STARI is Cow Relapsing Fever; Exceptionally Scarey U.S. Stupidity
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Subject: STARI is Cow Relapsing Fever; Exceptionally Scarey U.S.
Stupidity
Date: Jan 24, 2011 8:05 AM
ARTICLE BELOW- CORRECTION RE STARI
======================================
STARI is Cow Relapsing Fever.
Here is the CDC officer Alan
Barbour's patent for it:
http://www.actionlyme.org/CENTRAL_LYME_RICO_PATENTS.htm
That's how you know "Lyme Disease" is
a ruse. A strawman. The real name
of the disease is Relapsing Fever, and
of course it is all over the country:
http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id=138
And as far as "Lyme" being the new
AIDS, that's correct. OspA suppresses
the immune system, allowing for all
kinds of junk to not only to grow
undetected (tolerizes to fungal infections
in the blood), but activates virals that
were latent:
http://www.actionlyme.org/101016.htm
Mice and ticks might even be passing
along the Mousie Mononucleosis to
humans. (Seriously.)
Anyone can go to MedLine and look this
stuff up. The only item of information
that was rare was the exact structure of
HIV gp120 and OspA.
The crooks have still not told us what
OspA is, and Allen Steere still has
not explained to us how OspA results
in "HLA-linked-hypersensitivity bad-knee."
[Clifford Harding, Dave Dorward and
Dave Persing have, however, shown what
it is.]
Not since 1975, has Allen Steere ever
scientifically explained how this occurs.
And IDSA has never demonstrated what OspA
is/does, except when Gary Wormser reported
that OspA suppressed the immune system in
2001:
http://www.actionlyme.org/101016.htm
These facts don't get into the MSM for
many reasons but one of them is that a
lot of what drives "journalists" is being
the owner of some BREAKING! scoop. And
no "journalist" owns this.
The same applies re Lyme "activism."
And Now! look what happened:
http://www.nytimes.com/2011/01/23/health/policy/23drug.html?hpw&pagewanted=print
All of the ^^ DHHS and BigPharma have
admitted that they have no clue
what's a "brain" drug and why.
That's very funny because ILADS is
made up of mostly psychiatrists and
now they REALLY can't claim they know
what they're doing or selling.
CONCLUSION: America, private or public,
doesn't know what is a drug or what is a
disease.
I think I might phone that into Janet
Napolidykimo and tell her I'm scared uh dat!!!
http://www.dhs.gov/files/reportincidents/counterterrorism.shtm
KMDickson
http://www.actionlyme.org
http://www.relapsingfever.org
==================================================
Researchers: Florida doctors reluctant to diagnose Lyme disease
ADVERTISEMENT
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By KEITH MORELLI | The Tampa Tribune
Published: January 24, 2011
vote
nowBuzz up!
For more than two years, Dolores Claesson has fought a microscopic
enemy, a germ passed into her 17-year-old daughter, Sofia, by a sesame
seed-size tick.
If caught early, Lyme disease could have been easily treated, said
Dolores Claesson, who runs a support group and manages a widespread
network of Lyme disease patents and researchers. But because the
malady has not really found a home in Florida yet, she said, doctors
here are reluctant to diagnose it.
And some medical researchers agree, saying many doctors simply are
complying with a study by the Infectious Diseases Society of America
that warns against over-diagnosing Lyme disease because its symptoms
are so complex and mimic other ailments.
In Sofia's case, doctors misdiagnosed her disease and mistreated it,
stretching her sickness from days to months and eventually years. Now,
her immune system is depleted and she is a perfect host to any virus
that comes along, her mom said. Just this week, the teen spent eight
hours in a doctor's office getting an intravenous antibiotic drip.
In October 2008, Sofia contracted a high fever, a sore throat and her
doctor said it was mono, Dolores Claesson said, and referred the teen
to other physicians.
"A pediatric physician said it was fatigue syndrome," Claesson said,
"that it was hormonal and common among high achieving girls. He told
me to take her on a 20-minute walk three times a week and she would be
fine." The doctor also advised Claesson to take her daughter to a
psychiatrist.
After a while, Sofia developed warts on bottoms of her feet and began
sleeping 20 hours a day, her mom said.
"In all," she said, "we saw about 20 doctors."
None thought of Lyme disease.
"This is normal." Claesson said. "They don't know about it. They don't
know the signs and symptoms. In the Northeast, it's different. But
here in Florida, doctors don't know about it and don't know how to
diagnose it. They don't know how to treat it.
