Essential Ionizing Radiation Protection

With the growing concern of radiation heading our way, the #1 question on everybody’s mind this week is "What can we do to protect ourselves?"

Whether the danger is imminent or not, it’s clear that We Must Be Prepared.

“If ever there was a time for life style change, coupled with a demand for clean, unadulterated food, water and the protection and

support of the supplements that you need now and will need for the rest of your life, it is now. And if ever there was a time to call for the total banning of the two most dangerous misapplications of science in human history, GMOs and nuclear power, that time was yesterday. We missed yesterday so today is the time, and tomorrow and all the tomorrows that these disasters still allow us.” Dr. Rima

Japan's Reactors Are Leaking Radioactive Waste Which Is

Heading Towards the US and Europe

Radiation detoxification:

1) Potassium iodide KI or KIO3, Lugol’s solution works. Iodine has low toxicity: most people are iodine deficient so

high doses are advised. Just a couple (2 to 4) per day sipped in juice. Foods that may prevent the body from using iodine are: turnip, cabbage, mustard greens, cassava root, soybeans, pine nuts and millet. These foods are called goitrogens and excessive consumption can cause goiters so if you are using them temporarily, eat them raw. Iodine is sold as a dietary supplement, but if sold to protect the thyroid from radioactive iodine emitted by a reactor accident might be considered a "prescription drug" so remember, you are obtaining it to supplement your diet.

2) Sulfur containing, thiol rich compounds like MSM and foods like asparagus. Use Innerlight's Mycodetox I and II.

3) Alkalizing green diet and agents such as pH Miracle's pHour salts, pHlush salts and pHlavor salts (pHour salts which contains sodium, magnesium, potassium and calcium bicarbonate away from food, lemon juice in water).

4) Drink 4 to 6 liters of clean, pure and ionized water at a pH of over 9.5 and -250 mV, everyday. Put 5 drops of pH Miracle's Activator in all drinking water.

Minimum radiation doses which damage tissue

The relative sensitivity of various body tissues gives a good idea of the wide range of symptoms the body would likely experience due to heavy doses of radiation. The radiation exposure numbers below represent the minimum damaging doses for body tissues. The unit of dose is the “gray” (abbreviated Gy) which is roughly equivalent to a sievert. The gray represents the absorption of an average of one joule of energy per kilogram of mass in the target material and this new unit has officially replaced the “rad,” an older unit (One gray equals 100 rads):

Fetus–2 grays (Gy).

Bone marrow–2 Gy.

Ovary–2-3 Gy.

Testes–5-15 Gy.

Lens of the eye–5 Gy.

Child cartilage–10 Gy.

Adult cartilage–60 Gy.

Child bone–20 Gy.

Adult bone–60 Gy.

Kidney–23 Gy.

Child muscle–20-30 Gy.

Adult muscle–100+ Gy.

Intestines–45-55 Gy.

Brain–50 Gy.

5) Intravenous chelation or oral supplement your diet with Glutathione, N-acetyl-cysteine and L-taurine. These powerful antioxidants are said to remove radioactive heavy metals. If the contamination is ongoing, the chelation needs to continue.

Acute Radiation Sickness Symptoms

Nausea and vomiting

Diarrhea

Skin burns (skin reddening)

Weakness

Lethargy and fatigue

Loss of appetite (anorexia)

Fainting

Dehydration

Inflammation of tissues (swelling, redness or tenderness)Hemorrhages under the skin

Bleeding from your nose, gums or mouth

Anemia (low red blood cell count)

Hair loss (usually from just the scalp)

Decrease in platelets

6) L-Glutamine may help rebuild the gut if the GI tract is damaged

7) If the blood systen is impacted, pH Miracle Greens, liquid chlorophyll and green fruit and vegetables will be helpful in building new healthy red blood cells and useful to rebuild the white blood cells.

Cancer may strike about 4.5% of people exposed to radiation in the 1-Gy range, and one-quarter of those individuals will likely contract leukemia. Data from Hiroshima residents showed an increased frequency of lymphocyte chromosomal transmutations after the blast and workers involved in the Chernobyl cleanup showed a 20% increase in transmutation frequency.

All of the well-known cancer preventives become critically important. Radiation damages the alkaline buffering system which protects us from cancer and inserts an agent which damages our genetic make-up leading, much as GMOs do, to foreign proteins being coded for by that damaged DNA. The biochemical (i.e., nutritional) protections like abundant antioxidants, avoiding acidic toxins (including GMOs and chemically produced food, dental and other x-rays, TSA scanners, etc.) become crticially important at this time. The danger of "ionizing radiation" exposure is not just short term. When the reactors are capped and controlled, you will still be dealing with the long term dangers associated with acidic "ionizing radiation" exposure, in essence, for the rest of your life.

Physical safety and protection during a radiation emergency

1) Close all doors and windows and fireplace dampers (exposed to outside air).

2) Turn off all fans, air conditioners and heating units that bring in air from the outside (since it may be contaminated).

3) Bring the family and pets inside.

4) Move to an inner room or basement because it affords much higher radiation shielding.

If you are advised to evacuate, follow the directions provided and leave the area as quickly as possible; it may not be possible to self-shield at home, but if that is possible, that may be your safest option. If you have to leave, take along a flashlight, portable radio, batteries, first-aid kit, supply of sealed alkaline food and water, can opener, nutritional supplements, and sufficient cash and credit cards.

Protective Steps to Take

1) Iodine supplements are effective in blocking thyroid uptake of radioactive Iodine, but have NO OTHER PROTECTIVE EFFECT – NONE! If you do not have Potassium Iodide tablets or supplement-grade iodine, use tincture of Iodine by painting it on your skin: paint 8 ml of a 2 percent tincture of Iodine on the abdomen or forearm approximately 2 hours prior to contamination. That would be now. Do it daily until further notice. You will probably notice a general increase in your general health and well-being, as many people are chronically Iodine deficient; but do not over do it!. Do not drink or swallow other forms of iodine because they are poisonous. Do not drink Betadine or iodine water purification tablets!

2) Take 1, 130 mg. tablet of KI or KIO3 every 24 hours. Reduce dose based on the weight of children. Nursing and pregnant women should take the adult dose and infants should receive 1/8 tablet.

3) Cobalt 60 is believed to be drawn out of the body with an Epsom Salts bath or our Deep Sea Hawaiian Salts, available soon at www.phmiracle.com

Instructions: Dissolve 1 pound of Deep Sea Hawaiian sea salt or rock salt and 1 pound of sodium bicarbonate soda in a warm bath and soak into an alkaline bath water until the bath becomes cool. This usually takes about 20-25 minutes. Afterward, do not shower or rinse the Deep Sea Hawaiian salt off your body for 4-8 hours.

4) A pH Miracle Activator bath is believed to remove heavy metals (a serious problem in nuclear reactor accidents) and chemical contaminants. Take 1 two ounce bottle of pH Miracle Activator and empty into a warm bath and soak for at least 20-25 minutes. Do not wash off for at least 4 hours and make sure you use sufficient alkaline water at a pH of 9.5.

5) A pH Miracle pHour Salts Bath Instructions: Just add 1 cup of pHour salts to a tub of hot water — as

can be tolerated — and once again soak in it until the water becomes cool or body temperature. Don’t wash off for at least 4 hours and make sure you’re using sufficient water. Use a lot of alkaline water and do not increase the amount of bleach.

