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| October 24, 2010
American Medical Association Release "Morgellons
is systemic"
Small Bowel Capsule Findings Suggest that
Morgellon's Disease has an Organic Basis
and is Not Psychosomatic in Origin!
Daniel Chao, MD, David Cave, MD, PhD University of Massachusetts Medical Center,
Worcester, MA.
Purpose: Background: Morgellon's disease is a poorly described,
severe ulcerative skin condition that histologically
is consistent with dermatitis artefacta.
It has therefore been dismissed as a psychosomatic
disorder, much as was the case with ulcerative
colitis in the period from 1930 to 1960.
We present the first case of a patient with
Morgellon's syndrome who had additional
findings suggesting that it is a systemic
disease.
Case report: A 65 year old white female presents to us
with an unexplained iron deficiency anemia.
She had a history of systemic lupus and a
2 year history of severe skin ulcerations. The ulcers contained
fragments of black material. She had been
seen by multiple specialists who told her
that the lesions were self-inflicted and
that she should get psychiatric care. Physical
exam was of note for numerous papules with
erythematous, ulcerated centers measuring
2 to 12 mm located on the trunk, back, upper
and lower limbs and outer ear canal.
The ulcers were notable for sharply angulated
corners and clearly demarcated edges. She
had extensive scarring on her arms and legs.
Her labs were notable for a hemoglobin of
9.1 g/dL with MCV 83.3, serum albumin 3.4,
and ESR 32. ANA was negative. She had recently
completed a course of intravenous iron. A video capsule was performed. This showed
denuded villous patches in the jejunem, which
were unusual for their sharply angulated
appearance, similar to her skin lesions.
Small bowel biopsies were normal. Skin biopsy
showed hemorrhage and non-specific inflammation.
Histology of the black debris from her ulcers
suggested vegetable matter. Repeat capsule
examination 6 months later showed spontaneous
resolution of the denuded patches. Occlusion
treatment on one limb led to some improvement.
Discussion: This patient demonstrated cutaneous ulceration
consistent with Morgellon's syndrome,
but she had co-existing evidence for systemic
disease with iron deficiency, low albumin
and small bowel villous changes consistent
with a mild enteritis. This is the first
time that evidence for systemic disease has
been demonstrated in association with what
has previously been considered a disorder
limited to the skin. Further investigations
are warranted in a larger patient population.
ADDED: Latest news from an Australian Morgellons
sufferer
New, deadly and so far incurable Murine leukemia
retrovirus found in immunocompromised individuals
and now also in Morgellons sufferers. They
don`t know much about MLV-XMRV and contamination
processes except that it can be given by
blood transfusion and animals. This was initially
a virus found only on mice but it has mutated
and adapted to humans. Therefore I must repeat it again: you need to test not only bacterial infections
but also fungal and viral infections followed
with appropriate treatments. |
|
(Please click on the red arrow to this text
and source)  Hi has anyone seen my post ;A LITTLE INFO
ABOUY ME; if so ; have yiu shared a simular
incident; or does anything sound familiar?
pls reply .
Posted by kelly pollard on May 3, 2011 at 1:38pm
Whoever it was (think i remember from D.
Prince?!) that used Fixadent on the lesions
on their head should be elevated to sainthood!
Ran out of my Pascalite Pak, which is fabulous,
so resorted to the Fixadent morning and night
after cleaning my scalp. Amazing! The vermin
come up for air and get instantly trapped,
suffocate and die. Each morning and evening
I use the lice comb to lift everything off,
which until this was extraordinarily painful
no matter what I had been applying. The … Continue
Posted by Nancy J. Levy on April 30, 2011 at 12:48pm
THERE SHOULD BE A TAB WITH CLEAR INSTRUCTIONS
like do i always sign in by clicking 'sign
out' ? and more info on tabs exp; FORUM?
MAIN? BLOGS/ DISSCUSSIONS/ etc;. and how
do I get these q;s answerd without being
a pain when im just learning and to whom
do i ask? also i dont understand re; bottom
of this page ; what is the difference between
' save as post' or pubish or draft!
