Colloidal Silver Has Mainstream Medicine «Singing the Blues» (The
Best Years in Life) The widespread mainstream media coverage of the «blue man» Paul Karason and his rare skin condition known as Argyria
is part of a series of largely misleading and sensationalized scare
stories about the dangers of colloidal silver turning a person’s skin
blue.
Although the Karason story did not appear to originate from
mainstream medicine or the FDA, there is little doubt that they have
welcomed it with open arms and have been quick to trot out «medical
experts» and past FDA warnings to help «sing the blues» about colloidal
silver.
The truth is that mainstream medicine has a very good reason
to cry long and loud about colloidal silver, because it does represent a
very real danger – a danger to the huge profits of the pharmaceutical
industry’s patented antibiotics.
Silver has been used effectively by mankind to fight germs and
ailments for thousands of years, and the instances of modern use of
colloidal silver turning people’s skin blue are so rare as to be almost
non-existent – and unlike thousands of prescribed and approved
over-the-counter mainstream medications including the common aspirin,
silver has never killed anyone.
As a matter of fact, almost all of the relative handful of reported
instances have involved one or more of the following: older silver
products that contained as much as 10% or more silver (compared to mere
parts per million in modern colloidal silver), silver nitrate, home made
colloidal silver that was contaminated with salt, and silver that has
been consumed continuously in very large quantities over a very long
period of time.
In the case of Karason, he made his own ionic silver at home for
almost two decades and for many years consumed a quart or more per day. I
daresay that any prescribed or over-the-counter medication whose
recommended dosage was a couple of teaspoons a day would do far worse
than turn a person blue if they drank a quart or more of it a year! For
the sake of comparison, drinking a quart or more per day of colloidal
silver would be like a person taking several bottles of aspirin a day, a
practice that would be lethal in short order.
Karason actually appears to enjoy his notoriety as the Papa Smurf
blue man, and even though he sings the praises of how colloidal silver
saved his life and the many ailments he believes it cured, the focus of
attention is on his blue skin – a condition that is actually reversible
with proper diet and herbal cleanses despite mainstream claims to the
contrary.
What is also true about colloidal silver is that it is far safer,
more effective and less expensive than the marginally effective and side
effect laden mainstream antibiotics – and has mainstream and university
studies proving it dating back to the early 1900′s. The best
and strongest of the FDA approved antibiotics are effective for a
handful of bacteria at best, whereas colloidal silver is supremely
effective against just about every kind of single celled pathogen,
including bacteria, fungal growths and viruses (which antibiotics are
often wrongly prescribed for, despite the fact that antibiotics have no
effect on viruses).
If the public were told the truth, a rarity when it comes to
mainstream drugs versus natural competition, colloidal silver would
represent a huge threat to literally billions of dollars of profits and
so it is no wonder that mainstream medicine and their allies in the
mainstream media are once again loudly singing the blues – just as they
have repeatedly done in the past with misleading stories and studies
about a great many popular natural plants, supplements, vitamins and
minerals that represent threats to mainstream drug profits because they
are safer, more effective and less expensive alternatives to the
unnatural, side effect laden, hugely expensive and marginally effective
synthetics created in the labs of the powerful world pharmaceutical
empire.
While there are a great many natural threats to mainstream profits,
whose use and track records of safety and effectiveness date back
hundreds and even thousands of years, perhaps no natural alternative to
mainstream drugs represents as big of a threat to industry profits as
colloidal silver, and it is no coincidence that colloidal silver has
been placed at the very top of the FDA/mainstream medicine hit list.
However, when it comes to warning and scaring people away from
silver, both the mainstream medical industry and the FDA have serious
credibility problems. First of all, silver has a history of safe and
effective use dating back thousands of years. In addition, it
continues to be widely used today, including being used by NASA, the US
military and Potters for Peace for water purification, being used as a
germicidal agent by hospitals and medical suppliers and was recently
incorporated into a new line of hospital pajamas to prevent the spread
of infection, to name just a few of its present day uses.
The biggest credibility problem of all for mainstream medicine and
the FDA regarding silver is likely how they both approved and embraced
silver for medicinal use at one time – yet now would have us believe
that silver is both ineffective and dangerous. At one time silver
products were very much in favor with both mainstream medicine and the
FDA. No fewer than 34 different prescribed over-the-counter medications
containing silver were not only widely sold by industry, they were also
approved by the very same FDA which now seeks to warn us of its dangers
and have us believe it is ineffective.
What changed their minds? Perhaps the obvious answer can be found in
the fact that silver fell out of favor at the very same time that
patented sulfa drugs and patented antibiotics created in drug company
labs came on the market. Once that happened, the non-patentable silver
was no longer a tool for healing, but a threat to profits.
Zealous protection of mainstream approved drugs and suppression of
natural competition is nothing new -look at the estimated 100,000 or
more deaths caused by Vioxx before the FDA finally
removed it from the market. Look at the ridiculous actions of the FDA
when it threatened Washington cherry growers for telling the truth about
the health benefits of eating cherries, or at the storm trooper actions
against the makers of Charantia (bitter melon) tea in Florida who dared
put references to some of the 650 plus PubMed studies and citations
about bitter melon on their website.