During these baths, it is advisable to sip 1/2 teaspoon of phour Salts (sodium bicarbonate) in warm water with radioactive fallout. I recommend a stronger mixture of drinking an 8-ounce glass of water containing ¼-teaspoon natural Deep Sea Hawaiian sea salt (pH Miracle brand) and ¼-teaspoon pH Miracle pHour Salts. According to the severity, drink every 2-3 hours and each glass is to be taken with 4 capsules of pH Miracle's pHlush. If you are experiencing symptoms in the head, sinuses, chest, glands, neck, throat, then add ¼-teaspoon of fresh organic lemon juice to the mixture. Once again, don’t shower for at least 4 hours after the bath.

6) pH Miracle's Terra Cleanse montmorillonite clay baths are important detoxification strategies. Follow the instructions on the product. Do not do detox baths more than once a day. You can also take 1 scoop of the pH Miracle Terra Cleanse in 3 to 4 ounces of alkaline water and sip while take a detox bath.

7) Organic, uncontaminated wakame, kombu and other seaweed, Hokkaido pumpkin, and pH Miracle's Deep Sea Hawaiian salt are traditionally held to be protective against radiation, as the clinical results of atsuichiro Akizuki, M.D in a hospital outside of Nagasaki showed.

8) All acidic forms of sugars and sweets suppress the immune system for up to 6 hours and MUST BE AVOIDED at all costs.

9) 5 grams of pH Miracle green powder per day is protective against radiation sickness, according to the clinical experiences of doctors in Russia following Chernobyl. In fact, Russian health authorities declared that wheat and barley grasses accelerates the evacuation of radionuclides from the human body. Wheat and barley grasses found in the pH Miracle Greens contains large amounts of beta carotene, a compound which prevents acid damage to cells and is useful in treating and prevention of cancer, and free iron, which helps people recover from the anemia which leads to a great many of the radiation-related problems following exposure.

10) Wheat and barley grass contained in the pH Miracle Greens also contains high proportions of metallo-thionine compounds which combine with radioactive metals so they can be eliminated.

11) Sodium alginate (Alginic acid) is found in kelp, bladderwrack and Nori seaweed. Their consumption allowed many Japanese atomic bomb victims to survive since Sodium alginate binds with radioactive strontium. If this is accurate, kelp with its Iodine content may be doubly beneficial in the current circumstances.

12) Eating members of the kelp family, including kombu, sea palm, wakame, nori is a very, very good idea, but it must not come from the Pacific AFTER this radiation accident! Liquid chlorophyll is said to have a radioprotective effect because it is held to absorb gamma rays emitted from the radioactive particles in your body following contamination. A chlorophyll rich diet increases the survival of experimental animals after lethal doses of radiation.

13) I do not recommend zeolyte compounds because they are highly acidic with a pH of 1 to 2, and contain a toxic aluminum compounds.

14) The Schuessler cell salts contained in all of my InnerLight products which will be needed after radiation exposure are contained in my Mega-Multi Vitamin:

Calcarea Phosphorica (Phosphate of Lime), abbreviated as Calc. Phos

Kali Phosphoricum (Phosphate of Potash or Potassium) or Kali. Phos

Magnesia Phosphorica (Magnesium Phosphate) or Mag. Phos.

Natrum Phosphoricum (Phosphate of Soda) or Nat. Phos.

Ferrum Phosphoricum (Phosphate of Iron) or Fer. Phos.

Natrum Sulphuricum (Sulphate of Soda) or Nat. Sulph.

Kali Sulphuricum (Sulphate of Potash) or Kali. Sulph.

Calcarea Sulphurica (Sulphate of Lime) or Calc. Sulph.

Kali Muriaticum (Chloride of Potash) or Kali. Mur.

Natrum Muriaticum (Sodium Chloride) or Nat. Mur.

Calcium Fluorica (Fluoride of Lime) or Calc. Fluor.

Silicea (Silica)

.

Ralph Fucetola JD has an Interesting site, with a USA map of radiation detectors updated every 3 minutes: http://www.radiationnetwork.com/

Cesium 137 is a serious problem and is currently being emitted by the radiation contamination in Japan. Foods high in Calcium and Potassium are very helpful in replacing it and helping it to be eliminated from the body.

15) Vitamin D is depleted by Strontium 90 so extra pH Miracle Vitamin D3 is a very good idea. Lots of Vitamin D3 — at least 50,000 IU per day is generally a good idea for supporting the immune system. Iodine, Zinc, Calcium and Sulfur are important supplements as well to prevent their radioactive counterparts from becoming part of your biology. I strongly recommend our pH Miracle high potency mineral supplement, called pH Miracle Minerals and MSM called MycoDetox II on a daily basis except when you are having a chelation treatment. Other minerals which are both protective and important on their own for healthy functioning includes selenium, vanadium and boron.

16) Nutrients should be taken in high potency supplements as well including lycopene, beta carotene (mentioned above) and, of course, the grand daddy of all the acid quenchers, high doses of glutathione, NAC, and alpha lipoic acid. I would suggest taking 2 500 mg capsules of pH Miracle Gluthathione, 1 capsule of NAC 3 times a day and 1 capsule of R-factor lipoic acid 3 times a day. To potentiate Gluathione take 1 capsule of phosphotidyl choline 3 times a day. All of these products are available by going to: wwww.phmiracle.com Our pH Miracle baby organically sprouted Soy protein powder, which contains high amounts of cysteine, are also often given to cancer patients (one tablespoon daily) because of their high cysteine content which allows the body to make more anti-oxidant glutathione.

17)

Chlorophyll-containing foods and supplements containing wheat, barley, and kamut grass found in the pH Miracle greens should be added to all alkaline water with 5 drops of Activator and 1 ounce of liquid chlorophyll.

Chlorophyll closely resembles human blood and is used to cleanse, detoxify, purify and heal many conditions. It prevents bacterial and yeast growth or transformations from existing body cells, detoxifies heavy metals from the body, increases wound healing, detoxifies the liver and other organs, deodorizes the body, removes putrefactive bacteria from the colon, aids healing of 11 types of skin diseases, relieves ulcers, gastritis, pancreatitis and other inflammatory conditions, helps heal gum diseases, and inhibits radiation and the metabolic activation of many carcinogens. Many studies have reported the protective effects of chlorophyll on irradiated animals.

18)

Coenzyme Q10 or the pH Miracle Co-Factor 10

This substance protects against many chemicals and radiation, offering immense benefits to the supporting of the immune system and retarding the aging process caused by acidosis. Sufferers of heart problems, high blood pressure, angina, and obesity often find this substance to be helpful in managing symptoms. Natural levels decline with age; therefore, supplementation is needed. Try our liquid Co-Factor 10 at least 3 times a day as directed.

19)

Proanthocyanadins (Grape seed extract/Pycnogenol)

Considered to be one of the most powerful antioxidants or free acid scavengers, grape seed extract helps counteract stress, pollution and radiation. I would recommend taking InnerLight's Pronogenol, 2 capsules 3 times a day.

20) Wheat and Barley Grass Powders

Wheat and b

arley grass is a totally alkaline food. It contains all of the nutrients required for life, vitamins, minerals, alkaline buffers and other proteins (amino acids), essential fatty acids and chlorophyll. Wheat and barley grass has thousands of living phyto-nutriients (a special protein). Phyto-nutrients are nature’s biological catalysts that initiate all the chemical transformations in the body. Over 3,000 phyto-nutrients have been identified. They are required for every transformation in the body – digestion, cell respiration, bodily movements, thinking processes, detoxification, cancer control, fat, protein and carbohydrate metabolism, etc.

The normal daily amount of pH Miracle Greens which contains wheat and barley and even kamut grass is 1-3 teaspoons (1 tsp = 2 grams) in 1 liter of water and drinking a minimum of 4 liters a day.

