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Morgellons Fits Profile Of An ET Organism
by Samuel Feldman
6-25-6
http://www.schmoo.co.uk/morgellons.htm
Dear Jeff...
I've assembled a lot of data on
Morgellons and now believe the
preponderance of evidence suggests we are, in fact, dealing with an
off-planet issue. Please read the material below. Thanks for your
heroic work and boundless courage.
Sam
Read this:
"Most amazing, says Louis, the cells can reproduce under conditions
that usually kill life.
"These cells can be cultured at high
temperature (about 600° F) and pressure conditions and at high
temperature their growth rate (i.e. multiplication) can be very
fast.
"The details on replication are being submitted to another
journal."
So, I then read these articles:
And then I read this one:
Temperature and Pressure Experimentation With Red Rain Cells
"Over several months, Dr. Louis began experimenting with different
temperatures to see if the cells would respond. As the temperature
rose, he saw more activity. Eventually he got up to 300 degrees
Celsius, which is about 600 degrees Fahrenheit. He also increased
the pressure to 300 pounds per square centimeter. It is assumed that
normal Earth life would die at such a high temperature and pressure.
But the red-walled cells in the Kerala rain water seemed to thrive."
So, what we have in Kerala is scientific data that compels us to
do... and do so quickly... the same experiments on Morgellons fibers.
If Morgellons is, in fact, an ET 'organism' of some kind, we are
facing something that is perhaps threatening to all life on the
planet Earth. ALL life.
Kind regards, Sam Feldman
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Morgellons - Weird 'Alien' Bug Hits Thousands In US
by Samuel Feldman
6-25-6
"I think we are a looking at a major problem that has been
unrecognized in humanity right now."
-- Dr. William Harvey
NASA
Over 1000 people in Texas, Florida and California are saying that
they are suffering from a nasty new skin complaint, but doctors are
telling them they are 'delusional'.
It is a weird 'bug' which sounds like something from an 'X Files'
script, but it seems to be real, despite official denials from the
US medical establishment.
No one knows what it is, and most people suffering from it are told
they are suffering from 'Delusional Parasitosis' by their doctors.
However, now there is mounting evidence that it is the doctors and
the US medical establishment who are 'delusional', not their
unfortunate patients.
There are currently over 1,100 hundred known cases in the U.S.,
mostly in Texas, Florida and California of what is being called 'Morgellons',
and it is spreading.
Bugs crawling under your skin
Victims feel like bugs are crawling under their skin. They have
little blue fibers, and black specks and white threads coming out of
their skins. Under the skin, those fibers are connected to what
appears to be a cluster of fibers or in some instances, parasitic
looking organisms.
One Morgellons patient Eric Roberson said, 'It's almost like they're
intertwined with your muscle tissue,"
"The lesions start out as bumps that are itchy, little round raised
bumps. The fibers are quite alarming." said another.
"When you lay down, as soon as your head hits the pillow, your hair
starts crawling," says Becky Bailey.
"It gives you the sensation that you have worms under your skin or
rats crawling on you," says Miles Lawrence.
Another victim, Becky Bailey moved out of her Austin, Texas home and
into a trailer hoping to escape the bugs that torment her.
"We
ripped out our carpet and burned our carpet and furniture and move
out into our R-V and they were still on me."
A victim in California Dillon King committed suicide because he
could not stand the feeling of bugs crawling under his skin any
longer. His mother is quoted:
"The hardest thing was seeing him just
get worse all the time".
King's fiancée, Elizabeth Strong, says she thinks he picked up some
kind of 'weird infection', and that she's now beginning to show the
same symptoms.
"It started as a small sore and kept spreading," she
said.
The Morgellons Research Foundation, which is campaigning for more
research to be done, reports that unexplained hair loss, as well as
a hardening or thickening of skin is also a common symptom and that
many people report lymphedema, profound fatigue, and joint pain.
Objects described as granules are often found associated with skin
lesions as well and several victims have had lymph nodes surgically
removed due to obstruction.