Hopefully if this sends and if someone responds
Youll see Im actually usually inteligent
… Continue
Posted by kelly pollard on April 26, 2011 at 4:34pm — 1 Comment
Has anyone noticed how the morgies sparkle
when you burn them? It's become the way
I know that what I have destroyed was indeed
one of the bad guys. It has been suggested
that these things have a trace amount of
silver in them - which provides the spark...
or maybe they have aluminum in them..which
is what they are supposedly spraying out
of the chemliners.. I believe this accounts
for why we seem to have so many forest fires
that are so hard to extinguish. Aluminum
is a component in many… ...
(Please click red arrow to full text and
site)
             
Archive: Skin Parasites & Healing Clay
Date: Novemeber 21, 2002 From: Undisclosed Format: Email To: Eytons' Earth Research Modifications: Syntax, Format
My name is [ name removed ]. I have a very
strange disease, which is shared by thousands
of people in this counry.
Please see The Morgellons Filarial Research Organization and The National Association for People with Unidentified
Skin Parasites. In 1998 a doctor prescribed Permethrin
for me over the phone because I said I had
a rash and diarhea. He decided that I had
scabies even though he did not examine me.
The use of Permethrin caused a cutaneous
larval migration that resulted in terrible
skin lesions. I suffered with these for months.
When the doctor finally saw me he said he
did not know what was wrong but gave me Erythromycin
and Ultravate skin cream, which made things
worse.
I finally saw a naturopathic doctor who gave
me bentonite clay to use as a paste on the
lesions. This cleared them up. Many, many
people are suffering from this disease and
are being told that they are delusional by
doctors who do not know what this is or will
not say. I have a lot more info and would
be glad to help your research in any way
that I can. Please look at the sites I mentioned.
I would also like to know how much bentonite
to use internally. This disease involves
more than the skin.
Thank you.
[ More ]
There is very interesting reading here on
this "hair" and "fiber"
disease, dating back hundreds of years. Blood
tests on the little boy who provided the
specimens for many of these pictures will
be in tomorrow. I am going to send separately
high mag images of what these fibers look
like. Preliminary testing indicates a highly
unusual and primitive fungus with "loose"
DNA.
A blood smear from this child, taken at night,
contained what was identified as a strongyle-type
or onchocerca-type worm by a PhD in biology.
When the CDC received this, they said it
did not look like a parasite to them. I am
attaching the story of what happened to my
jackson chameleons after exposure to my well
water.
Although we now have a kinetico water system,
my pets and I still have many symptoms. I
have not, however, had any lesions since
1998. This disease affects cold and warm-blooded
animals, insects, birds and people. Some
people think it may be related to volcanic
eruptions, such as Mt. St. Helens. Other
people think it the military doing testing.
I tend to think these organisms have always
been around and maybe they only bother us,
unintentionally, when they themselves get
sick or when we are sick, from pollution,
etc. They are really incredible little creatures.
How miraculous to be able to pull a hair
from your head and watch it dart its little
sense organ at your skin, as if testing for
safety, or to see it coil and stretch out,
or swim in the water!
Of course, the many painful external and
internal symptoms are not nice. Some people
have had serious visual deterioration and
pulmonary and heart trouble. Some people
with lesions on their faces will not go out
or shop late at night so others will not
see them. It is heartbreaking.
When you think about all these people suffering
with these terrible symptoms and being met
by the medical profession with disinterest,
hostility or outright persecution, and being
told that they are delusional, it is incomprehensible.
I went to one medical doctor who refused
to look at my lesions or examine me, even
though I begged him in tears, and then called
mental health and told them I was mutilating
myself.
So I had a call from them asking me why I
was "mutilating myself." If something
as inexpensive as bentonite could provide
a solution or alleviate symptoms, what a
blessing this would be. I will keep you posted.
Thank you for your very kind letter.

Date: May 26, 2006 From: Jason @ Eytons Earth Format: Email To: List Group Modifications: Syntax, Format RE: Recent reported outbreaks of Morgellons
Disease in the Bay Area, California
My opinion is that these types of conditions
are real. I don't believe that there
is a single cause, but rather, a group of
conditions that are not easily diagnosed
that share many of the same symptoms ( hence
Morgellons Disease ). The first time I came
in contact with such a case, a whole family
was infected, including their cat. This was
somewhere around nine years ago.
