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DIFFERENT TECHNIQUES

DIFFERENT TECHNIQUES.

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DIFFERENT TECHNIQUES

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  1. DIFFERENT TECHNIQUES • KNOTT ‘S TECHNIQUE: Blood extraction is performed by a peristaltic pump. The patients vein is canalized and blood extraction proceeds via a sterile closed tubing circuit that runs through a pump and into an irradiation cuvette where the blood is exposed to UV Photons. From there the blood continues to a sterile receiving bottle. When all the blood collected is irradiated and contained in the bottle, the pump is reversed and the blood is once again irradiated before returning to the patient. • SYRINGE TECHNIQUE: This technique employs a 60cc syringe without a needle, which is connected to sterile tubing, which is in turned connected to a 9cm long cuvette and from there to the canalized vein of the patient. Blood is extracted by pulling back on the syringe and then reinfusion occurs by syringe injection. This motion back and forth is repeated 3 to 4 times depending on the volume of blood needed. Safety measure are greatly lacking in this type of procedure. • ELDESON TECHNIQUE: Utilized by THERAKOS of Johnson and Johnson. Here a patient’s vein is canalized and blood is extracted by pump action to a plasma separator. The whole blood is separated into Plasma and Serum. The Plasma continues via sterile tubing to the irradiation chamber; from there the blood is reconstituted into whole blood and reinfused back into the patient. This procedure takes 4:50 minutes and is very costly.

  2. FERNANDEZ TECHNIQUE:Dr. Fernandez developed a blood irradiation process which is extremely efficient, viable, safe and dependable. In our technique the patients vein canalization and blood extraction is performed by conventional methods, such as those employed by the RED CROSS. After collection is completed, the blood bag is connected to the irradiator and to a disposable sterile tubing kit and to the PCI-Cuvette. The blood is then pumped via a peristaltic pump at a precise flow rate; this guarantees precise dosage. The blood then flows to an irradiation chamber via a sterile spiral cuvette and is exposed to the exact dosage of UV photons. The blood then continues to a secondary collection bag. Once the irradiation process is complete (aprox. 3-7 minutes) and the collection bag is full, is it disconnected from the disposable kit and placed on an IV pole to be reinfused to the patient by conventional transfusion methods. Dr. Fernandez utilizes a blood administration kit with a 70micron filter to avoid any clots from being reinfused. • The PCI-1 has a special feature which is a memory chip that contains the patients complete medical history and dosage prescription provided by the attending physician. This chip must be inserted into a USB port on the machine in order for treatment to be initiated. This safety precaution avoids mistakes in dosage and assures patient and medical personnel safety. The blood never comes into contact with the ambient and the patient is never attached to the machine. Procedure takes 25 minutes.

  3. Mechanisms of Action • the illumination of the blood in the treatment chamber destroys or alters bacteria and viruses in the extracted blood in such a way as to provoke a reaction by the immune system upon its return to the body, which in turn destroys most or all of the other bacteria or virus in the body • the activation of 4-5 percent of the blood then spreads throughout the entire volume of the blood upon reinfusion, and the induced secondary emissions (biophotons are emitted by the activated cells. An incoming photon in photon therapy excites an electron to a higher energy level. When the electron drops back to its original level, it in turn emits a secondary photon.) destroy virus, bacteria, and-in autoimmune diseases-activated white blood cells. It is not clear to what extent the secondary emissions in photon therapy are immediate (fluorescent) or delayed (phosphorescent) • the treatment itself, though quite modest in intensity, has an impact on the autonomic nervous system (hence the frequent instances of flushing of the skin) and is perceived as a threat/stimulus by the entire immune system, which springs into action and thereby contributes to destroying bacteria or virus.

  4. Bacteria and viruses are more vulnerable to biophotonic emissions than are somatic cells. Photon therapy forms pyrimidine dimers and otherwise disrupts the DNA of microorganisms. In contrast, as long as somatic cells are not metabolically active, they have the capability of withstanding modest amounts of biophotons emitted by blood cells. • Photon therapy stimulates the activity of white blood cells; on the other, excess amounts destroy various white blood cells. This second point suggests a reason why photon therapy seems so effective against autoimmune diseases. In autoimmune disorders it appears that the metabolically active T-cells and other immune cells absorb much greater numbers of biophotons than ordinary body cells, and this destroys them, thus slowing down or stopping the disease. Activated T-cells in particular are prone to absorb secondary biophotons following photon therapy as a source of energy just as they absorb at a very high rate glucose and other energy-bearing molecules.

  5. BACTERIAL MEMBRANE DESTRUCTION This picture proves that bacterium are susceptible to destruction once exposed to UV pulse modulation irradiation. Viruses which are smaller than bacteria are readily destroyed by fragmentation.

  6. Rationale and Method of Treatment The Knott technique of blood irradiation (approved by the American Blood Irradiation Society) achieves the following physiologic objectives: ·         Increases the blood oxygen level ·         Increase phagocytosis (white blood cell activity) ·         Relieves toxemia, ·         Decreases edema (swelling) ·         Controls nausea and vomiting. The treatment consists of withdrawing blood from the patient and by use of the Knott hemo-irradiator, exposing it to radiant energy between the wave lengths of 2,399 and 3,900 angstrom units as it passes through the irradiation unit at a predetermined rate. The blood is returned to the patient through the needle used for the initial venipuncture (IV). The entire system is “closed” meaning the patient’s blood never leaves the tubing or the bottle and is simply returned back into the vein after passing through the UV device. Treatment requires 15-60 minutes depending on the amount of blood treated and how fast the blood flows. After the treatment, 15 minutes of rest is required, after which time the patient may resume whatever activity is permitted by his or her Woodlands Healing Research Center physician.

  7. Viral Infections ·         Poliomyelitis , polio-encephalitis, myelitis ·         Hepatitis: infectious, serum ·         Influenza ·         Common upper respiratory disease ·         Herpes simplex, Herpes zoster ·         Mononucleosis, Mumps, Measles Bacterial Infections ·         Pneumonia ·         Septicemia (staphyloccocus, streptococcus, pneumococcus) ·         Wound Infections, lymphatic infections (lymphangitis) ·         Peritonitis ·         Typhoid Fever ·         Recurrent skin infections (furunculosis, carbunulosis) Inflammatory Conditions ·         Acute thrombophlebitis, fibrositis, bursitis, nephritis, iritis, uveitis, cholecystitis, pancreatitis ·         Rheumatoid arthritis Circulation Conditions ·         Varicose and diabetic ulcers ·         Peripheral vascular disease ·         Gangrene ·         Vascular headaches Others ·         Non-healing Wounds and Fractures ·         Pemphigus ·         Emphysema ·         Adjunctive cancer treatment (Germany) Indications: According to the Foundation For Blood Irradiation, Inc, UBI has been found useful in treating:

  8. The results of treatment included: • inactivation of toxins • destruction and inhibition of growth of bacteria • increase in the oxygen-combining power of the blood and oxygen transportation to organs • activation of steroid hormones • vasodilation • activation of white blood cells • stimulation of cellular and humoral immunity • stimulation of fibrinolysis • decreased viscosity of blood • improved microcirculation • stimulation of corticosteroid production • decreased platelet aggregation

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