The fibers have been analyzed by FTIR (Fourier Transform Infrared
Spectroscopy) and have been identified as cellulose. Since true
fungi are not able to synthesize cellulose, the Foundation is
currently focused on the 'Oomycetes' class of fungus-like organisms.
Apparently 'Pythium insidiosum' is the only Oomycete which has been
documented to cause human infections.
Skeptic doctors and the 'Matchbox Sign'
Morgellons victim Jane Waldoch, a nurse for 24 year says she finds
fibers that look like crunched up bugs in her sheets every morning.
They come from the dozens of sores that cover her arms, legs, back
and neck.
She began collecting samples of what was coming out of her skin. She
thought it would help her doctors diagnose this bizarre and painful
skin condition. She was wrong.
Doctors took it as a sign that Jane was delusional.
"One of the hallmark clues to
delusional parasitosis is what they
call the matchbox sign. I guess in the older days people would take
their samples in little match boxes to their physician," she says.
Mary Leitao, a biologist and the executive director of the
Morgellons Research Foundation, said doctors have become,
"a brick
wall. They have their answer, and they aren't open to discussing the
possibility they could be wrong." "They are so smug and sure they are right," she said.
Dr. Peter Lynch of the University of California, a dermatologist for
40 years, is one of the few skeptical experts who have been willing
to even talk on the record. Other have ignored emails and telephone
calls.
He said,
"If there were a peer-reviewed study, with 15 or 20
patients who have the same exact thing in their skins, then maybe
I'd believe it,"
"When fiberglass curtains first came out, many people with skin
conditions were diagnosed with delusions of parasitosis (DOP). But
studies showed these patients had tiny (fiberglass particles) in
their skin."
"Anecdotal evidence doesn't carry much weight," Lynch said. "There
are many anecdotes of alien abductions, but that doesn't mean they
are true. And as for the pictures, you can see pictures of the Loch
Ness Monster on the Internet, too."
Leitao and other members of the
Morgellons Research Foundation are
not impressed with these arguments and point to the mounting
evidence.
Californian microbiologist Jenny Haverty for example, has done
research on the mystery malady. Her findings point to something very
definitely physical going on.
"I accepted specimens from four different people in four different
counties in the Bay Area, and I looked at them very carefully over
and over again under the microscope," she said.
"The colors and
shapes of the fibers of each individual were very, very similar."
She reports that tests on similar fibers taken those of several
other patients in the Bay Area show them to be tiny tubes of
protein. But how and why the filaments are formed remains a mystery
for now.
Evidence of link to Lyme Disease
Evidence is beginning to mount linking Morgellons to Lyme Disease
which can be caught from tick bites.
Ginger Savely, a medical practitioner in Austin Texas, says she's
seeing more and more patients in her clinic with the symptoms.
Quoted in a local newspaper she said "Talking about it just sounds
crazy, but there are just a lot of things that come out of their
skin."
Savely specializes in Lyme Disease and believes there may be a link.
She says that about 10 percent of her patients with chronic Lyme
disease have symptoms of Morgellons. He theory is that people with
the tick-borne Lyme Disease have weaker immune systems, and may be
more vulnerable to the Morgellons infection.
The Morgellons Research Foundation says that forty-four people with Morgellons have tested positive for
Borrelia burgdorferi (Bb), the
bacteria which causes Lyme Disease.
They believe that an infection with Borrelia burgdorferi (Bb) may
alter the individual's immune system and allow this unknown organism
to become an opportunistic coinfection.
Ancient Engine of An Unrecognised 'Borreliosis' Pandemic?
A former NASA physician and epidemiologist based in Houston also
believes there is an infectious bacteria at the heart of this
problem.
Dr. William Harvey is the current chairman of the NASA Education
Advisory Committee. He has documented more than 565 of these (Borreliosis)
cases in Texas and says 94% of (those with Morgellons' skin lesions)
have tested positive for the bacteria associated with Lyme disease,
or Borreliosis.
"I think we are a looking at a major problem that
has been unrecognized in humanity right now."
Harvey co-authored a published medical study concluding the bacteria
Borrelia burgdorferi, associated with Lyme disease, could be at the
heart of a widely unknown misdiagnosed infection.