The health department was called in to their
house, but they could not identify a parasite
or any other type of organism. One would
definately have thought the entire family,
including the cat, was insane.
However, I approached the situation with
the assumption that there was an infection
of some sort. Yes, these people were VERY
mentally and emotionally disturbed. However,
I figured that if I were experiencing what
they were, I would likely be disturbed as
well. On top of that, I'd never seen
a psychotic cat before. The cat spent quite
a bit of time just running around in circles.
The individual that had asked for my help
complained about tiny "jumping threads"
he could never see. He'd been tortured
with this predicament for several years,
describing a sensation of bugs crawling under
his skin.
I had him leave the environment, and coat
his entire body ( including the hair/head
) with natural bentonite clay. In very short
order ( an hour ) he experienced the first
moments of relief from this condition in
years.
However, after a time, the sensations would
return ( a day or more ). He would get temporary
relief by repeating the clay coating on his
body... Once, he did the clay therapy daily
for two weeks and experienced complete relief
during this time. However, it wasn't
practical for him to continue due to work,
etc.
I hypothesized that it may have been a parasitic
condition, with a 3 week ( or longer ) life
cycle. IF a parasitic infection, based on
the complaints, I assumed it lived on the
skin, or just beneath the skin, possibly
incubating in the ears or hair.
I traced his infection back to a neighbor
he once had who was an elderly woman originally
from a remote tribe in Africa. The individual
and his family had several unpleasant "neighborly"
encounters with this individual; shortly
thereafter became infected; then moved to
a new area of town in hopes of finding relief.
On studying old remedies, I found that garlic
was often used for parasites. Since I believed
the infection was a skin infection with external
body manifestations, I had the individual
shower very well, apply clay over the entire
body ( thinly coated but covering the skin
), and then allow the clay to dry. After
the clay dried, the individual showered,
and I tossed him a necklace with a few fresh
cloves of garlic ( peeled ).
Having doned his garlic necklace, he never
experienced discomfort again. I tried to
get him to get rid of the garlic necklace
( of course, he always used more fresh garlic
after a few days ) after a few months. However,
he was terrified of a relapse, and did not
want to be without it.
I saw this individual late last year; he
was perfectly fine, yet still wearing the
garlic necklace.
This was a very strange situation ( I still
shake my head in amazement when considering
the memory ), but I was pleased that years
of suffering for this individual had been
ended -- and permanently.
My experience with bentonite, montmorillonite
and french illite clays is extensive, especially
considering skin conditions. The only condition
I have not seen a positive response to is
conditions caused by substances such as Agent
Orange, although long term topical treatment
with clays made with fine quality colloidal
waters may even impact these so-called "jungle
rot" conditions.

A Sufferer's Report on a Unique Alternative
Treatement for Morgellon's Disease Please note that we have not tested this
method, this came from a report posted on
a health email list
For any of you following the mystery, or
who knows about using alfalfa.... This was
posted on a morgellons site today......................
I have been Morgellons sufferer for over
ten years.
Recently, I discovered, quite by accident,
something that is literally making it disappear
from my BODY.
As I am sure fellow sufferers can relate
to, over the years, I have experimented with
various "super baths," filling
the tub with hot water and puttibng in things
like lemons ...
(Please click red arrow to full text and
site)
Terrifying, painful, exhausting. When I have
spoken with people who identify as having
Morgellons disease, these are the words I
hear. Most researchers and medical professionals
consider Morgellons Disease (MD) to be synonymous
with Delusory Parasitosis (DP), a false,
unshakable belief that insects are living
in or on your skin or inside your body. Yet,
several small, concerted groups work to express
it as a distinct medical condition.
Red and blue fibers, described as "Morgellons
fibers".
MD was first described in academic literature
in 2005, when an unidentified number of patients
described itching, crawlingsensations, lesions,
and the eruption of red and blue fibers and
“granules” from their skin. Most
had Lyme disease, and MD was thought to be
significantly related to that (Savely &
Leitao, 2005). Recently, agrobacterium was
indicted as the new culprit, when two self-identified
MD patients with scleroderma were found to
have increased amounts of cellulose-protein
complex in their connective tissue (Savely
& Stricker, 2007, Harvey et al, 2009).
