Health insurance premiums are driven by the success or failure of actual health recovery maintenance and the costs required to deliver of service. Harris L. Coulter, Ph.D., of Washington, DC, and editor of the 8th edition of the HPUS,is an internationally renowned medical historian and author of over 30 books and essays, which include: THE DIVIDED LEGACY, a four volume epochal history of medicine, which covers its origins to present day.
“Society today is paying a heavy price in disease and death for the monopoly granted the medical profession in the 1920’s. In fact, the situation peculiarly resembles that of the 1830s when physicians relied on bloodletting, mercurial medicines, and quinine, even though knowing them to be intrinsically harmful. And precisely the same arguments were made in defense of these medicines as are employed today, namely, that the benefits outweigh the risks. In truth, the benefits accrue to the physician, while the patient runs the risks.”-Harris Coulter, Ph.D., (Divided Legacy Vol 3)
There is no question we need reform in the areas of disease elimination improvements in Health, better delivery of health care when it is needed and health insurance parity. Personally, am all for reform, but let those reforms ring with the clarity of Truth and illuminate our way through the fog obfuscation.
Overall chemo-therapy and radiation are documented to be an absolute failure in the so-called war against cancer. The long-term survival rate of cancer patients using orthodox therapies remains abysmal and the statistical reportage is obfuscated.
Refer to: New England Journal of Medicine, “Progress Against Cancer,” May 8, 1986 by John C. Bailar, III and Elaine M. Smith, and a ten-year follow-up “The War on Cancer” which appeared in Lancet, May 18th, 1996, by Michael B. Spoorn. Therein is published in leading medical journals, but they remain as the only therapies and pharmaceutical companies enjoy federal mandate.
Stated simply you cannot poison a sick person well.
HEALTH CARE REFORM is a meme used to numb the mind and sway political process but has little or nothing to do with health and certainly is neither, reform in the ways the public perceives, nor what they dearly need.
Merely by changing who and how much they profit for health services is only a small fraction of the underlying problem and ultimately it’s you who pay. Current Congressional debates will not offer true reform of our systemic disease CARE, but strengthen insurance profits and control.
The fruit of the healthcare tree, while certainly abundant, is altogether rotten, because the roots are corrupted by disease. If the Food and Drug Administration which regulates both FOOD and drugs while having far reaching powers that are beyond the Constitution of the United States of America, is powerless to effectuate the genuine change required to modify the so-called health industry.
Nor can the FDA provide the reforms by its far reaching power and control, then how can we expect it to come from mandates from an under educated over lobbied congress?
Give credit where due, the FDA has been effective in causing millions of tones of ground meat and spinach. A little too late perhaps as the FDA has done nothing to stop chemical companies from pouring oceans of deadly toxic, and known carcinogens on our crops.
“Water and air, the two essential fluids on which all life depends, have become global garbage cans” ~ Jacques Cousteau
HOW CAN YOU HAVE HEALTH IF WE DON’T HAVE CLEAN WATER AND AIR?
We must stop poisoning our earth with unnecessary toxic chemicals, which leaches out the elements and minerals building blocks of the cells of our bodies, and support and teach the farmers on bio-dynamic farming.
Why is there no respect for and replication of how the Hunzas and several other tribes on earth, wholive to be well over 120, and disease free.
These tribes drink the water which comes off of the slow grinding of the glacier across mountain terrain and gives minute quantities of every element and every mineral. Their cells have
access to all the natural building blocks of life and therefore remain impervious to invasion and disease.
Health and Old Age Places with High Longevity: Hunza Pakistan the area of Hunza in Pakistan which has a high level of longevity. A Guide to Shangri-La: The Leading Longevity Sites on Earth.
For Americans and the world at large where the crop land is awash in chemicals the minerals and elements are leached out of the soil and the roots of our food crops are have no way to chelate them so that we can digest them into our bodies.
What follows is a well known symptom called pica, and we are constantly looking for something to eat to satisfy the hunger of the cells and this leads to obesity and disease on a national scale.
There are solutions, but the FOOD administration, has done nothing to listen to, study, implement, nor promote the use of Bio-Dynamic Farming, which is proven to produce greater volumes of crops far healthier and do not poison our water aquifers.
One fairly recent proactive move; the FDA and the FTC have enforced the little known Federal Law under USC Title 21 Part 56, INFORMED CONSENT. This activity is evidenced by the too frequent drug commercials and advertisements. To name one example the anti depressant drug, ABILIFY, is known to cause death and suicide.