The FDA persecutions and prosecutions of cherry farmers, bitter
melon, and a long line of other natural alternatives points out just how
extreme the protection of the big drug companies’ products and profits
really is. Consider this: other than issues of national security, only
in natural health is it a crime to tell the truth due to the way the FDA
has construed their rules and definitions to protect industry.
For example, if a company were to advertise that vitamin C was a cure
for scurvy, as everyone knows is true, that company could be prosecuted
for selling unapproved drugs. The same would be true if a company
printed a testimonial from someone who reported health benefits due to
vitamin C, or any other vitamin, mineral, supplement or non FDA approved
drug.
For example, only the makers of FDA approved drugs can use the word
cure, or even imply any health benefits without the FDA considering the
product a drug. The catch is that in order to be FDA approved, no matter
how many PubMed cited studies or other studies have been performed, and
no matter how much of a history of hundreds or thousands of years and
users, the FDA only approves drugs that go through its specific approval process – one that costs hundreds of billions of dollars.
When it comes to natural alternatives, spending such money on a
natural product is prohibitive, since it could not be patented and could
be freely and cheaply sold by any number of competitors and it would be
virtually impossible to ever recover all the costs of getting the
natural product approved. Though the process is purported to be one
which protects the public from unsafe medicines (and we see how well
that worked for the hall of shame list of drugs like Vioxx, Avandia,
etc.), the net effect of the FDA’s drug definitions and approval process
is to exclude natural competition and insure that only the patentable
and profitable synthetics created in drug company labs can be approved
and marketed as having health benefits.
An example of such one-sided treatment favoring industry came in the
following news story about a lawsuit filed against the FDA by Public
Citizen after the FDA ignored years of complaints about the dangers of
ruptured tendons caused by one of the drug industry’s most powerful and
profitable antibiotics:
WASHINGTON, D.C. – Despite long-standing evidence that
fluoroquinolone antibiotics can cause tendon ruptures, the Food and Drug
Administration (FDA) has failed to increase its warnings to patients
and physicians about the dangers of the medicines, Public Citizen told a
federal court Thursday.
Public Citizen sued in the U.S. District Court for the District of
Columbia, asking the court to force the FDA to act upon a petition the
consumer group filed with the agency 16 months ago. The FDA has failed
to respond to the petition, which asked the agency to put a «black box»
warning on fluoroquinolone antibiotics (such as Cipro, Levaquin and
others) to make doctors and patients more aware of the risk of serious
tendon injury before tendons actually rupture.
The petition also urged the FDA to send a warning letter to
physicians, as well as require an FDA-approved medication guide to be
dispensed when prescriptions are filled. Public Citizen contends that
the FDA is violating the Administrative Procedure Act by not acting upon
the petition.
Stronger warnings could lead to earlier intervention and prevent
needless injuries by allowing doctors to switch patients to other
antibiotics, said Dr. Sidney Wolfe, director of Public Citizen’s Health
Research Group.
«While the FDA sits idly by and ignores the problem, more people will
suffer serious tendon ruptures that could have been prevented,» Wolfe
said. «The current warning is buried in a long list of possible adverse
reactions and is far too easy to miss.»
From November 1997 through December 2005, the FDA received
262 reports of tendon ruptures, mainly of the Achilles tendon, 258 cases
of tendinitis and 274 cases of other tendon disorders in patients using
fluoroquinolone antibiotics. An additional 74 tendon ruptures have
subsequently been reported to the FDA for a total of 336. Because only a
small fraction of cases are typically reported to the FDA, the actual
number of ruptures and other tendon injuries attributable to the
antibiotic is much higher (Source: Healthy News).
One can only imagine the FDA’s reaction if 336 tendon ruptures had
been reported for those who take the best antibiotic and pathogen
destroyer on the planet – colloidal silver. No doubt, they would have
raided the manufacturer with storm troopers and shut it down years ago,
just as they have done many times with the manufacturers and sellers of
other natural competitors to drug company products.
In conclusion, as far as I can tell, not one single instance of
Argyria has been attributed to properly made colloidal that was not
consumed in amounts that were up to hundreds of times the recommended
dosage, that has not stopped the FDA from continuing to «sing the blues»
about silver or from going after those who make and sell colloidal
silver products, not because silver represents a whit of threat to human
health but rather because it represents a threat to the inflated bottom
line profits of the mainstream drug manufacturers.
Finding out who the FDA really serves is a simple task – all you have
to do is follow the money. But don’t simply take my word, let a noted
past FDA commissioner tell you very clearly what the FDA is really
about:
«The FDA ‘protects’ the big drug companies and are
subsequently rewarded, and using the government’s police powers they
attack those who threaten the big drug companies. People think that the
FDA is protecting them.
It isn’t.
What the FDA is doing and what the public thinks it is doing are as different as night and day.»
Dr. Herbert Ley
Former U.S. FDA Commissioner
For important related articles:
Utopia Silver’s Fight for Health Freedom
http://www.tbyil.com/Utopia_Silver.htm
Why Does Mainstream Medicine Attack Colloidal Silver?
http://www.tbyil.com/MM-vs-ColloidalSilver.htm
Merck, other Pharma Companies helped fund activist groups who petitioned the EPA to regulate nano-silver as a pesticide
http://www.tbyil.com/EPA_Petition_Funding.htm
By Tony M. Isaacs