A multi-systemic medical framework for MD
with immunodeficiency problems has been described
(Harvey et al, 2009).
Lesions, attributed to Morgellons Disease.
.
The majority of physicians and researchers
consider MD to be synonymous with DP (Murase,
Woo & Koo, 2006), with the difference
that it is not believed to be parasites,
but about the fibers and granules (Robles
et al, 2008). In response, proponents of
MD as amedical condition herald it as different
from DP, citing a “lack of pre-existing
psychopathology” (Savely & Stricker,
2007). Yet, a study by Harvey et al (2009)
found 25 self-diagnosed MD participants all
had previous diagnoses of DP, and 23 had
other previous diagnoses, including bipolar
disorder, attention-deficit disorder, and
obsessive-compulsive disorder, the symptoms
of which coincided with the onset of their
MD symptoms. These psychological diagnoses
have many somatic connections, and their
medications commonly have side effects of
itching, crawling, and tingling sensations
(Hinkle, 2000), indicating that a psychological
composition of MD is very likely.
Some will disagree with a psychological conceptualization
of MD, and firmly believe that this is a
distinct medical condition. In fact, a DP
diagnosis is not always accurate, such as
with cutaneous myiasis, where fly larvae
inhabits the skin of a person (Barros et
al, 2010). Medical and scientific knowledge,
and identification of new pathogens, diseases,
and treatments, continually occur.
The burden of proof is on the advocates for
MD to be a distinct medical condition. In
my opinion, mental health should be recognized
as the possible, if not probable foundation
of MD. Fibers and granules of dirt and debris
are everywhere. Increased cellulose-protein
complex in two patients who also have scleroderma
is still distant from being definitive. Harvey’s
study found many vague health anomalies,
yet the autoimmune problems sound like what
one would expect from intense stress (Khansari
et al, 1990). What would be more stressful
than the real or perceived experience of
an infestation of the most personal and offensive
kind, the body?
Dr. Harvey recommends that we be open and
skeptical, and I agree. The CDC is in the
data-analysis stage of an investigation of
MD through Kaiser in Northern California.
As a scientist and as a person who is aware
of the suffering of people with these experiences,
I look forward to the results.
Sarah Bione-Dunn is a doctoral candidate
in clinical psychology at Alliant International
University. She expects her degree in June,
2010.
de Barros N, D’Avila MS, de Pace Bauab
S, Issa FK, Freitas FJ, Kim SJ, Chala LF,
& Cerri GG (2001). Cutaneous myiasis
of the breast: mammographic and us features-report
of five cases. Radiology, 218 (2), 517-20 PMID: 11161171
Harvey WT, Bransfield RC, Mercer DE, Wright
AJ, Ricchi RM, & Leitao MM (2009). Morgellons
disease, illuminating an undefined illness:
a case series. Journal of medical case reports, 3 PMID: 19830222
Hinkle, N. (2000). Delusory Parasitosis.
American Entomologist, 46 (1), 17-25
Khansari, D., Murgo, A., & Faith, R.
(1990). Effects of stress on the immune system
Immunology Today, 11, 170-175 DOI: 10.1016/0167-5699(90)90069-L
Murase JE, Wu JJ, & Koo J (2006). Morgellons
disease: a rapport-enhancing term for delusions
of parasitosis. Journal of the American Academy of Dermatology,
55 (5), 913-4 PMID: 17052509
Robles DT, Romm S, Combs H, Olson J, &
Kirby P (2008). Delusional disorders in dermatology:
a brief review. Dermatology online journal, 14 (6) PMID: 18713583
Savely G, & Leitao MM (2005). Skin lesions
and crawling sensations: disease or delusion?
Advance for nurse practitioners, 13 (5), 16-7 PMID: 15898309
Savely VR, Leitao MM, & Stricker RB (2006).
