Xanax - as you invoked my name, I find it necessary to clarify what I tried to say in my u2u.
I do believe you are on the right track here - but you are muddying the waters (perhaps irreparably) by bickering.
You need to focus on the research - and for the record - I'm with ZZZ on this one: corporate financed sources are spurious, even when they're
hawking "natural" cures. You need to use the National Institutes of Health PubMed database. [When you search, just add +PMID to your string]
So while you have provided evidence to support your hypothesis, you have
not proved it, as ZZZ says.
You are NOT going to find support for your global hypothesis in the scientific literature, and WILL need to prove your case from the ground up. IMO -
the evidence exists. You just need to do the work - and
not rely on others' summaries.
To prove your case, you will need to integrate proofs derived from medical and scientific research, with an added politico-economic analysis. Also,
you need to start with the premise that most, if not all, modern diseases arise from an original underlying infection with the same protein.
Your main obstacle is that most medical and scientific research results are privately owned, protected by Intellectual Property Rights laws,
and generally inaccessible. However, recent Open Source and Open Access movements now are bringing taxpayer funded research into the public domain
- so there's stuff out there, if you know how to look, and what to look for.
Here's a (very) quick and dirty outline to help you get started:
A. Break down your medical research to cover the 4 primary treatment modalities:
1. Drugs
2. Surgery
3. Organ replacement, including transplant and regrowth
4. Cell therapies, including bone marrow transplants, which are the only stem cell therapy available to ordinary people (on a limited basis, generally
not covered by insurance as "experimental")
Document what treatments exist, what's covered by insurance, and what's
not covered by insurance. You will find that the main obstacles to
early diagnosis, and effective preventive treatment ("cure"), result from limits on insurance coverage. So once you have identified the medical
realities - in scientific detail - you might want to look at the business associations between the pharmaceutical giants and global insurance and
reinsurance corporations.
If you do your homework - you will be able to prove that:
1. Modern diseases start with a protein that interferes with stem cell differentiation and development, and destroys tissue by causing cell mutations.
This protein targets different cells and tissues depending on a variety of factors, termed "catalytic cofactors." The only way to effectively treat
modern disease is to go straight to the protein, and nip the diseases in the bud before they progress and create complications ("clinical symptoms",
and new protein mutations (re-categorized as 'different' diseases).
2. Insurance policies specifically preclude early diagnosis, and only cover treatments targeted to complications that arise after underlying disease
has progressed. This is called a "cost-effective treatment strategy" - which relies first on treating secondary symptoms with drugs; second,
removing diseased tissue surgically; and third, removing destroyed organs or glands if possible, and replacing said destroyed body parts, if
necessary.
3. Insurance companies justify tiered "cost-effective treatment strategies" because most modern diseases are very slowly progressive, often taking
decades to become life threatening - they say that early diagnosis and intervention is "medically unnecessary." [Also search "medical necessity"]
NOTE:The costs arising from chronic debilitation and early disability - which results from non-diagnosis and non-treatment - are off-loaded
onto victims, and sometimes, governments.
4. Massive cleanup efforts are required to remove disease-causing proteins from food and water; also, industrial practises need to be redesigned to
prevent environmental contamination with synthetically created "catalytic cofactors." ...These considerations should lead you towards an
investigation of the financial connections between Big Pharma, the insurance industry,
and the chemical industry - you might start with Merck
and I.G. Farben.
Your research into treatments should review the treatment's history. For example:
1. Prior to penicillin's monopoly, bacteriophages were used with great success to treat bacterial infection - and because they are 'natural
bacterial predators,' have the ability to evolve right along with bacteria. Political intervention killed the bacteriophage industry to promote
penicillin and help establish the monopoly for anti-bacterial drugs. We now are paying the price. ...FYI - political intervention
still is
protecting the antibacterial drug monopoly, and suppressing the re-creation of a bacteriophage industry.
"The war against bacteria is not something that can be won by humans," Sulakvelidze says. "If you try to wipe them out, they will always return.
Only they will be stronger."
They're called phages. And they eat drug-resistant bacteria for breakfast.
Also see:
Investigator Lawrence Broxmeyer MD sees the possibility of bacteriophages as the antimicrobrials of the
future.