An alkaline body can heal itself … but it needs your help. It’s important to pay close attention to the foods and dietary supplements you consume. Here’s why.

Diet and your body’s susceptibility to radiation are closely entwined. Radiation and pollutants destroy vitamins A, C, E, K several N vitamins, essential fatty acids, calcium and the endocrine glands. If your body lacks calcium or potassium and other nutrients, it will more readily absorb the radioactive elements that are similar in structure to these nutrients.

Your best bet is to eat alkalizing, natural, fresh, organic (as much as possible) unprocessed foods, avoiding, all sugar, all animal protein, all grains, all dairy products, all acidic drinks including coffee and tea.. Here is a list of widely recommended foods and food supplements that can help to balance your body chemistry. This list is by no means exhaustive, but it will give you a good starting place.

1)

Calcium/magnesium

The New England Journal of Medicine reported that calcium may prevent pre-cancerous cells from becoming cancerous. It also protects against strontium 90 (similar structure to calcium) and other radioisotopes.

2)

Vitamin A or beta carotene

This vitamin manufactures antibodies, maintains and protects mucus membranes, and protects the thymus gland, the master gland of the immune system. It helps guard against tumor formation and cancerous cells, as well as reverses aging process of the skin caused by acids and their reaction with ultraviolet light.

3)

Vitamin E

Neutralizes harmful acidic "ionizing radiation" radicals and protects delicate tissue membranes.

4)

Zinc

Helps strengthen the T-cell-producing thymus gland. Aim for 50 to 100 mg daily of the Nutrient Bridge which would be 2 capsules 3 times a day.

5) Selenium

Selenium buffers the acids that cause cancer and protects against acidic carcinogens, by helping to produce an alkaline buffer called glutathione peroxidase.

Protective Foods

1)

Cruciferous alkalizing vegetables (cabbage, Brussels sprouts, broccoli, turnips, cabbage, spinach, cauliflower, and greens such as kale).

This family of alkalizing vegetables contain substances that inhibit breast and colon cancer cell growth. Cabbage and other cruciferous vegetables also contain dithiolthiones, a non-toxic group of compounds that have antioxidant, anti-cancer and anti-radiation properties.

Sources include dark, leafy vegetables (broccoli, spinach, kale, Swiss chard, ro¬maine, endive, chicory, escarole, watercress, col¬lard, mustard and dandelion greens), dark yellow and orange vegetables (carrot, sweet potatoes, yams, pumpkins, winter squash) and fruit (avocado, lemon, lime, peppers, jicama, tomato, cucumbers).

2)

Sea vegetables and their products

Sodium alginate, a non-nutritious extract from Pacific seaweed used to bind and detoxify heavy metals from the body (such as lead, mercury, cadmium, etc.), and agar, used as a thickening agent instead of gelatin or corn starch, will protect the human body from radiation effects. They also reduce absorption of strontium 90 by 50-80%

3)

Kelp and dulse, excellent natural sources of iodine, help protect against radioactive iodine. When the diet is adequately supplied with organic iodine (as in kelp), radioiodine is not as readily absorbed by the thyroid or the ovaries. Kelp contains 150,000 mcg of iodine per 100 grams (32 ounces). The RDA of iodine is 150-200 mcg. A reasonable daily dose of kelp would be 1-2 teaspoons of granules or 5-10 tablets.

4)

Foods containing a natural Vitamin A

Such as lima beans, asparagus, tomatoes, onions and spinach), fruit, (avocado, grapefruit, lemon and lime plus the white under the peel and pulps of sweet fruit like oranges), all unsprouted seeds (especially sunflower, sesame and pumpkin), all nuts (especially almonds and hazel nuts), leafy cherry flowers, apple blossoms, and all grasses, such as wheat, barley, kamut, straw and dog grasses.

5)

Essential fatty acids, GLA and EPA

EFAs are essential for proper functioning of the immune system and protects against the acids that cause cancer. Food sources include flax seed oil, hemp seed oil, and borage seed oil. I would suggest 2 to 3 tablespoons of our pH Miracle Omega 3, 6 and 9 to help protect against "ionizing radiation." You can order by going to: www.phmiracle.com

But wherever you do, protect yourself!!!!!! Read the pH Miracle Revised and Updated and especially study the protocol for good health, energy and vitality in Chapter 11.

More about → Essential Ionizing Radiation Protection

How To Protect Yourself From Nuclear Fallout and Ionizing Radiation

How do you protect yourself from the nuclear fallout of "ionizing radiation" coming our way NOW!!! from Japan that can cause serious illness and disease?

It is important to understand that "ionizing radiation," that can cause destructive body tissue damage from nuclear radiation exposure is the "effect" of nuclear radiation, which is caused by the removal of electrons from atoms, creating hydrogen ions or protons or environmental acids that can destroy animal or human life!

In the case of nuclear radiation or "ionizing radiation," tissue damaging hydrogen ions or acids from the environment can lead to serious illness and disease, causing cancer, leukemia and neurological disease, just to name a few!

Oxidation or fermentation is either the loss of electrons or the gain of protons or hydrogen ions (H+). All acids are proton or hydrogen ion (H+) donors, and therefore oxidizing or fermenting agents to the blood and tissues. When the body tissues are exposed to strong "ionizing radiation" or acids, whether from the environment (Japan's Fukushima Daiichi Nuclear Power Station), or from diet or from metabolism they can cause body tissue damage leading to serious illness and disease.

I

just received these video reports about the nuclear meltdown at the Fukushima Daiihi Nuclear Power Plant in Japan due to the earthquakes and tsunami. The radiation leakage from this nuclear plant is coming to the United States, Canada and other countries NOW!!!! PLEASE TAKE HEED AND WATCH ALL THE VIDEOS AND SEE THE LINKS BELOW NOW AND BE INFORMED. http://www.youtube.com/watch?v=WEsHbN-75e8&em_link=4aa1cfdd-8fd2-4ceb-8199-f6a6e3cbfead TO COMBAT THE ACIDIC EFFECTS OF "IONIZING RADIATION," YOU WILL NEED TO IMMEDIATELY START TAKING pHour Salts formula by pH Miracle, which contains reducing agents of "ionizing radiation" or acids in the form of sodium, magnesium, potassium and calcium bicarbonate. http://phmiracleliving.com/p-221-phour-salts.aspx I have also prepared a special formulation of mineral salts from the deep sea in Hawaii, called Liquid Mineral Gold, which contains iodine as well as high concentrations of alkalizing mineral salts to protect the endocrine system, including the thyroid from destructive "ionizing radiation." http://phmiracleliving.com/p-211-phlavor.aspx Finally, I would suggest drinking pH Miracle Greens, eating liberal amounts of green fruit and vegetables and especially drink electron-rich ionizing water made from our Chanson Water Ionizers. http://www.phmiracleliving.com/p-562-ultra-water-pack.aspx http://www.phmiracleliving.com/p-558-ph-miracle-greens.aspx Bottom line - To protect yourself from "ionizing radiation" you must maintain the alkaline design of the body with an alkaline lifestyle and diet. Read The pH Miracle Revised and Updated to learn how to protect yourself from hydrogen ions or acid created from "ionizing radiation." http://www.phmiracleliving.com/p-552-the-ph-miracle-revised-and-updated.aspx

More about → How To Protect Yourself From Nuclear Fallout and Ionizing Radiation

The Cause Of Polio - Mass Acidic Poisoning

Polio in the United States - Graphic Timeline: US 1870 - 1998

This graph shows polio in the United States in a context rarely (if ever) portrayed since Biskind, the environmental context. "DDT" and "DDT-like chemicals" are selected for this graph as the least complex way to represent the a broad overview of the evolution of the technology of, and potential for, mass poisoning. Some prominent organochlorines are chlorobenzene, PCBs (polychlorinated biphenyls) and DDT (dichloro-diphenyl-trichloroethane). Chlorobenzene is a precursor, a foundational compound used in the production of many industrial organochlorines. In the U.S., high production of chlorobenzene began in 1915, soon after the beginning of World War I.