"I want my kid fixed," she said. "Doctors here are like ostriches
putting their heads in the sand. It's been 27 months of pure hell,"
she said.
Over the past couple of years, Claesson, who has an educational
background in biochemistry but chose a career in business, is host to
a Lyme disease support group that includes 400 researchers, doctors
and victims in 40 countries.
"We're lepers," Claesson said. "We can't get any treatment. It's
bankrupted people. We are the new HIV/AIDS patients and we are being
ignored by physicians and if they do let us know we have Lyme disease,
they tell us to go to New York. We can't all fly to New York for
treatment."
She said her daughter, who has missed much of the past two years of
school, likely contracted the disease during a recent trip to Europe.
She understands that doctors here are not familiar with the disease.
They are pressured to diagnose something during short office visits
and most of the time, the patient actually suffers from the flu, she
said. Lyme disease symptoms are complicated, she said, and often look
like the common flu.
"Doctors have only 10 minutes to make a diagnosis," she said. "Mostly,
it's hit or miss with cures."
At 42, Shawn Ingram should be at the peak of his career as a paramedic
firefighter. Instead, he's holed up in his house, on full disability
because of Lyme disease.
He's been sick for 12 years and was diagnosed with Lyme disease eight
years ago.
"Back then, I had no idea what was going on," he said. "Being in the
medical field and 30 years old, I was gangbusters. I was a nothing-can-
harm-me kind of guy."
One day he came down with a bad flu, he said. "It never went away."
Fatigue, exhaustion set in.
"My mental clarity was gone," he said. "Now, I don't have endurance
and some days just walking though the house is taxing."
A Florida native, Ingram said he thinks he was bitten by a tick
somewhere in Central Florida, perhaps when he was fighting brush
fires.
Doctors in Florida passed him around, unable to diagnose what was
wrong, he said. "It took me about three years to find a doctor," he
said. "I even went to the Mayo clinic in Jacksonville. In those three
years, I saw about 18 doctors. I saw infectious disease specialists, a
cardiologist and internal medicine specialists."
They guessed at different maladies, he said. Chronic fatigue syndrome
and fibromyalgia topped the list.
Lyme disease, at the time, just didn't happen in Florida, he said.
"Nobody was really treating it," said Ingram of Tampa, "until I got
diagnosed eight years ago."
Finally, he found a local doctor who drew blood and sent it to a
specialized laboratory in California. The results: Lyme disease, he
said.
Since then, he has reached out to people with Lyme disease, offering
whatever support he could.
"I've seen people recover from it and I've seen people not recover
from it," he said. "If it's caught early, it is a treatable disease.
But, the medical system in Florida needs to be educated; doctors in
Florida need to be educated."
Lyme disease was first documented in the United States in 1975 and is
named for the town in Connecticut where some of the first cases
occurred. Experts say that over 16,000 cases a year have been reported
in the United States since1993, mostly in the Northeast.
By comparison, incidents of West Nile Virus across the nation average
nearly 1,700 a year.
A tick-born disease similar to Lyme is sweeping across the
southeastern United States. According to the Centers for Disease
Control and Prevention, the southern tick-associated rash illness
(STARI) is caused by the lone-star tick.
But, unlike Lyme disease, STARI has not been linked to arthritic,
neurological or chronic symptoms.
While the cause of STARI is unknown, studies have shown that is not
caused by Borrelia burgdorferi, the bacterium that causes Lyme
disease, the CDC reported.
Carol Fisch is a medical researcher living in Sarasota who has devoted
much of her work to Lyme disease. Diagnosed with Lyme disease 18 years
ago in Michigan, she said she was sick for five years before doctors
correctly discovered what was ailing her.
Now, she heads a support group for Lyme disease victims.
"The disease is spreading faster than wildfire," she said. While many
cases diagnosed here originate in other states, Florida is home to
ticks that carry Lyme disease, she said.
She admits that Lyme disease is complex. Symptoms caused by pathogens
that are difficult to detect vary widely and in some cases are
indistinguishable from other diseases.
"The way it will show itself may be different in different people,"
she said. "A lot has to do with genetics.
"Physicians need to be aware that it's here," she said. "For every
case that is diagnosed, 100 are misdiagnosed."
Across Florida, Lyme disease cases have more than tripled since 2007,
according to the Florida Department of Health's Office of Statistics
and Assessments, though the numbers are not staggering.