2. Most modern drugs are targeted to proteins - but focus on later-stage secondary symptoms. This means that the drugs target secondary proteins that
are produced by the body in response to disease, or are a mutation of the original infectious protein. Either way, even the most expensive
state-of-the-art drugs do
not target the protein causing the underlying disease - only proteins responsible for secondary effects. ...And most
drugs are themselves "catalytic cofactors" that trigger new mutations, and speed progression of the underlying disease.
proteinology - the scientific study of proteins or of the protein status of the body. [Ed. Note: Much more narrow than proteomics, which is concerned
with protein development, interractions, mutations, etc.]
Dorlands -
Merck Source
Ie., see:
Proteinology: Commercial pharmaceutical applicationsdo note the rumors saying that the island where Kuru was "discovered" was
purposefully infected, to see how protein-related disease spread and progressed.
Review current treatment alternatives:
1. Pay special attention to "personalized medicine" - including proteomics, metabolomics, and bioinformatics.
2. Consider the fact that treatments for protein-related diseases are now being marketed as "anti-aging therapies" - which are not covered
by insurance.
3. Take a look at the illegal trade in organs, and the "organ farms," where humans of all ages are imprisoned so doctors can harvest their organs as
needed. [Search Thomas Gordan, organ hunters, organ harvesting, etc.]
4. Think about how "stem cell farms" might operate - and who might have the financial ability to access treatments using the harvested stem
cells.
5. Research 'natural remedies' that block prion multiplication in the body - green tea, sage, curcurim (sp.?, in curry), and antihistamines top the
list.
Finally, but perhaps most critically:
1. You will find that new virulent diseases now are appearing at a horrifically rapid rate. Ie., "Doctors know C. difficile flourish after
patients take certain antibiotics. Now it seems any antibiotic can bring on the disease. ..."Something happened 18 to 24 months ago, ..."
said Dr. Mark Miller, chief of infectious diseases at Montreal's Jewish General Hospital."
www.cbc.ca...
calgary.cbc.ca...
2. Virtually all of these diseases arise from the ability of a protein called "a-smooth muscle actin" to access
any living cell, and thus,
cross species and kingdom barriers with ease - which allowed mutations to occur unhindered over the past century, and resulted in the now
uncontrollably rapid mutation rate.
3. Medical science canNOT treat or cure these new infectious diseases, mainly because current treatment modalities and industrial processes actually
create them.
4. There are solutions, and there is hope, but not without full disclosure, and honesty from our governments.
The following articles will help you get a handle on the complexities inherent in your hypothesis, and to develop a more comprehensive framework.
Also, all the articles have some specific references that will be useful to you. Again, while you can use others' work to help develop your personal
understanding, you MUST focus primarily on the
credible articles listed in PubMed as references to support your contentions:
[url=http://www.atsnn.com/story/151455.html]Eli Lilly Disses Blockbusters, Plugs Personalized Medicine: Medicaid Chokes" target="_blank" class="postlink" rel="nofollow">
3. Stem cell therapies go straight to the protein causing the underlying disease - and they work. The known history of cell therapy starts in 1912
with Dr. Kuettner - in 1931 Dr. Paul Nichans advertised cell therapies using non-human embryonic stem cells. Note that the first officially recognized
protein-related disease was fibromuscular dysplasia (1938, Leadbetter and Burkland) - which is not really a disease in its own right, but rather, the
stage where "a-smooth muscle actin" uses the vascular and immune systems to spread through the body. Review Linus Pauling's work on the immune
system in 1940, and his work on the actin protein's 'a' and 'b' conformations in 1950 - do not fail to note that Pauling was blacklisted by the
FBI for being a "commie," who thereby destroyed his credibility in America. Review the work on "teleomeres" done by the Nazis and in US
laboratories dominated by eugenics sympathizers in the 1940's. ...Research publicly available information on "fibroblasts" and embryonic stem cell
research conducted in the early 1950's - and outline the cryogenic storage facilities built in the USA in the early 1960's for the wealthy to store
their own "young" stem cells, for later use in autologic transplants. ...Do not overlook Gadjusek and other scientists researching proteins
associated with infectious disease in the 1950's - and
do note the rumors saying that the island where Kuru was "discovered" was
purposefully infected, to see how protein-related disease spread and progressed.
Review current treatment alternatives:
1. Pay special attention to "personalized medicine" - including proteomics, metabolomics, and bioinformatics.
2.
Consider the fact that treatments for protein-related diseases are now being marketed as "anti-aging therapies" - which are not covered
by insurance.