This graph is a compilation of new cases per year (not incidence, as portrayed elsewhere herein). The data for the last half of the 20th century was gathered from U.S. Vital Statistics. The very earliest numbers, from 1887 to about 1904, and the postpolio numbers, are interpolated from the general historical commentary regarding those periods (see bibliography on Homepage and NYC Health Commissioner Haden Emerson's compilations). While the graph is not perfectly accurate, due to changing methods of diagnoses and record-keeping within the medical system, it does give a reliable overall picture of polio cases in terms of known literature and records.

The source for the U.S. and Swiss discoveries of paralysis in calves is from Van Nostrand's Encyclopedia of Science and Engineering (1995), vol. 5, p1725. The phrase "Pesticides As A Panacea: 1942-1962" is a subtitle found in Encyclopedia Britannica, Macropaedia (1986). Refer to other graphs (Overview) for specific pesticide comparisons with polio incidence.

In 1915 Hooker Electrochemical began massive, unprecedented production of chlorobenzene (8,200 metric tons per year) and Dow Chemical began large-scale production soon thereafter. Chlorobenzenes are the basis for picric acid explosive used in World War I. They have also been used in the manufacture of wood treatments, war gas, herbicides, insecticides, bactericide, moth control, and polymer resins. (Mono)chlorobenzene is the base compound for DDT production. Currently in the U.S., 15 million pounds of p-dichlorobenzene production goes into room deodorants. According to Duesberg, CDC's investigation into Legionnaires disease ignored toxic cause and created a new false field of study regarding the Legionella bacterium.

The sudden surge of chlorobenzene production coincides in time and place (1915, Niagara Falls) to be considered as probable cause for the epidemic of central nerve system diseases that followed the next year in the New York City region. This epidemic lasted only six months, June to November, with 82% of the cases occurring in just 8 weeks. While polio literature terms this a world-wide polio epidemic, it was peculiarly a phenomena of the U.S. and was especially prominent in the New York City region. This is strange behavior for a supposedly predatory poliovirus, in an era, a continent, wholly unprotected by miracle vaccines.

The number of new cases for 1916 (40,485) were calculated by multiplying the U.S. incidence rate by the U.S. population. The number seems too high because of Naomi Rogers' statements that worldwide new cases in 1916 were 27,000, that two-thirds of world polio new cases were in the U.S. and that New York City new cases were 9,000. While this discrepancy exists, the data is still useful for showing relative case numbers and/or incidence for the early 20th century.

Both polio epidemics occurred two years after the beginning of a world war, if we use the dates of the epidemics, 1916 and 1942.

DDT and "DDT-like chemicals" are used to represent the major organochlorine pesticides and organochlorines of similar neurotoxic character. Most of the industrial organochlorines can produce CNS disease symptoms similar to polio. Refer to the Overview for graphs on DDT and other neurotoxic pesticides compared to polio incidence.

Critique of Dominant Images

It certainly appears, from the graph, that the vaccination programs arrived a few years too late to be credited for declining polio case numbers. The programs were close enough, however, for media to shoehorn them into their historical position. This quote from Time Magazine (March 28, 1994) is a typical example:

The great postwar epidemic peaked in the U.S. in 1952, when more than 20,000 children were paralyzed by polio and it tapered off in the early '60s, after the Salk vaccine and then the Sabin oral version were introduced.

This smooth, loaded phrase, framed with glossy photos and clever captions, goes down like lubricated jello. However, if we contain our admiration, and review the actual data, we realize that the great polio epidemic actually occurred from 1942 (or gradually, beginning decades earlier) to 1962, that is, it was not a "postwar epidemic". The epidemic declined not "in the early '60s", but a full decade earlier, in the early 1950s. Polio cases per year did not "taper off... after the Salk vaccine" as Time would have us believe -- new cases per year dove resolutely downward two years before the Salk vaccine field trials and four years before the vaccination programs were firmly underway. The decline of polio actually occurred after heated discussions regarding the dangers of DDT that began with in-house government/industry reviews of DDT in 1951, following Biskind and other's criticism of pesticides which began in 1949. These discussions were followed by a phase-out through industry compliance, a huge shift of sales to third-world countries, a phase-in of less-persistent pesticides, which was facilitated by legislation in 1954 and 1956, a renewed public image regarding the proper use and dangers of pesticides, the cancellation of DDT registration by 1968, and eventually the official ban of many of the persistent organochlorine pesticides by 1972 (in U.S. and developed countries).

Notice that while pesticide production directly correlates with new polio cases per year through every peak and valley, the Salk vaccine enters only after polio's decline. Salk's point of entry is not sufficient evidence to be routinely offered as proof for the victory of vaccines over the poliovirus, as Time implies, and as implied by Hayes and Laws, and virtually all other presentations of polio history in whatever media or educational forum.

The molecular biologist, Peter Duesberg, in his attempt to give Modern Medicine some credence with regard to virus causality (before refuting HIV causality with AIDS), apparently felt he could assume, in Inventing the AIDS Virus, that,

...the sudden, frightening polio epidemic that exploded in the Western nations, brought home by troops returning from the Pacific theater in 1945.

Yet a glance at the graph show his statement to be inaccurate. Polio was entrenched in the U.S. long before returning troops, and the increased polio cases per year correlate much more consistently with pesticide production (see Overview) than returning troops. A rise in new cases per year that peaked in 1945 can be clearly attributed to the government's release of war surplus DDT to the public market in 1945, not vague data about "troops returning from the Pacific theater in 1945". The troops were heavily treated with DDT years before the U.S. civilian population and as can be expected, in light of the acidic poison-theory, the troops suffered unusually high polio incidence rates when compared to the non-treated populations where they were stationed, and soldiers based in the U.S. (Biskind). The unusual drama and rash assumption that fills this excerpt of Duesberg's writings gives a sense that he has taken the whole package of ingrained polio images for granted.

Pesticide Phase-out and Vaccinations

DDT and BHC were phased out from the developed nations and at the same time vaccination programs were dramatically credited with saving these countries from the ravages of the poliovirus (see Homepage). However, the banned pesticides continued with higher than ever total distribution in the under-developed countries thanks to W.H.O.'s anti-mosquito campaigns, where to this day acute flaccid paralysis (AFP), polio, and DDT/BHC still prevail. DDT application, DDT phase-out programs, and polio vaccination programs are all being directed in these countries concurrently by the World Health Organization with little or no success.

Registration for DDT was canceled in 1968. and DDT was banned by the EPA in 1972 -- after the major organochlorines (DDT, BHC) had been gradually phased out of the U.S. market by the chemical industry and replaced with the less environmentally persistent pesticides, the organophosphates.

Post-polio

Pesticides

In 1983, via new legislation, DDT was allowed back into the U.S. marketplace, but only in pesticide blends. Within only a few months of this re-entry, a new kind of polio epidemic suddenly occurred. It was labeled "post-polio", the re-emergence of polio symptoms in former victims. This has involved approximately 600,000 victims and is the graph above. Like most of the data, this correlation is not even a whisper in the mainstream media.