In 2007, 30 Lyme disease diagnoses were reported in Florida and that
jumped to 88 in 2008. In 2009, the last year available, Florida
recorded 110 cases of Lyme disease.
In 2009, Hillsborough County's 11 reported Lyme disease cases tied
Sarasota and Lee counties for the most among Florida's 67 counties.
The county only had one case reported in 2007 and two in 2008.
KMDickson
Lipanj
CONCLUSION: America, private or public,
doesn't know what is a drug or what is a
disease.
Did you ever hear the expression from some of foreignors "DUMB
AMERICANS" but not dumb when it comes to making fools of people -
taking consulting? payoffs. You know what I mean --they sure are dumb -
jerks when the disease was known in Europe for over 100 yrs.....but
also in other items one lady I used to work with used the expression
"Dumb like a FOX."
rosap...@gmail.com
tell them all to start eating soursop fruit and lotsa tumeric (1
tablespoon 4 times a day for a month) and lotsa garlic (1 clove chewed
fresh and raw twice a day) and ginger(fresh and chewed raw and about a
dollop or two twice daily).
and lotsa fresh water.
and take dry saunas followed by a brush scrub all over the body and a
nice cold shower.
oh, also------------->>
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EHSI: Stem Cell Breakthrough May Bring Much in Store for NASA
Bioreactor
HOUSTON, Feb 01, 2011 (BUSINESS WIRE) -- A new study, revealing that
heart stem cells from children with congenital heart disease were able
to rebuild the damaged heart in the laboratory, could provide a new
outlet for Emerging Healthcare Solutions' (EHSI) NASA bioreactor.
Sunjay Kaushal, MD, PhD, surgeon in the Division of Cardiovascular
Thoracic Surgery at Children's Memorial Hospital and assistant
professor of surgery at Northwestern University Feinberg School of
Medicine, headed the study. It appears in the February issue of the
medical journal Circulation, and prompts a potential therapy option
that sidesteps the need for a heart transplant in children born with
defects.
Cells were obtained from patients ranging in age from a few days after
birth to 13 years who were undergoing routine congenital cardiac
surgery. The study found that the implanted cardiac stem cells are
functional and have the potential for use in repairing the damaged
heart. EHSI President and CEO Cindy Morrissey said on Monday that the
company's NASA bioreactor could be useful in creating the healthy stem
cell cultures necessary to stage clinical trials of similar
procedures.
"It takes millions of cells to regenerate a working organ," Morrissey
said. "These types of procedures, where large numbers of stem cells
are needed for the therapy, are exactly the kind of projects perfectly
suited to our NASA bioreactor's capabilities."
EHSI's Intrifuge Rotary Cell Culture System(TM) is a rotating-wall
bioreactor originally designed by NASA to facilitate the growth of
human cells in simulated weightlessness. Cell cultures--including
cardiac stem cells--grown inside the bioreactor look and function much
closer to human cells grown within the body than cell cultures grown
in Petri dishes, which are essentially flat.
Last December, EHSI acquired a license to use the bioreactor to expand
(or multiply) stem cell cultures in Germany, China, Panama and
elsewhere around the globe. Stem cell expansion is essential to the
research planned by EHSI's biotech subsidiary, CelulasGenetica,
including its current endeavor to develop a revolutionary new cure for
liver disease known as the Rutherford Procedure. It could also prove
essential to childhood cardiac therapeutics made possible by this
recent study.
Emerging Healthcare Solutions is taking a worldwide approach to
developing new stem cell treatments. Earlier this month, EHSI acquired
CelulasGenetica, a Central American leader in stem-cell technology
acquisition and development. In November, Morrissey established EHSI
business offices in Frankfurt, Germany, and Warsaw, Poland. Those
offices will allow the company to maintain long-term relationships
with some of the world's foremost stem-cell researchers and
entrepreneurs based in Central and Western Europe.
EHSI invests in technology developed to compete in the stem-cell
research industry alongside Teva Pharmaceutical Industries Ltd.
(TEVA); Allergan, Inc. (AGN); Alexion Pharmaceuticals, Inc. (ALXN);
and Forest Laboratories, Inc. (FRX).
About Emerging Healthcare Solutions, Inc.
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profits of emerging breakthrough medical technologies. The Company
believes the secret of leveraging future value for its shareholders is
the proper timing of its investment in promising new medical
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For more information, please visit .
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