In 2003 Harvey published his research in the medical journal Medical
Hypotheses. His article 'Lyme Disease: Ancient Engine of an
Unrecognized Borreliosis Pandemic', suggests that the bacteria
associated with Lyme disease is much more widely distributed.
"The yet-unrecognized form appears to have a broader clinical
presentation, wider geographic distribution, and vastly greater
prevalence," Harvey wrote in his report.
He says research suggests it attacks the immune system in a specific
way rendering it susceptible to these unusual organisms.
"The lab
tests that we do are predictably showing certain immune damage and
it is consistent from patient to patient to patient to patient."
Harvey believes the bacteria is the bigger problem. But the
so-called parasites, which have yet to be clinically proven in a
controlled laboratory setting, do have highly unusual
characteristics as seen through a scanning electron microscope.
Harvey says some of the "filaments" have been confirmed as the
infectious yeast Candida tropicalis and that doctors can easily see
the physical symptoms in people who are branded "delusional." He
says when patients complain that "fibers" are coming out of their
skin sores, physicians should investigate.
"All the doctors have to do is buy a 30X hand-held microscope from
Radio Shack and look," Harvey said. "The facts speak for
themselves."
Microscopic bug called 'Collembolan' could also be involved
The 'National Pediculosis Association' in Boston, Massachusetts,
originally created to increase awareness about head lice and protect
children from pesticides has also done some research. They teamed up
with the Oklahoma State Department of Health to study Morg. They
took skin samples from 20 patients who claim they have the bugs, but
were diagnosed by their doctors as delusional. Researchers found
collembolan, a microscopic bug, in 18 of the 20 patients.
Collembola feed on algae, bacteria and decaying matter. They thrive
in wet or damp surroundings, and can be found under leaky kitchen or
bathroom sinks, swimming pools, and the soil of potted plants.
The report has been published in the journal of the New York
Entomological Association.
Who is really delusional?
So, it seems there is in fact a real bug, or even a 'willing
coalition' of bugs at large in the United States attacking innocent
citizens, despite official denials. It also seems that it is the US
medical establishment that is 'delusional', not their unfortunate
patients. Either that, or they are lieing through their bleached
white teeth. Or possibly both.
Back to Contents
Morgellons - Mysterious
Ecto-Parasites
SafeSolutionsInc.com
6-24-6
A mysterious skin disease is currently spreading across America, and
doctors are searching for answers on how to stop the epidemic.
The disease, called Morgellons Disease, is a parasite-like infection
that literally makes the infected person's skin crawl. The disease
has already been found in thousands of patients in Florida , Texas
and California.
"I would lay in the bed and it felt like an army of ants just
crawling over the bed, all over my body," says one Morgellons
Disease sufferer.
"It never goes away," says another. "It doesn't die, it doesn't
leave."
What sounds like a science fiction movie is actually real life for
the unlucky people who have contracted the disease which leaves
painful sores all over the body. The sores ooze blue fibers, white
threads and little black specks of sand-like material.
The worst part, patients say, is the creepy and constant sensation
of bugs crawling under their skin.
Also discouraging, is the patient's treatment by doctors, who have
little knowledge about the disease, and in specific cases have
lacked compassion for the sufferers.
"I was so humiliated from the three doctors that I went to, that I
just refused to go back," said on patient.
Becky Bailey moved out of her Austin, Texas home and into a trailer
hoping to escape the bugs that torment her.
"We ripped out our carpet and burned our carpet and furniture and
move out into our R-V and they were still one me."
Without medical help, suffering families researched their symptoms
on their own by way of the internet. Finally, they were able to put
a name to their pain Morgellons.
The sickly skin disease has actually been around for centuries. In
1935, an English physician wrote a paper about Morgellons including
excerpts from medical journals from the 1600's, describing the
disease.
Unfortunately, not much was known then about Morgellons -- and not
much has been learned in the more than 400 years since.
