Cancer Cure Booklet

This booklet, Cancer Cure by Carol A. Morrison, M.D., F.A.C.C., Kathy P. Fairbanks, Ph.D. and Dr. William Donald Kelley, D.D.S., M.S., includes a chapter, FOR DOCTORS ONLY, The Kelley Metabolic Cancer Cure Program: Its Scientific Basis by Professor Kathy P. Fairbanks, Ph.D. (Embryology), that contains priceless knowledge.

ABOUT DR. W. D. KELLEY...

Creating health has been the life’s work of Dr. William Donald Kelley. With degrees obtained from Baylor University, University of Alabama and University of West Virginia in dentistry, orthodontics, chemistry, education physiology and with a strong background in nutrition, he is uniquely qualified to design the holistic metabolic programs that have been so successful with his patients, most of whom were suffering from such degenerative diseases as cancer, heart disease, allergies and arthritis.

Formerly an orthodontist, Dr. Kelley is a metabolic researcher and the creator of four of holistic medicine’s most advanced concepts: Non-Specific Metabolic Therapy®, the Science of Optimum Health®, Metabolic Ecology® and Metabolic Typing® concept which Linda Clark of the prestigious Price-Pottenger Foundation calls: “The most important nutritional discovery in the last 150 years”.

Dr. Kelley first applied his metabolic programs, complete systems aimed at improving the function of the total body, stimulating the immune response and preventing further health breakdowns, on his own family. He helped his children overcome serious allergy and asthma problems and solved his own health problem, metastasized pancreatic cancer, which is generally considered incurable. Upon being told that he couldn’t recover with conventional therapies, he intensified his study of metabolic medicine, attempting to find a way his own body could eliminate the disease. Ridding himself of his disease was only the first of many “impossible” jobs that Dr. Kelley has done in the last 38 years.

Dr. Kelley is a man of no small ambition. “If we don’t change the whole coarse of health care, we won’t have accomplished a thing”, he was recently quoted as saying. To accomplish this, he works on a consulting basis with several research organizations and a rapidly growing nationwide network of doctors who chose his methods.

Chapter I

FOR DOCTORS ONLY,

YOU, WHO SLEPT THROUGH EMBRYOLOGY CLASSES.

From: William Donald Kelley, D.D.S., M.S.

The Kelley Metabolic Cancer Cure Program:

Its Scientific Basis

by

Professor Kathy P. Fairbanks, Ph.D. (Embryology)

During the time that the trophoblast cells are aggressively infiltrating the maternal tissue, the inner cell mass is organizing itself into a three part disc, shaped like a flying saucer. These three parts of the disc are called the three primary germ layers, or the ectoderm, the endoderm and the mesoderm. Each of these three layers becomes a different part of the human body. The ectoderm becomes the skin, the brain, and the nerves. "Ecto" means surface, and indeed these cells become the surface covering of the body, and the nerves which are the interface of the body with the outside world. The endoderm becomes the linings of many organs, such as the lungs, the intestines, liver, and pancreas. "Endo" means within, and indeed these cells become almost all of the linings of the body. The mesoderm becomes the muscles, blood, bone, and the reproductive organs. "Meso" means middle, and these mesoderm cells, which form as the middle layer of the disc, become the vast majority of the cells of the body, forming almost all of the different cell types.

This process of organ formation involves extensive migration of certain cells from the disc to their future sites. The

mesoderm cells come from an area on the disc known as the primitive streak. Under a microscope, a dark streak progresses visibly along the center of the disc from the tail end to the head end of the disc. This primitive streak is caused as ectodermal cells drive down into the middle of the disc, like the filling of a sandwich, becoming mesodermal cells in the process. This migrating of ectodermal cells becoming mesodermal cells happens very early in development, between two weeks and three weeks after the trophoblasts begin invading the uterus of the mother. These migrating cells, which come from the primitive streak, are pleuripotent. The mesoderm cells are called pleuripotential, because under different circumstances they are able to follow more than one pathway of development. In other words, mesoderm cells can potentially form many kinds of tissue. They are cells which are closest in nature to the unruly aggressive trophoblastic cells that have formed the placenta.

