The Stowe Foundation
Mechanisms of HYDRATE8X
Hydration and the Aquaporin Channel
Peter Agre, a Nobel Prize recipient, outlines that fact that water molecules pass through the aquaporin channels one molecule at a time. That concept is not in conflict with structured water in the bulk phase. In fact, I use Peter Agre's work to support why structured water absorbs more readily through the membrane channels. Each water molecule, each H20 has a specific orbital relationship between the position of the hydrogen proton and the oxygen molecule. Each proton H+ is attached to the oxygen O (-2) through a covalent bond. There are two protons, H+ and one oxygen (-2) that give water its divalent properties. It is the spatial relationship or the orbital positioning of the two protons to the oxygen atom that gives the water molecule its divalent charge characteristics. The water molecule will be slightly positive on one side of the H20 molecule and slightly negative on the other side. Not many molecules are divalent, but water is because of the relationship of where the hydrogen protons exist in relationship to the oxygen.
The spatial relationship of the protons to each other, within a single water molecule, is called the water bond angle. The water bond angle is controlled by the energy of the covalent bond. Each hydrogen proton, H+, in each water molecule, H2O, is attached to the oxygen molecule through a covalent bond. Change the strength of the covalent bond between the hydrogen proton and the oxygen atom and you will change the water bond angle, the relationship of the two protons to each other. Change the water bond angle and you will change the divalent characteristics of the individual water molecule. Change the divalent characteristics of the water molecule and you will change the conductivity of the water. The reverse is true as well.
The only way to measure a change of conductivity of the water is to change the divalent characteristics of the water molecule or add an ionic substance, which is not part of our structured water technology. Now the nuclear magnetic resonance (NMR) of the water molecule, also measures the spatial relationship between the protons, H+ and the oxygen. It is called shielding. In this case the water molecule is dimagnetic as well as divalent. You measure the response of the water molecule to an imposed magnetic field. The only way to change the NMR reading of a water molecule is to change the position of the H+ protons.
The position of the H+ protons is solely controlled by the covalent bond that exists between the H+ protons and the oxygen molecule. The covalent bond controls all of the properties of the water molecule. That applies to each single water molecule. The physical properties of each single water molecule determine how easily each single water molecule can pass through the aquaporin channel. If you look closely at Peter Agre's work you will see that the there is a positive charge on the membrane wall one half of the way through the aquaporin channel. This is illustrated on the attached power points. That positive charge of the membrane wall is pulling on the negative charge of the water molecule. It pulls the water molecule into the aquaporin channel. The divalent characteristics of each single water molecule will influence the ability of a single water molecule to be pulled into the channel.
During the process that creates the structured water, we create a water molecule that can efficiently pass through the aquaporin channel. In the bulk phase of the water, single water molecules will link together through the process known as hydrogen bonding. That is where the hydrogen protons of one water molecule bond to the oxygen molecule of another nearby or neighbor water molecule. Hydrogen bonding is very different then covalent bonding. Hydrogen bonding occurs between water molecules and covalent bonding occurs within the water molecule.
When the covalent bonds are of a specific energy level, the hydrogen protons will have a very defined relationship to the oxygen molecule. That relationship will define how well the hydrogen proton can be shared with another nearby oxygen molecule or how well hydrogen bonding can be achieved. Sharing the protons is the same thing as being a proton donor. In any event, when you have the right energy levels in the covalent bonds within the water molecule, you will get the levels of hydrogen bonding between the water molecules that produce a linkage that is predominantly between six water molecules at a time. This is a dynamic equilibrium that simply reflects the propensity of water molecules to undergo hydrogen bonding.
The six sided structure is simply an offshoot of changing the covalent bond inside the water molecule. Changing the covalent bond and hence the water bond angle of each individual water molecule changes the physical properties of the water. That is what all the analytical properties tests show. The tests were performed at certified test facilities. Everyone else has to add a chemical to change the surface tension. Everyone else has to add something to change the viscosity. Everyone else has to add something to change the pH. The fact is we do not add anything to the water and yet we dramatically change the physical properties.
We accomplish this by using energy (magnetic, electrical and adiabatic compression) to change the covalent bond between the hydrogen proton and the oxygen molecule within the water molecule itself. In essence we reposition the hydrogen proton to a new stable orbital and it establishes a new equilibrium with the oxygen. You then have a new covalent bond and an entirely different water molecule. We alter the fundamental understanding of water. Not all water is created equal.
The single water molecule we create tends to agglomerate or self associate or hydrogen bond with other water molecules in units of six. The water then has vastly different physical properties with no additives. The individual water molecules have the right di-electric and di-magnetic constants to efficiently pass through the electromagnetic fields of the membrane walls. There is no discrepancy with anyone's understanding of water absorption into the cells, it just happens faster and more efficiently. In essence our technology simply changes the covalent bond between the hydrogen proton and the oxygen. We move both of the hydrogen protons to another stable orbital. That is why I call it quantum physics. At the end of the day we have simply created a new water molecule. The new water molecule has properties that can be measured and quantified. That is our proof.
The clinical study on diabetics shows that the new water has beneficial effects on the human body.