What is known, is that many of people who may have it, suffer from
these symptoms: constant itching/crawling sensation, chronic
fatigue, brain fog or attention deficit hyperactivity disorder,
bipolar disorder, depression, joint swelling or hair loss.
What you should do if you have these symptoms, is as puzzling as the
disease itself.
One woman in Pittsburgh, PA made it her mission to find out what
causes and what will cure this bizarre disease.
Mary Leitao is a biologist and the creator the Morgellons Research
Foundation in Pittsburgh.
Her goal is to get State Health Agencies and the Center for Disease
Control (CDC) to study this disease.
"It's inhumane that these people have been allowed to go home and
have been forced to research this day in and day out for years on
their own," says Leitao.
Leitao's motivations come from her 6 year old boy Drew. Four years
ago, he began to feel the itch.
"He started describing bugs. He said, mommy, bugs, and he would
scratch."
Then came the sores that shed the fibers. Mary took drew to the
doctor and the doctor said it was nothing to worry about.
"I was going to find an answer, or I was going to have to take my
life, that's all there was too it."
Doctors don't know what causes the disease, who is at risk and
exactly how many people may be suffering. The Morgellon Foundation
says they have about 12 hundred people registered on their site.
Those are only people who have a computer and happened to find them
online.
In Jacksonville, more than a dozen cases have been found.
For Anne Dill, standing in her backyard, looking over the lake is
physically and emotionally painful.
This silence and solitude serves as a constant reminder of what her
family is facing.
"We're going to lose everything, our house, our dreams," says Dill.
Five years ago, the dills bought their dream home in Lake City. They
spent most of their free time at their lake with friends, and
thought life was pretty close to perfect.
Then, three years ago, Anne, her husband and their four children all
got very sick at the very same time.
They think they have Morgellons, even though they have no idea how
they would have contracted it.
Morgellons is an unusual parasite-like skin disease, which produces
irritating sores all over the body.
These sores ooze blue fibers, white threads and little black specks
of sand-like material.
The Dills say they're also plagued with a constant, creepy crawling
feeling of bugs under their skin.
However, the most agonizing symptom is the chronic fatigue. The
Dills are so tired and so weak, they spend nearly all of their time,
at home.
The father, Tom Dill is the sickest. Along with the Morgellons, he's
developed signs of Lou Gehrig's disease. It's a neurological
disorder that robbed him of his muscle control. He's now bound to a
wheelchair and has trouble speaking. Tom doesn't know if his two
conditions are related. That has him worried about his children.
"I don't want to believe that what happened to me, happened to
them."
But answers are hard to come by. In fact, doctors tell them the
"bugs" they feel and sores they see, are only in their minds. In
medical terms, they are delusional parasitosis.
"I don't know how a doctor couldn't see that, it's ridiculous, I can
see it, I know there's something there, I'm like a freshman in high
school and I know that there's something wrong."
Doctor Hardesh Garg is an internal medicine specialist in
Jacksonville. He isn't surprised by the reaction the dills have been
getting from doctors.
"A lot of times, not all of us, who feel like, if it doesn't exist
in my medical book, it really doesn't exist and it must be a figment
of your imagination," says Garg.
Doctor Garg has never seen a patient with Morgellons. However, he
says this skin condition needs to be studied.
"Until we know what's causing it, can't say if it's infectious or
not or how dangerous it is."
No doctors on the First Coast or Florida could be found who know
anything about Morgellons. However, not all hope is lost. One
medical professional in Austin, Texas may have found a clue to the
Morgellon's mystery.
Ginger Savely is a nurse practitioner who specializes in treating
the tick borne Lyme disease. She also has first hand experience with
the mystery disease.
"Right now I think I have about twenty eight Morgellons patients,"
says Savely.
According to Savely, the anti-biotics she gives to patients with
Lyme are also working on some Morgellon's patients.
But this treatment is also unproven, and since doctors don't know if
it's contagious, the Dills say their home is now their prison.
So, the Dills spend a lot of quality time together. Five year old
Hanna has been one of the Dill's secrets to survival, as her love
for singing songs keeps the family entertained.