This broad developmental potential of the pleuripotential cells becomes more and more restricted and checked as the tissues acquire the specialized control mechanisms to guide the cells in their development. Increasingly complicated migrations of cells occur as the body of the new human is forming. For instance in the ectoderm, neural cells migrate in myriad directions and become specialized neurons. This regimentation of a cell’s capabilities must occur in order to form, for example, a bone cell as opposed to a muscle cell in the mesoderm. Such regimentation comes about in response to cues from the immediate surroundings, including the nearby tissue. The precision and coordination required for correct development is dependent upon these interactions. Thus, nearby tissues influence development of certain cells, probably by signals carried by certain protein molecules. Interestingly enough, these signals must also occur at certain precise times, so that a delay in these signals may lead to the failure of correct interactions, leading to various kinds of defects. Many of these defects cause the death of the developing embryo, and some lead to birth defects.

The intricate and precise orchestration of the formation of a normal human from the original inner cell mass is a miracle of precision timing and maturation of these pleuripotential cells. Every normal human contains varying numbers of cells, which have not completed their correct migrations, thereby leaving "sleeping" pleuripotential cells scattered throughout the body. When these pleuripotential cells are activated through genetic, environmental or nutritional factors, a tumor cell mass, similar to the invasive trophoblastic cell mass, can begin to form. This cancerous tumor may contain various types of tissue, such as chips of bone or hair. These scattered pleuripotential cells are normally prevented from becoming a cancerous tumor through circulating protein molecules, which keep their growth in check. It has been theorized that when a human body does not have enough of these patrolling molecules, the pleuripotential cell grows in an unrestrained fashion, becoming a carcinoma.

In summary, the early embryo has two cell types: the trophoblast and the embryoblast. The embryoblast becomes the three germ cell types: the ectoderm, the endoderm, and the mesoderm. The mesodermal cells are pleuripotential, with a vast ability to become many different kinds of cells. Some of these remain "sleeping" dispersed throughout the tissues of the body.

How Do Enzymes Work?

Enzymes are normally produced by the pancreas to help digest the food that enters the small intestine from the stomach. Different kinds of enzymes work on protein, on fats, or on starch and sugar. By the action of these powerful enzymes, large particles of protein, fat or starch are broken down into smaller and smaller pieces, until they are small enough to pass through the wall of the small intestine and be used in the human body for nourishment. Enzymes remaining in the small intestine serve there to digest food coming into the intestine from the stomach. These enzymes in the intestine also can be absorbed through the wall of the small intestine into the body, and travel in the blood stream to distant locations in the body where they are needed.

Why don’t these powerful enzymes start dissolving the very tissues that they are passing through? How can these enzymes travel to the tumor and only digest the cancer, without harming the person’s body in which the cancer is growing? The secret to how the enzyme can tell the difference between “good tissues and bad tissues” lies in a difference as small as the difference between your right hand and your left hand. Almost all the billions of tiny molecules in the body are either right-handed or left-handed. As an example of right and left handedness, let’s look at a pair of mittens. In a pair of mittens you find one for the right hand and one for the left hand. They are mirror images of each other, but if you tried to put the right-handed mitten down on top of the left-handed mitten, they would not match. In a mysterious way, the human body uses only right-handed sugar molecules but only left-handed protein molecules.

The above paragraph has discussed right-handed sugar molecules and left-handed protein molecules. Logic raises the question where are the mirror image substances? Where are the left-handed sugar molecules and the right-handed protein molecules? These are found within the placenta, which is made of trophoblasts. These are also found within the trophoblast-like tumor cells. What difference does this make for the enzyme trypsin?

We know that the enzyme trypsin acts on cooked left-handed proteins and living (non-cooked) right-handed proteins. Normally, when we eat a meal, the cooked left-handed proteins, which we eat, are digested in the small intestine by the trypsin released by the pancreas. Trypsin does not act on the organs of the human body, because these are living left-handed protein. However, trypsin is very effective at breaking down living right-handed proteins. And where did we say living right-handed proteins could be found? These living right-handed proteins are the substance comprising the cancerous tumor. So, the trypsin can travel via the bloodstream to the tumor, and its action there is on the protein mass that makes up the tumor. It breaks down the protein mass of the tumor and “liquefies” it.