Central nervous system diseases other than polio continue in the U.S. and throughout the world: acute flaccid paralysis, chronic fatigue syndrome, encephalitis, meningitis, muscular sclerosis, and rarely in humans, rabies.

The harsh realities of government policy are stated in Casarett and Doull's Toxicology (1996):

Although government agencies and industry have been slow in their reevaluation of a vast array of pesticides in use, reassessment often comes in the wake of or concomitant with some recently disclosed adverse environmental or health effect.

This after-the-fact approach to pesticide poisoning is puzzling enough without questioning Casarett and Doull's careful usage of the words: "often", "some", "recently", and "disclosed".

The acidic environmental correlations of post-polio are overlooked. Searching PubMed has been in vain. Recently, however, I found online a paper entitled "The Environmental Aspects Of The Post Polio Syndrome". It's website modification date is May, 1999. This article establishes a strong correlation between environmental factors and post-polio (see http://www.aehf.com/articles/A56.htm).

By searching PubMed on "environment and post-polio" a listing for the above article was found:

Rea WJ, Johnson AR, Fenyves E, Butler J.
Related Articles

The environmental aspects of the post-polio syndrome.
Birth Defects Orig Artic Ser. 1987;23(4):173-81. No abstract available.
PMID: 3620615; UI: 87299998

No other similar articles were found, and no abstract was available, although it presumably could be ordered from PubMed.

Poliovirus Presence In Post-Polio

According to immunity and vaccination theories, if anyone should be immune to polio, it should be former polio victims, however, numerous studies of post-polio victims have found evidence of active poliovirus.

From NIH's PubMed, four studies:

PMID: 7611631, UI: 95336052 (London, May, 1995) This study also quotes "a previous study"
PMID: 7611630, UI: 95336051 (Bethesda, MA, May, 1995)
PMID: 8818905, UI: 96415998 (Lyon, France, Aug., 1996)

Polio images are projected as if this data doesn't exist. It does not appear that money is being funneled into these kinds of studies.

Farr's Law

Farr's Law requires, for an epidemic to be a valid example of contagion, that the epidemic increase its incidence rates exponentially. Since polio has been ubiquitous since the beginning of human history, its incidence rate should have peaked long ago and universal immunity conferred, if immunity was ever required, and if the poliovirus was actually a predator.

Polio's non-compliance with Farr's Law is explained by viropathologists with a unique argument, the inverse of the argument usually given to support germ theory. The argument is that the poliovirus, which has been intimate with mankind since the beginning of history, suddenly became estranged from humans because of modern hygiene, and thus humans lost their natural immunity to the virus. So it is modern hygiene and the resulting lack of exposure to the virus that is said to have caused the polio epidemics to rage as never before.

It is interesting that for only one brief moment, viropathologists are willing to become eco-nutritional types who appreciate the value of natural breast feeding and the importantance of the internal microbiological ecology conferred positively upon humans by dirt.

Three different promotions of their inverse argument follow:

(1) The prominent book on polio history by Naomi Rogers, where the inverse argument resides in the title, Dirt and Disease: Polio Before FDR. The language style here is popular.

(2) In Textbook of Child Neurology (1995), John H. Menkes promotes the inverse argument with scientific language style:

Poliomyelitis... is less likely to be symptomatic in areas with inadequate sanitation, because poor sanitization is conducive to exposure at an age when lingering transferred maternal immunity can attenuate the clinical picture. (p420)

(3) In the propaganda film, A Paralyzing Fear: The Story of Polio in America. This was funded by the government and pharmaceutical firms and released in 1998.

The New York Times (March 4, 1998) reviews the film. It reinforces the fundamental tenets of polio culture, beginning with a quotation from a section that portrays a "vintage film clip":

"My name is virus poliomyelitis," intones a cultivated, sinister male voice, as a camera pans over fair-weather clouds from which a hollow shadow emerges carrying the silhouette of a crutch. "I consider myself quite an artist, a sort of sculptor," the voice continues. "I specialize in grotesques, twisting and deforming human bodies. That's why I'm called The Crippler."

Having dramatically demonized the poliovirus, the medical cavalry rides to the rescue:

...the epidemics grew steadily worse each year, with the number of new cases climbing from 5,000 in 1933 to 59,000 in 1952. Salvation came in 1954 with the Salk vaccine...

And the inverse argument is now fit to print:

The irony of the rise of polio in the 20th century, the movie reports, is that its prevalence was a result of improved sanitation. In grubbier times, babies and very young children developed antibodies to the disease, which had been around forever. A cleaner environment left increasing numbers of children with no natural immunity.

So The New York Times review concisely presents the standard polio images: the predatory virus, paralytic horror, epidemics, salvation via the Salk vaccine, and a unique exception from Farr's Law. I doubt anyone at NYT actually wrote the piece, rather that it was supplied to the journalist as a suggested article, to be adjusted to the author's style, thus essentially a customized press release.

Graphic Timeline: U.S. 1912-1970

The graph provides greater detail for the U.S. period of 1912-1970, and summarizes the vaccination issues mentioned above.

The Epidemic Intelligence ServiceDuesberg's Inventing The AIDS Virus (1996):[The CDC's] disease-control mission was increasingly being regarded as obsolete, prompting serious discussions about abolishing the CDC altogether.The situation changed in 1949 when the CDC brought on board Alexander Langmuir, an associate professor at the Johns Hopkins University School of Hygiene and Public Health. Langmuir was the CDC's first VIP, bringing with him both his expertise in epidemiology (the statistical study of epidemics) and his high-level connections -- including his security clearance as one of the few scientists privy to the Defense Department's biological warfare program...

...Langmuir and talked public officials and Congress into giving the CDC contingent powers to deal with potential emergencies... In July of 1951 he assembled the first class of the Epidemic Intelligence Service (EIS), composed of twenty-three young medical or public health graduates. After six weeks of intensive epidemiological training, these EIS officers were assigned for two years to hospitals or state and local health departments around the country. Upon completing their field experience, EIS alumni were free to pursue any career they desired, on the assumption that their loyalties would remain with the CDC and that they would permanently act as its eyes and ears. The focus of this elite unit was on activism rather than research and was expressed in its symbol -- a shoe sole worn through with a hole. According to British epidemiologist Gordon Stewart, a former CDC consultant, the EIS was nicknamed the "medical CIA."

The Director Of Polio Research

The National Foundation For Infantile Paralysis (NFIP) used the "The March Of Dimes" to fund its polio research which lead to the Salk vaccine field trials in 1954. The Director Of Polio Research was Dr. Henry Kumm.

According to the brief sketch in American Journal of Digestive Diseases, May 1953, Dr. Kumm was born in Wiesbaden, Germany. He came to the U.S. via Britain and became an American citizen in 1945. He had spent 23 years on the staff of the Rockefeller Foundation for Medical Research before joining the NFIP in July, 1951.

In April 1953, Dr. Kumm replaced Dr. Harry M. Weaver as Director Of Polio Research at NFIP.

During World War II he had served as civilian consultant to the Surgeon General of the U.S. Army in Italy, directing field studies for the use of DDT against malarial mosquitoes in the marshes near Rome and Naples.

As Dr. Kumm is a prominent DDT consultant, there is definitely a conflict of interest for this key player in polio research.

Earlier in his career Dr. Kumm worked extensively on transmission modes of the disease, yaws. He also worked with the Jamaican Yaws Commission. Scobey refers to allegations that arsenic injection treatments for yaws had caused an epidemic of polio in Samoa in 1936.

It is not presently known to what extent these events also could have compromised Dr. Kumm's position regarding polio.