To our detriment and demise, the FDA has a tunnel vision partisan perspective and always reactive, rarely proactive when a patient actually dies from using an FDA approved drug, they routinely avoid any blame and state “there is no conclusive evidence to prove it was because of the drug.” No drug company is ever charged with a crime and no executives, nor doctors, are criminally charged for manufacturing, nor for prescribing the drugs.
WHY? Because the drugs are FDA approved so it would mean they are culpable.
However, when a substance derived and used by another Healing Art, i.e. Homeopathy, is found to be highly effective in combating and eliminating a disease such as cancer, or reversing the side effects of AIDS, a stroke, or Cystic Fibrosis, to name a few, the FDA routinely states there is no scientific evidence to support the claims moves swiftly to prosecute to the fullest extent of the law.
We must continue to strengthen the education of the public on sound fundamentals of health maintenance.
We must allow for access and coverage to all branches of the Healing Arts. This is known as the ECLECTIC. The allopathic cartel are not the arbiters of truth, nor have they proven to be honorable stewards, nor have they provided viable solutions where other forms of healing arts have been successful, in some cases thousands of years.
The problem is that over the past 67 years, a Federal Agency, the Food and Drug Administration, created in 1938 as an agency to ensure that Food, Drugs and Cosmetics moving in interstate commerce, were pure, unadulterated, contained what was stated on the label and safe for human consumption.
Over the years the FDA has undergone a metamorphosis and has become a threat to the civil liberties and public health of Americans, as well as added incredibly to the cost of the products it regulates.
The FDA has a long history of using the resources of the agency to conduct Gestapo type raids on medical clinics, terrorizing patients, staff and practitioners, seizing quantities of vitamins, manuals and harmless natural products, issues completely inaccurate, indeed, deliberately mendacious publicity releases slandering practitioners, nutritional products and innovative drugs and has so far departed from the purposes for which it was created as to become a menace to both the public’s health and their civil liberties.
Under 80 or more years of Allopathic domination, the standardized American health care system is unable to:
(1)Control the resurgence of Tuberculosis in the country;
(2)Control the rising rate of Cancer deaths;
(3)Control the rising rate of coronary artery deaths;
(4)Lower the infant mortality rate;
(5)Find an effective cure for AIDS.
There are available answers to all these deficiencies, but none of them are embraced in Allopathic Doctrine.
The question presented is, if there is any legal control over this vast agency and any way citizens can take legal action to cause the agency to be brought under control and be forced to comport itself in accordance with the intent of Congress in creating it, and the additional question of whether or not citizens who have been harassed by its Ultra Vires activities may sue for damages or other relief.
If such legal action is possible, is such legal action the best, or the sole means which can or should be employed to bring the agency under control.
A further question may be what or who is responsible for the agency getting out of control and what, if anything, can be done to ensure that the agency does not get out of control in the future and once again become a menace to society.
The agency in question, the Food and Drug Administration, is an out of control bureaucracy, undertaking to perform some proper regulatory functions but devoting many of its resources to illicit functions not contained in its enabling legislation and not permissible under the constitution.
The agency [which was] directed by Commissioner David Kessler, M.D, JD, who assumed the position after the enforced resignation of Joe Young, PhD, has done little to change its behavior except put on a fresh face from time to time.
An investigation revealed widespread corruption with many officials, taking large bribes, not to mention every member of Congress who are heavily lobbied by industries it was supposed to regulate, and the entire agency was demoralized and ineffective.
The agency has openly and notoriously formed “partnership” with private trade associations and special interest groups for the purpose of aiding and abetting non-price predation in the health care market.
The agency has lawful jurisdiction over some Foods, Drugs and medical devices which are in interstate commerce and has no jurisdiction over the practice of medicine or other healing professions.
Despite this rather clear distinction, the agency repeatedly attempts to interfere with health care practitioners by means of its enforcement powers and by liaison with state regulatory agencies, and by conducting Gestapo type raids on the offices and clinics of health care practitioners who practice in Schools of Practice other than the Allopathic School and by attempting to suppress the use of techniques of healing and of products for use in health care which are not within its regulatory jurisdiction.