As further explanation, this cancerous tumor needs an enzyme with which it can digest the organ or tissue of the human where the tumor is located. It uses human tissue as food. To obtain its needed enzyme, the tumor itself makes the enzyme! This tumor-made enzyme is called “malignin” which does digest human protein. Malignin is a cancer growth stimulator. Malignin stimulates growth of a cancerous tumor, thereby producing more malignin, causing increased tumor growth which makes further malignin in a progressively expanding growth sequence. Thus, a growing cancer tumor continually makes increasing amounts of its own growth stimulator in a progressively expanding sequence. This malignin is the mirror image enzyme to trypsin. In other words, trypsin and malignin are mirror images of each other, as your right hand and left hand are mirror images of each other. As trypsin acts on living right-handed protein, namely the tumor mass, so malignin acts only on living left-handed proteins, namely human tissue.

Trypsin in sufficient quantities can begin to break down the cancerous tumor but not fully digest the cancerous tumor. During the breakdown process, trypsin produces some intermediate proteins and needs a second enzyme to complete their digestion, i.e. “liquefaction”. Therefore, to be successful, the enzyme treatment for cancerous tumors must include both of these enzymes in sufficient quantities to render the products of tumor digestion harmless.

These enzymes work by traveling through the bloodstream to the site of the tumor and digesting the specific protein of the tumor mass, without harming the body’s tissues at all. This fascinating story of the matching right and left handed molecules, trypsin and malignin, was explained almost a century ago by a Scottish professor by the name of John Beard, D.Sc. He published his work in London in 1911. His revolutionary book was entitled, The Enzyme Treatment of Cancer and Its Scientific Basis. At that time some cancers were treated by direct injection of the enzymes near the cancer mass. Now, we realize that injecting the enzymes is unnecessary, since swallowing capsules containing the enzymes will also work. Trypsin will only digest the protein of the tumor, thus it can safely travel through the body. The ability to target the tumor in such a specific and successful manner makes the use of surgery, radiation, and chemotherapy obsolete.

Kathy P. Fairbanks, Ph.D.

Kathy P. Fairbanks, Ph.D.

Note by Dr. Kelley:

Professor Fairbanks’ scientific presentation above is pure truth and scientific without error. Any clinician who challenges this should start all over with his education — in high school biology.

I first read Dr. Beard’s book in May 2000. However, by 1962 I had developed my successful protocol and was free of cancer. I accept Professor Fairbanks’ most significant contribution to the understanding of my program that should help the clinicians who stand up for proper treatment of those suffering with cancer.

The missing factors in Dr. Beard’s and Professor Fairbanks’ understanding are the enzyme activators which have made my program so successful for the past 40 years. It has been my experience, that without the complete program including the enzyme activators, success will be limited to approximately 52%

A malignant tumor mass (in error called cancer) always starts as one cell (a normal trophoblast).This tumor (a false placenta) produces its own “Malignin”. Malignin is an enzyme which accelerates growth of a malignant (cancer) tumor. It acts physiologically in its own positive feedback loop. In other words, the more Malignin produced by the tumor the more normal tissue is digested causing the production of more Malignin, thereby further accelerating growth and gross enlargement and spreading of the tumor. This is the “nasty scenario” of how Malignin acts in a vicious circle of progressively expanding tumor growth (false placenta) as in normal placental development.

The Pancreatic enzymes supplied in the “Kelley Metabolic Program” includes massive amounts of “Trypsin”. Trypsin is a three-dimensional mirror image of Malignin. Trypsin fights against Malignin. Large quantities of Trypsin in the bloodstream stop Malignin’s acceleration of tumor growth. Also, the non-growing tumor can now be recognized by the human body’s defensive warriors, white blood cells and antibodies. These defensive warriors engulf the liquefied dead non-growing tumor debris from the digestive activity of the enzyme Trypsin. Trypsin only digests non-normal tissue cells and dietary proteins. Trypsin does not attack or digest normal live human cells and proteins.

SECRET WEAPON

The disturbing parameter of the false placenta (malignant tumor mass) is its secret weapon. This weapon is the ability of the tumor mass to disguise itself inside of a surrounding layer of starch carbohydrate. When a person’s normal immunological defense mechanisms come in contact with this starch capsule, these defense mechanisms recognize the starch capsule as normal tissue and  do not attack it for removal from the body.

As explained above, the Pancreatic enzymes in the Kelley Program include large amounts of Trypsin, which stops tumor growth. Also included among these enzymes is Amylase, which does normally digest  starch. In my experience, these combinations of Pancreatic enzymes destroy and strip away about 97% of such starch capsules, thereby enabling tumors to be recognized, digested, liquefied and removed from persons’ bodies via their blood streams.

