Your Blood is Your Life
Blood carries much more importance than just being a vehicle for the distribution of nutrients and oxygen. Our blood is the most precious thing we have in the body. It carries all our thoughts, emotions, and memories and makes them available to every part of the body. Blood is the creator of life in our body and is different in every person. Each of us has a unique design of blood type, which is co-responsible for the uniqueness of our physical structure and personality. The categorization of blood into a few groups ignores this fundamental uniqueness of every human being.
There is only one type of blood for one person in the world. Blood carries decoded DNA, which knows what nutrients need to be sent where. It knows of and responds to all our needs, discrepancies, strengths, and weaknesses. The blood is filled with patterns and geometric designs that reorganize themselves according to our state of consciousness. Every new desire, feeling, or intention reprograms the blood instantly and all the parts of the body it is in contact with. When you take on another person’s blood you also take on his genetic information and part of his personality. The immune system can easily get depressed when foreign DNA (or several kinds of DNA if the blood comes from various donors) suddenly and unexpectedly enters a person’s blood through a transfusion. In many cases, the immune system is not able to fight off the many viral particles and toxins that are present in the donor’s blood.
The quality of our blood changes according to our thoughts, feelings, and emotions. Negative thoughts create toxic blood whereas happy thoughts make healthy blood. Fearful thoughts, for example fill your blood with adrenaline, loving thoughts flood it with interleukins. Both literally move your heart but with contrary effects. The adrenaline-shot causes panic to the heart; the interleukin-shot creates emotions of happiness in the heart and protects you against cancer.
Having a blood transfusion may create confusion and chaos within the body and mind. On the other hand, refusing a blood transfusion and not resorting to alternatives may put your life in danger. If you need a blood transfusion but prefer an alternative method contact the Blood Transfusion Society in your country. They may be able to put you in touch with a practitioner who is experienced in any of the above transfusion procedures. If you pretend to be a Jehovah’s Witness the hospital will arrange for an alternative approach.
Microcurrent therapy or blood electrification is the use of a very gentle current of electricity to cleanse the blood.
Despite the fact that electricity was used quite extensively as a health therapy in the 19th Century; that many patents have been filed proving the effectiveness of electricity for health and that microcurrents are used in the food industry to destroy pathogens … it is still not a mainstream medical tool.
Research at Albert Einstein College of Medicine in New York in 1991 piqued Bob Beck's interest in microcurrent therapy. This research involved the application of microcurrents to blood in the lab. The microcurrents neutralized the HIV virus … and other pathogens as well.
The research was first announced to the First International Symposium on Combination Therapies on March 14, 1991. The research was also reported in the March 30, 1991 issue of Science News:
"William D. Lyman and his colleagues found that exposure to 50 to 100 microamperes of electricity—comparable to that produced by a cardiac pacemaker—reduced the infectivity of the AIDS virus (HIV) by 50 to 95 percent. Their experiments, described March 14 in Washington, D.C., at the First Inter–national Symposium on Combination Therapies, showed that the shocked viruses lost the ability to make an enzyme crucial to their reproduction, and could no longer cause the white cells to clump together—two key signs of virus infection."
The researchers anticipated a microcurrent device would be developed for implant or that a dialysis approach would be used with microcurrents applied as blood was circulated outside of the body. William Lyman was also interviewed on Quirks and Quarks, a Canadian network radio program on March 30, 1991 about their promising research. Despite the fact they had found an inexpensive way to cleanse blood, their research was dropped.
Two sources for their research remain: US Patent #5,188,738 filed in 1993 and in 1996 the research paper was published in a medical journal, Surgical Technology International.