THE BUREAUCRATIC ANTI-COMPETITIVE CAMPAIGN
WHICH POSSIBLY INADVERTENTLY or INTENTIONALLY CREATES GENOCIDE
This claim is born of deliberate suppression of health technologies which are non-toxic, effective and inexpensive; to name only a few in critical areas, these include:
I. CARDIOVASCULAR DISEASES
EDTA Chelation – Adrenal Cortical Extract
II. STROKE PREVENTION AND REHABILITATION
Oxidative Therapies / Hyperbaric Chamber / Ozone
Human Growth Hormone
III. CANCER AND AIDS
IAT, Laetrile, L-Arginine, Black & Yellow Salves, Gerson Therapy, 714-X, Homeotherapeutics, Krebiozen, Essiac, Immunostim, anti-neoplastic, Honey, Glixoxide, Ricci Therapies and many others, too numerous to mention here.
THE STATE AND FEDERAL AGENCIES INVOLVED IN ANTICOMPETITIVE ACTIVITY
California (most active)
Department of Consumer Affairs
State Board of Medicine
State Board of Dental examiners
State Board of Osteopathic Examiners
State Board of Chiropractic Examiners
Food and Drug Branch
Attorney General’s Office
San Diego City Attorney’s Office
Other States (Generic)
State Board of Medical Examiners
State Board of Dental Examiners
Attorney General’s Office
Private Organizations Involved
Pharmaceutical Advertising Council
National Council Against Health Fraud (and affiliated organizations)
National Federation of State Boards of Medical Examiners
NCI – National Cancer Institute
CDC – Centers for Disease Control
FDA – Food and Drug Administration
NIH – National Institutes of Health
American Heart Association
American Cancer Society
Memorial Sloan Kettering Institute
American College of Allergy
Roswell, et al
In HEALTH UNITED STATES, an annual publication by the federal government, our national death rate from cancer is approximately 2,500,000 people per year and the rate is rising. Assuming a cost of $80,000 to $160,000 per person over the last 20 years, that figure represents $200,000,000 to $370,000,000 per year and 50,000,000 lives, or $4 TRILLION to $7.5 TRILLION dollars funneled from our collective economy into the hands of the medical pharmaceutical cartel. Is it any wonder, then, why we cannot find a cure?
In addition One of the first targeted, the FDA, or “Big Medicine,” since the early 1900’s, in this country was Dr. Royal Raymond Rife. His powerful evolutionary microscope, capable of shattering cancer cells and viruses with radio frequency vibrations, was destroyed and his books burned by federal authorities and he was imprisoned.
Some other embattled pioneers include, but are certainly not limited to: The healing arts of Ethno botany, Naturopathy Chiropractic and Acupuncture and Chelation, which all met intense resistance and violent opposition by federally protected orthodoxy.
Dietmar Schildwaechter, Ph.D., MD, was invaded in his home office in a militant style by state and federal authorities in the late 1980’s for introducing a cure for squamous cell cancer, which was proven in a 20-year study in Germany.
Andrew Ivy, MD, a pillar of the A.M.A., who came back from Germany after participating as a panelist in the Nuremberg war crime trials with a cure for cancer called Krebiozen, had his career shattered.
Bruce Halstead, MD;
Warren Levin, MD;
Vincent Speckhart, MD;
Royal Raymond Rife, MD
Wilhelm Reich, MD;
Jossef Issels, MD; and Max Gerson, MD;
Joseph Gold, MD,
Emmanuel Revici, MD;
Stanislaw Burzynski, MD;
James Privitera, MD;
Ed McCabe, author of Oxygen Therapies, jailed for 547 days; a best selling author.
Hulda Clark, ND;
There too many more which are not listed here. These gifted pioneers brought relief to a suffering humanity and were ruthlessly attacked by medical authorities and scientific dogma. Each paid a high price but distinguished themselves by their courage and resolves to stand up for their convictions, even in the face of overwhelming opposition, loss of license and jail. For a closer look at the inner workings, read: THE CANCER INDUSTRY: the Classic Expose ‘on the Cancer Establishment, by Ralph W. Moss, Ph.D.
The FDA regularly approves dangerous, often lethal pharmaceuticals. The side effects of these potentially deadly, or harm causing pharmaceutical drugs can only be fully discovered by wide-spread use. This is despite the average $250-500,000,000 and 15 years to bring these drugs to market, including phase trial tests, trying to prove the elusive “efficacy” requirement of the F.D. &C. Act.
Typically, after one of their highly publicized “wonder” drugs fails, causes death or serious side effects, no FDA official nor PAC member company president, research assistant, corporate official, company doctor, nor testing lab will be subjected to raid, investigation, indictment or jail term.
