficult-to-diagnose condition or who are in fact suffering from delusional parasitosis, the separate reality of which it shouldn't hurt to acknowledge, it has a very high potential for turning into the opposite of help.

And the worst part of that is: Based on the available information, however flawed it is, it does look to me very much like what's being called Morgellons does represent at least one serious and unidentified chronic medical condition. And very probably more than one.

So it's kind of dreadful that there aren't really any better options than the MRF. As well as tragic that people with serious chronic and non-imaginary medical conditions can so easily be dismissed as having a delusional disorder. Especially since the most likely upshot of that is that they'll end up taking some gruesome atypical neuroleptic, the benefits of which aren't exactly either universal or free of potentially debilitating side-effects, even for people who actually do have delusional disorders.

Nevertheless. If I were in their circumstances, I wouldn't want my welfare to be either contingent or dependent on an organization with as many risks and shortcomings as the MRF.

It's a sad and dangerous world we live in. Isn't it.

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Postby Et in Arcadia ego » Mon Feb 23, 2009 2:34 pm

Everything looks creepy under a microscope. That website offers nothing but a bunch of crappy photos that are totally unverifiable.

"Morgellon's" if it exists at all probably has a very mundane cause behind it, like a combination of net-fed neurosis and *some* form of semi-exotic parisotosis. As far as catering to paranoia culture, its sits right at the top of the pile next to TI's.

Sometimes the internet is all the disease a person requires.
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Postby catbirdsteed » Mon Feb 23, 2009 3:21 pm

The Center for Disease Control is taking and agnostic stance too. Good to know they are not as susceptible to fearmongering and unfettered paranoia as I am.[':wink:']


http://www.cdc.gov/unexplaineddermopath ... _info.html

Department of Health and Human Services, Centers for Disease Control and Prevention

Unexplained Dermopathy (aka "Morgellons")

Unexplained Dermopathy (aka "Morgellons") > General Information
General Information

Recently, the Centers for Disease Control and Prevention (CDC) has received an increased number of inquiries regarding an unexplained skin condition which some refer to as “Morgellons.” Persons who suffer from this unexplained skin condition report a range of cutaneous (skin) symptoms including crawling, biting and stinging sensations; granules, threads, fibers, or black speck-like materials on or beneath the skin; and/or skin lesions (e.g., rashes or sores). In addition to skin manifestations, some sufferers also report fatigue, mental confusion, short term memory loss, joint pain, and changes in vision.

The cause of this condition is unknown, and the medical community has insufficient information to determine whether persons who identify themselves as having this condition have a common cause for their symptoms or share common risk factors.

To assist in learning more about this condition, CDC is conducting an epidemiologic investigation. To learn more about the investigation, please refer to the following link: CDC's Unexplained Dermopathy Investigation. CDC held a telebriefing for the press on January 16,2008 to announce the epidemiologic investigation. To read the complete transcript of the telebriefing, refer to this link: http://www.cdc.gov/media/transcripts/2008/t080116.htm


But c2w? why Morgellons Research Foundation.? I certainly did not mention them, mainly Mayo Clinic and Billboard, oh, and wikipedia. Do they seem like the mouthpiece for this "condition"? They are not ranked very high on a simple scroogle search? Granted, this emerging condition is possibly full of the spookiest bullshit and paranoia anywhere, but it might behoove a truly skeptical tone (et in Arcadia ego) to take on the more established (reputable?) players rather than engage in patent dismissal- ism.
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Postby Avalon » Mon Feb 23, 2009 4:45 pm

The 1955 Swedish paper is alarming reading. It mentions use of DDT and mercury in attempting to rid the springtail infestation, and mentions in passing caterpilars of butterflies found in the vulva in another case, believed to have come there via eggs on the end of a douche bag nozzle.

Ladies, you have been warned. Leave not thy nozzles in the garden for that spring-like freshness.
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Postby crikkett » Mon Feb 23, 2009 4:51 pm

Ugh. This thread makes me itch.

/running away
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Postby brekin » Mon Feb 23, 2009 5:08 pm

This has been keeping me up at night....

http://www.telegraph.co.uk/news/worldne ... cured.html
http://www.msnbc.msn.com/id/26406111/
http://www.usatoday.com/news/health/200 ... cure_N.htm
Doctor seeks help for Indonesian 'Treeman'

Image


When dermatologist Anthony Gaspari first saw photos of Dede, the Indonesian fisherman who has come to be known worldwide as "the Treeman," he figured they must be a hoax.
The photos are all over the Internet. They show a man in his mid-30s whose skin is covered with bark-like lesions. And instead of fingers or toes, he appears to have roots sprouting from his arms and legs.

But staffers from Discovery Health, the cable channel, assured him Dede was real. Suspecting the man might have a rare pre-cancerous skin condition that Gaspari, chair of dermatology at the University of Maryland, had described in a scientific journal, they invited him to meet Dede.

Intrigued, Gaspari twice has flown nearly 24 hours from Baltimore to Jakarta and then driven three hours to Bandung. From there, it was an hour-long car ride, a half-hour boat ride across a lake and a half-hour hike to get to Dede's rural village. The first trip was in June 2007, the second this past March.


"In some ways, it's the modern-day Elephant Man," says Gaspari, referring to the 19th-century deformed Englishman named Joseph Merrick. "On the one hand, you're horrified to see how badly disfigured this individual is. Then on the other hand, how could this happen? There's a curiosity factor."

In person, Gaspari could see that Dede did not have the rare skin disorder that the Disovery Health team had suspected. A molecular analysis of biopsies of the growths on his body found they were caused by the human papillomavirus, or HPV.

Some HPV types cause genital warts, some can lead to cervical cancer, but scores of others cause common warts, the harmless little growths that sometimes pop up on the knees, face, fingers or other part of the body that are likely to be injured.

In people with healthy immune systems, common warts eventually clear up on their own. But Gaspari found that Dede has chronically low levels of disease-fighting white blood cells called CD4 cells. Low CD4 counts characterize AIDS, but Dede repeatedly has tested negative for HIV, the virus that causes AIDS, Gaspari says. Instead, he says, Dede, who has otherwise been healthy, must have inherited a rare flaw in his immune system.

Dede's is probably not the first such case in the world, Gaspari says, but "we just don't see patients living that long and going untreated that many years (thought to be 20) with that severe disease."

Ideally, Gaspari says, the Indonesian government would allow Dede to come to the USA for treatment with drugs such as antiviral medications to help his immune system fend off the HPV.

The next-best scenario, he says, would be for the Indonesian doctors to bring more specimens from Dede to his lab in Baltimore, where they could work together to identify his underlying genetic mutation and develop appropriate treatments.
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Postby kool maudit » Mon Feb 23, 2009 6:15 pm

this information, if true, is too horrible to process.
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