Timeline: U.S. 1945-1957

1945, DDT was released to public and aggressively promoted, against FDA advice.
March, 1949, Biskind's "Poisoning and the Elusive 'Virus X'" was published.

April, 1949, Biskind's study on neuropsychiatric manifestations of DDT was published.

1949 (approx.), Biskind was attacked with blatantly false data.

December 12, 1950, Biskind presented "Statement" on DDT to the House Of Representatives.

1950 and 1951, pesticide discussions began with government and industry.

May, 1951, Scobey's "Is The Public Health Law Responsible For The Poliomyelitis Mystery?", was published.

July, 1951 the first Epidemic Intelligence Service (EIS) class was assembled. EIS agents began movement into key positions -- in hospitals, government health departments, and media.
July, 1951 leading DDT consultant, Dr. Kumm, joined the NFIP, as Director Of Polio Research.

1952 Formulation of the polio vaccine begins. Tens of millions of doses of polio vaccines produced from virus grown in monkey cells infected with SV-40 (Simian Virus #40). Scientists 'perform experiments in laboratories to determine the correct doses of antigen and supplementary chemicals to use in the polio vaccine. (Ironically, since the scientific premise of vaccination is faulty, a 'correct dose of antigen and chemicals' does not exist).

April, 1952, Scobey's "Statement" on the "Poison Cause Of Poliomyelitis And Obstructions To Its Investigation" to the House Of Representatives was published.

1952, U.S. DDT/milk studies found DDT causal for paralysis in calves.

1952, DDT and other persistent pesticides began rapid phase-out in U.S. and other developing countries.

1953, Swiss DDT/milk studies found DDT causal for paralysis in calves.

March 26, 1953, Salk vaccine discovery announced, after evaluation of 600 vaccinated persons (Patenting The Sun).

April, 1953, leading DDT consultant, Dr. Kumm, appointed by Basil O'Connor to Director of Polio Research for NFIP.

May, 1953, Biskind alleged conspiracy:

...virtually the entire apparatus of communication, lay and scientific alike, has been devoted to denying, concealing, suppressing, distorting and attempts to convert into its opposite, the overwhelming evidence. Libel, slander and economic boycott have not been overlooked in this campaign. (Archive Of Pediatrics)

1954, Salk vaccine field trials began. 423,000 second grade children were vaccinated.

1954 Salk vaccine begins to be given to school children in Philadelphia.

1954 Parke-Davis pharmaceutical company combines the DPT shot with Polio vaccine. The new combination of four vaccines is called Quadrigen. (See 1959).

1954 Reward of $30,000 offered to anyone who proves polio vaccine not a fraud. Not one person was able to claim the reward.

1954 Mrs. Oveta Culp Hobby, Secretary of Health, Education and Welfare, allows a press photo to be taken during a ceremony declaring Salk vaccine safe.

1954 Polio rate caused by the vaccine accelerates ten-fold in Massachusetts.

1954 Eli Lilly company begins renovation of a five-story building in Indianapolis in July 1954 for the production of Salk vaccine. It is in full production by October of 1954. Wyeth, Parke-Davis and others follow suit.

March, 1955, Salk vaccine field trial declared "successful", HEW licensed the Salk vaccine. Salk promoted as "hero".

April 12, 1955, Salk vaccine began on large scale.

April 12-25, Walter Winchell, radio personality, warned of impending vaccine disaster.

1955 Georgia State public health officers meet in Atlanta (May 1955) to discuss
what was going wrong with the Salk vaccine program. A U.S. Public Health scientist at the meeting told the group that 'he was not permitted to disclose what had happened because it would jeopardize the investment of the pharmaceutical firms in the vaccine program.'

April 25, vaccination program encountered disaster via faulty vaccines manufactured by the Cutter Laboratory in California, which were discovered by EIS. The incidence rate (17 per 100,000 for one month) was higher than with that found with other manufacturer's vaccines, yet this rate was not at all an impossibility since incidence rates of over 400 per 100,000 per month were found in Detroit in 1958. The EIS found 204 Cutter polio cases, by assuming contagion, and then highly publicized these cases (Jane Smith, Patenting The Sun) though only 79 cases were documented (Fields Virology). It was decided that because Cutter did not filter its vaccine thoroughly, that tissue particles had contributed to allergic reactions and live polioviruses. Vaccinations were halted. May 13, vaccination program resumed "piecemeal". Eventually over 5 million persons were vaccinated. Salk was demoted to "mere technician". CDC and EIS assumed control of vaccinations.

1955 Idaho brings its Salk vaccination program to a halt on July 1, 1955.

Utah does the same on July 12, 1955.

1955 Massachusetts reports 642% increase in polio since vaccinations began in 1954 with vaccination of 130,000 children. In response, the National Foundation for Infantile Paralysis states that the increase in cases was due to the fact that 'no children were vaccinated there.'

1955 Massachusetts bans the sale of Salk vaccine.'

1955 US Surgeon General Scheele admits in a closed session of the AMA that 'Salk polio vaccine is hard to make and no batch can be proven safe before given to children'. Despite this fact, the public is told that the vaccine is safe. The government announces that it has the intention to vaccinate 57 million people before August 1955.

August 1, 1955, the "aggressive" James Shannon was promoted to director of NIH. He was formerly against the private control of polio research and vaccination programs.

Late 1955, March Of Dimes announced that since 1938 it had contributed $74,000,000 towards poliovirus research and $174,700,000 towards treatments for virus-diagnosed polio cases.

1955 American Cancer Society advertising circular states 'cancer will strike one of every four persons now living. More children from 3 to 15 years of age die of cancer than from any other disease.' (50 years before, cancer was unheard of in children). According to the ACS, they are predicting 6.4 million deaths from cancer, compared with 128,000 in 1933--an increase of 6.2 million cases in 22 years. Vaccination, pesticide use and chemical pollution are the main factors that have increased since 1933.

1956, the Gallup Poll claims that public confidence in the Salk vaccine is 36%. NFIP and the Salk vaccine are in a "valley". Vaccines are thoroughly tested by federal government, yet vaccination programs continue in the U.S.

1956-1957, NIH, under James Shannon, "takes over polio research".

1956 Seventeen states in the United States reject their government-supplied Salk polio vaccine.

1956 US government appropriates $53.6 million to 'aid states in providing free vaccine to people under 20 years of age'.

1956 Idaho health director Peterson states that polio only struck vaccinated children in areas where there had been no cases of polio since the preceding autumn. In 90% of the cases, the paralysis occurred in the arm in which the vaccine had been injected.

1956 American Public Health Service announces 168 cases of polio and 6 deaths among those vaccinated. Censorship is then imposed on the reporting of reactions to Salk vaccine.

1956 Oral polio vaccine developed further by Sabin.

1956 The US Public Health Service and the National Foundation for Infantile Paralysis (Rockefeller) put on a drive to 'sell' Salk polio vaccine to the public.

1957, Salk vaccine promoted heavily, implemented in Canada and England.

By the end of 1958, 72,000,000 had been inoculated. Infants under 5 comprised 51.7% of all paralytic polio cases. Only 55% of persons, below age 40 were vaccinated (52 million). The poliovirus could not be associated with 26% of the non-paralytic polio cases, nor could it be associated in 14% of the paralytic cases. Considering that 47.5% of the cases were non-paralytic, this translates to 42% that could not be protected by the Salk vaccine because their polio was not caused by the poliovirus. This is an argument that all polio is not caused by the poliovirus.

1959, "Federal action" is used against a chiropractor to prevent dissemination of anti-vaccination information through the U.S. mail (CDC, Polio Packet, 1959).