Bob Beck's genius found a simple way to apply these same microcurrents to blood without invading the body. He developed a system to place electrodes over the radial and ulner arteries on the wrist. Over the years, while enjoying the fruits of a successful career as an acclaimed physicist, Robert (Bob) C. Beck, D.Sc. maintained an interest in electro-therapy for health. When he heard that medical researchers had disabled viruses cultured in a laboratory with the application of microcurrents of electricity, his considerable intellect and ingenuity were aroused. While the medical researchers suggested the application of microcurrents similar to dialysis with the blood flowing out and then back into the body, Bob Beck developed a system to apply microcurrents to blood without invading the body. He developed a simple system for applying these microcurrents by placing electrodes over the wrist arteries. After considerable experimentation on himself, friends, acquaintances and a few individuals diagnosed with AIDS, all reaped some health benefit.
The results of a study conducted at the University of Washington are rather startling and indicate there should be a great upswing in microcurrent research. Researchers tested the microcurrent output of the Hulda Clark Zapper on white blood cells and leukemia cells. Keep in mind the Zapper is designed as a frequency unit. To generate frequencies, however, microcurrents are produced—usually minimal. The Zapper output proved safe on white blood cells while the Zapper proved to slow the growth of the leukemia cells in culture. The Zapper output is only 0.14 milliamp of a low-intensity time-varying electric current. This is much less than units used in The Beck Protocol.
Microcurrents are produced when frequencies are generated. The reverse is also true. When generating microcurrents, a frequency is produced. The Silver Pulser is designed as a microcurrent unit but it does emit frequency. The frequency matches that of the earth—1/2 of the Schumann frequency of 7.83 Hz.
Application of gentle microcurrents by electrodes placed on the skin is proving to be a valuable tool to help restore health.
FOR MORE INFO AND HOW TO DO IT SEE LINK BELOW
Anemia
“Building” blood can be the single most important task for you. If you have already begun getting transfusions, you know there is something terribly wrong with your blood-building organ—your bone marrow. It all hinges on iron.
Iron is more precious than gold to your body, as well as to bacteria, our iron “burglars.” They try to get it for themselves. The body’s strategy to keep it away from looting bacteria is to tie it tightly to two proteins: transferrin and lactoferrin
(“fer” means iron.)
Transferrin is the protein molecule that transports iron in the blood like a custom-made raft. It must sail on this raft to the bone marrow where it is used to make hemoglobin. If other metals take over this raft, iron can’t find its way to the bone marrow. Lactoferrin is another raft, but found in milk, tears, bone marrow, saliva, bronchial secretion, intestines, bile, urine, cervical mucous—obviously to keep iron away from the bacteria that enjoy living in these fluids. Both transferrin and lactoferrin are missing in cancer patients. This could be due to missing xanthine oxidase, a common oxidizer enzyme.
Making xanthine oxidase is somehow dependent on xanthine. Xanthine is one of the purines (quite similar to nucleic acid bases) typically missing in cancer patients due to clostridium bacteria. To restore your purines you must kill the invading clostridium bacteria. As soon as this is done, within twenty-four hours, everything is back in place. And transferrin is busily transporting iron again from your body’s storage piles.
Lactoferrin must be eaten before it gets reestablished. It is present in raw cows’ or goats’ milk and is not destroyed by sterilizing. Even one glass a week keeps lactoferrin reinstated. Goat milk does not have malonic acid and need not have vitamin C added.
To get your lactoferrin, choose a small beef bone with marrow in it. Place in water or broth. Boil 5 minutes. Then add HCl drops to sterilize. Eat it at least once a week. It is a delicacy.
Iron is necessary for your body in many ways, besides making hemoglobin for your red blood cells. Muscle activity depends on myoglobin—much like hemoglobin; it contains iron. Detoxification of cholesterol, hormones, assorted amines, even industrial chemicals that have entered the body is done by enzymes called cytochrome P-450s. They require iron. Nearly half the enzymes in the Krebs cycle need iron. The enzymes catalase, peroxidase and various dehydrogenases also contain iron.
Iron must not be in competition with copper, either. Copper water pipes and copper seeping from metal or plastic dental ware keep blood iron levels too low. So even when transferrin and lactoferrin are present, your body may be starved for iron.
Yet cancer patients cannot simply be given iron supplements...even if blood levels are low. It could do more harm than good.