To the trauma and suffering to the patients and their families and the productive work force, it comes with a hefty price tag.
Both Gaston Naessens and Dietmar Schildwaechter, Ph.D., MD, spent the last 40 years perfecting independent blood tests, which are able to pre diagnose any type of cancer and immune disorders up to two years prior to their onset, with a 1% margin of error. The industrial average false/negative ratio remains extremely high by comparison, yet these new tests are ignored or met with resistance.
THE RELEVANT SERVICE MARKET AND SUBSTITUTABLE ECONOMIC COMPETITORS
The Eclectic Practice of Medicine*
In 1906, Dr. Rolla Thomas completely revised the 1866 teaching manual by John Milton Scudder, and revised it yet again in 1907. This was the culmination of a thirty-year frenzy of published creativity at the Eclectic Medical Institute in Cincinnati, Ohio, and was the main teaching text at that school until the1930s…the college closed in 1939.
“…it were better for the doctor if he can forget that his patient has typhoid fever, pneumonia, dysentery, or whatever he may have, and study the conditions that are present. This may be wrongs of the circulation, of the nervous system, of the secretions, of digestion, of assimilation, or wrongs of the blood, but whatever the basal lesion, it must be overcome if the patient is to be benefited by medication.”
THE MONOPOLIZATION OF MEDICINE
The health care industry during the Progressive Era is well documented in academic studies and can reasonably be accepted as a given here without describing in great detail how or why it occurred. However, it was funded largely by the Rockefeller and Carnegie fortunes and was done to guarantee a dominant place in health care for the products of the petrochemical industry.
The Allopathic School of Medical Practice was picked to become the dominant survivor of the monopolization because it was:
(1) Numerically the largest,
(2) Had no well established system of doctrines which made it antagonistic to the use of a system of therapeutics based on petrochemical therapeutics,
(3) Was represented by a fairly well organized and active Trade Association which was receptive to a take over by the funders,
(4) Urgently needed a large infusion of cash and political influence to stop the growing public acceptance of its economic rivals and competitors,
(5) Had little to offer its members without such an infusion of cash and political influence,
(6) Were headed by a staff which welcomed any help – motivated by absolutely no idealism and almost entirely by avarice, the staff of the AMA was easy to enlist in the monopolization and proved extremely efficient – particularly Morris Fishbein, whose role was pivotal and whose service spanned several decades of the monopolization.
One of the chief monopolization strategies was through take over of medical education and the schools or universities which offered this. There were several hundred which offered a two year course in Allopathic Medicine and granted the M.D. degree, which was the sole credential necessary for practice at that time.
Competitive medical universities operated by Homeopathic and Eclectic interests were fewer, but at least 75 existed – some well established and endowed.
The monopolist could have selected any of these; they were all easy targets, but the Allopathic School of Practice had a void in its therapeutic system which made it ideal for the monopolist and the Homeopathic and Eclectic Schools had therapeutic systems which offered little room for the
incorporation of petrochemical technology.
Many Americans, at least those who could afford to do so, went abroad for their medical education, initially to England or Scotland but eventually to Germany where State supported Universities had better facilities and foreign students who could and would pay tuition to augment the salaries of the faculty were welcomed to the extent that lectures were offered in English as well as German to facilitate and accommodate these foreign scholars.
To a man, the initial faculty of John’s Hopkins, the first of the Medical Universities to be established and funded by the monopolists were graduates of German Universities and brought to the University both the medical and the political orientations gained as students at German universities, which they passed on to the students of John’s Hopkins, most of whom went out to become the faculties of other American medical colleges and further incorporate both the medical and the political orientations of German universities into the graduates of American Medical Universities funded by the monopolists. Those orientations remain a part of Allopathic medicine in the United States today.
This is primarily important in considering the role of the Allopathic School in genocidal activity, which the German medical profession entered into without protest between 1934 and 1945 under the National Socialist Regime in Germany.
Federal control started in earnest around 1938 with the Pure Food, Drug and Cosmetic Act and this became what it is today in 1962 with the Kefauffer Amendments to that Act, which amendments included for the first time, an efficacy requirement which gave the FDA far more power to control both drugs and information about drugs.
The Federal Act was not intended to give the agency any control over the practice of medicine or other health care professions and both its language and many decisions of Federal Courts make that clear. Nevertheless, the agency has made and continues to make increasing excursions into attempts to control the practice of medicine.
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