The mystery of Morgellons disease: infection
or delusion? American journal of clinical dermatology,
7 (1), 1-5 PMID: 16489838
Savely, V., & Stricker, R. (2007). Morgellons
disease: the mystery unfolds Expert Review of Dermatology, 2 (5), 585-591 DOI: 10.1586/17469872.2.5.585
(Please click red arrow to full text and
site)
Morgellons: A hidden epidemic or mass hysteria?
It's a mysterious condition that affects
tens of thousands worldwide. But what is
it?
Optical image of what sufferers are adamant
are morgellons fibres in skin samples - are
they made up of alien matter, or are
everyday materials the more likely explanation?
Photograph: Vitaly Citovsky/Suny at Stony
Brook
It all started in August 2007, on a family
holiday in New England. Paul had been watching
Harry Potter And The Order Of The Phoenix with his wife and two sons, and he had started
to itch. His legs, his arms, his torso –
it was everywhere. It must be fleas in the
seat, he decided.
But the 55-year-old IT executive from Birmingham
has been itching ever since, and the mystery
of what is wrong with him has only deepened.
When Paul rubbed his fingertips over the
pimples that dotted his skin, he felt spines.
Weird, alien things, like splinters. Then,
in 2008, his wife was soothing his back with
surgical spirit when the cotton swab she
was using gathered a curious blue-black haze
from his skin. Paul went out, bought a £40
microscope and examined the cotton. What
were those curling, coloured fibres? He Googled
the words: "Fibres. Itch. Sting. Skin."
And there was his answer. It must be: all
the symptoms fitted. He had a new disease
called morgellons. The fibres were the product of mysterious
creatures that burrow and breed in the body.
As he read on, he had no idea that morgellons
would turn out to be the worst kind of answer
imaginable.
Morgellons was named in 2001 by an American
called Mary Leitao, whose son complained of sores around his
mouth and the sensation of "bugs".
Examining him with a toy microscope, Leitao
found him to be covered in unexplained red,
blue, black and white fibres. Since then,
workers at her Morgellons Research Foundation
say they have been contacted by more than
12,000 affected families. Campaign group
the Charles E Holman Foundation states there are sufferers in "every
continent except Antarctica". Thousands
have written to Congress demanding action.
In response, more than 40 senators, including
Hillary Clinton, John McCain and a pre-presidential Barack Obama, pressured the Centres For Disease Control And Prevention (CDC) to investigate; in 2006, it formed
a special taskforce, setting aside $1m to
study the condition. Sufferers include folk
singer Joni Mitchell, who has complained of "this weird
incurable disease that seems like it's
from outer space... Fibres in a variety of
colours protrude out of my skin: they cannot
be forensically identified as animal, vegetable
or mineral. Morgellons is a slow, unpredictable
killer – a terrorist disease. It will
blow up one of your organs, leaving you in
bed for a year."
So it's new, frightening and profoundly
odd. But if you were to seek the view of
the medical establishment, you'd find
the strangest fact about this disease: morgellons
doesn't exist.
I meet Paul in a pub in a Birmingham suburb.
He shows me pictures he's collected of
his fibres. On his laptop, a grim parade
of images flicks past. There are sores, scabs
and nasal hairs, each magnified by a factor
of 200. In each photo there is a tiny coloured
fibre on or in his skin.
"Is it an excrement?" he asks.
"A byproduct? A structure they live
in?" A waitress passes with a tray of
salad as he points to an oozing wound. "Is
it a breathing pipe?"
Paul absent-mindedly digs his nails into
a lesion just below the hem of his shorts.
Little red welts pepper his legs and arms,
some dulled to a waxy maroon, others just
plasticky-white scar tissue.
He has seen an array of experts – GPs,
allergy doctors, infectious diseases clinicians
and dermatologists. Most end up agreeing
with the skin specialist to whom he first
took samples of his fibre-stained cotton:
his sores are self-inflicted and he suffers
from delusions of parasitosis (DOP), a psychiatric condition in which
people falsely believe themselves to be infested.
This particular form of DOP is thought to
be unique, in that it's spread through
the internet. Whereas in the past, episodes of mass hysteria
were limited to small communities –
perhaps the most famous being the witch panic
in Salem, Massachusetts in the 1690s – today, imagined symptoms can spread
much farther on the web.
Paul is not convinced by this diagnosis.