It has been my experience that the starch capsules on about 3% of malignant tumor masses are not destroyed and stripped away by the combinations of Pancreatic enzymes supplied in the Kelley Metabolic Program. Instead, such tumor masses become encapsulated within an inert fibrous sheath. The immune system ignores these fibrous encapsulated masses indefinitely while proceeding to repair and rebuild a ravished body. Although, as explained above our Pancreatic enzymes have large quantities of Amylase, the starch carbohydrate digesting enzyme, in about 3% of human bodies the enzymes do not recognize these starch capsules as foreign. This unusual non removal of such starch capsules in about 3% of human bodies is a subject of my further study. These unusual starch fibrous sheathed capsules are sometimes broken down by non pancreatin digestive enzymes such as our “Digest +” or “Wobenzyme” when taken along with our Pancreatic enzymes.

Respectfully,

Dr. Kelley

William Donald Kelley, D.D.S., M.S.

Medical Missionary to the most pagan peoples on earth — Americans.

“I have a friend losing the lung cancer battle. Does your program help those in later states of cancer? Chemo and radiation have not worked for him.” Houston, Texas

Dr. Kelley’s answer:

There is only one solution to any cancer.— The Kelley Metabolic Program. In reviewing the medical literature today from 1889 it has been well established, “there is no cure for cancer after it has been interfered with. All cancer reacts by increased growth to any injury mechanical or surgical, chemical, or thermal.” The 1985 Memorial Sloan-Kettering Review of several thousands of my patients stated that “cure rate of the Kelley Program was only 93% after the physicians had used Surgery, Chemotherapy and Radiation” Of course this is the highest “cure rate” in medical history. Exception was “pancreatic cancer” at 100% “cure rate”.

The denial of the KELLEY METABOLIC CANCER CURE PROGRAM is the denial of truth and all known scientific proven understanding. This denial is common among the Orthodox and Alternative medical communities. “Cure” is not in their vocabulary; only “Treatment” for financial gain. Cancer victims are “expendable as in experimental animals.”

Should your friend, at this late terminal stage, choose to use our program and can follow the protocol exactly for six months, there is a possibility for help. There is nothing else that offers the remote possibility of success.

God still runs this world in spite of our trying to commit suicide with all the force within us. At least your friend will know he has finally chosen the only possible successful procedure. He and his family can rest assured of this, not blaming themselves for not running around trying everything some idiot tells them about. This is the only solution. Nothing else has ever worked and anything else is not based upon scientific truth.

All successes and all failures of all cancer cures and of all orthodox and all alternative programs fall within, and are scientifically and rationally accounted for in our Metabolic Paradigm.

Dr. Kelley

Chapter II

Dr. Kelley’s Pancreatic Cancer Patients

The Pancreatic Study

INTRODUCTION

The second parameter of the review dramatically supports the final paragraph at the end of the previous chapter. In the second parameter of the study, there was a 100% cure rate for pancreatic cancer patients who carefully, faithfully and completely followed Dr. Kelley’s Metabolic Protocol.

The orthodox medical cure rate for pancreatic cancer is 0%. Although the following study includes only a very few pancreatic cases for various reasons and whims of the reporting journalist, it is the most significant and successful pancreatic cancer study in the world to date. This study alone proves Dr. Kelley’s objective, the Kelley Metabolic Cancer Paradigm is the only scientific basis and protocol for a cancer cure.

THE STUDY

Twenty-two (22) patients were selected for the study. Seventeen (17) of these patients had died. Five (5) patients were cured.

COMPLIANCE

Compliance, which is how rigorously each patient followed his or her metabolic program, was determined from several sources. Interviews with patients, family members, physicians, supplement purchases and Dr. Kelley’s notes.

          Ten of the twenty-two (22) patients had consulted Dr. Kelley only once, and had never followed the Metabolic Program, not even for a single day. All patients died.

          Another seven (7) patients pursued their Metabolic Program only partially and sporadically, for periods of time ranging from four weeks to 13. All these patients, too, were dead. None of these patients had used the Kelley Metabolic Program at all during the three months prior to their death.

