One of the more controversial medical mysteries lately is to be
studied by the CDC.
Morgellons is reported to be a strange skin disease
characterized by open lesions on the skin that give the sufferers
what they call the feeling of insects crawling on them. Many in
the medical community had been classifying this as a psychotic
disease, but now several places are studying it as a
"real" disease because of the confirmation of
"fibers" that apparently grow at the lesion site. It
was at first thought that the fibers were just small textile
fibers stuck to the wounds, but now they have been apparenty
found underneath unbroken skin.
" The
Centers for Disease Control and Prevention is launching a study
of Morgellons disease that may target South Texas where more than
100 people are suffering from the illness."..more
there
I read through the advocate and debunker sites a few months ago since it sounded so strange and interesting. I was taken aback by the common reaction of the medical community to just dismiss the symptoms. Had I not experienced the same dismissal for something so common as a collapsed disk in my neck, I would not have believed the doctors could be so callous. Unfortunately, doctors are human, and are not (usually) scientists. So anything they see that doesn't fit their prejudices is immediately dimissed as not medical in nature. At least now some real scientific method is being applied to this malady. And phycological or not, maybe these folks can get some real relief.
-- "Curiosity was framed; ignorance killed the cat." -- Author unknown
actually, I can't find any evidence the CDC or anyone else of credibility is looking into this. Going to a real doctor with textile or any other kind of fibres in a wound would result in immediate wound cleaning, so I'm thinking this a hoax, not a case of callous doctors.
Just as gonig to a good doctor with a collapsed disk or neck pain would not result in dissmisal. Sounds like you went to bad ones.
I recently contracted all the symptoms of Morgellon's, I had
a vacation home in the Florida gulf region, and believe this
unknown pathogen comes from this area and various other areas
around bodies of salt water, oceans, etc.
I called the CDC today, and listened to what they are doing as
per their pre-recorded public information line at 1-800-311-3435,
Ext. 6, for the group of people in Oakland, CA and am very
concerned. From the information I have gathered all
throughout the various stages of this disease - and by listening
to the tests that the CDC are performing to make a
determination - they will NOT find the pathogen.
"I believe I know what the pathogen is" - I left the
CDC this message today, 7/10/08, and whether anyone over there
responds, well.... I believe that they are somewhat
concerned however, this could be a matter of funding, that
possibly, the Government is not allowing the CDC to study this on
a larger spectrum to find what IS actually going on here.
I am in Atlanta, GA, I have been to 7 doctors and three Emergency
Rooms, and put on a pill for Tourette's Syndrome called Orap
- to "shut me up" and make me quit complaining about my
"imaginary" symptoms, a heavy "downer" that
keeps the Morgellon patient from being able to doctor themselves,
function, make doctor's appointments or even
drive. I do NOT have Tourette's Syndrome!
Every doctor I have seen is assuming that the patient is
delusionary and or psychotic. When you read about
"delusionary parasitosis" the first step the doctors
are supposed to take - is to determine if it is a REAL
infestation or NOT. However, every doctor that I have seen,
has not looked at a single sore - taken any blood, as requested,
nor looked at any body part with any detail. I have
been trying since April 29, to get some help.
Dogs are treated better than this in our country! This is a
shame to the Medical Professionals - that at this time there are
a reported 18,000 people with this, and the CDC is not taking a
count, this number could be doubled or tripled? - that are all
having the same symptoms. And all of them are considered
"delusionary", how can 18,000 people all be having the
same delusion?
If anyone is out there suffering, like I am - I have good
information on how to keep this under control until we can make
"them" realize - what this is. You can email me
homebizs@aol.com.
I am sorry for your suffering. The medical community reacton to
all this has been pathetic and unconscionable. The CDC and some
other studies are just trying to figure out what the heck it is
at best, they have not even begun to get a clue about a cure.
Those of us afflicted can not wait, so we must help each other.
After a year and a half of intense suffering and researching the
efforts of others, I feel that I am on the road to complete
irradtication. Here is what has helped me.
1. Metronidazole topical cream (also known as Flagyl). I
discovered this by accident, believing it might be Demodex mites,
which have similiar symptons. Not a cure per se, but definitely
helped heal during the open sore stage.
2. Collidal silver. You have probably seen the ConnieM video. If
not you may want to google it. Avoid silver proptein or ionic
silver (they can cause a side effect of turning blue! only 10
people in the US have it, but if it happens to you it's 100%,
right)... you need a high grade true colloidal silver .... the
darker yellow in color the better. Nutrasilver company is
recommended. Research on your own so you know for yourself.