3. Take a look at the illegal trade in organs, and the "organ farms," where humans of all ages are imprisoned so doctors can harvest their organs as
needed. [Search Thomas Gordan, organ hunters, organ harvesting, etc.]
4. Think about how "stem cell farms" might operate - and who might have the financial ability to access treatments using the harvested stem
cells.
5. Research 'natural remedies' that block prion multiplication in the body - green tea, sage, curcurim (sp.?, in curry), and antihistamines top the
list.
Finally, but perhaps most critically:
1. You will find that new virulent diseases now are appearing at a horrifically rapid rate. Ie.,
"Doctors know C. difficile flourish after
patients take certain antibiotics. Now it seems any antibiotic can bring on the disease. ..."Something happened 18 to 24 months ago, ..."
said Dr. Mark Miller, chief of infectious diseases at Montreal's Jewish General Hospital."
www.cbc.ca...
calgary.cbc.ca...
2. Virtually all of these diseases arise from the ability of a protein called "a-smooth muscle actin" to access
any living cell, and thus,
cross species and kingdom barriers with ease - which allowed mutations to occur unhindered over the past century, and resulted in the now
uncontrollably rapid mutation rate.
3. Medical science canNOT treat or cure these new infectious diseases, mainly because current treatment modalities and industrial processes actually
create them.
4. There are solutions, and there is hope, but not without full disclosure, and honesty from our governments.
The following articles will help you get a handle on the complexities inherent in your hypothesis, and to develop a more comprehensive framework.
Also, all the articles have some specific references that will be useful to you. Again, while you can use others' work to help develop your personal
understanding, you MUST focus primarily on the
credible articles listed in PubMed as references to support your contentions:
[url=http://www.atsnn.com/story/151455.html]Eli Lilly Disses Blockbusters, Plugs Personalized Medicine: Medicaid Chokes
[url=http://www.atsnn.com/story/133261.html]Personalized Medicine: The End of Blockbuster Drugs?
Sick Dog Gets $45,000 Stem Cell Transplant
Bush Signs Quarantine Orders for Bird Flu
Polarization Prevents US Cloning Ban
Bhopal in Slow Motion
Connections: Health, Finance and the US Treasury
Military Says Terrorists Might Use Bird Flu as Bioweapon
WHO Pushes for Bird Flu Vaccine Production
Neuro-Marketing: Straight to the Brain
New Bankruptcy Bill Protects Rich: Squeezes Troops, Everyone Else
Poison DUst: Depleted Uranium Kills
US Health Care Tab Ready to Explode
U.S. Still Silencing Scientists
Smoke, Mirrors, and Gulf War Syndrome
New Test Finds Mad Cow Before Symptoms Appear
Obesity and Mad Cow Disease
Mad Cow Madness
Bush Pushes to Limit Class-Action Suits
The New Military: Robots with Human DNA
The New Military: Microbots
Did Chemical and Drug Industries Create Mad Cow?
Mad Cow-causing Prions Found in All Organs
Mad Cow in Cosmetic Implants?
"Mad Cow" Spreading in Deer and Elk
"Mad Cow" Disease Uses Immune System to Spread in Body
The Final Solution
A Military-Governmental-Industrial Conspiracy?
Winds of Change: Science Goes Open Source
Stepping Down from the Ivory Tower
Prescription Drug Marketing Misleads Public
Health Care Crisis Debate Heats Up Behind the Scenes
Threat Analysis: Genetically Engineered Stealth Bio-weapons
Flu Vaccine Technology: Who's Blocking its Use?
Kerry Claims 100 Million Americans Chronically Debilitated
UK, US Criticized by Scientists
Fears of Terrorism Hide Real Biological Attack, Assault on Voting Rights
Merck and Vioxx: A Twisted Tale of Cover-ups, Pork and Profits
NIH Bypasses Need for Open Access Legislation
Population Control Bioweapon? Medical Accident? What is Fibromuscular Dysplasia
(FMD)?
Also see:
Green Medicine
EDIT: Somehow
a section keeps getting copied and inserted - although it does NOT EXIST except in the final copy. ...I cannot delete it. Please
ignore.
...Tried again - doesn't show up where I can cut it. Must be a glitch. Maybe a gremlin.
[edit on 17-9-2005 by soficrow]
[edit on 17-9-2005 by soficrow]