Recently researchers have been uncovered who have just published a
study on an unknown skin disease with the exact same symptoms.
It is promising research that points to a critter that could be
lurking in your home, and research the Dills may feel that every
family should look into.
Since the CBS47 investigation began digging into the Morgellons
mystery, dozens of people on the First Coast have been in contact,
desperately looking for help.
One of these people is a nurse who lives in Saint John's Country.
Her story is a striking example of how most patients with this
bizarre skin disease are shut out by their doctors.
At the end of another exhausting day for Jane Waldoch,
"I go to bed
at 8:30 , 9 o'clock. I feel like a little old lady and I'm 51 years
old."
Jane's fatigue is one of the many symptoms she has of the mystery
skin disease, some call Morgellon's.
As a nurse for 24 years, her first reaction was to see a doctor.
However, that is where her trouble began.
"I'm absolutely disappointed, disillusioned and very, very angry at
the medical community," says Waldoch.
In the past year, she's been referred to all kinds of doctors.
"Internal medicine, multiple dermatologists, infectious disease,
then it went to Rheumatology, Endocrinology, Neurology..." she says.
The doctors saw the sores, but couldn't figure out what was causing
them.
"They'd look at me and say, 'Its dry skin, quit worrying about it.'
I'm saying, 'This is the weirdest dry skin I've ever seen in my
life!'"
Still, she followed doctors' orders, and took her medications; all
two dozen bottles of them.
But none of these drugs worked. So Jane began collecting samples of
what was coming out of her skin. She thought it would help her
doctors diagnose this bizarre and painful skin condition.
She was wrong.
Doctors took it as a sign that Jane was delusional.
"One of the hallmark clues to delusional parasitosis is what they
call the matchbox sign. I guess in the older days people would take
their samples in little match boxes to their physician," she says.
Mary Leitao from the Morgellons foundation says patients would do
this to prove they were telling the truth.
Jane says she finds fibers that look like crunched up bugs in her
sheets every morning. They come from the dozens of sores that cover
her arms, legs, back and neck.
"I never thought I'd be in this position, of being embarrassed with
who I am, and what I look like."
However, Jane is coming forward, hoping her story will help find a
cure, especially for the youngest victims.
Jane is not the only case of the mystery disease found on the first
coast. More than 100 people have confirmed they have been suffering
from the exact same symptoms, some for as long two decades. Many of
them have been diagnosed with delusions of parasitosis.
One research foundation estimates that there are more than
13-hundred people across the country with Morgellons symptoms.
The true number may be a lot higher.
Mary Leitao is a biologist and the executive director of the
Morgellons Foundation. The foundation is studying this mysterious
skin disease.
They call it Morgellons -- because it looks and sounds exactly like
an infection doctors wrote about in the 1600's.
However, 400 years later, these stories don't add up to a diagnosis.
However, researchers may be getting the help they need to find a
major breakthrough.
Deborah Altschuler is the president of the National Pediculosis
Association in Boston, Massachusetts. The foundation was created to
increase awareness about head lice and protect children from
pesticides. Altschuler has been studying a disease that sounds exactly like
Morgellons disease.
"People were calling us with very similar symptoms from all over the
country," says Altschuler.
The NPA teamed up with the Oklahoma State Department of Health to
study the creepy crawlers.
They took skin samples from 20 patients who claim they have the
bugs, but were diagnosed by their doctors as delusional.
Researchers found collembolan, a microscopic critter, in 18 of the
20 patients.
Collembola feed on algae, bacteria and decaying matter. They thrive
in wet or damp surroundings, and can be found under leaky kitchen or
bathroom sinks, swimming pools, and the soil of potted plants.
The report was published in the journal of the New York
Entomological Association. However, it wasn't enough evidence to get
the centers for disease control to take action.
The CDC told Altschuler that the collembola was not a danger to
humans, even though she says the CDC has shown her no specific study
to prove it.
The Morgellons Foundation says it was also shot down by the CDC.
If the research on the collembola is right, researchers still have
to figure out how serious these critters are to your health, and
they have to find out how to kill them.
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