          Patients failed to follow the Metabolic Program, or followed it incompletely, for a number of reasons. One patient, who died the day after visiting Dr. Kelley, was too sick to begin. Another patient, whose disease had already bankrupted him, could not afford the supplements. Several patients gave up on the regime because their physicians strongly opposed Dr. Kelley’s approach. In addition, several found the lifestyle changes, the diet and detoxification too unappealing.

The reasons for non-compliance can be listed as follows:

          Five of the twenty-two patients followed the full Metabolic regimen as prescribed, and for periods ranging from two to ten years. Each enjoyed a complete regression of disease, and four were still alive when this report was published (1987). One patient died after 11 1/2 years of Alzheimer’s Disease, and of course cancer free.

Grouping of Pancreatic Cancer cases

 Group I

CONCLUSIONS

As described, one extremely ill patient died the day after consulting Dr. Kelley. Otherwise, based on the evaluation of the medical records, the patients in one group were not significantly sicker than those in any other group when first seen by Dr. Kelley.

          Dr. Kelley has repeatedly told all cancer patients they should follow the full program for at least several years to regain good health. Nevertheless, the mean survival time for those who followed the Metabolic Program only partially, and usually briefly, is 4.8 times greater than the survival time of patients who never began the Metabolic Program.

          Finally, the data allow an estimation of Dr. Kelley’s success rate with pancreatic cancer. In this calculation, only those patients who followed the full Metabolic Program are considered. This is appropriate: in any controlled clinical trial of a chemotherapeutic drug, subjects who deviate from the protocol must be discounted, even if they do well.

So, Dr. Kelley’s success rate, in this particular series of patients — considering only those who used the full program — is 100%.

The journalist used a relatively small number of patients. Nonetheless, this is an impressive outcome; no oncologist in the Orthodox or Alternative medical communities anywhere in the world can match these results.

It requires the failure of the pancreas from two to four years to develop a Malignant Tumor Mass — which the Medical Community in total error calls “CANCER”.

The Kelley Metabolic Program

As stated in Chapter III, Dr. Kelley’s Original Metabolic Medicine’s Cancer Cure Program works well with any cancer condition. In reality, his paradigm is the only scientific solution for any and all types of cancer. In failing to understand what cancer is, the Orthodox Medical Establishment has classified and named well over 200 different types of cancers. Fortunately for the cancer victim, there is only one metabolic malfunction, or as some say, disease process — the simple malfunction of one’s production and delivery of adequate pancreatin.

          The proper and effective therapeutic protocol for cancer consists of five broad areas of procedures that the cancer victim him/her self must address for a complete and permanent cure or remission.

Yes, many orthodox as well as alternative procedures supply some portion of these necessary parts of our paradigm. Their successes, although few, are easily accounted for. The person and/or his/her physician supplies, by accident, chance or guesses the necessary part of our Metabolic Paradigm. Likewise, their non-success is explained by their failure to provide the complete metabolic protocol

1.     Necessary nutrients, vitamins and minerals to activate one’s own pancreatin production.

2.     Additional pancreatin intake of adequate quantity and quality.

3.     Proper detoxification and clean-up of one’s contaminated and blocked metabolic functions and pathways.

4.     Dietary changes necessary and compatible with one’s genetic metabolic requirements

5.     The all-important intake of good safe water.

The Swift Kick

Many a time God Almighty has opened the door of opportunity to us that would be best for us and serve His purposes (the reason for our existence). All too often we peek-in and turn away to our own detriment. Occasionally, if we are blessed, He kicks us through it; our bottoms hurting, a whole new world opens to us.

                                     And so it is.

Chapter III

A Review of

Dr. Kelley’s Cancer Patients

The Medical Establishment has for many years endeavored to discredit Dr. Kelley’s most successful Cancer Paradigm developed in 1963.

A medical journalist obtained authorization under the guidance and direction of Dr. Robert A Good, Ph.D., M.D., President of Memorial Sloan Kettering Cancer Center in New York City to review Dr. Kelley’s records. The objective of the Medical Establishment was to prove beyond a shadow of doubt that Dr. Kelley was an unorthodox quack. Dr. Kelley’s objective was to prove beyond a shadow of doubt that the Kelley Paradigm is the only scientific basis for the Cure of Cancer. Dr. Kelley had some 33,000 well-documented medical records of his cancer patients. The documentation was so overwhelming this study continued for over five years.