Prices can vary.
3. I also use a water machine that treats water by opening the
angle of the Hydrgen to 114 degrees. I have used this for a
month, with unbelievable results. The biting and itching has
stopped. I am just trying to clear up residual skin problems now.
Again, please research for yourself, I have no stake in any
of these companies. Just reporting what is working for me. The
basis for this inventor is to get more oxegen into the
system, as this angle in hydrogen (H2o) has been collasping over
time. You can read about this and judge for yourself www.johnellis.com. This machine is
pricey, he is very nice and will work with you. To me it has
been worth it's weight in gold.
4. The only other thing I have read about with definite results
has been ultra-violoet therapy. Because the incredible trama to
my skin caused a secondary condition called Vitiligo (lose
of skin pigmentation), my dermatologist has agreed to these
treatments that I am about to begin. Because I have no inusrance
the drug company (there is a drug you take along with the
treatments) will supply it for free. The sessions then will only
be $5.00 each. If you are in this posision without insurance,
press the doctor to pursue the free medication for you.
I did not have the blue fibers appearing externally that everyone
spoke of (my friends would call evrytime there was something on
TV about it and say "this is what you have!"). I always
dismissed it because I did not see the fibers. What I did
have in the center of every sore was a tiny little sesamee like
kernel. When I removed them, hte sores healed faster. After
researching more, I discoverd that this is one of the more
obsure symptoms others were experiencing. The final test for me
was when I got a hand held black light and left it against my arm
for a few minutes. The littel white spots under the floresence
began to unfurl into little thread like worms of varying lengths.
They seem to be drawn out and attrached to this light. If anyone
you know is doubting you, show them this test!
It is right off the Xfiles and rather unnerving ... but pretty
convincing as well. Possibly not so far fetched. Lets face it,
many governments have been doing bio-chemical warefare
experiments for years. That is just a fact. Who knows what is out
there, or what is gone wrong. You never heard of any of this
stuff just a few decades back.
Most importantly, do not give up hope. You are not delusional,
and there are always answers. The human spirit is astounding. Tap
deeply into your courage, rely on the strength of your faith, and
know you are not alone in this struggle.
Hmm, note that the fibers are incredibly fluorescent... imaginge what a patient would look like under a strong black light...
On a more serious note, knowing more about this disease could be incredibly useful. Once a cure is found, perhaps the disease could be somehow harnessed to produce thread in factories, outside of human hosts. Might revolutionize the textile industry, or produce lighter forms of rope... provided it has decent tensile strength.
However, a cure is obviously a higher priority - I can't imagine having those symptoms.
I've seen reports that this is just a clever marketing ploy for the movie "A Scanner Darkly". Go to the CDC web page (http://www.cdc.gov/) and do a search of their site for "morgellons" and NOTHING comes up.
Is there anything out there NOT directly related to that guy at OSU?
Good grief. If this is just marketing, expect a backlash. This "viral marketing" and "creating a buzz" can lead to some bizarre things.
In any case, I see at least 7 independent listings in Google News. I also found something called the Morgellons Research Foundation which seems to have a very limited look to it. They claim articles going back to 2004. If this is buzz marketing, it must be deep, long term stuff. It may also be an elaborate hoax. I'm beginning to notice that the news reporters report on members of the previously listed "Research Foundation."
Heh, I wasted an evening of insomnia looking this up some time ago.
I could not find a single reputable source on it. Many people who are addicted to amphetemines end up experiencing symptoms like this. Once they are off the meth for some time, the systems go away.
Sleep deprived people on meth have internet access too and will search far and wide on google for anything matching their symptoms...
Turns out a lot of meth users are computer users and know how to throw up a few web sites about their "disease".
I certainly understand any skeptisism regarding the questioning whether Morgellons is true illness. I will also say that I am an educated person with a master degree, have run several marathons and have never been addicted to meth or the like. I have this didease. It is the most bizarre and unbelievable illness I could possibly imagine, and I would also have a hard time believing anyone who told me the stories that I could tell. I don't tell the stories to anyone, not even my husband. Yes, he knows a great deal but sometimes it is so strange I don't even begin to share a "latest" issue. I am hoping the day will soon come where I can get rid of this, help people like myself, and like you. We can't know what we don't know.
Hey I think you are the one on meth! up late at night responding to something that has no concern to you but to be a jerk. There are hundreds of people that have the same exact symptoms but have never met. What do you think that we all got together and made this shit up? Keep tweeking moran. Itried to kill myself over this shit and I am a mechanical engineer. Do you really think I have nothing better to do " If I had insomnia but to rag on people in need of treatment?" Get a life and go back to pumping your gas for min. wage. punk !