Mechanism of Hydration and the Aquaporin Channel
Immune therapy must be tailored to each individual patient. There is no magic bullet waiting to be discovered that can be patented and then mass marketed that will be the answer to diabetes, to cancer, to heart disease, to emphysema. These are all complex breakdowns of the immune system. They all result from the PITTS Syndrome. Each diabetic has a different combination of factors that leads to the breakdown of the pancreas. The patient’s individual score on the PITTS Syndrome determines what parts of Applied BioLogics are required for that patient to heal. For example, any advance in the treatment of infections will have major implications for the diabetic who wants to heal. Infections are the “I” of the PITTS Syndrome. There is substantial evidence that many type II diabetics have a viral infection of the pancreas. Eliminate the virus and the pancreas functions like it should to produce insulin. The same can be said for pancreatic flukes, which are parasites. Eliminate the parasites and pancreatic function can return. The point is you have to know what microorganism is affecting the pancreas.
The presence of heavy metals and other toxins also play an enormous role in diabetes, because toxins like to accumulate in the fatty tissue of the body and the pancreas is a fatty tissue. Cadmium is a heavy metal present in cigarettes. Mercury, a heavy metal toxin, is in our tuna.
We are bombarded with chemicals in our cosmetics and skin care products. Any biological product or medicine that can help detoxify the body will support reversing the PITTS Syndrome.
Chemotherapy is a toxin, the first “T” of the PITTS Syndrome. Many cancer patients become diabetic while undergoing treatment. It is mandatory to detoxify a cancer patient following chemotherapy or radiation if you expect normal body function to return. Each toxin requires its own pathway of elimination. The Foundation is constantly looking at the technology of detoxification.
In the area of detoxification, the liver is the key organ of the body. Even our own hormones can become toxic to the body when the hormones get out of balance. The liver eliminates circulating hormones from the blood to keep everything in balance. Insulin is a hormone and must compete with every other hormone in the body. If the liver malfunctions, hormones get out of balance. The diabetic is often resistant to his own insulin because of hormone imbalances related to liver problems. Any drug or performance enhancing steroid or alcohol that is toxic to the liver will cause severe complications for the diabetic. The interaction between toxins and the liver is a key factor of the PITTS Syndrome and Applied Biologics. Medicine has spent almost no capital resources on detoxification procedures. In fact they have resisted very powerful detox protocols such as chelation therapy. Chelation therapy removes heavy metals from the body and can vastly improve the body’s ability to heal. This procedure has benefited many diabetic patients following the concepts of immune therapy.
But stress, the “S” of the PITTS Syndrome and emotional trauma, the second “T” of PITTS can also bring profound hormone imbalances. Stress and emotional trauma put the adrenal glands into the fight or flee syndrome. There is a demand put on the body to produce extra energy. Hormones produced in the adrenal glands create this demand. The adrenal glands are the major organs of the endocrine system that respond to emotional trauma and stress.
The energy demand created by the adrenal glands can only be satisfied from the stores of blood glucose. Blood glucose can only enter the cells of the body to produce energy when the pancreas produces insulin. Both the adrenal glands and the pancreas become fatigued and lose their ability to perform when exposed to long-term chronic stress. Adult onset diabetes is not too far behind. The ability of adult stem cells to revitalize the pancreas, the adrenal glands and the liver becomes a vital issue to the diabetic. Adult stem cells can be transplanted to the patient by an infusion catheter or by an IV protocol to get a systemic rejuvenation of the body. The IV protocol can be investigated at the BioTherapy Research Institute without the need for a catheterization lab. There is no requirement for a surgical team. Adult stem Cells combined with Applied BioLogics will provide an answer to type II diabetes. Combine adult stem cells with gene therapy and you will get an answer to type I diabetes.
Within the field of adult stem cells, there is fascinating research about the ability of adult stem cells to reverse type I genetic diabetes. Adult stem cells contain the DNA of the patient. Type I diabetes is a genetic defect of the pancreas. By correcting the genetic defect of the DNA in the harvested adult stem cells prior to the expansion step, the stem cells that are transplanted back into the patient’s pancreas will be free of the genetic defect. When the pancreas is revitalized with the repaired transplanted adult stem cells, the patient is no longer diabetic because insulin production has been restored. This type of research holds fascinating promise for correcting genetic disease. The Stowe Foundation can provide research grants to other institutions under our 501c3 status. We carefully target our grants to projects that advance the concepts of immune therapy. However, the BioTherapy Research Institute is the heart and soul of the Stowe Foundation. The Foundation will eventually manage the Applied BioTherapy Center of San Diego where clients can come to receive immune therapy on a fee for service basis. The fees generated at the BioTherapy Center will help underwrite the costs of the Foundation.
The Stowe Foundation is conducting an investigational study into a new biologic response modifier that has shown promise against soft tissue cancers. By ridding the body of the cancerous process, it is then possible to transplant stem cells into the afflicted organ to repair the damage. The same concept applies to infections. Immune therapy based on autologous vaccines and biologic response modifiers to destroy pathogens prepares the body for the transplant procedure. If the body is highly toxic due to the presence of heavy metals and chemicals, then the BioTherapy Institute can administer very advanced detoxification procedures prior to the stem cell transplant. It is the BioTherapy Research Institute that applies the immune therapy protocols developed by the Stowe Foundation and our affiliated research and development teams spread throughout major universities and private research institutions.