SPECIALIZED TESTING FOR EARLY DETECTION CANCER AND CHRONIC ILLNESS


Typical Western ways of testing for cancer are CT scans, MRI’s, PET scans, and Mammograms. VERY IMPORTANT TO NOTE, IT IS PHYSICALLY IMPOSSIBLE FOR ANY OF THESE VISUAL EVALUATIONS TO DETERMINE IF IT IS A CANCEROUS OR FUNGAL MASS, OR “TUMOR”.

Unfortunately all too often people are misdiagnosed. Several years ago the CDC admitted that over 3 million people had been misdiagnosed in the last 30 years, the majority of them being women for breast cancer from a mammogram The CA Profile test is designed to not only be accurate for cancer activity but also the rate of metastasis, if any. The Cancer Profile test is also totally non-invasive with only a blood and urine sample that can be collected at any local hospital or collection site.

The Cancer Profile


The Cancer Profile™ is based on the premise that detectable biochemical changes occur in the human body during its transition into a cancerous state. It is comprised of 7 tests:

  • HCG (human chorionic gonadotropin) chemiluminescence assay serum
  • HCG urine quantitative
  • PHI (phosphohexose isomerase enzyme)
  • CEA (carcinoembryonic antigen)
  • GGTP (gamma-glutamyltranspeptidase
  • TSH (thyroid-stimulating hormone)
  • DHEA-S (dehydroepiandrosterone sulfate)

An Accepted Standard Of Care For Over 20 Years


The CA Profile test, or Cancer Profile test, has been an accepted standard of care for cancer diagnosis for over 20 years for showing ACTUAL out of control cancer cell activity in the entire body down to as little at 2800 active cells, not just what they may or may not have found in a biopsy. To put that in perspective, the smallest “mass” any of the visual scans like a CT, PET, MRI, or Mammogram can detect is about the size of a small green pea, and by that time IF it is cancerous at all a person has likely had out of control cancer activity for between 3 to 7 years.

When you order the CA Profile, not only do you get the most advanced cancer test available today, you have an opportunity to combine the cancer test with advanced full body remote scanning. This means from the comfort of your home in approximately two hours we can provide a complete scan for analysis, and review including: The underlying cause of disease; What are contributing factors to the cancer present in the body and what will it take to lower that risk? are there Dental issues that are lowering the immune system that are affecting disease? are Mycotoxins and Lyme present? What are the emotional root causes, other toxins and heavy metals that may be suppressing the immune system, plus the location of Toxic Foci (high concentrations of toxins).

The CA Profile© Includes The Following Tests

HCG (Human chorianic gonadotropin) intact (IRMA) and intact plus, HCG beta, core, and its fragments (IMM) are normally made by the embryonic origin trophoblast cells. However, It may be present in most, if not all, types of cancer. These two procedurally totally different methods are being used to ascertain the validity of the often very low amount of the hormone in the blood. The IRMA is immunoradiometric assay, and the IMM is chemiluminescence. The tests will detect extremely low levels of the hormone, and are specific for it 98-99%. The IRMA test will measure down to 0.3 mIU/mL, and IMM to 0.2 mIU/mL. Dr.Schandl named this tumor marker “the pregnancy and/or malignancy hormone.” HCG suppresses the immune system, starts and enhances DNA, RNA of protein synthesis, and generally it is produced under anaerobic cellular conditions by the trophoblast.

The HCG Urine test was studied and introduced at American Metabolic Laboratories. This test is now included in our Cancer Profile. It must be noted that American Metabolic Laboratories’ Urine-HCG Test may be the one and only one of its kind for being quantitative down to less than 1.1 mIU/mL detection level. This test, unlike Doctor Navarro’s for instance, requires about 0.5 mL of urine without any treatment, in its natural form. It is totally specific for the HCG hormone even in minute quantities. The old method requires acetone denaturation and extraction that yields a conglomerate of HCG, LH, FSH, and TSH hormones. All of the four structurally very similar hormones are precipitated by the harsh treatment and will add on to the reported HCG value. Postmenopausal women and older men with high LH and/or FSH, and hypothyroid individuals with high TSH may yield elevated “HCG” values. However, this hormone species is actually HCG-like (HCG-L) with one-half biological activity when compared to pregnancy or tumor generated HCG.

PHI enzyme channels cells into anaerobic metabolism, i.e. fermentation. This kind of cellular survival is what cancer cells favor. The more energy generating metabolic pathway is oxidative phosphorilation. This is the pathway normal cells require in the presence of oxygen. Hence, more oxygen is less cancer, and less oxygen is more cancer. PHI is called the autocrine motility factor, i.e. malignancy or cancer spread factor. This means it is one of the major causes of metastatic spread.

CEA is a broad spectrum cancer marker. It is the carcinoembryonic antigen. It can be elevated in all sorts of cancers. It is very prevalent in cancers of the breast, colon, and rectum. Like all the others, it is an independent cancer marker that by itself may be sufficient as a diagnostic adjunct.

GGTP is the most sensitive test for the liver, however, it may be elevated in diseases of the heart, lungs, and kidneys. It is not a tumor marker however, it may be elevated in cancer patients as a result of either cancer spread or toxic therapy.

TSH or thyroid stimulating hormone regulates basic metabolic rate, i.e. oxygen utilization. A high level, i.e. hypothyroidism, may be a prelude to cancer. Chemotherapy frequently causes this anaerobic condition by injuring the thyroid gland.

DHEA-S is the “adrenal anti stress, pro immunity, longevity hormone”, according to Dr. Schandl. The immune system is impaired without adequate amounts of this hormone. Most, if not all cancer patients and those in the process of developing cancer have very low or no DHEA in their blood.

HCG IRMAMay be elevated in cancer, stress-related to cancer, a developing cancer, or pregnancy. It will detect only intact hormone. It may not detect HCG-LNormal: Less than 1 mIU/mL; gray zone: up to 3.0 mIU/mL
HCG IMMMay be elevated in cancer, stress-related to cancer, a developing cancer, or pregnancy. It measures intact and all other molecular forms of the hormone, including HCGL-S (HCG-like)Normal: Less than 1mIU/mL; gray zone: up to 3.0 mIU/mL
***HCG UrineMay be elevated in cancer, stress-related to cancer, a developing cancer, pregnancy, or the presence of HCG like substance (HCGL)Normal: 0.0 – 1.0; gray zone 1.1 – 3.8 mIU/mL
PHIElevations may warn of a developing cancer; cancer; active AIDS, acute viral disease, acute heart, liver, or muscle diseaseNormal: Less than 34 U/L; gray zone: up to 40.00 U/L
GGTPDiseases of the liver, pancreas, and the biliary system. Also heart, lung, kidney ailmentsNormal: Females less than 29 IU/L, Males less than 35 IU/L
TSHThyroid stimulating hormone, for thyroid and oxygen metabolism.Normal: 0.4 – 4.0 mcIU/mL
DHEA-SAdrenal anti-stress, immunity, and longevity hormone; low or zero in most cancer patientsNormal: Females 35 – 430 mcg/dL, Males 80-560 mcg/dL. Results must be interpreted in reference to a person’s age
CEACarcinoembryonic antigen may be elevated in any malignancyNormal: Less than 3.0 ng/mL; gray zone is 3.1 – 5.0 ng/mL

*** Laboratory studies indicated that urinary HCG -IRMA was negative in 99% of the tested subjects. This means that very little, if any, tumor generated HCG was filtered out. The urine should be tested by the IMM method, however, because tumor originated ß and fragments can be present that the IRMA method excludes.