The suffering that many people associate with this condition is best addressed by a careful, objective scientific analysis. Considering the complexity of this condition, we believe that a measured and thorough approach offers the best chance for finding useful answers.
To learn more about this condition, CDC is conducting an epidemiologic investigation. CDC has awarded a contract to Kaiser Permanente's Northern California Division of Research to assist CDC in the investigation of this condition. The study is being designed and led by CDC.
The primary goals of the investigation are to help us learn more about who may be affected with this condition, the symptoms they experience, and to generate hypotheses about factors that may contribute to it. The investigation will involve: determining the clinical and epidemiologic features of this condition; assessing the histopathology of skin biopsies from affected patients; characterizing foreign material such as fibers or threads obtained from persons with the condition; and estimating rates of illness among the study population.
South Texas has always been, for some strange reason, a hotbed of bizarre pseudo-medical conditions. There is an entire town (Wimberly, TX) to the west of Austin where a large number of such patients live. There is an entire sub-culture involved in this stuff and apparently by word of mouth or through support groups, the area has been a magnet for such diagnoses. During the years I was on the faculty at the UT medical school in San Antonio, I saw many patients with the trendy diagnoses of the time, including so-called "20th century allergy." These patients described chronic fatigue plus poor concentration and a constellation of somatic symptoms including evanescent rashes and migratory pains as a result of "multiple chemical sensitivities." Paints, synthetic anything, food chemicals, anything that was named with a combination of letters and numbers, all were culprits. Many victims lived in houses in which they had coated the interior walls with aluminum foil and only ventured out swaddled in cotton clothes and wraps from head to toe, like some bizarre burkha.
Many of these patients had diagnosable psychiatric disorders and none had any definable medical diagnosis (at least from the point of this mainstream allopathic Western physician). As far as I know, they are still up there, holed up in their houses. The same syndrome has been present for as long as there are medical texts: neurasthenia, chronic Epstein-Barr syndrome, "chronic Lyme Disease," chronic fatigue syndrome, and others. The names change, but any practicing physician can recognize these patients. Further, there are many such patients diagnosed with other recognized syndromes, such as lupus for example, that do not have that disease but have been diagnosed inappropriately, both through carelessness on the MD as well as the patent's seeking a diagnosis.
The "fibers" are an interesting feature of theis condition. I cannot find it now, but there was a link on a Morgollon's thread on Kuro5hin to a study where EM and mass spectrometry of these fibers showed they were either fabric or skin, drawn into fibers by rubbing, itching, or other repetitive action.
Listen, This is not Lyme or any of the other diseases. This (taken from somebody who has it) disease is the devil. People joke about it further up the page of being able to be seen in a black light. Well guess what? At my work People are always talking behind my back about thinking I'm some weirdo because I'm basically glowing. If we aren't going through enough. I mean this is painfull and lets not forget annoying. So if you people that are on here to ridicule us who have it don't have anything better to do than to stay up on your free time and tormenting the tormented, well then I would probably pick morgellons over what you have. Shallow hearted nobody. Thank you : )
I am concerned about researchers putting so much focus on the fibers. I have suffered with morgellons for more than 4 years and can tell you there are fibers. I have yet to see any like OSU has photographed. The fiber comes out of my skin in huge amounts all over my body, especially around the eyes,nose, ears, and mouth.The color is usually black, yellow or white. There is a sticky substance with millions of glitter-sand like particles all over my body. There is a parasite present and I have learned how to control legions, but I have significant scarring promently on my face. I don,t seek treatment any longer because I got tired of being humilated. L-lysine helps so that makes me think there is a viral component. Antibiotics help but quit working after a couple of weeks. Lindane just makes you sick. I believe I am a reasonable person, but Morgellons is real even if some people are exploiting it. E-mail me if you have any questions, the only way it can be proven is by legitimate research.
CDC to Study Morgellons
One of the more controversial medical mysteries lately is to be studied by the CDC. Morgellons is reported to be a strange skin disease characterized by open lesions on the skin that give the sufferers what they call the feeling of insects crawling on them. Many in the medical community had been classifying this as a psychotic disease, but now several places are studying it as a "real" disease because of the confirmation of "fibers" that apparently grow at the lesion site. It was at first thought that the fibers were just small textile fibers stuck to the wounds, but now they have been apparenty found underneath unbroken skin.
" The Centers for Disease Control and Prevention is launching a study of Morgellons disease that may target South Texas where more than 100 people are suffering from the illness."..more there