To the present, the Salk vaccination program is promoted as victorious, and serves as a proof for the poliovirus theory. It also serves to bolster all other germ theories (regarding predatory microbes) and the general image of Modern Medicine. The pesticide theory is characterized as irresponsible and dangerous.

Needless to say, the charge that DDT predisposed to poliomyelitis was dropped after the disease was controlled through the use of vaccines. ...such irresponsible claims could produce great harm and, if taken seriously, even interfere with scientific search for true causes and realistic means of preventing the conditions in question. (Hayes and Laws (1991))

However, Hayes and Laws statement, above, is invalid because, 1) The vaccination programs are irrelevant to the decline of polio, while 2) pesticides correlate perfectly with polio, and 3) Dr. Biskind did not drop his charges, he alleged conspiracy "to convert into its opposite, the overwhelming evidence." The often published Biskind evidently was relegated to self-publishing after 1955.

Summary

The non-funded, ostracized theory of poison causality far exceeds all other theories in simplicity, exactitude, and directness regarding correlations within all data areas: dosage, physiology, etiology, epidemiology, economics, and politics.The historical non-relationship between vaccination and paralyitic polio can be viewed graphically, in terms of the official numbers:

Note: Persistent (low

biodegradability) pesticides are shown above.

See Salk Efficacy Index for method.

More about → The Cause Of Polio - Mass Acidic Poisoning

HIV/AIDS Can Be Reversed With Diet

HIV/AIDS always involves yeast and yeast always involves mycotoxins.

HIV/AIDS always involves yeast and yeast always involves mycotoxins or metabolic acids from yeast. I am saying it twice so you remember! You cannot have a suppressed immune system without metabolic, dietary or lifestyle acid. ACID equals pain and pain equals acid. ACID equals dis-ease and dis-ease equals ACID. You cannot separate the two. NOW we can say HIV/AIDS equals an acidic lifestyle and diet and an acidic lifestyle and diet equals HIV/AIDS. Clear the acid and you remove the symptom orHIV/Aids syndrome. NO MORE HIV/AIDS. The attached picture is the blood of a patient doing AIDS for over ten years. After 3 months of living the pH Miracle Lifestyle and Diet - NO MORE HIV titers in the blood and the next picture is how his blood looks NOW!

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Breaking News! Heart Dis-Ease & Stroke Linked To An Acidic Diet!

An article in today’s Telegraph, details startling new research that claims that “the leading cause of heart disease and stroke has been linked for the first time to a person’s diet and chemicals in the urine”.

Wow! A link between diet & health.

The study is apparently the first to link blood pressure to a person’s metabolic fingerprint.

Metabolic fingerprint is a catchy way of describing the the unique acidic metabolites that are left behind by specific cellular processes. In this case, the scientists were looking at the metabolites (small molecules) found in urine, which reveal the way food is broken down in the body.

Getting to the point.

Western diets (rich in acidic animal meat, high in the acid alcohol and low in fibre) are bad because they compromise the delicate pH balance of the blood and tissues.

People who eat a diet high in acid producing animal protein (indicated by the metabolite alanine being present in urine) have higher blood pressure, eat more calories, have higher cholesterol and body mass indexes.

People who eat diets higher in starches such as rice (indicated by the metabolite formate) have lower blood pressure and ingest fewer calories.

People who have a healthier root system or intestinal villi (destroyed by antibiotic use, increased by green foods and green drinks and indicated by the presence of hippurate in the urine) also have lower blood pressure. Hippurate is also present in the urine of individuals with low levels of alcohol intake and higher levels of dietary fibre.

While comparing the metabolic fingerprints of study participants in the U.K., United States, China and Japan, the scientists concluded that test subjects from the U.K. and the U.S.A. have similar genetic and metabolic profiles. In contrast, while the Chinese and Japanese participants had similar genetic profiles, they had different metabolic fingerprints.

What was most interesting was the comparison of the native Japanese participants with those Japanese individuals living in the U.S.A..

Japanese-Americans displayed a typical American metabolic fingerprint; indicating that lifestyle has a stronger effect on blood pressure & heart disease than genetics.

To summarize:

It does matter what you eat and drink. The food and the liquids you ingest do determine your over-all health. I have found that eating a diet high in chlorophyll, healthy polyunsaturated oils, drinking alkaline water at a pH of 9.5 and including liberal amounts of mineral salts can prevent heart attacks and strokes and keep your lymphatic and cardiovascular system clear, strong and healthy. In fact, I just had my heart and peripheral vascular system tested and the tests showed I have the heart and the cardiovascular system of a healthy 18 year old. I know that as a 60 year old exercising everyday, drinking greens, eating lots of healthy fats and including liberal amounts of alkalizing salts made the difference. On top of all this, I feel great!

More about → Breaking News! Heart Dis-Ease & Stroke Linked To An Acidic Diet!

Supplemental Hydrogen Peroxide - Good or Bad for the Body?

The controversy over the widespread use of hydrogen peroxide continues despite current research confirming the rejection of hydrogen peroxide as a nutritional supplement or therapeutic agent.

The following is a scientific critique of some recent publications advocating the use of hydrogen peroxide.

OVER VIEW

Atomic or nascent oxygen has been shown to be of great value in the eradication and retrograding biological transformations or pleomorphic micro-organisms such as bacteria, yeast and mold. These biological transformations and their waste products can create highly toxic acids causing dis-ease in man. These micro-organisms typically do not contain alkaline buffers to neutralize oxygen byproducts resulting from the utilization of electrons in the presence of oxygen and therefore cannot protect themselves. These alkaline buffers that can protect cells from being retrograded include catalase, superoxide dismautase and nascent oxygen.

Many substances are capable of releasing nascent oxygen such as chloride oxides, ozone, hydrogen peroxide and iodine compounds including sodium per iodate. A comparison may be made of these substances on the basis of their stability and toxicity as well as their pharmaconetic properties (how it reacts in the body). Using the above examples, Ozone (O3), releases its oxygen very rapidly (short half-life) while chloride oxides remain effective over a much longer period of time (such as the main ingredient in Prime pH or Activator - sodium chlorite). Hydrogen peroxide (H2O2) has a relative short half-life as well as stimulating the release of alkaline buffers such as OH- and SO- or hydroxyl ions or superoxide ions for the purposes of buffering toxic acidic waste products from metabolism of body cells or micro-organisms. Sodium peridate is a rich source of oxygen however, the byproduct, iodine, is highly toxic to the body cells causing them to retrograde into bacteria or yeast.

COMPARISON OF SOME COMMONLY USED OXIDANTS

Here are the important points to remember:

(1) Oxides of Chloride (CLO2) (CLO) (CLO3) etc.

These remarkable substances have been in use for almost 100 years to reverse the endogenous acids that cause human dis-ease. The major problem, however, has been their instability, resulting in equilibrium compounds such as chlorine, chlorate and hypochlorite. The ability to stabilize chloride oxides has been one of the major breakthroughs of my research in the last few years making it possible not only to use these oxides for oral use but in the injectable form as well.

The distinction between nascent (atomic) and molecular (atmospheric) oxygen is that the two nascent oxygen's that combine to form molecular oxygen (O2) are bound to each other, whereas in a carrier of atomic oxygen (CLO2), the two oxygen atoms are bound to a their atom (chlorine) but not to each other. This molecular structure makes possible the release of the highly active form, nascent oxygen (O1). The general pattern of this molecular structure is also found in other carriers of nascent oxygen.

Water is chlorinated with molecular chlorine (CL2), in which two atoms of chlorine are bound to each other. In oxides of chlorine, there is present only one chlorine which, upon release of the oxygen, becomes chloride (CL-), always naturally present in the blood and used by the body as an antioxidant to buffer dietary and metabolic acid.