Legally, the definition for a cancer cure is that a patient must be free of cancer five years after initial diagnosis. The study was approached from two general parameters. The first parameter was for all types of cancer. The results indicated a 93% cure rate, after their physicians dismissed the patients, stating that no further orthodox medical therapy could be helpful for them. In other words, their disease processes had exceeded the therapeutic limits of orthodox medicine and they could no longer be helped. Thus the standard Orthodox Death Sentence — go home and die.

Dr. Kelley often states, “It is possible to cure only 97% of Cancer Patients as in 3% of those diagnosed with cancer, the patient has a death wish, or more frequently the next of kin (wife, husband, parents, children) have a death wish for the cancer patient”.

The conditions for success for 97% of cancer patients are two in nature. One, the patient must have at least six months of time to get well into the Kelley Program and two, one must follow the protocol exactly and faithfully. After the first six months, there is an excellent prognosis for recovery. The cancer patient’s road to success is difficult and usually takes an additional 18 months of intense therapy, which can only be accomplished by the patient. When recovery has been gained, one must keep in mind that diet and pancreatic support are mandatory for the remainder of one’s cancer free life.

A Preliminary Review of many cancer types using

Dr. Kelley’s Cancer Program

          Dr. Kelley’s Metabolic Cancer Cure Program is effective on all types of cancer, for cancer is only a simple metabolic malfunction.

          The wide range of types of cancer confirms the effectiveness of Dr. Kelley’s Metabolic Cancer Cure Program. This study was in 1988, and most of the individuals remain alive and well. However, free of cancer, a few of them have died from other diseases or accidents.

	Tumor type	#Pts. on			#Deceased		#Survival times in years to   present while on program.
	Adenoidal	1			0		2
	Adrenal	1	0					1
	Basal cell	1	0					3
	Bile duct	1	0					5
	Bladder	2	0					5,6
	Bone	2	0					5,6
	Breast	30	3					1,1,1,2,2,3,3,3,4,4,4,4,4,4, 4,4,4,5,5,5,5,5,6,6,7,7,8,8, 8,10
	Cervical	3	0					2,3,4
	Choriocarcinoma	1	0					2
	Colon (all advanced)	15		0		1,1,2,3,3,5,5,6,6,7,8,8,8, 10,13
	Ewing’s sarcoma	1	1					2
	Fibrous Histiocytoma	(1)	0					5
	Hodgkin’s	4	0					1,1,3,10
	Leukemia (unclassified)	1	0					8
	Leukemia, acute    lymphocytic	2	0					1/2,2
	Leukemia, acute    myelocytic	2	0					4,5
	Leukemia chronic   Lymphocytic	1	0					1
	Lung	6	2					2,3,4,6,8,8
	Lymphoma  (unclassified)	14	1					1,1,2,2,2,3,3,4,5,5,5,5,5,13
	Melanoma	5	2					1,3,4,4,6
	Metastatic adrenocarcinoma	2	0					6,6
	Multiple myeloma	(2)	0					1,3
	Ovarian	3	0					2,5,8
	Pancreatic, 4 diagnosed at                       exploratory	8	0					1,3,3,4,5,7,8,8
	Parotid	1	0					5 ½
	Plasmacytoma	(1)	0					9
	Prostate	8	0					½,2,3,3,3,4,4,8
	Rhabdomyosarcoma	(1)	0					4
	Seminoma	1	0					5
	Skin	6	0					1,2,2,3,3,8
	Small intestine	(2)	0					3, 7 ½
	Stomach	2	0					4 1/2,6
	Trophoblastic	(1)	0
	Urethral	1	0					3 ½
	Uterus	6	0					3,3,6,7,8,10

We have lost it!

          We have lost credibility with  the general public. We have done this with malice aforethought. We are losing 2,739 cancer victims each and every day. We are not only ignorant, but we chose to remain so for fear of the multi-national Pharmaceutical/Medical establishment. This is pure fraud and murder.

          It has been over 100 years that the Cure for Cancer has been available to the medical communities, yet we continue to play our game of deception, plunder and murder.

          History is filled to the brim with documented facts, wherein the most educated of society have turned in the presence of truth, running to witchcraft, old wife’s tales, accepted treatments in ignorance and fear of the “establishment of their day”.