To be useful, iron must be in its special state, called ferrous. There is no benefit in having a large pile of iron in the ferric state. (“Ferrous” has an “o” like “good,” to help you remember.) This is why the correct form of an iron supplement is ferrous, as in ferrous gluconate. Even this cannot be given safely.
While transferrin and lactoferrin move iron from place to place, ferritin, stores it.
Ferritin is a roundish ball of protein with tiny holes in the sides. Protein is sticky. Ferritin balls stick to old, worn out red blood cells, persuading them to give up their iron atoms which slip into the tiny holes to be trapped inside as ferric iron.
But here, ferric iron can do no harm, even though thousands of molecules pile up inside. Ferritin is equipped to handle it just like a hive is designed to hold bees. Ferritin then proceeds to store this rather dangerous iron until it can be recycled. This occurs mainly in the spleen and liver. But all cells have some ferritin; it is in their lysosomes.
Unfortunately, ferritin has an enemy, asbestos. Our bodies are riddled with tiny tufts of asbestos. We have inhaled some, no doubt, but we have eaten most of it in food. Our bodies are able to excrete a great deal of it in spite of its needle-like shapes. But the body uses ferritin, our sticky iron-storage protein, to coat and bundle-up these asbestos tufts. That bursts open your ferritin molecules.
Ferritin is full of recycled iron waiting to be converted to the ferrous form. Both reducers, cysteine and vitamin C, can do
Undoubtedly asbestos has oxidized cysteine and vitamin C, ruining their reducing power. But a supplement of methyl sulfonyl methane (popularly called MSM), a strong reducing agent, can substitute for them, and in just a few days reduce enough ferric to ferrous iron to correct the anemia and save the day.
Lanthanide metals block the availability of iron even when large stock-piles of iron exist. The lanthanides simply stick to them magnetically and both are removed together by wearing a weak magnet.
A lot can go wrong with iron! And it’s not over yet. Even if you fix all the problems mentioned so far, iron may still be secretly stolen by a silent chelator of iron: This is a very large molecule, similar to other PAHs that are made by Ascaris. Phenanthroline travels throughout the body attracting iron to itself, which turns it into ferroin.
And considering that phenanthroline is powerful enough to suck the iron right out of the center of enzyme molecules, it can probably suck up our “good” copper the same way. Double harm is being done. Simply killing Ascaris gets rid of the ferroin and phenanthroline.
With parasites and other toxins gone, the iron level promptly rises and may reach forty from a value below 35 in the first five days, getting to a more normal level of 50 to 60 in three weeks.
The moral of the story is: chances are you have plenty of iron already so you should only take an iron supplement in a life threatening situation. Excess iron could be dangerous.
The low iron level in cancer has been known a very long time and is referred to as “anemia of chronic disease,” which includes “anemia of malignancy.” The same things that cause cancer cause anemia, namely parasites, dyes, and toxic metals. It is, more accurately, “anemia from Ascaris, Clostridium, copper, germanium, lanthanide and asbestos toxicity.” It is the unavailability of iron in the midst of plenty (of iron) that strangles the cancer patient’s metabolism and ultimately causes fatality in roughly half the failing cases, not the tumors themselves. Fortunately when you clean up the causes of cancer, you automatically clean up the causes of this anemia.
Cancer sufferers have to be especially careful about taking iron supplements because some research indicates inorganic iron (including ferrous gluconate) promotes tumor growth. Yet, as stated already, exceptions to this rule exist, and when the blood level falls below 20 while at the same time the RBC is below 3.5, we supply it as ferrous gluconate, 33 mg (one a day for only 5 days).
All anemic persons should:
Kill clostridium bacteria to restore purines, including xanthine, so xanthine oxidase can be made again, restoring transferrin.
Restore lactoferrin by drinking raw milk (which you sterilize) or eating bone marrow.
Never drink water from copper plumbing; remove metal dental materials from your mouth.
Use safe sweeteners. Sugar has asbestos which damages ferritin.
Take MSM to reduce ferric iron into good ferrous iron.
Kill Ascaris to eliminate phenanthroline which robs iron.