He carries an alcohol hand gel everywhere
he goes, has four showers a day and steam-cleans
his clothes. The stress leaves him exhausted,
short-tempered. He has difficulty concentrating
or applying himself at work. His lowest points
have been "pretty much feeling like
ending it. Thinking, could I go through with
it? Probably. It's associated with the
times the medical profession have dismissed
me. It's just… I can't see
myself living for ever with this."
Has he mentioned these thoughts to his doctor?
"No, because talking about things like
that adds a mental angle – supports
the prognosis of DOP. And it's absolutely
a physical condition. I mean, look!"
The evidence on his computer does appear
convincing. Much thinner than his body hair,
the fibres seem to be protruding from his
sores. But what are they? And how did they
get there? To find out, I'm heading to
the 4th Annual Morgellons Conference in Austin, Texas, to meet a molecular biologist who
doesn't believe the medical consensus.
Rather, he argues, the forensic tests he's
commissioned on the fibres point to something
altogether more unworldly.
In spring 2005, Randy Wymore, associate professor
of pharmacology at Oklahoma State University, stumbled across an article about morgellons.
Reading about the fibres sufferers believed
were the byproduct of some weird parasite,
but which were dismissed by dermatologists
as humdrum environmental detritus, he thought,
"But this should be easy to figure out."
He emailed sufferers, requesting samples,
then compared them with samples of cotton,
nylon, carpets and curtains. Examining them
under the microscope, he got a shock. The
sufferers' fibres looked utterly different.
Wymore arranged for fibre analysis at the
Tulsa police department's forensic laboratory.
Moments into his tests, a detective with
28 years' experience of this sort of
work murmured, "I don't think I've
ever seen anything like this." The morgellons
particles didn't match any of the 800
fibres on their database, nor the 85,000
known organic compounds. He heated one fibre
to 600C and was astonished to find it didn't
burn. By the day's end, Wymore concluded,
"There's something real going on
here. Something we don't understand at
all."
Last year, he approached several commercial
laboratories to run further tests, but the
moment they discovered the job was related
to morgellons, firm after firm backed out.
Finally, Wymore found a lab prepared to take
the work. It is these results that will be
revealed during the course of the two-day
conference.
.....
(Please click red arrow for text and site)
   Go To The Bottom Of Page For AMA Article....
American Medical Association (AMA) News Release;
“Morgellons is Systemic” –
Far Too Many Suicides
Small Bowel Capsule Findings Suggest that
Morgellon’s Disease has an Organic
Basis and is Not Psychosomatic in Origin!
Morgellons Lesions with Blue Fiber
Daniel Chao, MD, David Cave, MD, PhD University of Massachusetts Medical Center,
Worcester, MA.
Purpose: Background: Morgellon’s disease
is a poorly described, severe ulcerative
skin condition that histologically is consistent
with dermatitis artefacta. It has therefore
been dismissed as a psychosomatic disorder,
much as was the case with ulcerative colitis
in the period from 1930 to 1960. We present
the first case of a patient with Morgellon’s
syndrome who had additional findings suggesting
that it is a systemic disease. continue reading… .....
(Please click on the red arrow to this text
and source)
"Whoever it was (think i remember from
D. Prince?!) that used Fixadent on the lesions
on their head should be elevated to sainthood!
Ran out of my Pascalite Pak, which is fabulous,
so resorted to the Fixadent morning and night
after cleaning my scalp. Amazing! The vermin
come up for air and get instantly trapped,
suffocate and die. Each morning and evening
I use the lice comb to lift everything off,
which until this was extraordinarily painful
no matter what I had been applying. The …
"
(see this article below)
"...There is no cause; however, there
is prevention and relief to be had. If our
internal terrain is failing, lacking: minerals,
vitamins, amino acids, PH, healthy gut flora,
and oxygen and if we are not staying hydrated,
eating nutritiously and strengthening positive
emotions we then become prime target for
disease. Of course, there is some catalyst,
or vector probably a fungal element from
GMO pharming or something, but it will not
take hold in those with a strong terrain
and we can all strengthen our terrain and
become at least "symptom free",
I hesitate to use the word cured."
(Click on the red arrow to this article)
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