It should also me mentioned that the body generates nascent oxygen in the mixed function oxidase system for oxidative purposes and to buffer metabolic, respiratory and/or dietary acids to help maintain the alkaline design of the body or delicate pH balance of the body fluids at 7.365. Therefore the degradation products, chloride and nascent oxygen, are to be found naturally in biological systems for maintaining pH or alkaline design of the body.

Since the mechanism for buffer endogenous acids by nascent oxygen has been demonstrated by my research both in vitro and in vivo and involves a mechanism so fundamental to life processes it:

(1) cannot result in biological transformations of healthy body cells, including blood cells into bacteria, yeast or mold, and,

(2) does not damage human, animal or plant cells which are equipped to handle oxidative processes or metabolic, respiratory or dietary acid.

For these reasons buffering metabolic, respiratory and/or dietary acids and preventing the biological transformation of human, animal or plants cells into bacteria, yeast and mold and even retrograding these anaerobic micro-organisms by nascent oxygen (Prime pH or Activator which contains sodium chlorite and produces nascent oxygen) are superior adjunctive to use of any traditional therapies, including the use of antibiotics, vaccinations or hydrogen peroxide.

ADVANTAGES OF CHLORIDE OXIDES OVER OTHER KNOWN OXIDANTS ARE:

(1) The base compound is non-toxic at over 10 times the normal therapeutic levels.
(2) A rich source of electron rich nascent oxygen or atomic oxygen (O1) of two atoms per molecule compared to only one atom for hydrogen peroxide.
(3) The pH of this compound is 12.3 with an oxidative reduction potential of over -450 mV compared to hydrogen peroxide with a pH of 3.2 and an oxidative reduction potential of +274 mV.
(4) The major degradation compound (chloride ion) is non-toxic and a normal blood and body constituent in comparison to hydrogen peroxide which release 2 atoms of hydrogen causing acidification to the blood and tissues potentially leading to human dis-ease.
(5) The half-life of nascent oxygen in the body is approximately 12 hours compared to hydrogen peroxide which is 6 hours.
(6) Does not initiate the release of alkaline buffers from body cells where hydrogen peroxide does cause the release of oxygen alkaline buffers to neutralize the two hydrogen ions released from the hydrogen peroxide.

(2) OZONE

Ozone has the shortest half-life of the commonly used oxidants and because of its known toxicity to lung tissue in particular, is a major problem. The major use of ozone is the ozonation of blood in vitro which is common in Europe.

(3) Hydrogen Peroxide (H2O2)

Hydrogen peroxide has moderate to low source of nascent oxygen (one atom per molecule) with the disadvantage of high toxicity from the release of two hydrogen ions and a short half-life. It enters the body's own defense system against micro-organisms and metabolic, respiratory and/or dietary acids by causing the T-cells to release anti-oxidants in buffering the increased hydrogen ions.

Blood concentration Must be Kept Extremely Low

Hydrogen peroxide is a natural body product produced and released by lymphocytes and, for this reason, many feel unjustifiably that this indicates its use as a treatment. The facts are the body generates peroxide for highly specific purposes and in very small quantities. This substance, for example, is generated by T-cells for buffering increased acids from micro-organisms and is produced only when triggered to do so by the presence of these toxic acidic waste products. Almost all cells of the body generate peroxide, and unwanted byproducts, as a result of oxygen metabolism. An indication of just how unwanted is borne out by the biochemical mechanisms which universally present to buffer acids as soon as they are produced. Each and every red blood cell contains the bio-factor catalase, (the most efficient alkaline buffer known) to buffer and neutralize any acid as soon as it is created. It has been estimated that one molecule of catalase can decompose approximately 42,000 molecules of hydrogen peroxide in one second at zero degrees, in mammalian tissues. Other body cells contain not only catalase but glutathione to keep the concentration of peroxide at a concentration not greater than 10 -8 (0.00034%), an extremely low value.

Reduced Life Span

Research has shown a direct correlation between life span and the amount of catalase actually present to buffer the hydrogen ions in hydrogen peroxide. Subjects with less catalase and shorter life spans.

Conclusion:

(1) The use of hydrogen peroxide in a research clinical environment with competent researchers who understand the dangers of peroxide is legitimate scientific inquiry. However, peroxide is counter indicated in patients who may have cancer, Epstein-Bar, atherosclerosis, diabetes, or in those who simply want to live longer because of the increased release of hydrogen ions which decreases the pH of the body tissues. This increase of acids from the release of hydrogen ions may cause a cancerous condition or make a cancerous condition worse. The use of hydrogen peroxide is not prudent and I am no longer recommending its use.

(2) Various stabilized chloride oxides release nascent oxygen, which among other things, oxidizes environmental chemicals, supports white blood cell activity in buffering metabolic, respiratory and/or dietary acids and is devastating to anaerobic mirco-organism, such as bacteria, yeast and mold, at levels which are completely non-toxic to the human, animal or plant body.

(3) Chloride oxides such as the product Prime pH or Activator releases alkaline buffers which help to maintain the alkaline design of the body by buffering the acids from the functions of the body.

More about → Supplemental Hydrogen Peroxide - Good or Bad for the Body?

TOMORROW is my Birthday and here is my GIFT to YOU!!

TOMORROW is my Birthday and here is my GIFT to YOU!!

For my Birthday I decided to give a gift to all my friends on Facebook who have given so much to me, Shelley and our family. The gift is a line of avocado products, including avocado oil (Avocado oil plain, Avocado oil with lime or lemon, Avocado oil with garlic, and Avocado oil with Olive oil), avocado moisturizer, avocado lip balm, avocado shampoo, avocado conditioner, avocado liquid soap and avocado bar soap.

All of these products are made from our organically grown avocados from our Ranch in Valley Center, California and pressed on the only cold pressed oil press in all of the United States. That makes my avocado products the only avocado oil cold-pressed and bottled in the USA!!! All of my avocado products are ALL vegan, non-GMO, and certified organic.

The products that we currently have available on our website are the Avocado oil and the Avocado oil with lime. www.phmiracleliving.com Today and on my Birthday (March 6th) I am giving away a free bottle of your choice of the pH Miracle Avocado oil or Avocado oil with lime.

All you need to do to receive your Birthday gift from me on my birthday is send me your name, mailing address, contact phone number and email address to: Dr Robert O Young, The pH Miracle Living Center, 16390 Dia Del Sol, Valley Center, California, 92082. You can also drop me a message on Facebook or my email at: robert.young@phmiracle.com

The only cost you will pay will be the shipping and handling cost. You can order your free bottle of Avocado oil by going to my website at: www.phmiracle.com. Once you are at my website go to the "Food and Kitchen" section under the heading "Browse Products." Scroll down and you will find my avocado oil. Select the Avocado oil and go ahead and order. When you checkout simply enter "Coupon Code." That's it. We will then send you out your free bottle of the most incredible tasting oil in the world.

I know you will love my Avocado oil and my other avocado products and I hope to see them in stores around the world soon.

Keep in mind I have the only cold-pressed avocado oil that is certified organic in the world! This is a unique and special product and I am so thankful to live at a time when I can introduce these products to everyone.

Thank you all my friends for your love and support over the years and I look forward to sharing my birthday gift of our new avocado product line with you.

I have limited supplies so go to my website below as soon as you can so you will be assured to receive your gift.

http://phmiracleliving.com/p-239-avophat-gourmet-avocado-oil.asp

More about → TOMORROW is my Birthday and here is my GIFT to YOU!!