          In the early 1800’s thousands of women died of “child birth fever”. Dr. Semmelweis’ protocol of washing of hands and instruments earned him a room in an insane asylum. It was not until the 1940’s it became standard procedure to clean-up. Then “child birth fever” ceased  to be the leading cause of maternal death.

          It will take a massive revolt from the general public before this deplorable condition is corrected. Thousands of cancer victims must say NO to their physicians and hospitals for the use of Surgery, Chemotherapy and Radiation. These procedures have never been successful for treating cancer. They will never be successful.

          The good news is that the revolt has started in Texas. This revolt is scaring the medical communities. By the 1^st week in August 2001 the Ft. Worth Star Telegram newspaper printed a major article about the public losing faith in the area medical community.

          Yes, we have lost it — we doctors have lost our credibility with the public. Once it is lost it will probably take the current generation of physicians dying off and maybe one or two more generations before medicine’s treatment of metabolic and degenerative disease credibility is regained.

Chapter IV

Do I Have Cancer?

          Do I have cancer? Am I going to die? How long do I have to live? Is my cancer growing? Will I ever get well? Am I getting worse? How long have I got? Has my cancer stopped growing? Where do I find out? Why hasn’t my doctor told me? These are the questions we get bombarded with daily.

          Yes, we have the answers to these questions! Dr. Kelley has  found, and scientific publications by the thousands support, that cancer starts about 13 years before your doctor announces, “you probably have cancer, let us run some tests.” This is 13 years too late. It is 13 years after the fact. It is always too expensive. It could well be deceptive and inaccurate!

          Let us look at the current medical establishment’s diagnostic procedures. Legally, in dealing with cancer, biopsy is the accepted test or report. This only tells you the tissue they are examining is malignant or not malignant. All tests are not 100% accurate. Also in biopsy the surgeon could have failed to obtain a correct sample —thus resulting in a false negative report. Dr. Schandl’s Cancer Profile can indicate metabolic changes many years before diagnosis could be made by any other method. A positive result means either a developing cancer or an existing cancer.

          All other “cancer tests” that we know anything about DO NOT MEASURE CANCER. They all measure something else. Even Dr. Kelley’s “Self-Test” only indicates pancreatic function, immune system function and toxicity. From this we are forced to calculate or assume a malignant condition is present, or not present, or will become clinical within a two year time period.

LABORATORY TESTS

          The most accurate health evaluation system we have ever used is Dr. Emil Schandl’s “CA Profile©”. Dr. Kelley has used it for 25 years and recommends the use of it to all the doctors and technicians he teaches. It gives the health care professional and the patient alike the true and correct answers to their questions in a most understandable format.

          The “Cancer Profile” is a metabolic evaluation of what is really going on in your body. Are you really cancer free? Do you already have cancer? If you have cancer it may take 10 to 12 years for it  to develop to the size your health care professional can recognize it. Now you may ask “is there anything I can do to reverse an early cancer condition”?

          The use of Dr. Schandl’s “CA Profile©, a Metabolic Cancer Profile” and the Kelley Metabolic Program are the procedure of choice should one want to build health. Preventing degenerative disease processes, living a healthy life is certainly within your ability to attain. You only need know-how, and the dedication to do it.

          It is both amusing and tragic to us to see on national television and in many communities the local T-V stations, big campaigns for women to “self-examine their breast” for cancer. By the time they or their physician find a malignant tumor mass they have had cancer from 4 to 13 years. At this point the cancer has metastasized. The orthodox cure rate of metastasized cancer is 1 in 1000.

How to Obtain Dr. Schandl’s CA Profile©

                    With the current cancer rate of one out of two. It is a very good investment to take the CA Profile© test immediately. If you have been diagnosed by your physician as having cancer, take the CA Profile© test immediately. This will serve as a base line for future evaluations and monitor the progress of your recovery, relieving anxiety and stress. If you have not been diagnosed by your physician as having cancer, take the CA Profile© test immediately. This serves as a stress relief and gives you time to “build your health”.

1.     Call the American Metabolic Laboratories @ 1-954-929-4814. Request a patient CA Profile package.

2.     If you have a cooperative health care provider: Medical Doctor, Osteopath, Dentist, Chiropractor, Naturopath or other, they can sign the BLOOD TEST REQUISITION FORM for the test.

3.     If you do not have a cooperative health care provider, fill out the REQUEST FOR PHLEBOTOMY sent i